Key result
IV ritodrine is associated with maternal and fetal side effects but shows no neonatal harm.
Why the study?
The materno-fetal and neonatal effects of intravenous ritodrine therapy for premature labor were not fully characterized.
Does intravenous ritodrine therapy for premature labor cause deleterious effects on the mother and perinate?
Observational (n=57)
Does intravenous ritodrine therapy for premature labor cause deleterious effects on the mother and perinate?
Intravenous ritodrine for premature labor causes significant maternal and fetal side effects but does not appear to have deleterious effects on the neonates.
May warrant caution with ritodrine due to side effects; leaves open neonatal safety in observational data.
The materno-fetal and neonatal effects of ritodrine were studied in 37 women treated for premature labor with intravenous (i.v.) ritodrine. Marked cardiovascular, respiratory, and biochemical side effects of therapy were seen in the mothers and tachycardia was noted in the fetuses. The neonates of 18 women in whom ritodrine successfully postponed delivery were delivered with good Apgar scores and their admission vital signs and nursery courses were benign. Ritodrine failed to delay delivery more than a week in 19 mothers. There were no differences between their newborns and 20 control neonates in admission vital signs, blood gases, blood chemistries, complete blood counts, platelet counts, peak bilirubin, or duration of oxygen therapy. This study revealed no deleterious effects on neonates delivered after maternal ritodrine therapy despite significant maternal and fetal effects.
No takes yet. Share an insight, caveat, or question.
Hancock et al. (1985) conducted an observational in Premature labor (n=57). Intravenous ritodrine vs. Control neonates was evaluated on Neonatal outcomes including admission vital signs, blood gases, blood chemistries, complete blood counts, platelet counts, peak bilirubin, or duration of oxygen therapy. Intravenous ritodrine therapy for premature labor caused significant maternal and fetal side effects but revealed no deleterious effects on neonates compared to controls.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: