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L-Arginine in the treatment of valproate overdose - five clinical cases.

Authors :
Schrettl V
Felgenhauer N
Rabe C
Fernando M
Eyer F
Source :
Clinical toxicology (Philadelphia, Pa.) [Clin Toxicol (Phila)] 2017 Apr; Vol. 55 (4), pp. 260-266. Date of Electronic Publication: 2017 Feb 03.
Publication Year :
2017

Abstract

Background: Valproic acid and its metabolites - particularly valproyl-CoA - are inhibitors of the enzyme N-acetylglutamate synthetase. The amino acid l-arginine can stimulate N-acetylglutamate synthetase activity and could be potentially used therapeutically to correct hyperammonemia caused by valproate therapy or overdose. Severely valproic-acid-poisoned patients are usually treated with l-carnitine or hemodialysis in order to decrease hyperammonemia. We herein report of five cases, in which l-arginine was administered.<br />Methods: Observational study on five cases. Patients with hyperammonemia (i.e., ammonia 80 > μg/dL) and symptoms consistent with valproate overdose (i.e., drowsiness, coma) were selected for treatment with l-arginine. Data was collected retrospectively.<br />Results: l-Arginine decreased ammonia levels in a close temporal relation (case I ammonia in EDTA-plasma [μg/dL] decreased from 381 to 39; case II from 281 to 50; case III from 669 to 74; case IV from 447 to 56; case V from 202 to 60). In cases I and II, hemodialysis was performed and l-carnitine was given before the administration of l-arginine. In case III, hemodialysis was performed after the administration of l-arginine was already started. In cases IV and V, treatment with l-arginine was the sole measure to decrease ammonia levels in plasma.<br />Conclusion: The results suggest that l-arginine may be beneficial in selected cases of valproate overdose complicated by hyperammonemia. l-Arginine could extend our conventional treatment options for valproic acid overdose.

Details

Language :
English
ISSN :
1556-9519
Volume :
55
Issue :
4
Database :
MEDLINE
Journal :
Clinical toxicology (Philadelphia, Pa.)
Publication Type :
Academic Journal
Accession number :
28152637
Full Text :
https://doi.org/10.1080/15563650.2017.1284333