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Anesth Analg 2004;99:207-211
© 2004 International Anesthesia Research Society
doi: 10.1213/01.ANE.0000121308.26125.B0


CRITICAL CARE AND TRAUMA

Supplemental Oxygen and Carbon Dioxide Each Increase Subcutaneous and Intestinal Intramural Oxygenation

Jebadurai Ratnaraj, MD*, Barbara Kabon, MD*, Michael R. Talcott, DVM{dagger}, Daniel I. Sessler, MD{ddagger}, and Andrea Kurz, MD§

Departments of *Anesthesiology and {dagger}Veterinary Surgical Services, Washington University, St. Louis, MO; the {ddagger}Outcomes Research Institute and Departments of Anesthesiology and Pharmacology, University of Louisville, Louisville, KY; and §the Department of Anesthesiology, University of Bern, Switzerland and the Department of Anesthesiology and Intensive Care Medicine, University of Vienna, Vienna, Austria

Address correspondence and reprint requests to Dr. Kurz, Department of Anesthesiology, University of Bern, 3010 Bern, Switzerland. Address email to kurza{at}notes.wustl.edu

Oxidative killing by neutrophils, a primary defense against surgical pathogens, is directly related to tissue oxygenation. We tested the hypothesis that supplemental inspired oxygen or mild hypercapnia (end-tidal PCO2 of 50 mm Hg) improves intestinal oxygenation. Pigs (25 ± 2.5 kg) were used in 2 studies in random order: 1) Oxygen Study: 30% versus 100% inspired oxygen concentration at an end-tidal PCO2 of 40 mm Hg, and 2) Carbon Dioxide Study: end-tidal PCO2 of 30 mm Hg versus 50 mm Hg with 30% oxygen. Within each study, treatment order was randomized. Treatments were maintained for 1.5 h; measurements were averaged over the final hour. A tonometer inserted in the subcutaneous tissue of the left upper foreleg measured subcutaneous oxygen tension. Tonometers inserted into the intestinal wall measured intestinal intramural oxygen tension from the small and large intestines. Oxygen 100% administration doubled subcutaneous oxygen partial pressure (PO2) (57 ± 10 to 107 ± 48 mm Hg, P = 0.006) and large intestine intramural PO2 (53 ± 14 to 118 ± 72 mm Hg, P = 0.014); intramural PO2 increased 40% in the small intestine (37 ± 10 to 52 ± 25 mm Hg, P = 0.004). An end-tidal PCO2 of 50 mm Hg increased large intestinal PO2 approximately 16% (49 ± 10 to 57 ± 12 mm Hg, P = 0.039), whereas intramural PO2 increased by 45% in the small intestine (31 ± 12 to 44 ± 16 mm Hg, P = 0.002). Supplemental oxygen and mild hypercapnia each increased subcutaneous and intramural tissue PO2, with supplemental oxygen being most effective.

IMPLICATIONS: Tissue oxygenation is the primary determinant of oxidative killing rate by neutrophils. Increasing inspired oxygen concentration from 30% to 100% or increasing end-tidal PCO2 from 30 mm Hg to 50 mm Hg increased both subcutaneous or intestinal intramural tissue oxygenation, with supplemental oxygen being most effective. Either treatment is thus likely to reduce the risk of infection.




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Lippincott, Williams & Wilkins Anesthesia & Analgesia® is published for the International Anesthesia Research Society® by Lippincott Williams & Wilkins with the assistance of Stanford University Libraries' HighWire Press®. Copyright 2006 by the International Anesthesia Research Society. Online ISSN: 1526-7598   Print ISSN: 0003-2999 HighWire Press
Copyright © 2004 by the International Anesthesia Research Society.