Department of Pharmaceutical Outcomes and Policy, University of Florida College of Pharmacy, HPNP Building Room 3325, 1225 Center Drive, Gainesville, FL, 32610, USA.
Division of Infectious Diseases, Department of Medicine and Center for Clinical Epidemiology and Biostatistics, Center for Pharmacoepidemiology Research and Training, Department of Biostatistics, Epidemiology, and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Dig Dis Sci. 2020 Nov;65(11):3159-3174. doi: 10.1007/s10620-019-06037-z. Epub 2020 Jan 14.
Despite the high efficacy and safety associated with direct-acting antivirals (DAAs), access to HCV treatment has been frequently restricted because of the high DAA drug costs.
To (1) compare HCV treatment initiation rates between HCV monoinfected and HCV/HIV coinfected patients before (pre-DAA period) and after (post-DAA period) all-oral DAAs became available; and to (2) estimate the HCV treatment costs for payers and patients.
A retrospective analysis of the MarketScan Databases (2009-2016) was conducted for newly diagnosed HCV patients. Multivariable logistic regression was used to estimate the odds ratio (OR) of initiating HCV treatments during the pre-DAA and post-DAA periods. Kruskal-Wallis test was used to compare drug costs for dual, triple and all-oral therapies.
A total of 15,063 HCV patients [382 (2.5%) HIV coinfected] in the pre-DAA period and 14,896 [429 (2.9%) HIV coinfected] in the post-DAA period were included. HCV/HIV coinfected patients had lower odds of HCV treatment uptake compared to HCV monoinfected patients during the pre-DAA period [OR, 0.59; 95% confidence interval (CI), 0.45-0.78], but no significant difference in odds of HCV treatment uptake was observed during the post-DAA period (OR, 1.08; 95% CI, 0.87-1.33). From 2009 to 2016, average payers' treatment costs (dual, $20,820; all-oral DAAs, $99,661; p < 0.001) as well as average patients' copayments (dual, $593; all-oral DAAs $933; p < 0.001) increased significantly.
HCV treatment initiation rates increased, especially among HCV/HIV coinfected patients, from the pre-DAA to the post-DAA period. However, payers' expenditures per course of therapy saw an almost fivefold increase and patients' copayments increased by 55%.
尽管直接作用抗病毒药物(DAAs)具有较高的疗效和安全性,但由于 DAA 药物费用较高,HCV 治疗的可及性经常受到限制。
(1)比较全口服 DAAs 可用之前(DAA 前时期)和之后(DAA 后时期) HCV 单感染和 HCV/HIV 合并感染患者开始 HCV 治疗的比率;(2)估算支付方和患者的 HCV 治疗费用。
对 MarketScan 数据库(2009-2016 年)进行了一项新诊断 HCV 患者的回顾性分析。采用多变量逻辑回归估计 DAA 前和 DAA 后时期开始 HCV 治疗的优势比(OR)。Kruskal-Wallis 检验用于比较双重、三重和全口服治疗的药物费用。
在 DAA 前时期纳入了 15063 例 HCV 患者[382 例(2.5%)HIV 合并感染],在 DAA 后时期纳入了 14896 例[429 例(2.9%)HIV 合并感染]。与 HCV 单感染患者相比,HCV/HIV 合并感染患者在 DAA 前时期接受 HCV 治疗的可能性较低[OR,0.59;95%置信区间(CI),0.45-0.78],但在 DAA 后时期接受 HCV 治疗的可能性无显著差异(OR,1.08;95% CI,0.87-1.33)。从 2009 年到 2016 年,支付方的平均治疗费用(双重治疗,20820 美元;全口服 DAA 治疗,99661 美元;p<0.001)以及患者的平均 copayment(双重治疗,593 美元;全口服 DAA 治疗,933 美元;p<0.001)均显著增加。
从 DAA 前时期到 DAA 后时期,HCV 治疗的起始率增加,尤其是在 HCV/HIV 合并感染患者中。然而,每个疗程的支付方支出增加了近五倍,患者 copayment 增加了 55%。