The proposed practice of ''evidence-based medicine,'' which calls for
careful clinical judgment in evaluating the ''best available evidence,
'' should be differentiated from the special collection of data regard
ed as suitable evidence. Although the proposed practice does not seem
new, the new collection of ''best available'' information has major co
nstraints for the care of individual patients. Derived almost exclusiv
ely from randomized trials and meta-analyses, the data do not include
many types of treatments or patients seen in clinical practice; and th
e results show comparative efficacy of treatment for an ''average'' ra
ndomized patient, not for pertinent subgroups formed by such cogent cl
inical features as severity of symptoms, illness, comorbidity, and oth
er clinical nuances. The intention-to-treat analyses do not reflect im
portant post-randomization events leading to altered treatment; and th
e results seldom provide suitable background data when therapy is give
n prophylactically rather than remedially, or when therapeutic advanta
ges are equivocal. Randomized trial information is also seldom availab
le for issues in etiology, diagnosis, and prognosis, and for clinical
decisions that depend on pathophysiologic changes, psychosocial factor
s and support, personal preferences of patients, and strategies for gi
ving comfort and reassurance. The laudable goal of making clinical dec
isions based on evidence can be impaired by the restricted quality and
scope of what is collected as ''best available evidence.'' The author
itative aura given to the collection, however, may lead to major abuse
s that produce inappropriate guidelines or doctrinaire dogmas for clin
ical practice. (C) 1997 by Excerpta Medica, Inc.