How to assess pharmacogenomic tests for implementation in the NHS in England

Author:

Sanghvi Sonali12ORCID,Ferner Robin E.34ORCID,Scourfield Andrew4,Urquhart Robert2,Amin Sejal12,Hingorani Aroon D.5,Sofat Reecha67ORCID

Affiliation:

1. North Central London NHS Integrating Pharmacy & Medicines Optimisation Team London UK

2. Clinical Support Services Division University College London Hospitals NHS Foundation Trust London UK

3. School of Clinical and Experimental Medicine University of Birmingham Birmingham UK

4. Department of Clinical Pharmacology University College London Hospitals NHS Foundation Trust London UK

5. Institute of Cardiovascular Science, Centre for Clinical Department of Clinical Pharmacology and Therapeutics and the UCL BHF Research Accelerator University College London London UK

6. Health Data Research London UK

7. Department of Pharmacology and Therapeutics University of Liverpool Liverpool UK

Abstract

AbstractAimsPharmacogenomic testing has the potential to target medicines more effectively towards those who will benefit and avoid use in individuals at risk of harm. Health economies are actively considering how pharmacogenomic tests can be integrated into health care systems to improve use of medicines. However, one of the barriers to effective implementation is evaluation of the evidence including clinical usefulness, cost‐effectiveness, and operational requirements. We sought to develop a framework that could aid the implementation of pharmacogenomic testing. We take the view from the National Health Service (NHS) in England.MethodsWe used a literature review using EMBASE and Medline databases to identify prospective studies of pharmacogenomic testing, focusing on clinical outcomes and implementation of pharmacogenomics. Using this search, we identified key themes relating to the implementation of pharmacogenomic tests. We used a clinical advisory group with expertise in pharmacology, pharmacogenomics, formulary evaluation, and policy implementation to review data from our literature review and the interpretation of these data. With the clinical advisory group, we prioritized themes and developed a framework to evaluate proposals to implement pharmacogenomics tests.ResultsThemes that emerged from review of the literature and subsequent discussion were distilled into a 10‐point checklist that is proposed as a tool to aid evidence‐based implementation of pharmacogenomic testing into routine clinical care within the NHS.ConclusionOur 10‐point checklist outlines a standardized approach that could be used to evaluate proposals to implement pharmacogenomic tests. We propose a national approach, taking the view of the NHS in England. Using this approach could centralize commissioning of appropriate pharmacogenomic tests, reduce inequity and duplication using regional approaches, and provide a robust and evidence‐based framework for adoption. Such an approach could also be applied to other health systems.

Publisher

Wiley

Subject

Pharmacology (medical),Pharmacology

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