Multicenter randomized controlled trial of terlipressin versus sclerotherapy in the treatment of acute variceal bleeding:: The TEST study

被引:119
|
作者
Escorsell, A
Del Arbol, LR
Planas, R
Albillos, A
Bañares, R
Calès, P
Pateron, D
Bernard, B
Vinel, JP
Bosch, J
机构
[1] Univ Barcelona, Hosp Clin, Dept Med, IDIBAPS,Liver Unit,IMD, E-08036 Barcelona, Spain
[2] Univ Barcelona, Hosp Clin, Dept Med, IDIBAPS,Endoscopy Unit, E-08036 Barcelona, Spain
[3] Univ Alcala de Henares, Hosp Ramon y Cajal, Dept Gastroenterol, Madrid, Spain
[4] Univ Alcala de Henares, Clin Puerta Hierro, Dept Gastroenterol, Madrid, Spain
[5] Hosp Badalona Germans Trias & Pujol, Dept Gastroenterol, Badalona, Spain
[6] Univ Complutense Madrid, Hosp Gen Gregorio Maranon, Dept Gastroenterol, Madrid, Spain
[7] CHU Angers, Angers, France
[8] CHU Jean Verdier, Intens Care Unit, Bondy, France
[9] CHU Pitie Salpetriere, Paris, France
[10] CHU Purpan, Toulouse, France
关键词
D O I
10.1053/jhep.2000.16601
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Failure to control bleeding and early rebleeding account for the high mortality associated with variceal hemorrhage in cirrhosis. We compared endoscopic sclerotherapy to terlipressin, a drug that effectively controls acute bleeding while reducing in-hospital mortality. This multicenter randomized controlled trial included 219 cirrhotic patients admitted for endoscopy-proven acute variceal bleeding and randomized to receive repeated injections of terlipressin during 6 days (n = 105) or emergency sclerotherapy (n = 114). Success was defined as obtaining control of bleeding (24-hour bleeding-free period during the first 48 hours) and lack of early rebleeding (any further bleeding from initial control to 5 days later) and survival during the study. Both groups were similar at inclusion. Failure rate for terlipressin was 33% and 32% for sclerotherapy (not significant [NS]). Early rebleeding was responsible for 43% and 44% of failures, respectively. This high efficacy was observed in both Child-Pugh class A + B and Child-Pugh class C patients. Both treatments were similar regarding transfusion requirements, in-hospital stay, and 6-week mortality (26 vs. 19 patients). Side effects appeared in 20% of patients receiving terlipressin and in 30% of those on sclerotherapy (P = .06); being serious in 4% and 7%, respectively (NS). In conclusion, terlipressin and sclerotherapy are equally highly effective therapies achieving the initial control of variceal bleeding and preventing early rebleeding. Both treatments are safe, but terlipressin is better tolerated. Therefore, terlipressin may represent a first-line treatment in acute variceal bleeding until the administration of elective therapy, especially in hospitals where a skilled endoscopist is not available 24 hours a day.
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收藏
页码:471 / 476
页数:6
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