Key result
Superior mesenteric artery vasopressin infusion achieved permanent control of variceal hemorrhage in 100% of Child's class A, 62% of class B, and 33% of class C patients.
Why the study?
Does superior mesenteric artery vasopressin infusion effectively control variceal bleeding in patients with liver disease?
Observational (n=39)
Does superior mesenteric artery vasopressin infusion effectively control variceal bleeding in patients with liver disease?
The effectiveness of superior mesenteric artery vasopressin infusion for variceal hemorrhage is highly dependent on the severity of underlying liver disease and clotting function.
Answers are grounded in this paper and cite their sources.
Lower success in advanced disease warrants caution; leaves open randomized confirmation for variceal hemorrhage.
Liver function and clotting tests were evaluated in 39 patients with variceal bleeding prior to superior mesenteric artery vasopressin infusion. In six patients with mild hepatic dysfunction (Child's class A), permanent control of hemorrhage was achieved in all six and all survived the hospitalization. In 21 patients with moderate dysfunction (Child's class B), permanent control of hemorrhage was achieved in 13 (62%) and temporary control for 24 hr or longer in the remaining eight (38%). Survival in class B was 67% (14 of 21). In only four of 12 patients with severe hepatic dysfunction (Child's class C) was control of hemorrhage achieved (33 percent). None of these patients survived. Therapeutic failure also was associated with clotting derangements and the initial bleeding rate. It is concluded that the effectiveness of vasopressin in variceal hemorrhage is a function of the underlying liver disease and derangements in clotting function.
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Sl et al. (1977) conducted an observational in Variceal bleeding (n=39). Superior mesenteric artery vasopressin infusion was evaluated on Permanent control of hemorrhage. Superior mesenteric artery vasopressin infusion achieved permanent control of variceal hemorrhage in 100% of Child's class A, 62% of class B, and 33% of class C patients.
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