TY - JOUR
T1 - Routine use of fentanyl infusions for pain and stress reduction in infants with respiratory distress syndrome
AU - Orsini, A. J.
AU - Leef, K. H.
AU - Costarino, A.
AU - Dettorre, M. D.
AU - Stefano, J. L.
PY - 1996
Y1 - 1996
N2 - Objective: To determine whether fentanyl infusions given to premature infants with respiratory distress syndrome reduce stress and improve long- and short-term outcome. Methods: Twenty premature infants undergoing mechanical ventilation for respiratory distress syndrome were randomly assigned, in a double-blind fashion, to receive fentanyl by continuous infusion or a volume-matched placebo infusion. A behavioral state score was used to assess the infants' behavior. Cortisol and 11-deoxycortisol levels were measured as physiologic markers of stress. Urinary 3-methyl histidine/creatinine molar ratio was determined and the fractional excretion of urea was measured to assess catabolic state. Ventilatory indexes were recorded for each infant. Results: Infants receiving fentanyl showed significantly lower behavioral state scores (p <0.04) and lower heart rates (p <0.001) than those receiving placebo. 11 -Deoxycortisol levels were lower in the fentanyl group on days 3, 4, and 5 of the study (p <0.003). 3-Methyl histidine/creatinine ratios and fractional excretion of urea were not significantly different between the two groups. On the third day of the study, infants receiving fentanyl required a higher ventilator rate (p <0.01), higher peak inspiratory pressures (p <0.001), and higher positive end-expiratory pressure (p <0.0001) than those receiving placebo. There was no difference in long-term outcome with respect to the incidence of bronchopulmonary dysplasia, intraventricular hemorrhage, or sepsis or with respect to the duration of ventilator use. Conclusions: Although there was a reduction in stress markers in the infants receiving fentanyl, we were unable to demonstrate an improvement in catabolic state or long-term outcome. In addition, the infants receiving fentanyl required higher ventilatory support in the early phase of respiratory distress syndrome than did those receiving placebo.
AB - Objective: To determine whether fentanyl infusions given to premature infants with respiratory distress syndrome reduce stress and improve long- and short-term outcome. Methods: Twenty premature infants undergoing mechanical ventilation for respiratory distress syndrome were randomly assigned, in a double-blind fashion, to receive fentanyl by continuous infusion or a volume-matched placebo infusion. A behavioral state score was used to assess the infants' behavior. Cortisol and 11-deoxycortisol levels were measured as physiologic markers of stress. Urinary 3-methyl histidine/creatinine molar ratio was determined and the fractional excretion of urea was measured to assess catabolic state. Ventilatory indexes were recorded for each infant. Results: Infants receiving fentanyl showed significantly lower behavioral state scores (p <0.04) and lower heart rates (p <0.001) than those receiving placebo. 11 -Deoxycortisol levels were lower in the fentanyl group on days 3, 4, and 5 of the study (p <0.003). 3-Methyl histidine/creatinine ratios and fractional excretion of urea were not significantly different between the two groups. On the third day of the study, infants receiving fentanyl required a higher ventilator rate (p <0.01), higher peak inspiratory pressures (p <0.001), and higher positive end-expiratory pressure (p <0.0001) than those receiving placebo. There was no difference in long-term outcome with respect to the incidence of bronchopulmonary dysplasia, intraventricular hemorrhage, or sepsis or with respect to the duration of ventilator use. Conclusions: Although there was a reduction in stress markers in the infants receiving fentanyl, we were unable to demonstrate an improvement in catabolic state or long-term outcome. In addition, the infants receiving fentanyl required higher ventilatory support in the early phase of respiratory distress syndrome than did those receiving placebo.
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U2 - 10.1016/S0022-3476(96)70201-9
DO - 10.1016/S0022-3476(96)70201-9
M3 - Article
C2 - 8757574
AN - SCOPUS:0029836851
SN - 0022-3476
VL - 129
SP - 140
EP - 145
JO - Journal of Pediatrics
JF - Journal of Pediatrics
IS - 1
ER -