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کاردیولوژی - دکتر مددی

THE PATHOGENESIS OF VASCULAR

CALCIFICATION, NEW CLINICAL

DIAGNOSTIC MARKERS AND A NEW

CURATIVE NANOBIOTIC TREATMENT

FOR REVERSING ATHEROSCLEROSIS

IN HUMANS.

 

 Kajander EO1,2,3, Aho KM1, Maniscalco BS3, Mezo

GS3, 1University of Kuopio, Kuopio, 2Nanobac Oy, Kuopio, Finland; 3NanobacLabs Research Institute, Tampa, USA

Background: Atherosclerosis is an inflammatory disease stimulated by various infectious agents. Our hypothesis is that nanobacteria (Nanobacterium sanguineum, Ns), a new self-replicating infectious calcifying agent found in human blood, which causes life-long infections and adversely affects human cells, is causing atherosclerosis in the human vasculature. Clinical efficacy of a new targeted nanobiotic medication to reverse calcified atherosclerotic plaques and microvascular disease was evaluated in patients with advanced heart disease.

Methods (1) Ns was screened with immunohistochemical staining in human aortic calcific plaques and with prospective epidemiological survey on Ns markers (Ag and Ab) done by Nyyssönen, Kajander, Ciftcioglu and Salonen. (2) Ns lipid, mineral and protein components and biological interactions were analyzed with focus on atherosclerosis. (3) NanobacTX-ACES Clinical Study was undertaken to document the efficacy of the new nanobiotic, NanobacTX, to reverse coronary artery plaque calcification in 90 patients with well-documented coronary artery disease and high levels of coronary artery calcification. 4-month treatment outcome of NanobacTX was followed with EBCT Coronary Artery Calcification Scoring and with Ns markers in blood. Other medications or diet were not changed during the Study.

Results: Immunohistochemical staining detected Ns in 2 out of 4 aortic calcific plaques verifying results from the Mayo Clinic (Rasmunssen et al. JACC 39 Suppl: 206, 2002) and Puskas (Nanobacteria Minisymposium, http://www.nanobac.com/nbminisymp080301/page13.html). The Epidemiological Study found an association between Ns antigen and risk of MI and stroke. Ns biofilm contains Ca2+, unique lipopolysaccaride (LPS) and prothrombin, known active components of inflammatory and clotting processes. The NanobacTX-ACES Nanobiotic Study showed decreases in Coronary Artery Calcification EBCT scores by an average of 58% in Study subjects. Ns antigen and antibody showed a trend to rise at 2 months and to fall after 4 months.

Conclusions: Immunohistochemical staining showed presence of Ns in human aortic calcific plaques. Ns markers in blood have prognostic value for risk of MI and stroke. Ns contains components capable of stimulating immune cascades leading to local tissue/vascular wall inflammation and are risk factors for arterial and venous thrombus formation. Our earlier animal studies have revealed thrombus formation in large veins and arteries after Ns injection. Nanobiotic treatment with NanobacTX was effective in reversing coronary artery calcification. NanobacTX treatment caused initial increase in Ns markers leading to decline with concomitant improvement of atherosclerotic calcification scores in EBCT. Findings of the study open new insights to pathogenesis, diagnostics and treatment of atherosclerosis. Further research is clearly warranted.

In: XXIV Tampereen Lääkäripäivät 20.–22.3.2003 Luennot XXIV. Eds. Anttila S, Antonen J, Hutri-Kähönen N, Lahtela J, Tomas E, Anttila P. Lege Artis Oy, Tampere. Vammalan Kirjapaino Oy, Vammala 2003, p.330.

Kajander EO, Aho KM, Maniscalco BS, Mezo GS. THE PATHOGENESIS OF VASCULAR CALCIFICATION, NEW CLINICAL DIAGNOSTIC MARKERS AND A NEW CURATIVE NANOBIOTIC TREATMENT FOR REVERSING ATHEROSCLEROSIS IN HUMANS. 24th Tampere Medical Symposium, March 20-22, 2003, Tampere, Finland. The Organizing Committee of Tampere Medical Symposium 2003, Abstract Book, page 330 abstract No.2. Publisher Lege Artis Oy, Tampere.

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Mayo Clinic Zooms In On

 

Nanobacteria

 

TAMPA, Fla.—January 4, 2007 – Nanobac Pharmaceuticals, Inc. (OTCBB: NNBP)announces Scientists at Mayo, working under a collaborative agreement with NanobacPharmaceuticals Inc. have published an article in the Journal of Investigative Medicineregarding successfully isolating nanoparticles from human kidney stones in cell cultures.

The Mayo scientists also isolated proteins, RNA and DNA that appear to be associated with the nanoparticles or CNPs.

Entitled "Mayo Clinic Zooms In On Nanobacteria" the paper describes why the Mayo researchers say the findings could lead to solving the mystery of whether nanoparticles are viable living forms that can lead to disease - in this case, kidney stones. "We are looking at how kidney stones start as very small calcifications inside the kidney and then eventually grow into stones," said Mayo Clinic's John Lieske. "In the laboratory, we have isolated nanoparticles from kidney tissue and kidney stones, and have successfully propagated them in culture. This does not clearly confirm the role of nanoparticles in the formation of kidney stones, but it offers insight not otherwise known."

Intriguingly, the study cites evidence that the calcification process is not driven solely byphysical chemistry, but instead is influenced by specific proteins and cellular responses.

"There are at least two novel hypotheses here in terms of how stones might actually form.

One: an infectious agent. If that was the case, that would point us in the direction of using different kinds of treatments specific to an infectious agent.

Two: the idea that cells drive calcification. That would suggest other alternative therapies," added co-researcher Virginia Miller.

Dr. Maniscalco, co-chair of Nanobac, stated “We believed that CNPs play a major role in one of the most pervasive medical conditions in existence: calcification of arteries and organs. This study conducted by one of the lead medical and research facilities in the United States, lends credence to our beliefs.”

About Nanobac Pharmaceuticals: Nanobac Pharmaceuticals Inc. is dedicated to the discovery and development of products and services to improve human health through the detection and treatment of calcifying nanoparticles (CNPs), formerly known as nanobacteria. The company's pioneering research is establishing the pathogenic role of CNPs in soft tissue calcification, particularly in coronary artery, prostate and vascular disease.

Nanobac's drug discovery and development is focused on new and existing compounds that effectively inhibit, destroy or neutralize CNPs. Nanobac manufactures In Vitro Diagnostic (IVD) kits and reagents for detecting calcifying nanoparticles. IVD products include a line of assays, proprietary antibodies and reagents for uniquely recognizing CNPs. Nanobac's BioAnalytical Services works with biopharmaceutical partners to develop and apply methods for avoiding, detecting, and inactivating or eliminating CNPs from raw materials.

Nanobac Pharmaceuticals Inc. is headquartered in Tampa, Florida. For more information, visit our website at: http://www.nanobac.com.

Investors are cautioned that certain statements in this document, some statements in periodic press releases and some oral statements of Nanobac Pharmaceuticals, Inc. officials are "Forward-Looking Statements" within the meaning of the Private Securities Litigation Reform Act of 1995 (the "Act"). Forward-Looking statements include statements which are predictive in nature, which depend upon or refer to future events or conditions, which include words such as "believes," "anticipates," "intends," "plans," "expects," and similar expressions. In addition, any statements concerning future financial performance (including future revenues, earnings or growth rates),

ongoing business strategies or prospects, and possible future Nanobac Pharmaceuticals, Inc. actions, which may be provided by management, are also forward-looking statements as defined by the Act. Forward-Looking statements involve known and unknown risks, uncertainties, and other factors which may cause the actual results, performance or achievements of the Company to materially differ from any future results, performance or achievements expressed or implied by such forward-looking statements and to vary significantly from reporting period to reporting period. Although management believes that the assumptions will, in fact, prove to be correct or that actual future results will not be different from the expectations expressed in this report. These statements are not guarantees of future performance and Nanobac Pharmaceuticals, Inc. has no specific intention to update these statements.

Contact:

Nanobac Pharmaceuticals, Tampa

Brady Millican, 813-264-2241

or

Redwood Consultants

Jens Dalsgaard, 415-884-0348

Source: Nanobac Pharmaceuticals Inc.

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www.achd-library.com

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www.westodd.com

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سایت مایو     http://www.mayo.edu/cardiologyreview/
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کلیک کنید

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برای رجوع به سایت مربوطه می توانید در لینک زیر کلیک کنید

 

http://medicine.osu.edu/exam/*

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A (not so) brief history of electrocardiography.

Find out how electrocuting chickens (1775), getting laboratory assistants to put their hands in buckets of saline (1887), taking the ECG of a horse and following it to the slaughterhouse (1909), induction of indiscriminate angina attacks (1931), and hypothermic dogs (1953) have helped to improve our understanding of the ECG as a clinical tool. And why is the ECG labelled PQRST (1895)?

17th and 18th Centuries The harnessing of electricity, observations of its effects on animal tissues and the discovery of 'animal electricity'.
1600

William Gilbert
William Gilbert, Physician to Queen Elizabeth I, President of the Royal College of Physicians, and creator of the 'magnetic philosophy' introduces the term 'electrica' for objects (insulators) that hold static electricity. He derived the word from the Greek for amber (electra). It was known from ancient times that amber when rubbed could lift light materials. Gilbert added other examples such as sulphur and was describing what would later be known as 'static electricity' to distinguish it from the more noble magnetic force which he saw as part of a philosophy to destroy forever the prevailing Aristotlean view of matter. Gilbert W. De Magnete, magneticisique corporibus, et de magno magnete tellure. 1600
1646
Sir Thomas Browne, Physician, whilst writing to dispel popular ignorance in many matters, is the first to use the word 'electricity'. Browne calls the attractive force "Electricity, that is, a power to attract strawes or light bodies, and convert the needle freely placed". (He is also the first to use the word 'computer' - referring to people who compute calendars.)Browne, Sir Thomas. Pseudodoxia Epidemica: Or, enquiries Into Very Many Received Tenents, and Commonly Presumed Truths. 1646: Bk II, Ch. 1. London
1660
Otto Von Guericke builds the first static electricity generator.
1662

Descarte's reflex ©BIU
The work of Rene Descartes, French Philosopher, is published (after his death) and explains human movement in terms of the complex mechanical interaction of threads, pores, passages and 'animal spirits'. He had worked on his ideas in the 1630s but had abandoned publication because of the persecution of other radical thinkers such as Galileo. William Harvey had developed similar ideas but they were never published. Descartes R. De Homine (Treatise of Man); 1662: Moyardum & leffen, Leiden.
1664
Jan Swammerdam, a Dutchman, disproves Descartes' mechanistic theory of animal motion by removing the heart of a living frog and showing that it was still able to swim. On removing the brain all movement stopped (which would be in keeping with Descarte's theory) but then, when the frog was dissected and a severed nerve end stimulated with a scalpel the muscles twitched. This proved that movement of a muscle could occur without any connection to the brain and therefore the transmission of 'animal spirits' was not necessary.

Swammerdam's ideas were not widely known and his work was not published until after his death. However, he wrote many letters and his friend, Nicolaus Steno, did attack the Cartesian ideas in a lecture in Paris in 1665. Boerhaave published Swammerdam's 'Book of Nature' in the 1730s which was translated into English in 1758.

1668

electrical stimulation? ©BIU
Swammerdam refines his experiments on muscle contraction and nerve conduction and demonstrated some to notable figures such as the Grand-Duke Cosimo of Tuscany who was visiting Swammerdam's father's house on the Oude Schans in Amsterdam. One experiment suspended the muscle on a brass hook inside a glass tube with a water droplet to detect movement and 'irritated' the nerve with a silver wire. This produced movement of the muscle and it may have been due to the induction of a small electrical charge - although Swammerdam would have been unaware of this.

In the diagram opposite - a) glass tube, b) muscle, c) sliver wire, d) brass wire, e) drop of water, f) investigator's hand.

1729
Stephen Gray, English scientist, distinguishes between conductors and insulators of electricity. He demonstrates the transfer of static electrical charge to a cork ball across 150 metres of wet hemp thread. Later he found that the transfer could be achieved over greater distances by using brass wire.
1745

Leyden Jar
Dutch physicist Pieter van Musschenbroek discovers that a partly filled jar with a nail projecting from a cork in its neck can store an electrical charge. The jar is named the 'Leyden Jar' after the place of its discovery. Ewald Georg von Kliest of Pomerania invented the same device independently.

Using a Leyden jar in 1746, Jean-Antoine Nollet, French physicist and tutor to the Royal family of France sends an electrical current through 180 Royal Guards during a demonstration to King Louis XV.

1769
Edward Bancroft, an American Scientist, suggests that the 'shock' from the Torpedo Fish is electrical rather than mechanical in nature. He showed that the properties of the shock were similar to those from a Leyden jar in that it could be conducted or insulated with appropriate materials. The Torpedo fish and other species were widely known to deliver shocks and were often used in this way for therapeutic reasons. However, electrical theory at the time dictated that electricity would always flow through conductors and diffuse away from areas of high charge to low charge. Since living tissues were known to be conductors it was impossible to imagine how an imbalance of charge could exist within an animal and therefore animals could not use electricity for nerve conduction - or to deliver shocks. Furthermore, 'water and electricity do not mix' so the idea of an 'electric fish' was generally not accepted. Bancroft, E. An essay on the natural history of Guiana, London:T. Becket and P. A. de Hondt, 1769.
1773

John Walsh
John Walsh, fellow of the Royal Society and Member of Parliament, obtains a visible spark from an electric eel Electrophorus electricus. The eel was out of water as it was not possible to produce the spark otherwise. He used thin strips of tin foil and demonstrated his technique to many colleagues and visitors at his house in London. Unfortunately he never published his eel experiment though he did win the Copley medal in 1774 and 1783 for his work. The observations of Walsh, and Bancroft before him, added to the argument that some form of animal electricity existed. Walsh, J. On the electric property of torpedo: in a letter to Ben. Franklin. Phil. Trans. Royal Soc. 1773;63:478-489
1774
The Rev. Mr Sowdon and Mr Hawes, apothecary, report on the surprising effects of electricity in a case report of recovery from sudden death published in the annual report of the newly founded Humane Society now the Royal Humane Society. The Society had developed from 'The Institution for Affording immediate relief to persons apparently dead from drowning'. It was "instituted in the year 1774, to protect the industrious from the fatal consequences of unforseen accidents; the young and inexperienced from being sacrificed to their recreations; and the unhappy victims of desponding melancholy and deliberate suicide; from the miserable consequences of self-destruction."

A Mr Squires, of Wardour Street, Soho lived opposite the house from which a three year old girl, Catherine Sophia Greenhill had fallen from the first storey window on 16th July 1774. After the attending apothecary had declared that nothing could be done for the child Mr Squires, "with the consent of the parents very humanely tried the effects of electricity. At least twenty minutes had elapsed before he could apply the shock, which he gave to various parts of the body without any apparent success; but at length, upon transmitting a few shocks through the thorax, he perceived a small pulsation: soon after the child began to sigh, and to breathe, though with great difficulty. In about ten minutes she vomited: a kind of stupor, occaisioned by the depression of the cranium, remained for some days, but proper means being used, the child was restored to perfect health and spirits in about a week.

"Mr. Squires gave this astonishing case of recovery to the above gentlemen, from no other motive than a desire of promoting the good of mankind; and hopes for the future that no person will be given up for dead, till various means have been used for their recovery."

Since it is clear she sustained a head injury the electricity probably stimulated the child out of deep coma rather than providing cardiac defibrillation (see also 1788, Charles Kite). Annual Report 1774: Humane Society, London. pp 31-32
1775
Abildgaard shows that hens can be made lifeless with electrical impulses and he could restore a pulse with electrical shocks across the chest. "With a shock to the head, the animal was rendered lifeless, and arose with a second shock to the chest; however, after the experiment was repeated rather often, the hen was completely stunned, walked with some difficulty, and did not eat for a day and night; then later it was very well and even laid an egg." Abildgaard, Peter Christian. Tentamina electrica in animalibus. Inst Soc Med Havn. 1775; 2:157-61.
1786

Luigi Galvani
Italian Anatomist Luigi Galvani notes that a dissected frog's leg twitches when touched with a metal scalpel. He had been studying the effects of electricity on animal tissues that summer.

On 20th September 1786 he wrote "I had dissected and prepared a frog in the usual way and while I was attending to something else I laid it on a table on which stood an electrical machine at some distance from its conductor and separated from it by a considerable space. Now when one of the persons present touched accidentally and lightly the inner crural nerves of the frog with the point of a scalpel, all the muscles of the legs seemed to contract again and again as if they were affected by powerful cramps."

He later showed that direct contact with the electrical generator or the ground through an electrical conductor would lead to a muscle contraction. Galvani also used brass hooks that attached to the frog's spinal cord and were suspended from an iron railing in a part of his garden. He noticed that the frogs' legs twitched during lightening storms and also when the weather was fine. He interperated these results in terms of "animal electricity" or the preservation in the animal of "nerveo-electrical fluid" similar to that of an electric eel. He later also showed that electrical stimulation of a frog's heart leads to cardiac muscular contraction. Galvani. De viribus Electritatis in motu musculari Commentarius. 1791

Galvani's name is given to the 'galvanometer' which is an instrument for measuring (and recording) electricity - this is essentially what an ECG is; a sensitive galvanometer.

1788
Charles Kite wins the Silver Medal of the Humane Society (awarded at the first Prize Medal ceremony of the Society co-judged with the Medical Society of London) with an essay on the use of electricity in the diagnosis and resuscitation of persons apparently dead. This essay is often cited as the first record of cardiac defibrillation but the use of electricity suggested by Mr Kite is much different. For example, on describing a case of drowning from 1785 where resuscitation had been attempted with artificial respiration, warmth, tobacco, "volatiles thrown into the stomach, frictions, and various lesser stimuli" for nearly an hour, he then recalls the use of electricity. "Electricity was then applied, and shocks sent through in every possible direction; the muscles through which the fluid [electricity] passed were thrown into strong contractions." He concluded that electricity was a valuable tool that could determine whether or not a person, apparently dead, could be successfully resuscitated. Annual Report 1788: Humane Society, London. pp 225-244. Kite C. An Essay on the Recovery of the Apparently Dead. 1788: C. Dilly, London.
1792

Alessandro Volta
Alessandro Volta, Italian Scientist and inventor, attempts to disprove Galvani's theory of "animal electricity'" by showing that the electrical current is generated by the combination of two dissimilar metals. His assertion was that the electrical current came from the metals and not the animal tissues. (We now know that both Galvani and Volta were right.) To prove his theory he develops the voltaic pile in 1800 (a column of alternating metal discs - zinc with copper or silver - separated by paperboard soaked in saline) which can deliver a substantial and steady current of electricity. Enthusiasm in the use of electricity leads to further attempts at reanimation of the dead with experiments on recently hanged criminals. Giovani Aldini (the nephew of Galvani) conducts an experiment at the Royal College of Surgeons in London in 1803. The executed criminal had lain in a temperature of 30 F for one hour and was transported to the College. "On applying the conductors to the ear and to the rectum, such violent muscular contractions were executed, as almost to give the appearance of the reanimation". Aldini, J. Essai: Théorique et expérimental sur le Galvanisme, Paris (1804), Giovani Aldini. General Views on the Application of Galvanism to Medical Purposes Principally in cases of suspended Animation (London: J. Callow, Princes Street and Burgess and Hill, Great Windmill Street, 1819). Mary Shelly's Frankenstein was published in 1818. Louis Figuier, Les merveilles de la Science (Paris, 1867), p.653
1800 to 1895 The design of sensitive instruments that could detect the small electrical currents in the heart.
1819
While demonstrating to students the heating of a platinum wire with electricity from a voltaic pile at the University of Copenhagen, Danish physicist Hans Christian Oersted notices that a nearby magnetized compass needle moves each time the electrical current is turned on. He discovers electromagnetism which is given a theoretical basis (with remarkable speed) by André Marie Ampère.
1820
Johann (Johan) Schweigger of Nuremberg increases the movement of magnetized needles in electromagnetic fields. He found that by wrapping the electric wire into a coil of 100 turns the effect on the needle was multiplied. He proposed that a magnetic field revolved around a wire carrying a current which was later proven by Michael Faraday. Schweigger had invented the first galvanometer and announced his discovery at the University of Halle on 16th September 1820.
1825
Leopold Nobili, Professor of Physics at Florence, develops an 'astatic galvanometer'. Using two identical magnetic needles of opposite polarity, either fixed together with a figure of eight arrangment of wire loops (in earlier versions), or one moveable needle with a wire loop and one with a scale (in later versions), the effects of the earth's magnetic field could be compensated for. In 1827, using this instrument, he managed to detect the flow of current in the body of a frog from muscles to spinal cord. He detected the electricity running along saline moistened cotton thread joining the dissected frog's legs in one jar to its body in another jar. Nobili was working to support the theory of animal electricity and this conduction, transmitted without wires, he felt demonstrated animal electricity.
1838

Carlo Matteucci
Carlo Matteucci, Professor of Physics at the University of Pisa, and student of Nobili, shows that an electric current accompanies each heart beat. He used a preparation known as a 'rheoscopic frog' in which the cut nerve of a frog's leg was used as the electical sensor and twitching of the muscle was used as the visual sign of electrical activity. He also used Nobili's astatic galvanometer for the study of electricity in muscles typically inserting one galvanometer wire in the open end of the dissected muscle and the other on the surface of the muscle. He went on to try and demonstrate conduction in nerve but was unable to do so (since his galvanometers were not sensitive enough). Matteucci C. Sur un phenomene physiologique produit par les muscles en contraction. Ann Chim Phys 1842;6:339-341
1840
Dr Golding Bird, a Physician, accomplished chemist and member of the London Electrical Society, opens an electrical therapy room at Guy's Hospital, London treating a large range of diseases. Although the application of electricity was popular it was not considered a subject worthy of serious investigation. Because of Bird's reputation as a researcher electrical therapy achieved popularity amongst London Physicians including his mentor Dr Thomas Addison. Bird G. Lectures on Electricity and Galvanism, in their physiological and therapeutical relations, delivered at the Royal College of Physicians, in March, 1847 (Wilson & Ogilvy, London, 1847)
1843

Emil Du bois-Reymond
German physiologist Emil Du bois-Reymond describes an "action potential" accompanying each muscular contraction. He detected the small voltage potential present in resting muscle and noted that this diminished with contraction of the muscle. To accomplish this he had developed one of the most sensitive galvanometers of his time. His device had a wire coil with over 24,000 turns - 5 km of wire. Du Bios Reymond devised a notation for his galvanometer which he called the 'disturbance curve'. "o" was the stable equilibrium point of the astatic galvanometer needle and p, q, r and s (and also k and h) were other points in its deflection. Du Bois-Reymond, E. Untersuchungen uber thierische Elektricitat. Reimer, Berlin: 1848.
1850
Bizarre unregulated actions of the ventricles (later called ventricular fibrillation) is described by Hoffa during experiments with strong electrical currents across the hearts of dogs and cats. He demonstrated that a single electrical pulse can induce fibrillation. Hoffa M, Ludwig C. 1850. Einige neue versuche uber herzbewegung. Zeitschrift Rationelle Medizin, 9: 107-144
1856
Rudolph von Koelliker and Heinrich Muller confirm that an electrical current accompanies each heart beat by applying a galvanometer to the base and apex of an exposed ventricle. They also applied a nerve-muscle preparation, similar to Matteucci's, to the ventricle and observed that a twitch of the muscle occured just prior to ventricular systole and also a much smaller twitch after systole. These twitches would later be recognised as caused by the electrical currents of the QRS and T waves. von Koelliker A, Muller H. Nachweis der negativen Schwankung des Muskelstroms am naturlich sich kontrahierenden Herzen. Verhandlungen der Physikalisch-Medizinischen Gesellschaft in Wurzberg. 1856;6:528-33.
1858
William thompson (Lord Kelvin), Professor of Natural Philosophy at Glasgow University, invents the 'mirror galvanometer' for the reception of transatlantic telegraph transmissions. A small, freely rotating mirror, with magents stuck to its back is suspended in a fine copper coil and a reflected spot of light from this mirror 'amplifies' the small movements when electrical current is present. The whole apparatus was suspended in an air chamber and the pressure inside could be adjusted to vary the damping seen on the signals. This galvanometer was sensitive enough for transatlantic telegraphy.
1867
Thompson improves telegraph transmissions with the 'Siphon Recorder'. Before d'Arsonval (1880), Thompson uses a fine coil suspended in a strong magnetic magnetic field. Attached to the coil but isolated from it by ebonite (an insulator) was a siphon of ink. The siphon was charged with high voltage so that the ink was sprayed onto the paper that moved over an earthed metal surface. The siphon recorder could therefore not only detect currents it could also record them onto paper.
1869-70
Alexander Muirhead, an electrical engineer and pioneer of telegraphy, may have a recorded a human electrocardiogram at St Bartholomew's Hospital, London but this is disputed. If he had he is thought to have used a Thompson Siphon Recorder. Elizabeth Muirhead, his wife, wrote a book of his life and claimed that he refrained from publishing his own work for fear of misleading others. Elizabeth Muirhead. Alexander Muirhead 1848 - 1920. Oxford, Blackwell: privately printed 1926.
1872
French physicist Gabriel Lippmann invents a capillary electrometer. It is a thin glass tube with a column of mercury beneath sulphuric acid. The mercury meniscus moves with varying electrical potential and is observed through a microscope.
1872
Mr Green, a surgeon, publishes a paper on the resuscitation of a series of patients who had suffered cardiac and / or respiratory arrest during anaesthesia with chloroform. He uses a galvanic pile (battery) of 200 cells generating 300 Volts which he applied to the patient as follows "One pole should be applied to the neck and the other to the lower rib on the left side." Green T. On death from chloroform: its prevention by galvanism. Br Med J 1872 1: 551-3. Although this has been reported as an example of cardiorespiratory resuscitation it is unclear what the exact mechanism seems to be. It is unlikely to be electric cardioversion or external pacing. It seems to be another example of electrophrenic stimulation (See also Duchenne 1872).
1872

An 'electric' smile.

Guillaume Benjamin Amand Duchenne de Boulogne, pioneering neurophysiologist, describes the resuscitation of a drowned girl with electricity in the third edition of his textbook on the medical uses of electricity. This episode has sometimes been described as the first 'artificial pacemaker' but he used an electrical current to induce electrophrenic rather than myocardial stimulation. Duchenne GB. De l'electrisation localisee et de son application a la pathologie et la therapeutique par courants induits at par courants galvaniques interrompus et continus. [Localised electricity and its application to pathology and therapy by means of induced and galvanic currents, interrupted and continuous] 3ed. Paris. JB Bailliere et fils; 1872

1875
Richard Caton, a Liverpool Physician, presents to the British Medical Association in July 1875 in Edinburgh. Using a Thompson 'mirror galvanometer' in animals he shows it was possible to detect 'feeble currents of varying direction ... when the electrodes are placed on two points of the external surface, or one electrode on the grey matter and one on the surface of the skull'. This is the first report of the EEG (or electroencephalogram). Caton was proving another Physician's hypothesis, John Hughlings Jackson, who suggested in 1873 that epilepsy was due to excessive electrical activity in the grey matter of the brain. Caton R: The electric currents of the brain. BMJ 1875; 2:278, Mumenthaler, Mattle Eds. Neurology. 4th Edition. Stuttgart, Thieme: 2004.
1876
Marey uses the electrometer to record the electrical activity of an exposed frog's heart. Marey EJ. Des variations electriques des muscles et du couer en particulier etudies au moyen de l'electrometre de M Lippman. Compres Rendus Hebdomadaires des Seances de l'Acadamie des sciences 1876;82:975-977
1878
British physiologists John Burden Sanderson and Frederick Page record the heart's electrical current with a capillary electrometer and shows it consists of two phases (later called QRS and T). Burdon Sanderson J. Experimental results relating to the rhythmical and excitatory motions of the ventricle of the frog. Proc R Soc Lond 1878;27:410-414
1880
French physicist Arsène d'Arsonval in association with Marcel Deprez, improves the galvanometer. Instead of a magnetized needle moving when electrical current flows through a surrounding wire coil the Deprez-d'Arsonval galvanometer has a fixed magnet and moveable coil. If a pointer is attached to the coil it can move over a suitably calibrated scale. The d'Arsonval galvanometer is the basis for most modern galvanometers. Comptes rendus de l'Académie des sciences, 1882, 94: 1347-1350
1884
John Burden Sanderson and Frederick Page publish some of their recordings. Burdon Sanderson J, Page FJM. On the electrical phenomena of the excitatory process in the heart of the tortoise, as investigated photographically. J Physiol (London) 1884;4:327-338
1887
British physiologist Augustus D. Waller of St Mary's Medical School, London publishes the first human electrocardiogram. It is recorded with a capilliary electrometer from Thomas Goswell, a technician in the laboratory. Waller AD. A demonstration on man of electromotive changes accompanying the heart's beat. J Physiol (London) 1887;8:229-234
1889
Dutch physiologist Willem Einthoven sees Waller demonstrate his technique at the First International Congress of Physiologists in Bale. Waller often demonstrated by using his dog "Jimmy" who would patiently stand with paws in glass jars of saline.
1890
GJ Burch of Oxford devises an arithmetical correction for the observed (sluggish) fluctuations of the electrometer. This allows the true waveform to be seen but only after tedious calculations. Burch GJ. On a method of determining the value of rapid variations of a difference potential by means of a capillary electrometer. Proc R Soc Lond (Biol) 1890;48:89-93
1891
British physiologists William Bayliss and Edward Starling of University College London improve the capillary electrometer. They connect the terminals to the right hand and to the skin over the apex beat and show a "triphasic variation accompanying (or rather preceding) each beat of the heart". These deflections are later called P, QRS and T. Bayliss WM, Starling EH. On the electrical variations of the heart in man. Proc Phys Soc (14th November) in J Physiol (London) 1891;13:lviii-lix and also On the electromotive phenomena of the mammalian heart. Proc R Soc Lond 1892;50:211-214 They also demonstrate a delay of about 0.13 seconds between atrial stimulation and ventricular depolarisation (later called PR interval). On the electromotive phenomena of the mammalian heart. Proc Phys Soc (21st March) in J Physiol (London) 1891;12:xx-xxi
1893
Willem Einthoven introduces the term 'electrocardiogram' at a meeting of the Dutch Medical Association. (Later he claims that Waller was first to use the term). Einthoven W: Nieuwe methoden voor clinisch onderzoek [New methods for clinical investigation]. Ned T Geneesk 29 II: 263-286, 1893
1895 to date The first accurate recording of the electrocardiogram and its development as a clinical tool.
1895
Einthoven, using an improved electrometer and a correction formula developed independently of Burch, distinguishes five deflections which he names P, Q, R, S and T. Einthoven W. Ueber die Form des menschlichen Electrocardiogramms. Arch f d Ges Physiol 1895;60:101-123

Why PQRST and not ABCDE? The four deflections prior to the correction formula were labelled ABCD and the 5 derived deflections were labelled PQRST. The choice of P is a mathematical convention (as used also by Du Bois-Reymond in his galvanometer's 'disturbance curve' 50 years previously) by using letters from the second half of the alphabet. N has other meanings in mathematics and O is used for the origin of the Cartesian coordinates. In fact Einthoven used O ..... X to mark the timeline on his diagrams. P is simply the next letter. A lot of work had been undertaken to reveal the true electrical waveform of the ECG by eliminating the damping effect of the moving parts in the amplifiers and using correction formulae. If you look at the diagram in Einthoven's 1895 paper you will see how close it is to the string galvanometer recordings and the electrocardiograms we see today. The image of the PQRST diagram may have been striking enough to have been adopted by the researchers as a true representation of the underlying form. It would have then been logical to continue the same naming convention when the more advanced string galvanometer started creating electrocardiograms a few years later.

1897
Clement Ader, a French electrical engineer, reports his amplification system for detecting Morse code signals transmitted along undersea telegraph lines. It was never intended to be used as a galvanometer. Einthoven later quoted Ader's work but seems to have developed his own amplification device independently. Ader C. Sur un nouvel appareil enregistreur pour cables sous-marins. C R Acad Sci (Paris) 1897;124:1440-1442
1899

Karel Wenkebach
Karel Frederik Wenckebach publishes a paper "On the analysis of irregular pulses" describing impairment of AV conduction leading to progressive lengthening and blockage of AV conduction in frogs. This will later be called Wenckebach block (Mobitz type I) or Wenckebach phenomenon.
1899
Jean-Louis Prevost, Professor of Biochemistry, and Frederic Batelli, Professor of Physiology, both of Geneva discover that large electrical voltages applied across an animal's heart can stop ventricular fibrillation. Prevost JL, Batelli F: Sur quelques effets des descharges electriques sur le coeur des mammiferes. Acad. Sci. Paris, FR.: 1899; 129:1267-1268.

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1901
Einthoven invents a new galvanometer for producing electrocardiograms using a fine quartz string coated in silver based on ideas by Deprez and d'Arsonval (who used a wire coil). His "string galvanometer" weighs 600 pounds. Einthoven acknowledged the similar system by Ader but later (1909) calculated that his galvanometer was in fact many thousands of times more sensitive. Einthoven W. Un nouveau galvanometre. Arch Neerl Sc Ex Nat 1901;6:625-633
1902
Einthoven publishes the first electrocardiogram recorded on a string galvanometer. Einthoven W. Galvanometrische registratie van het menschilijk electrocardiogram. In: Herinneringsbundel Professor S. S. Rosenstein. Leiden: Eduard Ijdo, 1902:101-107
1903
Einthoven discusses commercial production of a string galvanometer with Max Edelmann of Munich and Horace Darwin of Cambridge Scientific Instruments Company of London.
1905
Einthoven starts transmitting electrocardiograms from the hospital to his laboratory 1.5 km away via telephone cables. On March 22nd the first 'telecardiogram' is recorded from a healthy and vigorous man and the tall R waves are attributed to his cycling from laboratory to hospital for the recording.
1905
John Hay of Liverpool, publishes pressure recordings from a 65 year old man showing heart block in which AV conduction did not seem to be impaired since the a-c intervals on the jugular venous waves was unchanged in the conducted beats. This is the first demonstration of what we now call Mobitz type II AV block. Hay J. Bradycardia and cardiac arrhythmias produced by depression of certain functions of the heart. Lancet 1906;1:138-143.
1906
Einthoven publishes the first organised presentation of normal and abnormal electrocardiograms recorded with a string galvanometer. Left and right ventricular hypertrophy, left and right atrial hypertrophy, the U wave (for the first time), notching of the QRS, ventricular premature beats, ventricular bigeminy, atrial flutter and complete heart block are all described. Einthoven W. Le telecardiogramme. Arch Int de Physiol 1906;4:132-164 (translated into English. Am Heart J 1957;53:602-615)
1906
Cremer records the first oesophageal electrocardiogram which he achieved with the help of a professional sword swallower. Oesophageal electrocardiography later developed in the 1970s to help differentiate atrial arrhythmias. He also records the first fetal electrocardiogram from the abdominal surface of a pregnant woman. Cremer. Ueber die direkte Ableitung der Aktionstrِme des menslichen Herzens vom Oesophagus und über das Elektrokardiogramm des Fِtus. Munch. Med. Wochenschr. 1906;53:811
1907
Arthur Cushny, professor of pharmacology at University College London, publishes the first case report of atrial fibrillation. His patient was 3 days post-op following surgery on an "ovarian fibroid" when she developed a "very irregular" pulse at a rate of 120 - 160 bpm. Her pulse was recorded with a "Jacques sphygmochronograph" which shows the radial pulse pressure against time - much like the arterial line blood pressure recordings used in Intensive Care today. Cushny AR, Edmunds CW. Paroxysmal irregularity of the heart and auricular fibrillation. Am J Med Sci 1907;133:66-77.
1908
Edward Schafer of the University of Edinburgh is the first to buy a string galvanometer for clinical use.
1909
Thomas Lewis of University College Hospital, London buys a string galvanometer and so does Alfred Cohn of Mt Sinae Hospital, New York. Thomas Lewis publishes a paper in the BMJ detailing his careful clinical and electrocardiographic observations of atrial fibrillation. At one point Lewis identified a fibrillating horse using the string galvanometer's electrocardigram recording. He then followed the horse to the slaughterhouse where he could visually confirm the fibrillating atrium. Lewis T. Auricular fibrillation: a common clinical condition. BMJ 1909;42:1528.
1909
Nicolai and Simmons report on the changes to the electrocardiogram during angina pectoris. Nicolai DF, Simons A. (1909) Zur klinik des elektrokardiogramms. Med Kiln 5;160
1910
Walter James, Columbia University and Horatio Williams, Cornell University Medical College, New York publish the first American review of electrocardiography. It describes ventricular hypertrophy, atrial and ventricular ectopics, atrial fibrillation and ventricular fibrillation. The recordings were sent from the wards to the electrocardiogram room by a system of cables. There is a great picture of a patient having an electrocardiogram recorded with the caption "The electrodes in use".James WB, Williams HB. The electrocardiogram in clinical medicine. Am J Med Sci 1910;140:408-421, 644-669
1911
Thomas Lewis publishes a classic textbook. The mechanism of the heart beat. London: Shaw & Sons and dedicates it to Willem Einthoven.
1912
Einthoven addresses the Chelsea Clinical Society in London and describes an equilateral triangle formed by his standard leads I, II and III later called 'Einthoven's triangle'. This is the first reference in an English article I have seen to the abbreviation 'EKG'.Einthoven W. The different forms of the human electrocardiogram and their signification. Lancet 1912(1):853-861
1918
Bousfield describes the spontaneous changes in the electrocardiogram during angina. Bousfield G. Angina pectoris: changes in electrocardiogram during paroxysm. Lancet 1918;2:475
1920
Hubert Mann of the Cardiographic Laboratory, Mount Sinai Hospital, describes the derivation of a 'monocardiogram' later to be called 'vectorcardiogram'. Mann H. A method of analyzing the electrocardiogram. Arch Int Med 1920;25:283-294
1920
Harold Pardee, New York, publishes the first electrocardiogram of an acute myocardial infarction in a human and describes the T wave as being tall and "starts from a point well up on the descent of the R wave". Pardee HEB. An electrocardiographic sign of coronary artery obstruction. Arch Int Med 1920;26:244-257
1924
Willem Einthoven wins the Nobel prize for inventing the electrocardiograph.
1924
Woldemar Mobitz publishes his classification of heart blocks (Mobitz type I and type II) based on the electrocardiogram and jugular venous pulse waveform findings in patients with second degree heart block. Mobitz W. Uber die unvollstandige Storung der Erregungsuberleitung zwischen Vorhof und Kammer des menschlichen Herzens. (Concerning partial block of conduction between the atria and ventricles of the human heart). Z Ges Exp Med 1924;41:180-237.
1926
A doctor from the Crown Street Women's Hospital in Sydney, who wished to remain anonymous, resuscitates a new-born baby with an electrical device later called a 'pacemaker'. The doctor wanted to remain anoymous because of the controversy surrounding research that artificially extended human life.
1928
Ernstine and Levine report the use of vacuum-tubes to amplify the electrocardiogram instead of the mechanical amplification of the string galvanometer. Ernstine AC, Levine SA. A comparison of records taken with the Einthoven string galvanomter and the amplifier-type electrocardiograph. Am Heart J 1928;4:725-731
1928
Frank Sanborn's company (founded 1917 and acquired by Hewlett-Packard in 1961 and since 1999, Philips Medical Systems) converts their table model electrocardiogram machine into their first portable version weighing 50 pounds and powered by a 6-volt automobile battery.
1929
Sydney doctor Mark Lidwill, physician, and Edgar Booth, physicist, report the electrical resuscitation of the heart to a meeting in Sydney. Their portable device uses an electrode on the skin and a transthoracic catheter. Edgar Booth's design could deliver a variable voltage and rate and was employed to deliver 16 volts to the ventricles of a stillborn infant.
1930
Wolff, Parkinson and White report an electrocardiographic syndrome of short PR interval, wide QRS and paroxysmal tachycardias. Wolff L, Parkinson J, White PD. Bundle branch block with short P-R interval in healthy young people prone to paroxysmal tachycardia. Am Heart J 1930;5:685. Later, when other published case reports were examined for evidence of pre-excitation, examples of 'Wolff Parkinson White' syndrome were identified which had not been recognised as a clinical entity at the time. The earliest example was published by Hoffmann in 1909. Von Knorre GH. The earliest published electrocardiogram showing ventricular preexcitation. Pacing Clin Electrophysiol. 2005 Mar;28(3):228-30
1930
Sanders first describes infarction of the right ventricle. Sanders, A.O. Coronary thrombosis with complete heart block and relative ventricular tachycardia: a case report, American Heart Journal 1930;6:820-823.
1931
Charles Wolferth and Francis Wood describe the use of exercise to provoke attacks of angina pectoris. They investigated the ECG changes in normal subjects and those with angina but dismissed the technique as too dangerous "to induce anginal attacks indiscriminately". Wood FC, Wolferth CC, Livezey MM. Angina pectoris. Archives Internal Medicine 1931;47:339
1931

first patented pacemaker
Dr Albert Hyman patents the first 'artificial cardiac pacemaker' which stimulates the heart by using a transthoracic needle. His aim was to produce a device that was small enough to fit in a doctor's bag and stimulate the right atrial area of the heart with a suitably insulated needle. His experiments were on animals. His original machine was powered by a crankshaft (it was later prototyped by a German company but was never successful). "By March 1, 1932 the artificial pacemaker had been used about 43 times, with a successful outcome in 14 cases." It was not until 1942 that a report of its successful short term use in Stokes-Adams attacks was presented. Hyman AS. Resuscitation of the stopped heart by intracardial therapy. Arch Intern Med. 1932;50:283
1932
Goldhammer and Scherf propose the use of the electrocardiogram after moderate exercise as an aid to the diagnosis of coronary insufficiency. Goldhammer S, Scherf D. Elektrokardiographische untersuchungen bei kranken mit angina pectoris. Z Klin Med 1932;122:134
1932
Charles Wolferth and Francis Wood describe the clinical use of chest leads. Wolferth CC, Wood FC. The electrocardiographic diagnosis of coronary occlusion by the use of chest leads. Am J Med Sci 1932;183:30-35
1934
By joining the wires from the right arm, left arm and left foot with 5000 Ohm resistors Frank Wilson defines an 'indifferent electrode' later called the 'Wilson Central Terminal'. The combined lead acts as an earth and is attached to the negative terminal of the ECG. An electrode attached to the positive terminal then becomes 'unipolar' and can be placed anywhere on the body. Wilson defines the unipolar limb leads VR, VL and VF where 'V' stands for voltage (the voltage seen at the site of the unipolar electrode). Wilson NF, Johnston FE, Macleod AG, Barker PS. Electrocardiograms that represent the potential variations of a single electrode. Am Heart J. 1934;9:447-458.
1935
McGinn and White describe the changes to the electrocardiogram during acute pulmonary embolism including the S1 Q3 T3 pattern. McGinn S, White PD. Acute cor pulmonale resulting from pulmonary embolism: its clinical recognition. JAMA 1935;114:1473.
1938
American Heart Association and the Cardiac Society of Great Britain define the standard positions, and wiring, of the chest leads V1 - V6. The 'V' stands for voltage. Barnes AR, Pardee HEB, White PD. et al. Standardization of precordial leads. Am Heart J 1938;15:235-239
1938
Tomaszewski notes changes to the electrocardiogram in a man who died of hypothermia. Tomaszewski W. Changements electrocardiographiques observes chez un homme mort de froid. Arch Mal Coeur 1938;31:525.

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1939
Langendorf reports a case of atrial infarction discovered at autopsy which, in retrospect, could have been diagnosed by changes on the ECG. Langendorf R. Elektrokardiogramm bei Vorhof-Infarkt. Acta Med Scand. 1939;100:136.
1942
Emanuel Goldberger increases the voltage of Wilson's unipolar leads by 50% and creates the augmented limb leads aVR, aVL and aVF. When added to Einthoven's three limb leads and the six chest leads we arrive at the 12-lead electrocardiogram that is used today.
1942
Arthur Master, standardises the two step exercise test (now known as the Master two-step) for cardiac function. Master AM, Friedman R, Dack S. The electrocardiogram after standard exercise as a functional test of the heart. Am Heart J. 1942;24:777
1944
Young and Koenig report deviation of the P-R segment in a series of patients with atrial infarction. Young EW, Koenig BS. Auricular infarction. Am Heart J. 1944;28:287.
1947
Gouaux and Ashman describe an observation that helps differentiate aberrant conduction from ventricular tachycardia. The 'Ashman phenomenon' occurs when a stimulus falls during the relative or absolute refractory period of the ventricles and the aberrancy is more pronounced. In atrial fibrillation with aberrant conduction this is demonstrated when the broader complexes are seen terminating a relatively short cycle that follows a relatively long one. The QRS terminating the shorter cycle is conducted 'more aberrantly' because it falls in the refractory period. The aberrancy is usually of a RBBB pattern. Gouaux JL, Ashman R. Auricular fibrillation with aberration simulating ventricular paroxysmal tachycardia. Am Heart J 1947;34:366-73.
1947
Claude Beck, a pioneering cardiovascular surgeon in Cleveland, successfully defibrillates a human heart during cardiac surgery. The patient is a 14 year old boy - 6 other patients had failed to respond to the defibrillator. His prototype defibrillator followed experiments on defibrillation in animals performed by Carl J. Wiggers, Professor of Physiology at the Western Reserve University. Beck CS, Pritchard WH, Feil SA: Ventricular fibrillation of long duration abolished by electric shock. JAMA 1947; 135: 985-989.
Wiggers CJ, Wegria R. Ventricular fibrillation due to single localized induction in condenser shock supplied during the vulnerable phase of ventricular systole. Am J Physiol 1939;128:500
1948
Rune Elmqvist, Swedish engineer who had trained as a doctor but never practiced, introduces the first ink jet printer for the transcription of analog physiological signals. He demonstrates its use in the recording of ECGs at the First International Congress of Cardiology in Paris in 1950. The machine (the mingograph) was developed by him at the company that later became Siemens. (Luderitz, 2002)
1949

modern 'Holter' Monitor
Montana physician Norman Jeff Holter develops a 75 pound backpack that can record the ECG of the wearer and transmit the signal. His system, the Holter Monitor, is later greatly reduced in size, combined with tape / digital recording and used to record ambulatory ECGs. Holter NJ, Generelli JA. Remote recording of physiologic data by radio. Rocky Mountain Med J. 1949;747-751.
1949
Sokolow and Lyon propose diagnostic criteria for left ventricular hypertrophy i.e. LVH is present if the sum of the size of the S wave in V1 plus the R wave in V6 exceeds 35 mm. Sokolow M, Lyon TP. The ventricular complex in left ventricular hypertrophy as obtained by unipolar precordial and limb leads. Am Heart J 1949;37:161
1950
John Hopps, a Canadian electrical engineer and researcher for the National Research Council, together with two physicians (Wilfred Bigelow, MD of the University of Toronto and his trainee, John C. Callaghan, MD) show that a coordinated heart muscle contraction can be stimulated by an electrical impulse delivered to the sino-atrial node. The apparatus, the first cardiac pacemaker, measures 30cm, runs on vacuum tubes and is powered by household 60Hz electrical current. Bigelow WG, Callaghan JC, Hopps JA. "General hypothermia for experimental intracardiac surgery." Ann Surg 1950; 1132: 531-539.
1953
Osborn, whilst experimenting with hypothermic dogs, describes the prominent J (junctional) wave which has often been known as the "Osborn wave". He found the dogs were more likely to survive if they had an infusion of bicarbonate and supposed the J wave was due to an injury current caused by acidosis. Osborn JJ. Experimental hypothermia: respiratory and blood pH changes in relation to cardiac function. Am J Physiol 1953;175:389.
1955
Richard Langendorf publishes the "rule of bigeminy" whereby ventricular bigeminy tends to perpetuate itself. Langendorf R, Pick A, Winternitz M. Mechanisms of intermittent ventricular bigeminy. I. Appearence of ectopic beats dependent upon the length of the ventricular cycle, the "rule of bigeminy." circulation 1955;11:442.
1956
Paul Zoll, a cardiologist, uses a more powerful defibrillator and performs closed-chest defibrillation in a human. Zoll PM, Linenthal AJ, Gibson P: Termination of Ventricular Fibrillation in Man by Externally Applied Countershock . NEJM 1956; 254: 727-729
1957

long QT syndrome
Anton Jervell and Fred Lange-Nielsen of Oslo describe an autosomal recessive syndrome of long-QT interval, deafness and sudden death later known as the Jervell-Lange-Nielsen syndrome. Jervell A, Lange-Nielsen F. Congenital deaf mutism, functional heart disease with prolongation of the QT interval and sudden death. Am Heart J 1957;54:59.
1958
Professor Ake Senning, of Sweden, places the first implantable cardiac pacemaker designed by Rune Elmqvist into a 43-year-old patient with complete heart block and syncope (Arne Larsson).
1959
Myron Prinzmetal describes a variant form of angina in which the ST segment is elevated rather than depressed. Prinzmetal M, Kennamer R, Merliss R, Wada T, Bor N. Angina pectoris. I. A variant form of angina pectoris. Am J Med 1959;27:374.
1960
Smirk and Palmer highlight the risk of sudden death from ventricular fibrillation particularly when ventricular premature beats occur at the same time as the T wave. The 'R on T' phenomenon. Smirk FH, Palmer DG. A myocardial syndrome, with particular reference to the occurrence of sudden death and of premature systoles interrupting antecedent T waves. Am J Cardiol 1960;6:620.
1963
Italian paediatrician C. Romano and Irish paediatrician O. Conor Ward (the following year) independently report an autosomal dominant syndrome of long-QT interval later known as the Romano-Ward syndrome. Romano C, Gemme G, Pongiglione R. Aritmie cardiache rare dell'eta pediatrica. Clin Pediatr. 1963;45:656-83.
Ward OC. New familial cardiac syndrome in children. J Irish Med Assoc. 1964;54:103-6
1963

Excercise ECG
Robert Bruce and colleages describe their multistage treadmill exercise test later known as the Bruce Protocol. "You would never buy a used car without taking it out for a drive and seeing how the engine performed while it was running," Bruce says, "and the same is true for evaluating the function of the heart." Bruce RA, Blackman JR, Jones JW, Srait G. Exercise testing in adult normal subjects and cardiac patients. Pediatrics 1963;32:742
Bruce RA, McDonough JR. Stress testing in screening for cardiovascular disease. Bull. N.Y. Acad Med. 1969;45:1288
1963
Baule and McFee are the first to detect the magnetocardiogram which is the electromagnetic field produced by the electrical activity of the heart. It is a method that can detect the ECG without the use of skin electrodes. Although potentially a useful technique it has never gained clinical acceptance, partly because of its greater expense. Baule GM, McFee R. Detection of the magnetic field of the heart. Am Heart J. 1963;66:95-96.
1966
Mason and Likar modify the 12-lead ECG system for use during exercise testing. The right arm electrode is placed at a point in the infraclavicular fossa medial to the border of the deltoid muscle, 2 cm below the lower border of the clavicle. The left arm electrode is placed similarly on the left side. The left leg electrode is placed at the left iliac crest. Although this system reduces the variability in the ECG recording during exercise it is not exactly equivalent to the standard lead positions. The Mason-Likar lead system tends to distort the ECG with a rightward QRS axis shift, a reduction in R wave amplitude in lead I and aVL, and a significant increase in R wave amplitude in leads II, III and aVF. Eur Heart J. 1987 Jul;8(7):725-33
1966

Torsade de pointes
François Dessertenne of Paris publishes the first case of 'Torsade de pointes' Ventricular Tachycardia. Dessertenne F. La tachycardie ventriculaire a deux foyers opposes variables. Arch des Mal du Coeur 1966; 59:263
1968
Journal of Electrocardiography, the Official Journal of the International Society for Computerized Electrocardiology and the International Society of Electrocardiology, is founded by Zao and Lepeschkin.
1968
Henry Marriott introduces the Modified Chest Lead 1 (MCL1) for monitoring patients in Coronary Care.
1969
Rosenbaum reviews the classification of ventricular premature beats and adds a benign form that arises from the right ventricle and is not associated with heart disease. This becomes known as the 'Rosenbaum ventricular extrasystole'. Rosenbaum MB. Classification of ventricular extrasystoles according to form. J Electrocardiol 1969;2:289.
1974
Jay Cohn, of University of Minnesota Medical School, describes the 'syndrome of right ventricular dysfunction in the setting of acute inferior wall myocardial infarction'. Cohn JN, Guiha NH, Broder MI. Right ventricular infarction. Am J Cardiol 1974:33:209-214
1974
Gozensky and Thorne introduce the term 'Rabbit ears' to electrocardiography. Rabbit ears describe the appearence of the QRS complex in lead V1 with an rSR' pattern (good rabbit) being typical of Right Bundle Branch Block and an RSr' (bad rabbit) suggesting a ventricular origin i.e. ventricular ectopy / tachycardia. Gozensky C, Thorne D. Rabbit ears: an aid in distinguishing ventricular ectopy from aberration. Heart Lung 1974;3:634.
1976
Erhardt and colleagues describe the use of a right-sided precordial lead in the diagnosis of right ventricular infarction which had previously been thought to be electrocardiographically silent. Erhardt LR, Sjogrn A, Wahlberg I. Single right-sided precordial lead in the diagnosis of right ventricular involvement in inferior myocardial infarction. Am Heart J 1976;91:571-6
1988
Professor John Pope Boineau of Washington University School of Medicine publishes a 30-year percpective on the modern history of electrocardiography. Boineau JP. Electrocardiology: A 30-year Perspective. Ah Serendipity, My Fulsome Friend. Journal of Electrocardiology 21. Suppl (1988): S1-9
1992

Brugada syndrome
Pedro Brugada and Josep brugada of Barcelona publish a series of 8 cases of sudden death, Right Bundle Branch Block pattern and ST elevation in V1 - V3 in apparently healthy individuals. This 'Brugada Syndrome' may account for 4-12% of unexpected sudden deaths and is the commonest cause of sudden cardiac death in individuals aged under 50 years in South Asia. The technology of the electrocardiogam, which is over 100 years old, can still be used to discover new clinical entities in cardiology. Brugada P, Brugada J. Right Bundle Branch Block, Persistent ST Segment Elevation and Sudden Cardiac Death: A Distinct Clinical and Electrocardiographic Syndrome. J Am Coll Cardiol 1992;20:1391-6
1992
Cohen and He describe a new non-invasive approach to accurately map cardiac electrical activity by using the surface Laplacian map of the body surface electrical potentials. He B, Cohen RJ. Body surface Laplacian ECG mapping. IEEE Trans Biomed Eng 1992;39(11):1179-91
1993

Mac 5000, 15-lead ECG
Robert Zalenski, Professor of Emergency Medicine, Wayne State University Detroit, and colleagues publish an influential article on the clinical use of the 15-lead ECG which routinely uses V4R, V8 and V9 in the diagnosis of acute coronary syndromes. Like the addition of the 6 standardised unipolar chest leads in 1938 these additional leads increase the sensitivity of the electrocardiogram in detecting myocardial infarction. Zalenski RJ, Cook D, Rydman R. Assessing the diagnostic value of an ECG containing leads V4R, V8, and V9: The 15-lead ECG. Ann Emerg Med 1993;22:786-793
1999
Researchers from Texas show that 12-lead ECGs transmitted via wireless technology to hand-held computers is feasible and can be interpreted reliably by cardiologists. Pettis KS, Savona MR, Leibrandt PN et al. Evaluation of the efficacy of hand-held computer screens for cardiologists' interpretations of 12-lead electrocardiograms. Am Heart J. 1999 Oct;138(4 Pt 1):765-70
2000
Physicians from the Mayo Clinic describe a new hereditary form of Short QT syndrome associated with syncope and sudden death that they discovered in 1999. Several genes have since been implicated. Gussak I, Brugada P, Brugada J, et al. Idiopathic short QT interval: a new clinical syndrome? Cardiology. 2000;94(2):99-102
2005
Danish cardiologists report the successful reduction in the time between onset of chest pain and primary angioplasty when the ECG of patients is transmitted wirelessly from ambulance to the cardiologist's handheld PDA (Personal Digital Assistant). The clinician can make an immediate decision to redirect patients to the catheter lab saving time in transfers between hospital departments. Clemmensen P, Sejersten M, Sillesen M et al. Diversion of ST-elevation myocardial infarction patients for primary angioplasty based on wireless prehospital 12-lead electrocardiographic transmission directly to the cardiologist's handheld computer: a progress report. J Electrocardiol. 2005 Oct;38(4 Suppl):194-8

Sources

  • Acierno. The History of Cardiology. 1994. New York: Parthenon.
  • Bibliotheque Inter-Universitaire de Medicine, Paris. Source of the images of 'Descarte's reflex' from De Hominis and Swammerdam's possible electrical stimulation of a nerve-muscle preparation.
  • Burchell HB. A centennial note on Waller and the first human electrocardiogram. Am J Cardiol 1987;59:979-983
  • Burnett J. The origins of the electrocardiograph as a clinical instrument. Medical History Supplement 5: 1985, 53-76. Published as a monograph. The emergence of modern cardiology. Bynum WF, Lawrence C, Nutton V, eds. Wellcome Institute for the History of Medicine:1985.
  • Cobb, Matthew. Exorcizing the animal spirits: Jan Swammerdam on nerve function. Nature Reviews, Neuroscience 2002;3:395-400
  • On Animal electricity: Being an Abstract of the Discoveries of Emil Du Bios-Reymond (translated). Edited by Dr Bence Jones. 1852. Churchill: London.
  • Fye WB. A history of the origin, evolution, and impact of electrocardiography. Am J Cardiol 1994;73:937-949
  • Geddes LA. Supplement. The Physiologist 1984;27(1):S-1
  • google.com, altavista.com, excite.com
  • Berndt Luderitz. History of the Disorders of Cardiac Rhythm. Third Edition. 2002. Blackwell Publishing.
  • Jaakko Malmivuo & Robert Plonsey: Bioelectromagnetism - Principles and Applications of Bioelectric and Biomagnetic Fields, Oxford University Press, New York, 1995
  • Nobel Institute. Presentation speech by Professor JE Johansson. The Nobel Prize in Physiology or Medicine 1924.
  • Pumphrey S. Latitude and the Magnetic Earth. Icon books, Cambridge: 2002. (see also the William Gilbert website)
  • Royal Humane Society, Annual Reports. Brettenham House, Lancaster Place, London, WC2 7EP.
  • Schamroth L. The 12 Lead Electrocardiogram. Blackwell Scientific Publications, Oxford: 1989.
  • Snellen HA. Willem Einthoven (1860-1927) Father of electrocardiography. Kluwer Academic Publishers, Dordrecht: 1995. with thanks to Kees Swenne
  • Titomir LI. The remote past and near future of electrocardiography: Viewpoint of a biomedical engineer. Bratisl Lek Listy 2000;101(5):272-279.
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The normal electrocardiogram.

ischaemic heart disease

Acute inferior myocardial infarction
Acute anterior myocardial infarction
Acute posterior myocardial infarction
Old inferior myocardial infarction
Acute myocardial infarction in the presence of LBBB

hypertrophy patterns

Left ventricular and left atrial hypertrophy - aortic stenosis
Mitral Stenosis
Right atrial hypertrophy
Left ventricular hypertrophy in the presence of left anterior hemiblock

atrioventricular (AV) block

First degree AV block
2 to 1 Atrioventricular block
Complete Heart Block
Complete heart block and atrial fibrillation

bundle branch block

Right Bundle Branch Block
Left anterior hemiblock
Left bundle branch block
'Trifascicular' block

supraventricular rhythms

Sinus bradycardia
Sinus tachycardia
Atrial Bigeminy
Atrial Premature Beat
Atrial fibrillation with rapid ventricular response
Atrial fibrillation with pre-existing LBBB
Atrial Flutter
Atrial flutter with 2:1 AV conduction
Wolff-Parkinson-White syndrome with atrial fibrillation (20k)

ventricular rhythms

Ventricular premature beats
Ventricular bigeminy
Idioventricular escape rhythm in Complete Heart Block
Ventricular tachycardia with clear AV dissociation
Ventricular tachycardia with subtle AV dissociation (20k)
Torsade de pointes ventricular tachycardia
Polymorphic Ventricular Tachycardia with an ICD
Ventricular Fibrillation

pacemakers

Ventricular pacemaker
Dual Chamber Pacemaker with an ICD

Wolff Parkinson White syndrome

WPW syndrome - left lateral pathway
WPW syndrome - anteroseptal pathway
Wolff-Parkinson-White syndrome with atrial fibrillation (20k)
Wolff-Parkinson-White syndrome with atrial fibrillation (another example)

miscellaneous

Implantable Cardioverter Defibrillator
Electrical Alternans - pericardial effusion
Long QT interval Romano-Ward Syndrome
Lown-Ganong-Levine Syndrome
Acute pulmonary embolus
Hyperkalaemia
Hypokalaemia
Piggy-back heart transplant
Digitalis effect

other

The electrical axis at a glance.
A brief history of electrocardiography
A page of comments and corrections for our book 'ECGs by Example'.

+ نوشته شده توسط دکتر شبنم مددی در دوشنبه پانزدهم مرداد 1386 و ساعت 13:16 |

Exam of the Heart

The major elements of the cardiac exam include observation, palpation and, most importantly, auscultation (percussion is omitted). As with all other areas of the physical exam, establishing adequate exposure and a quiet environment are critical. Initially, the patient should rest supine with the upper body elevated 30 to 45 degrees. Most exam tables have an adjustable top. If not, use 2 or 3 pillows. Remember that although assessment of pulse and blood pressure are discussed in the vital signs section they are actually important elements of the cardiac exam.

Observation: Assessment for distention of the right Internal Jugular vein (IJ) is a difficult skill. Its importance lies in the fact that the IJ is in straight-line communication with the right atrium. The IJ can therefore function as a manometer, with distention indicating elevation of Central Venous Pressure (CVP). This in turn is an important marker of intravascular volume status and related cardiac function. The focus here is on simply determining whether or not Jugular Venous Distention (JVD) is present. A discussion of the a, c and v waves that make up the jugular venous pulsations can be found elsewhere. These are quite difficult to detect for even the most seasoned physician.

Why is JVD so hard to assess? The IJ lies deep to skin and soft tissues, which can provide quite a bit of cover. Additionally, this blood vessel is under much lower pressure then the adjacent, pulsating carotid artery. It therefore takes a sharp eye to identify the relatively weak, transmitted venous impulses. A few things to remember:

  1. Think anatomically. The right IJ runs between the two heads (sternal and clavicular) of the sternocleidomastoid muscle (SCM) and up in front of the ear. This muscle can be identified by asking the patient to turn their head to the left and into your hand while you provide resistance to the movement. The two heads form the sides of a small triangle, with the clavicle making up the bottom edge. You should be able to feel a shallow defect formed by the borders of these landmarks. Note, you are trying to identify impulses originating from the IJ and transmitted to the overlying skin in this area. You can't actually see the IJ. The External Jugular (EJ) runs in an oblique direction across the sternocleidomastoid and, in contrast to the IJ, can usually be directly visualized. If the EJ is not readily apparent, have the patient look to the left and valsalva. This usually makes it quite obvious. EJ distention is not always a reliable indicator of elevated CVP as valves, designed to prevent the retrograde flow of blood, can exist within this vessel causing it to appear engorged even when CVP is normal. It also makes several turns prior to connecting with the central venous system and is thus not in a direct line with the right atrium.

    cardiac cvp

    Anatomy of the Neck Internal Jugular Anatomy

  2. Take your time. Look at the area in question for several minutes while the patient's head is turned to the left. The carotid artery is adjacent to the IJ, lying just medial to it. If you are unsure whether a pulsation is caused by the carotid or the IJ, place your hand on the patient's radial artery and use this as a reference. The carotid impulse coincides with the palpated radial artery pulsation and is characterized by a single upstroke timed with systole. The venous impulse (at least when the patient is in sinus rhythm and there is no tricuspid regurgitation) has three components, each associated with the aforementioned a, c and v waves. When these are transmitted to the skin, they create a series of flickers that are visible diffusely within the overlying skin. In contrast, the carotid causes a single up and down pulsation. Furthermore, the carotid is palpable. The IJ is not and can, in fact, be obliterated by applying pressure in the area where it emerges above the clavicle.
  3. Search along the entire projected course of the IJ as the top of the pressure wave (which is the point that you are trying to identify) may be higher then where you are looking. In fact, if the patient's CVP is markedly elevated, you may not be able to identify the top of the wave unless they are positioned with their trunk elevated at 45 degrees or more (else their will be no identifiable "top" of the column as the entire IJ will be engorged). After you've found the top of the wave, see what effect sitting straight up and lying down flat have on the height of the column. Sitting should cause it to appear at a lower point in the neck, while lying has the opposite effect. Realize that these maneuvers do not change the actual value of the central venous pressure. They simply alter the position of the top of the pulsations in relation to other structures in the neck and chest.
  4. Shine a pen light tangentially across the neck. This sometimes helps to accentuate the pulsations.
  5. If you are still uncertain, apply gentle pressure to the right upper quadrant of the abdomen for 5 to 10 seconds. This elicits Hepato-Jugular Reflux which, in pathologic states, will cause blood that has pooled in the liver to flow in a retrograde fashion and fill out the IJ, making the transmitted pulsations more apparent. Make sure that you are looking in the right area when you push as the best time to detect any change in the height of this column of blood is immediately after you apply hepatic pressure.
  6. Once you identify JVD, try to estimate how high in cm the top of the column is above the Angle of Louis. The angle is the site of the joint which connects the manubrium with the rest of the sternum. First identify the supra-sternal notch, a concavity at the top of the manubrium. Then walk your fingers downward until you detect a subtle change in the angle of the bone, which is approximately 4 to 5 cm below the notch. This is roughly at the level of the 2nd intercostal space. The vertical distance from the top of the column to this angle is added to 5cm, the rough vertical distance from the angle to the right atrium with the patient lying at a 45 degree angle. The sum is an estimate of the CVP. However, if you can simply determine with some accuracy whether JVD is present or not, you will be way ahead of he game! Normal is 7-9 cm.

bony structures of the chest

Bony Structures of the Chest


Angle of Louis 1 Angle of Louis 2

Finding the Angle of Louis:The wooden Q-tips highlight the different slopes of the sternum and manubrium. The point at which the
Q-tips cross is the Angle of Louis.

 

estimating cvp

Determining the CVP

Video of patient with markedly elevated central venous pressure.

Video simulation and discussion of central venous pressure.

Take some time to look across the left chest and try to identify the transmitted impulse caused by ventricular contraction, which may be apparent when contractions are particularly vigorous.

Palpation: The palm of your right hand is placed across the patient's left chest so that it covers the area over the heart. The heel should rest along the sternal border with the extended fingers lying below the left nipple. Focus on several things:

Palpation of the Precordium to Determine the Location of the PMI


cardiac pmi

  1. Can you feel a Point of Maximum Impulse (PMI) related to contraction at the apex of the underlying left ventricle? If so, where is it located? After identifying the rough position with the palm of your hand, try to pin down the precise location with the tip of your index finger. The normal sized and functioning ventricle will generate a penny sized impulse that is best felt in the mid-clavicular line, roughly at the 5th intercostal space. If the ventricle becomes dilated, most commonly as the result of past infarcts and always associated with ventricular dysfunction, the PMI is displaced laterally. In cases of significant enlargement, the PMI will be located near the axilla. Occasionally, the PMI will not localize to any one area, which does not necessarily indicate ventricular enlargement or dysfunction. Obesity and COPD may also limit your ability to identify its precise location. Palpating while the patient is in the left lateral decubitus position can make the PMI more obvious.
  2. What is the duration of the impulse? In the setting of hypertension or any other state of chronic pressure overload, the ventricle hypertrophies and the PMI becomes sustained (i.e. you feel the impulse for a longer period of time). This is actually pretty subjective and can be tough to detect. Note that hypertrophy and dilatation are not synonymous. They can exist separately or in conjunction with one another.
  3. How vigorous is the transmitted impulse? Processes associated with ventricular hypercontractility (e.g. compensated mitral regurgitation or aortic insufficiency that result in exceptionally large stroke volumes) generate an impulse of unusual vigor.
  4. Do you feel a thrill, a vibratory sensation produced by turbulent blood flow that is usually secondary to valvular abnormalities? The feeling is similar to that produced when you squeeze on a garden hose, partially obstructing the flow of water. The location of the thrill will depend on the involved valve (e.g. thrills caused by aortic stenosis are best felt toward the right upper sternal border). If a loud murmur is detected during auscultation, you may then go back and reassess for the presence of a thrill. In general, thrills are an uncommon finding.

    *Palpation of the precordium of a female patient is best done by placing the palm of your right hand directly beneath the patient's left breast such that the edge of your index finger rests against the inferior surface of the breast. Make sure that you tell that patient what you are about to do (and why) before actually performing this maneuver. Remember that with age tissue turgor often declines, causing the breasts to hang below the level of the heart.

  5. Carotid Artery Palpation: This is of greatest value during the assessment of aortic valvular and out flow tract disease (see below) and should thus be performed after auscultation so that you know whether or not these problems exist prior to palpation. However, for the sake of completeness it will be described here. The carotids can be located by sliding the second and third finger of either hand along the side of the trachea at the level of the thyroid cartilage (i.e. adams apple). The carotid pulsation is palpable just lateral to the groove formed by the trachea and the surrounding soft tissue. The quantity of subcutaneous fat will dictate how firmly you need to push. The pulsations should be easily palpable. Diminution may be caused by atherosclerosis, aortic stenosis, or severely impaired ventricular performance. Do not push on both sides simultaneously as this may compromise cerebral blood flow.

    ><img src=

Auscultation: The following anatomic pictures will aid you in understanding the principles of cardiac auscultation.

Internal anatomy Internal anatomy

Anatomic Relationship of Heart and LungsCardiac AnatomyCoronal Section of Heart Deep Coronal Section of Heart

  1. Become comfortable with your stethescope. There are multiple brands on the market, each of which incorporates its own version of a bell (low pitched sounds) and diaphragm (higher pitched sounds). Some have the diaphragm and bell on opposite sides of the head piece. Others have the bell and diaprhragm built into a single side, with the bell engaged by applying light pressure and the diaphragm engaged by pushing more firmly. Adult, pediatric, and newborn sizes also exist. And some combine adult and pediatric scopes into a single unit. Take the time to read the instructions for your particular model so that you are familiar with how to use it correctly. Several sample stethescopes are pictured below. It's worth mentioning that almost any commercially available scope will do the job. The most important "part" is what sits betwen the ear pieces!



    Adult Stethoscope

    Adult Stethoscope: Diaphragm and Bell
    Incorporated Into Single Side.

    Combination Adult & Pediatric Stethoscope

    Newborn Stethoscope

  2. Engage the diaphragm of your stethescope and place it firmly over the 2nd right intercostal space, the region of the aortic valve. Then move it to the other side of the sternum and listen in the 2nd left intercostal space, the location of the pulmonic valve. Move down along the sternum and listen over the left 4th intercostal space, the region of the tricuspid valve. And finally, position the diaphragm over the 4th intercostal space, left midclavicular line to examine the mitral area. These locations are rough approximations and are generally determined by visual estimation. In each area, listen specifically for S1 and then S2. S1 will be loudest over the left 4th intercostal space (mitral/tricuspid valve areas) and S2 along the 2nd R and L intercostal spaces (aortic/pulomonic valve regions). Note that the time between S1 and S2 is shorter then that between S2 and S1. This should help you to decide which sound is produced by the closure of the mitral/tricuspid and which by the aortic/pulmonic valves and therefore when systole and diastole occur. Compare the relative intensities of S1 and S2 in these different areas.

    Auscultation of the Heart

    normal chestchest auscultation

  3. In younger patients, you should also be able to detect physiologic splitting of S2. That is, S2 is made up of 2 components, aortic (A2) and pulmonic (P2) valve closure. On inspiration, venous return to the heart is augmented and pulmonic valve closure is delayed, allowing you to hear first A2 and then P2. On expiration, the two sounds occur closer together and are detected as a single S2. Ask the patient to take a deep breath and hold it, giving you a bit more time to identify this phenomenon. The two components of S1 (mitral and tricuspid valve closure) occur so close together that splitting is not appreciated.

    Heart sounds S1-S2
    Heart sounds physiologic splitting of S2

  4. You may find it helpful to tap out S1 and S2 with your fingers as you listen, accentuating the location of systole and diastole and lending a visual component to this exercise. While most clinicians begin asucultation in the aortic area and then move across the precordium, it may actually make more sense to begin laterally (i.e. in the mitral area) and then progress towards the right and up as this follows the direction of blood flow. Try both ways and see which feels more comfortable.

    Univeristy of Utah, Review of Cardiac Physiology

  5. Listen for extra heart sounds (a.k.a. gallops). While present in normal subjects up to the ages of 20-30, they represent pathology in older patients. An S3 is most commonly associated with left ventricular failure and is caused by blood from the left atrium slamming into an already overfilled ventricle during early diastolic filling. The S4 is a sound created by blood trying to enter a stiff, non-compliant left ventricle during atrial contraction. It's most frequently associated with left ventricular hypertrophy that is the result of long standing hypertension. Either sound can be detected by gently laying the bell of the stethoscope over the apex of the left ventricle (roughly at the 4th intercostal space, mid-clavicular line) and listening for low pitched "extra sounds" that either follow S2 (i.e. an S3) or precede S1 (i.e. an S4). These sounds are quite soft, so it may take a while before you're able to detect them. Positioning the patient on their left side while you listen may improve the yield of this exam. The presence of both an S3 and S4 simultaneously is referred to as a summation gallop.

    Listening for Extra Heart Sounds

     
    lateral auscultation

    Heart sounds S3
    Heart sounds S4

    Heart sounds summation gallop

  6. Murmurs: These are sounds that occur during systole or diastole as a result of turbulent blood flow. Traditionally, students are taught that auscultation is performed over the 4 areas of the precordium that roughly correspond to the "location" of the 4 valves of the heart (i.e. aortic valve area ='s the 2nd Right Intercostal Space, pulmonic valve area ='s the 2nd LICS, tricuspid valve area ='s 4th LICS, and mitral valve area ='s 4th LICS in the midclavicular line). This leads to some misperceptions. Valves are not strictly located in these areas nor are the sounds created by valvular pathology restricted to those spaces. So, while it might be OK to listen in only 4 places when conducting the normal exam, it is actually quite helpful to listen in many more when any abnormal sounds are detected. If you hear a murmur, ask yourself:
    1. Does it occur during systole or diastole?
    2. What is the quality of the sound (i.e. does it get louder and then softer; does it maintain the same intensity throughout; does it start loud and become soft)? It sometimes helps to draw a pictoral representation of the sound.
    3. What is the quantity of the sound? The rating system for murmurs is as follows:
      • 1/6… Can only be heard with careful listening
      • 2/6… Readily audible as soon as the stethescope is applied to the chest
      • 3/6… Louder then 2/6
      • 4/6… As loud as 3/6 but accompanied by a thrill
      • 5/6… Audible even when only the edge of the stethescope touches the chest
      • 6/6… Audible to the naked ear
        Most murmurs are between 1/6 and 3/6. Louder generally (but not always) indicates greater pathology.
    4. What is the relationship of the murmur to S1 and S2 (i.e. when does it start and stop)?
    5. What happens when you march your stethescope from the 2nd RICS (the aortic area) out towards the axilla (the mitral area)? Where is it loudest and in what directions does it radiate? By moving in small increments (i.e. listening in 8 or 10 places along the chest wall) you will be more likely to detect changes in the character of a particular murmur and thus have a better chance of determining which valve is affected and by what type of lesion.
  7. Auscultation over the carotid arteries (see under aortic stenosis for additional information): In the absence of murmurs suggestive of aortic valvular disease, you can listen for carotid bruits (sounds created by turbulent flow within the blood vessel) at this point in the exam. Place the diaphragm gently over each carotid and listen for a soft, high pitched "shshing" sound. It's helpful if the patient can hold their breath as you listen so that you are not distracted by transmitted tracheal sounds. The meaning of a bruit remains somewhat controversial. I was taught that bruits represented turbulent flow associated with intrinsic atherosclerotic disease… and that the disappearance of a bruit which was previously present was a sign that the lesion was progressing (i.e. further encroachment on the lumen of the vessel). However, a number of studies provide evidence that atherosclerotic disease is frequently absent when a bruit is present as well as the reverse situation. This is actually of clinical importance because recent data suggest that it may be beneficial to surgically repair carotid disease in patients who have significant stenosis yet have not experienced any symptoms (e.g. Transient ischemic attacks or strokes. Surgery in these settings has already proven to be beneficial). Thus, it is becoming increasingly important to determine the best way of identifying asymptomatic carotid artery disease... and carotid auscultation may, in fact, not be the mechanism of choice!

    The Auscultation Assistant is an excellent heart sound simulation site developed at UCLA. Press the "Back" button to return to this page.

      Blaufuss Multimedia Heart Sounds Tutorial. Press the "Back" button to return to this page.

    This University of Washington site also provides a variety of simulated heart sounds. Press the "Back" button to return to this page.

    In addition, there is an excellent heart sound tutorial CD ROM called, The Physiological Origins of Heart Sounds and Murmurs available at the OLR.

    Identifying the Most Common Murmurs:

    1. Systolic Murmurs: In the adult population, these generally represent either aortic stenosis or mitral regurgitation. To distinguish between them, remember the following:

    Murmurs of Aortic Stenosis (AS):

    1. Tend to be loudest along the upper sternal borders and get softer as you move down and out towards the axilla. There is, however, a phenomenon referred to at the Gallavardin Effect which can cause murmurs of AS to sound as loud towards the axilla as they do over the aortic region. When this occurs, the shape of the sound should be similar in both regions, helping you to distinguish it from MR (see below).
    2. Have a growling, harsh quality (i.e. get louder and then softer.. also referred to as a crescendo decrescendo, systolic ejection, or diamond shaped murmur). When the stenosis becomes more severe, the point at which the murmur is loudest (i.e. its peak intensity) occurs later in systole, as it takes longer to generate the higher ventricular pressure required to push blood through the tight orifice.

      Early peaking murmur
      Late peaking murmur

    3. Are better heard when the patient sits up and exhales.
    4. Are heard in the carotid arteries and over the right clavicle. Radiation to the clavicle can be appreciated by simply resting the diaphragm on the right clavicle. To assess for transmission to the carotids, have the patient hold their breath while you listen over each artery using the diaphragm of your stethescope. Carotid bruits can be confused with the radiating murmur of aortic stenosis. In general, carotid bruits are softer. Also, murmurs associated with aortic pathology should be audible in both carotids and get louder as you move down the vessel, towards the chest. In settings where carotid pathology coexists with aortic stenosis, a loud transmitted murmur associated with a valvular lesion may overwhelm any sound caused by intrinsic carotid disease, masking it completely.
    5. Carotid upstrokes refer to the quantity and timing of blood flow into the carotids from the left ventricle. They can be affected by aortic stenosis and must be assessed whenever you hear a murmur that could be consistent with AS. This is done by placing your fingers on the carotid artery as described above while you simultaneously listen over the chest. There should be no delay between the onset of the murmur, which marks the beginning of systole, and when you feel the pulsation in the carotid. In the setting of critical (i.e. very severe) aortic stenosis, small amounts of blood will be ejected into the carotid and there will be a lag between when you hear the murmur and feel the impulse. This is referred to as diminished and delayed upstrokes (a.k.a. parvus et tardus), as opposed to the full and prompt inflow which occurs in the absence of disease. Mild or moderate stenosis does not alter the character of carotid in-flow.
    6. Sub-Aortic stenosis is a relatively rare condition where the obstruction of flow from the left ventricle into the aorta is caused by an in-growth of septal tissue in the region below the aortic valve known as the aortic outflow tract. It causes a crescendo-decrescendo murmur that sounds just like aortic stenosis. As opposed to AS, however, the murmur is louder along the left lower sternal border and out towards the apex. This makes anatomic sense as the obstruction is located near this region. It also does not radiate loudly to the carotids as the point of obstruction is further from these vessels in comparison with the aortic valve. You may also be able to palpate a bisferiens pulse in the carotid artery (see under aortic insufficiency). Furthermore, the murmur will get softer if the ventricle is filled with more blood as filling pushes the abnormal septum away from the opposite wall, decreasing the amount of obstruction. Conversely, it gets louder if filling is decreased. This phenomenon can actually be detected on physical exam and is a useful way of distinguishing between AS and sub-aortic obstruction. Ask the patient to valsalva while you listen. This decreases venous return and makes the murmur louder (and will have the opposite effect on a murmur of AS). Then, again while listening, squat down with the patient. This maneuver increases venous return, causing the murmur to become softer. Standing will cause the opposite to occur. You need to listen for 20 seconds or so after each change in position to really appreciate any difference. Because the degree of obstruction can vary with ventricular filling, sub-aortic stenosis is referred to as a dynamic outflow tract obstruction. In aortic stenosis, the degree of obstruction that exists at any given point in time is fixed.

    Murmurs of Mitral Regurgitation (MR):

    1. Sound the same throughout systole.
    2. Generally do not have the harsh quality associated with aortic stenosis. In fact, they sound a bit like the "shshing" noise produced when you pucker your lips and blow through clenched teeth.
    3. Get louder as you move your stethescope towards the axilla.
    4. Will get even louder if you roll the patient onto their left side while keeping your stethescope over the mitral area of the chest wall and listening as they move. This maneuver brings the chamber receiving the regurgitant volume, the left atrium, closer to your stethescope, accentuating the murmur.
    5. Get louder if afterload is suddenly increased, which can be accomplished by having the patient close their hands tightly. MR is also affected by the volume of blood returning to the heart. Squatting increases venous return, causing a louder sound. Standing decreases venous return, thereby diminishing the intensity of the murmur.

    Mitral regurgitation

    Sometimes murmurs of aortic stenosis and mitral regurgitation co-exist, which can be difficult to sort out on exam. Moving your stethescope back and forth between the mitral and aortic areas will allow for direct comparison, which may help you decide if more then one type of lesion is present or if the quality of the murmur is the same in both locations, changing only in intensity (i.e. consistent with a one valve problem).

    2. Diastolic Murmurs: Tend to be softer and therefore much more difficult to hear then those occurring during systole. This makes physiologic sense as diastolic murmurs are not generated by high pressure ventricular contractions. In adults they may represent either aortic regurgitation or mitral stenosis, neither of which is too common. While systolic murmurs are often obvious, you will probably not be able to detect diastolic murmurs on your own until you have had them pointed out by a more experienced examiner.

    Aortic Regurgitation (AR); a.k.a. Aortic Insufficiency (AI):

    Cardiac Insufficiency

     
    1. Is best heard along the left para-sternal border, as this is the direction of the regurgitant flow.
    2. Becomes softer towards the end of diastole (a.k.a. decrescendo).
    3. Can be accentuated by having the patient sit up, lean forward and exhale while you listen.
    4. Occasionally accompanies aortic stenosis, so listen carefully for regurgitation in patients with AS.
    5. Will cause the carotid upstrokes to feel extraordinarily full as significant regurgitation increases ventricular pre-load, resulting in ejection of an augmented stroke volume. AI can also produce a double peaked pulsation in the carotids known as a bisferiens pulse, which is quite difficult to appreciate. Feeling your own carotid impulse at the same time that you're palpating the patient's may accentuate this finding. In cases of co-existent AS and AI, a bisferiens pulse suggests that the AI is the dominant problem. It may also be present with sub-aortic stenosis (see above), helping to distinguish it from AS.

    Mitral Stenosis (MS):

    1. Heard best towards the axilla
    2. Can be accentuated by having the patient role onto their left side while you listen with the bell of your sthethescope.
    3. Associated with a soft, low pitched sound preceding the murmur, called the opening snap. This is the noise caused by the calcified valve "snapping" open. It can, however, be pretty hard to detect.

    Auscultation, an ordered approach:
    Try to focus on each sound individually and in a systematic fashion. Ask yourself: Do I hear S1? Do I hear S2? What is their relative intensities in each of the major valvular areas? Is S2 split physiologically? Are there extra sounds before S1or after S2 (i.e. an S4 or S3)? Is there a murmur during systole? Is there a murmur during diastole? If a murmur is present, how loud is it? What is its character? Where does it radiate? Are there any maneuvers which affect its intensity? Remember that these sounds are created by mechanical events in the heart. As you listen, remind yourself what is happening to produce each of them. By linking auscultatory findings with physiology, you can build a case in your mind for a particular lesion.

    Interrelationship of Cardiac Events & Sounds

    Interrelationship of Caridac Events & Sounds

     
    This diagram courtesy of Dr. Wilbur Lew, Department of Medicine, San Diego VA Medical Center.

    A few final comments about auscultation:

    1. Pulmonic valve murmurs are rare in the adult population and, even when present, are difficult to hear due to the relatively low pressures generated by the right side of the heart.
    2. Tricuspid regurgitation (TR) is relatively common, most frequently associated with elevated left sided pressures which are then transmitted to the right side of the heart (though a number of other processes can cause TR as well). In this setting, both mitral and tricuspid regurgitation often co-exist. The murmur of MR is generally louder then that of TR, again due to the higher pressures on the left side of the heart. It can therefore be difficult to sort out if there is co-existent TR when MR is present. Try to listen along both the low left and right sternal borders (areas where the tricuspid valve is best assessed) and compare this to the mitral area. Move your stethoscope slowly across the precordium and note if there is any change in the character/intensity of the murmur. TR murmurs are also accentuated by inhalation, which increases venous return and therefore flow across the valve.
    3. Patients with COPD (emphysema) often have very soft heart sounds. Air trapping and subsequent lung hyperinflation results in a posterior-inferior rotation of the heart away from the chest wall and causes the interposition of lung between the chest wall and heart. In this setting, heart sounds can be accentuated by having the patient lean forward and fully exhale prior to listening. Furthermore, in any patient with particularly "noisy" breath sounds, it may be helpful to ask them to hold their breath (if they're able) while you examine the heart.
    4. Rubs: These are uncommon sounds produced when the parietal and visceral pericardium become inflamed, generating a creaky-scratchy noise as they rub together. The classic rub is actually made up of three sounds, associated with atrial contraction, ventricular contraction, and ventricular filling. In reality, its rare to hear all 3 components (more commonly, 2 are apparent). They can be accentuated by listening when the patient sits up, leans forward and exhales, bringing the two layers in closer communication. I feel compelled to mention this finding only because a common short hand for reporting the results of the cardiac exam comments on the absence of "Gallops, murmurs, or rubs," implying (incorrectly) that rubs are a frequent finding.
    5. If a patient has an abnormal heart sound due to a structural defect that has been quantified by echocardiography, make sure that you compare your findings to those identified during the study. This is a great way of learning!
    6. Don't get frustrated! Auscultation is a difficult skill to "master" and we are all continually refining our techniques. Take your time. Make sure the room is quiet. Be patient. Ask for help frequently. Read about particular murmurs and their pathophysiology when you encounter them. A number of the more subtle findings (e.g. an S3 or S4) can be very difficult to identify when the patient is tachycardic, a not uncommon scenario as this is one of the compensatory mechanisms for dealing with the dysfunction that has generated these findings in the first place. Re-examination after the patient has made clinical improvement may be more revealing.

In general, many of the above techniques are not used when examining every patient. If the exam is normal, it would be neither efficient nor revealing to put a patient through all of these maneuvers. The goal is to have a "bag of skills" at your disposal that you can reach into and employ to better define abnormalities when they present themselves.

+ نوشته شده توسط دکتر شبنم مددی در دوشنبه پانزدهم مرداد 1386 و ساعت 12:59 |

I HAVE HEART FAILURE


My face turned blue!
My eyes black,
When the doctor explained
I have a lack
Of strength in the muscles
Of my beating heart
‘Heart failure’, he called it
It hit me like a dart.

There was damage done
To my heart
But I was determined to make
A fresh start
I sat down with a pen
And chalked out a plan
That’s when I believe
My recovery began.

I read all there was
About the condition,
Surfed the internet until
There was clarity of vision.
It was clear that pills
Are now the mainstay
But the future is bright
Research leading the way.

I stuck to my pills
Never missing a dose
Side-effects came along
Adding to my woes;
I was resolved though
Not to give in
Fight it, I would
Until I win.

I checked my weight
Every day of the week
Daily walked half a mile
Felt my condition peak;
Plenty of support came
From the hospital staff
I was happy as ever
Often having a laugh.

That feeling has remained
Over many years
I still enjoy
The occasional beers,
To my friends I say
Let’s get together
Make our minds one
Fight this forever;
It’s a common disease
With a decent solution
If we team up
The battle is won.

Let’s spread the word
That we are coming
To beat the odds
To dance and sing
To remind all
That life is pure
And that prevention
Is better than cure.

+ نوشته شده توسط دکتر شبنم مددی در دوشنبه چهارم تیر 1386 و ساعت 10:54 |

Integrating Complementary Medicine Into Cardiovascular Medicine

A Report of the American College of Cardiology Foundation Task Force on Clinical Expert Consensus Documents (Writing Committee to Develop an Expert Consensus Document on Complementary and Integrative Medicine)

John H.K. Vogel, MD, MACC, Chair, Writing Committee Member, Steven F. Bolling, MD, FACC, Writing Committee Member, Rebecca B. Costello, PhD, Writing Committee Member, Erminia M. Guarneri, MD, FACC, Writing Committee Member, Mitchell W. Krucoff, MD, FACC, FCCP, Writing Committee Member, John C. Longhurst, MD, PhD, FACC, Writing Committee Member, Brian Olshansky, MD, FACC, Writing Committee Member, Kenneth R. Pelletier, MD(hc), PhD, Writing Committee Member, Cynthia M. Tracy, MD, FACC, Writing Committee Member, Robert A. Vogel, MD, FACC, Writing Committee Member, Robert A. Vogel, MD, FACC, Chair, Task Force Member, Jonathan Abrams, MD, FACC, Task Force Member, Jeffrey L. Anderson, MD, FACC, Task Force Member, Eric R. Bates, MD, FACC, Task Force Member, Bruce R. Brodie, MD, FACC, Task Force Member*, Cindy L. Grines, MD, FACC, Task Force Member, Peter G. Danias, MD, PhD, FACC, Task Force Member*, Gabriel Gregoratos, MD, FACC, Task Force Member*, Mark A. Hlatky, MD, FACC, Task Force Member, Judith S. Hochman, MD, FACC, Task Force Member*, Sanjiv Kaul, MBBS, FACC, Task Force Member, Robert C. Lichtenberg, MD, FACC, Task Force Member, Jonathan R. Lindner, MD, FACC, Task Force Member, Robert A. O’Rourke, MD, FACC, Task Force Member{dagger}, Gerald M. Pohost, MD, FACC, Task Force Member, Richard S. Schofield, MD, FACC, Task Force Member, Samuel J. Shubrooks, MD, FACC, Task Force Member, Cynthia M. Tracy, MD, FACC, Task Force Member* and William L. Winters, Jr, MD, MACC, Task Force Member*



    Preamble

 
This document was commissioned by the American College of Cardiology Foundation (ACCF) Task Force on Clinical Expert Consensus Documents (CECDs) to provide a perspective on the current state of complementary, alternative, and integrative medical therapies specifically as they relate to cardiovascular diseases (CVDs). It is intended to inform practitioners, payers, and other interested parties of many evolving areas of clinical practice and/or technologies associated with this topic that are widely available or new to the practice community. Topics chosen for coverage by CECD are so designated because the evidence base and experience with technology or clinical practice are not considered sufficiently well developed to be evaluated by the formal American College of Cardiology/American Heart Association (ACC/AHA) Practice Guidelines process. Often, the topic is the subject of considerable ongoing investigation.

The Task Force on CECDs recognizes that considerable debate exists regarding the clinical utility of alternative medicine practices. By their nature, alternative medicine practices differ widely in their scientific support. Despite this varying evidence base, these practices are widely employed by patients, including those with CVD. Many practitioners are not familiar with many alternative medicine techniques. Thus, the reader should view this CECD as the best attempt of the ACCF to inform and guide clinical practice in an area where rigorous evidence is not yet available or the evidence to date is not widely accepted. Where feasible, CECDs include indications or contraindications. The ACC/AHA Practice Guidelines Committee may subsequently address some topics covered by CECDs.

The Task Force on Clinical Expert Consensus Documents makes every effort to avoid any actual or potential conflicts of interest that might arise as a result of an outside relationship or personal interest of a member of the writing panel. Specifically, all members of the writing panel are asked to provide disclosure statements of all such relationships that might be perceived as real or potential conflicts of interest. These statements are reviewed by the parent task force and updated as changes occur. Please see Appendix I for the relationship with industry information pertinent to this document.

Robert A. Vogel, MD, FACC Chair, ACCF Task Force on Clinical Expert Consensus Documents


    I. Introduction

 Top
 Preamble
 I. Introduction
 II. Nutrition and supplements
 III. Mind/body and placebo
 IV. Acupuncture
 V. Bioenergetics (energy...
 V. Spirituality/Intentionality
 Staff
 Appendix I
 Appendix II
 References

 
Organization of Committee and Evidence Review.   The Writing Committee consisted of acknowledged experts in the field of complementary, alternative, and integrative medicine. Both the academic and private sectors were represented. The document was reviewed by five official reviewers nominated by the ACCF, representatives from the American Association of Critical Care Nurses, AHA, American Nurses Association, Preventive Cardiovascular Nurses Association, and the Society of Thoracic Surgeons, as well as 20 content reviewers nominated by the Writing Committee. This document will be considered current until the Task Force on CECDs revises or withdraws it from publication.

Background.   Alternative medical therapies encompass a broad spectrum of practices and beliefs (1). From a historical standpoint, they may be defined as, "...practices that are not accepted as correct, proper, or appropriate or are not in conformity with the beliefs or standards of the dominant group of medical practitioners in a society" (2). The Institute of Medicine (IOM) has recently reviewed complementary and alternative medical practices in the U.S. from a general viewpoint (3). This document will focus on cardiac aspects of complementary medicine. From a functional standpoint, alternative (also known as "complementary" or "integrative") therapies may be defined as interventions neither taught widely in medical schools nor generally available in hospitals (4). Ernst et al. (5) contend that "complementary medical techniques [complement] mainstream medicine by contributing to a common whole, by satisfying a demand not met by orthodoxy or by diversifying the conceptual frameworks of medicine." The terminology currently in use to describe these practices remains controversial. Many commonly used labels (e.g., "alternative," "unconventional," or "unproven") are judgmental and may inhibit the collaborative inquiry and discourse necessary to distinguish useful from useless techniques (6). Complementary and alternative medicine (CAM) is the language currently used by the National Institutes of Health (NIH) to describe this field of inquiry. The term "integrative medicine" has been used with increased frequency. Several recently published studies and editorials wrestle with the challenges of properly labeling and describing this field of inquiry (7–12). Herbs, vitamins, and non-herbal dietary products, as well as therapies conducted around issues such as spirituality, bioenergetics (i.e., acupuncture and energy fields), and mind/body, are all considered to be forms of complementary, alternative, or integrative medicine.

Purpose of This CECD.   The purpose of this CECD is to put the emerging area of CAM treatment and investigation into focus in order to enable the physician to provide better patient care in a meaningful and safe manner. The document will be concerned with the most recent advances and utilization of CAMs and therapies in a traditional cardiovascular practice.

In 2000, nearly 50% of all Americans sought the help of an alternative health care practitioner. This represents over 600 million visits (13). Nearly $30 billion was spent in the year 2001 on CAM (13,14). Many CAM interventions, including numerous herbal supplements, have been employed in an attempt to treat CVD. Of prime importance is putting CAM into perspective with its potential benefits and knowledge of important interactions with traditional cardiovascular medicines. In response to an enormous involvement in CAM, medical facilities have developed specialized CAM centers to investigate the potential benefits and integrate those benefits into routine care and lifestyle management.

The most complete and comprehensive findings to date on Americans’ use of CAM were released on May 27, 2004, by the National Center for Complementary and Alternative Medicine (NCCAM) and the National Center for Health Statistics (NCHS, part of the Centers for Disease Control and Prevention) (15). The new data came from a detailed survey on CAM included for the first time in 2002 in the National Health Interview Survey (NHIS). The NHIS, a survey done annually by the NCHS, interviews people in tens of thousands of American households about their health- and illness-related experiences.

The findings are yielding (and will continue to yield, through future analyses) a wealth of information on who uses CAM, what they use, and why. In addition, researchers can examine CAM use as it relates to many other factors such as age, race/ethnicity, place of residence, income, educational level, marital status, health problems, and the practice of certain behaviors that impact health (such as smoking cigarettes or drinking alcohol).

The survey showed that a large percentage of American adults are using some form of CAM—36% (15). When prayer specifically for health reasons is included in the definition of CAM, that figure rises to 62%. Dr. Stephen E. Straus, NCCAM Director, said, "The survey data will provide new and more detailed information about CAM use and the characteristics of people who use CAM. One benefit will be to help us target NCCAM’s research, training, and outreach efforts, especially as we plan NCCAM’s second five years, 2005 through 2009."

There is little doubt that CAM represents a revolution within our health care delivery system. Nevertheless, our traditional views of the medical establishment do not fully support CAM. There is a lack of significant instruction of CAM in medical schools, there is a paucity of CAM in most major hospitals, and there is little solid research published in peer-reviewed journals. Compensation by insurance companies for CAM is also an issue.

A recent report of the IOM entitled "Complementary and Alternative Medicine in the U.S." (3) described and characterized CAM therapies used by the American public. Additionally, the IOM sought to identify major scientific policy and practice issues related to CAM research and to the translation of validated therapies into conventional practice. In short, the report recommended that the same principles and standards of evidence of treatment effectiveness apply to all treatments, whether currently labeled as conventional medicine or CAM. Although randomized controlled trials (RCTs) remain the "gold standard" of evidence for treatment efficacy, the IOM noted that other study designs can be used to provide information about the effectiveness when RCTs cannot be done or may not be generalizable to CAM practice. Other acceptable clinical research designs included: preference RCTs (trials that include both randomized and non-randomized treatment arms); observational and cohort studies; case-control studies; studies of bundles (combinations) of therapies; studies that specifically incorporate, measure, or account for placebo or expectation effects; and attribute-treatment interaction analyses. Prioritization criteria were also proposed to assist researchers regarding which CAM therapies might warrant further investigation.

Integrating CAM into medicine must be guided by compassion, but enhanced by science, and made meaningful through solid doctor-patient relationships. Most importantly, CAM involves a commitment to the core mission of caring for patients on a physical, mental, and spiritual level. This document attempts to enable us to fulfill these objectives. A glossary of terms is contained in Appendix II. For additional information on CAM, please refer to www.acc.org for Appendix III: Internet Sources for Complementary Medicine Information and Appendix IV: Review of the Literature for Cardiovascular-Related Integrative Medicine.


    II. Nutrition and supplements

 Top
 Preamble
 I. Introduction
 II. Nutrition and supplements
 III. Mind/body and placebo
 IV. Acupuncture
 V. Bioenergetics (energy...
 V. Spirituality/Intentionality
 Staff
 Appendix I
 Appendix II
 References

 
This section provides a discussion of general nutrition and dietary supplements, including vitamins, minerals, and herbs that are related to the prevention and reduction of risk of CVD. Please see Appendix V at www.acc.org for a sample dietary supplement intake form.

Nutrition.   Diet is a major determinant of cardiovascular health. General nutrition affects body weight, lipoproteins, blood pressure, blood glucose, endothelial function, inflammation, and coagulation. Dietary modification is an important component of primary and secondary prevention of coronary heart disease (CHD) and hypertension. The essentials of proper nutrition include appropriate caloric intake and consumption of the essential macronutrients (carbohydrate, proteins, and fats) and micronutrients (vitamins, minerals). Specific nutrients can either accelerate or retard the development of CVD.

Obesity
Obesity contributes to CHD, diabetes, and hypertension (16). Obesity (body mass index [BMI] greater than 30 kg/m2) increased 50% in this country from 1991 to 1998 (17). Almost one-third of Americans are now obese and another one-third are overweight (BMI 25 to 30 kg/m2). The major cause of this recent increase in obesity is a 150 to 200 kcal increase in our daily caloric intake, mainly from snacks (18). A decrease in physical activity associated with more television viewing has also contributed. A third factor has been an increase in sugar consumption, which now averages 150 lbs per person per year (19). The latter factor has also contributed to an increased prevalence of type 2 diabetes.

Weight loss is often an important part of the management of CHD, diabetes, and hypertension (20). Excess weight increases low-density lipoprotein (LDL) cholesterol, triglycerides, and markers of inflammation, such as C-reactive protein; and decreases high-density lipoprotein (HDL) cholesterol. Even modest weight reduction can improve these atherogenic markers (20). Weight loss only occurs when caloric intake is less than caloric expenditure. The daily caloric requirement for sedentary and physically active individuals, respectively, is about 12 and 15 kcal per lb of ideal weight. A 3,500 kcal deficit results in approximately 1 lb of weight loss. On the average, a deficit or excess of 500 calories a day brings about weight loss or gain at the rate of 1 lb a week. Increasing physical activity also results in weight loss. One mile walked or jogged is equivalent to about 100 calories burned. The most successful weight loss programs use calorie restriction, exercise, counseling, and group support.

Extremely low-carbohydrate or ketotic diets have become popular for weight loss (21). Some randomized trials have found that obese individuals lose more weight on low-carbohydrate diets than on low-fat diets, although the difference is not uniformly significant (22,23). The mechanisms by which extremely low-carbohydrate diets facilitate weight loss include osmotic diuresis, glycogen and associated water depletion, anorexia due to ketosis, and exclusion of foods. Although LDL cholesterol decreases during the weight loss phase of low-carbohydrate dieting, levels return to baseline in the long term. Two benefits of extremely low-carbohydrate diets are a decrease in triglycerides and an increase in insulin sensitivity. The long-term cardiovascular effects of low-carbohydrate/high-fat diets are unknown, but epidemiologic data suggest that they would increase atherosclerosis (24).

Extremely low-fat diets have been used to treat established coronary artery disease (CAD) (25). One small study has demonstrated modest CAD regression (26). Extremely low-fat diets are difficult to apply widely. Low-fat diets are consistent with the general epidemiologic finding that atherosclerosis prevalence correlates with saturated fat intake, and more specifically, with trans fat intake. However, low-fat diets can increase small LDL particles. These diets also do not recognize the cardiovascular benefits that can be derived from omega-3 fatty acids. They also may increase triglyceride levels and decrease insulin sensitivity.

Macronutrients
Fatty acids can be generally characterized into saturated, trans, monounsaturated, and polyunsaturated classes depending on the number and configuration of double bonds. Saturated and trans fatty acids increase serum LDL cholesterol and directly impair endothelial function (27,28). Trans fatty acids also decrease HDL cholesterol (29). Considerable data suggest an association between dietary saturated and trans fats and CHD (24). Dietary cholesterol is also associated with CHD, but elevations in serum cholesterol are individually variable with dietary intake. Monounsaturated fatty acids have neutral effects on serum LDL and HDL cholesterol (30). Polyunsaturated fatty acids reduce HDL cholesterol, but their use in randomized trials is associated with decreased cardiovascular events (27).

Omega-3 fatty acids have three to six double bonds, the first one occurring between the third and fourth carbon from the methyl end. The omega-3 fatty acids have triglyceride-reducing, membrane-stabilizing, antiplatelet, and anti-inflammatory properties (31). Omega-3 fatty acids include alpha-linolenic, eicosapentaenoic, and decosahexaenoic acids. The former is contained in plant oils, whereas the latter two are contained in fish oils. Prospective randomized trials have demonstrated that consuming plant and fish omega-3 fatty acids reduces cardiovascular events, sudden death, and overall mortality (32).

Carbohydrates include monosaccharides, such as sugars, oligosaccharides, and polysaccharides or starches. Complex carbohydrates consist of starches and indigestible fiber. Fiber adds bulk to food and slows carbohydrate digestion. Soluble fiber in the form of psyllium, guar gum, and oat bran reduces serum LDL cholesterol (33). The blood glucose raising property of a food per 50 g of carbohydrate and per portion is measured by its glycemic index and load, respectively (34). High glycemic load foods such as cookies, rice, and potatoes increase serum triglycerides, decrease insulin sensitivity, and probably facilitate obesity.

Dietary recommendations
There are two types of dietary guidelines. The first type recommends specific quantities of macronutrients, such as less than 200 mg of cholesterol per day and less than 7% of calories as saturated fat, as in the AHA Step 2 diet (1). A second type recommends consumption and exclusion of specific foods, often in combination. An example is the recommendation to eat stanol/sterol ester margarines, soy products, soluble fiber, and walnuts or almonds to lower LDL cholesterol (33,35,36). The latter specific food portfolio recommendation has been found to lower LDL cholesterol more (29%) than an AHA Step 2 approach (8%) (37). In general, diets containing unsaturated fats, whole grains, fruits, vegetables, fish, and moderate alcohol are optimal for preventing heart disease (38,39). In October 2000, the AHA revised its dietary guidelines for Americans (1). The new guidelines retain the principles of the Step 1 and Step 2 diet but place emphasis on foods and an overall eating pattern (see the following text) rather than on percentages of food components such as fat.

The National Cholesterol Education Program (NCEP) has issued new practice guidelines on the prevention and management of high cholesterol in adults (40). The Third Adult Treatment Panel (ATPP III) of the NCEP further modified its dietary recommendations to include a more intense and effective eating plan than previously advocated. The new Therapeutic Lifestyle Changes (TLC) treatment plan complements that of the AHA guidelines and recommends less than 7% of calories from saturated fat and less than 200 mg of dietary cholesterol daily. Total allowed fat ranges from 25% to 35% of total daily calories provided that saturated fats and trans fatty acids are kept low. The ATP III encourages the use of foods that contain plant stanols and sterols or are rich in soluble fiber, to achieve greater LDL cholesterol-lowering power.

Mediterranean diet
The prevalence of CVD is considerably less in Mediterranean and Pacific Rim countries than in the U.S. at equivalent cholesterol levels (41). Common to such societies is a diet high in fruits, vegetables, beans, whole-grain carbohydrates, nuts, fish, and monounsaturated and polyunsaturated oils. Dairy products are consumed in low-to-moderate amounts and little red meat is eaten. Alcohol is consumed in moderation. The Lyon Diet Heart Study (42,43) tested the effectiveness of a Mediterranean-type diet, modified by substitution of an alpha-linolenic acid-enriched canola oil margarine for olive oil, on cardiovascular risk after a first myocardial infarction. After an average follow-up of 46 months, subjects following the modified Mediterranean-style diet had 72% fewer cardiovascular events and 60% lower all-cause mortality. Findings from the Lyon Diet Study have been reproduced recently using an Indo-Mediterranean diet in subjects with CHD (44). The intervention diet recommending increased consumption of fruits, vegetables, nuts, whole grains, and mustard and soybean oils reduced cardiovascular events by 45% and sudden cardiac death by 66%. Additionally, recommendations to increase fruit, vegetables, and low-fat dairy product consumption has been found to lower blood pressure in the Dietary Approaches to Stop Hypertension (DASH) study (45).

Summary of general nutritional recommendations

• Achieve and maintain ideal body weight by limiting foods high in calories and low in nutrient density, including those high in sugar, such as soft drinks and candy.
Eat a variety of fruits, vegetables, legumes, nuts, soy products, low-fat dairy products, and whole grain breads, cereals, and pastas.
• Eat baked or broiled fish at least twice per week.
• Choose oils and margarines low in saturated and trans fat and high in omega-3 fat, such as canola, soybean, walnut, and flaxseed oils, including those fortified with stanols and sterols.
• Avoid foods high in saturated and trans fats, such as red meat, whole milk products, and pastries.
If you drink alcohol, limit consumption to no more than 2 drinks per day for a man or 1 drink per day for a woman.
• Eat less than 6 g of salt or less than 2,400 mg of sodium per day.
• Be physically active. Get 30 min of exercise daily.

Bioactive Components in Foods.   Food components recommended for lowering the risk of CVD include plant sterols, soluble fiber, omega-3 fatty acids, nuts, and soy. Additional foods, such as garlic and teas, and moderate alcohol use will be discussed.

Omega-3 fatty acids
Individual fatty acids have remarkably diverse effects on coronary risk factors and vascular biology (41–45). Omega-3 and -6 fatty acids are essential nutrients. Dietary fatty acids affect eicosanoid products (e.g., thromboxanes, leukotrienes, prostaglandins) responsible for vasoregulation, inflammation, and coagulation. Omega-3 fatty acids may also affect CHD outcomes by decreasing triglyceride levels, ventricular arrhythmias, decreasing fibrinogen levels and platelet counts, modestly reducing blood pressures, and decreasing cell proliferation. Improvements in arterial compliance and endothelial function have also been documented with fish oil, a major supply of dietary omega-3 fatty acids. There are changes in autonomic tone (as observed by improvement in heart rate variability measures) and in mood (depression) (46).

Epidemiologic studies (47–51) have generally shown an inverse correlation between consumption of fish or other sources of dietary omega-3 fatty acids and cardiovascular events. Conversely, other epidemiologic studies (52–55) have failed to document the benefits of fish consumption. Good plant sources of the 18 carbon omega-3 fatty acid, alpha-linolenic acid, include flaxseed, canola, pumpkin seed, walnut, and soybean oil.

Omega-3 fatty acids have been tested in several secondary prevention trials. Four prospective, controlled intervention trials with either oily fish (56) or omega-3 fatty acid capsules (42,57,58) have demonstrated reduced cardiovascular events. However, in the DART trial, fish consumption reduced overall mortality early after myocardial infarction (MI) (56), but was associated with higher risk over the subsequent three years of the study (53). The GISSI-Prevenzione study is the largest of the controlled trials investigating omega-3 fatty acid supplements (1 g per day) and CHD risk. In this trial, total mortality was reduced by 20% and sudden death by 45% in an intention-to-treat analysis. Mortality was reduced through a decreased incidence in sudden death.

Studies published to date are mixed regarding a role for dietary omega-3 fatty acids in the prevention of restenosis after percutaneous coronary angioplasty (59–62). They have not been found to reduce coronary atherosclerosis progression to a significant extent (58,63). One study demonstrated that occlusion of aortocoronary venous bypass grafts was reduced after one year by daily ingestion of 4 g of fish-oil concentrate (64).

Stanol/sterol esters
Plant sterols or phytosterols have been known to have a cholesterol-lowering effect since the 1950s. The esterification of plant stanols renders them soluble in dietary fat, an effective vehicle for delivering plant stanols and sterols to the site of cholesterol absorption in the small intestine. Commercially available margarines that provide 3.4 to 5.1 g a day of plant stanol esters can significantly reduce serum total and LDL cholesterol levels without affecting HDL cholesterol or triglycerides (65–67). A decrease in LDL cholesterol levels of 9% to 20% can be achieved with consumption of approximately 2 g per day of plant sterol esters (36). In a randomized, eight-week placebo-controlled trial in 167 subjects, using plant stanol esters incorporated into an oil-based margarine, there was a significant reduction in serum total (12%) and LDL (17%) cholesterol levels in individuals taking a stable dose of a statin drug (68). No trials have studied the effects of stanol/sterol esters on cardiovascular risk. Stanol and sterol esters should be avoided by the rare individual with familiar sitosterolemia.

Garlic (Allium sativum)
Garlic is an herb that has been used for thousands of years as a food and spice. Garlic potentially affects plasma lipids, fibrinolytic activity, platelet aggregation, blood pressure, and blood glucose (69). Various formulations/preparations of garlic and different study designs have led to contradictory results. The Agency for Healthcare Research and Quality (AHRQ) (70) noted on review of 36 randomized trials modest, short-term effects of garlic supplementation on lipid and antithrombotic factors. Various garlic preparations led to small but significant reductions in total cholesterol at one month and at three months (range of average pooled reductions 11.6 to 24.3 mg/dl). Eight six-month controlled trials showed no significant reductions. Effects on clinical outcomes are not established, and effects on glucose and blood pressure are none to minimal. A similar meta-analysis conducted by Stevinson et al. (71) that included 13 randomized, placebo-controlled trials concluded that the use of garlic for hypercholesterolemia was of questionable value. Superko and Krauss (72) demonstrated in a randomized, placebo controlled trial in hypercholesterolemic subjects that garlic has no effect on major plasma lipoproteins and that it does not impact HDL subclasses, Lp(a), apolipoprotein B, postprandial triglycerides, or LDL subclass distribution.

Soy
Soy-based foods have cholesterol-lowering, estrogenic, and antioxidant properties. The mechanism underlying the cholesterol-lowering effect of soy is likely multifactorial. Soy-based foods reduce lipid oxidation, promote increased vascular reactivity, and improve arterial compliance (73). Favorable effects of soy phytoestrogens on lipid profiles, vascular reactivity, thrombosis, and cellular proliferation have been reported (74). Dietary intake of foods containing phytoestrogens is associated with a favorable cardiovascular risk profile as was demonstrated in 939 postmenopausal women participating in the Framingham Off-Spring Study (75). The consumption of soy protein can improve lipid profiles in hypercholesterolemic individuals above a background NCEP Step I diet. Soy decreases LDL cholesterol more in hypercholesterolemic individuals. Soy supplementation may also increase the levels of HDL cholesterol regardless of whether an individual is hypercholesterolemic or not. A meta-analysis of 38 trials of soy protein demonstrated reductions in total cholesterol of 9.3%, LDL cholesterol of 12.9%, and triglyceride levels of 10.5%, accompanied by an increase of 2.5% in HDL cholesterol (76). However, more recent studies in postmenopausal women fail to show improvements in plasma lipids (77). A recent placebo-controlled study in 108 men and 105 postmenopausal women randomized to either soy protein isolate or casein placebo for three months demonstrated an increase in levels of Lp(a) on soy supplementation with no improvement in indices of arterial function (78). Extracts of soy isoflavones given to human subjects do not result in cardiovascular benefits except for improvements in systemic arterial compliance (79).

The clinical benefit of isoflavones is unclear. In light of the recent findings about estrogen from the Women’s Health Initiative, the U.S. Preventive Services Task Force has stated that the evidence is inconclusive to determine whether phytoestrogens, such as soy isoflavones, are effective for reducing the risk of CVD (80).

Soluble fiber
Soluble or viscous fibers, such as oat bran, psyllium, guar, and pectin, are thought to reduce heart disease by lowering total and LDL cholesterol levels without affecting serum triglycerides. Conversely, insoluble wheat fiber and cellulose have no cholesterol-lowering effects unless used in the diet to replace foods supplying saturated fats or cholesterol (81). Increasing dietary fiber has been recommended as a safe and practical approach to cholesterol reduction. Large epidemiologic studies (82–84) have demonstrated a reduced risk for MIs and death from CHD in both men and women who consume higher amounts of dietary fiber. These studies provide strong support linking dietary fiber intake to protection from CHD. These data are supported by numerous ecological, cohort, case-comparison, population-based, and, most recently, clinical trials demonstrating an inverse relationship between dietary fiber consumption and atherosclerotic CVD (85).

The hypocholesterolemic effects of psyllium (86), guar gum (87), and oat bran (88) are documented by meta-analyses (89). A meta-analysis of 67 controlled trials studying the cholesterol lowering effect of four types of soluble fiber (oat, psyllium, pectin, and guar gum) reported small but significant reductions in total cholesterol (1.7 mg/dl per g soluble fiber) and LDL (cholesterol (1.9 mg/dl per g soluble fiber) (81). Hypercholesterolemic subjects with initially higher cholesterol levels experienced the most significant reductions. Triglycerides and HDL cholesterol were not significantly influenced by soluble fiber. The magnitude of lipid lowering was found to be similar for oat, psyllium, or pectin-based fibers.

Because of the favorable effect of soluble fiber on LDL cholesterol levels, the ATP III panel recommends that the diet be enriched by foods that provide a total of at least 5 to 10 g of soluble fiber daily (90). Dietary fiber also reduces blood pressure, obesity, insulin resistance, and clotting factors—all independent risk factors for CHD (85).

Nuts
The few studies that have looked at the consumption of whole nuts in relation to CHD have reported a consistent and substantial protective effect. Three of the largest nutritional epidemiologic prospective studies evaluating multiple population groups, ages, races, and gender have found a consistent inverse relationship between nut consumption and coronary risk (91–93).

The improvement in serum lipids associated with the consumption of nuts does not explain the magnitude of the CHD risk reduction of approximately 40% to 50% found in the epidemiologic studies. Nuts, especially walnuts and almonds, are high in arginine, magnesium, folate, plant sterols, and soluble fiber. Some nuts contain high levels of omega-3 essential fatty acids (e.g., walnuts), and they are an excellent source of vitamin E. In a prospective study of 86,016 women between the ages of 34 to 59 years, without previously diagnosed CHD, eating 5 oz of nuts per week was associated with a relative risk (RR) of 0.66 (95% confidence interval [CI] 0.47 to 0.93, p for trend = 0.005) of coronary events adjusted for risk factors and independent of fiber, fruit, and vegetable supplements (92). Recent prospective data from the Physicians’ Health Study demonstrated consumption of nuts two or more times a week significantly reduced the risk of sudden cardiac death (RR) of 0.53 (95% CI 0.30 to 092, p for trend = 0.01) and a RR of 0.70 (95% CI 0.50 to 0.98, p for trend = 0.06) for total CHD deaths compared with men who rarely or never consumed nuts (93). The association between nut consumption and sudden cardiac death became stronger after adjustment for lifestyle, cardiac risk factors, and diet. Like some nuts, canola oil and flaxseed oil are the richest known source of alpha-linolenic acid, an omega-3 fatty acid.

Tea
Tea drinking appears to be protective against CHD in a number of epidemiologic studies (94–97). In the older cohort of the Rotterdam Study, an inverse association was demonstrated between tea drinking and advanced aortic atherosclerosis (98). Data from a more recent follow-up of the Rotterdam Study highlighted a strong inverse relation between tea intake (greater than 375 ml/day) and MI with the relation being stronger in women than in men. The inverse association with tea drinking was stronger for fatal events than for nonfatal events. For flavonoid (quercetin + kaempferol + myricetin) intake, a strong association with MI was observed only in women (99). Results are inconclusive for clinical and case control studies. However, a recent prospective cohort study of 1,900 patients hospitalized with an acute MI followed for 3.8 years found a significantly reduced hazard ratio for subsequent total and cardiovascular mortality of 0.56 (95% CI 0.37 to 0.84) for heavy tea drinkers (more than 14 cups/week) compared to non-tea drinkers (100). A recent clinical study has shown that consumption of black tea improves brachial artery flow-mediated dilation in patients with CAD (101). Despite the favorable epidemiology and mechanistic investigations, no studies have prospectively documented a reduction in cardiovascular risk with tea drinking.

Alcohol
Epidemiologic studies have shown that the incidence of MI, angina pectoris, and coronary-related deaths are inversely related to moderate alcohol intake, as defined by 1 to 3 drinks daily. Although many mechanisms for this effect have been suggested, the best documented effect is an increase in HDL cholesterol by alcohol (102). Recent studies have shown that moderate drinkers are less likely to suffer ischemic stroke (103,104), peripheral vascular disease (105), and death following an acute MI (106). Cooper et al. (107) found that light-to-moderate drinkers with left ventricular systolic dysfunction had fewer adverse outcomes. In the Framingham Heart Study, Walsh et al. (108) found that the incidence of congestive heart failure was lower in subjects who consumed moderate amounts of alcohol. Abramson et al. (109) were able to demonstrate that subjects who consumed moderate levels of alcohol had a significantly lower risk of developing heart failure.

Moderate consumption of alcohol-containing beverages does not appear to result in significant morbidity; however, heavy alcohol consumption can result in cardiomyopathy, hypertension, hemorrhagic stroke, cardiac arrhythmia, and sudden death. Alcohol ingestion poses such a number of health hazards with irresponsible consumption that the AHA recommends that physicians and patients discuss the adverse and potentially beneficial aspects of moderate drinking (39).

Overview of dietary supplements
The Dietary Supplement Health and Education Act (DSHEA) of 1994 defined dietary supplements as a product (other than tobacco) intended to supplement the diet for such ingredients as vitamins, minerals, herbs, or other botanicals, amino acids, and substances such as enzymes, organ tissues, glandulars, and metabolites. Whatever their form, the DSHEA places dietary supplements in a special category under the general umbrella of "foods," not drugs, and requires that every supplement be labeled a dietary supplement. The establishment of dietary supplements as foods limited the Food and Drug Administration (FDA)’s premarketing regulatory authority and placed the FDA in a reactive, postmarketing role. Thus, for the FDA to remove a supplement from the market it most prove that the supplement presents a significant or unreasonable risk of injury or illness when used as recommended on the label. Recently, the IOM has urged that the U.S. Congress and federal agencies, in conjunction with industry, research scientists, consumers, and other stakeholders, amend DSHEA and the current regulatory practices for dietary supplements in an effort to improve product consistency and reliability (IOM, 2005). Just prior to the release of the IOM report on Complementary and Alternative Medicine in the U.S., the FDA announced three major regulatory initiatives designed to further implement DSHEA (http://www.cfsan.fda.gov/~lrd/fr04119a.html, docket no. 2004N-0458). These initiatives serve to inform the dietary supplement industry on a regulatory strategy involving the monitoring and evaluation of product and ingredient safety, assurance of product quality via good manufacturing practice (CGMP regulations), and monitoring and evaluation of product labeling. At the same time these new initiatives will give consumers a higher level of assurance about the safety of dietary supplement products and the reliability of their labeling.

Vitamin and Mineral Supplements.   Antioxidant vitamins
Antioxidant therapies are potentially useful in preventing both atherosclerosis and its complications by retarding LDL oxidation and by inhibiting the proliferation of smooth muscle cells, platelet adhesion and aggregations, the expression and function of adhesion molecules, and the synthesis of leukotrienes (110). Antioxidants may improve endothelial function, reduce ischemia, and stabilize atherosclerotic plaques to prevent plaque rupture (110).

Vitamin E
Primary Prevention Trials. A potential benefit of vitamin E in CHD is suggested by two large prospective epidemiologic trials, which found lower event rates in subjects who took at least 100 units of vitamin E per day (111,112). However, 50 mg of vitamin E in the Alpha-Tocopherol, Beta-Carotene (ATBC) cancer prevention trial of male smokers did not decrease nonfatal MIs, and increased hemorrhagic stroke (113,114). Vitamin E use was not associated with decreased stroke in the Health Professionals Follow-Up Study (115), the Nurses Health Study (112), and the Iowa Women’s Health Study (116). Most recently, the Collaborative Group of the Primary Prevention Project (PPP) found no decrease in cardiovascular events in 4,495 subjects with one or more risk factors after 3.6 years of synthetic vitamin E (300 units) therapy compared to none (117). These data have been confirmed by a recent pooled analysis of nine cohort studies (Pooling Project of Cohort Studies on Diet and Coronary Disease) in 293,172 subjects free of CHD. A lower CHD risk at higher intake of dietary vitamin E was present when adjusted for age and energy intake. However, supplemental vitamin E intake was found not to be significantly related to a reduced risk of CHD (118).

Secondary Prevention Trials. Only one of several controlled trials of vitamin E has shown a reduction in some aspect of cardiovascular risk. In the Cambridge Heart Antioxidant Study (CHAOS) (119) vitamin E reduced the risk of nonfatal MI, but not of fatal MI. The Heart Outcomes Prevention Evaluation (HOPE) study found no effect of vitamin E for several of primary and secondary CVD end points, including disease progression monitored by carotid ultrasound (120). The GISSI-Prevenzione trial (42) failed to show benefit from vitamin E supplementation on CHD or stroke in almost 8,000 patients. The Vitamin E Atherosclerosis Prevention Study (VEAPS) provided additional evidence that vitamin E supplementation (400 units) did not reduce the progression of atherosclerosis as evaluated by change in intimal medial thickness (121). A meta-analysis of seven randomized trials of vitamin E (50 units to 800 units) in 81,788 patients confirmed that vitamin E did not reduce mortality, decrease cardiovascular death, or cerebrovascular accident (122). A more recent and larger (135,967 participants in 19 clinical trials) meta-analysis that considered the dose dependent effects of vitamin E supplementation noted that at high dosage (400 units/day or more) a pooled risk difference of 34 per 10,000 persons (95% CI 5 to 63 per 10,000 persons, p = 0.022). However, it is unclear whether the investigators isolated the effects of vitamin E from those of other supplements. Most of the evidence for an elevated mortality risk came from two trials that administered vitamin E together with beta-carotene. It is uncertain whether an increased risk for death from high-dose vitamin E based on this most recent analysis of RCTs exists (123).

Vitamin C
Primary Prevention. When examined individually, most observational and prospective cohort studies do not demonstrate a relationship between vitamin C intake and CVD (124,125) and there have been no RCTs specifically examining the effects of vitamin C supplementation on cardiovascular end points (115,126). In the Iowa Women’s Health Study, women in the top quintile of vitamin C intake versus the lowest quintile had a nonsignificant increased risk for CHD mortality and a borderline significant trend toward increased stroke (127). Long-term use of vitamin C in a large prospective investigation was not associated with a reduced risk of stroke, as well (115). However, a more recent analysis from the Nurses’ Health Study indicates that women in the highest quintile of intake for vitamin C (greater than 360 mg per day from diet and supplements) compared with the lowest quintile (less than or equal to 93 mg per day), had a 27% lower risk for CHD, and women taking supplemental vitamin C had a 28% lower risk of nonfatal MI and fatal CHD compared with women who took no vitamin C (128). In the recent pooled analysis from the Pooling Project of Cohort Studies on Diet and Coronary Disease (118), those subjects with higher supplemental vitamin C intake (greater than 700 mg/day) had a 25% reduced risk of CHD. Nevertheless, the current consensus does not find a value for supplemental vitamin C in preventing heart disease (129).

Beta-carotene
Trials of beta-carotene have demonstrated no cardiovascular benefit, and one demonstrated an adverse clinical outcome. An increased incidence of lung cancer and CVD mortality were observed in the ATBC cancer prevention study (130). Beta-carotene supplementation was also associated with a slight increase in the frequency of angina pectoris (131). A meta-analysis of eight trials evaluating beta-carotene in 138,113 patients revealed a small but significant increase in all-cause mortality and cardiovascular death (128). Thus, beta-carotene supplementation is discouraged (1).

Combination Vitamin Trials. The Heart Protection Study (HPS) randomized 20,536 subjects at high risk for CHD to 40 mg simvastatin daily or placebo and vitamin E (600 mg), vitamin C (250 mg), and beta-carotene (20 mg) or placebo. After 5.5 years of study, no benefit from combination vitamin therapy was evident (132). A small RCT, the HDL Cholesterol Atherosclerosis Treatment Study (HATS), found that vitamin C (1 g), vitamin E (800 units), beta-carotene (50 mg), and selenium (100 mcg) reduced the benefit of simvastatin plus niacin therapy on CAD progression and cardiovascular events (133) suggesting a potential drug/supplement interaction affecting the efficacy of statin therapies. Lack of benefit for combination vitamin E (400 units) and vitamin C (500 mg) was also documented in 423 postmenopausal women with CAD participating in the Women’s Angiographic Vitamin and Estrogen (WAVE) trial (134).

In contrast to the aforementioned negative trials, the Antioxidant Supplementation in Atherosclerosis Prevention (ASAP) study of 440 hypercholesterolemic patients randomized to vitamins E and C, reported that combination therapy decreased the rate of atherosclerosis progression (especially in men) over a six-year period as measured by carotid artery intima-media thickness. This study selected subjects with high oxidative stress and maximized absorption of the antioxidants by giving them with meals (135).

In summary, aside from the recent pooled analysis of vitamin C cohort studies, the consensus of antioxidant vitamin study results do not support a cardiovascular benefit related to the use of vitamins E and C and beta-carotene (129).

Folic acid, vitamin B6, and vitamin B12
Elevated homocysteine levels are associated with increased risk of coronary artery and vascular disease. The mechanisms by which elevated homocysteine impairs vascular function are not completely understood, but may involve the stimulation of vascular smooth muscle cell growth and collagen synthesis, oxidative-endothelial injury and dysfunction, lipid peroxidation and platelet activation, and hypercoagulability (136). Intakes of folate, vitamins B6, and B12 are inversely related to homocysteine levels as all three vitamins are directly involved in the metabolism of homocysteine. Beginning in 1996 and mandatory in 1998, the FDA issued a regulation requiring all enriched grain products be fortified with folic acid (140 mcg/100 g serving portion), primarily for the reduction of congenital neural tube defects. The fortification of enriched grain product with folic acid has been associated with an improvement in the folate status of middle-aged and older adults (137). In the Framingham Offspring Study cohort, mean homocysteine levels decreased from 10.1 to 9.4 µmol/l with the introduction of fortified products (138).

Initial retrospective case-control studies (139–141) and prospective studies (142–147) suggested an inverse relationship between homocysteine and CVD. A recent meta-analysis, combining 30 prospective and retrospective studies, concluded that elevated homocysteine is less strongly related to ischemic heart disease and stroke risk in healthy populations than has been suggested (148). A meta-analysis of 14 prospective cohort studies, using the inclusion criterion of time to first cardiac or cerebrovascular event, found that elevated homocysteine levels moderately increased the risk of a first cardiovascular event, regardless of age and duration of follow-up (149).

In secondary prevention studies, two nonrandomized trials in patients with vascular disease found an inverse relationship between the intake of folic acid and vitamin B6 and vascular events (150). One study conducted in open-label fashion in 593 patients with coronary artery disease on statin therapy showed no benefit of folic acid in reducing cardiovascular events despite an 18% lowering in homocysteine levels (151–153).

Most recently, a trial of folic acid (1 mg), vitamin B12 (400 units), and pyridoxine (B6) (10 mg) found a significantly reduced homocysteine levels, rate of restenosis, and need for revascularization in a group of 553 CAD patients at one year of follow-up (151,152). A similar RCT of 626 patients treated with B-vitamin therapy following coronary stenting procedures, however, found increased rates of restenosis, particularly in patients receiving bare-metal stents and major adverse cardiac events in the vitamin treated group after one year of follow-up. The rate of restenosis in the homocysteine-lowering group was 35% compared with 27% in the group receiving placebo (154). Although striking differences exist between the study populations, it raises the potential of possible harm from use of high-dose B-vitamins. Strong evidence for a benefit for B vitamins in CVD is pending; there remain a number of ongoing trials, including WACS, SEARCH, PACIFIC, NORVIT, and CHAOS-2 (155).

Minerals
Magnesium
Magnesium metabolism is involved in insulin sensitivity and blood pressure regulation, and magnesium deficiency is common in both diabetes and hypertension. The links among magnesium, diabetes, and hypertension suggest the possibility that magnesium can affect CVD (156,157). Magnesium depletion is associated with electrocardiographic changes, arrhythmias, and increased sensitivity to cardiac glycosides (158). Epidemiologic studies have suggested that ingesting hard water that contains magnesium, consuming a diet higher in magnesium, or using magnesium supplements decreases CVD (159). The Honolulu Heart Program found a 1.7- to 2.1-fold excess risk of CHD among those subjects in the lowest versus highest quintile of magnesium intake after 15 years of follow-up (160). Similarly, epidemiologic evidence suggests that magnesium may play a role in regulating blood pressure (161–165). A recent meta-analysis of 20 randomized studies including both normotensive and hypertensive subjects detected a dose-dependent blood pressure reduction with magnesium supplementation (166). The DASH intervention study demonstrated that a diet of fruits and vegetables, which increased magnesium intake from an average of 176 to 423 mg per day, significantly lowered blood pressure in adults who were not classified as hypertensive (167). However, studies in hypertensive patients have led to conflicting results. Ascherio et al. (168) found an inverse correlation between the intake of magnesium and the risk of stroke.

Magnesium intake has been found to be inversely associated with carotid artery thickness in women but not in men (163). Oral magnesium therapy (365 mg twice daily for 6 months) in 187 patients with CAD demonstrated a 14% improvement in exercise duration combined with a decrease in exercise-induced chest pain compared to no change in the placebo group (169). In patients with congestive heart failure (CHF), a population at high risk for magnesium deficiency, oral magnesium replacement decreases the frequency of ventricular arrhythmias (170).

Dietary intakes of magnesium are suboptimal in the U.S. as evidenced by recent NHANES survey intake data (171). Diets rich in magnesium and magnesium supplementation may be helpful in preventing CVD, especially hypertension.

Other bioactive supplements
Coenzyme Q10
Coenzyme Q10 (CoQ10) is involved in oxidative phosphorylation and the generation of adenosine triphosphate (ATP). The CoQ10 acts as a free radical scavenger and membrane stabilizer. There have been over 40 controlled trials of the clinical effect of CoQ10 on CVD, a majority of which show benefit in subjective (quality of life, decrease in hospitalizations) and objective (increased left ventricular ejection fraction, stroke index) parameters. A recent review (172) and meta-analysis (173) have shown benefit of CoQ10 as adjunctive treatment in patients with CHF. The largest trial to date was a one-year, placebo-controlled study of CoQ10 in 651 New York Heart Association (NYHA) functional class III or IV CHF patients (174). These investigators found a significant decrease (38% to 61%) in the number of hospitalizations, incidences of pulmonary edema, and episodes of cardiac asthma. No differences in death rates were documented. However, two of the most recent placebo-controlled trials found that the addition of 100 to 200 mg/day of oral CoQ10 to conventional medical therapy did not result in significant improvement in left ventricular ejection fraction, peak oxygen consumption, exercise performance, or quality of life in patients with advanced heart failure (175,176).

A mortality benefit for CoQ10 has not been established in contrast to angiotensin-converting enzyme inhibitors, beta-blockers, and aldosterone antagonists. Case reports associate CoQ10 therapy with decreased internation normalized ratio (INR) in patients taking warfarin (177); however, CoQ10 had no effect on the INR in patients on warfarin in a randomized, double-blind, placebo-controlled, crossover trial (178). Caution is advised if patients are taking CoQ10 and warfarin. The HMG-CoA reductase inhibitors may inhibit the natural synthesis of CoQ10, and reduced levels of CoQ10 have been documented in small controlled clinical trials in patients on statin therapies (179). Reduced levels of CoQ10 may place the patient at increased risk for myopathy (180–183); however, studies of CoQ10 for decreasing myalgias and myositis are not definitive. One unique formulation of CoQ10 has received FDA Orphan Drug status for treating mitochondrial disorders. The value of CoQ10 in CVD and with statin use has not been clearly established.

L-carnitine
In 1986, the FDA-approved L-carnitine for use in primary carnitine deficiency, which manifests as a disruption in the transport of free fatty acids across the mitochondrial membrane for energy production. In myopathic carnitine deficiency, muscle weakness is paramount (184). Convincing evidence is lacking for the use of carnitine in patients without carnitine deficiency undergoing cardiac surgery, in patients with angina pectoris, acute myocardial infarction, shock, and peripheral vascular disease (185). Urinary carnitine excretion is known to be increased in patients with heart failure (186). Several clinical RCTs have evaluated the addition of L-carnitine to standard medial therapy for heart failure with mixed results (187–189). Significant improvements in maximum exercise times and ejection fractions were reported by Mancini et al. (190) in 60 patients with NYHA functional class II or III CHF who were randomized either to propionyl-L-carnitine (50 mg t.i.d.) or placebo for 180 days. Two other small trials reported similar results, and one trial showed improvement at a higher dose. In a double-blind randomized trial in 155 patients with claudication, a significant improvement in exercise treadmill performance (54% increased walking time) and functional status was achieved with oral propionyl-L-carnitine 2 g/day for 6 months (191). Differences in effect may be due to the dose and formulation of carnitine. In contrast, the investigators of the Study on Propionyl-L-Carnitine in Chronic Heart Failure did not show improved exercise tolerance on L-carnitine supplementation (187).

At present, it is unclear whether L-carnitine provides any benefit beyond well-established therapies. A more definitive answer will come from the Carnitine Ecocardiografia Digitalizzata Infarto Miocardico (CEDIM-2) trial, which will assess the efficacy of L-carnitine in approximately 4,000 patients with acute MI over six months (192). Supplements containing D- or DL-carnitine, often present in over the counter preparations and dietary supplements, should not be substituted for L-carnitine. Carnitine frequently causes nausea, pyrosis, dyspepsia, and diarrhea. Concomitant use of carnitine with warfarin may potentiate warfarin’s anticoagulant effects.

L-arginine
L-arginine is the precursor of nitric oxide (NO) and has been shown to improve coronary and brachial artery endothelial function and reduce monocyte/endothelial cell adhesion (193–195). In patients with recurrent chest pain, improvements in coronary blood flow in response to acetylcholine have also been documented. In hypercholesterolemic subjects, dietary supplementation with L-arginine over two weeks has been shown to normalize the adhesiveness of mononuclear cells (196) and reduce platelet aggregability (197). However, in a study in 30 patients with CAD, supplemental L-arginine did not affect measures of NO bioactivity and NO-regulated markers of inflammation (198).

There are a few documented reports of adverse effects from oral use of L-arginine. Several patients with hepatic impairment and a recent history of spironolactone use were reported to develop severe hyperkalemia upon initiation or arginine hydrochloride for management of metabolic alkalosis (199). Oral L-arginine appears to have potential benefit in CHD, but hard evidence for its value is currently not available.

Herbal Preparations.   In the U.S. today, herbs may be marketed as dietary supplements providing their intended use is not to diagnose, treat, cure, or prevent disease. A number of approved drug substances have their origin in plants, such as digoxin, atropine, reserpine, and amiodarone. However, only a few herbal products available in the U.S. have been tested for cardiovascular purposes: hawthorn (heart failure and coronary insufficiency), garlic (atherosclerosis), ginkgo (arterial occlusive disease), and horse chestnut (chronic venous insufficiency) (200). Few U.S. products benefit from rigorous characterization and standardization necessary for clinical study.

Hawthorn (Crataegus)
Hawthorn has positive inotropic effects and is a peripheral vasodilator. It increases myocardial perfusion and stroke volume and reduces afterload. Antiarrhythmic effects have been reported in an ischemia-reperfusion model. Orally, hawthorn leaf extract has been used for CHF, cor pulmonale, ischemic heart disease, arrhythmias, blood pressure reduction, atherosclerosis, and cerebral insufficiency (200). Preparations made from flowers with leaves are sold as a prescription medication in parts of Europe and Asia. For example, in Germany, hawthorn can be prescribed for "mild cardiac insufficiency."

Several double-blind clinical studies of patients diagnosed with heart failure have shown objective improvement in cardiac performance using bicycle ergometry (201,202) or spiroergometry. In one study, hawthorn was found to be as effective as captopril in improving exercise tolerance. Based on ergometric performance parameters, the minimum effective daily dose of hawthorn extract is 300 mg. In most trials, the maximum benefit was seen after 6 to 8 weeks of therapy. Weikl et al. (203) demonstrated an improvement in exercise performance in 136 stage II CHF subjects receiving 160 mg hawthorn special extract WS 1442 (leaves and flowers). The efficacy and safety of hawthorn extract WS 1442 (900 and 1,800 mg) were evaluated in a 16-week randomized, controlled trial in 209 patients with NYHA functional class III heart failure. The investigators found a dose-dependent effect of WS 1442 on enhancing exercise capacity and reducing heart failure-related signs and symptoms. The preparation was shown to be well-tolerated and safe (204). A recent pharmacokinetic study was conducted in 8 healthy subjects consuming 0.25 mg digoxin alone or with hawthorn extract WS 1442, which demonstrated no significant alterations in the pharmacokinetic parameters for digoxin (205). Clinical trials are underway in the U.S. to evaluate further the safety and efficacy of hawthorn in patients with heart failure.

Hawthorn may offer some advantages over digoxin in mild heart failure. Compared to digitalis, hawthorn has a wider therapeutic range, lower risk in case of toxicity, has less of an arrhythmogenic potential, is safer to use in renal impairment, and can be safely used with diuretics and laxatives (200). However, hawthorn can markedly enhance the activity of digitalis (206), and care should be taken when combining it with beta-blockers and class III antiarrhythmics.

Ginkgo biloba (ginkgo leaf extract)
Ginkgo has been used for relief of intermittent claudication in patients with peripheral arterial occlusive disease. Ginkgo leaf, obtained from the Ginkgo biloba tree, and its extracts, or GBE, contain several bioactive constituents including flavonoids, terpenoids, and organic acids. As with other phytomedicines, several constituents of ginkgo extracts may contribute to its therapeutic effect. The mechanism of benefit is unknown. Two meta-analyses of the efficacy of ginkgo leaf extract for the treatment of intermittent claudication concluded that only modest benefits resulted from its use (207,208). In the meta-analysis performed by Pittler and Ernst (207), eight randomized, placebo-controlled, double-blind studies involving a total of 415 participants were evaluated. All of the studies used pain-free walking distance as the primary outcome measure. Several different formulations of ginkgo were used with doses ranging from 120 to 160 mg a day. The majority of trials lasted 24 weeks. Statistical pooling of the results from the eight trials showed that ginkgo significantly increased pain-free walking distance by 34 m. The clinical relevance of this increase is unclear.

Ginkgo is considered relatively safe, with a few documented adverse effects being mild gastrointestinal upset and headache. Ginkgo has been reported to increase the risk of bleeding. The concomitant use with aspirin, non-steroidal anti-inflammatory drugs (NSAIDs), and anticoagulants, such as warfarin and heparin, is not advised. Ginkgo can increase blood pressure in patients taking thiazide diuretics (209). Ginkgo does not appear to interact or adversely affect concomitant therapy with cardiac glycosides, and it appears to provide a small benefit in the treatment of peripheral arterial disease.

Horse chestnut (Aesculus hippocastanum)
Horse chestnut seed extract (HCSE) contains escin, a triterpene glycoside, and the toxic glycoside aesculin, a hydroxycoumarin derivative that is used to treat venous insufficiency (210). A systematic review of 14 randomized, placebo-controlled trials (a total of 1,071 subjects) was recently completed evaluating the efficacy of HCSE for the treatment of chronic venous insufficiency. The HCSE was found to be superior to placebo and as effective as compression therapy in decreasing lower leg volume and leg circumference at the calf and ankle. Symptoms such as leg pain, pruritus, and feeling of fatigue and tenseness were also reduced (211). Side effects are uncommon, but gastrointestinal irritation and toxic nephropathy may occur (212).

Contraindications to use include hypersensitivity to escin or horse chestnut and renal or hepatic impairment (213). At present there is no human drug interaction data available, but the increased risk of bleeding due to the naturally occurring coumarin constituents is possible. Also, HCSE has been suspected of causing hypoglycemic effects (209). The German Commission E has approved the use of HCSE in chronic venous insufficiency. It may be effective in that role.

Guggulipid (guggul gum)
Guggulipid has a long history of use in Ayurvedic medicine, which is an ancient Indian system that uses an integrated approach (diet, lifestyle, herbs, exercise, and meditation) to the prevention and treatment of illness by maintaining harmony among the mind, body, and forces of nature. Both guggul and its purified extracts have been used as hypolipidemic agents in patients with ischemic heart disease, hypercholesterolemia, and obesity (214). Clinical studies performed in India have demonstrated that 25 mg of guggulsterone extracts t.i.d. may be an effective treatment for hypercholesterolemia and hypertriglyceridemia. Reductions in total cholesterol levels of approximately 24% and reductions in triglycerides of 16% to 23% have been reported (215,216). The majority of these trials were not randomized.

In one randomized, controlled study of 125 hyperlipidemic patients, a standardized extract of guggulsterone was compared with clofibrate with mean reductions in serum cholesterol and triglycerides of 11% and 16%, respectively (217). In the first randomized, controlled trial of guggulipid outside of India, 103 healthy adults with hypercholesterolemia given 1,000 or 2,000 mg guggulipid containing 2.5% guggulsterones experienced no improvement in their lipid levels. A hypersensitivity rash was reported in a small number of subjects (218). Effects of guggulipids on HDL were mixed. A standard dose is 75 to 100 mg of guggulsterones daily divided into three doses. Guggulipids can cause gastrointestinal upset, headache, mild nausea, belching, hiccups (209), and rash (218). Concomitant oral administration can reduce propranolol and diltiazem bioavailability and might reduce the therapeutic effects of these drugs (219). Although in vitro studies suggest a plausible mechanism of action for guggulipid as a cholesterol-lowering agent (220), definitive safety and efficacy data are lacking.

Red yeast rice (Monascus purpureas)
Red yeast is the rice fermentation product of a mixture of several species of Monascus fungi, principally Monascus purpureas. It contains monacolin K (lovastatin, mevinolin) and other HMG-CoA reductase inhibiting compounds. Red yeast has been used to reduce cholesterol levels (221,222). In a 12-week placebo-controlled study conducted in the U.S. in 83 healthy subjects with hyperlipidemia (222), 2.4 g of red yeast rice significantly reduced total cholesterol by 16%, LDL cholesterol levels by 22%, and total triglycerides by 7% compared with placebo. No serious side effects were reported, but additional longer-term studies are needed.

Red yeast should be treated as an HMG-CoA reductase inhibitor, with all the possible side effects, drug interactions, and precautions associated with this class of drugs. Red yeast rice is no longer marketed with standardized lovastatin levels in U.S. owing to legal issues, and it is now sold without lovastatin levels declared. Because of the availability of statins, its use is not recommended.

Policosanol
Policosanol is a sugar cane extract that contains a mixture of aliphatic alcohols. Lipid-lowering effects of policosanol have been shown in a variety of animal species; however, little is known about its mechanism of action or its exact composition. Over 1,000 subjects have been studied for periods of six weeks to one year in 15 randomized, placebo-controlled trials using policosanol (5 to 20 mg per day) for lipid lowering. At doses of 10 to 20 mg per day, significant reductions were observed for total cholesterol (17% to 21%) and LDL cholesterol (21% to 29%) with increases in HDL cholesterol (8% to 15%) (223). There are no data on efficacy determined by clinical end points. Although policosanol appears to be well-tolerated, caution should be exercised when combining policosanol with antiplatelet or anticoagulant agents, including garlic, ginkgo, and high doses of vitamin E (224), as policosanol has been shown to inhibit platelet aggregation in both healthy and diseased patients (225). The majority of the existing studies have been conducted in Cuba, and independent verification is needed before its use can be recommended.

Ephedra (Ma huang)
Ephedra, together with its principal alkaloid ephedrine, was one of the first of the Chinese herbal medicines to be used in Western medicine. Ephedra is used to treat bronchospasm, asthma, bronchitis, allergic disorders, and nasal congestion, or as a central nervous system stimulant (209). Ephedrine acts by stimulating alpha, beta-1, and -2 adrenergic receptors, and indirectly by releasing norepinephrine from body stores. The cardiovascular effects of ephedrine last 10 times longer than those of epinephrine and consist primarily of increased heart rate and peripheral vascular resistance. Ephedrine and related alkaloids have been associated with adverse cardiovascular events, including acute MI, severe hypertension, myocarditis, and lethal cardiac arrhythmias. Dietary supplements that contain ephedra alkaloids were widely promoted and used in the U.S. for weight loss and increased energy. Their use was associated with a number of adverse events, including MI, stroke, arrhythmias, and death (226), and in December 2003 the FDA announced a ban on the sale of ephedra products in the U.S. Of developing concern is the herbal Citrus aurantium, or bitter orange, which contains similar stimulant amines as ephedra and is now being marketed in weight loss products. The Joint National Committee (JNC)-7 guidelines list it as a possible cause of resistant hypertension (227). One case report of acute MI has been associated with its use as contained in a multi-ingredient weight loss product. Table 1 provides a list of herbs containing stimulants.


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Table 1. Herbs Containing Stimulants

 
Oleander (Nerium oleander/Thevetia peruviana)
Oral oleander was once used for treating mild heart failure, but is now considered too dangerous for medicinal use (209). All parts of the oleander plant contain the cardiac glycosides oleandrin, oleandroside, nerioside, and digitoxigenin, which have positive inotropic and negative chronotropic actions. Oleander poisoning resembles digitalis toxicity, with predominant symptoms of nausea and vomiting, and cardiac toxicity with conduction delays that may last up to three to six days. Reports suggest that yellow oleander toxicity can be reversed by infusion of antidigoxin Fab fragments. Use of this herb is contraindicated in patients on digoxin and should not be used with other cardiac glycoside-containing herbs (209). In view of the availability of digoxin, its use is not recommended.

Herb-Drug Interactions: What We Need to Know.   The increased use of herbal and phytomedicines by both health professionals and consumers has raised questions about herb-supplement and herb-drug interactions because herbs are making a resurgence in the U.S. market. Kaufman et al. (228) described the patterns of prescription and nonprescription drugs in the U.S. population, noting that:

• 14% of the population took supplements and herbals over the prior week
• 16% of prescription drug users also took herbs or supplements
• 40% of the population used one or more mineral or vitamin supplements

In 1997, an estimated 15 million adults took prescription medications along with herbal remedies and/or high dose vitamins (229). These individuals are potentially at risk for adverse herb-supplement or herb-drug interactions. The following tables delineate possible drug interactions with herbal or botanical products. Table 2 lists herbs that may potentiate the effect of cardiac glycosides and antiarrhythmics. Table 3 lists the potential adverse effects of herbal remedies and their major constituents. Table 4 lists potential interactions between some herbal medicinal products and cardiovascular drugs. Table 5 lists the interference of herbal products in therapeutic drug monitoring.


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Table 2. Loss of Serum Potassium, Which May Potentiate the Effects of Cardiac Glycosides and Antiarrhythmics

 

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Table 3. Potential Adverse Effects of Herbal Remedies and Their Major Constituents*

 

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Table 4. Potential Interactions* Between Some Herbal Medicinal Products and Cardiovascular Drugs

 

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Table 5. Laboratory Analysis and Treatment Guidelines for Specific Herbal Preparation and Their Critical Contaminants

 
Summary of recommendations for bioactive food components and dietary supplements
Supplements/interventions that can be recommended

1 Omega-3 supplements 1 to 2 g per day if insufficient omega-3 intake from fish
2 Stanol/sterol ester margarines (2 g per day)
3 Soluble fiber (5 to 20 g per day)
4 Soy foods and soy protein (equivalent to 25 g soy protein daily

Possibly useful for indications noted

1 Moderate alcohol intake (1/2 to 2 drinks per day—a drink is 5 oz of wine, 12 oz of beer or 1.5 oz of 80 proof whiskey) for cardiovascular risk reduction
2 Tea (1 to 2 cups daily) for cardiovascular risk reduction
3 Recommended dietary intake of magnesium (RDA adult men 420 mg; women 320 mg daily). Consider supplementation for those at risk (poor dietary intake or conditions that increase renal magnesium losses).
4 Folic acid supplementation (plus vitamins B6 and B12) if homocysteine is elevated.

Cannot recommend at this time (for some individuals in some situations, probably not harmful)

1 Folic acid supplementation if homocysteine is not elevated for vascular disease
2 Garlic for lipid lowering
3 Soy isoflavones for lipid lowering
4 L-arginine supplementation for nutritional support
5 CoQ10 for nutritional support
6 Hawthorn for mild heart failure
7 Ginkgo biloba for peripheral vascular disease
8 HCSE for peripheral vascular disease

Supplements/interventions not recommended (possibly harmful)

1 Levels exceeding the upper tolerable limits (IOM, 2001) for vitamins C (2,000 mg/day) and E (1,000 mg/day); and beta-carotene supplementation not recommended; limit to food sources.
2 Ephedra, oleander, and other herbs/botanicals with well-defined contraindications to cardiovascular drug and/or CVD conditions.

Related Alternative Therapy.   Chelation
Chelation therapy is a form of alternative medicine utilized in the treatment of atherosclerotic CVD. Over 800,000 patient visits were made for chelation therapy in the U.S. in 1997. Chelation therapy consists of a series of intravenous infusions containing disodium ethylene diamine tetraacetic acid (EDTA) in combination with other substances, such as vitamins. Use of EDTA has been found to be effective in chelating and removing toxic heavy metals from the blood (238). It is purported that the removal of polyvalent cations, notably calcium ions, can lead to the regression of atherosclerotic plaques by a yet undefined mechanism. Use of EDTA chelation therapy is FDA-approved in treating lead poisoning and toxicity from other heavy metals. The FDA has not approved the use of chelation therapy to treat CAD.

The bulk of the evidence supporting the use of EDTA chelation therapy is in the form of case reports and case series. A systematic review on chelation therapy for peripheral arterial occlusive disease has shown that chelation therapy is not superior to placebo and is associated with considerable risks (239). At present, the benefit of chelation therapy remains controversial as highlighted by a recent Cochrane Review (240) of five randomized controlled studies in small numbers of subjects evaluating outcomes of disease severity and subjective measures of improvement.

The ACC position statement reapproved in 1990 states "that there is insufficient scientific evidence to justify the application of chelation therapy for atherosclerosis on a clinical basis. At the present time, therefore, chelation therapy for atherosclerosis should be applied only under an investigation protocol."

In an effort to advance the evidence base for the use of chelation therapy, the NCCAM and the National Heart, Lung, and Blood Institute (NHLBI) have launched the first large-scale clinical trial to determine the safety and efficacy of EDTA chelation therapy in individuals with coronary artery disease. The five-year Trial to Assess Chelation Therapy (TACT) will involve over 2,300 patients at more than 100 research sites across the country. The study will determine whether EDTA chelation and/or high-dose vitamin supplements improve event-free survival, whether these are safe for use, improve the quality of life, and are cost-effective. The primary end point in the trial will be a composite of death, MI, stroke, hospitalization for angina, and coronary revascularization.


    III. Mind/body and placebo

 Top
 Preamble
 I. Introduction
 II. Nutrition and supplements
 III. Mind/body and placebo
 IV. Acupuncture
 V. Bioenergetics (energy...
 V. Spirituality/Intentionality
 Staff
 Appendix I
 Appendix II
 References

 
The Mind/Body Relationship and its Correlation to CVD.   Reviewing the mind/body relationship and its clinical correlates to CVD is a union of both the social and biological. Although physicians easily grasp measurable physiological phenomena (e.g., the concept of acid production, blood pressure elevation, and the angiographic narrowing of a coronary artery), it is much more difficult to understand social relationships, isolation, anger, depression, and their manifestation in disease. Sterling and Eyer (241) have illustrated how the development of modern society is associated with a disruption of human relationships. These disruptions cause chronic psychological arousal, which is defined as stress. The body’s physiological mechanisms are altered by chronic psychological arousal and this leads to pathology and disease.

The function of arousal is to help the individual "cope" with environmental demands. Coping may be defined as "contending" or "struggling." This behavior frequently requires excess physical or emotional energy to deal with a difficult situation. Studies have shown that patients entering a hospital for diagnostic tests have elevated norepinephrine, epinephrine, cortisol, and growth hormone levels (242–245). Because these patients have little control over their situation, there is little effective coping behavior. Under these circumstances, in which limited control over the environment is possible, the stress hormones are maximized. Likewise, students during examination periods demonstrate a rise in cortisol, epinephrine, serum blood sugar, cholesterol, and blood pressure levels. Under exam stress, these same students exhibit a decline in white blood cells (242,243,245–249). This drop in white blood cells in part explains the high rate of physical illness under stressful situations. Tax accountants have been shown to have large increases in serum cholesterol (independent of diet) and a decrease in blood clotting time during tax season (250). Arousal, and as a consequence stress, will be high not only among individuals with little control over life circumstances, but also among individuals with a high demand for performance. Arousal that results from a lack of control will frequently manifest with anger or fear. Although high-demand situations are frequently accompanied by anxiety, they may result in extreme pleasure if the coping style is successful. However, this success in the end does not mean that the metabolic costs to the body are less.

Impact of Stress on CVD Risk Factors.   In the Framingham Heart Study (251), hypertension was involved in over 80% of all cardiovascular deaths. In addition, hypertension was at least twice as strong a predictor of death as smoking or elevated blood cholesterol. Over 50 million Americans are currently hypertensive. In about 5%, a specific pathology such as a renal artery stenosis can be identified. In the remaining 95%, the blood pressure increase is not attributed to a specific pathology. Different mechanisms can contribute to the development of hypertension. Acute arousal leads to sympathetic stimulation and an increase in cardiac output. When arousal is maintained for long periods of time, the elevation in blood pressure remains even if the inciting stimulus is removed. At this stage, the hypertension is not sustained by increased cardiac output but by increased vascular resistance.

Stress may lead to hypertension through repeated blood pressure elevations and by increasing the amount of vasoconstricting hormones. Stress factors leading to hypertension include job strain, social environment, emotional stress, and white coat hypertension. Overall, studies conclude that, although stress does not directly cause hypertension, it can clearly affect its development. Stress leads to sympathetic nervous system activation with excessive amounts of cortisol, epinephrine, and aldosterone. The combination of increased cardiac output and vasoconstriction may transiently raise blood pressure. Feelings of frustration, exhaustion, and helplessness can activate the pituitary and adrenocortical hormones. Non-pharmacological treatments to manage stress such as meditation, acupuncture, biofeedback, and music therapy have been found to be effective in decreasing blood pressure and the development of hypertension (252).

Although not a substitute for pharmacological therapy, certain non-drug therapies offer support for individuals with hypertension. Steelman (253) studied the effect of tranquil music on blood pressure and anxiety in surgery patients. The experimental group listened to music during the intraoperative period. The control group received usual care. Music appeared to reduce blood pressure in the experimental group. Pender (254) studied the effect of progressive muscle relaxation (PMR) training in hypertensive patients. Those individuals who received PMR training reported less anxiety. Decreased anxiety correlated with decreased systolic blood pressure. Older African-Americans who were taught the transcendental meditation technique had a significant reduction in diastolic and systolic blood pressure (255).

Diabetes, like hypertension, remains an important risk factor for the development of CVD. Chronic arousal can contribute to diabetes in two ways. With arousal, there is an increase in catabolic hormones, most notably epinephrine, cortisol, growth hormone, and glucagon. These hormones antagonize the actions of insulin by mobilizing glucose, fatty acids, and protein breakdown. Furthermore, glucagon and norepinephrine act to suppress the secretion of insulin. The resulting hyperglycemia, hyperinsulinemia, and hyperlipidemia all accelerate pathology.

In addition to hypertension and diabetes mellitus, studies linking stress and cholesterol date back to the 1950s. These older studies suggest that stress associated with time pressure, repetitive assembly line work, and increased responsibility may raise serum cholesterol (250,256,257). Both cortisol and epinephrine have been linked in humans to serum cholesterol elevation. In many animal experiments, stress has accelerated atherosclerosis. Rabbits on a high-fat diet when stressed with electrical stimulation over 10 months have an increased number of atheromas in comparison with non-stressed controls. The administration of epinephrine to cholesterol-fed rabbits further intensifies lipid infiltration of the aortic intima. As mentioned previously, accountants show continuous monthly rises in cholesterol, despite maintaining a constant diet, which peaks at the end of the fiscal year (250).

Depression and the Development of CVD.   A growing body of evidence suggests that depression may predispose to cardiovascular events (258). Individuals with mental stress during daily life have twice the risk of myocardial ischemia. In addition, those patients with post-MI depression have higher mortality rates than non-depressed controls. Depression is common after acute MI and is associated with an increased risk of mortality for at least 18 months. One reason for this higher morbidity and mortality within the first few months following an MI is that depressed patients are less likely to follow recommendations to reduce further cardiac events.

Ziegelstein et al. (259) found that patients who were identified with at least mild-to-moderate depression or major depression reported lower adherence to a low-fat diet, regular exercise, and stress management. Individuals with major depression and/or dysthymia reported taking their medication less often than prescribed. Those findings, in part, explain why depression in the hospital is related to long-term prognosis in patients recovering from an MI.

In addition, acute MI patients with unstable angina who were identified as depressed in the hospital were more likely to experience cardiac death or nonfatal MI than other patients (259). The impact of depression on 430 patients with unstable angina (41.4% depressed) remained after controlling for other prognostic factors such as left ventricular ejection fraction and number of diseased vessels (260).

In addition to depression, other research suggests that social support may influence prognosis following an acute MI. In a study of 887 post-MI patients, Frasure-Smith et al. (261) found that 32% had mild-to-moderate depression. After one year, follow-up interviews were conducted and demonstrated that elevated Beck depression scores were related to cardiac mortality. The relationship between depression and cardiac mortality decreased with increasing support. Furthermore, of those one-year survivors who were depressed at baseline, higher baseline social support was related to greater than expected improvement in depression symptoms.

The Enhancing Recovery in Coronary Heart Disease Patients Study (ENRICHD) was sponsored by the NHLBI. The study enrolled 2,481 patients at 73 hospitals within 28 days of an MI; participants had major or minor depression, low social support, or both. Patients were assigned to either a "treatment" or "usual medical care" group (262). Cognitive therapy was provided by the treatment group for six months. At the end of six months, patients in the treatment group scored significantly better on the Hamilton depression (57% reduction in depression versus 47% reduction in the usual medical care group) scale. Likewise, patients low in social support demonstrated a 27% improvement in this parameter versus 18% for the usual care group. However, despite the treatment groups’ improvement in depression and social isolation, there was no improvement in heart disease survival.

Increased use of selective serotonin reuptake inhibitors (SSRIs) and their demonstrated safety in patients with CVD raises the question of whether early pharmaceutical treatment for depression in cardiac patients will improve clinical outcome (263–265). Yet despite this low-risk profile, very little research exists regarding the benefit of SSRIs in patients with CVD. The Sertraline Antidepressant Heart Randomized Trial (SADHART) has evaluated the efficacy and safety of sertraline therapy in patients with acute heart disease without evidence of statistically significant benefit (266). Until meaningful data are obtained, the use of antidepressants in cardiac patients requires a weighing of the risks versus potential benefit.

In addition to affecting lipids, enhancing weight loss and improving exercise tolerance, cardiac rehabilitation provides emotional support, reduces depression, improves quality of life scores, and decreases mortality by 25% (267–271). Such programs serve as the logical place to screen cardiac patients for psychosocial risk factors such as depression and anxiety. Once identified, appropriate intervention can be initiated.

In conclusion, although post-MI depression is a predictor of one-year cardiac mortality, high levels of social support appear to decrease the magnitude of depression. High levels of social support also predict improvements in depression symptoms over the first post-MI year in those individuals with baseline depression.

Summary of recommendations for mind/body relationship
Several complementary and alternative medicine techniques have been used as adjuncts to traditional therapies in the treatment of CVD as follows:

a Coronary artery disease
1 Stress reduction
2 Meditation
3 Group support

 
b Arrhythmias
1 Biofeedback
2 Stress management
3 Group support

 
c Pre-surgery
1 Guided imagery

 
d Cholesterol
1 Stress management
2 Meditation

 
e Congestive heart failure
1 Biofeedback
2 Group support

 
f Hypertension
1 Group support
2 Biofeedback
3 Meditation
4 Pet acquisition (272–277)

 

Placebo.   "Placebo," Latin for "I shall please," can be derived from a device, a drug, or complementary medicine modalities. A placebo is not necessarily a sham therapy but a potential response due to an interaction between the intent of the healer and the expectations of the patient. The response can be powerful, but the longevity of the response can vary by condition and type of placebo. Several reports in cardiology—BHAT (278), CHF-STAT trial (279), and the Coronary Drug Project (280)—have shown a remarkably strong effect regarding compliance with placebo. The reduction in mortality for those who take their placebo compared to those who are non-compliant is highly significant, but the mechanism (280) is unknown.

Shapiro (281) indicated that the physician was important in the dyadic dance of healing and proposed that perhaps doctors, independent of what they did, were actually potent placebos in their own right. He and others enumerated a number of specific variables that might endow some physicians with particular curative manna: enthusiasm for treatment, apparent warm feelings for the patient, confidence, and authority. Some physicians may be able to exhibit a placebo effect more intensely than others, but the mechanism for this and the extent of it are not understood.

The placebo effect has been described as a nonspecific psychological or psychophysiologic therapeutic effect, but this may not be correct and the response may be a crucial synergistic adjunct to any cardiovascular therapy. Placebos can elicit a real and substantial response, the extent of which is related to the type of the placebo, the condition being treated, and the response being elicited. No multivariate analysis has detected which specific patient characteristics are most associated with a profound placebo effect. The placebo response in major depression (282) ranges from 32% to 70% and can equal that of a drug intervention. After all, what occurs during psychotherapy is a form of placebo response. The importance of understanding the mechanisms responsible for the placebo response is crucial to understanding the basic nature of healing (283). Expectancy, beliefs, anxiety, hope, trust, and intent can alter outcomes regarding disease (284).

The placebo response may involve disease expression, specific neuroendocrine, neuronal and immune intermediary pathways, neuropeptides, enkephalins, endorphins, cholecystokinin, neurohormones (including glucocorticoids and prolactin), neurotransmitters (including 5-hydroxytryptamine, norepinephrine, dopamine), and other messengers such as nitric acid and prostaglandins. The power of expectancy of improvement was emphasized by controlled trials of arthroscopic surgery and of neurosurgery. Osteoarthritis of the knee responds as well to arthroscopic debridement, arthroscopic lavage, and placebo surgery. Similarly, sham neurosurgery improved Parkinson patients as well as cell implants and sham cardiovascular surgery improves patient chest pain as often as 90% of the time (285). It is, however, difficult to quantitate the benefit of either the placebo effect or sham procedure.

Hrobjartsson and Gotzsche (286) suggest there is little evidence that placebos in specific conditions, comparing no therapy to placebo therapy, had powerful clinical effects. Yet this is likely disease specific as many placebo-controlled studies showed enormous benefits of the placebo (282). Another form of the placebo response is relief to a patient when serious disease is excluded. Patients who have an evaluation ("tests") for atypical chest pain are less likely to be disabled than those who do not have such an evaluation (287).


    IV. Acupuncture

 Top
 Preamble
 I. Introduction
 II. Nutrition and supplements
 III. Mind/body and placebo
 IV. Acupuncture
 V. Bioenergetics (energy...
 V. Spirituality/Intentionality
 Staff
 Appendix I
 Appendix II
 References

 
Acupuncture has gained increasing acceptance by the lay public, partly as a result of increasing communication between the U.S. and China since the early 1970s (1,288). Texts on acupuncture date back to 206 BC, although the Yellow Emperor, Huang Di, the originator of traditional Chinese medicine lived in 2,697 BC (289). Acupuncture has been used for a wide variety of conditions, but it is most accepted for treatment of pain (290–293). Increasing evidence suggests that acupuncture may also be useful in treating patients with neurological disease, including disorders of the autonomic nervous system, hypertension, and other forms of CVD. The World Health Organization (WHO) has noted that acute infection and inflammation, dysfunction of autonomic nervous system, pain, and peripheral and central neurological diseases each represent conditions for which acupuncture may be indicated (291,292,294). The mechanism by which acupuncture is believed to benefit the subject is through its ability to modulate neural activity in several regions of the brain and thus reduce sympathetic outflow to the heart and vascular system (295).

There are four areas of CVD for which acupuncture eventually may be indicated. These include ischemic CVD, hypertension, heart failure, and arrhythmias. Studies from several groups, including Ballegaard (296) and Richter (297), have examined the role of acupuncture in treatment of patients with stable angina. Ballegaard, in an initial study, was unable to document a decrease in angina in humans as measured by a decrease in the rate of anginal attacks, consumption of nitroglycerin or exercise tolerance, comparing true acupuncture to sham acupuncture (296,298); the group concluded that true acupuncture cannot be distinguished from sham acupuncture in which needles were placed outside traditional meridians. Two other studies by the same group showed an acupuncture-related improvement in exercise capacity and rate-pressure product (299), particularly when acupuncture reduces sympathetic neural outflow (298). Separately, Richter (297) observed that acupuncture exerted a beneficial effect in patients with severe stable angina who had been aggressively treated with medical therapy. Manual acupuncture reduced the number of anginal attacks per week, the severity of chest pain, electrocardiographic evidence of myocardial ischemia, and increased the workload required to provoke angina in patients with CAD and stable angina (297). The latter study used a tablet placebo control. These studies involved small numbers of patients, were unblinded, and did not use the most appropriate sham controls.

Prolonged peripheral vasodilation, measured by peripheral thermography, occurs following electroacupuncture (297). Acupuncture or its non-invasive surrogate, transcutaneous electrical nerve stimulation (TENS), appears to influence peripheral blood flow in patients with Raynaud’s syndrome (300), skin flap survival in experimental preparations (301,302), and skin temperature in patients with polyneuropathy (303). The primary form of Raynaud’s cold-induced vasoconstriction, assessed by Doppler flowmetry and clinical symptoms, is reduced by acupuncture compared to sham treatment (300). Secondary forms of Raynaud’s appear to be less influenced by acupuncture. Survival of ischemic musculocutaneous skin flaps is increased in experimental preparations treated with either manual or electroacupuncture (301,302). Similarly, patients undergoing reconstructive surgery who are treated with TENS experience improved microvascular flow and reduced edema and capillary stasis relative to placebo TENS (304). Low-frequency TENS leads to a prolonged increase in skin temperature in patients with diabetic polyneuropathy (303). Most studies on the peripheral circulatory effects of acupuncture are small and were not blinded; confirmation of their observations is needed.

Several small trials suggest that hypertension may be improved by acupuncture (305–310). The magnitude of the effect of acupuncture on blood pressure in patients with hypertension is small but significant; reductions of 5 to 10 mm Hg have been noted. These and other small studies from outside the U.S. have led to funding of at least two ongoing clinical trials by the NCCAM to test the hypothesis that acupuncture can lower blood pressure in patients with hypertension.

Experimental studies indicate that acupuncture reduces demand-induced myocardial ischemia in felines (311), catecholamine- or stress-induced hypertension (312–315), or genetically associated hypertension (316). These studies also demonstrate that acupuncture limits myocardial ischemia by reducing myocardial oxygen demand rather than by increasing coronary blood flow in a feline model (311). Acupuncture also can inhibit ventricular extrasystoles induced by stimulating the hypothalamus (317), paraventricular nucleus (317) or following administration of BaCl2 (314).

The rationale for using acupuncture to treat myocardial ischemia, hypertension, and arrhythmias stems from its ability to inhibit sympathetic outflow (316). Numerous experimental studies have shown that acupuncture, particularly low frequency (2 to 4 Hz) electroacupuncture, causes the release of opioids in a number of regions in the hypothalamus, midbrain, and medulla (290,318–323) that are concerned with processing information that ultimately influences sympathetic neural activity. Thus, by releasing endorphins, endomorphins, or enkephalins (324), which act as neuromodulators that likely reduce function of excitatory neurotransmitters, acupuncture appears to be able to inhibit sympathetic outflow and clinical events associated with heightened sympathetic activity. Other neurotransmitters that might be associated with the influence of acupuncture on sympathetic neural activity important in cardiovascular regulation include gamma-aminobutyric acid (GABA), serotonin or 5-hydroxydopamine (5-HT), acetylcholine, and nociceptin (131). High-frequency electroacupuncture (100 Hz) may influence the cardiovascular system through another opioid neurotransmitter/neuromodulator, dynorphin (325).

Acupuncture can be stimulated either manually by simply inserting a needle in an acupuncture point, then either leaving it in place or twisting and thrusting the needle or by stimulating the needles with a small amount of electrical current at low frequency (2 to 4 Hz) (312,314). Electro-acupuncture appears to be the strongest form of acupuncture and can induce a long clinical response in rats lasting from 1 to 12 h (316). These responses have led to treatment regimens of 30 to 45 min of acupuncture administered two to three times per week for 2 to 4 weeks. Although there are no well-controlled studies in humans, there is a suggestion that one to four courses of 10 days’ treatment with acupuncture lowers blood pressure (5 to 25 mm Hg) in some (e.g., borderline and essential hypertension) but not in all types of hypertension (307–310). Many practitioners use manual acupuncture at several acupoints including acupoints within the same spinal segment, called "segmental acupuncture," or a combination of segmental and distant acupoints (i.e., auricular acupuncture). In the treatment of pain, there are numerous variations of these techniques, including inserting needles at myofascial trigger points and at the specific site of pain (326). There are no data on the efficacy of different techniques of acupuncture with respect to cardiovascular treatment.

Specific acupuncture points, such as the Neiguan or Zusanli acupoints, overlying the median and deep peroneal nerves, respectively, have been used extensively for treatment of cardiovascular abnormalities (317), although the issue of point specificity for treating specific organ system ailments requires further research. The NIH has published a consensus statement indicating that a number of issues related to acupuncture concerning its efficacy, sham effects, adverse reaction, acupuncture points, training and credentialing, and mechanisms of action need further exploration (294).

The response to acupuncture has been suggested to be related to the placebo effect (293). Because placebo effects can occur in as many as 40% of patients and because acupuncture seems to be efficacious in only approximately 70% of patients, there appears to be a narrow window between placebo and what might be a true response (i.e., 30% of patients) (327). Nevertheless, one mechanism of placebo appears to involve the endogenous opioid system (328). Most practitioners check for symptoms of tingling, local warmth, heaviness, or fullness, termed DeQi, to confirm proper placement of needles in acupoints. Such symptoms indicate stimulation of underlying neural pathways, but do not guarantee a true acupuncture versus a placebo response. Although experimental preparations circumvent this criticism, because the animals generally are anesthetized, clinical investigation in the future will need to include adequate sham controls to provide rigorous tests of the acupuncture hypothesis.

Worldwide, more than 40% of physicians recommend acupuncture to their patients and more than 15% of physicians want to add this modality to their therapeutic armamentarium (329). Although not required for licensed physicians, the practice of acupuncture by others, such as those trained in traditional Chinese medicine (i.e., acupuncturists), currently is regulated by more than 35 state boards in the U.S. Furthermore, the FDA regulates use of the disposable stainless steel acupuncture needles. Recently, a workshop held by the NHLBI and the NCCAM identified areas of needed research in complementary medicine in general and acupuncture specifically (330).

Areas of needed research in acupuncture include clinical efficacy, mechanisms of action, and side effects. Most authorities agree that the risk of an adverse event resulting from acupuncture is small, generally below 10% if performed by physicians. However, the risk of a serious event such as pneumothorax, the most common severe side effect, is significantly lower (2%), and although spinal cord lesions, hepatitis and HIV infections, endocarditis, arthritis, and osteomyelitis have been reported, they are rare. The risk of an adverse event for non-physician acupuncturists is higher (331), but again the risk of a serious event is low.


    V. Bioenergetics (energy medicine)

 Top
 Preamble
 I. Introduction
 II. Nutrition and supplements
 III. Mind/body and placebo
 IV. Acupuncture
 V. Bioenergetics (energy...
 V. Spirituality/Intentionality
 Staff
 Appendix I
 Appendix II
 References

 
Since ancient times, many cultures and religious disciplines have considered that an aura, a life force, a radiant energy field can emanate from, and surround, living things (332). This poorly understood vital energy (Hindu prana, Chinese qi, chi, and Japanese ki) associated with the soul, spirit, and mind, impinges on the potential boundaries of modern physics and the relationship of the mind to the physical world (333). Bioenergetics offers the possibility to harness a healing life force (334,335). The wide array of questionable energy-healing approaches opens the possibility of medical quackery that can put patients with serious underlying diseases at risk especially if standard, accepted, and effective therapies are overlooked.

Bioenergy, "life energy," is thought by some to influence mind/body, mind/mind (person to person) and mind/mind (person to infinite spirit) relationships (336) and is altered by conscious and unconscious efforts (336). Bioenergy is believed by some to affect psychological states and physiological processes of the nervous, endocrine, and immune systems (psychoneuroimmunology). It is likely that consciousness manifested as thought, emotion, memories, fears, and self-concept can create physical changes in the body, and this appears modulated by many circulating mediators such as tumor necrosis factor (TNF)-alpha, which may reduce or eliminate a reward response in animals and may be manifest by conditions such as MI. Blockers of TNF-alpha (etanercept) restore the reward response (337).

No sound scientific evidence demonstrates existence of bioenergy fields. Scientific or not, bioenergy concepts are deeply ingrained and has gained popularity. Out-of-hand dismissal of influence of bioenergetics by a physician may disrupt a relationship to a believing patient and cause the patient to turn elsewhere.

The mind can influence health, life, and death (338,339). Energy that facilitates connectedness, harmony, and health can be as simple as emotional release in the form of mirthful laughter or tears. Mirthful laughter can improve immune system functioning (340). This form of bioenergy can be harnessed to improve a patient’s well-being and outcome.

Belief in the benefit of treatment can improve outcome even if the treatment is a placebo. Controlled studies showing benefit of bioenergy approaches over placebo raise the issue of a potential mechanism of effect with functional magnetic resonance imaging (MRI) that can show blood flow changes during brain mapping.

Many cardiovascular symptoms are not treated easily with present medical therapy. Functional complaints, such as chest pain, palpitations, dyspnea, fatigue, and weakness not associated with measurable physical abnormalities are poorly understood, and methods to eliminate consequences could greatly improve health (286). Reinterpretation of the symptoms and their severity by the patient (mental energy) may have an influence on outcome. The real benefit of these treatments might be as an adjunct to improve patient optimism and outcomes by their psychosocial effects (280).

A sense of peace, serenity, calm, power, or emotional connection can have potent influence on outcomes (286). Removal of stress (not yet well defined) by a technique utilizing bioenergy may modify severe disabling symptoms even if the therapy has no proven benefit. Such an approach can be advocated as long as it does not exclude standard therapy and does not cause harm.

Methods to Study Bioenergy.   Although bioenergy may be immeasurable, patients—and therapists—will continue to use bioenergy approaches if convinced of their efficacy, no matter the resolve of a specific scientific, or medical community to discount benefits even if there is scientific demonstration of inefficacy. Adjusting bioenergy fields through acupuncture, therapeutic touch, Qi Gong, Johrei, Reiki, crystal therapy, and magnet therapy may improve health, but data are too preliminary to recommend any therapy (341). If they do have an effect, both the extent of benefit and the mechanisms responsible are unknown.

Traditional Chinese medicine encompasses folk practices based on mysticism and bioenergy (342). A recent analysis of 2,938 clinical trials reported in Chinese medical journals shows these data to be inconclusive (343). Chinese trials were qualitative, short-term, small, poorly controlled, rarely blinded, and contained inadequate data.

Forms of Bioenergetics.   The techniques share common features: focus on "bioenergy" by practitioners and "energy transfer" leads to beneficial effects.

Relaxation
Relaxation therapy in 192 men having two or more risk factors for CAD was associated with better outcomes compared to a control group (344). "Type A" persons tending to have a higher incidence of hypertension and death from CVD may benefit from a relaxation response (345–348). Progressive muscle relaxation techniques have been associated with improved cardiovascular outcomes, but data are still preliminary.

Yoga
Movements and positions in yoga and the breathing exercises can lower the blood pressure and alter breathing patterns (349). Among other improvements in physical fitness, yoga can increase absolute and relative maximal oxygen uptake by 7% and 6%, respectively, after eight weeks in a controlled setting (341). Yoga has been associated with improved heart rate variability and respiratory variables (350). There can be a decrease in sympathetic response (350,351) and changes in baroreflex sensitivity (352). Yoga may influence the progression and regression of atherosclerosis (353), and may beneficially alter the lipid profile (354), but the data are too preliminary to make a sound recommendation in favor of yoga.

Qi Gong
Qi Gong has increased dramatically. Qi means life-force energy and Gong is "practicing skill." Practitioners believe that vital energy circulates through "meridians," connecting all organs, and illness is an imbalance, or interruption, of Qi. Qi Gong is said to re-balance the energy (355).

Internal Qi Gong involving deep breathing, concentration, and relaxation is a self-discipline that trains body and mind to alter flow of "vital energy." In 76 post-MI patients, Qi Gong was associated with improvement in respiratory rate, heart rate, and respiratory sinus arrhythmia (356). In similar study, hospitalization was reduced in post-MI patients learning Qi Gong relaxation techniques (357). In hypertensive patients, Qi Gong was associated with an improvement in levels of prostoglandin (357).

"External Qi Gong" is performed by "masters" who claim to cure with energy from their fingertips. Control Qi is claimed to diagnose and cure various conditions (357). Qi Gong may influence and reduce respiratory rate, heart rate, blood pressure, and accentuate vagal tone demonstrated by changes in heart rate variability (358–360). However, th clinical significance and mechanisms are unclear (361).

Over 1,300 references on Qi Gong suggests benefit to treat hypertension, respiratory diseases, and cancer. For hypertension, lower stroke and mortality rates have been shown in preliminary studies (362). Qi Gong may benefit some patients with atherosclerotic obstruction of the lower extremities (363), and breathing approaches might influence symptoms in patients with mitral valve prolapse (364).

Reiki
Reiki is believed to use "healing energy" to enhance vitality, resiliency, and health for both practitioner and patient (365,366). There are over 500,000 practitioners. The technique’s most profound effect is deep relaxation. It works, supposedly, only if the receiver can detect the subtle, personal, unconscious energy. A practitioner "attuned" to the energy places his hands onto or just above the patient’s body at strategic points (chakras) to transfer energy. Channeling this energy is purported to have a positive effect, but scientifically demonstrable cardiovascular effects have not been shown (367).

Healing and therapeutic touch
Healing touch (HT) and therapeutic touch (TT) use the concept of energy fields (auras), energy centers (chakras), and energy tracts (medians) to empower healing similar to Reiki.

Healing touch, developed by Janet Mentgen, RN (368), is used extensively by nurses (68,000 participants in the U.S.) at all levels of health care, but it based on little supportive controlled data. Universal energy is believed to be channeled to work with human "energy fields" to restore harmony and balance. The technique utilizes the hands to clear, energize and balance the human energy fields, thus affecting physical, emotional, mental, and spiritual health.

Healing TT is a therapeutic intervention, an educational program, and an international organization that provides healing touch certification and formulates standards of practice (368).

In therapeutic touch, hands are used to direct healing energy. Healing supposedly results from transfer of "excess energy" from healer to patient. Therapeutic touch was conceived in the 1970s by Dolores Krieger (369). Therapeutic touch involves "centering" (align the healer to the patient’s energy level), "assessment" (hands detect forces from the patient), "unruffling the field" (sweeping stagnant energy downward to prepare for energy transfer), and energy transfer (from practitioner to patient) (370).

Therapeutic touch was evaluated in a meta-analysis by Astin et al. (371). Of the 11 trials reviewed, 7 showed a positive treatment effect and at least one outcome. These included a 17% decrease in anxiety in cardiac care unit (CCU) patients, reduced need for postoperative pain medication, and improved wound healing.

Healing TT may reduce anxiety but no sound scientific evidence supports the postulated "energy transfer" benefits claimed. Benefits reported may simply be a placebo effect, literally a "laying on of hands" (372).

Distance healing
Similar to TT and distance (intercessory) prayer, "distance healing" is energy transfer that is said to occur over very long distances. Beutler et al. (373) showed small but significant changes in diastolic blood pressure in a double-blind controlled study of distance healing. One study showed benefit of distance (blinded) prayer on autonomic tone based on skin conductance levels and "blood volume pulse" (373,374).

Applied kinesiology
This technique of kinesiology is performed by therapists using acupressure points and a muscle-testing method to diagnose nutritional and glandular "deficiencies," which are then "corrected" by manipulation or nutrition supplements. There is little substantiated supportive data.

Meditation
Meditation, not universally considered bioenergy therapy, can alter blood distribution in the brain observed by magnetic resonance imaging scans and can increase delta wave activity observed on the electroencephalogram. Rage behavior decreases. Transcendental meditation has been linked to reduction in cardiovascular mortality (375–382). It can lower blood pressure (383–385). Zen meditation has been associated with improved heart rate variability and slowing of respiratory rate (384). These data are preliminary and techniques cannot be recommended yet.

Vibrational medicine
Practitioners of vibrational medicine consider humans as dynamic energy systems ("body/mind/spirit" complexes). People are influenced by subtle emotional, spiritual, nutritional, and environmental energies that affect health (386). These concepts involve vibrational medicine: aromatherapy, chakra rebalancing, distance healing; flower essence therapy, homeopathy; Kirlian photography, moxibustion, orthomolecular medicine; past-life regression, radionics; and other unfounded approaches.

Magnetotherapy
"Magnetotherapy" is applied through the use of permanent or fluctuant magnetic fields, but there are no proven benefits for the CVD (387,388). Scherlag has been evaluating, in an animal model, low-level gauss fields to affect atrial arrhythmias in preliminary studies (389).

Homeopathy.   Water is believed to retain the memory of and be energized by compounds that existed in it. Scanning of water by MRI suggests there might be some, but no data has demonstrated health benefits for CVD (390). A meta-analysis of homeopathic treatments in the Lancet of more than 80 studies indicated, compared to placebo, that homeopathic treatments might be effective (391,392). Although the results were significant as a whole, concerning any one-disease entity, no significant treatment could be discerned. The therapies were not standardized.

Caveats.   Potential beneficial effects of these approaches may be in part due to an undefined psychological impact that might ultimately create a physiological effect. The approaches have not been tested for safety. There are no specific proven cardiovascular benefits from any of these therapies to treat disease.

Potential adverse influences may be the release of inhibitions causing anger, hostility, "negative" energy, or reduction of needed sympathetic tone. No bioenergy therapy has been shown to alter the natural course of CVD (392). These therapeutic approaches may appear to have benefit as an adjunct to standard medical therapies and for patients with severe functional, yet symptomatic, complaints, but actual benefits are difficult to measure. Bioenergy approaches should not be considered substitutes for standard medical care; they may offer false hope to patients and at an expensive price.

Practitioners and patients who use these techniques will likely continue to employ them even without a scientific foundation. Practitioner qualifications are difficult to measure (393).

"Benefits" may represent the natural course of a disease or the patient’s or therapist’s interpretation of the condition. Positive results may represent experimenter biases not obvious from the study design. Patients may undergo "energy healing" and be cured of a condition that they do not have or they may be misdiagnosed. A bioenergy practitioner might exaggerate or create an illusion of the benefit of therapy. Biases for, and against, bioenergy healing make it even more difficult to assess the quality of the data.

Ongoing studies including those funded by the NCCAM are evaluating energy healing approaches.

Recommendations.   Conditions for which bioenergy therapies are not contraindicated (but not specifically recommended) include:

1 If a bioenergy treatment does not interfere with standard, accepted, and proven therapy.
2 If standard therapies do not provide optimal symptomatic improvement, or for a condition that is potentially functional or has functional overlay.

No bioenergy therapy should be considered a substitute for standard, accepted, and approved therapies. If any bioenergy approach is considered, one should choose a practitioner who has a good reputation, appears to have good results, and is willing to work with medical professionals.


    V. Spirituality/Intentionality

 Top
 Preamble
 I. Introduction
 II. Nutrition and supplements
 III. Mind/body and placebo
 IV. Acupuncture
 V. Bioenergetics (energy...
 V. Spirituality/Intentionality
 Staff
 Appendix I
 Appendix II
 References

 
Spirituality in Cardiovascular Applications.   Anectdotally the will to live, a strong life force spirit or faith, a loving family or community, or the absence of these features has been considered related to outcomes in cardiovascular care. Synchrony between belief systems or other "connections" between patient and healer are also widely considered important on an intuitive basis.

Some indigenous master healers from various cultures and faiths assert that medicines and procedures constitute only about 20% of what heals and that 80% is mediated through the spirit (394,395). With remarkable uniformity across these healers, the "spirit" is considered an integral element of optimal diagnosis and therapy (396,397).

The ramifications of such claims, if even partly true, are staggering. It is currently impossible to assess the accuracy of such claims based on available data. The ubiquitous presence of spiritual beliefs and practices present since ancient times mandates systematic examination (339,398–407).

Intuitively, the role of spirituality in modern cardiovascular care offers both the potential to better understand and support patients who face cardiac death and provide new questions for therapeutic interventions. Thousands of observational, instructional, anecdotal, theological, and philosophical treatises suggest the potential impact of the spirit in health, including passages from the Bible, the Koran, the Upanishads, the transcribed teachings of Buddha and other religious literature.

Compendia.   A number of well-referenced overviews or comprehensive compendia of references have been compiled on scientific investigations into spiritual and religious practices correlated with cellular, physiologic, somatic and psychosomatic healing applications. These books and compendia can be found on the ACCF Web site as Appendix VI and include references using broad arrays of study designs with a heterogeneous nomenclature and definitions specific to the heart. Two consistent themes include epidemiologic observations that both personal and social spirituality have correlations with selected outcomes measures, and that spirituality, particularly prayer, may have efficacy in healing applications. Data quality, selection bias, interpretative bias, publication bias, and details of safety issues are not discernible from these compendia.

Review Articles and Meta-Analyses.   Various structured reviews and meta-analyses of spiritual descriptors and therapies and their correlations with clinical outcomes (not specific to cardiology) have also emerged in the peer review literature and can be found on the ACCF web site as Appendix VII. This literature overall is well summarized in the Astin et al. (371) recent meta-analysis of clinical studies involving spirituality. The researchers acknowledge that available reports were so heterogeneous in structure, methods, population, and end points measured that their attempt to perform a classical meta-analysis had to be "abandoned." The present writing group’s consensus overview of these reviews suggest:

1 The literature in this area is devoid of mechanistic insight and is heterogeneous as to the quality of study design.
2 There is no scientific evidence in the literature sufficiently definitive or compelling to provide a basis for specific recommendations on the use of spiritual intervention for healing purposes in a cardiology population.
3 There is a notable consistency across reports suggesting efficacy.
4 There are no obvious safety issues attendant to spiritual interventions.

Specific Reports of Spirituality and Cardiovascular Care.   Epidemiologic evidence correlating individual spiritual practice, involvement within a spiritual community, and of communities characterized by their spiritual practices with improved cholesterol levels, more normative blood pressure, other risk factor modulations, incidence of clinically recognized coronary disease, incidence of MI, post-coronary artery bypass graft (CABG) survival, and improved survival overall provides an intriguing context for other observations of psychosocial descriptors—including personality type, hostility, depression, isolation, and cardiac outcomes (408–418). As with all epidemiologic data, however, it remains unclear whether or not there is actually a causal relationship between these spiritual features and the clinical outcomes.

Reports of palliation of subjectively perceived stress and/or pain levels in patients admitted to the CCU or undergoing cardiac catheterization constitute another area intriguing both for its consistency and for its apparent overlap with the use of imagery, relaxation, and other biofield and energy healing techniques in similar patients (419–421). Only one preliminary report, however, has actually correlated such palliative end points with clinical outcomes (394–397,422).

Four prospective, randomized, double-blinded clinical trials examining the influence of off-site prayer on clinical outcomes in cardiac patients have been reported (394,395). In three of the studies, CCU patients were assigned either to off-site intercessory prayer or no prayer in addition to standard care. In two of the CCU studies, a combined index of hospital course and complications severity was derived specifically for study purposes (397). Although findings were reported as significantly improved in each cohort treated with off-site prayer, clinical interpretation of these findings is difficult. In the third CCU study (396), no significant differences existed in clinical outcomes, although the study was powered to a higher treatment effect than may have been observed. The fourth study was a feasibility pilot examining an array of CAM practices in patients with acute coronary syndromes undergoing invasive catheterization and angioplasty (396). Using major adverse cardiac events (MACE) and blindly analyzed continuous electrocardiographic evidence of post-angioplasty ischemia, absolute reductions were observed in the prayer group relative to the standard therapy group; however, these difference did not reach statistical significance (423). Two additional prospective, multicenter clinical studies of double blind off-site prayer in patients undergoing CABG and percutaneous coronary intervention, respectively, have completed enrollment and will soon be reported (422).

Key Issues in Spirituality Applied to Cardiovascular Care.   Support versus spiritual therapy
Careful consideration must be given to the important differences between rendering spiritual support for patients and families and the study of experimental, directed spiritual therapy.

Spiritual support constitutes the response of the health care system to the self-perceived spiritual needs of the patient and family. Access to a chapel, the presence of a chaplain, awareness of and sensitivity to spiritual and ethnic preferences—spiritual support services can broadly be seen as the health care system’s readiness and sensitivity to needs identified by patient and family, particularly in the face of life-threatening illness. Spiritual support might be a component of therapy focused on recovery from illness, or it may be involved as tools for coping, for grief, or for transcendence of impending death. It is generally appropriate for spiritual support services to be assessed and advanced through a quality assurance/quality improvement (QA/QI) process. External agencies appropriate for overview of QA/QI include the Joint Commission for Hospital Accreditation.

Spiritual therapy implies a healing objective actively sought and documented through experimental intervention. Formal research protocols, Institutional Review Board processes, and informed consent from patients are appropriate. Specific considerations of methodology, mechanism, dose and dose response, and other aspects fundamental to work with any new therapeutic agent in cardiology patients are all applicable. Peer-review grant funding for spiritual therapy protocols is currently identifiable at the NCCAM and other agencies at the NIH. New standards and recommendations for study in this area have recently been published (424–429).

Spirituality and religion
"Religion," the "religious," and the "spiritual" are terms used synonymously to refer to that which connects the mortal being to the highest sense of meaning and order at a transpersonal level. In other usage, the term "religion" implies established ethnic and cultural groups, and in some cases evokes the concept of a divinity, whereas "spiritual" implies a more generic attribute.

Unique baseline spirituality patient descriptors
Epidemiologic evidence is compelling that baseline spirituality descriptors characterized by established questionnaires are associated with certain cardiac outcomes (417). In one report, the degree of the spirituality effect was equivalent to a history of cigarette smoking (430). Further study and especially prospective multivariate models will be important to better understand the predictive information content of baseline spirituality in conjunction with other classical cardiac predictors of outcome (e.g., age, ejection fraction, gender).

Methods and spiritual therapy
No discrete measurements report intensity or "dose" of spiritual therapies. Qualitative features include descriptions of the practice itself, the content of the prayer, meditation, intention or imagery used, the experience level of the practitioner, any notable ethnic affiliations, and/or the use of ancillary components such as music, soft abdominal breathing, humming or chanting, a prescribed body posture or the like. Quantitative features, such as the number of individuals praying, the duration of the prayers, and the proximity to the patient, are also of potential interest.

Mechanism of action and surrogate measures
"Divine intervention," "life force," "love," "joy," and "spirit" all share a common feature—the absence of any satisfactory mechanistic explanation as to how they operate in health or disease. Three explanations are widely discussed:

1 These forces are divine, and so cannot be comprehended, particularly within a deterministic model.
2 These forces cannot be measured because they do not exist.
3 These forces are self-evident, and we simply have not yet developed measurement tools.

In the absence of discrete measurements or appreciable mechanisms of action, and in the presence of spiritual practice imbued in the culture of patients, families, communities, and health care staff, a pure control group for spirituality trials is difficult, if not impossible, to develop. Thus, studies in this area can currently examine incremental, but not absolute, therapeutic effects.

Safety and efficacy end points in spiritual therapy studies
Selection of efficacy end points for study in this area must be consistent with the population studies. For patients with very advanced heart disease, where end of life issues may become ascendant over mortality per se, the influence of spiritual interventions on end of life measures would be a reasonable approach.

Conversely, if spiritual therapy shows a therapeutic effect it may be capable of causing harm. As with any new therapy whose mechanism is undefined, it is unreasonable to simply assume safety and study efficacy—addressing safety, with Data Safety Monitoring Boards, should be formally included in trials as a safety and efficacy study design.

Similarly, as research with potential safety issues attendant, clinical trials applying spiritual intervention to cardiology patients as an investigational therapy should do so with the informed consent of the patient.

Sensitivity, privacy, and ethics
Spiritual matters constitute one of the most private and personal areas for both patients and staff. Sensitivity to the broad array of belief systems and to the highly symbolic nature of certain terms, concepts, or icons is paramount to develop spiritual support systems and studies of spiritual therapy. Incorporation of spiritual assessments as part of standard nursing admission procedures or the acquisition of spirituality survey information in conjunction with research protocols must be conducted with strict attention to whether the patient finds the queries objectionable and to the confidentiality of the material and with informed consent.

Cultural preconceptions and bias regarding spirituality are substantial, with some issues that are primarily philosophical, not subject to scientific study or resolution, and likely to be contentious when discussed broadly. Crucial issues include:

How do we know when God answers prayer?
• Does one religion have more powerful prayer?
• How would a negative study of prayer be interpreted?
• Is death a negative end point?
• Is technology necessary in the setting of true faith?

It seems reasonable to examine spiritual therapy as an adjunct to modern technology, not as competition or a replacement for standard care. It is reasonable to assess the safety and efficacy of spiritual interventions with reasonable but rigorous science and clinical trial designs. It is reasonable to investigate physiologic signals that might provide either a marker of the presence of spiritual influence or even a key to mechanisms through which spiritual influence is mediated.

Extension of dialogue across the disciplines and constituencies concerned with spiritual support and spiritual therapy is timely and important.

Delivery Roles, Accreditation, and Certification Standards.   Optimal spiritual support or therapy requires considerable re-thinking regarding the relative roles of the patient, the family, the community, the clergy, and hospital staff. As Don Carlos Peete stated in his 1955 book The Psychosomatic Genesis of Coronary Artery Disease: "I believe the most successful physician will instill into his patient hope, courage, and patience. He can do so only if he has these virtues himself. The discipline necessary to face the responsibilities that are ours as individuals and as a people can be attained only when we understand and use both the spiritual and physical laws in our daily lives" (311,323,324).

Summary and General Recommendations.   Spiritual needs, influences, and therapeutic claims are ancient and ubiquitous. Spirituality issues are pertinent to patients with heart disease. Recommendations include:

1 Development of health care responsive to the spiritual needs of patients and families.
2 No practice guidelines for spiritually based therapy in cardiovascular care can be currently recommended.
3 Clinical research of spiritual interventions in cardiology settings is reasonable, should be conducted as safety and efficacy trials, and ethically must include the informed consent of patients.
4 The use of unique baseline descriptors of spirituality in clinical trials is suggested.
5 Development of a common nomenclature, use of standardized measures, and detailed methodological descriptions in clinical trials of spiritual interventions are recommended.

The cultivation of multidisciplinary forums on concepts of spirituality and healing, delivery roles, practice standards, and certification issues is suggested.


    Staff

 Top
 Preamble
 I. Introduction
 II. Nutrition and supplements
 III. Mind/body and placebo
 IV. Acupuncture
 V. Bioenergetics (energy...
 V. Spirituality/Intentionality
 Staff
 Appendix I
 Appendix II
 References

 
Christine W. McEntee, Chief Executive Officer

Dawn R. Phoubandith, MSW, Associate Director, ClinicalPolicy and Documents

Ana Patricia Jones, Senior Coordinator, Clinical Policy and Documents


    Appendix I

 Top
 Preamble
 I. Introduction
 II. Nutrition and supplements
 III. Mind/body and placebo
 IV. Acupuncture
 V. Bioenergetics (energy...
 V. Spirituality/Intentionality
 Staff
 Appendix I
 Appendix II
 References

 
Relationships with industry

Writing committee members were asked to identify all relationships with industry that were relevant—or could be perceived as relevant—to this document. One member, Dr. Kenneth Pelletier, declared that he had past (not current) research grants with Medtronic and Merck. The other authors of this document declared that they had no relevant relationships with industry pertinent to this topic.


    Appendix II

 Top
 Preamble
 I. Introduction
 II. Nutrition and supplements
 III. Mind/body and placebo
 IV. Acupuncture
 V. Bioenergetics (energy...
 V. Spirituality/Intentionality
 Staff
 Appendix I
 Appendix II
 References

 
Glossary

Acupressure.   Acupressure is an ancient Asian healing art that uses the fingers to press key points on the surface of the skin. Practitioners believe this stimulates the body’s immune system to self heal. When stimulated, these points may relieve muscular tension and promote the release of endorphins—neurochemicals that relieve pain. Acupressure uses the same points and meridians (patterns of energy flow) as acupuncture, but instead of needles it treats with gentle, firm pressure of fingers and hands.

Acupuncture.   Acupuncture is a treatment based on an ancient Chinese medicine. Acupuncture places extremely thin, sharp needles (that are sometimes connected to a low-voltage power source) along a network of "lines of energy" or meridians on the body surface. Chinese medicine practitioners believe these meridians conduct energy throughout the body. However, recent (Western) evidence indicates that the needles stimulate sensory nerves underlying meridians to alter neurotransmitter release in regions of the central nervous system concerned with regulation of the autonomic nervous system and hence the heart and blood vessels. Acupuncture is believed by clinicians practicing traditional Chinese medicine (TCM) to balance the opposing forces of yin and yang, keep the normal flow of energy unblocked, and maintain or restore health to the body and mind (http://nccam.nih.gov/health/acupuncture/#glossary, accessed September 18, 2002). Eastern scientists have translated these TCM concepts into a neurophysiologic paradigm in which acupuncture, by evoking the release of inhibitory neurotransmitters (endorphins, enkephalins, and possibly endomorphins) in the hypothalamus, midbrain, and medulla, in turn, reduces activity of premotor neurons concerned with sympathetic outflow to the heart and vascular system (1).

AHA dietary guidelines.   October 2000 revision of the AHA dietary guidelines to Americans (1).

Applied kinesiology.   This chiropractic technique is performed by therapists, using acupressure points and a muscle-testing method. Practitioners believe they are able to diagnose nutritional and glandular "deficiencies" that are then "corrected" by manipulation or nutrition supplements.

Atkins diet.   Developed by Dr. Robert Atkins, this diet limits carbohydrates to 20 g initially for rapid weight loss. This is done by eliminating high carbohydrate foods such as bread, potatoes, pasta, fruit, juices, and candy. Fats and proteins are the main source of fuel on this diet. Meat, eggs, butter, and most cheeses can be eaten without restriction.

Bioenergy (bioenergetics).   Bioenergetics is a loosely collected series of healing "disciplines" that attempt to harness natural forces and powers to influence natural healing processes. Bioenergy fields are thought to be altered by conscious and unconscious efforts (330). Bioenergy medicine uses bioenergy (HT and TT, Qi Gong, Johrei, Reiki, crystal therapy, relaxation therapy, distance healing, applied kinesiology, and magnet therapy) to heal (431).

Biofeedback.   Biofeedback (BF) techniques are treatment methods that use monitoring instruments of various degrees of sophistication. The BF techniques provide patients with physiologic information that allows them to reliably influence psychophysiological responses of two kinds: 1) responses not ordinarily under voluntary control, and 2) responses that ordinarily are easily regulated, but for which regulation has broken down. Technologies that are commonly used include electromyography (EMG BF), electroencephalography, thermometers (thermal BF), and galvanometry (electrodermal BF) (432).

Crystal therapy.   Practitioners believe that crystals contain or possess energy fields that can be used to heal. Practitioners believe that each crystal is associated with different energy fields or emotions.

Distance healing.   There is much overlap among TT, distance healing, and distance prayer. Spiritual healing practiced when the patient is not present is called distance healing and is similar to prayer. It can be practiced in groups or individually.

Guided imagery.   A patient is asked to focus deliberately on a particular image in order to "relax, manage stress, or alleviate a specific symptom" (433). Key to this therapy is that the patient is in control of the image and can redirect it. The image does not have to be physiologically true, as in the case of a cancer patient imagining being free of cancer, or even real in the sense that the patient has or would ever experience what the image depicts. Imagery may be just simple visualization or a sensory perception such as a smell, a touch, or a sound (325,434,435). Although imagery uses the conscious mind, it may also be utilized to tap into the unconscious or less conscious mind.

Ho’oponopono.   This Hawaiian approach alleges to find the divine within oneself to remove stress and release problems. It involves repentance and "transmutation" to provide spiritual freedom, love, peace, and wisdom (431).

Hydrotherapy.   The concept behind this technique is that water is "energized" by compounds in extremely dilute amounts. Practitioners believe that water retains the memory of the compounds that existed in it. This may reflect dilute amounts of the retained original compound.

Hypnosis.   Hypnotic techniques induce states of selective attentional focusing or diffusion combined with enhanced imagery. They are often used to induce relaxation and also may be a part of cognitive behavioral therapy. The techniques have both pre- and post-suggestion components. The pre-suggestion component involves attentional focusing through the use of imagery, distraction, or relaxation, and has features that are similar to other relaxation techniques. Subjects focus on relaxation and passively disregard intrusive thoughts. The suggestion phase is characterized by introduction of specific goals; for example, analgesia may be specifically suggested. The post-suggestion component involves continued use of the new behavior following termination of hypnosis (431).

Magnetotherapy.   This therapy is applied through the use of permanent or fluctuant magnetic fields.

Meditation.   Meditation is a self-directed practice for relaxing the body and calming the mind. Various meditation techniques are in common use; each has its own proponents. Meditation generally does not involve suggestion, autosuggestion, or trance (436,437).

Mediterranean diet.   This is a diet high in fruits, vegetables, bread and other cereals, potatoes, beans, nuts, and seeds. Olive oil is an integral part of the diet and is an important source of monounsaturated fat. Dairy products, fish, and poultry are eaten in low to moderate amounts and little red meat is consumed. Up to four eggs are consumed weekly and wine is drunk with meals in low to moderate amounts.

Mental physics.   This is purported to be a practical, holistic, futuristic science that manifests "hidden meaning" of the Bible and involves "astral travel;" aura reading chanting; meditation, pranayama ("deep scientific breathing exercises"); "pranic therapy" (a variant of channeling); reflexology; shiatsu; and individualization of diet according to "chemical type" (438).

Mind/body.   Mainstream mind-body medicine, as defined by Chiarmonte (438a), is "based on the premise that mental or emotional processes (the mind) can affect physiologic function (the body)." Lazar (438b) elaborates on this point further, saying that mind-body medicine is an integrative discipline that examines the relationship between psychological states and psychological interventions and between physiology and pathophysiological processes. Conversely, most practitioners of CAM—which takes a different approach to mind/body medicine—hold that the mind’s impact on the body is not unidirectional; rather, there is an integrated process in which both mind and body affect each other (439).

Music therapy.   Music therapy is the prescribed use of music by a qualified person to effect positive changes in the psychological, physical, cognitive, or social functioning of individuals with health or educational problems (440).

Nutrition.   This concerns cardioprotective diets, including AHA Step I and Step II; Mediterranean; NCEP ATP III; DASH, low-fat and low-sugar diets. Also includes garlic, nuts, teas, and alcohol use.

Placebo.   A placebo is defined as an inert or innocuous treatment that works not because of the therapy itself but because of its suggestive effect. It is considered a mind/body modality, but with some distinct differences. Placebo therapy depends on the power of a patient’s belief that the therapy will be effective (431).

Pranic psychotherapy.   Pranic psychotherapy includes removal and disintegration of "traumatic psychic energy," disintegration of "negative elementals" ("bad spirits"), and creation of a "positive thought entity."

Progressive muscle relaxation (PMR).   Progressive muscle relaxation focuses on reducing muscle tone in major muscle groups. Each of 15 major muscle groups is tensed and then relaxed in sequence.

Qi Gong.   Qi is life force energy and Gong is "practicing skill." Practitioners of Qi Gong believe that vital energy circulates through "meridians," connecting all organs. Illness is attributed to an imbalance, or interruption, of Qi. Qi Gong is said to re-balance "yin" and "yang" (365).

Internal Qi Gong. Involves deep breathing, concentration, and relaxation. It is a self-discipline that trains body and mind to alter flow of "vital energy," for self-reliance and adjustment, to cure disease, and to strengthen and prolong life.
External Qi Gong. Affects things outside one’s body. It is performed by "masters" who claim to cure with energy released from their fingertips.

Reiki.   Rei is "universal," or "spiritual," and Ki is "life force energy." It is a form of laying on the hands (431).

Relaxation.   Relaxation techniques are a group of behavioral therapeutic approaches that differ widely in their philosophical bases as well as in their methodologies and techniques. Their primary objective is the achievement of nondirected relaxation, rather than direct achievement of a specific therapeutic goal. They all share two basic components: 1) repetitive focus on a word, sound, prayer, phrase, body sensation, or muscular activity, and 2) adoption of a passive attitude toward intruding thoughts and a return to the focus. These techniques induce a common set of physiologic changes that result in decreased metabolic activity. Relaxation techniques may also be used in stress management (as self-regulatory techniques) and have been divided into deep and brief methods (441).

Reversal diet.   The Ornish reversal diet consists of 10% fat and is combined with a program of smoking cessation, aerobic exercise, stress management training and psychological support.

Spirituality.   Spirituality can be defined as a belief system focusing on intangible elements that impact vitality and meaning to life’s events (431). In the absence of insight into the mechanism, the entire area of spirituality and cardiovascular health remains highly anecdotal, intuitive and speculative. As patients and families of loved ones who have heart disease face mortality in a very personal and immediate way, however, there is widespread interest in how cardiologists think about and approach spiritual issues in practice and in research.

Supplements.   The Dietary Supplement Health and Education Act (DSHEA) of 1994 defined dietary supplements as a product (other than tobacco) intended to supplement the diet that bears or contains one or more of the following ingredients: vitamins, minerals, herbs, or other botanicals, amino acids, and substances such as enzymes, organ tissues, glandulars, and metabolites. Whatever their form, DSHEA places dietary supplements in a special category under the general umbrella of "foods," not drugs, and requires that every supplement be labeled a dietary supplement (http://www.cfsan.fda.gov/~dms/ds-oview.html, accessed September 18, 2002). Other examples include antioxidants, plant sterols, soluble fiber, omega-3 fatty acids and soy; herbs, such as Ginkgo biloba, guggulipid, and HCSE; and other supplements, such as, L-arginine, L-carnitine, and CoQ10.

Therapeutic touch.   Practitioners believe that their hands are used to direct healing energy. Healing supposedly results from transfer of "excess energy" from healer to patient.

Transcendental meditation.   Transcendental meditation focuses on a "suitable" sound or thought (the mantra) without attempting to actually concentrate on the sound or thought.

Vibrational medicine.   Considers humans as dynamic energy systems ("body/mind/spirit" complexes). The dynamic energy system, the life force, is influenced by subtle emotional, spiritual, nutritional, and environmental energies. Health and illness originate in "subtle energy systems."

Yoga.   Developed in India, yoga is a psycho-physical discipline with roots dating back about 5,000 years. Today, most yoga practices in the West focus on the physical postures, termed "asanas," breathing exercises called "pranayama," and meditation (source: http://www.yogasite.com/yogafaq.html#What).

Zen meditation.   This technique is a form of Buddhism originating in Asia; it teaches that desires are the primary cause of suffering. Meditative absorption in which all dualistic distinctions are eliminated (source: http://healing.about.com/cs/zen/index.htm?terms=zen+meditation) (236).


    Footnotes

 
The recommendations set forth in this report are those of the Writing Committee and do not necessarily reflect the official position of the American College of Cardiology Foundation.

When citing this document, the American College of Cardiology Foundation would appreciate the following citation format: Vogel JHK, Bolling SF, Costello RB, Guarneri EM, Krucoff MW, Longhurst JC, Olshansky B, Pelletier KR, Tracy CM, Vogel RA. Integrating complementary medicine into cardiovascular medicine: a report of the American College of Cardiology Foundation Task Force on Clinical Expert Consensus Documents (Writing Committee to Develop an Expert Consensus Document on Complementary and Integrative Medicine). J Am Coll Cardiol 2005;46:184–221.

Copies: This document is available on the World Wide Web site of the American College of Cardiology (www.acc.org). Reprints of this document may be purchased for $10 each by calling 1-800-253-4636, ext. 694, or by writing to the American College of Cardiology, Educational Services, 9111 Old Georgetown Road, Bethesda, MD 20814-1699.

Permissions: Multiple copies, modification, alteration, enhancement, and/or distribution of this document are not permitted without the express permission of the American College of Cardiology Foundation. Please direct requests to: copyright_permissions@acc.org .

* Former members of Task Force Back

{dagger} Former chair of Task Force Back


    References

 Top
 Preamble
 I. Introduction
 II. Nutrition and supplements
 III. Mind/body and placebo
 IV. Acupuncture
 V. Bioenergetics (energy...
 V. Spirituality/Intentionality
 Staff
 Appendix I
 Appendix II
 References

 

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