Evidence map›Paper›PMID 30621445›Full record

ArticleThe Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association2019

Methods and Challenges in a Cohort Study of Infants and Toddlers With Craniofacial Microsomia: The Clock Study.

Daniela V Luquetti, Matthew L Speltz, Erin R Wallace, Babette Siebold, Brent R Collett, Amelia F Drake, Alexis L Johns, Kathleen A Kapp-Simon, Sara L Kinter, Brian G Leroux and 4 more

Open access · greenAbstract read
In one paragraph

Article in The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Establishing an International Interdisciplinary Research Network in Craniofacial Microsomia: The CARE Program.The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association · 2024
    Article
  4. Article
  5. Early Experiences of Parents of Children With Craniofacial Microsomia.Journal of obstetric, gynecologic, and neonatal nursing : JOGNN · 2024
    Article
  6. Review
  7. Psychosocial and Health-Related Experiences of Individuals With Microtia and Craniofacial Microsomia and Their Families: Narrative Review Over 2 Decades.The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association · 2023
    Review
  8. Article
  9. Cognitive, Motor, and Language Development of Preschool Children With Craniofacial Microsomia.The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association · 2021
    Article
  10. Behavioral Adjustment of Preschool Children With and Without Craniofacial Microsomia.The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association · 2021
    Article
  11. Article
  12. Observational
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

14 authors at 6 institutions in 1 country.

Daniela V Luquetti1 Seattle Children's Research Institute, Seattle, WA, USA.
Matthew L Speltz1 Seattle Children's Research Institute, Seattle, WA, USA.
Erin R Wallace1 Seattle Children's Research Institute, Seattle, WA, USA.
Babette Siebold1 Seattle Children's Research Institute, Seattle, WA, USA.
Brent R Collett1 Seattle Children's Research Institute, Seattle, WA, USA.
Amelia F Drake4 University of North Carolina, Chapel Hill, NC, USA.
Alexis L Johns5 Children's Hospital Los Angeles, Los Angeles, CA, USA.
Kathleen A Kapp-Simon6 Shriners Hospitals for Children, Chicago, IL, USA.
Sara L Kinter1 Seattle Children's Research Institute, Seattle, WA, USA.
Brian G Leroux8 University of Washington School of Dentistry, Seattle, WA, USA.
Leanne Magee9 Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Susan Norton1 Seattle Children's Research Institute, Seattle, WA, USA.
Kathleen Sie1 Seattle Children's Research Institute, Seattle, WA, USA.
Carrie L Heike1 Seattle Children's Research Institute, Seattle, WA, USA.
Seattle Children's Hospital · USUniversity of Washington · USChildren's Hospital of Los Angeles · USChildren's Hospital of Philadelphia · USShriners Hospitals for Children - Chicago · USUniversity of North Carolina at Chapel Hill · US

Funding

Transform Dissemination and Implementation Science in CTSA ProgramsUL1TR002319 · NCATS · UNIVERSITY OF WASHINGTON · PI John K. Amory · 2017 to 2026
$100.0M
Institute of Translational Health SciencesUL1TR000423 · NCATS · UNIVERSITY OF WASHINGTON · PI DISIS, MARY L. · 2012 to 2016
$49.4M
CFM: Longitudinal Outcomes in Children pre-Kindergarten (CLOCK)R01DE022438 · NIDCR · SEATTLE CHILDREN'S HOSPITAL · PI HEIKE, CARRIE LYN, SPELTZ, MATTHEW LOUIS · 2012 to 2018
$4.7M
NCATS NIH HHS UL1 TR000423NCATS NIH HHS UL1 TR002319NIDCR NIH HHS R01 DE022438
6 · The paper itself

Abstract

objectiveThe Craniofacial microsomia: Longitudinal Outcomes in Children pre-Kindergarten (CLOCK) study is a longitudinal cohort study of neurobehavioral outcomes in infants and toddlers with craniofacial microsomia (CFM). In this article, we review the data collection and methods used to characterize this complex condition and describe the demographic and clinical characteristics of the cohort.

settingCraniofacial and otolaryngology clinics at 5 study sites.

participantsInfants with CFM and unaffected infants (controls) ages 12 to 24 months were recruited from the same geographical regions and followed to age 36 to 48 months.

methodsPhenotypic, neurodevelopmental, and facial expression assessments were completed during the first and third waves of data collection (time 1 and time 3, respectively). Medical history data were taken at both of these time points and during an intermediate parent phone interview (time 2).

resultsOur cohort includes 108 cases and 84 controls. Most cases and controls identified as white and 55% of cases and 37% of controls identified as Hispanic. Nearly all cases had microtia (95%) and 59% had mandibular hypoplasia. Cases received extensive clinical care in infancy, with 59% receiving care in a craniofacial clinic and 28% experiencing at least one surgery. Study visits were completed at a study site (92%) or at the participant's home (8%).

conclusionsThe CLOCK study represents an effort to overcome the challenges of characterizing the phenotypic and neurodevelopmental outcomes of CFM in a large, demographically and geographically diverse cohort.

Indexed as

Congenital MicrotiaGoldenhar SyndromeChild, PreschoolCohort StudiesFemaleHumansInfantLongitudinal StudiesMaleTreatment OutcomeUnited Statescohortcraniofacial microsomiahemifacial microsomiamethodsoculoauriculovertebral spectrum

Identifiers

PMID30621445
PMCPMC6996714
OpenAlexW2908577271

What OpenQuestion holds

Textmetadata
LicenceTDM
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.