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Phenobarbital prior to preterm birth for preventing neonatal periventricular haemorrhage
Caroline A Crowther1, Danielle D Crosby, David J Henderson-Smart
1ARCH: Australian Research Centre for Health of Women and Babies, Discipline of Obstetrics and Gynaecology, The University of Adelaide, Women's and Children's Hospital, 72 King William Road, Adelaide, South Australia, Australia, 5006.
Insights
Prenatal phenobarbital administration to mothers at risk of preterm birth did not prevent periventricular haemorrhage (PVH) in infants. The drug also did not reduce neurodevelopmental abnormalities, but increased maternal sedation.
Area of Science:
- Neonatal Medicine
- Obstetrics
- Pharmacology
Background:
- Preterm infants face risks of periventricular haemorrhage (PVH).
- Phenobarbital is investigated for its potential to prevent brain injury by managing blood pressure and flow in neonates.
Purpose of the Study:
- To evaluate the efficacy and safety of maternal phenobarbital administration for preventing infant PVH in cases of imminent very preterm birth.
- To assess potential benefits and harms to both mother and infant.
Main Methods:
- A systematic review and meta-analysis of randomized controlled trials (RCTs) was conducted.
- Searched the Cochrane Pregnancy and Childbirth Group's Trials Register for relevant studies up to March 2008.
- Assessed trial eligibility, quality, and extracted data on neonatal and maternal outcomes.
Main Results:
- Initial analyses of nine trials (1752 women) suggested phenobarbital reduced all grades of PVH (RR 0.65) and severe PVH (RR 0.41).
- However, these benefits were primarily driven by low-quality trials; higher-quality trials showed no significant effect on PVH rates.
- No differences in neurodevelopmental abnormalities were observed at 18-24 months or seven years. Maternal sedation was more frequent (RR 2.06).
Conclusions:
- Current evidence does not support the prophylactic use of maternal phenobarbital to prevent infant PVH or childhood neurological disability.
- Maternal sedation is a potential adverse effect.
- Future research should prioritize robust neurodevelopmental outcome assessments.
Background:
Preterm infants are at risk of periventricular haemorrhage. Phenobarbital might prevent ischaemic injury or reduce fluctuations in blood pressure and blood flow in the brain.
Objectives:
To assess the benefits and harms of giving phenobarbital to women at risk of imminent very preterm birth with the primary aim of preventing periventricular haemorrhage in the infant.
Search Strategy:
We searched the Cochrane Pregnancy and Childbirth Group's Trials Register (31 March 2008).
Selection Criteria:
Randomised trials with reported data that compared neonatal and maternal outcomes following prenatal exposure to phenobarbital, with outcomes in controls with or without placebo.
Data Collection And Analysis:
We independently assessed trial eligibility and quality and extracted data. We included eligible trials in the initial analysis and prespecified sensitivity analyses to evaluate the effect of trial quality.
Main Results:
Nine trials (1752 women) were included. Analyses of all included trials showed a significant reduction in the rates of all grades of periventricular haemorrhage (PVH) (risk ratio (RR) 0.65, 95% confidence interval (CI) 0.50 to 0.83; nine trials; 1591 women) and severe grades PVH (3 and 4) (RR 0.41, 95% CI 0.20 to 0.85; eight trials; 1527 women) in infants whose mothers had been given prenatal phenobarbital. These results were influenced by trials of poor quality which contributed excessive weight in the analysis due to their higher rates of severe PVH. When only the two higher quality trials were included, these beneficial effects disappeared for all grades of PVH (RR 0.90, 95% CI 0.75 to 1.08; two trials; 945 women), and severe grades of PVH (RR 1.05, 95% CI 0.60 to 1.83; two trials; 945 women).No difference was found in the incidence of neurodevelopmental abnormalities at paediatric follow up at 18 to 24 months or seven years of age between children born to mothers given prenatal phenobarbital and children not so exposed. Maternal sedation was more likely in women receiving phenobarbital (RR 2.06, 95% CI 1.79 to 2.37; one trial; 576 women).
Authors' Conclusions:
The evidence in this review does not support the use of prophylactic maternal phenobarbital administration to prevent periventricular haemorrhage in preterm infants or to protect them from neurological disability in childhood. Phenobarbital administration may lead to maternal sedation. If any future trials are carried out, they should measure neurodevelopmental status at follow up.
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