Healthcare Utilization and Costs of Care in Patients With Irritable Bowel Syndrome With Constipation or Chronic Idiopathic Constipation After Initiating Oral Therapies: Real-World Analysis in the US Medicare Population

IF 3.4 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Eric Shah, Tsung-Ying Lee, Zachary Baldwin, Jens Kort, Masakazu Ando, Steven W. Champaloux, Mena Boules, Yuri Sanchez Gonzalez
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引用次数: 0

Abstract

Introduction

Irritable bowel syndrome with constipation (IBS-C) and chronic idiopathic constipation (CIC) are common functional intestinal disorders which impact all age groups, yet there is limited comparative evidence on the economic benefits of treatment of these conditions on the elderly. We assessed differences in healthcare resource utilization (HCRU) and total costs of care among Medicare-insured patients initiating linaclotide, lubiprostone, or plecanatide after 1 year.

Methods

Retrospective analysis from the Merative™ MarketScan® Medicare Database (January 2017–September 2023), including adult patients who initiated a qualifying IBS-C/CIC medication (linaclotide, lubiprostone, plecanatide) (index date defined as date of initiation) and had at least 6 months of pre-index and 12 months of post-index continuous benefit coverage under fee-for-service Medicare plans. For HCRU and all-cause total cost (medical + pharmacy) outcomes, 12-month comparisons were characterized via count (for HCRU) or cost ratios between linaclotide and lubiprostone, and linaclotide and plecanatide. Generalized linear regression models adjusting for key baseline patient characteristics and 6-month pre-index HCRU and cost were used to estimate differences in outcomes at 12 months between treatment groups.

Results

A total of 7916 Medicare patients were included in the analysis, of whom 5773 initiated linaclotide, 1856 initiated lubiprostone, and 287 initiated plecanatide. After adjusting for key patient characteristics and pre-index HCRU, count ratios > 1 demonstrated that patients who received lubiprostone versus linaclotide had significantly greater HCRU (P < 0.05) at 12 months. After 12 months follow-up, adjusted all-cause total costs of care were significantly lower among patients who received linaclotide versus lubiprostone or plecanatide, largely driven by lower all-cause medical costs observed in patients who received linaclotide (P < 0.05).

Conclusion

These findings suggest that linaclotide treatment may be associated with lower total healthcare costs compared to lubiprostone and plecanatide for patients initiating IBS-C/CIC-related drugs in Medicare populations.

肠易激综合征合并便秘或慢性特发性便秘患者在开始口服治疗后的医疗保健利用和护理成本:美国医疗保险人群的真实世界分析
肠易激综合征伴便秘(IBS-C)和慢性特发性便秘(CIC)是影响所有年龄组的常见功能性肠道疾病,但关于老年人治疗这些疾病的经济效益的比较证据有限。我们评估了医疗保险患者在1年后开始使用利那洛肽、鲁比前列酮或普莱那肽的医疗资源利用率(HCRU)和总护理成本的差异。方法:回顾性分析Merative™MarketScan®Medicare数据库(2017年1月- 2023年9月),包括开始使用符合条件的IBS-C/CIC药物(利那洛肽、鲁比前列酮、plecanatide)(指数日期定义为起始日期)的成年患者,并且在指数前和指数后至少有6个月的持续受益覆盖。对于HCRU和全因总成本(医疗+药房)结果,通过利那洛肽和鲁比前列酮、利那洛肽和普莱卡纳肽之间的HCRU计数或成本比进行12个月的比较。采用调整关键基线患者特征和6个月前指数HCRU和成本的广义线性回归模型来估计治疗组之间12个月结局的差异。结果:共有7916例Medicare患者纳入分析,其中利那洛肽5773例,鲁比前列酮1856例,plecantide 287例。在调整了关键患者特征和指数前HCRU后,计数比率bbbb1表明,接受鲁比前列石治疗的患者比接受利那洛肽治疗的患者有更大的HCRU (P)。结论:这些发现表明,在医疗保险人群中,对于开始使用IBS-C/ cic相关药物的患者,与鲁比前列石和普莱纳肽相比,利那洛肽治疗可能与更低的总医疗成本相关。
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来源期刊
Advances in Therapy
Advances in Therapy 医学-药学
CiteScore
7.20
自引率
2.60%
发文量
353
审稿时长
6-12 weeks
期刊介绍: Advances in Therapy is an international, peer reviewed, rapid-publication (peer review in 2 weeks, published 3–4 weeks from acceptance) journal dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of therapeutics and interventions (including devices) across all therapeutic areas. Studies relating to diagnostics and diagnosis, pharmacoeconomics, public health, epidemiology, quality of life, and patient care, management, and education are also encouraged. The journal is of interest to a broad audience of healthcare professionals and publishes original research, reviews, communications and letters. The journal is read by a global audience and receives submissions from all over the world. Advances in Therapy will consider all scientifically sound research be it positive, confirmatory or negative data. Submissions are welcomed whether they relate to an international and/or a country-specific audience, something that is crucially important when researchers are trying to target more specific patient populations. This inclusive approach allows the journal to assist in the dissemination of all scientifically and ethically sound research.
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