1991
DOI: 10.1177/014107689108400224
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A Report–Chronic Fatigue Syndrome: Guidelines for Research

Abstract: Report of a consensus meeting held at Green College.

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Cited by 818 publications
(603 citation statements)
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“…In total, 641 patients were recruited into the PACE trial from secondary-care specialist CFS clinics in the UK, all of whom met the Oxford criteria for CFS (6 months of disability, with fatigue as a principal symptom, not otherwise explained by other diagnoses) (Sharpe et al 1991). Participants were assessed by a research assistant for the presence of the international CDC criteria for CFS (Reeves et al 2003) and diagnostic criteria for fibromyalgia (Wolfe et al 2010).…”
Section: Methodsmentioning
confidence: 99%
“…In total, 641 patients were recruited into the PACE trial from secondary-care specialist CFS clinics in the UK, all of whom met the Oxford criteria for CFS (6 months of disability, with fatigue as a principal symptom, not otherwise explained by other diagnoses) (Sharpe et al 1991). Participants were assessed by a research assistant for the presence of the international CDC criteria for CFS (Reeves et al 2003) and diagnostic criteria for fibromyalgia (Wolfe et al 2010).…”
Section: Methodsmentioning
confidence: 99%
“…The trial included participants meeting the Oxford criteria for CFS [4], which require fatigue as the principal symptom, accompanied by significant disability and without an exclusionary medical or psychiatric diagnosis. All participants were assessed by specialist doctors to exclude other medical diagnoses [18].…”
Section: Entry Criteria and Primary Outcomesmentioning
confidence: 99%
“…It involves comparing the patient's symptoms and history with diagnostic criteria; the Oxford criteria [4], the International 1994 criteria [3], and the National Institute for Health and Care Excellence (NICE) criteria [2].…”
Section: Introductionmentioning
confidence: 99%
“…Despite accumulating evidence recognising it as affecting 250,000 people in the UK [4], controversy surrounding this diagnosis is reflected in CFS/ME patient experiences of feeling stigmatised and marginalised [5]. Two main diagnostic criteria commonly used to diagnose CFS/ME [6] are those of the CDC (Centers for Disease Control and Prevention, US) [1] and Oxford [7], with the former most commonly used in the UK [8].…”
Section: Introductionmentioning
confidence: 99%