Zhou Chen, Chen Yang, Liu Jiacheng, Shi Qin, Xiong Bin
Department of Radiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, Hubei, China.
Hubei Province Key Laboratory of Molecular Imaging, Wuhan, 430022, Hubei, China.
J Interv Med. 2022 Feb 26;5(1):37-39. doi: 10.1016/j.jimed.2021.12.006. eCollection 2022 Feb.
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.
我们报告了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两例肝性脑病病例。靶向药物诱导的肝毒性和抗血管生成作用可能导致氨代谢失衡,从而使血氨水平升高。TIPS使部分肝脏血液供应分流,加重肝脏损害,并将富含氨的肠内血液分流至体循环。这些可能是TIPS后分子靶向药物导致肝性脑病的机制。当临床医生为接受过TIPS的患者选择分子靶向治疗作为二线或三线靶向治疗时,也应考虑药物性肝性脑病的后果。