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Drug adherence to biologic DMARDS with a special emphasis on the benefits of subcutaneous abatacept

Authors Malaviya, Ostör A

Received 23 March 2012

Accepted for publication 28 April 2012

Published 15 August 2012 Volume 2012:6 Pages 589—596

DOI https://doi.org/10.2147/PPA.S23786

Review by Single-blind

Peer reviewer comments 3


Anshuman P Malaviya,1 Andrew JK Östör1,2

1
Rheumatology Clinical Research Unit, Addenbrooke's Hospital, Cambridge, UK; 2School of Clinical Medicine, University of Cambridge, Cambridge, UK

Abstract: Major advances in drug development have led to the introduction of biologic disease-modifying drugs for the treatment of rheumatoid arthritis, which has resulted in unprecedented improvement in outcomes for many patients. These agents have been found to be effective in reducing clinical signs and symptoms, improving radiological damage, quality of life, and functionality, and have also been found to have an acceptable safety profile. Despite this, drug adherence is unknown, which has huge health care and health-economic implications. Local and national guidelines exist for the use of biologics; however, its varied use is widespread. Although this may in part reflect differences in prescribing behavior, patient preference plays a key role. In this review we will explore the factors that contribute to patient preference for, and adherence to, biologic therapy for rheumatoid arthritis with emphasis on the subcutaneous preparation of abatacept, a T-cell costimulatory molecule blocker. Overall, subcutaneous administration is preferred by patients and this may well improve drug adherence.

Keywords: subcutaneous administration, self-injectable, abatacept, rheumatoid arthritis, preference, adherence, compliance, biologic DMARD

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