Cai Jennifer, Preblick Ronald, Zhang Qiaoyi, Kwong Winghan Jacqueline
Associate Director, Health Economics & Outcomes Research, Daiichi Sankyo, Inc, Parsippany, NJ.
Director, Health Economics & Outcomes Research, Daiichi Sankyo, Inc, Parsippany, NJ.
Am Health Drug Benefits. 2014 Nov;7(8):444-51.
Clinical guidelines recommend parenteral anticoagulation therapy with an early initiation of warfarin therapy for the treatment of patients with acute venous thromboembolism (VTE) and the prevention of recurrence.
To evaluate the outpatient utilization of parenteral anticoagulant therapy and warfarin among patients with VTE, and to examine the effects of parenteral anticoagulant use and the time to warfarin initiation from VTE diagnosis on the risk for VTE recurrence.
The Truven Health MarketScan Commercial Claims Database was used to identify patients aged 18 to 64 years who had an outpatient claim for deep-vein thrombosis or pulmonary embolism between January 2010 and December 2011 (ie, index date) and had no VTE diagnosis or treatment during the 12 months before the index date, had no hospital or emergency department VTE claim within 7 days after the index outpatient VTE claim, and had received warfarin <30 days after the index date. A recurrent VTE event was defined as a VTE-related emergency department visit or hospitalization within 8 to 365 days after the index date. A Cox proportional hazards model was used to estimate the adjusted hazard ratio (HR) associated with VTE recurrence risk related to parenteral anticoagulant use and warfarin initiation timing.
A total of 5820 patients were included in the study (mean age, 50.5 years); of these, 45% were female. A total of 75.7% (4403) of the patients receiving warfarin also received a parenteral anticoagulant, and the median time from VTE diagnosis to warfarin initiation was 5 days for parenteral anticoagulant users compared with 11 days for nonusers. Parenteral anticoagulant use was associated with a 49% recurrent VTE risk reduction (HR, 0.51; 95% confidence interval [CI], 0.43-0.60; P <.001). Each day of delayed warfarin initiation from the diagnosis of acute VTE was associated with a 1% increase in the risk for VTE recurrence (HR, 1.01; 95% CI, 1.01-1.02; P = .003).
Overall, 1 in 4 patients with VTE who had received warfarin in the outpatient setting did not receive parenteral anticoagulation therapy. Among those who received warfarin, its initiation was not always timely, despite its positive effects on reducing VTE recurrence. These findings highlight the potential quality-of-care concerns associated with the failure to use or the delayed implementation of guideline-recommended VTE treatment, and the need to improve compliance with clinical guidelines in the treatment of patients with VTE.
临床指南推荐采用肠外抗凝治疗,并尽早开始华法林治疗,用于治疗急性静脉血栓栓塞症(VTE)患者并预防复发。
评估VTE患者肠外抗凝治疗和华法林的门诊使用情况,并研究肠外抗凝剂的使用以及从VTE诊断到开始使用华法林的时间对VTE复发风险的影响。
使用Truven Health MarketScan商业索赔数据库,识别2010年1月至2011年12月期间(即索引日期)有门诊深静脉血栓形成或肺栓塞索赔记录、在索引日期前12个月内无VTE诊断或治疗记录、在索引门诊VTE索赔后7天内无医院或急诊科VTE索赔记录且在索引日期后<30天接受华法林治疗的18至64岁患者。复发性VTE事件定义为索引日期后8至365天内与VTE相关的急诊科就诊或住院。采用Cox比例风险模型估计与肠外抗凝剂使用和华法林起始时间相关的VTE复发风险的调整后风险比(HR)。
共有5820名患者纳入研究(平均年龄50.5岁);其中45%为女性。接受华法林治疗的患者中,共有75.7%(4403名)也接受了肠外抗凝剂治疗,肠外抗凝剂使用者从VTE诊断到开始使用华法林的中位时间为5天,而非使用者为11天。使用肠外抗凝剂与VTE复发风险降低49%相关(HR,0.51;95%置信区间[CI],0.43 - 0.60;P <.001)。从急性VTE诊断开始,华法林起始时间每延迟一天,VTE复发风险增加1%(HR,1.01;95%CI,1.01 - 1.02;P =.003)。
总体而言,在门诊接受华法林治疗的VTE患者中,四分之一未接受肠外抗凝治疗。在接受华法林治疗的患者中,尽管其对降低VTE复发有积极作用,但其起始并不总是及时的。这些发现凸显了与未使用或延迟实施指南推荐的VTE治疗相关的潜在医疗质量问题,以及改善VTE患者治疗中遵循临床指南情况的必要性。