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Medication therapy management and adherence among US renal transplant recipients

BACKGROUND: Medication therapy management (MTM) services among patient populations with a range of disease states have improved adherence rates. However, no published studies have examined the impact of Medicare Part D MTM eligibility on renal transplant recipients’ (RTRs) immunosuppressant therapy...

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Autores principales: Chisholm-Burns, Marie A, Spivey, Christina A, Tolley, Elizabeth A, Kaplan, Erin K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4854272/
https://www.ncbi.nlm.nih.gov/pubmed/27175070
http://dx.doi.org/10.2147/PPA.S104646
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author Chisholm-Burns, Marie A
Spivey, Christina A
Tolley, Elizabeth A
Kaplan, Erin K
author_facet Chisholm-Burns, Marie A
Spivey, Christina A
Tolley, Elizabeth A
Kaplan, Erin K
author_sort Chisholm-Burns, Marie A
collection PubMed
description BACKGROUND: Medication therapy management (MTM) services among patient populations with a range of disease states have improved adherence rates. However, no published studies have examined the impact of Medicare Part D MTM eligibility on renal transplant recipients’ (RTRs) immunosuppressant therapy (IST) adherence. This study’s purpose was therefore, to determine the effects of Medicare Part D MTM on IST adherence among adult RTRs at 12 months posttransplant. METHODS: Cross-sectional analyses were performed on Medicare Parts A, B, and D claims and transplant follow-up data reported in the United States Renal Data System. The sample included adult RTRs who were transplanted between 2006 and 2011, had graft survival for 12 months, were enrolled in Part D, and were prescribed tacrolimus. IST adherence was measured by medication possession ratio for tacrolimus. MTM eligibility was determined using criteria established by the Centers for Medicare and Medicaid Services. Descriptive statistics were calculated. Adherence was modeled using multiple logistic regression. RESULTS: In all, 17,181 RTRs were included. The majority of the sample were male (59.1%), and 42% were MTM-eligible. Mean medication possession ratio was 0.91±0.17 (mean ± standard deviation), with 16.83% having a medication possession ratio of <0.80. MTM eligibility, sex, age, and number of prescription drugs were significantly associated with adherence in the full model (P<0.05). MTM-eligible RTRs were more likely to be adherent than those who were not MTM-eligible (odds ratio =1.13, 95% confidence interval 1.02–1.26, P=0.02). CONCLUSION: The findings provide evidence that access to MTM services increases IST adherence among RTRs.
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spelling pubmed-48542722016-05-12 Medication therapy management and adherence among US renal transplant recipients Chisholm-Burns, Marie A Spivey, Christina A Tolley, Elizabeth A Kaplan, Erin K Patient Prefer Adherence Original Research BACKGROUND: Medication therapy management (MTM) services among patient populations with a range of disease states have improved adherence rates. However, no published studies have examined the impact of Medicare Part D MTM eligibility on renal transplant recipients’ (RTRs) immunosuppressant therapy (IST) adherence. This study’s purpose was therefore, to determine the effects of Medicare Part D MTM on IST adherence among adult RTRs at 12 months posttransplant. METHODS: Cross-sectional analyses were performed on Medicare Parts A, B, and D claims and transplant follow-up data reported in the United States Renal Data System. The sample included adult RTRs who were transplanted between 2006 and 2011, had graft survival for 12 months, were enrolled in Part D, and were prescribed tacrolimus. IST adherence was measured by medication possession ratio for tacrolimus. MTM eligibility was determined using criteria established by the Centers for Medicare and Medicaid Services. Descriptive statistics were calculated. Adherence was modeled using multiple logistic regression. RESULTS: In all, 17,181 RTRs were included. The majority of the sample were male (59.1%), and 42% were MTM-eligible. Mean medication possession ratio was 0.91±0.17 (mean ± standard deviation), with 16.83% having a medication possession ratio of <0.80. MTM eligibility, sex, age, and number of prescription drugs were significantly associated with adherence in the full model (P<0.05). MTM-eligible RTRs were more likely to be adherent than those who were not MTM-eligible (odds ratio =1.13, 95% confidence interval 1.02–1.26, P=0.02). CONCLUSION: The findings provide evidence that access to MTM services increases IST adherence among RTRs. Dove Medical Press 2016-04-28 /pmc/articles/PMC4854272/ /pubmed/27175070 http://dx.doi.org/10.2147/PPA.S104646 Text en © 2016 Chisholm-Burns et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Chisholm-Burns, Marie A
Spivey, Christina A
Tolley, Elizabeth A
Kaplan, Erin K
Medication therapy management and adherence among US renal transplant recipients
title Medication therapy management and adherence among US renal transplant recipients
title_full Medication therapy management and adherence among US renal transplant recipients
title_fullStr Medication therapy management and adherence among US renal transplant recipients
title_full_unstemmed Medication therapy management and adherence among US renal transplant recipients
title_short Medication therapy management and adherence among US renal transplant recipients
title_sort medication therapy management and adherence among us renal transplant recipients
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4854272/
https://www.ncbi.nlm.nih.gov/pubmed/27175070
http://dx.doi.org/10.2147/PPA.S104646
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