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Intra‐pulmonary shunt and pulmonary gas exchange during exercise in humans
Author(s) -
Stickland Michael K.,
Welsh Robert C.,
Haykowsky Mark J.,
Petersen Stewart R.,
Anderson William D.,
Taylor Dylan A.,
Bouffard Marcel,
Jones Richard L.
Publication year - 2004
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jphysiol.2004.069302
Subject(s) - shunt (medical) , medicine , pulmonary artery , cardiology , perfusion , hypoxic pulmonary vasoconstriction , cardiac output , pulmonary shunt , arterial blood , anesthesia , lung , hemodynamics
In young, healthy people the alveolar–arterial P O 2difference (A‐aDO 2 ) is small at rest, but frequently increases during exercise. Previously, investigators have focused on ventilation/perfusion mismatch and diffusion abnormalities to explain the impairment in gas exchange, as significant physiological intra‐pulmonary shunt has not been found. The aim of this study was to use a non‐gas exchange method to determine if anatomical intra‐pulmonary (I‐P) shunts develop during exercise, and, if so, whether there is a relationship between shunt and increased A‐aDO 2 . Healthy male participants performed graded upright cycling to 90% while pulmonary arterial (PAP) and pulmonary artery wedge pressures were measured. Blood samples were obtained from the radial artery, cardiac output was calculated by the direct Fick method and I‐P shunt was determined by administering agitated saline during continuous 2‐D echocardiography. A‐aDO 2 progressively increased with exercise and was related to ( r = 0.86) and PAP ( r = 0.75). No evidence of I‐P shunt was found at rest in the upright position; however, 7 of 8 subjects developed I‐P shunts during exercise. In these subjects, point bi‐serial correlations indicated that I‐P shunts were related to the increased A‐aDO 2 ( r = 0.68), ( r = 0.76) and PAP ( r = 0.73). During exercise, intra‐pulmonary shunt always occurred when A‐aDO 2 exceeded 12 mmHg and was greater than 24 l min −1 . These results indicate that anatomical I‐P shunts develop during exercise and we suggest that shunt recruitment may contribute to the widened A‐aDO 2 during exercise.