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Efficacy of L-Ornithine L-Aspartate in Acute Liver Failure: A Double-Blind, Randomized, Placebo-Controlled Study

Acharya, Subrat Kumar, Bhatia, Vikram, Sreenivas, Vishnubhatla, Khanal, Shankar, Panda, Subrat Kumar·2009·Gastroenterology

Abstract

Background & aims In acute liver failure (ALF), high blood ammonia levels have been documented that correlate with mortality and complications. L-ornithine L-aspartate (LOLA) reduces ammonia levels by increasing hepatic ammonia disposal and its peripheral metabolism. Present study evaluated efficacy and ammonia lowering effect of LOLA in ALF. Methods This study was placebo-controlled and blinded. We randomized 201 patients with ALF between January 2005 and October 2007 to either placebo or LOLA infusions (30 g daily) for 3 days. Arterial ammonia was measured at baseline and daily for 6 days. The primary end point was improvement in survival. The study followed CONSORT guidelines and was registered at the ClinicalTrials.gov (Identifier: NCT00470314). Results There was no reduction in mortality with LOLA treatment (mortality: 33.3% in placebo and 42.4% in LOLA; relative risk of death 1.27; 95% CI: 0.88-1.85; P = .204). By multivariate analysis, ammonia levels were an independent predictor of survival. There was significant decrease in ammonia levels in both groups with time (P Conclusions LOLA infusion did not lower the ammonia or improved survival in ALF.

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Crossref · 10.1053/j.gastro.2009.02.050

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Metadata

Authors
Acharya, S. K., Bhatia, V., Sreenivas, V., Khanal, S., & Panda, S. K.
Venue
Gastroenterology
Publisher
Elsevier BV
Published
2009-06
Volume
136
Issue
7
Pages
2159-2168
ISSN
0016-5085
Cited by
173
References
0
Language
en

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