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Anticonvulsants for preventing mortality and morbidity in full term newborns with perinatal asphyxiaEvans DJ, Levene MI, Tsakmakis M
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SummaryIt is unclear whether giving anticonvulsants to newborn babies soon after possible birth asphyxia at term is safe and effective. More studies are needed.Seizures (or convulsions) are common following birth asphyxia. These seizures may worsen the brain injury. In theory, anticonvulsant medication given to babies soon after possible birth asphyxia may improve outcome by preventing seizures and protecting the brain. Anticonvulsant drugs are not without side effects and there are concerns that they might impair brain development. The studies included in this review involved relatively small numbers of babies and few studies assessed developmental outcome. At present, there is insufficient information on which to base recommendations about the effectiveness of giving anticonvulsants to newborn babies soon after possible birth asphyxia.
This is a Cochrane review abstract and plain language summary, prepared and maintained by The Cochrane Collaboration, currently published in The Cochrane Database of Systematic Reviews 2008 Issue 3, Copyright © 2008 The Cochrane Collaboration. Published by John Wiley and Sons, Ltd.. The full text of the review is available in The Cochrane Library (ISSN 1464-780X).
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October 26. 1998 AbstractBackgroundSeizures are common following perinatal asphyxia and may exacerbate secondary neuronal injury by increasing cerebral metabolic demand, causing fluctuations in oxygenation and perfusion, and triggering the release of excitatory neurotransmitters. Anticonvulsant therapy has been used in infants with perinatal asphyxia in order to prevent seizures. However, long term anticonvulsant therapy may lead to inhibition of brain development. Therefore, the routine use of anticonvulsant therapy to prevent seizures following perinatal asphyxia needs to be evaluated. ObjectivesTo assess the effect of administering anticonvulsants to infants of 37 weeks gestation or more following perinatal asphyxia on death or subsequent severe neurodevelopmental disability and/or the prevention of seizures. Search strategyRelevant randomised controlled trials were identified using a combination of electronic database searches, hand searches and a search of the Cochrane Controlled Trials Registry. Selection criteriaAll randomised or quasi-randomised controlled clinical trials that reported data comparing the following outcomes: mortality, neurodevelopmental disability, neonatal seizures and adverse events, following anticonvulsant therapy in term infants (37 weeks or more) compared to controls (with or without placebo) following perinatal asphyxia. Data collection and analysisMethodological quality and validity of studies were assessed without consideration of the results. Data relevant to the outcome were extracted and analysed. Main resultsSeven randomised or quasi-randomised controlled trials that met the selection criteria were included. No studies were of sufficient methodological quality and size to demonstrate a valid, clinically significant change in the risk of mortality or severe neurodevelopmental disability. A meta-analysis combining five studies comparing barbiturates with conventional therapy following perinatal asphyxia demonstrated no difference in risks of death, severe neurodevelopmental disability, or the combined outcome of death or severe neurodevelopmental disability. Authors' conclusionsAt the present time, anticonvulsant therapy to term infants in the immediate period following perinatal asphyxia cannot be recommended for routine clinical practice, other than in the treatment of prolonged or frequent clinical seizures. Any future studies should be of sufficient size to have the power to detect clinically important reductions in mortality and severe neurodevelopmental disability. |