Key result
Low-dose doxapram hydrochloride reduced apnea frequency by approximately 90% in premature infants without causing QT or PR prolongation, arrhythmia, or changes in the QT/RR slope.
Why the study?
Does low-dose doxapram hydrochloride reduce apnea episodes without causing cardiac conduction disorders in premature very-low-birth-weight infants with AOP?
Observational (n=15)
Does low-dose doxapram hydrochloride reduce apnea episodes without causing cardiac conduction disorders in premature very-low-birth-weight infants with AOP?
Low-dose doxapram hydrochloride effectively reduces apnea in premature infants without causing adverse cardiac conduction effects such as QT prolongation.
May support low-dose doxapram for apnea of prematurity without conduction risks; hypothesis-generating and requires randomized confirmation.
Doxapram hydrochloride, a respiratory stimulant, has several undesirable side effects during high-dose administration, including second-degree atrioventricular (AV) block and QT prolongation. In Japan, this drug is contraindicated for newborn infants. Recent studies, however, have demonstrated the efficacy and safety of doxapram therapy for apnea of prematurity (AOP) using lower doses than those previously tested. As a result, approximately 60% of Japanese neonatologists continue to use this drug. This study used surface ECG recordings to assess the cardiac safety of low-dose doxapram hydrochloride (0.2 mg/kg/h) in fifteen premature very-low-birth-weight infants with idiopathic AOP. Cardiac intervals and number of apnea episodes were compared before and after drug administration. Low-dose doxapram hydrochloride resulted in approximately 90% reduction in the frequency of apnea without side effects. None of the infants developed QT or PR prolongation, arrhythmia, or other conduction disorders. In addition, there was no change in the slope of QT/RR before versus after administration of doxapram hydrochloride. We conclude that low-dose administration of doxapram hydrochloride did not have any undesirable effects on myocardial depolarization and repolarization.
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Miyata et al. (2007) conducted an observational in Idiopathic apnea of prematurity (AOP) (n=15). Doxapram hydrochloride vs. Before drug administration was evaluated on Cardiac intervals (QT/RR slope) and number of apnea episodes. Low-dose doxapram hydrochloride reduced apnea frequency by approximately 90% in premature infants without causing QT or PR prolongation, arrhythmia, or changes in the QT/RR slope.
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