Matthai William H, Hursting Marcie J, Lewis Bruce E, Kelton John G
University of Pennsylvania Medical School, 39th and Market Sts WS 392, Philadelphia, PA 10104, USA.
Thromb Res. 2005;116(2):121-6. doi: 10.1016/j.thromres.2004.11.006. Epub 2004 Dec 8.
Heparin therapy is not recommended for patients with a history of heparin-induced thrombocytopenia (HIT), except in specialized situations, because this treatment can lead to severe reactions including thrombocytopenia and thrombosis. However, the optimal management of patients with a history of HIT requiring acute anticoagulation has not yet been clarified because of the lack of prospective studies. We evaluated the safety and efficacy of argatroban, a direct thrombin inhibitor, as an anticoagulant in patients with a history of HIT needing acute anticoagulation.
Thirty-six patients with a history of serologically confirmed HIT were treated prospectively with argatroban [median (5th-95th percentile) dose of 2.0 (1.0-4.3) microg/kg/min for 4.0 (0.7-8.4) days]. Prospectively defined endpoints included successful anticoagulation (therapeutic activated partial thromboplastin time), and bleeding, new thromboembolic events, or other adverse effects during therapy or within 30 days following its cessation.
All patients required acute anticoagulation with the most common admission diagnoses being deep venous thrombosis or pulmonary embolism (n=13) and chest pain or acute coronary syndrome (n=12). Eleven patients had previously received argatroban therapy for HIT; one patient underwent two treatment courses of argatroban for a history of HIT. The median (5th-95th percentile) time between the past diagnosis of HIT and initiation of argatroban was 7.5 (0.4-114.6) months. All evaluable patients were successfully anticoagulated. No patient had major bleeding, new thromboembolic events, or other adverse effects. There were no adverse events related to reexposure.
Argatroban can provide safe and effective anticoagulation, on initial or repeat exposure, in patients with a history of HIT.
肝素诱导的血小板减少症(HIT)患者不建议使用肝素治疗,特殊情况除外,因为这种治疗可能导致严重反应,包括血小板减少和血栓形成。然而,由于缺乏前瞻性研究,HIT病史患者急性抗凝的最佳管理方案尚未明确。我们评估了直接凝血酶抑制剂阿加曲班作为抗凝剂用于需要急性抗凝的HIT病史患者的安全性和有效性。
36例血清学确诊的HIT病史患者接受阿加曲班前瞻性治疗[中位(第5-95百分位数)剂量为2.0(1.0-4.3)μg/kg/min,持续4.0(0.7-8.4)天]。前瞻性定义的终点包括成功抗凝(治疗性活化部分凝血活酶时间),以及治疗期间或停药后30天内的出血、新的血栓栓塞事件或其他不良反应。
所有患者均需要急性抗凝,最常见的入院诊断为深静脉血栓形成或肺栓塞(n=13)以及胸痛或急性冠状动脉综合征(n=12)。11例患者先前因HIT接受过阿加曲班治疗;1例患者因HIT病史接受了两个疗程的阿加曲班治疗。上次HIT诊断至开始使用阿加曲班的中位(第5-95百分位数)时间为7.5(0.4-114.6)个月。所有可评估患者均成功抗凝。无患者发生大出血、新的血栓栓塞事件或其他不良反应。无与再次暴露相关的不良事件。
阿加曲班在初次或再次使用时,可为有HIT病史的患者提供安全有效的抗凝作用。