4.3 Article

Respiratory symptom o Swiss people with primary ciliary dyskinesia

Journal

ERJ OPEN RESEARCH
Volume 8, Issue 2, Pages -

Publisher

EUROPEAN RESPIRATORY SOC JOURNALS LTD
DOI: 10.1183/23120541.00673-2021

Keywords

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Funding

  1. Swiss National Science Foundation Ambizione fellowship [PZ00P3_185923]
  2. Swiss National Science Foundation [320030B_192804]
  3. Lung League Bern
  4. European Respiratory Society
  5. ERN-LUNG (PCD core)
  6. Swiss National Science Foundation (SNF) [PZ00P3_185923, 320030B_192804] Funding Source: Swiss National Science Foundation (SNF)

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This study is the first to describe patient-reported PCD symptoms. The consistent collection of standardized clinical data will allow us to better characterize the phenotypic variability of the disease and study disease course and prognosis.
Background Mostly derived from chart reviews, where symptoms are recorded in a nonstandardised manner, clinical data about primary ciliary dyskinesia (PCD) am inconsistent, which leads to missing and unreliable information. We assessed the prevalence and frequency of respiratory and ear symptoms and studied differences by age and sex among an unselected population of Swiss people with PCD. Methods We sent a questionnaire that included items from the FOLLOW-PCD standardised questionnaire to all Swiss PCD registry participants. Results We received questionnaires from 74 (86%) out of 86 invited persons or their caregivers (median age 23 years, range 3-73 years), including 68% adults (>= 18 years) and 51% females. Among participants, 70 (94%) reported chronic nasal symptoms; most frequently runny nose (65%), blocked nose (55%) or anosmia (38%). Ear pain and hearing problems were reported by 58% of the participants. Almost all (99%) reported cough and sputum production. The most common chronic cough complications were gastrooesophageal reflux (n=11; 15%), vomiting (n=8; 11%) and urinary incontinence (n=6; 8%). Only nine (12%) participants reported frequent wheeze, which occurred mainly during infection or exercise, while 49 (66%) reported shortness of breath, and 9% even at rest or during daily activities. Older patients reported more frequent nasal symptoms and shortness of breath. We found no difference by sex or ultrastructural ciliary defect. Conclusion This is the first study to describe patient-reported PCD symptoms. The consistent collection of standardised clinical data will allow us to better characterise the phenotypic variability of the disease and study disease course and prognosis.

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