Studies on intragastric PCO2 at rest and during exercise as a marker of intestinal perfusion in patients with chronic heart failure

Eur J Heart Fail. 2004 Jun;6(4):403-7. doi: 10.1016/j.ejheart.2004.03.002.

Abstract

Aims: The aim of this study was to investigate mesenteric ischaemia by determining intragastric PCO(2) (iPCO(2)) with gastric tonometry during rest and exercise stress testing in patients with chronic heart failure (CHF). In CHF inflammatory immune activation is hypothesized to result from a chronic endotoxin challenge due to bacterial translocation of hypoperfused intestinal mucosa.

Methods and results: In 10 patients with CHF and ten healthy controls a tonometry catheter was inserted into the stomach. IPCO(2) was measured at rest and during bicycle exercise every 5 min. At rest arterial pCO(2) (aPCO(2)), intragastric pCO(2) (iPCO(2)) and the intragastric/arterial gap did not differ between patients and controls. During low level exercise (25 W), patients showed an increase in iPCO(2) compared to resting iPCO(2), whereas controls did not show an increase in iPCO(2) (change in iPCO(2): 12+/-2% vs. 1+/-0.4%, P<0.001). In CHF, iPCO(2) during peak exercise was 25+/-3% higher than at rest, compared to controls (increase 2+/-1, P<0.0001).

Conclusions: Patients with CHF already at low level exercise develop an increase in iPCO(2). This is likely to reflect hypoperfusion of the intestinal mucosa, which may contribute to the development of bacterial translocation.

Publication types

  • Comparative Study

MeSH terms

  • Biomarkers / analysis
  • Biomarkers / blood
  • Carbon Dioxide / metabolism*
  • Chronic Disease
  • Exercise / physiology*
  • Exercise Test
  • Female
  • Germany
  • Heart Failure / metabolism*
  • Heart Failure / physiopathology*
  • Humans
  • Lactic Acid / metabolism
  • Lipopolysaccharide Receptors / metabolism
  • Male
  • Manometry
  • Middle Aged
  • Perfusion*
  • Potassium / blood
  • Prospective Studies
  • Regression Analysis
  • Rest / physiology*
  • Sodium / blood
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Biomarkers
  • Lipopolysaccharide Receptors
  • Tumor Necrosis Factor-alpha
  • Carbon Dioxide
  • Lactic Acid
  • Sodium
  • Potassium