Phenobarbital, primidone and sodium valproate in the prophylaxis of febrile convulsions
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Published on: June 25, 2016
Insights
Phenobarbital, primidone, and sodium valproate showed similar efficacy in preventing febrile convulsions. However, specific sodium valproate dosing regimens impacted its prophylactic effectiveness, with b.i.d. administration being less effective than t.i.d.
Area of Science:
- Pediatric Neurology
- Clinical Pharmacology
Background:
- Febrile convulsions are common in children.
- Effective prophylactic treatment is crucial to prevent recurrence.
Purpose of the Study:
- To compare the efficacy of phenobarbital, primidone, and different sodium valproate dosing regimens in preventing febrile convulsions.
- To investigate the impact of dosing frequency and daily dosage on sodium valproate's prophylactic effect.
Main Methods:
- A study involving 196 children with febrile convulsions.
- Treatment groups included phenobarbital, primidone, and various sodium valproate regimens (20-25 mg/kg/day b.i.d., 20-25 mg/kg/day t.i.d., 30 mg/kg/day b.i.d.).
- One-year recurrence rates of febrile convulsions were analyzed.
Main Results:
- No statistically significant difference in recurrence rates was observed among phenobarbital, primidone, and the studied valproate groups.
- The sodium valproate regimen of 20-25 mg/kg/day b.i.d. demonstrated a relatively inferior prophylactic effect compared to other valproate regimens.
- Higher daily fluctuations in plasma levels and lower minimum plasma levels were noted with b.i.d. dosing and lower daily dosages of sodium valproate.
Conclusions:
- Phenobarbital, primidone, and sodium valproate are similarly effective in preventing febrile convulsions.
- Dosing frequency and daily dosage significantly influence the prophylactic efficacy of sodium valproate.
- Twice-daily (b.i.d.) administration of sodium valproate may be less effective than thrice-daily (t.i.d.) administration due to plasma level fluctuations.
Abstract:
Of 196 children with febrile convulsions, 6.9 were placed on phenobarbital, 4-5 mg/kg/day b.i.d., and 32 on primidone, 15-20 mg/kg/day b.i.d. The remaining 95 children were given sodium valproate; the dosage was 20-25 mg/kg/day b.i.d. in 38 of them, 20-25 mg/kg/day t.i.d. in 24 of them, and 30 mg/kg/day b.i.d. in 33 patients. Recurrence rate of febrile convulsions during one year were not statistically different among these five groups. However, the dosage regimen of valproate of 20-25 mg/kg/day b.i.d. was relatively inferior to the other regimens of valproate in the prophylactic effect. This may be explained by the facts that when the same daily dosage of sodium valproate was given, the daily fluctuation of plasma levels was greater with the b.i.d.-regimen than with the t.i.d.-regimen, and that when the dosage interval was the same, the minimum plasma level of the day was lower with the smaller daily dosage regimen than with the larger one.
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