Evidence map›Paper›PMID 42592871›Full record

ReviewPediatric pulmonology2026

Primary Ciliary Dyskinesia: A Suggested Pathway to Transition From Pediatric to Adult Care.

Abel De Castro, Melanie Sue Collins, Raksha Jain, Jennifer B Walsh, Juliana Alba-Suárez, Yadira M Rivera-Sánchez

Abstract readReview
In one paragraph

Review in Pediatric pulmonology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Abel De CastroUniversity of Texas Southwestern Medical Center, Dallas, Texas, USA.ORCID https://orcid.org/0009-0001-4300-2773
Melanie Sue CollinsUniversity of Connecticut School of Medicine/Connecticut Children's, Hartford, Connecticut, USA.
Raksha JainUniversity of Texas Southwestern Medical Center, Dallas, Texas, USA.
Jennifer B WalshUniversity of Texas Southwestern Medical Center, Dallas, Texas, USA.ORCID https://orcid.org/0009-0000-6861-8331
Juliana Alba-SuárezUniversity of Texas Southwestern Medical Center/Dallas Children's Health, Dallas, Texas, USA.
Yadira M Rivera-SánchezUniversity of Texas Southwestern Medical Center/Dallas Children's Health, Dallas, Texas, USA.ORCID https://orcid.org/0000-0003-0625-4741

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary ciliary dyskinesia (PCD) is a rare, genetically heterogeneous disorder characterized by motile ciliary dysfunction that impairs mucociliary clearance. Symptoms of PCD can include unexplained neonatal respiratory issues, chronic sino-otopulmonary symptoms, recurrent infections, bronchiectasis, and subfertility. It is expected that the number of adult patients with PCD is four times higher than the number of pediatric patients. There are no established guidelines for transitioning individuals with PCD from pediatric to adult clinics. Although the exact prevalence is difficult to determine, it is estimated that up to 13% of adults with non-CF bronchiectasis have PCD. The Six Core Elements of Health Care Transition, developed by Got Transition, funded by the National Alliance to Advance Adolescent Health, and endorsed by the American Academy of Pediatrics, the American Academy of Family Physicians, and the American College of Physicians, can serve as a framework for transitioning PCD patients to adult care. Programs implementing the Six Core Elements have significantly reduced care dropouts during adolescence and early adulthood and increased engagement in care in early adulthood. PCD has been the subject of growing research aimed at improving diagnostic methods, treatments, and awareness, leading to earlier and more accurate diagnoses in both children and adults. Additionally, more adult PCD centers are seeking accreditation from the PCD Foundation and collaborating with pediatric centers to ensure continuity of care. Although many chronic diseases, such as cystic fibrosis (CF), inflammatory bowel disease (IBD), and, more recently, sickle cell disease, have established transition guidelines, PCD presents unique challenges that affect the transition process, as discussed in this work. We outline a pathway for transitioning pediatric patients with PCD to adult care.

Indexed as

Kartagener SyndromeTransition to Adult CareAdolescentAdultChildHumans

Identifiers

PMID42592871
PMCPMC13470829

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.