Effect of continuous hemofiltration on hemodynamics, lung inflammation and pulmonary edema in a canine model of acute lung injury

Intensive Care Med. 2003 Nov;29(11):2034-42. doi: 10.1007/s00134-003-2017-3. Epub 2003 Oct 14.

Abstract

Objective: This study examined whether continuous hemofiltration favorably affects cardiopulmonary variables, lung inflammation, and lung fluid balance in a canine model of oleic acid induced acute lung injury.

Methods: Eleven pentobarbital-anesthetized dogs were randomly divided into a control (mechanical ventilation, MV) group (n=6) and a MV plus hemofiltration (HF) group (n=5). All animals received an intravenous injection of oleic acid (0.09 ml/kg) to induce acute lung injury. Continuous arterial-venous hemofiltration (blood flow 100 ml/min, ultrafiltration rate at 50-65 ml kg(-1) h(-1)) was started after establishment of oleic acid induced acute lung injury and continued for 4 h. Hemodynamics, lung mechanics, gas exchange, lung fluid balance, lung histology, and the level of plasma cytokines were assessed.

Results: After 240 min of HF treatment there was a significant increase in cardiac output, reduction in pulmonary arterial pressure, and improvement in both oxygenation and lung mechanics. Also, in the HF group the lung wet-to-dry weight ratio was significantly reduced. Histologically, HF reduced edema and inflammatory cell infiltration in the lung. There was also a significantly greater decrease in plasma IL-6 and IL-8 levels in the HF group than in group receiving MV alone.

Conclusions: In a canine model of acute lung injury continuous HF improved cardiopulmonary function, reduced pulmonary edema, decreased lung permeability and inflammation, and decreased the plasma concentration of proinflammatory cytokines.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Albumins / analysis
  • Analysis of Variance
  • Animals
  • Biopsy
  • Blood Gas Analysis
  • Bronchoalveolar Lavage Fluid / chemistry
  • Cytokines / blood
  • Disease Models, Animal*
  • Dogs
  • Female
  • Hemodynamics
  • Hemofiltration / instrumentation
  • Hemofiltration / methods*
  • Male
  • Oleic Acid
  • Pulmonary Edema / chemically induced
  • Pulmonary Edema / diagnosis
  • Pulmonary Edema / physiopathology*
  • Pulmonary Edema / therapy*
  • Pulmonary Gas Exchange
  • Random Allocation
  • Respiration, Artificial
  • Respiratory Distress Syndrome / chemically induced
  • Respiratory Distress Syndrome / diagnosis
  • Respiratory Distress Syndrome / physiopathology*
  • Respiratory Distress Syndrome / therapy*
  • Respiratory Mechanics
  • Severity of Illness Index
  • Single-Blind Method

Substances

  • Albumins
  • Cytokines
  • Oleic Acid