Effect of Magnesium Sulfate Given for Neuroprotection Before Preterm Birth
A Randomized Controlled Trial
- Caroline A. Crowther, MD, FRANZCOG;
- Janet E. Hiller, PhD;
- Lex W. Doyle, MD, FRACP;
- Ross R. Haslam, FRACP;
- for the Australasian Collaborative Trial of Magnesium Sulphate (ACTOMgSO4) Collaborative Group
- Author Affiliations: Departments of Obstetrics and Gynaecology (Dr Crowther) and Public Health (Dr Hiller), The University of Adelaide, and Department of Neonatal Medicine, Women's and Children's Hospital (Dr Haslam), Adelaide, South Australia; and Departments of Obstetrics and Gynaecology and Paediatrics, The University of Melbourne, The Royal Women's Hospital, Melbourne, Victoria, Australia (Dr Doyle).
Abstract
Context Prenatal magnesium sulfate may reduce the risk of cerebral palsy or death in very preterm infants.
Objective To determine the effectiveness of magnesium sulfate given for neuroprotection to women at risk of preterm birth before 30 weeks' gestation in preventing pediatric mortality and cerebral palsy.
Design, Setting, and Patients Randomized controlled trial at 16 tertiary hospitals in Australia and New Zealand with stratification by center and multiple pregnancy. A total of 1062 women with fetuses younger than 30 weeks' gestation for whom birth was planned or expected within 24 hours were enrolled from February 1996 to September 2000 with follow-up of surviving children at a corrected age of 2 years.
Interventions Women were randomly assigned to receive a loading infusion of 8 mL (4 g [16 mmol] of 0.5 g/mL of magnesium sulfate solution or isotonic sodium chloride solution [0.9%]) for 20 minutes followed by a maintenance infusion of 2 mL/h for up to 24 hours.
Main Outcome Measures Rates of total pediatric mortality, cerebral palsy, and the combined outcome of death or cerebral palsy at a corrected age of 2 years.
Results Data were analyzed for 1047 (99%) 2-year survivors. Total pediatric mortality (13.8% vs 17.1%; relative risk [RR], 0.83; 95% confidence interval [CI], 0.64-1.09), cerebral palsy in survivors (6.8% vs 8.2%; RR, 0.83; 95% CI, 0.54-1.27), and combined death or cerebral palsy (19.8% vs 24.0%; RR, 0.83; 95% CI, 0.66-1.03) were less frequent for infants exposed to magnesium sulfate, but none of the differences were statistically significant. Substantial gross motor dysfunction (3.4% vs 6.6%; RR, 0.51; 95% CI, 0.29-0.91) and combined death or substantial gross motor dysfunction (17.0% vs 22.7%; RR, 0.75; 95% CI, 0.59-0.96) were significantly reduced in the magnesium group.
Conclusions Magnesium sulfate given to women immediately before very preterm birth may improve important pediatric outcomes. No serious harmful effects were seen.
