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Clinical Trial
. 2001 May;119(5):1503-9.
doi: 10.1378/chest.119.5.1503.

Clinical correlation with changing radiographic appearance during partial liquid ventilation

Affiliations
Clinical Trial

Clinical correlation with changing radiographic appearance during partial liquid ventilation

D P Schuster et al. Chest. 2001 May.

Abstract

Study objectives: To evaluate the chest radiographic filling pattern associated with partial liquid ventilation (PLV) with the perfluorochemical perflubron (LiquiVent; Alliance Pharmaceutical Corp; San Diego CA) as a function of dose and timing.

Design: Post hoc review of chest radiographs by three independent observers with correlation to clinical variables.

Setting: Phase II randomized, uncontrolled, prospective, multicenter clinical trial.

Patients: Sixteen adult patients with diffuse bilateral infiltrates consistent with acute lung injury and a PaO(2)/fraction of inspired oxygen (FIO(2)) ratio < 300 with positive end-expiratory pressure of 13 cm H(2)O and FIO(2) > or = 0.5.

Interventions: All patients were treated with either a 10-mL/kg or 20-mL/kg loading dose of perflubron followed by maintenance dosing at 3-h intervals to protocol-determined levels.

Results: There was a significant relationship between inhomogeneous radiographic filling during the first 48 h of treatment and the use of the lower loading dose of perflubron. Inhomogeneous radiographic filling (in 5 patients) was associated with a lower high-dose/FIO(2) ratio at 24 h compared with the remaining patients. These differences resolved by 48 h. There were no other statistically significant correlations identified.

Conclusions: The radiographic appearance of PLV with perflubron appears to depend on the dose administered. Lower doses can be associated with both inhomogeneous radiographic filling and a transient deterioration in oxygenation during the first 24 to 48 h of treatment.

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