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Optimizing medicines management: From compliance to concordance

This expert article was written by Annie Cushing and Richard Metcalfe and first published in Therapeutics and Clinical Risk Management, Volume 3, Number 6, December 2007

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File type and size: PDF 0.280 MB
Publication size: 12 pages
Publication date: December 2007
Published by: Dove Medical Press
ThePharmYard product code: dove420

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AUTHORS:

Annie Cushing1
Richard Metcalfe2

1Clinical and Communication Skills Unit, Barts and the London, Queen Mary’s School of Medicine and Dentistry, University of London, London, England, UK
2Department of Neurology, Institute of Neurological Sciences, Southern General Hospital, Glasgow, Scotland, UK

ABSTRACT

Medication prescribed but not consumed represents a huge loss in drug and prescribing costs and an enormous waste of expensive medical time. In this article we discuss what is known about compliance and adherence, explore the concept of concordance and demonstrate its fundamental difference from both. Not all patients are ready or suitable for shared decision making in management of their condition, some still preferring a doctor-led decision but an increasing number want a partnership approach. By opening up and rebalancing the discussion about medication, we can expect a consultation which is more satisfying for both parties and flowing from this, more effective, focused prescribing of medication which is more likely to be adhered to by the patient. We examine the extent to which doctor and patient behaviors are currently compatible with this change of concept and practice, look at available consultation models which might be useful to the reflective practitioner and consider what actions on the part of the doctor and the healthcare system could promote medicine prescription and utilization in line with this new approach based on partnership.



ABOUT THE JOURNAL

Therapeutics and Clinical Risk Management

ISSN 1176-6336

An international, peer-reviewed journal of clinical therapeutics and risk management, focusing on concise rapid reporting of clinical studies in all therapeutic areas, outcomes, safety, and programs for the effective, safe, and sustained use of medicines.

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