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Merck
  • Phenytoin versus Leviteracetam for seizure prophylaxis after brain injury - a meta analysis.

Phenytoin versus Leviteracetam for seizure prophylaxis after brain injury - a meta analysis.

BMC neurology (2012-05-31)
Syed Nabeel Zafar, Abdul Ahad Khan, Asfar Ayaz Ghauri, Muhammad Shahzad Shamim
摘要

Current standard therapy for seizure prophylaxis in Neuro-surgical patients involves the use of Phenytoin (PHY). However, a new drug Levetiracetam (LEV) is emerging as an alternate treatment choice. We aimed to conduct a meta-analysis to compare these two drugs in patients with brain injury. An electronic search was performed in using Pubmed, Embase, and CENTRAL. We included studies that compared the use of LEV vs. PHY for seizure prophylaxis for brain injured patients (Traumatic brain injury, intracranial hemorrhage, intracranial neoplasms, and craniotomy). Data of all eligible studies was extracted on to a standardized abstraction sheet. Data about baseline population characteristics, type of intervention, study design and outcome was extracted. Our primary outcome was seizures. The literature search identified 2489 unduplicated papers. Of these 2456 papers were excluded by reading the abstracts and titles. Another 25 papers were excluded after reading their complete text. We selected 8 papers which comprised of 2 RCTs and 6 observational studies. The pooled estimate's Odds Ratio 1.12 (95% CI = 0.34, 3.64) demonstrated no superiority of either drug at preventing the occurrence of early seizures. In a subset analysis of studies in which follow up for seizures lasted either 3 or 7 days, the effect estimate remained insignificant with an odds ratio of 0.96 (95% CI = 0.34, 2.76). Similarly, 2 trials reporting seizure incidence at 6 months also had insignificant pooled results while comparing drug efficacy. The pooled odds ratio was 0.96 (95% CI = 0.24, 3.79). Levetiracetam and Phenytoin demonstrate equal efficacy in seizure prevention after brain injury. However, very few randomized controlled trials (RCTs) on the subject were found. Further evidence through a high quality RCT is highly recommended.

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Sigma-Aldrich
5,5-二苯基海因, ≥98%
USP
苯妥英, United States Pharmacopeia (USP) Reference Standard
Supelco
苯妥英标准液 溶液, 1.0 mg/mL in methanol, ampule of 1 mL, certified reference material, Cerilliant®
Supelco
苯妥英钠, Pharmaceutical Secondary Standard; Certified Reference Material
苯妥英钠, European Pharmacopoeia (EP) Reference Standard
苯妥英钠, European Pharmacopoeia (EP) Reference Standard