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Sodium Valproate versus Propranolol in paediatric migraine prophylaxis
M R Ashrafi1, R Shabanian, G R Zamani
1Department of Pediatric Neurology, Tehran University of Medical Sciences, Children's Medical Center, 62 Gharib Street, 14194 Tehran, Iran.
Insights
Sodium Valproate and Propranolol are effective for pediatric migraine prophylaxis. Both medications significantly reduced headache frequency, severity, and duration in children, with no significant difference between them.
Area of Science:
- Neurology
- Pediatrics
- Clinical Pharmacology
Background:
- Pediatric migraine is a common neurological disorder impacting children's quality of life.
- Effective prophylactic treatments are crucial for managing frequent migraine attacks in pediatric populations.
Purpose of the Study:
- To compare the efficacy of Sodium Valproate versus Propranolol for pediatric migraine prophylaxis.
- To evaluate the impact of these treatments on headache frequency, severity, and duration.
Main Methods:
- A randomized clinical trial involving 120 pediatric patients (3-15 years) with common migraine.
- Patients were randomized into two groups: Sodium Valproate (Group A) and Propranolol (Group B).
- The study included baseline, titration, and fixed-dose treatment periods.
Main Results:
- Both Sodium Valproate and Propranolol demonstrated significant efficacy in migraine prophylaxis.
- 72% of patients on Sodium Valproate and 69% on Propranolol achieved >50% reduction in monthly headache frequency.
- Both drugs significantly reduced headache severity and duration, with no statistically significant difference between the groups (p < 0.05).
Conclusions:
- Sodium Valproate and Propranolol are equally effective in the prophylaxis of common migraine in children.
- Both medications represent viable therapeutic options for reducing the burden of pediatric migraine.
Abstract:
In a randomized clinical trial the effect of Sodium Valproate in pediatric migraine prophylaxis was compared with that of Propranolol. One hundred and twenty patients with common migraine (migraine without aura) aged from 3 to 15 years who met the defined criteria enrolled into the study. Randomly the patients were divided in two groups of A and B, treating with sodium Valproate and Propranolol, respectively. Three phases of baseline period (phase I), titration and adjustment period (phases II) and fixed -dose treatment period (phase III) have been designed. A total of 57 patients in group A, and 58 patients in group B completed all phases of the trial. Seventy two percent of patients in group A and 69% of patients in group B have responded to Sodium Valproate and Propranolol, respectively, as a reduction of more than 50% in headache frequency per month. Further more both drugs have shown efficacy in reducing the severity and duration of headache and also better response to rescue medications (p value <0.01). There was no significant difference in all previously mentioned therapeutic effects between two groups (p value <0.05).
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