多发性骨髓瘤患者在 Vrd 化疗期间发生急性心肌梗死:临床病例

V. Ostrovskyi
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引用次数: 0

摘要

急性心肌梗死是一种危重病,发病率和死亡率都很高。与心肌梗死相关的急性心肌损伤的特点是心肌肌钙蛋白浓度迅速升高并随后下降。根据相关数据,多发性骨髓瘤患者属于静脉和动脉血栓形成的高危人群。因此,这些患者心血管并发症(包括心肌梗死)的发病率高于普通人群。变应性贫血的发生会减少心肌供氧,从而进一步加剧这一风险。此外,针对肿瘤性血液病的化疗也有可能引发心血管毒性并发症。多发性骨髓瘤治疗中常用的免疫调节剂药物,如沙利度胺和来那度胺,与来那度胺诱发的心肌梗死有关,这是一种普遍的不良反应。使用蛋白酶体抑制剂(如硼替佐米和卡非佐米)会增加发生心肌梗死的风险。本临床病例介绍了一名多发性骨髓瘤患者在使用来那度胺和硼替佐米的低累积化疗剂量期间发生急性心肌梗死的病例。这突出表明,在对高危多发性骨髓瘤患者进行每个特定化疗疗程之前,有必要加强临床、仪器和实验室监测。这种监测有助于及早发现化疗引起的心脏毒性反应,以便及时干预和处理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ACUTE MYOCARDIAL INFARCTION DURING VRD CHEMOTHERAPY IN A PATIENT WITH MULTIPLE MYELOMA: A CLINICAL CASE
Acute myocardial infarction is a critical condition associated with significant morbidity and mortality rates. Myocardial infarction-related acute myocardial injury is characterized by a rapid elevation and subsequent decline in cardiac troponin concentration. According to the relevant data patients with multiple myeloma are in a high-risk category for venous and arterial thrombosis. Therefore, the incidence of cardiovascular complications, which include myocardial infarction, in these patients is higher than in the general population. The development of metaplastic anemia further compounds this risk by diminishing myocardial oxygen supply. Moreover, chemotherapy for oncohematological diseases carries the potential for cardiotoxic cardiovascular complications. Immunomodulator drugs like Thalidomide and Lenalidomide, frequently utilized in multiple myeloma treatment, have been associated with Lenalidomide-induced myocardial infarction—a prevalent adverse effect. The use of proteasome inhibitors such as Bortezomib and Carfilzomib poses an increased risk for myocardial infarction development. This clinical case presents an instance of acute myocardial infarction in a multiple myeloma patient during low cumulative chemotherapy dosage, comprising Lenalidomide and Bortezomib. It underscores the necessity for enhanced clinical, instrumental, and laboratory monitoring before each specific chemotherapy course in high-risk multiple myeloma patients. Such monitoring facilitates the early detection of chemotherapy-induced cardiotoxic effects, allowing for timely intervention and management.
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