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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 |
Appears in Collections: | Άρθρα/Articles |
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