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化疗诱导的心脏毒性继发心脏骤停后5-氟尿嘧啶的重新引入

Reintroduction of 5-Fluorouracil Post-cardiac Arrest Secondary to Chemotherapy-Induced Cardiotoxicity.

作者信息

Wu Kathie, Bhattacharya Prianka

机构信息

Internal Medicine, Geisinger Medical Center, Danville, USA.

Hematology/Oncology, Geisinger Medical Center, Danville, USA.

出版信息

Cureus. 2023 Jan 26;15(1):e34232. doi: 10.7759/cureus.34232. eCollection 2023 Jan.

DOI:10.7759/cureus.34232
PMID:36852353
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9962189/
Abstract

5-fluorouracil (5-FU) has been known to have cardiotoxic side effects, including coronary vasospasm, myocardial infarctions, heart failure, arrhythmias, and cardiac arrest. These cases have been reported in patients with either known coronary disease or known risk factors. In cases of acute cardiotoxicity, cessation of fluoropyrimidines is recommended, and reintroduction of the medication is generally avoided. We present a case of a young patient with no known risk factors for coronary disease, who presented with an acute cardiac arrest suspected secondary to vasospasm from the administration of 5-FU for the treatment of rectal cancer and was successfully maintained on treatment with 5-FU post-arrest after transitioning from an infusion to bolus administration.

摘要

已知5-氟尿嘧啶(5-FU)具有心脏毒性副作用,包括冠状动脉痉挛、心肌梗死、心力衰竭、心律失常和心脏骤停。这些病例在患有已知冠状动脉疾病或已知风险因素的患者中均有报道。在急性心脏毒性的情况下,建议停用氟嘧啶,并且通常避免重新使用该药物。我们报告了一例年轻患者,该患者无已知的冠状动脉疾病风险因素,因直肠癌接受5-FU治疗后疑似因血管痉挛继发急性心脏骤停,在从静脉输注改为推注给药后,心脏骤停后成功继续使用5-FU进行治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e53/9962189/2c869477dde2/cureus-0015-00000034232-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e53/9962189/25a421aa6223/cureus-0015-00000034232-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e53/9962189/2c869477dde2/cureus-0015-00000034232-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e53/9962189/25a421aa6223/cureus-0015-00000034232-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e53/9962189/2c869477dde2/cureus-0015-00000034232-i02.jpg

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In vitro evidence that myocardial ischemia resulting from 5-fluorouracil chemotherapy is due to protein kinase C-mediated vasoconstriction of vascular smooth muscle.体外实验证据表明,5-氟尿嘧啶化疗引起的心肌缺血是由于蛋白激酶C介导的血管平滑肌血管收缩所致。
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