[Efficacy of decision support systems to improve medication safety - results of the evaluation of the "Arzneimittelkonto NRW"].
Wirksamkeit technischer Unterstützungssysteme zur Verbesserung der Arzneimitteltherapiesicherheit – Evaluationsergebnisse des Arzneimittelkontos NRW.
Arzneimitteltherapiesicherheit
Decision support systems
Entscheidungsunterstützende Systeme
Information technology
Informationstechnologie
Medication safety
Potentially inadequate medication
Potenziell inadäquate Verschreibungen
Journal
Zeitschrift fur Evidenz, Fortbildung und Qualitat im Gesundheitswesen
ISSN: 2212-0289
Titre abrégé: Z Evid Fortbild Qual Gesundhwes
Pays: Netherlands
ID NLM: 101477604
Informations de publication
Date de publication:
Nov 2019
Nov 2019
Historique:
received:
31
07
2018
revised:
04
10
2019
accepted:
14
10
2019
pubmed:
26
11
2019
medline:
20
12
2019
entrez:
26
11
2019
Statut:
ppublish
Résumé
Polypharmacy increases the risk of adverse drug reactions, especially in the elderly. Therefore, the reduction of potentially inadequate medication (PIM), an improvement in drug therapy safety and, in general, a more rational use of drugs is an objective of various interventions. The aim of this prospective single-arm interventional study is to investigate the potential of a decision support system (DSS; "Arzneimittelkonto NRW") to improve medication safety in outpatient care. 15 primary care physicians participating in the study recruited 874 patients. Prescription data and results of medication safety tests were available for 654 patients. Data of at least 12 months were available for 86% of these patients. PIM prevalence declined within 12 months (-11.3%), but not at a statistically significant level. The number of prescriptions after the introduction of the DSS is significantly below the prescription volume before the introduction of the DSS (-14.1%). Constantly high alteration rates of up to 85% were observed, for example, on drug interaction system warnings made by the DSS. Technical decision support systems have the potential to support a safer and cost-saving drug use. For the first time, this pilot study provides evidence for this in the context of standard outpatient care in Germany. However, further investigations are necessary to establish a robust body of evidence. A particular focus should be on the qualitative monitoring of the studies and the involvement of other actors in the care process.
Identifiants
pubmed: 31761651
pii: S1865-9217(19)30172-2
doi: 10.1016/j.zefq.2019.10.002
pii:
doi:
Types de publication
Journal Article
Langues
ger
Sous-ensembles de citation
IM
Pagination
80-89Informations de copyright
Copyright © 2019. Published by Elsevier GmbH.