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  3. Clinical manifestations in primary ciliary dyskinesia: systematic review and meta-analysis.
 

Clinical manifestations in primary ciliary dyskinesia: systematic review and meta-analysis.

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BORIS DOI
10.7892/boris.92900
Date of Publication
October 2016
Publication Type
Article
Division/Institute

Institut für Sozial- ...

Universitätsklinik fü...

Author
Goutaki, Myrofora
Institut für Sozial- und Präventivmedizin (ISPM)
Meier, Anna Bettina
Institut für Sozial- und Präventivmedizin (ISPM)
Halbeisen, Florian Samuelorcid-logo
Institut für Sozial- und Präventivmedizin (ISPM)
Lucas, Jane S
Dell, Sharon D
Maurer Schild, Elisabethorcid-logo
Institut für Sozial- und Präventivmedizin (ISPM)
Casaulta, Carmenorcid-logo
Universitätsklinik für Kinderheilkunde
Departement Klinische Forschung, Forschungsgruppe Pneumologie (Pädiatrie)
Jurca, Majaorcid-logo
Institut für Sozial- und Präventivmedizin (ISPM)
Spycher, Benorcid-logo
Institut für Sozial- und Präventivmedizin (ISPM)
Kühni, Claudia
Institut für Sozial- und Präventivmedizin (ISPM)
Subject(s)

600 - Technology::610...

300 - Social sciences...

Series
European respiratory journal
ISSN or ISBN (if monograph)
0903-1936
Publisher
European Respiratory Society
Language
English
Publisher DOI
10.1183/13993003.00736-2016
PubMed ID
27492829
Description
Few original studies have described the prevalence and severity of clinical symptoms of primary ciliary dyskinesia (PCD). This systematic review and meta-analysis aimed to identify all published studies on clinical manifestations of PCD patients, and to describe their prevalence and severity stratified by age and sex.We searched PubMed, Embase and Scopus for studies describing clinical symptoms of ≥10 patients with PCD. We performed meta-analyses and meta-regression to explain heterogeneity.We included 52 studies describing a total of 1970 patients (range 10-168 per study). We found a prevalence of 5% for congenital heart disease. For the rest of reported characteristics, we found considerable heterogeneity (I(2) range 68-93.8%) when calculating the weighted mean prevalence. Even after taking into account the explanatory factors, the largest part of the between-studies variance in symptom prevalence remained unexplained for all symptoms. Sensitivity analysis including only studies with test-proven diagnosis showed similar results in prevalence and heterogeneity.Large differences in study design, selection of study populations and definition of symptoms could explain the heterogeneity in symptom prevalence. To better characterise the disease, we need larger, multicentre, multidisciplinary, prospective studies that include all age groups, use uniform diagnostics and report on all symptoms.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/147999
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File(s)
FileFile TypeFormatSizeLicensePublisher/Copright statementContent
Goutaki EurRespirJ 2016.pdftextAdobe PDF426.75 KBpublished
Goutaki EurRespirJ 2016_manuscript&supplmat.pdftextAdobe PDF1003.59 KBacceptedOpen
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