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European Respiratory Society and American Thoracic Society guidelines for the diagnosis of primary ciliary dyskinesia

European Respiratory Society and American Thoracic Society guidelines for the diagnosis of primary ciliary dyskinesia
European Respiratory Society and American Thoracic Society guidelines for the diagnosis of primary ciliary dyskinesia

Primary ciliary dyskinesia (PCD) is caused by pathogenetic variants in more than 55 genes. PCD is associated with early-onset chronic wet cough and rhinosinusitis, laterality defects, middle ear disease and reduced fertility. The clinical presentation is heterogeneous, and diagnosis often relies on multiple tests. The American Thoracic Society (ATS) and European Respiratory Society (ERS) have previously developed separate guidelines for diagnosis. Here, ERS and ATS members systematically reviewed the literature on diagnostic tools used in practice and developed unified evidence-based guidelines for PCD diagnosis using Grading of Recommendations, Assessment, Development and Evaluations methodology, and a transparent process of decision-making using evidence-to-decision frameworks. The Task Force panel formulated three PICO (Patients, Intervention, Comparison, Outcome) questions and three narrative questions. The accuracies of high-speed video microscopy, immunofluorescence and nasal nitric oxide were compared to a reference test of transmission electron microscopy and/or genetics. The panel gives a strong recommendation for use of high-speed video microscopy, immunofluorescence and nasal nitric oxide as adjunct tests to transmission electron microscopy and/or genetics for PCD diagnosis. However, no adjunct test is suitable as a standalone test to diagnose PCD and no single adjunct or reference test is suitable to exclude PCD. Pursuing a genetic diagnosis is encouraged owing to the implications for management. The panel emphasises that tests should meet a minimum standard and proposes that patients are evaluated at a referral centre experienced in diagnosis. The pre-test probability based on symptoms should be considered when interpreting results.

0903-1936
Shoemark, Amelia
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Goutaki, Myrofora
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Kinghorn, Bre Anna
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Ardura-Garcia, Cristina
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Baz-Redón, Noelia
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Chilvers, Mark
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Davis, Stephanie D.
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De Brandt, Jana
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Dell, Sharon
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Dhar, Raja
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Dixon, Lucy
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Ferkol, Thomas
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Hogg, Claire
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Legendre, Marie
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Leigh, Margaret
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Lucas, Jane S.
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Manion, Michele
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Rumman, Nisreen
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Toews, Ingrid
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Labonte, Valerie
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Wee, Wallace B.
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Kouis, Panayiotis
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Horani, Amjad
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et al.
Shoemark, Amelia
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Goutaki, Myrofora
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Kinghorn, Bre Anna
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Ardura-Garcia, Cristina
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Baz-Redón, Noelia
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Chilvers, Mark
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Davis, Stephanie D.
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De Brandt, Jana
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Dell, Sharon
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Dhar, Raja
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Dixon, Lucy
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Ferkol, Thomas
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Hogg, Claire
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Legendre, Marie
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Leigh, Margaret
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Lucas, Jane S.
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Manion, Michele
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Rumman, Nisreen
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Toews, Ingrid
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Labonte, Valerie
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Wee, Wallace B.
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Kouis, Panayiotis
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Horani, Amjad
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Shoemark, Amelia, Goutaki, Myrofora and Kinghorn, Bre Anna , et al. (2025) European Respiratory Society and American Thoracic Society guidelines for the diagnosis of primary ciliary dyskinesia. The European respiratory journal, 66 (6), [2500745]. (doi:10.1183/13993003.00745-2025).

Record type: Article

Abstract

Primary ciliary dyskinesia (PCD) is caused by pathogenetic variants in more than 55 genes. PCD is associated with early-onset chronic wet cough and rhinosinusitis, laterality defects, middle ear disease and reduced fertility. The clinical presentation is heterogeneous, and diagnosis often relies on multiple tests. The American Thoracic Society (ATS) and European Respiratory Society (ERS) have previously developed separate guidelines for diagnosis. Here, ERS and ATS members systematically reviewed the literature on diagnostic tools used in practice and developed unified evidence-based guidelines for PCD diagnosis using Grading of Recommendations, Assessment, Development and Evaluations methodology, and a transparent process of decision-making using evidence-to-decision frameworks. The Task Force panel formulated three PICO (Patients, Intervention, Comparison, Outcome) questions and three narrative questions. The accuracies of high-speed video microscopy, immunofluorescence and nasal nitric oxide were compared to a reference test of transmission electron microscopy and/or genetics. The panel gives a strong recommendation for use of high-speed video microscopy, immunofluorescence and nasal nitric oxide as adjunct tests to transmission electron microscopy and/or genetics for PCD diagnosis. However, no adjunct test is suitable as a standalone test to diagnose PCD and no single adjunct or reference test is suitable to exclude PCD. Pursuing a genetic diagnosis is encouraged owing to the implications for management. The panel emphasises that tests should meet a minimum standard and proposes that patients are evaluated at a referral centre experienced in diagnosis. The pre-test probability based on symptoms should be considered when interpreting results.

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More information

Accepted/In Press date: 2 September 2025
e-pub ahead of print date: 18 December 2025
Additional Information: Publisher Copyright: Copyright ©The authors 2025. For reproduction rights and permissions contact permissions@ersnet.org.

Identifiers

Local EPrints ID: 510543
URI: http://eprints.soton.ac.uk/id/eprint/510543
ISSN: 0903-1936
PURE UUID: 1f169980-f5d7-4920-a99f-1cc25b9bcd25
ORCID for Jane S. Lucas: ORCID iD orcid.org/0000-0001-8701-9975

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Date deposited: 13 Apr 2026 16:42
Last modified: 14 Apr 2026 01:38

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Contributors

Author: Amelia Shoemark
Author: Myrofora Goutaki
Author: Bre Anna Kinghorn
Author: Cristina Ardura-Garcia
Author: Noelia Baz-Redón
Author: Mark Chilvers
Author: Stephanie D. Davis
Author: Jana De Brandt
Author: Sharon Dell
Author: Raja Dhar
Author: Lucy Dixon
Author: Thomas Ferkol
Author: Claire Hogg
Author: Marie Legendre
Author: Margaret Leigh
Author: Jane S. Lucas ORCID iD
Author: Michele Manion
Author: Nisreen Rumman
Author: Ingrid Toews
Author: Valerie Labonte
Author: Wallace B. Wee
Author: Panayiotis Kouis
Author: Amjad Horani
Corporate Author: et al.

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