Evidence map›Paper›PMID 41217813›Full record

ArticleInternational journal of language & communication disorders

Beyond Prevalence: Understanding the Relationship Between Early Anatomic Factors and the Likelihood for Cleft Speech Characteristics.

Kazlin Mason, Katelyn Kotlarek, Amy Davies, Yvonne Wren

Abstract read
In one paragraph

Article in International journal of language & communication disorders. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

1 citing paper in PubMed.

  1. Article
4 · The record

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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

4 authors.

Kazlin MasonDepartment of Human Services, University of Virginia, Charlottesville, Virginia, USA.ORCID 0000-0001-6839-9116
Katelyn KotlarekDivision of Communication Disorders, College of Health Sciences, University of Wyoming, Laramie, Wyoming, USA.ORCID 0000-0001-5974-3309
Amy DaviesBristol Dental School, University of Bristol, Bristol, UK.ORCID 0000-0001-7234-0539
Yvonne WrenBristol Dental School, University of Bristol, Bristol, UK.ORCID 0000-0002-1575-453X

Funding

The integrated Translational Health Research Institute of Virginia (iTHRIV): Using Data to Improve HealthUL1TR003015 · NCATS · UNIVERSITY OF VIRGINIA · PI BROWN, DONALD E, JOHNSTON, KAREN C. · 2019 to 2023
$20.3M
Institutional Career Development CoreKL2TR003016 · NCATS · UNIVERSITY OF VIRGINIA · PI PAPIN, JASON, WORRALL, BRADFORD B · 2019 to 2023
$3.9M
NCATS NIH HHS KL2 TR003016NCATS NIH HHS UL1 TR003015
6 · The paper itself

Abstract

purposeThis study investigates early anatomic determinants influencing the likelihood of cleft speech characteristics (CSCs) in children with cleft palate with or without lip involvement (CP+/-L). The primary objective was to identify critical anatomic factors within the first year of life that impact the presence of CSCs at Age 3.

methodsThe Cleft Collective Longitudinal Cohort Study of children born with a CP+/-L was utilized. Data from 293 children were included in the analyses. Anatomic variables, including cleft type, pre-operative cleft width and fistula status, were assessed in relation to CSCs. Logistic regression analyses were adjusted for confounding variables such as age, sex and hearing status.

resultsAt 36 months, 64.9% of children with cleft palate exhibited CSCs. Anterior CSCs were most common (36.2%), while passive CSCs were least common (16.0%). Cleft type strongly influenced CSC prevalence, with UCLP and BCLP associated with higher odds of any CSC. Wider clefts were associated with passive, non-oral and posterior CSCs. Fistula presence markedly increased the odds of CSCs, especially passive and posterior CSCs. Logistic regression analyses revealed strong associations between cleft type, cleft width, fistula and specific CSCs outcomes.

conclusionsThe multifactorial nature of CSC production in children with CP+/-L is underscored by distinct impacts of cleft type, pre-operative cleft width and fistula status. Early, individualized interventions are paramount, emphasizing the need for proactive measures, including effective fistula management and speech therapy. Prioritizing prevention strategies for children with anatomic risk factors may reduce the likelihood of producing CSCs, contributing to more typical speech development and optimizing long-term speech outcomes for affected children. WHAT THIS PAPER ADDS: What is already known on this subject Children with cleft palate, with or without lip involvement (CP+/-L), frequently develop speech sound disorders due to anatomic variations affecting the craniofacial complex. Previous research has identified a range of speech difficulties in these children, with variability in the prevalence and types of cleft speech characteristics (CSCs). Less is known about the precise multifactorial impact of specific anatomic factors and their influence on the likelihood of developing CSCs, necessitating further investigation. What this paper adds to existing knowledge This study identifies the multifactorial impact of early anatomic factors, including cleft type, cleft width and fistula status, on the likelihood of cleft speech characteristics (CSCs) at Age 3 in children with CP+/-L. This research enhances understanding of how these anatomical factors influence CSCs, offering valuable data to guide future studies and/or clinical practices aimed at optimizing speech development in children with cleft conditions. What are the potential or actual clinical implications of this work? The findings emphasize the importance of early and individualized speech assessments and interventions for children with cleft conditions, particularly those with wider clefts and fistulas. Early detection and timely surgical and therapeutic interventions could reduce the likelihood of CSCs, improving long-term speech outcomes and enabling more effective management plans tailored to the specific anatomic profiles for these children.

Indexed as

Cleft LipCleft PalateSpeech DisordersChild, PreschoolFemaleHumansInfantLongitudinal StudiesMalePrevalenceanatomyCleft Collectivecleft speech characteristicscraniofacial anomaliesfistulapalatoplastyspeech outcomes

Identifiers

PMID41217813
PMCPMC12604683

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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.