|
|
||||||||
Journal of Applied Physiology, Vol 77, Issue 1 441-451, Copyright © 1994 by American Physiological Society
ARTICLES |
R. H. Habib, R. B. Chalker, B. Suki and A. C. Jackson
Department of Biomedical Engineering, Boston University 02215.
We measured input impedance between 16 and 2,048 Hz in intubated subjects at functional residual capacity. The corresponding subglottal impedances (ZSG) were then computed using a model where the endotracheal tube was represented by a distributed-parameter two-port network. ZSG was well described by a model based on Horsfield's asymmetric airway geometry at total lung capacity (TLC) with nonrigid walls. The walls of the cartilaginous airways included separate cartilage and soft tissue compartments, whereas the noncartilaginous airway walls had only a soft tissue compartment. Both compartments consisted of a series resistance, inertance, and compliance, the values of which were computed from airway dimensions and wall material properties (viscosity, density, and Young's modulus). Airway wall thickness was determined by scaling an airway wall area-diameter relationship. Airway lengths and diameters were scaled from the Horsfield TLC values by a single factor and by an order-dependent sigmoidal curve, respectively. The estimated soft tissue viscosity and Young's modulus were 1.04 +/- 0.21 cmH2O.s and 593 +/- 319 cmH2O, respectively. Airway lengths and tracheal diameters were not statistically different from the Horsfield values. The estimated diameters of the more peripheral airways were significantly reduced compared with the Horsfield TLC values (e.g., approximately 40% at the terminal airway), which is consistent with the reduction in airway caliber when the lung deflates from TLC to functional residual capacity. These results indicate that high-frequency ZSG is sensitive to subglottal airway geometry and wall properties and that by use of appropriate structural models one can estimate airway geometry and airway wall parameters.
This article has been cited by other articles:
![]() |
C. Thamrin, P. D. Sly, and Z. Hantos Broadband frequency dependence of respiratory impedance in rats J Appl Physiol, October 1, 2005; 99(4): 1364 - 1371. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Kompis, H. Pasterkamp, and G. R. Wodicka Acoustic Imaging of the Human Chest Chest, October 1, 2001; 120(4): 1309 - 1321. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. Nassar, A. Jackson, and D. Carrier Entraining the natural frequencies of running and breathing in guinea fowl (Numida meleagris) J. Exp. Biol., May 1, 2001; 204(9): 1641 - 1651. [Abstract] [PDF] |
||||
![]() |
B. Louis, R. Fodil, S. Jaber, J. Pigeot, P.-H. Jarreau, F. Lofaso, and D. Isabey Dual assessment of airway area profile and respiratory input impedance from a single transient wave J Appl Physiol, February 1, 2001; 90(2): 630 - 637. [Abstract] [Full Text] [PDF] |
||||
![]() |
U. FREY, K. MAKKONEN, T. WELLMAN, C. BEARDSMORE, and M. SILVERMAN Alterations in Airway Wall Properties in Infants with a History of Wheezing Disorders Am. J. Respir. Crit. Care Med., June 1, 2000; 161(6): 1825 - 1829. [Abstract] [Full Text] |
||||
![]() |
H. L. Gillis and K. R. Lutchen Airway remodeling in asthma amplifies heterogeneities in smooth muscle shortening causing hyperresponsiveness J Appl Physiol, June 1, 1999; 86(6): 2001 - 2012. [Abstract] [Full Text] [PDF] |
||||
![]() |
U. FREY, M. SILVERMAN, R. KRAEMER, and A. C. JACKSON High-frequency Respiratory Impedance Measured by Forced-Oscillation Technique in Infants Am. J. Respir. Crit. Care Med., August 1, 1998; 158(2): 363 - 370. [Abstract] [Full Text] [PDF] |
||||
![]() |
U. Frey, B. Suki, R. Kraemer, and A. C. Jackson Human respiratory input impedance between 32 and 800 Hz, measured by interrupter technique and forced oscillations J Appl Physiol, March 1, 1997; 82(3): 1018 - 1023. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Visit Other APS Journals Online |