Screening and Follow-up Babies with Hearing Impairment

Background: Hearing loss in newborns or congenital deafness can be caused by failure to develop one or more parts of the auditory system or cessation of the development process at a certain stage.Method: This research is included in the type of analytical observational research using a cross-sectional study design. The research was conducted at Audiology Outpatients, Dr. Soetomo Academic Hospital Surabaya. The parents of the baby agreed that their child would be included in the research (informed consent). Meanwhile, the exclusion criteria were external and middle ear disorders, OAE, AABR and BERA examinations could not be carried out due to non-technical factors, the patient’s condition was unstable, and the results of the first examination showed PASS.Results: Based on gender, the majority were boys with 18 babies (60%) compared to girls with 12 babies (40%). The most common hearing loss screening results were Pass, namely 23 people (76.7%) in the right ear and 24 people (80%) in the left ear. The history of disease which is a risk factor is asphyxia, namely 26 people (87%) and 4 people (13%) with jaundice.Conclusion: Our research revealed that there were still patients with Refer results. Therefore, screening and follow-up for babies at risk of hearing loss.

Institutions

Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2025-03-21
DOI
https://doi.org/10.5281/zenodo.15063311
Primary Topic
Hearing, Cochlea, Tinnitus, Genetics
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Screening and Follow-up Babies with Hearing Impairment

Zenodo (CERN European Organization for Nuclear Research)
Hearing, Cochlea, Tinnitus, Genetics
article

Screening and Follow-up Babies with Hearing Impairment

article en

Abstract

Background: Hearing loss in newborns or congenital deafness can be caused by failure to develop one or more parts of the auditory system or cessation of the development process at a certain stage.Method: This research is included in the type of analytical observational research using a cross-sectional study design. The research was conducted at Audiology Outpatients, Dr. Soetomo Academic Hospital Surabaya. The parents of the baby agreed that their child would be included in the research (informed consent). Meanwhile, the exclusion criteria were external and middle ear disorders, OAE, AABR and BERA examinations could not be carried out due to non-technical factors, the patient’s condition was unstable, and the results of the first examination showed PASS.Results: Based on gender, the majority were boys with 18 babies (60%) compared to girls with 12 babies (40%). The most common hearing loss screening results were Pass, namely 23 people (76.7%) in the right ear and 24 people (80%) in the left ear. The history of disease which is a risk factor is asphyxia, namely 26 people (87%) and 4 people (13%) with jaundice.Conclusion: Our research revealed that there were still patients with Refer results. Therefore, screening and follow-up for babies at risk of hearing loss.

Zenodo (CERN European Organization for Nuclear Research)
Universitas Airlangga (ID)
Reduced inequalities
Openalex Percentile: Top 50%
Hearing, Cochlea, Tinnitus, Genetics
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.