Real-world persistence and adherence to glucagon-like peptide-1 receptor agonists among obese commercially insured adults without diabetes.

IF 2.3 4区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Patrick P Gleason, Benjamin Y Urick, Landon Z Marshall, Nicholas Friedlander, Yang Qiu, R Scott Leslie
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引用次数: 0

Abstract

Background: In 2014, the US Food and Drug Administration approved the first glucagon-like peptide-1 (GLP-1) receptor agonist product, liraglutide injection, for obesity treatment. Many GLP-1 obesity treatment clinical trials report significant weight loss and medication adherence at more than 85%. Little is known about the real-world GLP-1 obesity treatment adherence, persistence, and switch rates.

Objective: To measure GLP-1 therapy persistence, adherence, and switch rates in a real-world cohort of members without diabetes using these drugs for obesity treatment.

Methods: Integrated pharmacy and medical claims data from 16.5 million average monthly commercially insured membership were used to identify obese members without diabetes newly initiating GLP-1 therapy between January 1, 2021, and December 31, 2021. Members were required to be continuously enrolled 1-year before and after the GLP-1 therapy start date and aged 19 years of age or older. Persistence was measured as no greater than or equal to 60-day gap with allowance for GLP-1 switching. Adherence was measured as the proportion of days covered (PDC) and members with a PDC greater than or equal to 80% were considered adherent. GLP-1 product switching was also assessed descriptively.

Results: 4,066 commercially insured obese members without diabetes that newly initiated GLP-1 therapy met all study criteria. The mean age was 46 years, and 81% were female. Overall, GLP-1 persistence was 46.3% at 180 days and 32.3% at 1 year. The highest and lowest persistence rates at 1 year were observed for semaglutide (Ozempic) at 47.1% and liraglutide (Saxenda) 19.2%, respectively. Average PDC during the 1-year assessment was 51.0% with 27.2% adherent to therapy and 11.1% switched GLP-1 drugs.

Conclusions: This GLP-1 weight loss treatment real-world analysis, among obese individuals without diabetes, found poor 1-year persistence and adherence and low rates of switching between products. These findings will aid in assessing products cost-effectiveness, understanding obesity care management program needs, forecasting future GLP-1 use and cost trends, and negotiating GLP-1 pharmaceutical manufacturer value-based purchasing agreements.

无糖尿病的肥胖商业保险成年人对胰高血糖素样肽-1 受体激动剂的实际坚持和依从性。
背景:2014 年,美国食品和药物管理局批准了首个用于肥胖治疗的胰高血糖素样肽-1(GLP-1)受体激动剂产品--利拉鲁肽注射液。许多 GLP-1 肥胖治疗临床试验报告显示,患者体重明显减轻,服药依从性超过 85%。但人们对现实世界中 GLP-1 肥胖治疗的依从性、持续性和转换率知之甚少:目的:测量现实世界中使用 GLP-1 治疗肥胖症的非糖尿病患者的 GLP-1 治疗坚持率、持续率和转换率:方法:利用平均每月 1650 万名商业保险会员的综合药房和医疗索赔数据,确定 2021 年 1 月 1 日至 2021 年 12 月 31 日期间新开始 GLP-1 治疗的无糖尿病肥胖会员。会员必须在 GLP-1 治疗开始日期前后 1 年连续投保,且年龄在 19 岁或以上。持续性的衡量标准是在允许 GLP-1 转换的情况下,间隔期不大于或等于 60 天。依从性以覆盖天数比例(PDC)来衡量,PDC 大于或等于 80% 的成员被视为依从性良好。还对 GLP-1 产品转换进行了描述性评估:有 4,066 名无糖尿病的商业保险肥胖会员新近开始接受 GLP-1 治疗,符合所有研究标准。平均年龄为 46 岁,81% 为女性。总体而言,GLP-1 180 天的持续率为 46.3%,1 年的持续率为 32.3%。在 1 年的持续率中,塞马鲁肽(Ozempic)最高,为 47.1%;利拉鲁肽(Saxenda)最低,为 19.2%。1年评估期间的平均PDC为51.0%,其中27.2%坚持治疗,11.1%更换GLP-1药物:这项 GLP-1 减肥治疗真实世界分析发现,在无糖尿病的肥胖人群中,1 年的持续性和依从性较差,产品间的转换率较低。这些发现有助于评估产品的成本效益,了解肥胖症护理管理计划的需求,预测未来 GLP-1 的使用和成本趋势,以及协商 GLP-1 制药生产商基于价值的采购协议。
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来源期刊
Journal of managed care & specialty pharmacy
Journal of managed care & specialty pharmacy Health Professions-Pharmacy
CiteScore
3.50
自引率
4.80%
发文量
131
期刊介绍: JMCP welcomes research studies conducted outside of the United States that are relevant to our readership. Our audience is primarily concerned with designing policies of formulary coverage, health benefit design, and pharmaceutical programs that are based on evidence from large populations of people. Studies of pharmacist interventions conducted outside the United States that have already been extensively studied within the United States and studies of small sample sizes in non-managed care environments outside of the United States (e.g., hospitals or community pharmacies) are generally of low interest to our readership. However, studies of health outcomes and costs assessed in large populations that provide evidence for formulary coverage, health benefit design, and pharmaceutical programs are of high interest to JMCP’s readership.
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