Evidence map›Paper›PMID 37672503›Full record

ArticlePloS one2023

Medical imaging utilization and associated radiation exposure in children with down syndrome.

Emily C Marlow, Jonathan M Ducore, Marilyn L Kwan, Erin J A Bowles, Robert T Greenlee, Jason D Pole, Alanna K Rahm, Natasha K Stout, Sheila Weinmann, Rebecca Smith-Bindman and 1 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 21% 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.

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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 9 institutions in 3 countries.

Emily C MarlowDepartment of Surveillance & Health Equity Science, American Cancer Society, Kennesaw, Georgia, United States of America.
Jonathan M DucoreDepartment of Pediatrics, University of California, Davis, California, United States of America.
Marilyn L KwanDivision of Research, Kaiser Permanente Northern California, Oakland, California, United States of America.
Erin J A BowlesKaiser Permanente Washington Health Research Institute, Kaiser Permanente Washington, Seattle, Washington, United States of America.ORCID 0000-0001-6287-7391
Robert T GreenleeMarshfield Clinic Research Institute, Marshfield Clinic Health System, Marshfield, Wisconsin, United States of America.
Jason D PoleCentre for Health Service Research, University of Queensland, Brisbane, Australia.ORCID 0000-0002-0413-5434
Alanna K RahmDepartment of Genomic Health, Geisinger, Danville, PA, United States of America.ORCID 0000-0003-2513-9298
Natasha K StoutDepartment of Population Medicine, Harvard Medical School, Boston, Massachusetts, United States of America.ORCID 0000-0002-7946-5649
Sheila WeinmannKaiser Permanente Center for Health Research, Portland, Oregon, United States of America.ORCID 0000-0002-7696-0070
Rebecca Smith-BindmanDepartment of Biostatistics and Epidemiology, University of California, San Francisco, California, United States of America.
Diana L MigliorettiKaiser Permanente Washington Health Research Institute, Kaiser Permanente Washington, Seattle, Washington, United States of America.ORCID 0000-0002-5547-1833
Kaiser Permanente · USKaiser Permanente Washington Health Research Institute · USAmerican Cancer Society · USGenomic Health (United States) · USHarvard University · USLee University · USMarshfield Clinic · USThe University of Queensland · AUUniversity of California, Davis · US

Funding

Risk of Pediatric and Adolescent Cancer Associated with Medical ImagingR01CA185687 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KWAN, MARILYN L, MIGLIORETTI, DIANA L · 2015 to 2019
$10.0M
Group Health Cancer Research Program Research Specialist AwardR50CA211115 · NCI · KAISER FOUNDATION RESEARCH INSTITUTE · PI BOWLES, ERIN JANELLE AIELLO · 2017 to 2021
$919k
NCI NIH HHS R01 CA185687NCI NIH HHS R50 CA211115
6 · The paper itself

Abstract

objectiveTo evaluate the frequency of medical imaging or estimated associated radiation exposure in children with Down syndrome.

methodsThis retrospective cohort study included 4,348,226 children enrolled in six U.S. integrated healthcare systems from 1996-2016, 3,095 of whom were diagnosed with Down syndrome. We calculated imaging rates per 100 person years and associated red bone marrow dose (mGy). Relative rates (RR) of imaging in children with versus without Down syndrome were estimated using overdispersed Poisson regression.

resultsCompared to other children, children with Down syndrome received imaging using ionizing radiation at 9.5 times (95% confidence interval[CI] = 8.2-10.9) the rate when age <1 year and 2.3 times (95% CI = 2.0-2.5) between ages 1-18 years. Imaging rates by modality in children <1 year with Down syndrome compared with other children were: computed tomography (6.6 vs. 2.0, RR = 3.1[95%CI = 1.8-5.1]), fluoroscopy (37.1 vs. 3.1, RR 11.9[95%CI 9.5-14.8]), angiography (7.6 vs. 0.2, RR = 35.8[95%CI = 20.6-62.2]), nuclear medicine (6.0 vs. 0.6, RR = 8.2[95% CI = 5.3-12.7]), radiography (419.7 vs. 36.9, RR = 11.3[95%CI = 10.0-12.9], magnetic resonance imaging(7.3 vs. 1.5, RR = 4.2[95% CI = 3.1-5.8]), and ultrasound (231.2 vs. 16.4, RR = 12.6[95% CI = 9.9-15.9]). Mean cumulative red bone marrow dose from imaging over a mean of 4.2 years was 2-fold higher in children with Down syndrome compared with other children (4.7 vs. 1.9mGy).

conclusionsChildren with Down syndrome experienced more medical imaging and higher radiation exposure than other children, especially at young ages when they are more vulnerable to radiation. Clinicians should consider incorporating strategic management decisions when imaging this high-risk population.

Indexed as

Down SyndromeRadiation ExposureChildHumansInfantRadiographyRetrospective StudiesTomography, X-Ray Computed

Identifiers

PMID37672503
PMCPMC10482278
OpenAlexW4386493352

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.