TY - JOUR
T1 - Impact of Cost-Sharing Increases on Continuity of Specialty Drug Use
T2 - A Quasi-Experimental Study
AU - Li, Pengxiang
AU - Hu, Tianyan
AU - Yu, Xinyan
AU - Chahin, Salim
AU - Dahodwala, Nabila
AU - Blum, Marissa
AU - Pettit, Amy R.
AU - Doshi, Jalpa A.
N1 - Funding Information:
Dr. Doshi has served as a consultant or member of an advisory board for Alkermes, Inc., Boehringer Ingelheim, Forest Laboratories, Ironwood Pharmaceuticals, Merck & Co. Inc., and Shire, receiving honoraria; has had grants from Amgen Inc., Merck & Co. Inc., Pfizer Inc., Janssen Biotech, Sanofi, Regeneron, Humana, Pharmaceutical Research and Manufacturers of America (PhRMA), and the National Pharmaceutical Council; and has a spouse who holds stocks in Merck & Co. Inc. and Pfizer Inc. Dr. Chahin has received a grant from Pharmaceutical Research and Manufacturers of America (PhRMA) Foundation. Dr. Dahodwala has received grant funding from the National Institutes of Health, Parkinson’s Foundation, The Michael J. Fox Foundation, The Parkinson Council, AbbVie, and Medtronic. Dr. Pettit has received consulting fees from Alkermes, Inc., unrelated to the topic of this article. Drs. Li, Hu, Yu, and Blum have no conflicts to report. Disclaimer: None.
Funding Information:
research agreement funded by Pfizer Inc. The funding source, however, had no role in the design and conduct of the study, data analysis, decision to publish, or preparation and review of the manuscript. The University of Pennsylvania’s Center for Pharmacoepidemiology Research and Training supported the use of the Cerner Multum Lexicon NDC database. The authors would like to thank Vrushabh P. Ladage, BS, for his editorial assistance with the manuscript. Drs. Hu, Yu, and Chahin were employees at the University of Pennsylvania at the time of conduct of the study.
Publisher Copyright:
© Health Research and Educational Trust
PY - 2018/8
Y1 - 2018/8
N2 - Objective: To examine the impact of cost-sharing increases on continuity of specialty drug use in Medicare beneficiaries with multiple sclerosis (MS) or rheumatoid arthritis (RA). Data Sources/Study Setting: Five percent Medicare claims data (2007–2010). Study Design: Quasi-experimental study examining changes in specialty drug use among a group of Medicare Part D beneficiaries without low-income subsidies (non-LIS) as they transitioned from a 5 percent cost-sharing preperiod to a ≥25 percent cost-sharing postperiod, as compared to changes among a disease-matched contemporaneous control group of patients eligible for full low-income subsidies (LIS), who faced minor cost sharing (≤$6.30 copayment) in both the pre- and postperiods. Data Collection/Extraction Methods: Key variables were extracted from Medicare data. Principal Findings: Relative to the LIS group, the non-LIS group had a greater increase in incidence of 30-day continuous gaps in any Part D treatment from the lower cost-sharing period to the higher cost-sharing period (MS, absolute increase = 10.1 percent, OR = 1.61, 95% CI 1.19–2.17; RA, absolute increase = 21.9 percent, OR = 2.75, 95% CI 2.15–3.51). The increase in Part D treatment gaps was not offset by increased Part B specialty drug use. Conclusions: Cost-sharing increases due to specialty tier-level cost sharing were associated with interruptions in MS and RA specialty drug treatments.
AB - Objective: To examine the impact of cost-sharing increases on continuity of specialty drug use in Medicare beneficiaries with multiple sclerosis (MS) or rheumatoid arthritis (RA). Data Sources/Study Setting: Five percent Medicare claims data (2007–2010). Study Design: Quasi-experimental study examining changes in specialty drug use among a group of Medicare Part D beneficiaries without low-income subsidies (non-LIS) as they transitioned from a 5 percent cost-sharing preperiod to a ≥25 percent cost-sharing postperiod, as compared to changes among a disease-matched contemporaneous control group of patients eligible for full low-income subsidies (LIS), who faced minor cost sharing (≤$6.30 copayment) in both the pre- and postperiods. Data Collection/Extraction Methods: Key variables were extracted from Medicare data. Principal Findings: Relative to the LIS group, the non-LIS group had a greater increase in incidence of 30-day continuous gaps in any Part D treatment from the lower cost-sharing period to the higher cost-sharing period (MS, absolute increase = 10.1 percent, OR = 1.61, 95% CI 1.19–2.17; RA, absolute increase = 21.9 percent, OR = 2.75, 95% CI 2.15–3.51). The increase in Part D treatment gaps was not offset by increased Part B specialty drug use. Conclusions: Cost-sharing increases due to specialty tier-level cost sharing were associated with interruptions in MS and RA specialty drug treatments.
KW - Medicare
KW - chronic illness
KW - observational data/quasi-experiments
KW - pharmaceuticals: prescribing/use/costs
UR - http://www.scopus.com/inward/record.url?scp=85050387409&partnerID=8YFLogxK
U2 - 10.1111/1475-6773.12744
DO - 10.1111/1475-6773.12744
M3 - Article
C2 - 28736929
AN - SCOPUS:85050387409
SN - 0017-9124
VL - 53
SP - 2735
EP - 2757
JO - Health services research
JF - Health services research
ER -