Department of Pharmacy, Wake Forest Baptist Medical Center, Winston-Salem, NC, USA.
Eur J Haematol. 2017 Oct;99(4):332-335. doi: 10.1111/ejh.12921. Epub 2017 Jul 25.
To evaluate the efficacy and safety of direct oral anticoagulant (DOAC) therapy in hospitalized patients with suspected heparin-induced thrombocytopenia (HIT).
Retrospective cohort study of adult patients prescribed apixaban, dabigatran, or rivaroxaban for the treatment of acute HIT from January 1, 2013 to January 1, 2017. Eligibility requirements included an intermediate or high pretest probability for HIT (4T score≥4) and a positive IgG-specific anti-PF4/heparin complex assay. The primary outcome measure was the composite of newly diagnosed venous or arterial thromboembolism, gangrene, or amputation due to critical limb ischemia during hospitalization.
A total of 12 patients were included for analysis, five of which experienced HIT-related thrombosis prior to initiation of DOAC therapy. Seven patients received parenteral therapy with argatroban prior to initiation of DOAC treatment. Nine patients were treated with apixaban while three received rivaroxaban for an average of 9.33 days while hospitalized. Zero patients experienced the primary outcome of HIT-related thrombosis, and no patients experienced major bleeding post DOAC initiation. All patients achieved platelet recovery while receiving DOAC therapy.
In this small retrospective study of adult patients treated for acute HIT, treatment with DOAC therapy was not associated with in-hospital thrombotic or hemorrhagic events.
评估直接口服抗凝剂(DOAC)治疗疑似肝素诱导血小板减少症(HIT)住院患者的疗效和安全性。
这是一项回顾性队列研究,纳入了 2013 年 1 月 1 日至 2017 年 1 月 1 日期间因急性 HIT 而接受阿哌沙班、达比加群或利伐沙班治疗的成年患者。入选标准包括 HIT 的中高度预测试验概率(4T 评分≥4)和 IgG 特异性抗 PF4/肝素复合物检测阳性。主要观察指标是住院期间新发静脉或动脉血栓形成、坏疽或因严重肢体缺血导致的截肢,以及因 HIT 相关血栓形成导致的复合结局。
共有 12 例患者纳入分析,其中 5 例在开始 DOAC 治疗前发生 HIT 相关血栓形成。7 例患者在开始 DOAC 治疗前接受了阿加曲班的静脉治疗。9 例患者接受了阿哌沙班治疗,3 例患者接受了利伐沙班治疗,平均住院时间为 9.33 天。没有患者发生 HIT 相关血栓形成的主要结局,也没有患者在开始 DOAC 治疗后发生大出血。所有患者在接受 DOAC 治疗时均实现了血小板恢复。
在这项针对急性 HIT 成年患者的小样本回顾性研究中,DOAC 治疗与住院期间的血栓或出血事件无关。