Evidence map›Paper›PMID 22183286›Full record

ArticleBrazilian journal of otorhinolaryngology

Audiological and genetics studies in high-risk infants.

Maria Francisca Colella-Santos, Maria de Fátima de Campos Françozo, Christiane Marques do Couto, Maria Cecilia Marconi Pinheiro Lima, Tatiana Guilhermino Tazinazzio, Arthur Menino Castilho, Edi Lucia Sartorato

Abstract read
In one paragraph

Article in Brazilian journal of otorhinolaryngology. 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

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

1 citing paper in PubMed.

  1. The effects and outcomes of electrolyte disturbances and asphyxia on newborns hearing.International journal of pediatric otorhinolaryngology · 2013
    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

7 authors.

Maria Francisca Colella-SantosCurso de Fonoaudiologia, Faculdade de Ciências Médicas, Unicamp.
Maria de Fátima de Campos Françozo
Christiane Marques do Couto
Maria Cecilia Marconi Pinheiro Lima
Tatiana Guilhermino Tazinazzio
Arthur Menino Castilho
Edi Lucia Sartorato

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

unlabelledHearing is one of the main ways with which one person can contact the external world; it plays a key role in their integration with society.

aimThe objective of this study was to analyze the results of the hearing, medical and genetic evaluation of high-risk infants who failed the newborn hearing screening. MATERIALS AND

methodsClinical and experimental study. We assessed thirty-eight neonates, with ages between one and six months. The infants underwent the following procedures: medical interview; immittance testing; Brainstem Auditory Evoked Potential; Transient Evoked Otoacoustic Emission and otorhinolaryngological evaluation. DNA extraction from the oral mucosa was performed for genetic studies using the protocol method adapted from the Human Genetics Lab of the CBMEG/UNICAMP.

resultsRegarding gender and presence of risk factors, significant statistically differences were not found in normal hearing infants and in those with hearing loss. Concerning gestational age, term infants were more affected by hearing loss. Hearing loss was identified in 58% of the sample, conduction hearing loss represented 31.5% (12/38) and neurossensory 28.9% of cases. There were none of the genetic mutations most commonly seen in cases with a genetic etiology.

conclusionHearing loss was identified in the majority of High-risk infants.

Indexed as

Audiometry, Evoked ResponseCross-Sectional StudiesEvoked Potentials, Auditory, Brain StemFemaleGestational AgeHearing Loss, ConductiveHearing Loss, SensorineuralHumansInfantInfant, NewbornMaleOtoacoustic Emissions, SpontaneousRisk FactorsSeverity of Illness IndexSex Factors

Identifiers

PMID22183286
PMCPMC9443818

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.