Evidence map›Paper›PMID 37158261›Full record

ArticleThe Laryngoscope2023

Otolaryngologic Manifestations of Trisomy 13 and Trisomy 18 in Pediatric Patients.

Jalen Benson, Candace Stewart, Margaret A Kenna, A Eliot Shearer

Open access · greenAbstract read
In one paragraph

Article in The Laryngoscope, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

2 citing papers in PubMed, 11 citations in OpenAlex.

  1. Sleep-disordered breathing in children with neurodisabilities.European respiratory review : an official journal of the European Respiratory Society · 2026
    Review
  2. Prevalence and clinical characterization of oral clefts in patients with chromosome trisomy 18.Revista paulista de pediatria : orgao oficial da Sociedade de Pediatria de Sao Paulo · 2024
    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

4 authors at 1 institution in 1 country.

Jalen BensonDepartment of Otolaryngology & Communication Enhancement, Boston Children's Hospital, Boston, Massachusetts, USA.
Candace StewartDepartment of Otolaryngology & Communication Enhancement, Boston Children's Hospital, Boston, Massachusetts, USA.
Margaret A KennaDepartment of Otolaryngology & Communication Enhancement, Boston Children's Hospital, Boston, Massachusetts, USA.ORCID 0000-0003-0851-9272
A Eliot ShearerDepartment of Otolaryngology & Communication Enhancement, Boston Children's Hospital, Boston, Massachusetts, USA.ORCID 0000-0002-5324-4805
Boston Children's Hospital · US

Funding

Genetic Analysis and Manipulation Core (GAEC)P50HD105351 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI SCOTT Loren POMEROY, MUSTAFA SAHIN · 2021 to 2026
$9.4M
SEQuencing a Baby for an Optimal Outcome (SEQaBOO)R01DC015052 · NIDCD · BRIGHAM AND WOMEN'S HOSPITAL · PI MORTON, CYNTHIA CASSON · 2016 to 2020
$3.8M
Development of Genome Editing as Treatment for Genetic Hearing LossR01DC016875 · NIDCD · MASSACHUSETTS EYE AND EAR INFIRMARY · PI CHEN, ZHENG-YI · 2019 to 2023
$3.0M
Spiral Ganglion Health: from Genomics to Gene TherapyK08DC019716 · NIDCD · BOSTON CHILDREN'S HOSPITAL · PI SHEARER, AIDEN ELIOT · 2021 to 2025
$965k
NICHD NIH HHS P50 HD105351NIDCD NIH HHS K08 DC019716NIDCD NIH HHS K08DC019716NIDCD NIH HHS R01 DC015052NIDCD NIH HHS R01DC015052NIDCD NIH HHS R01 DC016875NIDCD NIH HHS R01DC016875
6 · The paper itself

Abstract

objectiveThe survival rate of patients with trisomy 13 and trisomy 18 has increased dramatically over the past two decades. We sought to comprehensively describe the otolaryngologic clinical characteristics and procedures required for these patients at our institution.

methodsWe performed algorithmic identification of patients with a diagnosis of trisomy 13 and trisomy 18 for whom the otolaryngology service provided inpatient or outpatient care at our institution between the dates of February 1997 and March 2021.

resultsOf the 47 patients studied, 18 patients had a diagnosis of trisomy 13, and 29 had a diagnosis of trisomy 18. Complete trisomy was present in 44% (8/18) of trisomy 13 patients and 55% (16/29) of trisomy 18 patients. 81% of patients were living at the time of the study. About 94% (44/47) of patients required consultation with another specialty in addition to Otolaryngology. Overall, the most common diagnoses among this cohort were gastroesophageal reflux disease (47%), dysphagia (40%), otitis media (38%), and obstructive sleep apnea (34%). Nearly three-quarters (74%) of patients studied required an otolaryngologic procedure. The most common surgical procedure was tonsillectomy and/or adenoidectomy. Patients with trisomy 18 were significantly more likely to have external auditory canal stenosis and obstructive sleep apnea whereas patients with trisomy 13 were more likely to have cleft lip and palate.

conclusionsPatients with a diagnosis of trisomy 13 or 18 often require multidisciplinary management and the range of required care spans the breadth of otolaryngology. LEVEL OF EVIDENCE: 4 Laryngoscope, 133:1501-1506, 2023.

Indexed as

Cleft LipCleft PalateOtolaryngologySleep Apnea, ObstructiveTonsillectomyAdenoidectomyChildHumansRetrospective StudiesTrisomy 13 SyndromeTrisomy 18 SyndromeEdwards SyndromePatau Syndrometrisomy 13trisomy 18

Identifiers

PMID37158261
PMCPMC10169904
OpenAlexW4292491167

What OpenQuestion holds

Textmetadata
LicenceTDM
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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.