The Use of Decomposition Methods in Real-World Treatment Benefits Evaluation for Patients with Type 2 Diabetes Initiating Different Injectable Therapies: Findings from the INITIATOR Study

被引:7
|
作者
Brekke, Lee [1 ]
Buysman, Erin [1 ]
Grabner, Michael [2 ]
Ke, Xuehua [2 ]
Xie, Lin [3 ]
Baser, Onur [3 ,4 ,5 ]
Wei, Wenhui [6 ]
机构
[1] Optum, 11000 Optum Circle, Eden Prairie, MN 55344 USA
[2] HealthCore Inc, Wilmington, DE USA
[3] STATinMED Res, Ann Arbor, MI USA
[4] Univ Michigan, Ann Arbor, MI 48109 USA
[5] MEF Univ, Sch Econ Adm & Social Sci, Istanbul, Turkey
[6] Sanofi US, Bridgewater, NJ USA
关键词
choice; decomposition analysis; insulin glargine; liraglutide; personalized medicine; real-world; type; 2; diabetes; BLINDER-OAXACA DECOMPOSITION; HEALTH-CARE; MANAGEMENT; ASSOCIATION; STATEMENT; POSITION; OUTCOMES; VISITS;
D O I
10.1016/j.jval.2017.05.019
中图分类号
F [经济];
学科分类号
02 ;
摘要
Background: Determining characteristics of patients likely to benefit from a particular treatment could help physicians set personalized targets. OBJECTIVES: To use decomposition methodology on real-world data to identify the relative contributions of treatment effects and patients' baseline characteristics. METHODS: Decomposition analyses were performed on data from the Initiation of New Injectable Treatment Introduced after Antidiabetic Therapy with Oral-only Regimens (INITIATOR) study, a real-world study of patients with type 2 diabetes started on insulin glargine (GLA) or liraglutide (LIRA). These analyses investigated relative contributions of differences in baseline characteristics and treatment effects to observed differences in 1-year outcomes for reduction in glycated hemoglobin A1c (HbA1c) and treatment persistence. RESULTS: The greater HbA1c reduction seen with GLA compared with LIRA (-1.39% vs. -0.74%) was primarily due to differences in baseline characteristics (HbA1c and endocrinologist as prescribing physician; P < 0.050). Patients with baseline HbA1c of 9.0% or more or evidence of diagnosis codes related to mental illness achieved greater HbA1c reductions with GLA, whereas patients with baseline polypharmacy (6-10 classes) or hypogylcemia achieved greater reductions with LIRA. Decomposition analyses also showed that the higher persistence seen with GLA (65% vs. 49%) was mainly caused by differences in treatment effects (P < 0.001). Patients 65 years and older, those with HbA1c of 9.0% or more, those taking three oral antidiabetes drugs, and those with polypharmacy of more than 10 classes had higher persistence with GLA; patients 18 to 39 years and those with HbA1c of 7.0% to less than 8.0% had higher persistence with LIRA. CONCLUSIONS: Although decomposition does not demonstrate causal relationships, this method could be useful for examining the source of differences in outcomes between treatments in a real-world setting and could help physicians identify patients likely to respond to a particular treatment. Copyright (C) 2017 International Society for Pharmacoeconomics and Outcomes Research (ISPOR). Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:1252 / 1259
页数:8
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