Interdevice agreement in respiratory resistance values by oscillometry in asthmatic children

Francine M Ducharme, Imane Jroundi, Guillaume Jean, Guillaume Lavoie Boutin, Christiane Lawson, Benjamin Vinet, Francine M Ducharme, Imane Jroundi, Guillaume Jean, Guillaume Lavoie Boutin, Christiane Lawson, Benjamin Vinet

Abstract

Background: With several commercially available devices measuring respiratory impedance by oscillometry, the agreement between values obtained on different instruments or frequencies remains unclear. Our aim was to examine the agreement between resistance and reactance parameters on two oscillometry instruments using different waveforms.

Methods: We conducted a prospective cross-sectional study in asthmatic children aged 3-17 years. Reproducible oscillometry measurements were obtained in random order, by blinded operators, at three modes: 5-10-15-20-25 Hz (5-25 Hz) multifrequency mode on the MasterScreen impulse oscillometry system, and both 5-25 Hz multifrequency mode and 7 Hz monofrequency on the tremoFlo C-100 airwave sinusoidal system. Resistance, reactance and within-breath parameters were examined using the intraclass correlation coefficient (ICC), paired t-test, linear regression and Bland-Altman method.

Results: Of 50 participants, 44 and 38 completed between-device and within-frequency measurements, respectively. Between-device measurements at 5-25 Hz showed high (ICC 0.88-0.91) and good (ICC 0.69-0.87) agreement in resistance and reactance, respectively, but with an absolute within-patient difference (≥0.05 kPa·L-1·s-1) and proportional bias (≥30% per kPa·L-1·s-1) in all parameters and oscillatory frequencies, apart from resistance at 5 Hz. A significant proportional bias was documented in most within-breath parameters at 5 versus 7 Hz on tremoFlo.

Conclusion: Observed differences in resistance and reactance suggest the need for instrument- and frequency-specific paediatric normative values.

Conflict of interest statement

Conflict of interest: F.M. Ducharme reports nonfinancial support (donation of the tremoFlo device) from Thorasys Inc. during the conduct of the study. Conflict of interest: I. Jroundi reports receiving a Canadian Francophonie Scholarship Program (CFSP) postdoctoral scholarship during the conduct of the study. Conflict of interest: G. Jean has nothing to disclose. Conflict of interest: G. Lavoie Boutin has nothing to disclose. Conflict of interest: C. Lawson has nothing to disclose. Conflict of interest: B. Vinet has nothing to disclose.

Figures

FIGURE 1
FIGURE 1
Patient selection from screening to analysis. IOS: MasterScreen impulse oscillometry system. #: in seven patients, the coefficient of variation of repeated measures exceeded 15%, whereas in one patient, the mean of three values was recorded, but the individual values were lost, preventing confirmation of the coefficient of variation.
FIGURE 2
FIGURE 2
a–l) Bland–Altman plots of absolute differences between tremoFlo and MasterScreen impulse oscillometry system (IOS) measurements versus the mean of the two measurements in resistance R (left panels) at a) 5, c) 10, e) 15, g) 20, i) 25 and k) 5–20 Hz and in reactance X (right panels) at b) 5, d) 10, f) 15, h) 20, j) 25 and l) 5–20 Hz in 38 patients with reproducible IOS measurements. MD: mean difference. In each plot, the black solid horizontal line represents the absolute within-patient MD between parameters measured on the tremoFlo minus those on the IOS, with 95% of all absolute differences contained within the black dashed horizontal lines. These values are indicated as MD (95% CI) in kPa·L−1·s−1 at the top of each plot: values >0 indicate that tremoFlo measurements were higher than IOS measurements and vice versa. The magnitude and direction of the proportional bias is depicted by the green linear regression line with the 95% confidence interval and is indicated as β (95% CI) at the bottom of each plot.
FIGURE 2
FIGURE 2
a–l) Bland–Altman plots of absolute differences between tremoFlo and MasterScreen impulse oscillometry system (IOS) measurements versus the mean of the two measurements in resistance R (left panels) at a) 5, c) 10, e) 15, g) 20, i) 25 and k) 5–20 Hz and in reactance X (right panels) at b) 5, d) 10, f) 15, h) 20, j) 25 and l) 5–20 Hz in 38 patients with reproducible IOS measurements. MD: mean difference. In each plot, the black solid horizontal line represents the absolute within-patient MD between parameters measured on the tremoFlo minus those on the IOS, with 95% of all absolute differences contained within the black dashed horizontal lines. These values are indicated as MD (95% CI) in kPa·L−1·s−1 at the top of each plot: values >0 indicate that tremoFlo measurements were higher than IOS measurements and vice versa. The magnitude and direction of the proportional bias is depicted by the green linear regression line with the 95% confidence interval and is indicated as β (95% CI) at the bottom of each plot.
FIGURE 3
FIGURE 3
a–d) Bland–Altman plots of absolute differences between tremoFlo at 5 and 7 Hz versus the mean of the two measurements in resistance R and reactance X in 44 patients with reproducible measurements for a) R and b) X and in 42 patients for c) ΔR and d) ΔX. MD: mean difference. In each plot, the black solid horizontal line represents the absolute MD, with 95% of all absolute differences contained within the black dashed horizontal lines. These values are indicated as MD (95% CI) in kPa·L−1·s−1 at the top of each plot: values >0 indicate that tremoFlo measurements at 5 Hz are higher than at 7 Hz and vice versa. The magnitude and direction of the proportional bias is depicted by the green linear regression line with the 95% confidence interval and is indicated as β (95% CI) at the bottom of each plot.

References

    1. Beydon N. Pulmonary function testing in young children. Paediatr Respir Rev 2009; 10: 208–213.
    1. Beydon N, Davis SD, Lombardi E, et al. . An official American Thoracic Society/European Respiratory Society statement: pulmonary function testing in preschool children. Am J Respir Crit Care Med 2007; 175: 1304–1345.
    1. Ducharme FM, Davis GM. Respiratory resistance in the emergency department: a reproducible and responsive measure of asthma severity. Chest 1998; 113: 1566–1572.
    1. Rosenfeld M, Allen J, Arets BH, et al. . An official American Thoracic Society workshop report: optimal lung function tests for monitoring cystic fibrosis, bronchopulmonary dysplasia, and recurrent wheezing in children less than 6 years of age. Ann Am Thorac Soc 2013; 10: S1–S11.
    1. Debley J, Filbrun AG, Subbarao P. Clinical applications of pediatric pulmonary function testing: lung function in recurrent wheezing and asthma. Pediatr Allergy Immunol Pulmonol 2011; 24: 69–76.
    1. Ducharme FM, Davis GM. Measurement of respiratory resistance in the emergency department: feasibility in young children with acute asthma. Chest 1997; 111: 1519–1525.
    1. Frei J, Jutla J, Kramer G, et al. . Impulse oscillometry: reference values in children 100 to 150 cm in height and 3 to 10 years of age. Chest 2005; 128: 1266–1273.
    1. Dencker M, Malmberg LP, Valind S, et al. . Reference values for respiratory system impedance by using impulse oscillometry in children aged 2–11 years. Clin Physiol Funct Imaging 2006; 6: 247–250.
    1. Nowowiejska B, Tomalak W, Radliński J, et al. . Transient reference values for impulse oscillometry for children aged 3–18 years. Pediatr Pulmonol 2008; 43: 1193–1197.
    1. Malmberg LP, Pelkonen A, Poussa T, et al. . Determinants of respiratory system input impedance and bronchodilator response in healthy Finnish preschool children. Clin Physiol Funct Imaging 2002; 22: 64–71.
    1. Lee JY, Seo JH, Kim HY, et al. . Reference values of impulse oscillometry and its utility in the diagnosis of asthma in young Korean children. J Asthma 2012; 49: 811–816.
    1. Amra B, Soltaninejad F, Golshan M. Respiratory resistance by impulse oscillometry in healthy Iranian children aged 5–19 years. Iran J Allergy Asthma Immunol 2008; 7: 25–29.
    1. Park JH, Yoon JW, Shin YH, et al. . Reference values for respiratory system impedance using impulse oscillometry in healthy preschool children. Korean J Pediatr 2011; 54: 64–68.
    1. AlBlooshi A, AlKalbani A, Narchi H, et al. . Respiratory function in healthy Emirati children using forced oscillations. Pediatr Pulmonol 2018; 53: 936–941.
    1. Tanimura K, Hirai T, Sato S, et al. . Comparison of two devices for respiratory impedance measurement using a forced oscillation technique: basic study using phantom models. J Physiol Sci 2014; 64: 377–382.
    1. Zimmermann SC, Watts JC, Bertolin A, et al. . Discrepancy between in vivo and in vitro comparisons of forced oscillation devices. J Clin Monit Comput 2018; 32: 509–512.
    1. Hall GL, Sly PD, Fukushima T, et al. . Respiratory function in healthy young children using forced oscillations. Thorax 2007; 62: 521–526.
    1. Liu AH, Zeiger R, Sorkness C, et al. . Development and cross-sectional validation of the Childhood Asthma Control Test. J Allergy Clin Immunol 2007; 119: 817–825.
    1. Nathan RA, Sorkness CA, Kosinski M, et al. . Development of the asthma control test: a survey for assessing asthma control. J Allergy Clin Immunol 2004; 113: 59–65.
    1. Koo TK, Li MY. A guideline of selecting and reporting intraclass correlation coefficients for reliability research. J Chiropr Med 2016; 15: 155–163.
    1. Bland JM, Altman DG. Statistical methods for assessing agreement between two methods of clinical measurement. Lancet 1986; 1: 307–310.
    1. Hellinckx J, Cauberghs M, De Boeck K, et al. . Evaluation of impulse oscillation system: comparison with forced oscillation technique and body plethysmography. Eur Respir J 2001; 18: 564–570.
    1. Oostveen E, De Soomer K, Otte JA, et al. . Instrument variability in the measurement of respiratory resistance. Eur Respir J 2014; 44: Suppl. 58, P1823.
    1. Put W, Baars J, van der Grinten CPM. Comparing 3 forced oscillation devices in different subject groups. Eur Respir J 2016; 48: Suppl. 60, PA3613.
    1. Sato S, Hirai T, Tanimura K, et al. . Comparison of three devices for respiratory impedance measurement using forced oscillation technique: basic study using phantom models. Am J Respir Crit Care Med 2015; 191: A2100.
    1. Zimmermann S, Lyon J, Bertolin A, et al. . Within-breath resistance and reactance and short-term repeatability in two forced oscillation technique devices. Eur Respir J 2015; 46: Suppl. 59, PA2276.
    1. Timmins SC, Coatsworth N, Palnitkar G, et al. . Day-to-day variability of oscillatory impedance and spirometry in asthma and COPD. Respir Physiol Neurobiol 2013; 185: 416–424.
    1. Oostveen E, MacLeod D, Lorino H, et al. . The forced oscillation technique in clinical practice: methodology, recommendations and future developments. Eur Respir J 2003; 22: 1026–1041.
    1. Watts JC, Farah CS, Seccombe LM, et al. . Measurement duration impacts variability but not impedance measured by the forced oscillation technique in healthy, asthma and COPD subjects. ERJ Open Res 2016; 2: 00094-02015.
    1. Skylogianni E, Douros K, Anthracopoulos MB, et al. . The forced oscillation technique in paediatric respiratory practice. Paediatr Respir Rev 2016; 18: 46–51.
    1. Komarow HD, Myles IA, Uzzaman A, et al. . Impulse oscillometry in the evaluation of diseases of the airways in children. Ann Allergy Asthma Immunol 2011; 106: 191–199.
    1. Calogero C, Simpson SJ, Lombardi E, et al. . Respiratory impedance and bronchodilator responsiveness in healthy children aged 2–13 years. Pediatr Pulmonol 2013; 48: 707–715.

Source: PubMed

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