Barriers and facilitators for systematically registering adverse drug reactions in electronic health records:a qualitative study with Dutch healthcare professionals

Background: Systematically registering ADRs in electronic health records (EHRs) likely contribute to patient safety as it enables the exchange of drug safety data. Currently, ADRs registrations by healthcare professionals (HCPs) is suboptimal. This study aimed to identify barriers and facilitators perceived by HCPs to register ADRs systematically in EHRs. Research Design and Methods: A qualitative study with individual interviews was conducted among specialist physicians and hospital pharmacists from 10 different Dutch hospitals. A semi-structured interview guide was used to identify experienc... Mehr ...

Verfasser: Geeven, Isa P. A. C.
Jessurun, Naomi T.
Wasylewicz, Arthur T. M.
Drent, Marjolein
Spuls, Phyllis I.
Hoentjen, Frank
van Puijenbroek, Eugène P.
Vonkeman, Harald E.
Grootens, Koen P.
van Doorn, Martijn B. A.
van den Bemt, Bart J. F.
Bekker, Charlotte L.
Dokumenttyp: Artikel
Erscheinungsdatum: 2022
Reihe/Periodikum: Geeven , I P A C , Jessurun , N T , Wasylewicz , A T M , Drent , M , Spuls , P I , Hoentjen , F , van Puijenbroek , E P , Vonkeman , H E , Grootens , K P , van Doorn , M B A , van den Bemt , B J F & Bekker , C L 2022 , ' Barriers and facilitators for systematically registering adverse drug reactions in electronic health records : a qualitative study with Dutch healthcare professionals ' , Expert opinion on drug safety , vol. 21 , no. 5 , pp. 699-706 . https://doi.org/10.1080/14740338.2022.2020756
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-29048195
Datenquelle: BASE; Originalkatalog
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Link(s) : https://research.vumc.nl/en/publications/95976d5c-021e-4c6d-85e6-25ed56c2d039