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Redistribution of microcirculatory blood flow within the intestinal wall during sepsis and general anesthesia

Luzius B Hiltebrand1, Vladimir Krejci, Marcus E tenHoevel

  • 1Department of Anesthesia, University of Berne, Inselspital, Berne, Switzerland.

Anesthesiology
|February 28, 2003
PubMed
Abstract

Insights

In early septic shock, intestinal mucosal blood flow is maintained despite reduced overall flow. This suggests autoregulation protects the gut lining by redirecting blood from the muscle layer to the mucosa.

Area of Science:

  • Physiology
  • Sepsis Research
  • Gastrointestinal Medicine

Background:

  • Intestinal mucosal hypoperfusion is a critical issue in sepsis, potentially leading to organ failure.
  • Impaired autoregulation of microcirculatory blood flow in the gut is implicated in sepsis and surgical complications.

Purpose of the Study:

  • To investigate microcirculatory blood flow in the gastrointestinal tract during early septic shock in a porcine model.
  • To assess the autoregulation of intestinal mucosal blood flow during sepsis.

Main Methods:

  • Used ultrasound transit time flowmetry for superior mesenteric artery blood flow and laser Doppler flowmetry for mucosal and muscularis microcirculatory blood flow in pigs.
  • Induced sepsis via fecal peritonitis and managed fluid resuscitation to transition between hypodynamic and hyperdynamic states.

Main Results:

  • During hypodynamic sepsis, cardiac output, mesenteric artery flow, and gastric mucosal blood flow decreased significantly. Muscularis blood flow in the stomach, jejunum, and colon also dropped substantially.
  • Jejunal and colonic mucosal blood flow remained stable during the hypodynamic phase.
  • In hyperdynamic sepsis, cardiac output and mesenteric artery flow increased threefold. Mucosal blood flow rose above baseline, while muscularis flow in the jejunum and colon remained depressed.

Conclusions:

  • Autoregulation of intestinal mucosal microcirculatory blood flow appears largely intact during early septic shock in this model.
  • Blood flow redistribution from the intestinal muscularis to the mucosa may explain the preserved mucosal perfusion.

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