Background
There has been considerable controversy regarding how to name and
define the illnesses known as myalgic encephalomyelitis (ME) and chronic
fatigue syndrome (CFS). The IOM report has proposed a new clinical criteria
and name for this illness, but aspects of these recommendations have been
scrutinized by patients and scientists.
Purpose
It is possible that both empiric and consensus approaches could be
used to help settle some of these diagnostic challenges. Using patient
samples collected in the United States, Great Britain, and Norway
(N=556), the current study attempted to categorize patients using
more general as well as more restricted case definitions.
Results
Overall, the outcomes suggest that there might be four groupings of
patients, with the broadest category involving those with chronic fatigue
(N=62), defined by 6 or more months of fatigue which can be cannot
be explained by medical or psychiatric conditions. A second category
involves those patients that have chronic fatigue that can be explained by a
medical or psychiatric condition (N=47). A third category involves
more specific criteria that have been posited both by the IOM report, a
Canadian Clinical Case criteria, a ME-ICC criteria and a more empiric
approach. These efforts have specified domains of substantial reductions of
activity, post-exertional malaise, neurocognitive impairment, and sleep
dysfunction (N=346). Patients with these characteristics were more
functionally impaired than those meeting just chronic fatigue criteria,
p < .05. Finally, those meeting even more
restrictive ME criteria proposed by Ramsay, identified a smaller and even
more impaired group, p < .05.
Discussion
The advantages of using such empirical and consensus approaches to
develop reliable classification and diagnostic efforts are discussed.