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Acute antimanic efficacy and safety of intravenous valproate loading therapy: an open-label study.

Abstract
This open-label study investigated whether acute antimanic effects and safety of intravenous valproate loading therapy is superior to oral valproate loading. Eighteen patients with DSM-IV diagnosis of either bipolar affective disorder or schizomania who met the study criteria were recruited (9 in the intravenous and 9 in the oral valproate group). Psychopathology was assessed with the scale for manic and mixed states on days 0 and 4. A checklist was used for the assessment of side effects. The results showed about 36% reduction in total mean manic scores with intravenous valproate loading; however, statistically, the degree of reduction in manic scores was comparable between the groups. A nonsignificant increase in the rate of adverse events was noted in the intravenous group. Despite its limitations, this study suggests that acute antimanic effects of both intravenous and oral valproate loading are comparable.
AuthorsK Jagadheesan, Harpreet S Duggal, Subash Chandra Gupta, Somuya Basu, Sanjeev Ranjan, Rajiv Sandil, Sayeed Akhtar, S Haque Nizamie
JournalNeuropsychobiology (Neuropsychobiology) Vol. 47 Issue 2 Pg. 90-3 ( 2003) ISSN: 0302-282X [Print] Switzerland
PMID12707491 (Publication Type: Clinical Trial, Comparative Study, Controlled Clinical Trial, Journal Article)
CopyrightCopyright 2003 S. Karger AG, Basel
Chemical References
  • Antimanic Agents
  • Valproic Acid
Topics
  • Administration, Oral
  • Adolescent
  • Adult
  • Antimanic Agents (adverse effects, therapeutic use)
  • Bipolar Disorder (drug therapy)
  • Diagnostic and Statistical Manual of Mental Disorders
  • Drug Evaluation
  • Humans
  • Injections, Intravenous (methods)
  • Male
  • Middle Aged
  • Schizophrenia (drug therapy)
  • Statistics, Nonparametric
  • Time Factors
  • Treatment Outcome
  • Valproic Acid (adverse effects, therapeutic use)

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