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      ERS Task Force guideline for the diagnosis of primary ciliary dyskinesia

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          Abstract

          The diagnosis of primary ciliary dyskinesia is often confirmed with standard, albeit complex and expensive tests. In many cases, however, the diagnosis remains difficult despite the array of sophisticated diagnostic tests. There is no ‘gold standard’ reference test. Hence, a task force supported by the European Respiratory Society has developed this guideline to provide evidence-based recommendations on diagnostic testing, especially in the light of new developments in such tests, and the need for robust diagnoses of patients who might enter randomised controlled trials of treatments. The guideline is based on pre-defined questions relevant for clinical care, a systematic review of the literature, and assessment of the evidence using the GRADE (Grading of Recommendations, Assessment, Development and Evaluation) approach. It focuses on: clinical presentation, nasal nitric oxide, analysis of ciliary beat frequency and pattern by high-speed video-microscopy analysis, transmission electron microscopy, genotyping and immunofluorescence. It then used a modified Delphi survey to develop an algorithm for the use of diagnostic tests to definitively confirm and exclude the diagnosis of PCD; also to provide advice when the diagnosis is not conclusive. Finally, this guideline proposes a set of quality criteria for future research on the validity of diagnostic methods for PCD.

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          Author and article information

          Journal
          8803460
          3682
          Eur Respir J
          Eur. Respir. J.
          The European respiratory journal
          0903-1936
          1399-3003
          9 July 2018
          04 January 2017
          January 2017
          20 July 2018
          : 49
          : 1
          : 1601090
          Affiliations
          [1 ]Primary Ciliary Dyskinesia Centre, University Hospital Southampton NHS Foundation Trust, Southampton, UK
          [2 ]University of Southampton Faculty of Medicine, Academic Unit of Clinical and Experimental Medicine, Southampton, UK
          [3 ]Primary Ciliary Dyskinesia Centre, Department of Woman and Child Health (SDB), University of Padova, Italy
          [4 ]Institute of Social and Preventive Medicine, University of Bern, Switzerland
          [5 ]Department of Paediatrics, Inselspital, University Hospital of Bern, University of Bern, Switzerland
          [6 ]Telethon Kids Institute, The University of Western Australia, Subiaco, Australia
          [7 ]Dept. of Pediatrics/ Respiratory Medicine, Erasmus University, Rotterdam, The Netherlands
          [8 ]Division of Respiratory Medicine, The Hospital for Sick Children, Departments of Pediatrics and Institute of Health Policy Management and Evaluation, University of Toronto, Toronto, Ontario, Canada
          [9 ]Division of Paediatric Pulmonology and Allergology, Department of Paediatrics and Adolescent Medicine, Medical University of Graz, Graz, Austria
          [10 ]Service de Génétique et Embryologie Médicales, Centre de Référence des Maladies Respiratoires Rares, Hôpital Armand Trousseau, Assistance Publique - Hôpitaux de Paris (AP-HP), Paris, France
          [11 ]Inserm UMR_S933, Sorbonne Universités (UPMC Univ Paris 06), Paris, France
          [12 ]Centre for PCD Diagnosis and Research,Department of Infection, Immunity and Inflammation, University of Leicester, Robert Kilpatrick Clinical Sciences Building, Leicester Royal Infirmary, Leicester, UK
          [13 ]Departments of Paediatrics and Paediatric Respiratory Medicine, Imperial College and Royal Brompton Hospital, London UK
          [14 ]Experimental Otorhinolaryngology Research Group, Department of Neurosciences, KULeuven, Leuven, Belgium.
          [15 ]ENT Department, University Hospitals Leuven, Leuven, Belgium
          [16 ]University of North Carolina at Chapel Hill, Chapel Hill, NC, USA
          [17 ]Paediatric Department, Sapienza University of Rome, Italy
          [18 ]Danish PCD & chILD Centre, CF Centre Copenhagen, Paediatric Pulmonary Service, Department of Paediatrics and Adolescent Medicine, Copenhagen University Hospital, Rigshospitalet, Denmark
          [19 ]Department of Pediatrics, University Hospital Muenster, Muenster Germany
          [20 ]AP-HP, Hôpital Kremlin-Bicetre, service d’ORL et de chirurgie cervico-faciale, Le Kremlin-Bicetre, 94275, France;
          [21 ]Université Paris-Sud, Faculté de Médecine, Le Kremlin-Bicêtre, F-94270, France
          [22 ]Paediatric Department, Second Faculty of Medicine, Charles University and Motol University Hospital, V Úvalu 84, 150 06 Prague 5, Czech Republic
          [23 ]Patient Representative, PCD Family Support Group, Registered Charity No. 104 9931 Ref: PCD150624FC01 , UK
          [24 ]Iberoamerican Cochrane Center, Barcelona, Spain
          [25 ]German speaking European Patient Association based in Germany “Kartagener Syndrom und Primäre Ciliäre Dyskinesie e. V.”
          [26 ]Pediatric Pulmonology, Department of Translational Medical Sciences, Federico II University, Azienda Ospedaliera Universitaria Federico II, Naples, Italy
          Author notes
          Corresponding Author; Jane S Lucas. Primary Ciliary Dyskinesia Centre, University Hospital Southampton NHS Foundation Trust, Southampton, SO16 6YD. UK. jlucas1@ 123456soton.ac.uk
          Article
          PMC6054534 PMC6054534 6054534 nihpa979979
          10.1183/13993003.01090-2016
          6054534
          27836958
          a9c94b05-614c-4e0b-83a0-2164670183f4
          History
          Categories
          Article

          immunofluorescence,genetics,ciliary function,nitric oxide,diagnosis,primary ciliary dyskinesia

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