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四种凝血因子浓缩物(4F-PCC)治疗因子 Xa 抑制剂相关出血患者的安全性、疗效和成本:一项回顾性研究。

Safety, efficacy, and cost of four-factor prothrombin complex concentrate (4F-PCC) in patients with factor Xa inhibitor-related bleeding: a retrospective study.

机构信息

Medical University of South Carolina, 150 Ashley Avenue, Charleston, SC, 29425, USA.

出版信息

J Thromb Thrombolysis. 2019 Aug;48(2):250-255. doi: 10.1007/s11239-019-01846-5.

Abstract

Oral factor Xa (fXa) inhibitor-related bleeding is a concerning drug safety problem. There is considerable controversy surrounding available reversal strategies. The recently approved reversal agent andexanet alfa has limited data, an unclear safety profile, and imparts a substantial financial burden. This has led to the off-label use of four-factor prothrombin complex concentrates (4F-PCC) for this indication. This study aimed to assess the safety and efficacy of 4F-PCC for the management of major bleeding related to oral fXa inhibitors. This observational, retrospective study included adult patients admitted from 2014 to 2018 who received 4F-PCC (Kcentra) for fXa inhibitor-related major bleeding. Efficacy was assessed using criteria described by Sarode et al. Secondary outcomes included the incidence of thromboembolism, mortality, and a cost analysis comparing 4F-PCC to andexanet alfa for reversal of oral fXa inhibitors. Thirty-one patients received 4F-PCC for major bleeding associated with apixaban (55%) or rivaroxaban (45%). Intracranial hemorrhage (58%) and pericardial effusion (16%) accounted for the majority of bleeding events. Most patients received a single weight-based 4F-PCC dose of 25 units/kg (38.7%) or 50 units/kg (51.6%). Effective hemostasis was achieved in 80.6% of patients. Five patients (16%) died due to acute bleeding and no thromboembolic events were observed. Administration of 4F-PCC was effective for most patients requiring emergent reversal of anticoagulation with apixaban or rivaroxaban and was associated with a low risk of thromboembolic events. Considerable cost differences limit the use of andexanet alfa and may warrant further study of 4F-PCC for fXa inhibitor reversal.

摘要

口服因子 Xa(fXa)抑制剂相关出血是一个令人关注的药物安全问题。现有的逆转策略存在很大争议。最近批准的逆转剂andexanet alfa 数据有限,安全性不明,且带来巨大的经济负担。这导致了四种因子凝血酶原复合物浓缩物(4F-PCC)在该适应证中的非适应证使用。本研究旨在评估 4F-PCC 用于管理与口服 fXa 抑制剂相关的大出血的安全性和有效性。这是一项观察性、回顾性研究,纳入了 2014 年至 2018 年因 fXa 抑制剂相关大出血而接受 4F-PCC(Kcentra)治疗的成年患者。采用 Sarode 等人描述的标准评估疗效。次要结局包括血栓栓塞发生率、死亡率以及比较 4F-PCC 与 andexanet alfa 逆转口服 fXa 抑制剂的成本分析。31 例患者因接受阿哌沙班(55%)或利伐沙班(45%)治疗而发生大出血而接受了 4F-PCC 治疗。颅内出血(58%)和心包积液(16%)占大多数出血事件。大多数患者接受了单次体重剂量的 4F-PCC(25 单位/kg,38.7%)或 50 单位/kg(51.6%)。80.6%的患者实现了有效的止血。5 例(16%)患者因急性出血死亡,未观察到血栓栓塞事件。4F-PCC 对大多数需要紧急逆转阿哌沙班或利伐沙班抗凝的患者有效,且血栓栓塞事件风险低。显著的成本差异限制了 andexanet alfa 的使用,可能需要进一步研究 4F-PCC 用于 fXa 抑制剂逆转。

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