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The Journal of Thoracic and Cardiovascular Surgery, Vol 95, 712-716, Copyright © 1988 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
GF Nieman, AM Paskanik and CE Bredenberg
Positive end-expiratory pressure (PEEP) increases arterial carbon dioxide
tension and alveolar dead space by reducing alveolar capillary perfusion.
The two likely mechanisms by which PEEP reduces alveolar capillary
perfusion are reduction of cardiac output or compression of pulmonary
capillaries within interalveolar septa, or both mechanisms. This study
attempts to quantitate the impact of each of these mechanisms on alveolar
capillary perfusion in anesthetized dogs by restoring cardiac output to
baseline values with dextran 70 infusion after application of 15 cm H2O
PEEP. Alveolar capillary perfusion was assessed directly through the
visceral pleura by in vivo photomicroscopy. PEEP resulted in a fall in
cardiac output and alveolar capillary perfusion with a concomitant rise in
alveolar dead space- tidal volume ratio and arterial carbon dioxide
tension. Infusion of dextran 70 returned the cardiac output to baseline
levels but only slightly increased alveolar capillary perfusion. Both dead
space/tidal volume ratio and arterial carbon dioxide tension remained
significantly elevated with PEEP even with normal cardiac output.
Microscopically, alveolar capillaries appeared compressed and flattened by
PEEP, which indicated a mechanical interruption of blood flow.
Extra-alveolar vessels remained perfused with PEEP. PEEP increased dead
space/tidal volume ratio 36%; restoration of cardiac output reduced dead
space/tidal volume ratio only 7% and did not return alveolar capillary
perfusion to baseline levels. These data indicate that most of the reduced
alveolar perfusion with PEEP results from direct compression of alveolar
capillaries and not from reduced cardiac output.
ARTICLES
Effect of positive end-expiratory pressure on alveolar capillary perfusion
Department of Surgery, State University of New York Health Science Center at Syracuse 13210.
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