| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
Canadian Journal of Anesthesia, Vol 42, 547-553, Copyright © 1995 by Canadian Anesthesiologists' Society
ARTICLES |
P Zhang, A Ohara, T Mashimo, H Imanaka, A Uchiyama and I Yoshiya
Department of Anesthesiology, Osaka University Medical School, Japan.
Xenon (Xe) may cause an increase in airway resistance due to its high density and viscosity. The object of this study was to examine the effects of Xe on pulmonary resistance using dog models with normal and methacholine-treated airways. During anaesthesia 22 mongrel dogs' tracheas were intubated and the lungs were mechanically ventilated with 70% N2/30% O2 as a control gas. The gases 70% nitrous oxide (N2O), 50% N2O, 70% Xe and 50% Xe were administered in a random order for 25 min. Bronchoconstriction was produced by a continuous infusion of methacholine, 0.22 mg.kg-1.hr-1. Pulmonary resistance (RL) was calculated by the isovolume method using flow at the airway opening, volume and transpulmonary pressure. In normal dogs, RL breathing 70% Xe (mean +/- SEM, 0.84 +/- 0.12 cm H2O.L-1.sec-1) was greater (P < 0.05) than with 70% N2O, 50% N2O or control gas (0.61 +/- 0.08, 0.59 +/- 0.06 and 0.62 +/- 0.06 cmH2O.L-1.sec-1). Breathing 50% Xe the RL (0.77 +/- 0.10 cmH2O.L-1.sec-1) was not different from 50% N2O or control. Methacholine infusion increased RL 3.92 +/- 1.98 (mean +/- SD) times. The RL breathing 50% Xe (2.55 +/- 0.44 cmH2O.L-1.sec-1) was not greater than during 50% N2O or control (2.08 +/- 0.33 and 2.13 +/- 0.33 cmH2O.L-1.sec-1) in methacholine-treated dogs. The data suggest that inhalation of high concentrations of Xe increases airway resistance, but only to a modest extent in dogs with normal or methacholine-treated airways.
This article has been cited by other articles:
![]() |
E. A. Hoffman and D. Chon Computed Tomography Studies of Lung Ventilation and Perfusion Proceedings of the ATS, December 1, 2005; 2(6): 492 - 498. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. D. Sanders, D. Ma, and M. Maze Xenon: elemental anaesthesia in clinical practice Br. Med. Bull., February 22, 2005; 71(1): 115 - 135. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Schwarzkopf, T. Schreiber, E. Gaser, N.-P. Preussler, L. Hueter, H. Schubert, H. Rek, and W. Karzai The Effects of Xenon or Nitrous Oxide Supplementation on Systemic Oxygenation and Pulmonary Perfusion During One-Lung Ventilation in Pigs Anesth. Analg., February 1, 2005; 100(2): 335 - 339. [Abstract] [Full Text] [PDF] |
||||
![]() |
J.-H. Baumert, M. Reyle-Hahn, K. Hecker, R. Tenbrinck, R. Kuhlen, and R. Rossaint Increased airway resistance during xenon anaesthesia in pigs is attributed to physical properties of the gas Br. J. Anaesth., April 1, 2002; 88(4): 540 - 545. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. Preckel, D. Ebel, J. Mullenheim, J. Fra{beta}dorf, V. Thamer, and W. Schlack The Direct Myocardial Effects of Xenon in the Dog Heart In Vivo Anesth. Analg., March 1, 2002; 94(3): 545 - 551. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |