Junqi Gou, Chaohui Liu, Mingjian Lang, Fengyou Yao
Department of Cardiology, Geriatric Diseases Institute of Chengdu/Cancer Prevention and Treatment Institute of Chengdu, Chengdu Fifth People's Hospital (The Second Clinical Medical College, Affiliated Fifth People's Hospital of Chengdu University of Traditional Chinese Medicine), Chengdu, China.
Front Pharmacol. 2025 Aug 22;16:1618693. doi: 10.3389/fphar.2025.1618693. eCollection 2025.
Avatrombopag, a thrombopoietin receptor agonist (TPO-RA), is used for immune thrombocytopenia (ITP) but confers thrombotic risks. Acute myocardial infarction (AMI) as an adverse event is underreported.
A 58-year-old female with steroid-refractory ITP developed ST-elevation myocardial infarction (STEMI) 5 days after initiating avatrombopag monotherapy (20 mg/day). She had no history of traditional cardiovascular risk factors. Her platelet count increased from two to 122 × 10/L before AMI. Coronary angiography revealed thrombotic occlusion of the left ventricular posterior branch, treated with thrombus aspiration. Dual antiplatelet therapy was initiated, and avatrombopag was discontinued. The patient was discharged on day 10 post-AMI. At the 14-day follow-up, thrombocytopenia recurred (platelets 18 × 10/L), requiring avatrombopag re-initiation alongside aspirin. No further thrombosis occurred.
Avatrombopag monotherapy may induce rapid coronary thrombosis. Prophylactic antiplatelet therapy and maintaining platelets at 50-150 × 10/L are critical during TPO-RA treatment. This case highlights the need for thrombotic risk assessment before TPO-RA initiation.
阿伐曲泊帕是一种血小板生成素受体激动剂(TPO-RA),用于治疗免疫性血小板减少症(ITP),但存在血栓形成风险。急性心肌梗死(AMI)作为一种不良事件的报道较少。
一名58岁的女性,患有类固醇难治性ITP,在开始阿伐曲泊帕单药治疗(20mg/天)5天后发生ST段抬高型心肌梗死(STEMI)。她没有传统心血管危险因素的病史。在AMI发生前,她的血小板计数从2×10⁹/L增加到122×10⁹/L。冠状动脉造影显示左心室后支血栓性闭塞,采用血栓抽吸治疗。开始双联抗血小板治疗,并停用阿伐曲泊帕。患者在AMI后第10天出院。在14天的随访中,血小板减少症复发(血小板计数为18×10⁹/L),需要重新开始使用阿伐曲泊帕并联合阿司匹林治疗。未再发生血栓形成。
阿伐曲泊帕单药治疗可能会诱发快速冠状动脉血栓形成。在TPO-RA治疗期间,预防性抗血小板治疗以及将血小板维持在50-150×10⁹/L至关重要。该病例强调了在开始TPO-RA治疗前进行血栓形成风险评估的必要性。