Tranexamic acid may be a useful pharmacotherapy for endoscopically resistant small bowel angiodysplasia  

作　　者：Shunji Fujimori 

机构地区：[1]Department of Gastroenterology,Chiba Hokusoh Hospital,Nippon Medical School,Chiba 270-1694,Japan

出　　处：《World Journal of Gastroenterology》2023年第7期1131-1138,共8页世界胃肠病学杂志（英文版）

摘　　要：Small bowel angiodysplasia(SBAD)is reported to account for nearly 50%of cases of small bowel bleeding.When SBAD occurs frequently,it is difficult to treat all the angiodysplasias endoscopically,and gastrointestinal bleeding often recurs.Hormone therapy,somatostatin analogs,thalidomide and vascular endothelial growth factor(VEGF)-neutralizing antibodies have been reported to reduce gastrointestinal angiodysplasia(GIAD)bleeding.However,there is no strong evidence to recommend them.Also,there are no guidelines for their use.Hereditary hemorrhagic telangiectasia(HHT)is a hereditary disease caused by abnormalities in VEGF,resulting in multiple GIADs.A treatment guideline has been created for GIAD in HHT,and the use of tranexamic acid,an antifibrinolytic agent,is the first recommendation pharmacotherapy for GIAD with gastrointestinal bleeding that is difficult to treat endoscopically.It has been reported that fibrinolysis is accelerated in GIAD patients who are not HHT,similar to HHT patients.The use of tranexamic acid for gastric antral vascular ectasia in GIAD has been reported to be useful.However,there are very few reports of its use for SBAD.There are concerns with tranexamic acid use regarding the development of thrombosis/embolism,but there are few reports of such side effects.Future clinical trials including tranexamic acid for SBAD are desired.

关 键 词：ANGIODYSPLASIA INTESTINE Hereditary hemorrhagic telangiectasia Tranexamic acid Endoscopic treatment PHARMACOTHERAPY 

分 类 号：R574.5[医药卫生—消化系统]