Effect of doxapram on episodes of apnoea, bradycardia and hypoxaemia in preterm infants

Aim: To study the effect of doxapram on the frequency of apnoea, bradycardi a and hypoxaemia. Methods: Fifteen infants, median gestational age at birth 27 weeks (range 24-30), age at study 27 days (12-60), with greater than or equal to 6 episodes of bradycardia or hypoxaemia/6 h despite serum caffein e levels in the thera peutic range, received doxapram either intravenously (0.5-2 mg/kg/h) or orally (2-8 mg/kg every 2 h). Six-hour recordings of pul se oximeter saturation (SPO2), pulse waveforms, EGG, breathing movements an d nasal air-flow were performed immediately before as well as 1, 3 and 6 da ys after onset df treatment. Recordings were analysed for apnoea (greater t han or equal to 4 s), bradycardia (heart rate < 2/3 of baseline) and hypoxa emia (SPO2 less than or equal to 80%). Results: There was no difference bet ween enteral and intravenous administration; results are therefore presente d for the total group. Doxapram resulted in a significant decrease in the f requency of apnoea [22 (11-27) vs. 14 (7-23)/h, p < 0.01], bradycardia [3 ( 0-7) vs. 1 (0-3)/h, p < 0.01] and hypoxaemia [8 (0-18) vs. 2 (0-17)/h, p < 0.01] already after 1 day of treatment which was sustained throughout the 6 day study period. Side effects included an increase in the proportion of t ime spent awake [5 (0-24) vs. 12% (3-28), p < 0.01] and in gastric residual s [0% of feeding volume (0-5) vs. 4% (0-19), p < 0.05]. Enteral was switche d to intravenous doxapram in 3 of 9 infants because of gastrointestinal sid e effects. Conclusion: Doxapram substantially reduced the frequency of apno ea, bradycardia and hypoxaemia in these patients with caffeine-resistant ap noea of prematurity. Enteral administration, however, was not tolerated in a significant proportion (33%) of infants.