How Good Is "Evidence" from Clinical Studies of Drug Effects and Why Might Such Evidence Fail in the Prediction of the Clinical Utility of Drugs?
Promising evidence from clinical studies of drug effects does not always translate to improvements in patient outcomes. In this review, we discuss why early evidence is often ill suited to the task of predicting the clinical utility of drugs. The current gap between initially described drug effects...
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Veröffentlicht in: | Annual review of pharmacology and toxicology 2015-01, Vol.55 (1), p.169-189 |
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description | Promising evidence from clinical studies of drug effects does not always translate to improvements in patient outcomes. In this review, we discuss why early evidence is often ill suited to the task of predicting the clinical utility of drugs. The current gap between initially described drug effects and their subsequent clinical utility results from deficits in the design, conduct, analysis, reporting, and synthesis of clinical studies-often creating conditions that generate favorable, but ultimately incorrect, conclusions regarding drug effects. There are potential solutions that could improve the relevance of clinical evidence in predicting the real-world effectiveness of drugs. What is needed is a new emphasis on clinical utility, with nonconflicted entities playing a greater role in the generation, synthesis, and interpretation of clinical evidence. Clinical studies should adopt strong design features, reflect clinical practice, and evaluate outcomes and comparisons that are meaningful to patients. Transformative changes to the research agenda may generate more meaningful and accurate evidence on drug effects to guide clinical decision making. |
doi_str_mv | 10.1146/annurev-pharmtox-010814-124614 |
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In this review, we discuss why early evidence is often ill suited to the task of predicting the clinical utility of drugs. The current gap between initially described drug effects and their subsequent clinical utility results from deficits in the design, conduct, analysis, reporting, and synthesis of clinical studies-often creating conditions that generate favorable, but ultimately incorrect, conclusions regarding drug effects. There are potential solutions that could improve the relevance of clinical evidence in predicting the real-world effectiveness of drugs. What is needed is a new emphasis on clinical utility, with nonconflicted entities playing a greater role in the generation, synthesis, and interpretation of clinical evidence. Clinical studies should adopt strong design features, reflect clinical practice, and evaluate outcomes and comparisons that are meaningful to patients. 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subjects | bias clinical trials Clinical Trials as Topic - economics Clinical Trials as Topic - methods Clinical Trials as Topic - standards Clinical Trials as Topic - statistics & numerical data Conflict of Interest Data Interpretation, Statistical drug therapy Drug-Related Side Effects and Adverse Reactions - etiology Endpoint Determination Evidence-Based Medicine - economics Evidence-Based Medicine - methods Evidence-Based Medicine - standards Evidence-Based Medicine - statistics & numerical data Humans Patient Safety Patient Selection precision medicine prediction in pharmacology Quality Improvement Quality Indicators, Health Care Research Design - standards Research Design - statistics & numerical data Research Support as Topic Risk Assessment Risk Factors treatment effectiveness Treatment Outcome |
title | How Good Is "Evidence" from Clinical Studies of Drug Effects and Why Might Such Evidence Fail in the Prediction of the Clinical Utility of Drugs? |
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