Voriconazole vs isavuconazole治疗侵袭性曲霉病:美国医疗保险人群的回顾性分析(2017-2020)

IF 3.8 Q2 INFECTIOUS DISEASES
Therapeutic Advances in Infectious Disease Pub Date : 2025-06-27 eCollection Date: 2025-01-01 DOI:10.1177/20499361251347778
Sophea Chan, Laura Leigh Stoudenmire, Xianyan Chen, Duna Zhan, Andrés F Henao-Martínez, Daniel B Chastain
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引用次数: 0

摘要

背景:虽然isavuconazole (ISA)在治疗侵袭性曲霉病(IA)的临床试验中表现出与voriconazole (VCZ)的非劣效性,但现实世界的比较是有限的。目的:比较VCZ与ISA治疗IA患者的治疗完成度、不良事件、住院率和医疗费用。设计:回顾性队列研究,使用Merative MarketScan索赔数据(2017-2020)。方法:包括接受VCZ或ISA单药治疗的诊断为IA(国际疾病分类,第十次修订,临床修改(ICD-10-CM)代码)的成年人(大于或等于18岁)。治疗完成被定义为治疗时间大于或等于42天。描述性统计和逻辑回归用于评估抗真菌药物选择、不良事件、住院和治疗完成的结局和预测因素。结果:335例患者中,84% (n = 282)接受VCZ治疗,16% (n = 53)接受ISA治疗。基线特征具有可比性,尽管VCZ组有较高的医疗补助登记,而ISA组有更多的恶性肿瘤患者。治疗完成率具有可比性(92%,p = 1),中位治疗持续时间(VCZ: 120天,ISA: 112天,p = 0.95)。不良事件发生率无显著性差异(VCZ: 49%, ISA: 60%, p = 0.18),但ISA组cns相关事件发生率更高(16% vs 9%, p = 0.32)。VCZ与较低的门诊药房费用相关(中位数为1,596.68美元vs 11,000 0.66美元,p p = 0.01)。恶性肿瘤患者接受VCZ治疗的几率较低(OR 0.30, p = 0.001),年龄越小,治疗不完全的几率越高(OR 0.97, p = 0.035)。女性与不良事件风险增加有关。值得注意的是,VCZ的使用与不良事件的增加或治疗不完全无关。结论:尽管治疗时间和完成率相似,但VCZ治疗IA的频率是ISA的5倍。VCZ与较低的费用相关,并且不会增加不良事件或停药的风险。这些发现表明,VCZ仍然是IA的常用治疗方法,并且可能是更具成本效益的治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Voriconazole versus isavuconazole for invasive aspergillosis: a retrospective analysis in a medically insured U.S. population (2017-2020).

Background: While isavuconazole (ISA) has demonstrated non-inferiority to voriconazole (VCZ) for invasive aspergillosis (IA) in clinical trials, real-world comparisons are limited.

Objectives: To compare treatment completion, adverse events, hospitalizations, and healthcare costs in patients treated with VCZ versus ISA for IA.

Design: Retrospective cohort study using Merative MarketScan claims data (2017-2020).

Methods: Adults (⩾18 years) diagnosed with IA (International Classification of Diseases, Tenth Revision, Clinical Modification (ICD-10-CM) codes) who received VCZ or ISA monotherapy were included. Treatment completion was defined as ⩾42 days of therapy. Descriptive statistics and logistic regression were used to assess outcomes and predictors of antifungal selection, adverse events, hospitalizations, and treatment completion.

Results: Among 335 patients, 84% (n = 282) received VCZ and 16% (n = 53) received ISA. Baseline characteristics were comparable, although the VCZ group had higher Medicaid enrollment, and the ISA group had more patients with malignancy. Treatment completion rates were comparable (92% each, p = 1), as were median treatment durations (VCZ: 120 days, ISA: 112 days, p = 0.95). Adverse event rates were not significantly different (VCZ: 49%, ISA: 60%, p = 0.18), but CNS-related events occurred more frequently with ISA (16% vs 9%, p = 0.32). VCZ was associated with lower outpatient pharmacy costs (median $1,596.68 vs $11,000.66, p < 0.001) and total hospitalization costs (median $40,681.89 vs $121,545.89, p = 0.01). Malignancy was associated with lower odds of receiving VCZ (OR 0.30, p = 0.001), and younger age predicted higher odds of treatment incompletion (OR 0.97, p = 0.035). Female sex was associated with increased adverse event risk. Notably, VCZ use was not associated with increased adverse events or treatment incompletion.

Conclusion: VCZ was prescribed five times more frequently than ISA for IA, despite similar treatment durations and completion rates. VCZ was associated with lower costs and did not increase the risk of adverse events or treatment discontinuation. These findings suggest that VCZ remains commonly used and potentially more cost-effective treatment option for IA.

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CiteScore
5.30
自引率
8.80%
发文量
64
审稿时长
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