Evidence map›Paper›PMID 38072392›Full record

ArticleChest2024

Situs Ambiguus Is Associated With Adverse Clinical Outcomes in Children With Primary Ciliary Dyskinesia.

Kimberley R Kaspy, Sharon D Dell, Stephanie D Davis, Thomas W Ferkol, Margaret Rosenfeld, Scott D Sagel, Carlos Milla, Kenneth N Olivier, Andrew T Barber, Wallace Wee and 7 more

2 registry-linked trialsOpen access · greenAbstract readMulticenter Study
In one paragraph

Article in Chest, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 13% 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.

NCT00323167 completednot on this map

Rare Genetic Disorders of the Airways: Cross-sectional Comparison of Clinical Features, and Development of Novel Screening and Genetic Tests

TypeobservationalSponsorUniversity of North Carolina, Chapel HillRan2006 to 2012Enrolled367ConditionsKartagener Syndrome, Cystic Fibrosis, Pseudohypoaldosteronism, Primary Ciliary Dyskinesia
NCT02389049 completednot on this map

Research Genetic Testing for Primary Ciliary Dyskinesia Using a Panel of Genes

TypeobservationalSponsorUniversity of North Carolina, Chapel HillRan2015 to 2018Enrolled320ConditionsPrimary Ciliary Dyskinesia, Kartagener Syndrome
3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Nutrition and growth of primary ciliary dyskinesia patients: a systematic review.European respiratory review : an official journal of the European Respiratory Society · 2026
    Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Primary ciliary dyskinesia.Paediatrics & child health · 2025
    Article
  7. Article
  8. Article
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

17 authors at 8 institutions in 2 countries.

Kimberley R KaspyMcGill University Health Centre Research Institute, Montreal Children's Hospital, Montreal, QC.
Sharon D DellBC Children's Hospital, University of British Columbia, Vancouver, BC.
Stephanie D DavisDepartment of Pediatrics, Marsico Lung Institute, University of North Carolina School of Medicine, Chapel Hill, NC.
Thomas W FerkolDepartment of Pediatrics, Marsico Lung Institute, University of North Carolina School of Medicine, Chapel Hill, NC.
Margaret RosenfeldDepartment of Pediatrics, Seattle Children's Research Institute, University of Washington School of Medicine, Seattle, WA.
Scott D SagelDepartment of Pediatrics, University of Colorado School of Medicine, Aurora, CO.
Carlos MillaDepartment of Pediatrics, Stanford University, Palo Alto, CA.
Kenneth N OlivierDepartment of Medicine, Marsico Lung Institute, University of North Carolina School of Medicine, Chapel Hill, NC.
Andrew T BarberDepartment of Pediatrics, Virginia Commonwealth University, Richmond, VA.
Wallace WeeHospital for Sick Children, University of Toronto, Toronto, ON, Canada.
Feng-Chang LinDepartment of Biostatistics, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, NC.
Lang LiDepartment of Biostatistics, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, NC.
Emmanouil RampakakisMcGill University Health Centre Research Institute, Montreal Children's Hospital, Montreal, QC.
Maimoona A ZariwalaDepartment of Pathology/Lab Medicine, Marsico Lung Institute, University of North Carolina School of Medicine, Chapel Hill, NC.
Michael R KnowlesDepartment of Medicine, Marsico Lung Institute, University of North Carolina School of Medicine, Chapel Hill, NC.
Margaret W LeighDepartment of Pediatrics, Marsico Lung Institute, University of North Carolina School of Medicine, Chapel Hill, NC.
Adam J ShapiroMcGill University Health Centre Research Institute, Montreal Children's Hospital, Montreal, QC. Electronic address: adam.shapiro@muhc.mcgill.ca.
University of North Carolina at Chapel Hill · USMontreal Children's Hospital · CASeattle Children's Hospital · USStanford University · USUniversity of British Columbia · CAUniversity of Colorado Denver · USUniversity of Toronto · CAVirginia Commonwealth University · US

Funding

The Impact of COVID-19 on People Living with Rare Diseases and Their FamiliesU2CTR002818 · NCATS · CINCINNATI CHILDRENS HOSP MED CTR · PI Maurizio Macaluso, Michael Wagner · 2019 to 2026
$51.2M
NIH Prior Approval Process ProfessionalUL1TR002535 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2018 to 2022
$51.1M
Longitudinal Characterization of Respiratory Tract Exacerbations and Treatment Responses in Primary Ciliary DyskinesiaU54HL096458 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DAVIS, STEPHANIE DUGGINS, FERKOL, THOMAS W · 2009 to 2023
$20.0M
Yale Center for Mendelian GenomicsUM1HG006504 · NHGRI · YALE UNIVERSITY · PI GERSTEIN, MARK BENDER, GUNEL, MURAT · 2016 to 2020
$14.8M
Pathogenesis of PCD Lung DiseaseR01HL071798 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI KNOWLES, MICHAEL R · 2004 to 2021
$7.2M
Use of Tiered Genetic Sequencing and Specialty Referral for Identifying and Managing Rare Genetic Causes of Chronic Suppurative Respiratory DiseaseU01HL172658 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Alexandra Freeman, Kenneth N. Olivier · 2024 to 2026
$1.2M
NCATS NIH HHS U2C TR002818NCATS NIH HHS UL1 TR002535NHGRI NIH HHS UM1 HG006504NHLBI NIH HHS R01 HL071798NHLBI NIH HHS U01 HL172658NHLBI NIH HHS U54 HL096458
6 · The paper itself

Abstract

backgroundPrimary ciliary dyskinesia (PCD) is a rare disorder of motile cilia associated with situs abnormalities. At least 12% of patients with PCD have situs ambiguus (SA), including organ laterality defects falling outside normal arrangement (situs solitus [SS]) or mirror image inversion (situs inversus totalis [SIT]). RESEARCH QUESTION: Do patients with PCD and SA achieve worse clinical outcomes compared with those with SS or SIT? STUDY DESIGN AND

methodsThis cross-sectional, multicenter study evaluated participants aged 21 years or younger with PCD. Participants were classified as having SA, including heterotaxy, or not having SA (SS or SIT). Markers of disease severity were compared between situs groups, adjusting for age at enrollment and severe CCDC39 or CCDC40 genotype, using generalized linear models and logistic and Poisson regression.

resultsIn 397 participants with PCD (mean age, 8.4 years; range, 0.1-21), 42 patients were classified as having SA, including 16 patients (38%) with complex cardiovascular malformations or atrial isomerism, 13 patients (31%) with simple CVM, and 13 patients (31%) without cardiovascular malformations. Of these, 15 patients (36%) underwent cardiac surgery, 24 patients (57%) showed an anatomic spleen abnormality, and seven patients (17%) showed both. The remaining 355 participants did not have SA, including 152 with SIT and 203 with SS. Overall, 70 participants (17%) harbored the severe CCDC39 or CCDC40 genotype. Compared with participants without SA, those with SA showed lower median BMI z scores (P = .03), lower FVC z scores (P = .01), and more hospitalizations and IV antibiotic courses for acute respiratory infections during the 5 years before enrollment (P < .01). Participants with cardiovascular malformations requiring surgery or with anatomic spleen abnormalities showed lower median BMI z scores and more hospitalizations and IV therapies for respiratory illnesses compared with participants without SA.

interpretationChildren with PCD and SA achieve worse nutritional and pulmonary outcomes with more hospitalizations for acute respiratory illnesses than those with SS or SIT combined. Poor nutrition and increased hospitalizations for respiratory infections in participants with SA and PCD are associated with cardiovascular malformations requiring cardiac surgery, splenic anomalies, or both. TRIAL REGISTRY: ClinicalTrials.gov; Nos.: NCT02389049 and NCT00323167; URL: www. CLINICALTRIALS: gov.

Indexed as

Situs InversusAdolescentChildChild, PreschoolCiliary Motility DisordersCross-Sectional StudiesFemaleHeterotaxy SyndromeHumansInfantKartagener SyndromeMaleSeverity of Illness IndexYoung AdultheterotaxyKartagener syndromeprimary ciliary dyskinesiasitus ambiguus

Identifiers

PMID38072392
PMCPMC11110675
OpenAlexW4389502563

What OpenQuestion holds

Textmetadata
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.