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Successes & failures in medical history

By looking through medical history we see many examples of how progress has been made without the use of animals, how progress has been retarded due to animal-based research and how disasters have occurred because of it.

 

Photo courtesy PETA

Real progress:

The following advances in medical progress have all been achieved without the use of non-human animals:

Sanitation

In the mid to late 19th Century, death rates fell dramatically due to the decline in infectious diseases, including TB, bronchitis, pneumonia, influenza, whooping cough, measles, scarlet fever, diptheria, smallpox, cholera, typhoid, diarrhoea and dysentry. However the mortality for each of these infections were declining long before the introduction of antibiotics and immunization.  Instead they have been linked to public health measures and social legislation that have improved the living standards of working people, and to better understanding and availability of nutritional requirements.

Surgery

Surgery, particularly for wounds of the heart and chest during the Second World War became a common procedure, providing opportunity for many fundamental skills of heart surgery to be developed.

(The Wellcome Museum of the History of Medicine (Science Museum, London, 1986)

Lawson Tait has been recognised as one of the most brilliant surgeons in history and pioneered many of our present day surgical techniques. He was also a fierce critic of vivisection.  He was the first to successfully perform a cholecystectomy (gall bladder operation), removal of the appendix, operation on a case of ruptured ectopic pregnancy, and many abdominal operations. He was also a strong proponent of cleanliness during surgery, which during his time was not a common practice.

(Lawson Tait, Transactions of the Birmingham Philosophical Society, 20 April 1882)

Anaesthesia

Before the discovery of anaesthetics, the best surgeons were those who could perform painful operations in the shortest possible time. The introduction of anaesthesia was therefore considered to be a huge medical advance.

In the 1840’s, laughing gas parties and ‘ether frolics’ were popular entertainments amongst medical students. It was the recreational inhalation of ether that prompted Dr Crawford Long to suggest it’s use for surgical procedures. Further ‘partying’ led to the discovery of the properties of chloroform and others.

X-rays

Discovered by accident in 1895 by physics professor Wilhelm Rontgen. He was passing electrical discharges through a partially evacuated glass tube when he discovered by accident that highly penetrative but invisible rays were emitted from the tube. By putting his own hand in the path of the rays he learned that flesh but not bones was transparent to the rays.

(K. Walker, The Story of Medicine, Hutchinson, 1954)

Recessions:

The use of the following drugs/procedures were delayed for many years due to the misleading conclusions from animal-based research:

Penicillin

Discovered by Fleming in 1928 who found that bacteria would not grow on a culture medium accidentally contaminated by a mould. Even before this discovery however, mould on damp cheeses were used to make a plaster for infected wounds.  Fleming lost interest in his discovery when a sample was injected into rabbits and became deactivated by blood.

Many years later, the drug was resurrected by Oxford scientists Florey and Chain. Fleming wished to inject penicillin into the spine of a dangerously ill patient but the results of the administration were unknown. Florey tried the experiment on a cat, but due to a shortage of time it was also administered to the patient before the results of the cat test were available. The cat died, however the patient’s health improved.

Blood transfusions

Following the discovery of blood circulation in 1666, Richard Lower transferred blood from one dog to another. A year later, French physician Jean Denis transfused lambs blood into a boy.  After a number of patients died following the procedure, and a lawsuit brought against the Professor, no further attempts were made for more than a century. It wasn’t until the early part of the nineteenth century that it was realised that transfusions could only be sourced from human donors, and the method only became safe after the discovery of the main blood groups by Karl Landsteiner in 1900. The discovery was made by mixing human blood in test tubes and not through the use of animals.

(R. McGrew, Encyclopaedia of Medical History, MacMillan Press, 1985)

Digitalis

The beneficial effects of digitalis for the treatment of heart conditions were known for many years however it’s widespread use was delayed because animal experiments indicated a dangerous rise in blood pressure.

(M.Beddow Bayly, The Futility of Experiments on Living Animals, NAVS, 1962)

Iron Sorbitol

Used as a treatment for iron deficiency anaemia. It was originally injected into the muscles of rats and rabbits and found to cause sarcomas at the site of injection. 20 years after the initial research on rats it revealed no real hazard during clinical experience.

(M. Weatherall, Nature, 387-390, 1 April 1982)

Disasters:

The following drugs were all ‘successfully’ tested on animals, yet produced widespread damage when applied to humans:

Thalidomide

Probably the most infamous drug disaster, marketed in 1957 by Chemie Grunenthal, and in 1958 by the Distillers Company, as a sedative and to treat morning sickness in pregnant women. Initially caused peripheral neuritis - numbness and cold, severe muscular cramps, weakness of the limbs and lack of coordination. In the following years it was found to cause damage to the human foetus, resulting in 10,000 children born crippled and deformed with missing limbs.

Clioquinol

The main ingredient in Ciba Geigy’s anti-diarrhoea drugs caused an epidemic of disease in Japan in the 1960s. It was banned in Japan in 1970 and then removed from the world market in 1982 (12 years later!). At least 10,000 people, and possibly up to 30,000, fell victim to SMON (subacute myelo-optic neuropathy), a disease which causes numbness, weakness in the legs, paralysis, eye problems including blindness, all due to nerve damage.

(Lancet, 534, 5 March 1977)

Eraldin

Marketed by ICI in the 1970s for the treatment of heart conditions it was thoroughly tested on animals which gave no indication of the tragedy it would cause.  Withdrawn in 1976 after it was found to cause serious eye damage, including blindness, and 23 deaths. Over 1,000 patients received compensation for the damage it caused.

(G.R.Venning, British Medical Journal, 199-202, 15 January, 1983)

Isoprenaline aerosol inhalers

During the 1960s at least 3,500 young British asthma sufferers died following it’s use.

(W.H.Inman in Monitoring for Drug Safety, W.H.Inman, Ed., MTP Press Ltd, 1980)

Opren

An arthritis drug introduced in 1980 by Eli Lilly after safely passing animal tests.

It was withdrawn in August 1982 after being found to be highly toxic in humans, with 3,500 reports of harmful effects including 61 British deaths, mainly through liver damage in the elderly..

(British Medical Jornal 459-460, 14 August, 1982)

Zomax

An anti-inflammatory drug marketed in 1980 to treat post-operative pain. It was withdrawn in 1983 after deaths from severe allergic reactions.

(The Guardian, 9 March 1983)

Osmosin

A slow release drug to treat arthritis caused 40 deaths in the UK alone and was withdrawn in 1983 after only ten months.

(R.D.Mann, Modern Drug Use, MTP Press Ltd., 1984)

Flosint

Marketed by Farmitalia Carlo Erba, was withdrawn after 12 months after Britain’s Committee on Safety of Medicines received reports of 217 adverse reactions.

Zelmid

Anti-depressant drug marketed by Astra in 1982.Withdrawn in 1983 after 300 reports of adverse reactions, including convulsions, liver damage, neuropathies and Guillain-Barre syndrome.

(R.D.Mann, Modern Drug Use, an Enquiry on Historical Principles, MTP Press Ltd, 1984)

Anti-inflammatory drugs phenylbutazone and oxyphenbutazone are responsible for an estimated 10,000 deaths worldwide.

(Estimate by Dr Sidney Wolfe, director of the Ralph Nader Health Research Group, Lancet, 353, 11 February, 1984)

And even more recently (July 2002), over nine million women worldwide who have been prescribed Premarin as a hormone replacement therapy have now been advised that it has been found to greatly increase the risk of breast cancer, heart disease, strokes and blood clots in the lungs.  Premarin was introduced in 1942 by Wyeth-Ayerst and is one of the most prescribed drugs in the United States.  In Australia, 300,000 women have been urged to seek advice from their doctor.

(PETA - www.menopauseonline.org/whi.html)

This list is by no means exhaustive. It merely serves as a snapshot to illustrate how dangerously misleading the use of non-human animals can be in medical research when results are applied to human conditions. 

One can wonder how far we may have progressed had it not been for the delays and deviations caused by animal-based research.

 

Copyright © 2004 AAHR
Last modified: June 23, 2005