Effects of growth and breed on direct static measurements of chest wall compliance in cattle

1997 ◽  
Vol 62 (1) ◽  
pp. 1-5 ◽  
Author(s):  
D Desmecht ◽  
F Rollin ◽  
A Linden ◽  
P Lekeux
Keyword(s):  
Chest Wall ◽  
Chest Wall Compliance ◽  
Wall Compliance

Low-frequency respiratory mechanical impedance in the rat

1987 ◽  
Vol 63 (1) ◽  
pp. 36-43 ◽  
Author(s):  
Z. Hantos ◽  
B. Daroczy ◽  
B. Suki ◽  
S. Nagy
Keyword(s):  
Frequency Dependence ◽  
Chest Wall ◽  
Low Frequency ◽  
Mechanical Impedance ◽  
Total Resistance ◽  
Low Frequencies ◽  
Chest Wall Compliance ◽  
Before And After ◽  
Airway Opening ◽  
Wall Compliance

modified forced oscillatory technique was used to determine the respiratory mechanical impedances in anesthetized, paralyzed rats between 0.25 and 10 Hz. From the total respiratory (Zrs) and pulmonary impedance (ZL), measured with pseudorandom oscillations applied at the airway opening before and after thoracotomy, respectively, the chest wall impedance (ZW) was calculated as ZW = Zrs - ZL. The pulmonary (RL) and chest wall resistances were both markedly frequency dependent: between 0.25 and 2 Hz they contributed equally to the total resistance falling from 81.4 +/- 18.3 (SD) at 0.25 Hz to 27.1 +/- 1.7 kPa.l–1 X s at 2 Hz. The pulmonary compliance (CL) decreased mildly, from 2.78 +/- 0.44 at 0.25 Hz to 2.36 +/- 0.39 ml/kPa at 2 Hz, and then increased at higher frequencies, whereas the chest wall compliance declined monotonously from 4.19 +/- 0.88 at 0.25 Hz to 1.93 +/- 0.14 ml/kPa at 10 Hz. Although the frequency dependence of ZW can be interpreted on the basis of parallel inhomogeneities alone, the sharp fall in RL together with the relatively constant CL suggests that at low frequencies significant losses are imposed by the non-Newtonian resistive properties of the lung tissue.

scholarly journals CAN THEORETICAL VALUES FOR CHEST WALL COMPLIANCE BE USED IN ARDS PATIENTS?

2015 ◽  
Vol 3 (Suppl 1) ◽  
pp. A999
Author(s):  
GQ Chen ◽  
M Xu ◽  
XL Chen ◽  
N Rittayamai ◽  
M Kim ◽  
...  
Keyword(s):  
Chest Wall ◽  
Chest Wall Compliance ◽  
Wall Compliance

Developmental changes in chest wall compliance in infancy and early childhood

1995 ◽  
Vol 78 (1) ◽  
pp. 179-184 ◽  
Author(s):  
C. Papastamelos ◽  
H. B. Panitch ◽  
S. E. England ◽  
J. L. Allen
Keyword(s):  
Chest Wall ◽  
Respiratory System ◽  
Respiratory Muscles ◽  
Lung Compliance ◽  
Developmental Changes ◽  
System Function ◽  
Manual Ventilation ◽  
Chest Wall Compliance ◽  
Wall Stiffness ◽  
Wall Compliance

Development of chest wall stiffness between infancy and adulthood has important consequences for respiratory system function. To test the hypothesis that there is substantial stiffening of the chest wall in the first few years of life, we measured passive chest wall compliance (Cw) in 40 sedated humans 2 wk-3.5 yr old. Respiratory muscles were relaxed with manual ventilation applied during the Mead-Whittenberger technique. Respiratory system compliance (Crs) and lung compliance (Cl) were calculated from airway opening pressure, transpulmonary pressure, and tidal volume. Cw was calculated as 1/Cw = 1/Crs - 1/Cl during manual ventilation. Mean Cw per kilogram in infants < 1 yr old was significantly higher than that in children > 1 yr old (2.80 +/- 0.87 vs. 2.04 +/- 0.51 ml.cmH2O–1.kg-1; P = 0.002). There was an inverse linear relationship between age and mean Cw per kilogram (r = -0.495, slope -0.037; P < 0.001). In subjects with normal Cl during spontaneous breathing, Cw/spontaneous Cl was 2.86 +/- 1.06 in infants < 1 yr old and 1.33 +/- 0.36 in older children (P = 0.005). We conclude that in infancy the chest wall is nearly three times as compliant as the lung and that by the 2nd year of life chest wall stiffness increases to the point that the chest wall and lung are nearly equally compliant, as in adulthood. Stiffening of the chest wall may play a major role in developmental changes in respiratory system function such as the ability to passively maintain resting lung volume and improved ventilatory efficiency afforded by reduced rib cage distortion.

μ-Opioid receptor agonist effects on medullary respiratory neurons in the cat: evidence for involvement in certain types of ventilatory disturbances

2003 ◽  
Vol 285 (6) ◽  
pp. R1287-R1304 ◽  
Author(s):  
Peter M. Lalley
Keyword(s):  
Tidal Volume ◽  
Chest Wall ◽  
Opioid Receptor ◽  
Membrane Properties ◽  
Respiratory Neurons ◽  
Opioid Agonist ◽  
Chest Wall Compliance ◽  
Wall Compliance ◽  
Μ Opioid Receptor ◽  
Synaptic Drive

μ-Opioid receptor agonists depress tidal volume, decrease chest wall compliance, and increase upper airway resistance. In this study, potential neuronal sites and mechanisms responsible for the disturbances were investigated, dose-response relationships were established, and it was determined whether general anesthesia plays a role. Effects of μ-opioid agonists on membrane properties and discharges of respiratory bulbospinal, vagal, and propriobulbar neurons and phrenic nerve activity were measured in pentobarbital-anesthetized and unanesthetized decerebrate cats. In all types of respiratory neurons tested, threshold intravenous doses of the μ-opioid agonist fentanyl slowed discharge frequency and prolonged duration without altering peak discharge intensity. Larger doses postsynaptically depressed discharges of inspiratory bulbospinal and inspiratory propriobulbar neurons that might account for depression of tidal volume. Iontophoresis of the μ-opioid agonist DAMGO also depressed the intensity of inspiratory bulbospinal neuron discharges. Fentanyl given intravenously prolonged discharges leading to tonic firing of bulbospinal expiratory neurons in association with reduced hyperpolarizing synaptic drive potentials, perhaps explaining decreased inspiratory phase chest wall compliance. Lowest effective doses of fentanyl had similar effects on vagal postinspiratory (laryngeal adductor) motoneurons, whereas in vagal laryngeal abductor and pharyngeal constrictor motoneurons, depression of depolarizing synaptic drive potentials led to sparse, very-low-frequency discharges. Such effects on three types of vagal motoneurons might explain tonic vocal fold closure and pharyngeal obstruction of airflow. Measurements of membrane potential and input resistance suggest the effects on bulbospinal Aug-E neurons and vagal motoneurons are mediated presynaptically. Opioid effects on the respiratory neurons were similar in anesthetized and decerebrate preparations.

A pinhole method for measuring chest wall compliance

1983 ◽  
Vol 54 (4) ◽  
pp. 1157-1160
Author(s):  
J. L. Grant ◽  
D. P. Moulton
Keyword(s):  
Chest Wall ◽  
Respiratory Muscles ◽  
Esophageal Pressure ◽  
Repeated Measurements ◽  
Needle Valve ◽  
Chest Wall Compliance ◽  
Pressure Line ◽  
Wall Compliance ◽  
The Subject

We describe a method of measuring chest wall compliance (Cw) that readily detects whether respiratory muscles are relaxed. The method simulates a normal slow sigh, with the subject exhaling through a needle valve. Cw is calculated from the slope of the volume-esophageal pressure line. With relaxed subjects, repeated measurements yield similar slopes. When subjects cannot relax, the volume-pressure line is irregular and variable. In 26 subjects who could relax, Cw averaged 0.208 +/- 0.05 (SD) l/cmH2O.

Relationship between chest wall and pulmonary compliance and age

1965 ◽  
Vol 20 (6) ◽  
pp. 1211-1216 ◽  
Author(s):  
Charles Mittman ◽  
Norman H. Edelman ◽  
Arthur H. Norris ◽  
Nathan W. Shock
Keyword(s):  
Chest Wall ◽  
The Elderly ◽  
Lung Compliance ◽  
Positive Pressure ◽  
Age Difference ◽  
Elastic Recoil ◽  
Chest Wall Compliance ◽  
Pulmonary Compliance ◽  
Lung Compartment ◽  
Wall Compliance

Chest wall and pulmonary compliance were measured in 42 normal males aged 24—78 years. Measurements were made using the static method and the positive-pressure breathing method of Heaf and Prime. Chest wall compliance decreased significantly with age. Pulmonary compliance measured at functional residual capacity was similar in old and young subjects. As lung volume increased pulmonary compliance decreased more in the young than in the old. The latter age difference may result from a loss of lung elastic recoil in the elderly or may be due totally to the age difference in chest wall compliance. The observed age differences in lung compartment volumes can largely be accounted for by the decrease in chest wall compliance. aging; chest wall compliance; lung compliance; static measurement of compliance; positive-pressure measurement of compliance; lung volumes; residual volume Submitted on July 17, 1964

Respiratory mechanics in normal bonnet and rhesus monkeys

1979 ◽  
Vol 46 (1) ◽  
pp. 166-175 ◽  
Author(s):  
P. C. Kosch ◽  
J. R. Gillespie ◽  
J. D. Berry
Keyword(s):  
Chest Wall ◽  
Mammalian Species ◽  
Lung Volumes ◽  
Chest Wall Compliance ◽  
Wide Range ◽  
Residual Capacity ◽  
Static Mechanical ◽  
Wall Compliance ◽  
Trapped Gas ◽  
Gas Volume

We measured lung volumes and quasi-static volume-pressure relationships in 22 normal upright bonnet (Macaca radiata) and 12 rhesus (M. mulatta) monkeys. In comparison with interspecies pulmonary function/body weight regressions our monkeys' lung volumes are larger and their lungs are considerably more compliant, but their chest wall compliance is similar to a wide range of mammalian species. However, chest wall compliance of our monkeys was found to be considerably less than that of other more commonly used experimental mammals such as dogs, cats, and rodents. The monkey chest walls were found to be about four times as stiff (3.3 +/- 0.1 (ml/cmH2O)/kg), whereas their lungs were nearly twice as compliant (9.2 +/- 0.7 (ml/cmH2O)/kg) compared to those of supine beagle dogs. Thus, their stiff chest wall sets their functional residual capacity (64.1 +/- 1.2% TLC30) at a much larger percentage of total lung capacity (TLC30) than that of the supine beagle dog (33.8% TLC30). Residual volume (13.2 +/- 1.9% TLC30) equaled the trapped gas volume after bilateral thoracotomy and was set by airway closure. We found more hysteresis area in the chest wall than in the lungs. Our measurements indicate that the static mechanical behavior of the respiratory system of the monkey compares well to man and that the monkey has considerable merit as an animal model for human respiratory function and disease research.

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