阿加曲班(一种直接凝血酶抑制剂)对抗磷脂抗体综合征、肝素诱导的血小板减少症和COVID-19肺炎患者维持抗凝治疗的新型监测和剂量调整

Christine E Ryan, Kelly A Newman, Russel J Roberts, Galit H Frydman, Rachel P Rosovsky
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引用次数: 0

摘要

对于需要全身抗凝的患者,需要可靠的监测方法来确保抗凝维持在正确的治疗窗口内,患者得到适当的治疗。当滴定直接凝血酶抑制剂(DTI),稀释凝血酶时间(dTT)的测量已被证明是更可靠和准确的比活化部分凝血酶活时间(aPTT)的测量,因此往往首选的DTI评估。然而,当两种dTT测量都不容易获得且aPTT测量不可靠时,临床需要出现。病例总结:一名57岁女性,既往有抗磷脂抗体综合征、肝素性血小板减少症及多发深静脉血栓和肺栓塞病史,因缺氧性呼吸衰竭入院,并插管治疗。用阿加曲班代替她的家庭药物华法林。然而,患者在基线时aPTT值延长,并且我们机构的夜间dTT测定有限。一个由血液学和药学临床医生组成的多学科团队创建了一个修改的患者特异性aPTT靶标范围,并相应地调整了阿加曲班的剂量。随后aPTT值在修改后的靶标范围内与治疗dTT值相对应,表明治疗抗凝成功实现并维持。另外,采用一种新的研究性即时检测方法对患者血液样本进行回顾性评估,该方法检测并量化了阿加曲班的抗凝作用。结论:在aPTT测量不可靠的患者中,使用DTI治疗抗凝可以通过修改患者特异性aPTT靶标范围来实现。早期验证一种用于DTI监测的研究性快速检测替代方案是有希望的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Novel Monitoring and Dose Adjustment of Argatroban, a Direct Thrombin Inhibitor, to Maintain Therapeutic Anticoagulation in a Patient With Antiphospholipid Antibody Syndrome, Heparin-Induced Thrombocytopenia, and COVID-19 Pneumonia.

Novel Monitoring and Dose Adjustment of Argatroban, a Direct Thrombin Inhibitor, to Maintain Therapeutic Anticoagulation in a Patient With Antiphospholipid Antibody Syndrome, Heparin-Induced Thrombocytopenia, and COVID-19 Pneumonia.

Novel Monitoring and Dose Adjustment of Argatroban, a Direct Thrombin Inhibitor, to Maintain Therapeutic Anticoagulation in a Patient With Antiphospholipid Antibody Syndrome, Heparin-Induced Thrombocytopenia, and COVID-19 Pneumonia.

In patients who require systemic anticoagulation, a reliable monitoring method is required to ensure anticoagulation is maintained within the correct therapeutic window and patients are treated appropriately. When titrating direct thrombin inhibitors (DTIs), dilute thrombin time (dTT) measurements have been demonstrated to be more reliable and accurate than activated partial thromboplastin time (aPTT) measurements and thus often the preferred DTI assessment. However, a clinical need arises when both dTT measurements are not readily available and aPTT measurements are unreliable.

Case summary: A 57-year-old woman with a history of antiphospholipid antibody syndrome, heparin-induced thrombocytopenia, and multiple prior deep venous thromboses and pulmonary emboli was admitted with COVID-19 pneumonia and intubated due to hypoxic respiratory failure. Argatroban was initiated in place of her home medication warfarin. However, the patient had a prolonged aPTT value at baseline and overnight dTT assay measurements were limited at our institution. A multidisciplinary team of hematology and pharmacy clinicians created a modified patient-specific aPTT target range and argatroban dosing was titrated accordingly. Subsequent aPTT values in the modified target range corresponded to therapeutic dTT values, indicating therapeutic anticoagulation was successfully achieved and maintained. Patient blood samples were additionally evaluated retrospectively using an investigational novel point-of-care test that detected and quantified the argatroban anticoagulant effect.

Conclusions: Therapeutic anticoagulation with a DTI in a patient with unreliable aPTT measurements can be achieved with use of a modified patient-specific aPTT target range. Early validation of an investigational rapid testing alternative for DTI monitoring is promising.

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