gms | German Medical Science

23. Jahrestagung des Deutschen Netzwerks Evidenzbasierte Medizin e. V.

Deutsches Netzwerk Evidenzbasierte Medizin e. V.

01. - 03.09.2022, Lübeck

Use of an electronic medication management support system in patients with polypharmacy in general practice: results of a quantitative process evaluation of the AdAM trial

Meeting Abstract

  • Robin Brünn - Goethe-Universität, Institut für Allgemeinmedizin, Deutschland
  • Dorothea Lemke - Goethe-Universität, Institut für Allgemeinmedizin, Deutschland
  • Jale Basten - Ruhr-Universität, Abteilung für Medizinische Informatik, Biometrie und Epidemiologie, Deutschland
  • Petra Kellermann-Mühlhoff - BARMER, Produktstrategie /-entwicklung, Deutschland
  • Juliane Köberlein-Neu - Bergische Universität Wuppertal, Bergisches Kompetenzzentrum für Gesundheitsökonomik und Versorgungsforschung, Wuppertal, Deutschland
  • Christiane Muth - Universität Bielefeld, AG Allgemein- und Familienmedizin, Bielefeld, Deutschland; Goethe-Universität, Institut für Allgemeinmedizin, Deutschland
  • Marjan van den Akker - Goethe-Universität, Institut für Allgemeinmedizin, Deutschland

Evidenzbasierte Medizin für eine bedarfsgerechte Gesundheitsversorgung. 23. Jahrestagung des Deutschen Netzwerks Evidenzbasierte Medizin. Lübeck, 01.-03.09.2022. Düsseldorf: German Medical Science GMS Publishing House; 2022. Doc22ebmPOS-2_3-03

doi: 10.3205/22ebm102, urn:nbn:de:0183-22ebm1024

Published: August 30, 2022

© 2022 Brünn et al.
This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 License. See license information at http://creativecommons.org/licenses/by/4.0/.


Outline

Text

Background/research question: Polypharmacy is associated with increased risks of adverse drug events due to medication errors. General practitioners (GPs) often lack a comprehensive overview of their patients’ medication due to prescriptions by specialists. This process evaluation investigates implementation and use of a computerized decision-support system (eMMa), granting full access to patients’ medical treatments, within a GP setting.

Methods: Evaluating implementation and use of eMMa is based on the Medical Research Council Guidance and its process evaluation framework. The process evaluation uses pseudonymized logbook entries of eMMa and comprises four dimensions: Reach examines to which extent the intended study population was included. Dose, Fidelity, and Tailoring examine how eMMa was used by GPs. The analyses were mainly explorative and descriptive.

Results: Study participants corresponded to the target population, although patients in greater need of care were treated less frequently. Despite GPs identifying and correcting prescription errors according to eMMa recommendations, both the intended intervention intensity and intervention goal of the process evaluation were rarely fulfilled.

Conclusion: The results of the process evaluation show that the implemented system has only been used in a subset of targeted patients and that only part of the recommendations have been followed. This must be taken into account when considering the effects of the intervention on patient-relevant outcomes. Furthermore, underreporting may have occurred since documentation of monitoring and changes in pharmacotherapy was not enforced. An improved use of eMMa could be achieved through more intensive training, data exchange of the software with practice information systems and collaboration in interprofessional teams, for example by involving pharmacists, which is substantiated in the literature.

Competing interests: Keine