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Improvement of arterial oxygenation by selective infusion of prostaglandin E 1 to ventilated lung during one‐lung ventilation
Author(s) -
Chen T.L.,
Ueng T.H.,
Huang C.H.,
Chen C.L.,
Haung F.Y.,
Lin C.J.
Publication year - 1996
Publication title -
acta anaesthesiologica scandinavica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.738
H-Index - 107
eISSN - 1399-6576
pISSN - 0001-5172
DOI - 10.1111/j.1399-6576.1996.tb04381.x
Subject(s) - medicine , anesthesia , oxygenation , lung , hypoxic pulmonary vasoconstriction , ventilation (architecture) , pulmonary artery , vasoconstriction , arterial blood , vascular resistance , cardiac output , cardiology , hemodynamics , mechanical engineering , engineering
Background :One‐lung anesthesia provides a better surgical field for thoracic procedures but also impairs the arterial oxygenation and venous admixture. During one‐lung ventilation, pulmonary vasoconstriction is assumed to be present within both ventilated and collapsed lungs. We propose that arterial oxygenation could be optimized by offsetting the vasoconstriction within the microcirculation of ventilated lung. Method :In an anesthetized dog model, incremental doses of prostaglandin E 1 (PGE 1 ) were selectively infused into the main trunk of the pulmonary artery of the ventilated lung after one‐lung ventilation for 60 min (PGE 1 group, n=9). Arterial oxygenation and calculated venous admixture (Qs/Qt) was also assessed in a time‐course control group (Control group, n =5). During two‐lung ventilation (FIO 2 : 0.66), arterial PO 2 and venous admixture was 44.22 ± 3.5 kPa and 10.7±2.3%, respectively. One‐lung ventilation (FIO 2 : 0.66) with left lung collapsed reduced arterial PO 2 to 11.6±1.7 kPa and increased venous admixture to 40.7±5.8% (P<0.001). Venous O 2 tension also decreased from 6.3±0.7 kPa to 5.0±0.6 kPa with a slight increase in mean pulmonary artery pressure and pulmonary vascular resistance (P <0.05). Results : During selective infusion of PGE 1 at a dose of 0.04 to 0.2 μg kg ‐1 min ‐1 , there was a dose‐dependent improvement in arterial PO 2 with a parallel reduction of venous admixture during one‐lung ventilation. Arterial PO 2 increased to a maximum of 23.0±4.3 kPa, and the venous admixture decreased significantly to a minimum of 27.4±4.2% by PGE 1 at a dose of 0.04‐0.4 μg kg ‐1 min ‐1 (P<0.01). PGE 1 resulted in a small increase in cardiac output and decreases of pulmonary pressure and pulmonary vascular resistance at a relatively high dose of 0.4 μg kg ‐1 min ‐1 during selective infusion (P<0.05). Conclusion: These results suggest that a selective pulmonary artery infusion of PGE 1 to the ventilated lung within the dose range of 0.04‐0.4 μg kg ‐1 min ‐1 is practical and effective to improve arterial oxygenation and reduce venous admixture during one‐lung ventilation.