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  3. Late Diagnosis of Infants with PCD and Neonatal Respiratory Distress.
 

Late Diagnosis of Infants with PCD and Neonatal Respiratory Distress.

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BORIS DOI
10.7892/boris.147133
Date of Publication
September 4, 2020
Publication Type
Article
Division/Institute

Institut für Sozial- ...

Contributor
Goutaki, Myrofora
Institut für Sozial- und Präventivmedizin (ISPM)
Universitätsklinik für Kinderheilkunde
Halbeisen, Florian Samuelorcid-logo
Institut für Sozial- und Präventivmedizin (ISPM)
Barbato, Angelo
Crowley, Suzanne
Harris, Amanda
Hirst, Robert A
Karadag, Bülent
Martinu, Vendula
Morgan, Lucy
O'Callaghan, Christopher
Ozçelik, Ugur
Scigliano, Sergio
Ucros, Santiago
Yiallouros, Panayiotis
Schulzke, Sven M
Kühni, Claudia
Institut für Sozial- und Präventivmedizin (ISPM)
Universitätsklinik für Kinderheilkunde
Subject(s)

600 - Technology::610...

300 - Social sciences...

Series
Journal of clinical medicine
ISSN or ISBN (if monograph)
2077-0383
Publisher
MDPI
Language
English
Publisher DOI
10.3390/jcm9092871
PubMed ID
32899853
Uncontrolled Keywords

laterality defect neo...

Description
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.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/55450
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File(s)
FileFile TypeFormatSizeLicensePublisher/Copright statementContent
Goutaki JClinMed 2020.pdftextAdobe PDF1.03 MBAttribution (CC BY 4.0)publishedOpen
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