Initial Tocolytic Therapy for Preterm Labor
For women in preterm labor between 24-34 weeks gestation, tocolytic therapy is recommended primarily to delay delivery for 48-72 hours to allow for administration of antenatal corticosteroids and maternal transfer to a tertiary care facility with appropriate neonatal intensive care capabilities. 1
First-Line Tocolytic Options
- Nifedipine is recommended as a reasonable first-line tocolytic agent due to its effectiveness in delaying delivery, favorable side effect profile compared to beta-mimetics, and association with improved neonatal outcomes 2, 3
- Initial dosing regimen: 10 mg nifedipine capsules orally every 15 minutes up to 40 mg in the first hour, followed by 20 mg slow-release nifedipine at 90 minutes 4
- Calcium channel blockers like nifedipine have been shown to decrease adverse neonatal outcomes by significantly delaying delivery and are associated with fewer maternal side effects than beta-mimetics 2, 3
Alternative Tocolytic Options
- Indomethacin may be considered as a reasonable first choice for acute tocolysis in gestational ages less than 32 weeks, but prolonged use (>48 hours) should be avoided 2
- Atosiban (oxytocin receptor antagonist) has an excellent maternal and fetal safety profile but has not been shown to significantly reduce neonatal complications 2, 5
- When compared with calcium channel blockers, atosiban results in fewer maternal adverse effects but may be less effective at prolonging gestation 3
Magnesium Sulfate Considerations
- While magnesium sulfate is sometimes used as a tocolytic, evidence for its effectiveness is controversial 2, 6
- Its primary benefit in the periviable period is for fetal neuroprotection, reducing the incidence of cerebral palsy when administered before anticipated early preterm birth 1
- Important safety considerations with magnesium sulfate include:
Duration and Limitations of Tocolysis
- Tocolytic therapy generally does not significantly lengthen gestational age beyond seven days 2
- Despite the ability to delay delivery temporarily, no tocolytic has been consistently shown to improve overall neonatal outcomes or reduce the overall rate of preterm birth 1
- The primary benefit remains gaining time for corticosteroid administration and maternal transfer to appropriate facilities 1
Clinical Monitoring During Tocolysis
- For magnesium sulfate: monitor deep tendon reflexes, respiratory rate (should remain ≥16 breaths/min), urine output (maintain at ≥100 mL over 4 hours), and serum magnesium levels 7
- For nifedipine: monitor maternal blood pressure and heart rate due to potential hypotensive effects, though these are less severe than with beta-mimetics 3
- Continuous fetal monitoring should be maintained during acute tocolysis 1