Document Detail


Treatment of infantile spasms with sodium valproate followed by benzodiazepines.
MedLine Citation:
PMID:  17957923     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
OBJECTIVE: To review the result of the infantile spasms' treatment with sodium valproate followed by nitrazepam or clonazepam. STUDY DESIGN: Descriptive retrospective study. SETTING: Srinagarind Hospital, Department of Pediatrics, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand. MATERIAL AND METHOD: Twenty-four infantile spasms admitted between January 1994 and December 2003 were analyzed. The inclusion criteria were the patients with infantile spasms clinically diagnosed by the pediatric neurologist, having hypsarrhythmic pattern EEG, and receiving sodium valproate with or without nitrazepam or clonazepam. The patients who had an uncertain diagnosis, incomplete medical record, or that were incompletely followed up were excluded. Data were collected on sex, age at onset of seizure, type of infantile spasms, associated type of seizure, predisposing etiological factor, neuroimaging study, and the result of treatment including cessation of spasms, subsequent development of other seizure types, quantitative reduction of spasms, relapse rates of spasms, psychomotor development, and adverse effects of AEDs. RESULTS: The mean age at onset was 177 days. The male-to-female ratio was 1:1.2. There were 13 cryptogenic (54.2%) and 11 symptomatic (45.8%) infantile spasms. The most common predisposing etiological factors in symptomatic cases were hypoxic ischemic encephalopathy (45.5%) and microcephaly (36.4%), respectively. Ten patients received sodium valproate (41.7%), another 10 received sodium valproate with clonazepam (41.7%), and four received sodium valproate with nitrazepam (16.7%). Both, the complete cessation rate and the 50% reduction of spasms rate were 45.8%. The duration to complete cessation was 70 days. The relapse rate was 18.2%. The rate of delayed psychomotor development was 83.3%. The mean duration of follow-up was 49.6 months. CONCLUSION: The authors propose to use sodium valproate concomitantly with benzodiazepines, especially clonazepam, in situations such as unavailability, intolerability, or adverse effects of ACTH or vigabatrin, or in a patient who does not respond to ACTH or vigabatrin.
Authors:
Narong Auvichayapat; Sompon Tassniyom; Sutthinee Treerotphon; Paradee Auvichayapat
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Journal of the Medical Association of Thailand = Chotmaihet thangphaet     Volume:  90     ISSN:  0125-2208     ISO Abbreviation:  J Med Assoc Thai     Publication Date:  2007 Sep 
Date Detail:
Created Date:  2007-10-25     Completed Date:  2007-12-06     Revised Date:  2008-11-21    
Medline Journal Info:
Nlm Unique ID:  7507216     Medline TA:  J Med Assoc Thai     Country:  Thailand    
Other Details:
Languages:  eng     Pagination:  1809-14     Citation Subset:  IM    
Affiliation:
Division of Pediatric Neurology, Department of Pediatrics, Faculty of Medicine, Khon Kaen University, Khon Kaen 40002, Thailand. anaron@kku.ac.th
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MeSH Terms
Descriptor/Qualifier:
Adrenocorticotropic Hormone / drug effects
Anticonvulsants / therapeutic use*
Benzodiazepines / administration & dosage,  therapeutic use*
Clonazepam / therapeutic use
Drug Therapy, Combination
Female
Humans
Infant
Male
Nitrazepam / therapeutic use
Retrospective Studies
Spasm / drug therapy*
Spasms, Infantile / drug therapy*
Time Factors
Valproic Acid / administration & dosage,  therapeutic use*
Vigabatrin / therapeutic use
Chemical
Reg. No./Substance:
0/Anticonvulsants; 12794-10-4/Benzodiazepines; 146-22-5/Nitrazepam; 1622-61-3/Clonazepam; 60643-86-9/Vigabatrin; 9002-60-2/Adrenocorticotropic Hormone; 99-66-1/Valproic Acid
Comments/Corrections
Comment In:
J Med Assoc Thai. 2007 Oct;90(10):2244   [PMID:  18041449 ]

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