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Canadian Clinical Working Case Definition Review

Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: Clinical Working Case Definition, Diagnostic and Treatment Protocols

The Canadian Expert Consensus Panel Clinical Case Definition for ME/CFS by Dr Bruce Carruthers et al. The 2003 Canadian Expert Consensus Panel clinical case definition more accurately represents the true symptomatology and manifestations of the disease than all other current case definitions. As The M.E. Society of America explain:

The Canadian Expert Consensus Panel has published a medical milestone, the first clinical case definition for the disease known as myalgic encephalomyelitis/chronic fatigue syndrome. This definition is clearly a vast improvement over the CDC's 1994 Fukuda criteria, which led to misunderstanding in both research and treatment modalities by making "fatigue" a compulsory symptom but by downplaying or making optional the disease's hallmark of post-exertional sickness and other cardinal ME/CFS symptoms. In sharp contrast to the Fukuda criteria, this new clinical case definition makes it compulsory that in order to be diagnosed with ME/CFS, a patient must become symptomatically ill after exercise and must also have neurological, neurocognitive, neuroendocrine, dysautonomic, and immune manifestations. In short, symptoms other than fatigue must be present for a patient to meet the criteria. This case definition, which incorporates some of the current research on dysautonomia, cardiac, and immune problems, was published in the Journal of Chronic Fatigue Syndrome, Vol. 11 (1) 2003. ([Online]).

It is true however that along with many excellent features in these guidelines there are also some very serious weak points and drawbacks in the text (the treatment section is very weak and flawed and along with every definition of the illness written since 1988 when the ‘fatigue’ myth was created to obfuscate the true nature of the illness for political and financial gain these guidelines also unfortunately still use the medically inaccurate terminology of ‘fatigue’ for example).

Despite its imperfections however, the Canadian Guidelines remain overall vastly superior to all other definitions of the illness in existence. In contrast to the Oxford, Holmes and Fukuda (and other) recent definitions the Canadian Guidelines describes an illness that is recognisable as M.E. finally which makes these guidelines a vitally important new tool for M.E. specialists, researchers and patients around the world. M.E. is a distinct, recognisable entity that can be diagnosed relatively early in the course of the disease, providing the physician has some experience with the illness. The new Canadian Guidelines now also make diagnosis easier than ever before even for those with no experience with the illness.

In addition to the need for government funding for research into M.E. however, funding is also necessary to formulate a truly accurate case definition for M.E. (not 'ME/CFS'). One which is not tainted by the bogus concept of ‘fatigue’ or by psychological bias and which has been produced by true M.E. experts. Until that time however, the Canadian Guidelines are far superior to the many 'CFS' definitions and should be used to the exclusion of all others.

Read some excellent comments and critiques of the Guidelines online at:

 

These texts are each essential reading for anyone with an interest in M.E.

For more information on this topic see: The Definitions of M.E.

For more on the various texts (and tests) which may be useful in diagnosing M.E. see: Testing for M.E.

See Smoke and Mirrors for a discussion of why the disease category of 'CFS' must be abandoned.


Availability of the Guidelines

 





Quotes/Excerpts from the text

ME/CFS has developed following a blood transfusion. Within days or weeks of the initiating event, patients show a progressive decline in health and develop a cascade of symptoms.

Canadian Expert Consensus Panel Clinical Case Definition for ME/CFS

 

In a group of 752 patients, 4.5% had a blood transfusion a few days to a week prior to developing acute onset ME/CFS.

Canadian Expert Consensus Panel Clinical Case Definition for ME/CFS p79

 

Patients who suffered an acute onset showed significantly more dysregulation of the immune system than those patients whose onset was gradual.

Canadian Expert Consensus Panel Clinical Case Definition for ME/CFS p77

 

ME/CFS occurs in both epidemic and sporadic forms.

Canadian Expert Consensus Panel Clinical Case Definition for ME/CFS

 

Comments from the Canadian Guidelines on Cognitive Behavior Therapy (CBT) and Graded Exercise Therapy (GET) This excerpt is taken from pages 46-49 of the article "Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: Clinical Working Case Definition, Diagnostic and Treatment Protocols" which appeared in the Journal of Chronic Fatigue Syndrome, Vol. 11(1) 2003, pp. 7-115, by Carruthers et al

An excerpt:

Two hypotheses have been presented as underlying the CBT model of chronic fatigue syndrome (105). The first hypothesis "assumes that the pathophysiology of CFS is largely irreversible, but considers that a fine-tuning of the patient's understanding and coping behavior may achieve some improvement in his or her quality of life." The second hypothesis is based on the premise that the patient's impairments are learned due to wrong thinking, and "considers the pathophysiology of CFS to be entirely reversible and perpetuated only by the interaction of cognition, behavior, and emotional processes. According to this model, CBT should not only improve the quality of the patient's life, but could be potentially curative" (105).

There is much that is objectionable in the very value-laden second hypothesis, with its implied primary causal role of cognitive, behavioral and emotional processes in the genesis of ME/CFS. This hypothesis is far from being confirmed, either on the basis of research findings or from its empirical results.

Nevertheless, the assumption of its truth by some has been used to influence attitudes and decisions within the medical community and the general cultural and social milieu of ME/CFS. To ignore the demonstrated biological pathology of this illness, to disregard the patient's autonomy and experience and tell them to ignore their symptoms, all too often leads to blaming patients for their illness and withholding medical support and treatment.

Care must be taken not to classify patients experiencing chronic fatigue as ME/CFS patients unless they meet all the criteria for ME/CFS, as the outcomes for these two patient groups are substantially different.

A well informed physician empowers the patient by respecting their experiences, counsels the patients in coping strategies, and helps them achieve optimal exercise and activity levels within their limits in a common sense, non-ideological manner, which is not tied to deadlines or other hidden agenda.



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Copyright © by Jodi Bassett 2004 - 2008