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Published on: June 25, 2016
Prophylactic anticonvulsants for prevention of immediate and early postcraniotomy seizures
1Department of Surgery, Chang Gung Medical College & Chang Gung Memorial Hospital, Taipei, Taiwan, Republic of China.
Insights
This study found that phenytoin effectively reduced postoperative seizures in patients undergoing intracranial surgery. Prophylactic anticonvulsant administration before wound closure is recommended for urgent craniotomies.
Area of Science:
- Neurosurgery
- Pharmacology
- Clinical Neurology
Background:
- Postoperative seizures are a significant complication following intracranial surgery.
- Anticonvulsant prophylaxis aims to mitigate seizure risk in this patient population.
Purpose of the Study:
- To evaluate the efficacy of phenytoin in preventing early postoperative seizures after supratentorial intracranial surgery.
- To assess the achievement of therapeutic serum levels of phenytoin in surgical patients.
Main Methods:
- A randomized controlled trial involving 374 patients undergoing intracranial surgery.
- Intravenous phenytoin (15 mg/kg) administered preoperatively, followed by 5-6 mg/kg/day postoperatively for 3 days.
- A placebo group received identical treatment for comparison.
Main Results:
- Phenytoin administration resulted in significantly fewer immediate and early postoperative seizures compared to placebo (3 vs. 13 seizures).
- Therapeutic serum phenytoin levels (10-20 micrograms/mL) were achieved in 59.8% of treated patients.
- No postoperative hematomas were observed in patients experiencing seizures.
Conclusions:
- Phenytoin is effective in reducing the incidence of early postoperative seizures following supratentorial intracranial surgery.
- Prophylactic anticonvulsant administration should be considered, particularly for urgent craniotomies, with administration timed before wound closure to maintain therapeutic levels.
Abstract:
Phenytoin (15 mg/kg) was administered intravenously to 189 patients shortly before their intracranial, supratentorial surgery was completed. Intravenous phenytoin of 5-6 mg/kg/day in three divided doses was administered daily for the first 3 postoperative days. Therapeutic serum levels (10-20 micrograms/mL) were achieved in 113 (59.8%) patients. An equally constituted, randomized control group of 185 patients received a placebo under identical conditions. The group receiving phenytoin had only one immediate and two early postoperative seizures. The 185 controls had four immediate and nine early postoperative seizures. None of the follow-up computed tomography scans of the patients with seizures showed postoperative hematoma. One patient had a significant tension pneumocranium, a possible cause of postoperative seizures. To avoid a decrease in the serum anticonvulsant level due to intraoperative blood loss, it is suggested that for patients who need an urgent or emergent craniotomy, prophylatic anticonvulsant medication should be given at least 20 minutes before completion of wound closure.
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