Incremental effect of non-invasive oscillating device on chest physiotherapy in critically ill children: a cross-over randomised trial

Introduction Chest physiotherapy (CPT) and intrathoracic percussion ventilation have been recognised as to encourage dislodging the secretions; nonetheless, the tolerance to the procedure and its efficiency have not been proven to be sufficient.Method and analyses This study aims to examine the tole...

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Main Authors: Atsushi Kawaguchi, Gabrielle Bernier, Andy Adler, Philippe A Jouvet
Format: Article
Language:English
Published: BMJ Publishing Group 2020-10-01
Series:BMJ Open
Online Access:https://bmjopen.bmj.com/content/10/10/e038648.full
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spelling doaj-cf7976c667744559a4dac522bc52f4792021-05-06T09:30:40ZengBMJ Publishing GroupBMJ Open2044-60552020-10-01101010.1136/bmjopen-2020-038648Incremental effect of non-invasive oscillating device on chest physiotherapy in critically ill children: a cross-over randomised trialAtsushi Kawaguchi0Gabrielle Bernier1Andy Adler2Philippe A Jouvet3Pediatrics, University of Montreal, Montreal, Quebec, CanadaFaculty of Medicine, University of Montreal, Montreal, Quebec, CanadaSystems and Computer Engineering, Carleton University, Ottawa, Ontario, CanadaPediatrics, University of Montreal, Montreal, Quebec, CanadaIntroduction Chest physiotherapy (CPT) and intrathoracic percussion ventilation have been recognised as to encourage dislodging the secretions; nonetheless, the tolerance to the procedure and its efficiency have not been proven to be sufficient.Method and analyses This study aims to examine the tolerance, feasibility and physiological effects in airway clearance by using a novel extrathoracic non-invasive oscillating transducer device (NIOD) in critically ill children. A two-stage cross-over randomised controlled study in a paediatric intensive care unit in a Canadian Academic Children’s Hospital will be applied. Children under 24 months old, for whom CPT is prescribed for airway clearance, will be included. The study consists of two stages; (1) Stage 1 ‘Frequency Level’: we will apply two different frequencies of the NIOD (40 Hz vs 60 Hz) for 12 min each, on each patient 3 hours apart, and (2) Stage 2 ‘NIOD versus CPT’: we will implement NIOD and CPT alternatingly for 3 hours apart. The order of the procedures will be randomly allocated for each case. We will compare the average Δchanges of tidal lung volume measured by a 3D imaging system and regional lung functions using electrical impedance tomography, between the two different frequencies and between the NIOD periods and the CPT periods. We will also examine tolerance by seeing COMFORT Scales and related complications during the procedures. We estimate necessary sample size as 6 for each arm (Total 12 cases) for stage 1 and 48 cases for Stage 2, with power of 0.8 and alpha of 0.05.Ethics and dissemination This study has been approved by the Health Research Ethics Board of University of Montreal, Canada (REB number: 2020-2471). We will disseminate our findings through peer-reviewed publications and conference presentations in paediatric or/and critical care fields.Trial registration number ClinicalTrials.gov Registry (NCT03821389).https://bmjopen.bmj.com/content/10/10/e038648.full
collection DOAJ
language English
format Article
sources DOAJ
author Atsushi Kawaguchi
Gabrielle Bernier
Andy Adler
Philippe A Jouvet
spellingShingle Atsushi Kawaguchi
Gabrielle Bernier
Andy Adler
Philippe A Jouvet
Incremental effect of non-invasive oscillating device on chest physiotherapy in critically ill children: a cross-over randomised trial
BMJ Open
author_facet Atsushi Kawaguchi
Gabrielle Bernier
Andy Adler
Philippe A Jouvet
author_sort Atsushi Kawaguchi
title Incremental effect of non-invasive oscillating device on chest physiotherapy in critically ill children: a cross-over randomised trial
title_short Incremental effect of non-invasive oscillating device on chest physiotherapy in critically ill children: a cross-over randomised trial
title_full Incremental effect of non-invasive oscillating device on chest physiotherapy in critically ill children: a cross-over randomised trial
title_fullStr Incremental effect of non-invasive oscillating device on chest physiotherapy in critically ill children: a cross-over randomised trial
title_full_unstemmed Incremental effect of non-invasive oscillating device on chest physiotherapy in critically ill children: a cross-over randomised trial
title_sort incremental effect of non-invasive oscillating device on chest physiotherapy in critically ill children: a cross-over randomised trial
publisher BMJ Publishing Group
series BMJ Open
issn 2044-6055
publishDate 2020-10-01
description Introduction Chest physiotherapy (CPT) and intrathoracic percussion ventilation have been recognised as to encourage dislodging the secretions; nonetheless, the tolerance to the procedure and its efficiency have not been proven to be sufficient.Method and analyses This study aims to examine the tolerance, feasibility and physiological effects in airway clearance by using a novel extrathoracic non-invasive oscillating transducer device (NIOD) in critically ill children. A two-stage cross-over randomised controlled study in a paediatric intensive care unit in a Canadian Academic Children’s Hospital will be applied. Children under 24 months old, for whom CPT is prescribed for airway clearance, will be included. The study consists of two stages; (1) Stage 1 ‘Frequency Level’: we will apply two different frequencies of the NIOD (40 Hz vs 60 Hz) for 12 min each, on each patient 3 hours apart, and (2) Stage 2 ‘NIOD versus CPT’: we will implement NIOD and CPT alternatingly for 3 hours apart. The order of the procedures will be randomly allocated for each case. We will compare the average Δchanges of tidal lung volume measured by a 3D imaging system and regional lung functions using electrical impedance tomography, between the two different frequencies and between the NIOD periods and the CPT periods. We will also examine tolerance by seeing COMFORT Scales and related complications during the procedures. We estimate necessary sample size as 6 for each arm (Total 12 cases) for stage 1 and 48 cases for Stage 2, with power of 0.8 and alpha of 0.05.Ethics and dissemination This study has been approved by the Health Research Ethics Board of University of Montreal, Canada (REB number: 2020-2471). We will disseminate our findings through peer-reviewed publications and conference presentations in paediatric or/and critical care fields.Trial registration number ClinicalTrials.gov Registry (NCT03821389).
url https://bmjopen.bmj.com/content/10/10/e038648.full
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