Bleeding Esophagogastric Varices from Extrahepatic Portal Hypertension: 40 Years’ Experience with Portal-Systemic Shunt1
- 1 June 2002
- journal article
- research article
- Published by Wolters Kluwer Health in Journal of the American College of Surgeons
- Vol. 194 (6) , 717-728
- https://doi.org/10.1016/s1072-7515(02)01170-5
Abstract
Background: This article discusses the largest and longest experience reported to date of the use of portal-systemic shunt (PSS) to treat recurrent bleeding from esophagogastric varices caused by extrahepatic portal hypertension associated with portal vein thrombosis (PVT). Study Design: Two hundred consecutive children and adults with extrahepatic portal hypertension caused by PVT who were referred between 1958 and 1998 after recovering from at least two episodes of bleeding esophagogastric varices requiring blood transfusions were managed according to a well-defined and uniformly applied protocol. All but 14 of the 200 patients were eligible for and received 5 or more years of regular followup (93%); 166 were eligible for and received 10 or more years of regular followup (83%). Results: The etiology of PVT was unknown in 65% of patients. Identifiable causes of PVT were neonatal omphalitis in 30 patients (15%), umbilical vein catheterization in 14 patients (7%), and peritonitis in 14 patients (7%). The mean number of bleeding episodes before PSS was 5.4 (range 2 to 18). Liver biopsies showed normal morphology in all patients. The site of PVT was the portal vein alone in 134 patients (76%), the portal vein and adjacent superior mesenteric vein in 10 patients (5%), and the portal and splenic veins in 56 patients (28%). Postoperative survival to leave the hospital was 100%. Actuarial 5-year, 10-year, and 15-year survival rates were 99%, 97%, and 95%, respectively. Five patients (2.5%), all with central end-to-side splenorenal shunts, developed thrombosis of the PSS, and these were the only patients who had recurrent variceal bleeding. During 10 or more years of followup, 97% of the eligible patients were shown to have a patent shunt and were free of bleeding. No patient developed portal-systemic encephalopathy, liver function tests remained normal, liver biopsies in 100 patients showed normal architecture, hypersplenism was corrected. Conclusion: PSS is the only consistently effective therapy for bleeding esophagogastric varices from PVT and extrahepatic portal hypertension, resulting in many years of survival, freedom from recurrent bleeding, normal liver function, and no encephalopathy.Keywords
This publication has 49 references indexed in Scilit:
- Treatment of bleeding esophagogastric varices due to extrahepatic portal hypertension: Results of portal-systemic shunts during 35 yearsJournal of Pediatric Surgery, 1994
- Portasystemic Shunting Versus Liver Transplantation for the Budd-Chiari SyndromeAnnals of Surgery, 1991
- H-type shunt with an autologous venous graft for treatment of portal hypertension in childrenJournal of Pediatric Surgery, 1989
- Endoscopic sclerotherapy for portal hypertension due to extrahepatic obstruction: long-term follow-upGastrointestinal Endoscopy, 1989
- Endoscopic sclerotherapy for bleeding esophageal varices secondary to extrahepatic portal vein obstructionGastrointestinal Endoscopy, 1987
- Endoscopic Sclerotherapy versus Port Acaval Shunt in Patients with Severe Cirrhosis and Acute Variceal HemorrhageNew England Journal of Medicine, 1987
- Sclerotherapy after First Variceal Hemorrhage in CirrhosisNew England Journal of Medicine, 1984
- Portal obstruction in children. II. Results of surgical portosystemic shuntsThe Journal of Pediatrics, 1983
- Portal obstruction in children. I. Clinical investigation and hemorrhage riskThe Journal of Pediatrics, 1983
- Immediate and long-term results of superior mesenteric vein-inferior vena cava shunt for portal hypertension in childrenJournal of Pediatric Surgery, 1975