Marcos-Jubilar M, García Erce J A, Martínez-Calle N, Páramo J A, Martínez Virto A, Quintana-Díaz M
Hematology Service, Clínica Universidad de Navarra, Pamplona, Spain.
Banco de Sangre y Tejidos de Navarra, Pamplona, Spain.
Transfus Med. 2019 Aug;29(4):268-274. doi: 10.1111/tme.12621. Epub 2019 Jul 25.
To evaluate the effectiveness and safety of prothrombin complex concentrates (PCCs) in approved and off-label indications.
PCCs are approved for the urgent reversal of vitamin K antagonists (VKAs). Data concerning the efficacy, safety and dosing for off-label indications are limited, but they are included in massive bleeding protocols.
This was a retrospective review of cases treated with four-factor PCCs (4F-PCCs) between January 2009 and 2016. Efficacy end-points include: (i) VKA reversal efficacy assessed by international normalised ratio (INR) normalisation (<1·5) and (ii) clinical efficacy as bleeding cessation and/or decreased number of transfused blood components and 24-h mortality in bleeding coagulopathy. The safety end-point is the incidence of thromboembolic events.
A total of 328 patients were included (51·8% male, median age 78 years old). Indications were as follows: VKA reversal (66·6%), bleeding coagulopathy (30·5%) and direct anticoagulant (DOAC) reversal due to bleeding (2·5%). VKA reversal was effective in 97·1% of patients, and 76·5% demonstrated complete reversal (INR < 1·5); only 34·3% patients needed hemoderivatives. Prior to emergency procedures, PCCs achieved global responses in 83% of patients, with no bleeding complication during intervention. DOAC reversal was effective in 88·9% of patients. Bleeding cessation was associated with the dose administered (P = 0·002). In coagulopathy bleeding, haemorrhage cessation, established by the International Society of Thrombosis and Haemostais (ISTH) definition, occurred in 56·7% of massive bleeding events and in 42·5% of other coagulopathies; 24-h mortality was 30%, mainly related to active bleeding. Ten thrombotic episodes were observed (3·1%).
4F-PCC was effective as adjuvant treatment with an acceptable safety profile, not only for the emergent reversal of VKAs but also for refractory coagulopathy associated with major bleeding.
评估凝血酶原复合物浓缩剂(PCCs)在已批准和未批准适应症中的有效性和安全性。
PCCs被批准用于紧急逆转维生素K拮抗剂(VKAs)。关于未批准适应症的疗效、安全性和剂量的数据有限,但它们被纳入了大出血治疗方案中。
这是一项对2009年1月至2016年期间接受四因子PCCs(4F-PCCs)治疗的病例的回顾性研究。疗效终点包括:(i)通过国际标准化比值(INR)正常化(<1.5)评估的VKA逆转疗效,以及(ii)作为出血停止和/或输注血液成分数量减少以及出血性凝血病24小时死亡率的临床疗效。安全终点是血栓栓塞事件的发生率。
共纳入328例患者(51.8%为男性,中位年龄78岁)。适应症如下:VKA逆转(66.6%)、出血性凝血病(30.5%)和因出血导致的直接口服抗凝剂(DOAC)逆转(2.5%)。97.1%的患者VKA逆转有效,76.5%的患者实现完全逆转(INR<1.5);只有34.3%的患者需要血液制品。在急诊手术前,PCCs在83%的患者中取得了整体反应,干预期间无出血并发症。DOAC逆转在88.9%的患者中有效。出血停止与给药剂量相关(P=0.002)。在凝血病出血中,根据国际血栓与止血学会(ISTH)的定义确定的出血停止发生在56.7%的大出血事件和42.5%的其他凝血病中;24小时死亡率为30%,主要与活动性出血有关。观察到10次血栓形成事件(3.1%)。
4F-PCC作为辅助治疗有效,安全性可接受,不仅用于VKA的紧急逆转,也用于与大出血相关的难治性凝血病。