ReviewArchives of disease in childhood. Fetal and neonatal edition2004
Universal neonatal hearing screening moving from evidence to practice.
Review in Archives of disease in childhood. Fetal and neonatal edition, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.
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.
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.
Who cites it
22 citing papers in PubMed, 97 citations in OpenAlex.
- Targeted genetic screening for identifying carrier status and early-onset disease risks in Chinese newborns.Communications medicine · 2025Article
- Targeted gene sequencing and hearing follow-up in 7501 newborns reveals an improved strategy for newborn hearing screening.European journal of human genetics : EJHG · 2025Article
- Newborn concurrent hearing and genetic screening for hearing impairment: A systematic review and meta‑analysis.Experimental and therapeutic medicine · 2024Article
- Association between in vitro fertilization-embryo transfer and hearing loss: risk factors for hearing loss among twin infants in a cohort study.European journal of pediatrics · 2023Article
- Genetic Analysis of theFrontiers in genetics · 2022Article
- Article
- Preserving Inhibition during Developmental Hearing Loss Rescues Auditory Learning and Perception.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019Article
- Concurrent Hearing and Genetic Screening of 180,469 Neonates with Follow-up in Beijing, China.American journal of human genetics · 2019Article
- Cordblood-Based High-Throughput Screening for Deafness Gene of 646 Newborns in Jinan Area of China.Clinical and experimental otorhinolaryngology · 2015Article
- Showing Value in Newborn Screening: Challenges in Quantifying the Effectiveness and Cost-Effectiveness of Early Detection of Phenylketonuria and Cystic Fibrosis.Healthcare (Basel, Switzerland) · 2015Article
- Newborn hearing screening in the Campania region (Italy): early language and perceptual outcomes of infants with permanent hearing loss.Acta otorhinolaryngologica Italica : organo ufficiale della Societa italiana di otorinolaringologia e chirurgia cervico-facciale · 2013Article
- Frequency of Hearing Impairment among Full-term Newborns in Yazd, Iran.Iranian journal of pediatrics · 2013Article
- Universal neonatal hearing screening: Six years of experience in Qatar.Qatar medical journal · 2012Article
- Clinical practice: The approach to the deaf or hard-of-hearing paediatric patient.European journal of pediatrics · 2011Review
- A prospective, longitudinal study of the impact of GJB2/GJB6 genetic testing on the beliefs and attitudes of parents of deaf and hard-of-hearing infants.American journal of medical genetics. Part A · 2009Article
- Factors influencing parental decision about genetics evaluation for their deaf or hard-of-hearing child.Genetics in medicine : official journal of the American College of Medical Genetics · 2009Article
- Clinical comparison of the auditory steady-state response with the click auditory brainstem response in infants.Clinical and experimental otorhinolaryngology · 2008Article
- Ethnic differences in parental perceptions of genetic testing for deaf infants.Journal of genetic counseling · 2008Article
- Article
- Multiprofessional committee on auditory health: COMUSA.Brazilian journal of otorhinolaryngologyArticle
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Recent technological advances have made feasible universal newborn hearing screening and therefore early detection of permanent childhood hearing impairment. Over the past three years, new information has been published on whether early intervention is beneficial, the possibility of harm arising from newborn screening, and its cost. Dramatic progress has been made in the large scale implementation of universal screening in many parts of the western world.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.