分子靶向治疗引起经颈静脉肝内门体分流术(TIPS)后肝性脑病的病例报告和文献综述。

Chen Zhou , Yang Chen , Jiacheng Liu , Qin Shi , Bin Xiong
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引用次数: 1

摘要

我们报告了两例在我们中心经颈静脉肝内门体分流术(TIPS)后由分子靶向药物引起的肝性脑病。靶向药物诱导的肝毒性和抗血管生成作用可能会导致氨代谢失衡,从而升高血氨水平。TIPS会转移肝脏的部分血液供应,加重肝脏损伤,并将富含氨的血液从肠道分流到系统循环中。这些可能是TIPS后分子靶向药物引起肝性脑病的机制。当临床医生选择分子靶向治疗作为TIPS患者的第二或第三种靶向治疗时,还应考虑药物诱导的肝性脑病的后果。
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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Molecular targeted therapy causes hepatic encephalopathy in patients after Transjugular intrahepatic portosystemic shunt (TIPS): A case report and literature review

We report two cases of hepatic encephalopathy caused by molecular targeted drugs after the Transjugular intrahepatic portosystemic shunt (TIPS) procedure in our center. The liver toxicities and anti-angiogenic effects induced by targeted drugs may generate an imbalance in ammonia metabolism, elevating blood ammonia levels. TIPS diverts partial blood supply from the liver, aggravates liver impairment, and shunts ammonia-rich blood from the intestine into the systemic circulation. These may be the mechanisms leading to hepatic encephalopathy caused by molecular targeted drugs following TIPS. When clinicians choose molecular targeted therapy as the second or third targeted therapy for patients who have undergone TIPS, the consequence of drug-induced hepatic encephalopathy should also be considered.

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来源期刊
Journal of Interventional Medicine
Journal of Interventional Medicine Medicine-General Medicine
CiteScore
1.30
自引率
0.00%
发文量
32
审稿时长
68 days
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