Division of Research, Kaiser Permanente Northern California, 2000 Broadway, Oakland, CA, 94612, USA.
Department of Health Systems Science, Kaiser Permanente Bernard J. Tyson School of Medicine, Pasadena, CA, USA.
J Thromb Thrombolysis. 2022 Oct;54(3):470-479. doi: 10.1007/s11239-022-02695-5. Epub 2022 Aug 19.
Limited data exist in large, representative populations about whether the risk of thromboembolic events varies after receiving four-factor human prothrombin complex concentrate (4F-PCC) versus treatment with human plasma for urgent reversal of oral vitamin K antagonist therapy. We conducted a multicenter observational study to compare the 45-day risk of thromboembolic events in adults with warfarin-associated major bleeding after treatment with 4F-PCC (Kcentra®) or plasma. Hospitalized patients in two large integrated healthcare delivery systems who received 4F-PCC or plasma for reversal of warfarin due to major bleeding from January 1, 2008 to March 31, 2020 were identified and were matched 1:1 on potential confounders and a high-dimensional propensity score. Arterial and venous thromboembolic events were identified up to 45 days after receiving 4F-PCC or plasma from electronic health records and adjudicated by physician review. Among 1119 patients receiving 4F-PCC and a matched historical cohort of 1119 patients receiving plasma without a recent history of thromboembolism, mean (SD) age was 76.7 (10.5) years, 45.6% were women, and 9.4% Black, 14.6% Asian/Pacific Islander, and 15.7% Hispanic. The 45-day risk of thromboembolic events was 3.4% in those receiving 4F-PCC and 4.1% in those receiving plasma (P = 0.26; adjusted hazard ratio 0.76; 95% confidence interval 0.49-1.16). The adjusted risk of all-cause death at 45 days post-treatment was lower in those receiving 4F-PCC compared with plasma. Among a large, ethnically diverse cohort of adults treated for reversal of warfarin-associated bleeding, receipt of 4F-PCC was not associated with an excess risk of thromboembolic events at 45 days compared with plasma therapy.
关于在接受 4 因子人凝血酶原复合物浓缩物(4F-PCC)与用人血浆紧急逆转口服维生素 K 拮抗剂治疗后,血栓栓塞事件的风险是否存在差异,在大型代表性人群中仅有有限的数据。我们进行了一项多中心观察性研究,比较了在华法林相关大出血后接受 4F-PCC(Kcentra®)或血浆治疗的成年人在 45 天内血栓栓塞事件的风险。从 2008 年 1 月 1 日至 2020 年 3 月 31 日,从两个大型综合医疗服务提供系统中确定了因大出血而接受 4F-PCC 或血浆治疗以逆转华法林的住院患者,并根据潜在混杂因素和高维倾向评分进行了 1:1 匹配。从电子健康记录中确定了接受 4F-PCC 或血浆治疗后 45 天内的动脉和静脉血栓栓塞事件,并由医生审查进行裁决。在接受 4F-PCC 的 1119 名患者和接受无近期血栓栓塞史的血浆的 1119 名匹配历史队列中,平均(SD)年龄为 76.7(10.5)岁,45.6%为女性,9.4%为黑人,14.6%为亚裔/太平洋岛民,15.7%为西班牙裔。接受 4F-PCC 的患者中血栓栓塞事件的 45 天风险为 3.4%,接受血浆的患者中为 4.1%(P=0.26;调整后的危险比为 0.76;95%置信区间为 0.49-1.16)。与接受血浆治疗的患者相比,接受 4F-PCC 治疗的患者在治疗后 45 天的全因死亡风险较低。在一个大型、种族多样化的成年人群中,因逆转华法林相关出血而接受治疗的患者中,与接受血浆治疗相比,接受 4F-PCC 治疗与 45 天内血栓栓塞事件风险增加无关。