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系统性硬皮病相关肺动脉高压患者联合治疗的成本效益。

Cost-Effectiveness of Combination Therapy for Patients With Systemic Sclerosis-Related Pulmonary Arterial Hypertension.

机构信息

Centre for Health PolicyMelbourne School of Population and Global HealthThe University of Melbourne Parkville VIC Australia.

Department of Medicine The University of Melbourne at St Vincent's Hospital (Melbourne) Fitzroy VIC Australia.

出版信息

J Am Heart Assoc. 2021 Apr 6;10(7):e015816. doi: 10.1161/JAHA.119.015816. Epub 2021 Mar 24.

Abstract

Background To evaluate the cost-effectiveness of combination pulmonary arterial hypertension specific therapy in systemic sclerosis-related PAH. Methods and Results Health outcomes and costs were captured through data linkage. Health utility was derived from Medical Outcomes Study Short Form-36 scores. A probabilistic discrete-time model was developed to simulate lifetime changes in costs and health utility. Mortality was predicted using a Gompertz parametric survival model. For both treatment arms, the simulations were started using the same cohort of 10 000 patients. Probabilistic sensitivity analysis was performed using the Monte Carlo simulation with 1000 sets of sampled parameter values. Of 143 patients with systemic sclerosis-related pulmonary arterial hypertension, 89 were on monotherapy and 54 on combination therapy. Mean simulated costs per patient per year in monotherapy and combination therapy groups were AU$23 411 (US$16 080) and AU$29 129 (US$19 982), respectively. Mean life years and quality-adjusted life years from pulmonary arterial hypertension diagnosis to death of patients receiving monotherapy were 7.1 and 3.0, respectively, and of those receiving combination therapy were 9.2 and 3.9, respectively. Incremental costs per life year and quality-adjusted life year gained of combination therapy compared with monotherapy were AU$47 989 (US$32 920) and AU$113 823 (US$78 082), respectively. At a willingness-to-pay threshold of AU$102 000 (US$69 972) per life year gained, and of AU$177 222 (US$121 574) per quality-adjusted life year gained, the probability of combination therapy being cost-effective was 0.95. Conclusions The incremental cost per quality-adjusted life year gained of combination therapy compared with monotherapy was substantial in the base case analysis. Given the fatal prognosis of systemic sclerosis-related pulmonary arterial hypertension and the incremental cost per life year of AU$47 989 (US$32 920), combination therapy could be considered cost-effective in systemic sclerosis-related pulmonary arterial hypertension.

摘要

背景

评估肺动脉高压特定联合治疗方案在系统性硬化症相关肺动脉高压中的成本效益。

方法和结果

通过数据链接获取健康结果和成本。健康效用来自 Medical Outcomes Study Short Form-36 评分。开发了一个概率离散时间模型来模拟终生的成本和健康效用变化。使用 Gompertz 参数生存模型预测死亡率。对于两个治疗组,模拟都是从 10000 名患者的同一队列开始的。使用蒙特卡罗模拟进行概率敏感性分析,使用 1000 组抽样参数值。在 143 名系统性硬化症相关肺动脉高压患者中,89 名接受单一药物治疗,54 名接受联合治疗。在单一药物治疗和联合治疗组中,每位患者每年的平均模拟成本分别为 23411 澳元(16080 美元)和 29129 澳元(19982 美元)。接受单一药物治疗的患者从肺动脉高压诊断到死亡的平均寿命和质量调整生命年分别为 7.1 年和 3.0 年,接受联合治疗的患者分别为 9.2 年和 3.9 年。与单一药物治疗相比,联合治疗的增量成本每年每获得一个生命和质量调整生命年分别为 47989 澳元(32920 美元)和 113823 澳元(78082 美元)。在愿意支付的每年获得一个生命的 102000 澳元(69972 美元)和每年获得一个质量调整生命年的 177222 澳元(121574 美元)的阈值下,联合治疗具有成本效益的概率为 0.95。

结论

在基础病例分析中,与单一药物治疗相比,联合治疗的每质量调整生命年增量成本较高。考虑到系统性硬化症相关肺动脉高压的致命预后以及每年 47989 澳元(32920 美元)的增量成本,联合治疗可能在系统性硬化症相关肺动脉高压中具有成本效益。

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