Acute Coronary Syndrome in Essential Thrombocythemia and Polycythemia Vera.

IF 0.5 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS
Heart Views Pub Date : 2025-07-01 Epub Date: 2025-11-21 DOI:10.4103/heartviews.heartviews_81_25
Rasha Kaddoura, Dina Ahmed, Ahmed Rudwan, Ahmed Elyas, Mohamed A Yassin
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引用次数: 0

Abstract

Essential thrombocythemia (ET) and polycythemia vera (PV) are rare chronic myeloproliferative neoplasms that have hemostatic complications (i.e., thrombosis and hemorrhage), leading to morbidity and mortality. Treatment in ET or PV is directed toward preventing thrombotic consequences. However, the increased risk of bleeding may complicate antithrombotic therapy in these patients. Thrombosis may occur in both arterial and venous vascular beds. Arterial thrombosis, such as acute coronary syndrome (ACS), is more frequent than venous thrombosis. Both ET and PV can initially present as an ACS, the management of which is highly challenging in the absence of clinical guidelines that are dedicated to such patients. The management of ACS in patients with ET or PV has not been well described in literature. Herein, this review discusses the pathogenesis, characteristics, and management of ACS in patients with ET or PV.

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原发性血小板增多症和真性红细胞增多症的急性冠脉综合征。
原发性血小板增多症(ET)和真性红细胞增多症(PV)是一种罕见的慢性骨髓增生性肿瘤,具有止血并发症(即血栓形成和出血),可导致发病率和死亡率。治疗ET或PV是为了防止血栓的后果。然而,出血风险的增加可能使这些患者的抗血栓治疗复杂化。血栓形成可发生在动脉和静脉血管床。动脉血栓形成,如急性冠状动脉综合征(ACS),比静脉血栓形成更常见。ET和PV最初都可以表现为ACS,在缺乏专门针对此类患者的临床指南的情况下,其管理极具挑战性。在ET或PV患者中ACS的处理尚未在文献中得到很好的描述。本文就ET或PV合并ACS的发病机制、特点及治疗进行综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Heart Views
Heart Views CARDIAC & CARDIOVASCULAR SYSTEMS-
自引率
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发文量
28
审稿时长
28 weeks
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