Am. J. Respir. Crit. Care Med., Vol 149, No. 3, Mar 1994, 811-814.
Improvement in pulmonary hypertension and hypoxemia during nitric oxide inhalation in a patient with end-stage pulmonary fibrosis
RN Channick, RC Hoch, JW Newhart, FW Johnson and CM Smith
Pulmonary and Critical Care Division, University of California, San Diego Medical Center 92103.
A patient with severe interstitial pulmonary fibrosis, hypoxemia, pulmonary
hypertension, and cor pulmonale was given inhaled nitric oxide (NO)
followed by intravenous PGE1 to assess the reversibility of pulmonary
hypertension. During NO inhalation, there was marked reduction in pulmonary
vascular resistance, increased cardiac output, and dramatic improvement in
arterial oxygenation. There was no effect on systemic vascular resistance.
In contrast, intravenous PGE1 led to rapid arterial oxygen desaturation and
worsened dyspnea. The beneficial responses to inhaled NO in this patient
suggest that, even in severe chronic lung disease, reversible pulmonary
vasoconstriction is present. Inhaled NO thus has a potential therapeutic
role as a selective pulmonary vasodilator in patients with interstitial
pulmonary fibrosis and cor pulmonale.
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Copyright © 1994 American Thoracic Society
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