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Steven H Woolf a Department of Family Practice, Virginia
Commonwealth University, Fairfax, Virginia 22033, USA, b Center for
Quality of Care Research, University of Nijmegen, PO Box 9101, 6500 HB
Nijmegen, Netherlands, c School of Health and Related Research, University of
Sheffield, Sheffield S1 4DA, d Centre for Health Services
Research, University of Newcastle upon Tyne, Newcastle upon Tyne
NE2 4AA, e Health Services Research Unit, University of
Aberdeen, Aberdeen AB9 2ZD
Correspondence to: Professor Woolf
shwoolf@aol.com
| The first 150 words of the full text of this article appear below. |
Over the past decade, clinical guidelines have increasingly become a familiar part of clinical practice. Every day, clinical decisions at the bedside, rules of operation at hospitals and clinics, and health spending by governments and insurers are being influenced by guidelines. As defined by the Institute of Medicine, clinical guidelines are "systematically developed statements to assist practitioner and patient decisions about appropriate health care for specific clinical circumstances."1 They may offer concise instructions on which diagnostic or screening tests to order, how to provide medical or surgical services, how long patients should stay in hospital, or other details of clinical practice.
The broad interest in clinical guidelines that is stretching
across Europe, North America, Australia, New Zealand, and Africa (box)
has its origin in issues that most healthcare systems face: rising
healthcare costs, fueled by increased demand for care, more expensive
technologies, and an ageing population; variations in service delivery
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