Chen-Fuh Lam, P Vernon Van Heerden, John Blott, Brigit Roberts, Kenneth F Ilett
Journal: Journal of critical care 2004;19(1):48-53
PMID: 15101006
OBJECTIVES
To examine the effects of inhaled NONOates in patients with acute respiratory distress syndrome (ARDS).
DESIGN
Case-series, phase I clinical trial.
SETTING
A multidisciplinary intensive care unit in a tertiary teaching hospital.
PATIENTS
Five consecutive patients with ARDS (men; age range, 47-76 years).
MEASUREMENTS
DETA/NO (150 micromol) was aerosolized into the lungs of patients on mechanical ventilation via the endotracheal tube over 20 minutes. Hemodynamic parameters were measured and blood samples were taken before, during, and after inhalation.
RESULTS
Compared to baseline values, pulmonary vascular resistance decreased until the end of the study period (180 minutes) while intrapulmonary shunting decreased significantly up to 45 min after DETA/NO aerosol administration. Inhaled DETA/NO had no effect on the systemic circulation (systemic blood pressure or cardiac output).
CONCLUSIONS
Inhaled DETA/NO is a selective pulmonary vasodilator in patients with ARDS. However, a larger number of patients is required to confirm the findings of this pilot study.
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