Evidence map›Paper›PMID 32899853›Full record

ArticleJournal of clinical medicine2020

Late Diagnosis of Infants with PCD and Neonatal Respiratory Distress.

Myrofora Goutaki, Florian S Halbeisen, Angelo Barbato, Suzanne Crowley, Amanda Harris, Robert A Hirst, Bülent Karadag, Vendula Martinu, Lucy Morgan, Christopher O'Callaghan and 6 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03517865 (International Primary Ciliary Dyskinesia Cohort), which is not on this map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.0field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03517865 active not recruitingnot on this map

International Primary Ciliary Dyskinesia Cohort

TypeobservationalSponsorUniversity of BernRan2013 to 2080Enrolled3,400ConditionsPrimary Ciliary Dyskinesia, Kartagener Syndrome
3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Observational
  8. Chronic airway disease in primary ciliary dyskinesia-spiced with geno-phenotype associations.American journal of medical genetics. Part C, Seminars in medical genetics · 2022
    Review
  9. Clinical phenotypes of primary ciliary dyskinesia.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2022
    Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Genetic Testing for Neonatal Respiratory Disease.Children (Basel, Switzerland) · 2021
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 13 institutions in 10 countries.

Myrofora GoutakiInstitute of Social and Preventive Medicine, University of Bern, 3012 Bern, Switzerland.ORCID 0000-0001-8036-2092
Florian S HalbeisenInstitute of Social and Preventive Medicine, University of Bern, 3012 Bern, Switzerland.
Angelo BarbatoPrimary Ciliary Dyskinesia Centre, Department of Women's and Children's Health (SDB), University of Padova, 1848 Padova, Italy.
Suzanne CrowleyPaediatric Department of Allergy and Lung Diseases, Oslo University Hospital, 0372 Oslo, Norway.
Amanda HarrisPrimary Ciliary Dyskinesia Centre, NIHR Respiratory Biomedical Research Centre, University of Southampton, Southampton SO 16 6YD, UK.
Robert A HirstDepartment of Respiratory Sciences, College of Life Sciences, University of Leicester, Leicester LE1 7RH, UK.
Bülent KaradagDepartment of Pediatric Pulmonology, Marmara University, School of Medicine, Istanbul 34854, Turkey.ORCID 0000-0003-0605-8871
Vendula MartinuDepartment of Paediatrics, 2nd Faculty of Medicine, Charles University and University Hospital Motol, 38FQ+FX Prague, Czech Republic.
Lucy MorganDepartment of Respiratory Medicine, Concord Hospital Clinical School, University of Sydney, Sydney, NSW 2138, Australia.ORCID 0000-0001-6389-1953
Christopher O'CallaghanDepartment of Respiratory Sciences, College of Life Sciences, University of Leicester, Leicester LE1 7RH, UK.
Ugur OzçelikDepartment of Pediatric Pulmonology, Hacettepe University Faculty of Medicine, 06230 Ankara, Turkey.
Sergio SciglianoCentro Respiratorio, Hospital de Niños Ricardo Gutierrez, Buenos Aires C1425EFD, Argentina.
Santiago UcrosDepartamento de Pediatría, Fundación Santa Fe, Clínica de Neumología Pediátrica Compensar, Bogotá 12390, Colombia.
Panayiotis YiallourosMedical School, University of Cyprus, 596G+R2 Nicosia, Cyprus.
Sven M SchulzkeDepartment of Neonatology, University Children's Hospital Basel UKBB, 4056 Basel, Switzerland.
Claudia E KuehniInstitute of Social and Preventive Medicine, University of Bern, 3012 Bern, Switzerland.ORCID 0000-0001-8957-2002
University of Bern · CHUniversity of Leicester · GBCharles University · CZFundación Santa Fe de Bogotá · COHacettepe University · TRHospital General de Niños Ricardo Gutierrez · ARMarmara University · TROslo University Hospital · NOThe University of Sydney · AUUniversity Children’s Hospital Basel · CHUniversity of Cyprus · CYUniversity of Padua · ITUniversity of Southampton · GB

Funding

Department of Health NIHR300367Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung SNF 320030B_192804
6 · The paper itself

Abstract

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.

Indexed as

laterality defectneonatal respiratory distressorphan diseasesprimary ciliary dyskinesia

Identifiers

PMID32899853
PMCPMC7563976
OpenAlexW3083370257

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.