Endoscopic variceal ligation (EVL) is a new techniquedesigned to manage esophageal varices. The effect of sclerotherapy following repeated banding ligation remains unknown. Seventy-two patients with a history of esophageal variceal bleeding received regular EVL until variceal disappearance or until left with residual small varices. Subsequently, patients were randomized to receive sclerotherapy (Group 1, 37 patients) or serve as a control (Group 2, 35 patients). Group 1 received one to two sessions of low-dose sclerotherapy to achieve complete variceal disappearance. After a mean follow-up of 2 years, 4 months, recurrent esophageal varices developed in 14% of Group 1 and 43% of Group 2 (P F .02). Rebleeding was encountered in 8% of Group 1 versus 31% of Group 2 (P ؍ .01). One case of esophageal stricture (2.7%) was encountered in Group 1. Endoscopic injection sclerotherapy (EIS) has been well documented as a valuable tool to help control acute variceal bleeding, to prevent recurrent bleeding, and perhaps to improve survival. [1][2][3][4] However, it may be associated with substantial complications. 5 Endoscopic variceal ligation (EVL) has emerged in recent years as a new tool in the management of bleeding esophageal varices. 6 Controlled studies have demonstrated that EVL is superior to EIS in terms of obliterating esophageal varices, i.e., fewer treatment sessions are required with EVL than that with EIS. 7-11 On the other hand, varices, when reduced to minimal size by EVL, become inaccessible to EVL. Whether the addition of EIS may be of benefit to those patients remains unknown. This study was undertaken to investigate this issue.
PATIENTS AND METHODSBetween July 1991 and July 1993, patients with a history of esophageal variceal bleeding admitted to Veterans General HospitalKaohsiung were considered for enrollment. Patients admitted with acute esophageal variceal bleeding between January 1992 and July 1993 were included in a trial comparing EIS and EVL, which has been published elsewhere. 10 During the overlapping period, only patients who were admitted to prevent variceal rebleeding but not eligible for prior study were enrolled in the current study. In this study, all the patients were treated with repeated EVL, and then randomized to receive additional EIS or not. The patient population was different from the previous study. The aims of the current study were to observe whether recurrent varices and rebleeding could be reduced in patients receiving EIS following repeated EVL. The inclusion criteria of this study were: 1) patients were cirrhotic and had a history of esophageal variceal bleeding; and 2) patients received repeated EVL until variceal disappearance or until left with residual small varices (defined below). The exclusion criteria were: 1) association with gastric variceal bleeding; 2) association with malignancy, uremia, or other debilitating disease; and 3) history of sclerotherapy or shunt operation. -Blocker was not administered during the study. An informed consent was obtained from all o...