An international group of back pain researchers considered recommendations for standardized measures in clinical outcomes research in patients with back pain.
To promote more standardization of outcome measurement in clinical trials and other types of outcomes research, including meta-analyses, cost-effectiveness analyses, and multicenter studies.
Better standardization of outcome measurement would facilitate comparison of results among studies, and more complete reporting of relevant outcomes. Because back pain is rarely fatal or completely cured, outcome assessment is complex and involves multiple dimensions. These include symptoms, function, general well-being, work disability, and satisfaction with care.
The panel considered several factors in recommending a standard battery of outcome measures. These included reliability, validity, responsiveness, and practicality of the measures. In addition, compatibility with widely used and promoted batteries such as the American Academy of Orthopaedic Surgeons Lumbar Cluster were considered to minimize the need for changes when these instruments are used.
First, a six-item set was proposed, which is sufficiently brief that it could be used in routine care settings for quality improvement and for research purposes. An expanded outcome set, which would provide more precise measurement for research purposes, includes measures of severity and frequency of symptoms, either the Roland or the Oswestry Disability Scale, either the SF-12 or the EuroQol measure of general health status, a question about satisfaction with symptoms, three types of "disability days," and an optional single item on overall satisfaction with medical care.
Standardized measurement of outcomes would facilitate scientific advances in clinical care. A short, 6-item questionnaire and a somewhat expanded, more precise battery of questionnaires can be recommended. Although many considerations support such recommendations, more data on responsiveness and the minimally important change in scores are needed for most of the instruments.
From the *Center for Cost and Outcomes Research, the Department of Medicine, and the Department of Health Services, University of Washington, Seattle, Washington; the †University of Alberta, Edmonton, Alberta, Canada; ‡The Department of Epidemiology, Maastricht University, Maastricht, The Netherlands; §The Institute for Work and Health, Toronto, Ontario, Canada; ∥Keele University School of Postgraduate Medicine, Stoke-on-Trent, United Kingdom; the #EMGO Institute, Vrije University, Amsterdam, The Netherlands; the ††Finnish Institute of Occupational Health, Helsinki, Finland; the ‡‡National Primary Care Research and Development Centre, University of Manchester, Manchester, United Kingdom;§§Group Health Cooperative, Seattle, Washington; and ∥∥The Glasgow Nuffield Hospital, Glasgow, Scotland.
Supported in part by a grant (HS-08194) from the Agency for Health Care Policy and Research, Washington DC.
Presented in part at the Second International Forum for Primary Care Research on Low Back Pain, The Hague, The Netherlands, May 30-31, 1997.
Acknowledgment date: August 14, 1997.
First revision date: January 30, 1998.
Acceptance date: February 11, 1998.
Device status category: 1.
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