Case–non-case studies: Principle, methods, bias and interpretation - 22/03/19
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Summary |
Case–non-case studies are among the methods used to assess drug safety by analyzing the disproportionality of adverse drug reaction reports in pharmacovigilance databases. First used in the 1980s, the last few decades have seen a significant increase in the use of this study design. The principle of case–non-case studies is to compare the drug exposure of cases of an adverse reaction of interest with that of cases with other reported reactions and called “non-cases”. Their results are presented in the form of reporting odds ratio (ROR), the interpretation of which makes it possible to highlight pharmacovigilance signals. This article describes the principle of case–non-case studies, the calculation method of the ROR and its confidence interval, the different analytical modalities and how to interpret its results with regard to the advantages and limitations of this type of study.
Le texte complet de cet article est disponible en PDF.Keywords : Case–non-case studies, Disproportionality analysis, Reporting odds ratio, Pharmacovigilance, Pharmacoepidemiology, Bias
Plan
☆ | This manuscript is an updated translation of an article published in French by the same author in the journal Thérapie in 2018 (Therapie 2018;73:247–55). |
Vol 74 - N° 2
P. 225-232 - avril 2019 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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