Literature DB >> 2645081

Treatment of esophageal varices.

T L Rice1.   

Abstract

The pathophysiology and treatment of esophageal varices are reviewed. The cause of esophageal varices is generally thought to be portal hypertension. The most common cause of portal hypertension in the United States is alcoholic liver disease. Other etiologies of portal hypertension include portal vein thrombosis, schistosomiasis, and inferior vena caval obstruction by tumor or thrombus. Although short-term balloon tamponade and vasopressin infusion will control acute variceal hemorrhage, they do not affect the underlying problem and are not indicated for long-term treatment of esophageal varices. Surgical procedures either ablate varices or lower portal vein pressure. Portal-systemic shunts have emerged as the preferred surgical technique, but the superiority of total versus selective shunts is unclear. Pharmacological management can include administration of vasopressin, somatostatin, verapamil, or isosorbide dinitrate for short-term treatment or verapamil, isosorbide dinitrate, or propranolol for prolonged treatment. Use of sclerotherapy for treatment and prevention of hemorrhage from esophageal varices has grown recently. Because there are several sclerosing agents and combinations of agents available for use, assessing their relative safety and efficacy is difficult. Innovative approaches to management of varices include a shunt procedure involving the left lung, use of a tissue adhesive, and laser treatment. Because of its effectiveness and ease of administration, sclerotherapy appears to be a rational method of treatment for acute hemorrhage from esophageal varices.

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Year:  1989        PMID: 2645081

Source DB:  PubMed          Journal:  Clin Pharm        ISSN: 0278-2677


  1 in total

1.  Staging of portal hypertension and portosystemic shunts using dynamic nuclear medicine investigations.

Authors:  Mircea Dragoteanu; Ioan-A Balea; Liliana-A Dina; Cecilia-D Piglesan; Ioana Grigorescu; Stefan Tamas; Sabin-O Cotul
Journal:  World J Gastroenterol       Date:  2008-06-28       Impact factor: 5.742

  1 in total

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