ObjectiveTo date, studies of partial liquid ventilation (PLV) have examined its effects acutely in anesthetized and mechanically ventilated subjects. We set out to develop a model of prolonged PLV in awake, spontaneously breathing animals.DesignAnimal case seriesSettingCardiopulmonary physiology laboratory.SubjectsFifteen New Zealand white rabbits (3.2 +/- 0.39 kg).InterventionsAnimals were anesthetized and instrumented with a novel technique allowing percutaneously assisted placement of an intratracheal catheter with a subcutaneously tunneled externalized free end. After anesthetic recovery, PLV was performed in spontaneously breathing unsedated animals.Measurements and Main ResultsEvaporative losses were determined using a single 10 mL/kg perflubron dose (n = 5); hourly radiographs were obtained until residual perflubron was minimal. For prolonged PLV (n = 10), a 10-mL/kg initial perflubron dose was followed every 4 hrs with 5-mL/kg supplements. Radiographs were obtained immediately before and after perflubron administration and were scored (0-5) by a radiologist blinded to dosing regimen and time Interval. Data were analyzed with ANOVA and Student's t-test with correction for multiple comparisons. Initial filling was nearly complete (score = 4.8 +/- 0.42); lungs were maintained approximately half-filled through 4 hrs (score = 2.53 +/- 0.71). By 6 hrs, the majority of perflubron had evaporated (score = 1.75 +/- 0.53). Over 24 hrs, radiographs documented continuous perflubron exposure (postfill = 4.53 +/- 0.64, prefill = 3.40 +/- 0.71, average = 3.97 +/- 0.43); scores were comparatively higher after filling (after = 4.53 +/- 0.64, before = 3.4 +/- 0.71, p < .001). Left and right lung volumes were equivalent (left = 4.06 +/- 0.47, right = 3.89 +/- 0.39, p = .027). All animals survived the 24 hrs of PLV.ConclusionsPercutaneously assisted intratracheal cannulation with catheter exteriorization permits prolonged PLV in spontaneously breathing, unsedated animals. Continuous perfluorocarbon exposure with this method is reproducible, consistent, and well tolerated for 24 hrs in uninjured animals. (Crit Care Med 1999; 27:941-945)