airflow perturbation device
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2017 ◽  
Vol 07 (02) ◽  
pp. 53-61
Author(s):  
Mary Kate Montgomery ◽  
Allen Luk ◽  
Arthur T. Johnson ◽  
Jafar Vossoughi

CHEST Journal ◽  
2016 ◽  
Vol 150 (4) ◽  
pp. 1123A
Author(s):  
O Dene Lewis ◽  
Peter Whitesell ◽  
John Whitesell ◽  
Wesley Granger ◽  
Jafar Vossoughi ◽  
...  

2015 ◽  
Vol 24 (3) ◽  
pp. 470-479 ◽  
Author(s):  
Sally J. K. Gallena ◽  
Nancy Pearl Solomon ◽  
Arthur T. Johnson ◽  
Jafar Vossoughi ◽  
Wei Tian

Purpose An investigational, portable instrument was used to assess inspiratory (R i ) and expiratory (R e ) resistances during resting tidal breathing (RTB), postexercise breathing (PEB), and recovery breathing (RB) in athletes with and without paradoxical vocal fold motion disorder (PVFMD). Method Prospective, controlled, repeated measures within-subject and between-groups design. Twenty-four teenage female athletes, 12 with and 12 without PVFMD, breathed into the Airflow Perturbation Device for baseline measures of respiratory resistance and for two successive 1-min trials after treadmill running for up to 12 min. Exercise duration and dyspnea ratings were collected and compared across groups. Results Athletes with PVFMD had lower than control R i and R e values during RTB that significantly increased at PEB and decreased during RB. Control athletes' R e decreased significantly from RTB to PEB but not from PEB to RB, whereas R i did not change from RTB to PEB but decreased from PEB to RB. Athletes without PVFMD ran longer, providing lower dyspnea ratings. Conclusion Immediately following exercise, athletes with PVFMD experienced increased respiratory resistance that affected their exercise performance. The difference in resting respiratory resistances between groups is intriguing and could point to anatomical differences or neural adaptation in teenagers with PVFMD. The Airflow Perturbation Device appears to be a clinically feasible tool that can provide insight into PVFMD and objective data for tracking treatment progress.


2014 ◽  
Vol 57 (4) ◽  
pp. 1323-1329 ◽  
Author(s):  
Sally K. Gallena ◽  
Nancy Pearl Solomon ◽  
Arthur T. Johnson ◽  
Jafar Vossoughi ◽  
Wei Tian

Purpose In this study, the authors aimed to determine reliability of the airflow perturbation device (APD) to measure respiratory resistance within and across sessions during resting tidal (RTB) and postexercise breathing in healthy athletes, and during RTB across trials within a session in athletes with paradoxical vocal fold motion (PVFM) disorder. Method Prospective, repeated-measures design. The APD measured respiratory resistance during 3 baseline assessments in 24 teenage female athletes, 12 with and 12 without PVFM. Control athletes provided data at rest and following a customized exercise challenge during each of 3 sessions. Intraclass correlation coefficient (ICC) analysis assessed strength of relationships, and repeated-measures analysis of variance assessed differences across trials and sessions. Results ICC analyses confirmed strong correlations across RTB trials for inspiratory, expiratory, and mean respiratory resistance in both groups. Inspiratory resistance decreased ~5% between sessions for control participants; expiratory and mean respiratory resistances were stable. Data from control athletes across sessions and following rigorous exercise were strongly correlated when taken at comparable intervals. Conclusions APD-measured respiratory resistance, including separate assessments for the inspiratory and expiratory phases, has strong test–retest reliability during RTB and after exercising. This suggests that the APD is a useful measurement tool for the assessment of airway function in patients suspected of having PVFM.


2013 ◽  
Vol 2013 ◽  
pp. 1-11 ◽  
Author(s):  
J. Pan ◽  
A. Saltos ◽  
D. Smith ◽  
A. Johnson ◽  
J. Vossoughi

The airflow perturbation device (APD) has been developed as a portable, easy to use, and a rapid response instrument for measuring respiratory resistance in humans. However, the APD has limited data validating it against the established techniques. This study used a mechanical system to simulate the normal range of human breathing to validate the APD with the clinically accepted impulse oscillometry (IOS) technique. The validation system consisted of a sinusoidal flow generator with ten standardized resistance configurations that were shown to represent a total range of resistances from 0.12 to 0.95 kPa·L−1·s (1.2–9.7 cm H2O·L−1·s). Impulse oscillometry measurements and APD measurements of the mechanical system were recorded and compared at a constant airflow of 0.15 L·s−1. Both the IOS and APD measurments were accurate in assessing nominal resistance. In addition, a strong linear relationship was observed between APD measurements and IOS measurements (R2 = 0.999). A second series of measurements was made on ten human volunteers with external resistors added in their respiratory flow paths. Once calibrated with the mechanical system, the APD gave respiratory resistance measurements within 5% of IOS measurements. Because of their comparability to IOS measurements, APD measurements are shown to be valid representations of respiratory resistance.


CHEST Journal ◽  
2012 ◽  
Vol 142 (4) ◽  
pp. 783A
Author(s):  
Peter Whitesell ◽  
John Whitesell ◽  
Jafar Vossoughi ◽  
Arthur Johnson

2012 ◽  
Vol 97 (Suppl 2) ◽  
pp. A194-A195
Author(s):  
N. Rostami ◽  
M. Bautista ◽  
A. Johnson ◽  
J. Vossoughi ◽  
M. Kezsler

2012 ◽  
Vol 6 (1) ◽  
Author(s):  
Arthur T. Johnson ◽  
Jafar Vossoughi ◽  
James Pan

Author(s):  
James Pan ◽  
Andrew Saltos ◽  
Dan Smith ◽  
Arthur Johnson ◽  
Jafar Vossoughi

The airflow perturbation device (APD) has been developed as a portable, easy to use, and rapid-response instrument for noninvasively measuring respiratory resistance in humans. However, the APD has limited data validating it against established techniques; moreover, a method does not exist to standardize resistance measurement outputs between APD units. This study proposes a system that simulates the normal range of human breathing to validate the APD with the clinically accepted impulse oscillometry technique. Two respiratory resistance ranges were tested. The validation system consisted of a sinusoidal flow generator with ten standardized resistance configurations that were shown to represent a total range of resistances from 0.7000–9.4475 cmH2O·L−1·s−1. Impulse oscillometry (IOS) measurements and APD measurements of the calibration system were recorded and compared at a constant volumetric flow rate of 0.150 L·s−1. Both IOS and the APD consistently failed to estimate nominal resistance accurately. However, a strong second-order relationship was observed between APD measurements and IOS measurements (R2 = 0.997). Because of their comparability to IOS measurements, APD measurements are shown to be valid representations of respiratory resistance in a standard pneumatic model.


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