Beneficial short-term effect of autogenic drainage on peripheral resistance in childhood cystic fibrosis disease

Plamen Bokov, Michèle Gerardin, Géraldine Brialix, Emmanuelle Da Costa Noble, Romain Juif, Antonia Vital Foucher, Laurence Le Clainche, Véronique Houdouin, Benjamin Mauroy, Christophe Delclaux, Plamen Bokov, Michèle Gerardin, Géraldine Brialix, Emmanuelle Da Costa Noble, Romain Juif, Antonia Vital Foucher, Laurence Le Clainche, Véronique Houdouin, Benjamin Mauroy, Christophe Delclaux

Abstract

Background: Airway clearance techniques are supposed to be a necessary adjunct for the enhancement of impaired peripheral clearance in cystic fibrosis (CF). The objective was to assess the effect of one physiotherapy session (autogenic drainage: AD) on mucus clearance (sputum wet weight) and impulse oscillometry system (IOS) indices, including those obtained from extended Resistance-Inertance-Compliance (eRIC) modelling, considering the degree of bronchial congestion.

Methods: Thirty children with CF (median age: 12.7 years) in a stable condition prospectively underwent IOS measurements at baseline and after AD. They were divided in two groups: with (visual analog scale of bronchial congestion by the physiotherapist ≥ 5/10) and without (scale < 5/10) bronchial congestion. Paired-comparison of the effects of AD on airway resistance measurements was done with Wilcoxon test.

Results: The congestion scale correlated with the wet weight of sputum production during the session (Pearson test: p < 0.0001, R = 0.66). Ten children had bronchial congestion and 20 were without congestion. In the whole group, R5-20 Hz significantly decreased after AD (P = 0.049), which was related to a decrease in the children with congestion (P = 0.025), whereas it was not significantly modified in the children without congestion (P = 0.327). The eRIC model allowed the calculation of the peripheral resistance of the respiratory system, which also decreased in the children with congestion (P = 0.037), however, not modified in the children without congestion (P = 0.390).

Conclusion: One session of autogenic drainage has the ability to decrease peripheral resistance obtained from IOS measurements, more specifically in children with CF with moderate to severe bronchial congestion.

Trial registration: ClinicalTrials.gov Identifier: NCT04094441.

Keywords: Chest physiotherapy; Childhood; Cystic fibrosis; Impulse oscillometry; Lung model.

Conflict of interest statement

The authors declare that they have no competing interests.

© 2022. The Author(s).

Figures

Fig. 1
Fig. 1
Timeline of study procedures. IOS denotes impulse oscillometry system; VD denotes anatomical dead space; AD denotes autogenic drainage. 27/30 children performed spirometry after the AD session and among them 14 had a bronchodilator test (salbutamol 400 µg) due to airflow limitation
Fig. 2
Fig. 2
The impedance spectra obtained by fitting the model. Respiratory system resistance (upper panel) and reactance (lower panel) obtained by fitting the model (thick solid lines) to the baseline data of the experimental measurements represented by the median values and the 25th and 75th percentiles for each frequency (thin lines). Overall, the model adequately fitted experimental data
Fig. 3
Fig. 3
Indices of peripheral resistance assessed before and after AD. The upper panels describe R5-R20Hz resistance of the respiratory system before (left panel) and after (right panel) a single AD session. Box and whisker plots show median, 25th and 75th percentiles, and 10th and 90th percentiles in children with CF with (dark grey) and without (light grey) bronchial congestion. The middle panel describes individual data of the 30 children: black lines for the 10 children with bronchial congestion and light grey lines for the 20 children without bronchial congestion. To better highlight individual changes of R5–20 Hz, the Y-axis is a logarithmic base 10 scale. A significant decrease in the raw value of R5–20 Hz was observed in the children with bronchial congestion (P = 0.025) whereas it was not significant in those without congestion (P = 0.327). The lower panels describe RperipheralRS computed using eRIC model before (left panel) and after (right panel) a single AD session. Box and whisker plots show median, 25th and 75th percentiles, and 10th and 90th percentiles in children with CF with (dark grey) and without (light grey) bronchial congestion. The middle panel describes individual data of the 30 children: black lines for the 10 children with bronchial congestion and light grey lines for the 20 children without bronchial congestion. To better highlight individual changes of RperipheralRS, the Y-axis is a logarithmic base 10 scale. A significant decrease in RperipheralRS (P = 0.037) is evidenced after physiotherapy in the children with bronchial congestion, which was not significant in those without congestion (P = 0.390)

References

    1. Kirilloff LH, Owens GR, Rogers RM, Mazzocco MC. Does chest physical therapy work? Chest. 1985;88:436–444. doi: 10.1378/chest.88.3.436.
    1. Bateman JR, Newman SP, Daunt KM, Sheahan NF, Pavia D, Clarke SW. Is cough as effective as chest physiotherapy in the removal of excessive tracheobronchial secretions? Thorax. 1981;36:683–687. doi: 10.1136/thx.36.9.683.
    1. Warnock L, Gates A. Chest physiotherapy compared to no chest physiotherapy for cystic fibrosis. Cochrane Database Syst Rev. 2015;2015:CD001401.
    1. Castellani C, Duff AJA, Bell SC, Heijerman HGM, Munck A, Ratjen F, et al. ECFS best practice guidelines: the 2018 revision. J Cyst Fibros. 2018;17:153–178. doi: 10.1016/j.jcf.2018.02.006.
    1. Button BM, Wilson C, Dentice R, Cox NS, Middleton A, Tannenbaum E, et al. Physiotherapy for cystic fibrosis in Australia and New Zealand: a clinical practice guideline. Respirology. 2016;21:656–667. doi: 10.1111/resp.12764.
    1. McIlwaine M, Wong LT, Chilvers M, Davidson GF. Long-term comparative trial of two different physiotherapy techniques; postural drainage with percussion and autogenic drainage, in the treatment of cystic fibrosis. Pediatr Pulmonol. 2010;45:1064–1069. doi: 10.1002/ppul.21247.
    1. Sakarya A, Uyan ZS, Baydemir C, Anık Y, Erdem E, Gokdemir Y, et al. Evaluation of children with cystic fibrosis by impulse oscillometry when stable and at exacerbation. Pediatr Pulmonol. 2016;51:1151–1158. doi: 10.1002/ppul.23449.
    1. Bokov P, Bafunyembaka G, Medjahdi N, Bernard A, Essalhi M, Houdouin V, et al. Cross-sectional phenotyping of small airway dysfunction in preschool asthma using the impulse oscillometry system. J Asthma. 2021;58:573–585. doi: 10.1080/02770903.2020.1719133.
    1. McCormack P, Burnham P, Southern KW. Autogenic drainage for airway clearance in cystic fibrosis. Cochrane Database Syst Rev. 2017;10:CD009595.
    1. Burnham P, Stanford G, Stewart R. Autogenic drainage for airway clearance in cystic fibrosis. Cochrane Database Syst Rev. 2021;12:CD009595.
    1. Bokov P, Gerardin M, Le Clainche L, Houdouin V, Delclaux C. Impulse oscillometry indices to detect an abnormal lung clearance index in childhood cystic fibrosis. Pediatr Pulmonol. 2021 doi: 10.1002/ppul.25649.
    1. King GG, Bates J, Berger KI, Calverley P, de Melo PL, Dellacà RL, et al. Technical standards for respiratory oscillometry. Eur Respir J. 2020;55:1900753. doi: 10.1183/13993003.00753-2019.
    1. Gochicoa-Rangel L, Torre-Bouscoulet L, Martínez-Briseño D, Rodríguez-Moreno L, Cantú-González G, Vargas MH. Values of impulse oscillometry in healthy Mexican children and adolescents. Respir Care. 2015;60:119–127. doi: 10.4187/respcare.03374.
    1. Rodriguez Hortal MC, Hjelte L. Time point to perform lung function tests evaluating the effects of an airway clearance therapy session in cystic fibrosis. Respir Care. 2014;59:1537–1541. doi: 10.4187/respcare.02823.
    1. Miller MR, Hankinson J, Brusasco V, Burgos F, Casaburi R, Coates A, et al. Standardisation of spirometry. Eur Respir J. 2005;26:319–338. doi: 10.1183/09031936.05.00034805.
    1. Quanjer PH, Stanojevic S, Cole TJ, Baur X, Hall GL, Culver BH, et al. Multi-ethnic reference values for spirometry for the 3–95-yr age range: the global lung function 2012 equations. Eur Respir J. 2012;40:1324–1343. doi: 10.1183/09031936.00080312.
    1. Wallaert E, Perez T, Prevotat A, Reychler G, Wallaert B, Le Rouzic O. The immediate effects of a single autogenic drainage session on ventilatory mechanics in adult subjects with cystic fibrosis. PLoS ONE. 2018;13:e0195154. doi: 10.1371/journal.pone.0195154.
    1. Chow S-C, Shao J, Wang H. A note on sample size calculation for mean comparisons based on noncentral t-statistics. J Biopharm Stat. 2002;12:441–456. doi: 10.1081/BIP-120016229.
    1. Lee SW. Methods for testing statistical differences between groups in medical research: statistical standard and guideline of Life Cycle Committee. Life Cycle. 2022;2:e1. doi: 10.54724/lc.2022.e1.
    1. Rothman KJ. No adjustments are needed for multiple comparisons. Epidemiology. 1990;1:43–46. doi: 10.1097/00001648-199001000-00010.
    1. Phillips GE, Pike SE, Jaffé A, Bush A. Comparison of active cycle of breathing and high-frequency oscillation jacket in children with cystic fibrosis. Pediatr Pulmonol. 2004;37:71–75. doi: 10.1002/ppul.10358.
    1. Leemans G, Belmans D, Van Holsbeke C, Becker B, Vissers D, Ides K, et al. The effectiveness of a mobile high-frequency chest wall oscillation (HFCWO) device for airway clearance. Pediatr Pulmonol. 2020;55:1984–1992. doi: 10.1002/ppul.24784.
    1. Pfleger A, Steinbacher M, Schwantzer G, Weinhandl E, Wagner M, Eber E. Short-term effects of physiotherapy on ventilation inhomogeneity in cystic fibrosis patients with a wide range of lung disease severity. J Cyst Fibros. 2015;14:627–631. doi: 10.1016/j.jcf.2014.12.017.
    1. Knihtilä H, Kotaniemi-Syrjänen A, Pelkonen AS, Kalliola S, Mäkelä MJ, Malmberg LP. Small airway oscillometry indices: repeatability and bronchodilator responsiveness in young children. Pediatr Pulmonol. 2017;52:1260–1267. doi: 10.1002/ppul.23794.
    1. Park J-H, Lee JH, Kim H-J, Jeong N, Jang H-J, Kim H-K, et al. Usefulness of impulse oscillometry for the assessment of bronchodilator response in elderly patients with chronic obstructive airway disease. J Thorac Dis. 2019;11:1485–1494. doi: 10.21037/jtd.2019.03.34.
    1. Ren CL, Brucker JL, Rovitelli AK, Bordeaux KA. Changes in lung function measured by spirometry and the forced oscillation technique in cystic fibrosis patients undergoing treatment for respiratory tract exacerbation. Pediatr Pulmonol. 2006;41:345–349. doi: 10.1002/ppul.20390.
    1. Buchs C, Coutier L, Vrielynck S, Jubin V, Mainguy C, Reix P. An impulse oscillometry system is less efficient than spirometry in tracking lung function improvements after intravenous antibiotic therapy in pediatric patients with cystic fibrosis. Pediatr Pulmonol. 2015;50:1073–1081. doi: 10.1002/ppul.23301.
    1. Loukou I, Moustaki M, Deligianni A, Sardeli O, Douros K. Forced oscillation technique for monitoring the respiratory status of children with cystic fibrosis: a systematic review. Children (Basel) 2021;8:857.
    1. de Souza Simoni LH, Dos Santos DO, de Souza HCD, Baddini-Martinez JA, Santos MK, Gastaldi AC. Acute effects of oscillatory PEP and thoracic compression on secretion removal and impedance of the respiratory system in non-cystic fibrosis bronchiectasis. Respir Care. 2019;64:818–827. doi: 10.4187/respcare.06025.
    1. Gonçalves Wamosy RM, Castilho T, Almeida ACDS, de Assumpção MS, Ludwig Neto N, Schivinski CIS. Immediate effect of inhalation therapy combined with oscillatory positive expiratory pressure on the respiratory system of children with cystic fibrosis. Int J Clin Pract. 2021;75:e14659. doi: 10.1111/ijcp.14659.
    1. Mauroy B, Flaud P, Pelca D, Fausser C, Merckx J, Mitchell BR. Toward the modeling of mucus draining from human lung: role of airways deformation on air-mucus interaction. Front Physiol. 2015;6:214. doi: 10.3389/fphys.2015.00214.
    1. Barry PJ, Flume PA. Bronchodilators in cystic fibrosis: a critical analysis. Expert Rev Respir Med. 2017;11:13–20. doi: 10.1080/17476348.2017.1246358.
    1. Kartal Öztürk G, Eşki A, Gülen F, Demir E. Is Impulse oscillometry system a useful method for the evaluation and follow-up of patients with cystic fibrosis? Pediatr Allergy Immunol Pulmonol. 2021;34:15–22. doi: 10.1089/ped.2020.1317.
    1. Eber E, Oberwaldner B, Zach MS. Airway obstruction and airway wall instability in cystic fibrosis: the isolated and combined effect of theophylline and sympathomimetics. Pediatr Pulmonol. 1988;4:205–212. doi: 10.1002/ppul.1950040404.
    1. Gochicoa-Rangel L, Del Río-Hidalgo R, Hernández-Ruiz J, Rodríguez-Moreno L, Martínez-Briseño D, Mora-Romero U, et al. Validating reference equations for impulse oscillometry in healthy Mexican children. Respir Care. 2017;62:1156–1165. doi: 10.4187/respcare.05247.
    1. Arens R, Gozal D, Omlin KJ, Vega J, Boyd KP, Keens TG, et al. Comparison of high frequency chest compression and conventional chest physiotherapy in hospitalized patients with cystic fibrosis. Am J Respir Crit Care Med. 1994;150:1154–1157. doi: 10.1164/ajrccm.150.4.7921452.
    1. Marques A, Bruton A, Barney A. Clinically useful outcome measures for physiotherapy airway clearance techniques: a review. Phys Therapy Rev. 2006;11:299–307. doi: 10.1179/108331906X163441.

Source: PubMed

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