Saint Francis Hospital, Memphis, TN, USA.
Ann Pharmacother. 2014 Feb;48(2):286-91. doi: 10.1177/1060028013511060. Epub 2013 Nov 6.
To describe the diagnosis, management, and monitoring of a patient with heparin-induced thrombocytopenia (HIT) with thrombosis and simultaneous bleeding risk treated with argatroban and transitioned to intravenous (IV) warfarin secondary to the inability to administer enteral medications.
A 71-year-old man was admitted to the surgical intensive care unit (SICU) following aortic valve repair, coronary artery bypass, and ascending aortic aneurysm repair. On postoperative day 9, he was found to have a pulmonary embolism, and therapeutic heparin was started. The following day, his platelet count was found to have dropped precipitously. HIT was diagnosed, heparin was discontinued, and argatroban was initiated. On postoperative day 22, anticoagulation was discontinued because of massive gastrointestinal bleeding. On postoperative day 35, multiple venous thromboses were found, and argatroban was restarted. The patient developed a high-output enterocutaneous fistula, eliminating the option of enteral route of medication administration. The multidisciplinary SICU team transitioned the patient from argatroban to IV warfarin for long-term anticoagulation. The international normalized ratio was monitored and remained therapeutic throughout his admission without further thrombotic complications.
HIT occurs when antibodies develop to heparin-platelet factor 4 complexes, causing simultaneous hypercoagulability and thrombocytopenia. It is diagnosed based on both clinical factors and laboratory testing. Treatment includes discontinuation of all forms of heparin; initiation of a nonheparin anticoagulant, such as argatroban; and transition to warfarin.
IV warfarin is a therapeutic option for patients with malabsorption issues. A multidisciplinary team in an intensive care setting optimizes cost-effective, patient-centered, and safe care.
描述 1 例肝素诱导的血小板减少症(HIT)伴血栓形成和同时存在出血风险患者的诊断、治疗和监测,该患者因无法给予肠内药物而使用阿加曲班治疗,并随后因不能给予肠内药物而转换为静脉(IV)华法林。
1 名 71 岁男性,因主动脉瓣修复、冠状动脉旁路移植和升主动脉瘤修复后入住外科重症监护病房(SICU)。术后第 9 天,发现其患有肺栓塞,并开始使用治疗剂量的肝素。第 2 天,发现其血小板计数急剧下降。诊断为 HIT,停用肝素,并开始使用阿加曲班。术后第 22 天,因大量胃肠道出血而停止抗凝治疗。术后第 35 天,发现多处静脉血栓形成,重新开始使用阿加曲班。患者发生高输出肠外瘘,排除了肠内给药途径。多学科 SICU 团队将患者从阿加曲班转换为 IV 华法林进行长期抗凝治疗。国际标准化比值(INR)监测结果显示,在整个住院期间均保持治疗范围,且无进一步的血栓并发症。
当抗体形成于肝素-血小板因子 4 复合物时,会发生肝素诱导的血小板减少症(HIT),导致同时出现高凝状态和血小板减少症。其诊断基于临床因素和实验室检测。治疗包括停用所有类型的肝素;开始使用非肝素抗凝剂,如阿加曲班;并转换为华法林。
对于存在吸收不良问题的患者,IV 华法林是一种治疗选择。重症监护环境中的多学科团队可以优化具有成本效益、以患者为中心且安全的护理。