Abstract
Aims: To examine medication adherence and discontinuation in two separate groups of patients with schizophrenia or bipolar disorder (BD), who began receiving a long-acting injectable antipsychotic (LAI) versus those who changed to a different oral antipsychotic monotherapy.
Materials and methods: The Truven Health Analytics MarketScan Multi-State Medicaid claims database was used to identify patients with schizophrenia; Truven Health Analytics MarketScan Commercial and Medicaid claims databases were used to identify patients with BD. The analyses included adult patients (≥18 years) who either began receiving an LAI (no prior LAI therapy) or changed to a different oral antipsychotic (monotherapy). The first day of initiating an LAI or changing to a new oral antipsychotic was the index date. Linear and Cox regression models were conducted to estimate medication adherence (proportion of days covered [PDC]) and time to medication discontinuation (continuous medication gap ≥60 days), respectively. Models adjusted for patient demographic and clinical characteristics, baseline medication use, and baseline ED or hospitalizations.
Results: Patients with schizophrenia (N = 5638) who began receiving LAIs had better medication adherence (5% higher adjusted mean adherence) during the 1 year post-index period and were 20% less likely to discontinue their medication during the entire follow-up period than patients who changed to a different oral antipsychotic monotherapy, adjusting for differences between LAI users and oral users. Similarly, patients with BD (N = 11,344) who began receiving LAIs also had 5% better medication adherence and were 19% less likely to discontinue their medication than those using oral antipsychotics.
Limitations: Clinical differences unmeasurable in this database may have been responsible for the choice of LAI versus oral antipsychotics, and these differences may be responsible for some of the adherence advantages observed.
Conclusions: This real-world study suggests that patients with schizophrenia or BD who began receiving LAIs had better medication adherence and lower discontinuation risk than those who changed to a different oral antipsychotic monotherapy.
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Declaration of funding
This research was supported by Otsuka Pharmaceutical Development and Commercialization Inc. and Lundbeck.
Author contributions: All authors met the ICMJE criteria for authorship, including contributing to study concept and design, interpretation of the data, and to the drafting and critical review of the manuscript. E.C. further contributed to the analysis of the data. This manuscript has been read and approved by all authors.
Declaration of financial/other relationships
M.G. has disclosed that he is an employee of Otsuka Pharmaceutical Development and Commercialization Inc. T.Y., M.S.B. and E.C. have disclosed that they are employees of Partnership for Health Analytic Research LLC. A.H. and M.T. have disclosed that they are employees of Lundbeck.
Peer reviewers on this manuscript have received an honorarium from JME for their review work, but have no relevant financial or other relationships to disclose.
Acknowledgements
No assistance in the preparation of this article is to be declared.
Previous presentation: International Society for Pharmacoeconomics and Outcomes Research (ISPOR) 22nd Annual International Meeting, Boston, MA, May 2017.
Notes
Notes
1 Otsuka America Pharmaceuticals, Inc., Rockville, MD
2 Janssen Pharmaceuticals, Inc., Titusville, NJ
3 Alkermes, Inc., Waltham, MA
4 Janssen Pharmaceuticals, Inc., Titusville, NJ