A Randomized Controlled Trial of Propranolol Use During Ligation Program for Secondary Prophylaxis of Esophageal Variceal Bleeding

被引:2
作者
Chen, Wen-Chi [1 ,2 ,3 ]
Yang, Tsung-Chieh [2 ,4 ]
Lee, Pei-Chang [2 ,4 ]
Wang, Yen-Po [2 ,5 ]
Hou, Ming-Chih [2 ,4 ]
Lee, Fa-Yauh [2 ,4 ]
机构
[1] Kaohsiung Vet Gen Hosp, Dept Med, Div Gastroenterol & Hepatol, Kaohsiung, Taiwan
[2] Natl Yang Ming Chiao Tung Univ, Sch Med, Taipei, Taiwan
[3] Natl Sun Yat Sen Univ, Dept Postbaccalaureate Med, Kaohsiung, Taiwan
[4] Taipei Vet Gen Hosp, Dept Med, Div Gastroenterol & Hepatol, Taipei, Taiwan
[5] Taipei Vet Gen Hosp, Endoscopy Ctr Diag & Treatment, Taipei, Taiwan
关键词
cirrhosis; esophageal varices; portal hypertension; propranolol; BETA-BLOCKERS; ISOSORBIDE MONONITRATE; ENDOSCOPIC LIGATION; PORTAL-HYPERTENSION; IMPROVE SURVIVAL; PLUS NADOLOL; HEMORRHAGE; CIRRHOSIS; MANAGEMENT; SCLEROTHERAPY;
D O I
10.14309/ajg.0000000000002457
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
INTRODUCTION: Endoscopic variceal ligation (EVL) plus nonselective beta-blockers (NSBB) is the standard of care for secondary prophylaxis of esophageal variceal bleeding (EVB). This trial aimed to compare the rebleeding rates between EVL plus NSBB till eradication of esophageal varices (EEV) and EVL plus long-term NSBB. METHODS: After control of acute EVB, patients with cirrhosis were randomized into 2 groups, with group A patients receiving EVL plus propranolol till EEV, while group B patients received standard of care with continuation of propranolol. Recurrent varices were ligated at follow-up endoscopy in both groups. RESULTS: The median follow-up period was 23.0 months in group A (n = 106) and 23.6 months in group B (n = 106). Twelve patients (11.3%) in group A and 11 (10.4%) in group B had recurrent EVB. The difference in rebleeding rates and the 95% confidence interval (CI) was 0.9% (-7.5% to 9.3%). The upper 95% CI bound of the difference was within the margin of 13.2%, and the noninferiority of group A to group B was established. Thirty-eight patients (35.8%) in group A and 40 (37.7%) in group B had further decompensation, with the difference (95% CI) of -1.9% (-14.9% to 11.1%). Twenty-four patients (22.6%) in group A and 26 (24.5%) in group B expired, with the difference (95% CI) in mortality rates of -1.9% (-13.3% to 9.5%). DISCUSSION: EVL plus propranolol till EEV was noninferior to EVL plus continuing propranolol in secondary prophylaxis of EVB, but the impact on further decompensation and transplantation-free survival deserved further investigation.
引用
收藏
页码:278 / 286
页数:9
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