Shunt and ventilation-perfusion distribution during partial liquid ventilation in healthy piglets

Journal of Applied Physiology - Tập 82 Số 3 - Trang 933-942 - 1997
Elisabeth Mates1, J. Hildebrandt1, J. Craig Jackson1, Peter Tarczy‐Hornoch1, Michael P. Hlastala1
1Departments of Physiology and Biophysics, Medicine, and Pediatrics, University of Washington, Seattle, Washington 98195-6522

Tóm tắt

Mates, Elisabeth A., Jacob Hildebrandt, J. Craig Jackson, Peter Tarczy-Hornoch, and Michael P. Hlastala. Shunt and ventilation-perfusion distribution during partial liquid ventilation in healthy piglets. J. Appl. Physiol.82(3): 933–942, 1997.—Replacing gas in the lung with perfluorocarbon fluids (PFC) and periodically ventilating with a gas [partial liquid ventilation (PLV)] has been shown to improve oxygenation in models of respiratory distress syndrome. We hypothesized that the addition of PFC to healthy lungs would result in shunt, diffusion impairment, and increased ventilation-perfusion (V˙a/Q˙) heterogeneity. Previously, Mates et al. showed that O2 shunt and arterial-alveolar CO2 difference increased linearly with dose in piglets given graded intratracheal doses of PFC (10, 20, and 30 ml/kg followed by mechanical ventilation with 100% O2) (E. A. Mates, J. C. Jackson, J. Hildebrandt, W. E. Truog, T. A. Standaert, and M. P. Hlastala. In: Oxygen Transport to Tissue XVI, 1994, p. 427–435). Here we reportV˙a/Q˙ distribution in the same animals, showing a 50% increase inV˙a/Q˙ heterogeneity during PLV independent of PFC dose. Ventilation heterogeneity was the major factor in this increase, and there was no significant change in dead space ventilation. We also report on five animals given a single 20 ml/kg dose of PFC and followed for 3 h. They showed an increase in shunt during PLV but no change in arterial-alveolar CO2 difference.

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10.1126/science.152.3730.1755

10.1152/jappl.1993.75.6.2696

10.1097/00003246-199105000-00019

10.1016/S0022-3476(05)82457-6

10.1097/00003246-199503000-00022

10.1016/0022-3468(93)90608-N

10.1152/jappl.1984.56.1.1

10.1152/jappl.1978.44.2.258

10.1172/JCI107910

10.1203/00006450-198809000-00003

10.1097/00003246-199309000-00008

10.1016/S0022-3476(95)70461-2

10.1152/jappl.1986.60.1.154

10.1152/jappl.1980.49.2.262

10.1007/978-1-4615-1875-4_76

10.1007/978-1-4613-0333-6_75

Matthews W. H., 1978, Undersea Biomed. Res., 5, 341

10.1378/chest.69.1.79

Moskowitz G. D., 1973, Med. Instrum., 9, 28

10.1016/0034-5687(68)90058-3

10.1152/jappl.1993.74.2.951

10.1152/jappl.1973.35.1.117

Shaffer T. H., 1984, Pediatr. Res., 18, 47, 10.1203/00006450-198404001-00712

10.1152/jappl.1974.36.2.208

10.1203/00006450-197604000-00005

Tarczy-Hornoch P., 1995, Pediatr. Res., 37, 353A, 10.1203/00006450-199503000-00016

10.1021/je60059a015

10.1164/ajrccm/148.3.785

10.1152/jappl.1987.62.4.1740

10.1152/jappl.1974.36.5.600

10.1152/jappl.1974.36.5.588

10.1152/jappl.1992.72.3.1024