Contribution of physiotherapy in primary ciliary dyskinesia diagnostic

<bold>Background:</bold> In primary ciliary dyskinesia (PCD), an abnormal ciliary beating leads to impaired mucociliary clearance and mucus stasis within the airways. Chest physiotherapy aims to improve airway clearance. PCD diagnosis is difficult as there is no gold standard reference test, and a combination of different tests is currently used. Different clinical predictive tools exist and aim to predict the likelihood of a positive PCD diagnosis. However, the contribution of airway congestion’s evaluation by a physiotherapist in PCD diagnosis is unknown. <bold>Aim:</bold> To evaluate the role of airway congestion assessment in PCD diagnosis. <bold>Method:</bold> This is a retrospective study on 7 PCD patients and 7 non-PCD patients referred to our PCD diagnostic center and matched for age (mean age: 24.9±19.8 and 19.7±22.3 years, p=0.787). Each patient underwent a complete medical history and a chest physiotherapy session to assess the presence of airway congestion. We defined airway congestion as the detection of secretions within the lower airways by the physiotherapist, and chronic mucus hypersecretion (CMH) as the patient reported chronic wet cough or sputum production from chest on most days. <bold>Results:</bold> Airway congestion was found more frequently in PCD patients (85.7%) than in non-PCD patients (42.9%) but the difference was non-significant (p=0.266). Interestingly, we found no link between reported CMH and the detection of airway congestion by the physiotherapist (63.6% and 66.7% in patients with or without CMH, respectively, p= <0.999). <bold>Conclusions:</bold> Our pilot study showed that the assessment of airway congestion might contribute to PCD diagnosis, but larger studies on bigger cohorts are needed to confirm these preliminary results.

Authors

Institutions

Publication Details

Published
2024-09-14
DOI
https://doi.org/10.1183/13993003.congress-2024.pa3207
Primary Topic
Cystic Fibrosis Research Advances
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Contribution of physiotherapy in primary ciliary dyskinesia diagnostic

Céline Kempeneers, Adeline Jacquinet, Elisa Docampo Martínez, Doriane Calmès et al.
Cystic Fibrosis Research Advances
article

Contribution of physiotherapy in primary ciliary dyskinesia diagnostic

Céline Kempeneers, Adeline Jacquinet, Elisa Docampo Martínez, Doriane Calmès, Renaud Louis, Romane Bonhiver, Olivier Hougrand, Anne‐Lise Poirrier, Noémie Bricmont, Julie Harvengt, Françoise Guissard, Clara Pauly, R. Renson, Ammar El Kheir
article en

Abstract

<bold>Background:</bold> In primary ciliary dyskinesia (PCD), an abnormal ciliary beating leads to impaired mucociliary clearance and mucus stasis within the airways. Chest physiotherapy aims to improve airway clearance. PCD diagnosis is difficult as there is no gold standard reference test, and a combination of different tests is currently used. Different clinical predictive tools exist and aim to predict the likelihood of a positive PCD diagnosis. However, the contribution of airway congestion’s evaluation by a physiotherapist in PCD diagnosis is unknown. <bold>Aim:</bold> To evaluate the role of airway congestion assessment in PCD diagnosis. <bold>Method:</bold> This is a retrospective study on 7 PCD patients and 7 non-PCD patients referred to our PCD diagnostic center and matched for age (mean age: 24.9±19.8 and 19.7±22.3 years, p=0.787). Each patient underwent a complete medical history and a chest physiotherapy session to assess the presence of airway congestion. We defined airway congestion as the detection of secretions within the lower airways by the physiotherapist, and chronic mucus hypersecretion (CMH) as the patient reported chronic wet cough or sputum production from chest on most days. <bold>Results:</bold> Airway congestion was found more frequently in PCD patients (85.7%) than in non-PCD patients (42.9%) but the difference was non-significant (p=0.266). Interestingly, we found no link between reported CMH and the detection of airway congestion by the physiotherapist (63.6% and 66.7% in patients with or without CMH, respectively, p= <0.999). <bold>Conclusions:</bold> Our pilot study showed that the assessment of airway congestion might contribute to PCD diagnosis, but larger studies on bigger cohorts are needed to confirm these preliminary results.

University of Liège (BE), Centre Hospitalier Universitaire de Liège (BE)
Zero hunger
Openalex Percentile: Top 63%
Cystic Fibrosis Research Advances
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.