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Doxapram versus methylxanthine for apnea in preterm infants
1NSW Centre for Perinatal Health Services Research, Queen Elizabeth II Institute for Mothers and Infants, Building DO2, University of Sydney, Sydney, NSW, Australia 2006. dhs@mail.usyd.edu.au
The Cochrane Database of Systematic Reviews
|May 5, 2000
Summary
Doxapram and methylxanthine (theophylline) appear equally effective for treating recurrent apnea in preterm infants in the short term. However, these trials are small, so caution is advised regarding potential differences or less common side effects.
Area of Science:
- Neonatal Medicine
- Pharmacology
- Respiratory Medicine
Background:
- Recurrent apnea is prevalent in preterm infants, potentially causing hypoxemia and bradycardia requiring resuscitation.
- Doxapram and methylxanthine drugs are used to stimulate breathing and prevent apnea in neonates.
Purpose of the Study:
- To compare the efficacy of doxapram versus theophylline in reducing apnea and mechanical ventilation use in preterm infants.
- To assess the safety profile of doxapram compared to theophylline for apnea treatment in neonates.
Main Methods:
- Systematic review and meta-analysis of randomized or quasi-random trials comparing doxapram with methylxanthines for apnea treatment.
- Trials excluded infants with specific causes of apnea.
- Methodological quality assessed, data extracted and synthesized using relative risk and risk difference.
Main Results:
- No apparent difference in apnea incidence within 48 hours between intravenous doxapram and methylxanthine treatment.
- No infants required mechanical ventilation in either treatment group.
- No adverse effects were reported in the included trials.
Conclusions:
- Intravenous doxapram and methylxanthine show similar short-term effectiveness for apnea of prematurity.
- Small trial sizes limit the ability to exclude important differences in efficacy or less common side effects.
- Further large-scale studies are needed to clarify optimal use, identify responsive infants, and assess long-term outcomes and side effects.