Chronic Conditions and Behavioural Change Approaches to Medication Adherence: Rethinking Clinical Guidance and Recommendations.

adherence behavioural change chronic conditions clinical guidance knowledge translation

Journal

Patient preference and adherence
ISSN: 1177-889X
Titre abrégé: Patient Prefer Adherence
Pays: New Zealand
ID NLM: 101475748

Informations de publication

Date de publication:
2020
Historique:
received: 25 11 2019
accepted: 04 02 2020
entrez: 27 3 2020
pubmed: 27 3 2020
medline: 27 3 2020
Statut: epublish

Résumé

Patient adherence to medication is an ongoing concern for clinicians, obfuscating treatment efficacy and resulting in wastage of medicine, reduced clinical benefit, and increased mortality. Despite this, procedural guidance on how clinicians should best engage patients regarding their medicine-taking is limited in the United Kingdom. Adherence for chronic conditions is notably complex, requiring clear education, communication, and behavioural shifts to initiate and sustain daily regimens successfully. This article explores current clinician guidance on assuring patient adherence to medication within the National Health Service, comparing it to that provided for healthcare workers in the field of behavioural change. Outlining the inertia of the former and the progress of the latter, we consider what steps should be taken to address this deficit, including greater focus on patient concerns, as well as knowledge translation for healthcare professionals in future adherence research. Current United Kingdom clinical guidance for assuring patient adherence is largely outdated based on inconclusive evidence for best practice. However, efforts to encourage behavioural change in the public health setting demonstrate evidence-based success. Integrating knowledge generated around adherence behaviour and the practical application of adherence and behavioural change research, as well as funding for longer-term studies with a focus on clinical outcomes, may help to solidify the NICE guidance on adherence and further progress the field. This would require close involvement from patient groups and networks informing ethical aspects of study design and clinical implementation.

Identifiants

pubmed: 32210543
doi: 10.2147/PPA.S239916
pii: 239916
pmc: PMC7075430
doi:

Types de publication

Journal Article

Langues

eng

Pagination

581-586

Subventions

Organisme : HCRW_
ID : HCRW_RFPPB-16A-1296
Pays : United Kingdom

Informations de copyright

© 2020 Read et al.

Déclaration de conflit d'intérêts

The authors report no conflicts of interest in this work, financial or otherwise.

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Auteurs

Simon Read (S)

School of Healthcare Sciences, Cardiff University, Cardiff, Wales, UK.

James Morgan (J)

Cardiff and Vale University Health Board, Cardiff, Wales, UK.

David Gillespie (D)

Centre for Trials Research, Cardiff University, Cardiff, Wales, UK.

Claire Nollett (C)

Centre for Trials Research, Cardiff University, Cardiff, Wales, UK.

Marjorie Weiss (M)

School of Pharmaceutical Sciences, Cardiff University, Cardiff, Wales, UK.

Davina Allen (D)

School of Healthcare Sciences, Cardiff University, Cardiff, Wales, UK.

Pippa Anderson (P)

Swansea Centre for Health Economics, Swansea University, Swansea, Wales, UK.

Heather Waterman (H)

School of Healthcare Sciences, Cardiff University, Cardiff, Wales, UK.

Classifications MeSH