4.7 Article

Late Diagnosis of Infants with PCD and Neonatal Respiratory Distress

Journal

JOURNAL OF CLINICAL MEDICINE
Volume 9, Issue 9, Pages -

Publisher

MDPI
DOI: 10.3390/jcm9092871

Keywords

primary ciliary dyskinesia; neonatal respiratory distress; laterality defect; orphan diseases

Funding

  1. Swiss National Foundation [SNF 320030B_192804]
  2. EU FP7 project BESTCILIA
  3. Lung League of Bern
  4. Lung League of St Gallen
  5. Lung League of Vaud
  6. Lung League of Ticino
  7. Lung League of Valais
  8. Milena Carvajal Pro-Kartagener Foundation
  9. Ambizione fellowship by the Swiss National Foundation [PZ00P3_185923]
  10. Ministry of Health, Czech Republic [NV19-07-00210]
  11. NIHR GOSH BRC
  12. Swiss National Science Foundation (SNF) [PZ00P3_185923] Funding Source: Swiss National Science Foundation (SNF)

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Neonatal respiratory distress (NRD) is common among infants with primary ciliary dyskinesia (PCD), but we do not know whether affected neonates receive a timely diagnosis. We used data from the international PCD cohort and assessed the proportion of patients with PCD who had a history of NRD and their age at diagnosis, stratifying by presence of laterality defects. First we analyzed data from all participants diagnosed after 2000, followed by individuals from a subgroup diagnosed using stricter criteria. Among the 1375 patients in the study, 45% had a history of NRD and 42% had laterality defects. Out of the 476 children with definite PCD diagnosis, 55% had a history of NRD and 50% had laterality defects. Overall, 30% of children with PCD were diagnosed during the first 12 months of life. This varied from 13% in those with situs solitus and no NRD, to 21% in those with situs solitus and NRD, 33% in those with situs anomalies but no NRD, and 52% in those with both situs anomalies and NRD. Our results suggest that we need to improve our knowledge of the neonatal presentation of infants with PCD and apply it so that these patients will receive appropriate care sooner.

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