ABSTRACT. Objectives. To demonstrate that a period of partial liquid ventilation (PLV) with perflubron improves pulmonary function, without adverse events, in a select group of critically ill infants receiving extracorporeal life support (ECLS) with a high likelihood of mortality.Methods. This was an open-label, noncontrolled, phase I and II trial of PLV in two infants with congenital diaphragmatic hernia and four infants with acute respiratory distress syndrome (ARDS) who were failing to improve while receiving ECLS. PLV was performed by instilling and maintaining a functional residual capacity of sterile perflubron for 4 to 96 hours.Results. Four infants were successfully weaned off ECLS for at least 3 days, and two infants (both with ARDS) are long-term survivors after PLV. All infants demonstrated lung recruitment and improved lung compliance, and there were no adverse events related to PLV.Conclusions. The study suggests that perflubron PLV is safe, improves lung function, and recruits lung volume in critically ill infants receiving ECLS. PLV therapy for infants with ARDS seems to have a great deal of promise. Based on this and other phase I and II trials, studies of PLV on selected full-term infants before ECLS have been initiated. Pediatrics 1997;99(1). URL: http://www. pediatrics.org/cgi/content/full/99/1/e2; congenital diaphragmatic hernia, acute respiratory distress syndrome, partial liquid ventilation, extracorporeal life support.ABBREVIATIONS. ECLS, extracorporeal life support; ARDS, acute respiratory distress syndrome; CDH, congenital diaphragmatic hernia; PLV, partial liquid ventilation; FRC, functional residual capacity.Perfluorochemicals have been explored as respiratory media for more than 20 years in many animal models of respiratory disease and, more recently, in initial phase I and II human trials of liquid ventilation.1-7 These chemicals are very stable, have low surface tension, are generally insoluble in water or lipid, and are excellent solvents for respiratory gases. The effectiveness of liquid ventilation is achieved, in part, through recruitment of collapsed gas-exchanging units, increasing lung compliance, and cleansing the lung of pulmonary debris. Sterile perflubron (LiquiVent; Alliance Pharmaceutical Corp, San Diego, CA), is one of very few perfluorochemicals that is produced as a medical-grade drug. The compound has an impressive biocompatibility profile in animals and humans and is the only fluid that is approved by the Federal Food and Drug Administration for testing as a breathing agent. Perflubron has a high solubility for respiratory gases, a positive spreading coefficient on saline, and a low viscosity and is highly radiopaque on plain radiograph or computed tomographic imaging. 8,9 Recent advances in respiratory therapies for the critically ill neonates have expanded the treatment options for infants with severe respiratory failure. In those severely effected infants, extracorporeal life support (ECLS) may result in increased survival. Nevertheless, morbidity remains high, ...