Abstract | OBJECTIVE: STUDY DESIGN: Randomized, placebo-controlled trial. PLACE AND DURATION OF STUDY: Department of Gastroenterology and Hepatology, Sheikh Zayed Hospital, Lahore, from February to August 2005. METHODOLOGY: Cirrhotic patients with hyperammonemia and overt hepatic encephalopathy were enrolled. Eighty patients were randomized to two treatment groups, L-ornithine-L-aspartate (20 g/d) or placebo, both dissolved in 250 mL of 5% dextrose water and infused intravenously for four hours a day for five consecutive days with 0.5 g/kg dietary protein intake at the end of daily treatment period. Outcome variables were postprandial blood ammonia and mental state grade. Adverse reactions and mortality were also determined. RESULTS: Both treatment groups were comparable regarding age, gender, etiology of cirrhosis, Child-Pugh class, mental state grade and blood ammonia at baseline. Although, improvement occurred in both groups, there was a greater improvement in L-ornithine-L-aspartate group with regard to both variables. Four patients in the placebo group and 2 in L-ornithine-L-aspartate group died. CONCLUSION:
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Authors | Irfan Ahmad, Anwaar A Khan, Altaf Alam, Akif Dilshad, Arshad Kamal Butt, Farzana Shafqat, Kashif Malik, Shahid Sarwar |
Journal | Journal of the College of Physicians and Surgeons--Pakistan : JCPSP
(J Coll Physicians Surg Pak)
Vol. 18
Issue 11
Pg. 684-7
(Nov 2008)
ISSN: 1022-386X [Print] Pakistan |
PMID | 18983791
(Publication Type: Clinical Trial, Journal Article, Randomized Controlled Trial)
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Chemical References |
- Dipeptides
- Ammonia
- ornithylaspartate
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Topics |
- Adult
- Aged
- Ammonia
(blood)
- Cognition
- Dipeptides
(administration & dosage, therapeutic use)
- Female
- Health Status Indicators
- Hepatic Encephalopathy
(drug therapy, physiopathology)
- Humans
- Hyperammonemia
(drug therapy)
- Infusions, Intravenous
- Liver Cirrhosis
(complications, physiopathology)
- Male
- Middle Aged
- Postprandial Period
(drug effects)
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