http://www.tandfonline.com/doi/full/10.1080/09638288.2017.1383518?scroll=top&needAccess=true
Defining and measuring recovery from myalgic encephalomyelitis and chronic fatigue syndrome: the physician perspective
Andrew R. Devendorf ,Carly T. Jackson,Madison Sunnquist &Leonard A. Jason
Pages 1-8 | Received 06 May 2017, Accepted 19 Sep 2017, Published online: 05 Oct 2017
Abstract
Purpose: To inform an operationalised definition of recovery from myalgic encephalomyelitis (ME) and chronic fatigue syndrome (CFS) for research and practice. Without a consensus on defining and measuring recovery, there will continue to be controversy amongst researchers, clinicians, and patients when interpreting treatment outcomes.
Method: This study explores physicians’ views on recovery from ME and CFS. We conducted semi-structured interviews with 10 physician participants who are experts in the ME and CFS field. Our deductive thematic analysis, using a realist perspective, provided a framework for differentiating recovery and significant improvement.
Results: Physicians conceptualised recovery as complete symptom remission and a return to premorbid functioning (adjusted for with age), whereas they viewed significant improvement as a substantial reduction in symptoms with considerable functional gains, where patients may operate in daily life but still must cope or be treated.
Conclusions: Our findings provide recommendations and approaches for measuring: daily functioning, symptomatology, quality of life, and physical functioning.
Chronic illness, assessment, prognosis, physical functioning, psychosocial functioning, qualitative
Additional information
Funding
This study was funded by the Eunice Kennedy Shriver National Institute of Child Health and Human Development [grant number HD072208].