1. CHARACTERIZATION OF ACUTE RESPONSE TO SURVANTA® (BERACTANT) IN THE TREATMENT OF NEONATAL RDS † 1589
- Author
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Randy R. Miller, Leandro Cordero, Elizabeth M. Zola, and Robert A Shalwitz
- Subjects
Acute effects ,business.industry ,Blood gas measurements ,respiratory system ,respiratory tract diseases ,Anesthesia ,Pediatrics, Perinatology and Child Health ,medicine ,Breathing ,Dosing ,business ,Tidal volume ,Beractant ,Respiratory minute volume ,medicine.drug ,Oxygen saturation (medicine) - Abstract
Previously the acute pulmonary responses to Survanta were studied by monitoring intermittent changes in ventilatory and blood gas measurements. This study is designed to continuously characterize the acute response to Survanta during the 60 minutes following the initial dose administered to premature infants weighing 650-1500g diagnosed with significant RDS (a/A PO2≤ 0.3) prior to 2 hours of life. For the study duration (10 min prior to and 60 min following treatment) oxygen saturation, ventilator rate, and tidal volume are maintained within target ranges 93-98%, 45-60/min, and 5-7mL/kg, respectively. Survanta 4 mL/kg is administered intratracheally using a 5 Fr TrachCare MAC™ without interrupting ventilation. Software for the Drager Babylog 8000 ventilator allows continuous monitoring and recording of ventilator parameters, including FiO2, minute ventilation, MAP, and others. SaO2 is continuously monitored and recorded at 5 min intervals. Acute effects on FiO2 for the initial 9 patients indicate a marked linear decrease in FiO2(± SEM) during the 30 minutes following dosing, with a continued decline thereafter. The a/A PO2 ratio increased by two fold, and SaO2 was kept stable throughout. Other parameters are being evaluated. No administration side effects were observed. Enrollment is expected to total 40 infants.
- Published
- 1997
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