卡吡嗪对美国商业保险患者短期和长期残疾结果的实际影响。

IF 2.9 4区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Journal of Medical Economics Pub Date : 2025-12-01 Epub Date: 2025-03-04 DOI:10.1080/13696998.2025.2470014
Prakash S Masand, Mousam Parikh, Jamie Ta, Enrico Zanardo, Dominique Lejeune, Cristina Martínez, François Laliberté, Nadia Nabulsi
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引用次数: 0

摘要

目的:比较美国双相情感障碍(BP)、重度抑郁症(MDD)或精神分裂症谱系障碍(SCZ)患者在开始使用卡吡嗪之前和之后的全因和精神健康(MH)相关的短期和长期残疾休假和相关费用。方法:利用Merative MarketScan商业和健康与生产力管理(HPM)数据库(2016年1月至2021年12月)来识别诊断为BP、MDD或SCZ的成年人,这些成年人在基线(指数前12个月)和指数后≥3个月期间具有≥2次药房卡吡嗪索赔(首次索赔=指数)、≥3个月的卡吡嗪使用(辅助治疗MDD)和连续的商业保险覆盖和HPM资格。观察持续到卡吡嗪停药、保险或HPM资格结束、指数后1年或HPM数据可用性结束。评估了全因和mh相关的残疾索赔、天数和费用。使用比率比率(RR)比较基线与指数后的伤残索赔率(事件)和天数;使用平均成本差异来比较成本。比较由广义估计方程模型计算。在不同适应症中分别重复分析。结果:共489例患者(BP = 238, MDD = 233, SCZ = 18;平均年龄43.3岁;60.7%的女性;平均随访7.6个月)。cariprazine开始治疗后的全因致残率和天数分别比基线低29% (RR = 0.71 [95% CI = 0.57, 0.86])和28%(0.72[0.53,0.94])(两种ppp的局限性:对失业、无保险或有公共保险的患者的推广能力有限。结论:与开始使用卡吡嗪之前相比,使用卡吡嗪后致残事件、天数和平均费用显著降低。这些结果可以帮助理解卡吡嗪在这些患者的残疾管理中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The real-world impact of cariprazine on short- and long-term disability outcomes among commercially insured patients in the United States.

Aim: To compare all-cause and mental health (MH)-related short-term and long-term disability leaves and associated costs among patients in the United States with bipolar disorder (BP), major depressive disorder (MDD), or schizophrenia spectrum disorders (SCZ) before versus after cariprazine initiation.

Methods: Merative MarketScan Commercial and Health and Productivity Management (HPM) databases (January 2016 to December 2021) were utilized to identify adults diagnosed with BP, MDD, or SCZ with ≥2 pharmacy cariprazine claims (first claim = index), ≥3 months of cariprazine use (adjunctively for MDD), and continuous commercial insurance coverage and HPM eligibility during baseline (12 months pre-index) and ≥3 months post-index. Observation continued until cariprazine discontinuation, insurance or HPM eligibility end, 1 year post-index, or HPM data availability end. All-cause and MH-related disability claims, days, and costs were evaluated. Baseline versus post-index rates of disability claims (events) and days were compared using rate ratios (RR); costs were compared using mean cost differences. Comparisons were calculated from generalized estimating equation models. Analyses were replicated separately across indications.

Results: There were 489 patients overall (BP = 238, MDD = 233, SCZ = 18; mean age = 43.3 years; 60.7% female; mean follow-up = 7.6 months). All-cause rates of disability events and days following cariprazine initiation were 29% (RR = 0.71 [95% CI = 0.57, 0.86]) and 28% (0.72 [0.53, 0.94]) lower than baseline, respectively (both p < .05). MH-related rates of disability events and days were 40% (0.60 [0.43, 0.80]) and 43% (0.57 [0.34, 0.84]) lower, respectively (both p < .01). All-cause disability costs were $2,917 lower and MH-related disability costs were $2,482 lower than baseline (40% and 51% decrease, respectively; both p < .01). Results were similar for indication-specific analyses.

Limitations: Limited generalizability to patients who are unemployed, uninsured, or have public insurance.

Conclusions: Rates of disability events, days, and mean costs were significantly lower after versus before cariprazine initiation. These results can help contextualize cariprazine's role in managing disability for these patients.

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来源期刊
Journal of Medical Economics
Journal of Medical Economics HEALTH CARE SCIENCES & SERVICES-MEDICINE, GENERAL & INTERNAL
CiteScore
4.50
自引率
4.20%
发文量
122
期刊介绍: Journal of Medical Economics'' mission is to provide ethical, unbiased and rapid publication of quality content that is validated by rigorous peer review. The aim of Journal of Medical Economics is to serve the information needs of the pharmacoeconomics and healthcare research community, to help translate research advances into patient care and be a leader in transparency/disclosure by facilitating a collaborative and honest approach to publication. Journal of Medical Economics publishes high-quality economic assessments of novel therapeutic and device interventions for an international audience
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