Bancroft Tim, Lim Jonathan, Wang Cheng, Sander Stephen D, Swindle Jason P
Health Economics and Outcomes Research, Inc., Optum, Eden Prairie, Minnesota.
Health Economics and Outcomes Research, Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, Connecticut.
Clin Ther. 2016 Mar;38(3):545-56.e1-6. doi: 10.1016/j.clinthera.2016.01.008. Epub 2016 Feb 5.
This study compared health care resource utilization (HCRU), costs, and persistence among patients newly diagnosed as having nonvalvular atrial fibrillation (NVAF) and newly treated with dabigatran versus warfarin.
This retrospective claims-based study used data from a large US managed care organization. The earliest claim for dabigatran or warfarin during October 1, 2010 through October 31, 2011 was the index date, with cohort assignment based on index medication. Evidence of newly diagnosed NVAF within 30 days before the index date and no claims for oral anticoagulants during the 12-month preindex period were required. Cohorts were matched using propensity scores. Per-patient-per-month HCRU, costs, and persistence were calculated during the variable follow-up period of up to 12 months after the index date. Descriptive and multivariable analyses were used to examine differences in outcomes.
After matching, 869 patients per cohort were identified (mean age, 67.8 years; 40.4% female). Compared with warfarin, dabigatran had fewer per-patient-per-month emergency department (0.10 vs 0.13, P = 0.010), office (1.98 vs 2.96, P < 0.001), and outpatient (1.05 vs 1.48, P < 0.001) visits. Despite higher mean pharmacy costs for dabigatran (P < 0.001), mean total health care (P = 0.309) and medical costs (P = 0.568) were similar to warfarin. Persistence was higher with dabigatran versus warfarin (median, 204 vs 161 days; mean, 213.7 vs 195.5 days, P = 0.001).
Among patients newly diagnosed as having NVAF, those newly treated with dabigatran had lower HCRU, higher persistence, and similar total health care costs compared with those treated with warfarin.
本研究比较了新诊断为非瓣膜性心房颤动(NVAF)并开始使用达比加群与华法林治疗的患者的医疗资源利用(HCRU)、成本及治疗持续性。
这项基于索赔数据的回顾性研究使用了美国一家大型管理式医疗组织的数据。2010年10月1日至2011年10月31日期间最早的达比加群或华法林索赔日期为索引日期,根据索引用药进行队列分配。要求在索引日期前30天内有新诊断NVAF的证据,且在索引前12个月内无口服抗凝剂索赔记录。使用倾向得分对队列进行匹配。在索引日期后的长达12个月的可变随访期内计算每位患者每月的HCRU、成本及治疗持续性。采用描述性和多变量分析来检验结果差异。
匹配后,每个队列确定了869例患者(平均年龄67.8岁;40.4%为女性)。与华法林相比,达比加群每位患者每月的急诊科就诊次数(0.10对0.13,P = 0.010)、门诊就诊次数(1.98对2.96,P < 0.001)和门诊就诊次数(1.05对1.48,P < 0.001)更少。尽管达比加群的平均药房成本较高(P < 0.001),但平均总医疗成本(P = 0.309)和医疗成本(P = 0.568)与华法林相似。达比加群的治疗持续性高于华法林(中位数,204天对161天;平均值,213.7天对195.5天,P = 0.001)。
在新诊断为NVAF的患者中,与接受华法林治疗的患者相比,接受达比加群新治疗的患者HCRU更低、治疗持续性更高且总医疗成本相似。