The combination of partial liquid ventilation and inhaled nitric oxide in the severe oleic acid lung injury model

Chest. 1998 Jun;113(6):1658-66. doi: 10.1378/chest.113.6.1658.

Abstract

Study objectives: To elucidate the efficacy of the combination of inhaled nitric oxide (NO) and partial liquid ventilation (PLV) in ARDS.

Design: Prospective, randomized, controlled study.

Setting: A research laboratory at a university medical center.

Subjects: Thirty-two rabbits.

Interventions: Animals were anesthetized and ventilated via tracheostomy (tidal volume=40 mL; respiratory rate=25 breaths/min; fraction of inspired oxygen=0.99). After 0.08 mL/kg (0.071 g/kg) oleic acid was administered via the central venous route, animals were randomly divided into the following four groups depending on the ventilatory mode: (1) Gas ventilation (GV)-control group: GV was continued throughout the study; (2) GV-NO group: NO inhalation (10 ppm) was performed under GV; (3) PLV-control group: PLV using perflubron (15 mL/kg) was continued until the end of the study; and (4) PLV-NO group: NO inhalation (10 ppm) was performed under PLV.

Measurements and results: NO inhalation improved PaO2 in the PLV-NO group (from 133+/-20 to 167+/-23 mm Hg; p=0.0008), but not in the GV-NO group (from 67+/-6 to 63+/-9 mm Hg), although pulmonary vascular resistance decreased both in the GV-NO (from 4,604+/-328 to 4,337+/-322 dyne x s x cm(-5); p=0.0116) and the PLV-NO group (from 4,727+/-665 to 4,112+/-560 dyne x s x cm(-5); p=0.0036). (Data were expressed as mean+/-SEM.)

Conclusion: PLV augmented the effect of inhaled NO on pulmonary gas exchange. The combination of PLV and NO inhalation could be effective in severe ARDS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carbon Dioxide / blood
  • Fluorocarbons / administration & dosage*
  • Hemodynamics
  • Hydrocarbons, Brominated
  • Nitric Oxide / administration & dosage*
  • Oleic Acid
  • Oxygen / blood
  • Pulmonary Circulation
  • Pulmonary Edema / chemically induced
  • Pulmonary Edema / physiopathology
  • Pulmonary Edema / therapy*
  • Rabbits
  • Respiration, Artificial* / methods
  • Vascular Resistance

Substances

  • Fluorocarbons
  • Hydrocarbons, Brominated
  • Carbon Dioxide
  • Oleic Acid
  • Nitric Oxide
  • perflubron
  • Oxygen