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Cardiovascular

Different approaches to the assessment of adherence and persistence with cardiovascular-disease preventive medications

ORCID Icon, ORCID Icon, ORCID Icon, , ORCID Icon, & show all
Pages 1329-1336 | Received 19 Dec 2016, Accepted 31 Mar 2017, Published online: 19 May 2017
 

Abstract

Objective: To assess suitability and comparability of the most common methods of treatment adherence and persistence assessment, as applied to the same pharmacy dataset.

Methods: Data on drugs prescribed for cardiovascular primary prevention to participants in the Aragon Workers’ Health Study (AWHS) were collected from a regional electronic drug prescription database. Several different approaches were used to measure treatment adherence (with the medication possession ratio [MPR]) and proportion of days covered [PDC]) and persistence in new users by therapeutic subgroup. Defined daily dose (DDD) was used as a proxy of the number of days’ supply, or substituted with surrogate daily dose values.

Results: Higher mean adherence values and proportions of adherent patients were obtained using MPR versus PDC, with additional differences depending on the approach used. The proportion of adherent patients was lowest for oral antidiabetics (14.4%–30.6%) and highest for antihypertensives (70.2%–82.1%). The use of surrogate daily dose values increased adherence for antidiabetics and statins and decreased adherence for antihypertensives. After a 1 year follow-up, treatment persistence was observed for 21.1%, 58.7%, and 29.5% of antidiabetic, antihypertensive and statin users, respectively.

Conclusions: Our findings indicate that use of multiple measures of treatment adherence and persistence provides a more complete overview of medication use patterns, and certain limitations associated with DDD for some drug groups can be overcome with replacement by surrogate doses. The PDC indicator seems to provide a more accurate reflection of patient behavior and treatment continuity than the MPR. Any comparison of adherence/persistence should always consider the method used, variables analyzed, and corresponding data collection process.

Correction Statement

This article has been republished with minor changes. These changes do not impact the academic content of the article.

Transparency

Declaration of funding

The study received external funding from the Proyecto del Fondo de Investigacion Sanitaria, Instituto de Salud Carlos III, Spanish Ministry of Health, and Fondo Europeo de Desarrollo Regional(FEDER)(PI13/01668).

Author contributions: S.M. and E.M. conceived and designed the study; C.F. and S.M. analyzed and interpreted the data; S.M. wrote the draft of the paper and I.A., M.J.L., M.J.R., J.A. and E.M. participated in critical revision of the text. All authors approved the final version and assume accountability for all aspects of the study.

Declaration of financial/other relationships

S.M., I.A., C.F., M.J.L., M.J.R., J.A. and E.M. have disclosed that they have no significant relationships with or financial interests in any commercial companies related to this study or article.

CMRO peer reviewers on this manuscript have no relevant financial or other relationships to disclose.

Acknowledgements

The authors thank O. Howard for English-language editing of the manuscript.

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