Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.14279/3662
Title: Management of Primary Ciliary Dyskinesia in European Children: Recommendations and Clinical Practice
Authors: Strippoli, Marie Pierre Francoise 
Yiallouros, Panayiotis K. 
Frischer, Thomas H. 
Barbato, Angelo 
Snijders, Deborah 
Maurer, Elisabeth 
Lucas, Jane Sa A 
Eber, Ernst 
Karadag, Bulent 
Pohunek, Petr 
Zivkovic, Zorica M. 
Escribano, Amparo Fernandez 
O'Callaghan, Christopher Liam 
Bush, Andrew J. 
Kuehni, Claudia Elisabeth 
metadata.dc.contributor.other: Γιάλλουρος, Παναγιώτης
Major Field of Science: Medical and Health Sciences
Field Category: Clinical Medicine
Keywords: Bronchiectasis;Ciliary motility disorders;Diagnosis;Kartagener syndrome;Primary ciliary dyskinesia;Therapy
Issue Date: 1-Jun-2012
Source: European Respiratory Journal, 2012, vol. 39, no. 6, pp.1482-1491
Volume: 39
Issue: 6
Start page: 1482
End page: 1491
Journal: European Respiratory Journal 
Abstract: The European Respiratory Society Task Force on primary ciliary dyskinesia (PCD) in children recently published recommendations for diagnosis and management. This paper compares these recommendations with current clinical practice in Europe. Questionnaires were returned by 194 paediatric respiratory centres caring for PCD patients in 26 countries. In most countries, PCD care was not centralised, with a median (interquartile range) of 4 (2-9) patients treated per centre. Overall, 90% of centres had access to nasal or bronchial mucosal biopsy. Samples were analysed by electron microscopy (77%) and ciliary function tests (57%). Nasal nitric oxide was used for screening in 46% of centres and saccharine tests in 36%. Treatment approaches varied widely, both within and between countries. European region, size of centre and the country's general government expenditure on health partly defined availability of advanced diagnostic tests and choice of treatments. In conclusion, we found substantial heterogeneity in management of PCD within and between countries, and poor concordance with current recommendations. This demonstrates how essential it is to standardise management and decrease inequality between countries. Our results also demonstrate the urgent need for research: to simplify PCD diagnosis, to understand the natural history and to test the effectiveness of interventions.
URI: https://hdl.handle.net/20.500.14279/3662
ISSN: 13993003
DOI: 10.1183/09031936.00073911
Rights: © ERS 2012
Type: Article
Affiliation : University of Bern 
Universitätsklinik für Kinder- und Jugendheilkunde 
University of Padua 
University of Southampton 
Medical University of Graz 
Marmara University 
University Hospital Motol 
European University, Belgrade 
University of Valencia 
Great Ormond Street Hospital 
Royal Brompton Hospital 
Cyprus University of Technology 
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