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Diagnostic randomized controlled trials: the final frontier
Authors:Marc Rodger  Tim Ramsay  Dean Fergusson
Affiliation:1. Thrombosis Program, Division of Hematology, Department of Medicine, Faculty of Medicine, University of Ottawa, 501 Smyth Road, Ottawa, ON, K1H 8L6, Canada
2. Clinical Epidemiology Program, Ottawa Hospital Research Institute, 501 Smyth Road, Ottawa, ON, K1H 8L6, Canada
3. Department of Epidemiology and Community Medicine, Faculty of Medicine, University of Ottawa, 501 Smyth Road, Ottawa, ON, K1H 8L6, Canada
4. Ottawa Methods Centre, Ottawa Hospital Research Institute, 501 Smyth Road, Ottawa, ON, K1H 8L6, Canada
5. The Ottawa Hospital, Clinical Epidemiology Program, 501 Smyth Road, Box 201, Ottawa, ON, K1H 8L6, Canada
Abstract:
ABSTRACT: Clinicians, patients, governments, third-party payers, and the public take for granted that diagnostic tests are accurate, safe and effective. However, we may be seriously misled if we are relying on robust study design to ensure accurate, safe, and effective diagnostic tests. Properly conducted, randomized controlled trials are the gold standard for assessing the effectiveness and safety of interventions, yet are rarely conducted in the assessment of diagnostic tests. Instead, diagnostic cohort studies are commonly performed to assess the characteristics of a diagnostic test including sensitivity and specificity. While diagnostic cohort studies can inform us about the relative accuracy of an experimental diagnostic intervention compared to a reference standard, they do not inform us about whether the differences in accuracy are clinically important, or the degree of clinical importance (in other words, the impact on patient outcomes). In this commentary we provide the advantages of the diagnostic randomized controlled trial and suggest a greater awareness and uptake in their conduct. Doing so will better ensure that patients are offered diagnostic procedures that will make a clinical difference.
Keywords:
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