Hypoxic pulmonary vasoconstriction in systemic sclerosis and primary pulmonary hypertension

Chest. 1991 Mar;99(3):551-6. doi: 10.1378/chest.99.3.551.

Abstract

Reduction of pulmonary vascular resistance by a high inspired oxygen concentration is a common, but not universal phenomenon in patients with pulmonary vascular disease of varying etiology that may determine their response to long-term domiciliary oxygen therapy. We therefore determined changes in PVR during oxygen therapy in two patient populations not previously studied: systemic sclerosis (n = 8, mean age +/- SEM, 44.5 +/- 5.4 years) and primary pulmonary hypertension (n = 7, mean age +/- SEM 38 +/- 7.8 years). All patients were hypoxemic (arterial oxygen tension, on air 9.5 +/- 1.2 kPa for SSc and 8.3 +/- 0.6 kPa for PPH, p greater than 0.05). Right atrial pressure, pulmonary artery pressure, pulmonary artery occlusion pressure, systemic arterial pressure, PaO2 and cardiac output by thermodilution were measured at three, 20-min intervals while inspiring air and again after inspiring 60 percent oxygen for 30 min. The PVR fell significantly with oxygen in patients with SSc from 797.6 +/- 179.2 to 610 +/- 151.6 dynes/s/cm-5 (p less than 0.01), and this fall correlated with baseline PAP and PaO2 prior to oxygen therapy (r = 0.86, p less than 0.025; r = 0.77, p less than 0.05, respectively). In patients with PPH, there was no significant fall in PVR with oxygen (from 969 +/- 80.2 to 851.9 +/- 91.2 dynes/s/cm-5, p greater than 0.05) and no predictor of a vasodilator response in individual patients. In SSc, hypoxic pulmonary vasoconstriction contributes more consistently to elevated PVR than in patients with PPH.

Publication types

  • Comparative Study

MeSH terms

  • Adult
  • Blood Pressure / physiology
  • Carbon Dioxide / blood
  • Cardiac Output / physiology
  • Female
  • Humans
  • Hypertension, Pulmonary / physiopathology*
  • Hypoxia / blood
  • Hypoxia / physiopathology
  • Lung / blood supply*
  • Male
  • Middle Aged
  • Oxygen / blood
  • Oxygen Inhalation Therapy*
  • Pulmonary Artery / physiopathology
  • Scleroderma, Systemic / physiopathology*
  • Vascular Resistance / physiology
  • Vasoconstriction* / physiology

Substances

  • Carbon Dioxide
  • Oxygen