Dhillon Sohita
Wolters Kluwer Health Adis, Auckland, New Zealand.
Am J Cardiovasc Drugs. 2009;9(4):261-82. doi: 10.2165/1120090-000000000-00000.
Argatroban, a highly selective direct thrombin inhibitor, is indicated for use as an anticoagulant for the treatment and prophylaxis of thrombosis in patients with heparin-induced thrombocytopenia (HIT), and in patients undergoing percutaneous coronary intervention (PCI) who have, or are at risk for, HIT. Intravenous argatroban improved clinical outcomes and was generally well tolerated in adults with HIT or HIT with thrombosis syndrome (HITTS). In two pivotal, open-label, historically controlled studies in adults with HIT, the incidence of the primary composite endpoint (all-cause death, all-cause amputation, or new thrombosis) was significantly lower in argatroban recipients than in historical controls, and more argatroban recipients than historical controls stayed event-free during the study according to a Kaplan-Meier analysis. In adults with HITTS in these trials, although the incidence of the primary composite endpoint did not differ significantly between argatroban recipients and historical controls, a Kaplan-Meier analysis showed that more patients receiving argatroban than historical controls remained event-free during the study. Major and minor bleeding rates in argatroban recipients were generally similar to those in historical controls in these studies. Argatroban was also an effective anticoagulant in patients with HIT undergoing PCI in three small, uncontrolled trials, pooled data from which showed that most (>or=95%) patients achieved a satisfactory outcome of the PCI procedure and adequate anticoagulation (coprimary endpoints). It was generally well tolerated in these patients, with the incidence of major bleeding being <or=1.1%. The efficacy and safety of argatroban in pediatric patients has not been established. However, a small uncontrolled, preliminary study suggests that it may be useful in seriously ill pediatric patients requiring nonheparin anticoagulation.
阿加曲班是一种高度选择性的直接凝血酶抑制剂,适用于作为抗凝剂,用于治疗和预防肝素诱导的血小板减少症(HIT)患者以及接受经皮冠状动脉介入治疗(PCI)且患有HIT或有HIT风险的患者的血栓形成。静脉注射阿加曲班可改善临床结局,并且在患有HIT或伴有血栓形成综合征(HITTS)的成人中通常耐受性良好。在两项针对成人HIT患者的关键、开放标签、历史对照研究中,接受阿加曲班治疗的患者中主要复合终点(全因死亡、全因截肢或新血栓形成)的发生率显著低于历史对照,并且根据Kaplan-Meier分析,在研究期间接受阿加曲班治疗且无事件发生的患者比历史对照更多。在这些试验中患有HITTS的成人中,尽管接受阿加曲班治疗的患者与历史对照之间主要复合终点的发生率没有显著差异,但Kaplan-Meier分析表明,在研究期间接受阿加曲班治疗且无事件发生的患者比历史对照更多。在这些研究中,接受阿加曲班治疗的患者的主要和次要出血率通常与历史对照相似。在三项小型非对照试验中,阿加曲班在接受PCI的HIT患者中也是一种有效的抗凝剂,汇总数据显示,大多数(≥95%)患者PCI手术取得了满意的结果且抗凝充分(共同主要终点)。这些患者对阿加曲班通常耐受性良好,严重出血的发生率≤1.1%。阿加曲班在儿科患者中的疗效和安全性尚未确立。然而,一项小型非对照的初步研究表明,它可能对需要非肝素抗凝的重症儿科患者有用。