Treffer: [Use of the capture-recapture method to assess the frequency of "serious" adverse drug reactions: experience of Toulouse University Hospital].

Title:
[Use of the capture-recapture method to assess the frequency of "serious" adverse drug reactions: experience of Toulouse University Hospital].
Transliterated Title:
Utilisation de la méthode capture-recapture pour l'évaluation de la fréquence des effets indésirables "graves" médicamenteux: l'expérience du CHU de Toulouse.
Authors:
Montastruc JL; Laboratoire de pharmacologie médicale et clinique, Unité de pharmacoépidémiologie, EA 3696, Faculté de médecine, Toulouse. montastruc@cict.fr, Lugardon S, Desboeuf K, Fernet P, Lapeyre-Mestre M
Source:
Bulletin de l'Academie nationale de medecine [Bull Acad Natl Med] 2008 Feb; Vol. 192 (2), pp. 421-30; discussion 430-1.
Publication Type:
English Abstract; Journal Article
Language:
French
Journal Info:
Publisher: Académie nationale de médecine Country of Publication: Netherlands NLM ID: 7503383 Publication Model: Print Cited Medium: Print ISSN: 0001-4079 (Print) Linking ISSN: 00014079 NLM ISO Abbreviation: Bull Acad Natl Med Subsets: MEDLINE
Imprint Name(s):
Publication: Paris : Académie nationale de médecine
Original Publication: Paris, Masson.
Entry Date(s):
Date Created: 20080930 Date Completed: 20081114 Latest Revision: 20131121
Update Code:
20250114
PMID:
18819693
Database:
MEDLINE

Weitere Informationen

There is evidence that the methods classically used to identify and quantify adverse drug reactions (ADRs), based on spontaneous reporting or computerized medical databases, are not exhaustive. Spontaneous notifications to regional pharmacovigilance centers suffer from under-reporting Combining different sources could improve our knowledge of ADR frequency. The aim of this study was to estimate the incidence of serious ADRs handled in medical wards of a French university hospital, using data from the Programme de Medicalisation des Systemes d'Information (PMSI) and spontaneous reports recorded in the French Pharmaco Vigilance Database. The study period was the first 6 months of 2001. From the PMSI, we selected all hospitalization summaries that included an ICD-10 code related to a potential ADR. From the French Pharmaco Vigilance Database, we selected all serious ADRs that occurred during the study period and were reported by physicians working in the University Hospital. After identifying cases recorded in both sources, we applied the capture-recapture method in order to estimate the real number of ADRs. From the PMSI, we identified 274 different hospital stays involving an ADR. Out of 241 reports selected from the French Pharmaco Vigilance Database, we retained 151 ADRs for analysis. Fifty-two ADRs were found in both databases, giving an estimated total of 796 serious ADRs [95% confidence interval (CI) 638, 954], corresponding to 2.9% of inpatients (95% CI 2.3, 3.5) during the first half of 2001. This study confirms the lack of exhaustiveness of ADR reporting, whatever the data source, and underlines the value of merging data from different databases.