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首页> 外文期刊>Journal of Clinical Pharmacy and Therapeutics >Causality assessment of adverse drug reactions: comparison of the results obtained from published decisional algorithms and from the evaluations of an expert panel, according to different levels of imputability.
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Causality assessment of adverse drug reactions: comparison of the results obtained from published decisional algorithms and from the evaluations of an expert panel, according to different levels of imputability.

机译:药物不良反应的因果关系评估:根据可插补程度的​​不同,比较已发布的决策算法和专家小组的评估结果。

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OBJECTIVES: To evaluate agreement between causality assessments of reported adverse drug reactions (ADRs) obtained from decisional algorithms, with those obtained from an expert panel using the WHO global introspection method (GI), according to different levels of imputability and to evaluate the influence of confounding variables. METHOD: Two hundred reports were included in this study. An independent researcher used decisional algorithms, while an expert panel assessed the same ADR reports using the GI, both aimed at evaluating causality. Reports were divided according to the presence, absence or lack of information on confounding variables. RESULTS: The rates of concordance between assessments made using the algorithms and GI according to levels of imputability were: 45% for 'certain', 61% for 'probable', 46% for 'possible' and 17% for drug unrelated terms. When confounding variables were taken into account, the rates of concordance for the 'absence of information', 'lack of information' and 'presence of confounding variables' in the 'certain' group were 49, 69 and 7%, respectively. The corresponding values for the 'probable' group were 80, 68 and 24% and 30, 51 and 51%, respectively for the 'possible' group. CONCLUSION: Full agreement with global introspection was not found for any level of causality assessment. Confounding variables were found to be associated with low levels of agreement between decision algorithms and the GI method compromising the algorithms' sensitivity and specificity.
机译:目的:根据可插补程度的​​不同,评估从决策算法获得的报告的药物不良反应(ADR)与由专家小组使用WHO全球自省方法(GI)获得的因果关系评估之间的一致性,并评估令人困惑的变量。方法:本研究包括200份报告。一个独立的研究人员使用了决策算法,而一个专家小组则使用GI评估了相同的ADR报告,两者均旨在评估因果关系。根据是否存在混淆变量的信息来划分报告。结果:根据可插性水平,使用算法和GI进行的评估之间的一致性比率为:“确定”为45%,“可能”为61%,“可能”为46%,与药物无关的术语为17%。当考虑混杂变量时,“某些”组中“缺少信息”,“缺乏信息”和“存在混杂变量”的一致性比率分别为49%,69%和7%。 “可能”组的对应值分别为“可能”组的80%,68%和24%,以及30%,51%和51%。结论:在任何水平的因果关系评估中都未发现与全球自省的完全一致。发现混淆变量与决策算法和GI方法之间较低的一致性水平相关,从而损害了算法的敏感性和特异性。

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