Your new experience awaits. Try the new design now and help us make it even better

SYSTEMATIC REVIEW article

Front. Pharmacol.

Sec. Pharmacogenetics and Pharmacogenomics

Volume 16 - 2025 | doi: 10.3389/fphar.2025.1659875

This article is part of the Research TopicReviews in Pharmacogenetics and Pharmacogenomics: 2025View all articles

Implementation of pharmacogenetic testing in community pharmacies: A Scoping review

Provisionally accepted
  • 1Center for Research and Innovation in Clinical Pharmaceutical Sciences, Lausanne University Hospital and University of lausanne, Lausanne, Switzerland
  • 2Institute of Pharmaceutical Sciences of Western Switzerland, University of Geneva, University of Lausanne, Geneva, Switzerland
  • 3School of Pharmaceutical Sciences, University of Geneva, Geneva, Switzerland

The final, formatted version of the article will be published soon.

The field of pharmacogenetics (PGx) has expanded significantly in recent years, with growing evidence supporting its role in enhancing medication effectiveness and reducing adverse events. Yet, the integration of PGx into routine clinical practice remains limited. Community pharmacies hold a key position in the healthcare system, offering expert medication advice and maintaining close patient contact due to their accessibility. This context has driven research efforts to integrate PGx testing into healthcare systems in various countries. However, evidence on optimal strategies for embedding PGx services in this settings is still emerging. We conducted a scoping review to provide a comprehensive overview of the implementation of PGx testing in community pharmacies, focusing on both successful strategies and challenges. A systematic search of studies involving PGx testing in community pharmacies was conducted using PubMed, Embase, the Cochrane Library and Web of Science, including all publications up to February 2025. The search considered implementation outcomes: feasibility, acceptability, adoption, fidelity, appropriateness, cost, penetration and sustainability. The process and reporting followed the PRISMA recommendations for scoping reviews (PRISMA-ScR). Study findings were classified according to Proctor’s implementation outcomes. A total of 17 studies met the inclusion criteria and were included in the review. Key implementation variables were extracted from these studies. Feasibility was supported by a manageable time process and high technical success. The appropriateness of PGx was reflected in its ability to identify numerous medication-related issues. Adoption varied between patients and prescribers. While patient engagement was high, many sharing PGx results with other physicians, integration of PGx recommendations by prescribers was inconsistent. The intervention was generally well accepted, with high satisfaction among patients and pharmacists, although some physicians expressed concerns. This scoping review demonstrates the potential for PGx testing to become a viable part of routine care in community pharmacies. It highlight positive patient perceptions and provider willingness to adopt testing. However, it also identifies key barriers, including the need for standardized PGx guidelines, education for providers, and reimbursement policies. The study underscores the importance of patient education, seamless integration into pharmacy workflows, and continued research to support successful implementation.

Keywords: Pharmacogenetics, Scoping review, implementation science, communitypharmacy services, precision medicine

Received: 04 Jul 2025; Accepted: 02 Sep 2025.

Copyright: © 2025 Coumau, Coumau and Csajka. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Chantal Csajka, Center for Research and Innovation in Clinical Pharmaceutical Sciences, Lausanne University Hospital and University of lausanne, Lausanne, Switzerland

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.