Search results for "Audiometry"

showing 10 items of 89 documents

Hearing among 75-year-old people in three Nordic localities: A comparative study

2005

The aim of this study was to compare auditory functions and to analyse the prevalence of hearing impairment and the relationship of self-reported hearing disability with audiometric test results among 75-year-old people in three Nordic localities. The representative samples came from Glostrup, Denmark (n = 571), Goteborg, Sweden (n =450), and Jyvaskyla, Finland (n =388). The median pure-tone thresholds were rather similar in all three populations. The prevalence of moderate hearing impairment varied between 26% and 34% in men, and between 17% and 23% in women. The corresponding figures in the prevalence of self-reported hearing difficulties were 41%-57%, and 28%-37%. The self-reported diffi…

Linguistics and Languagemedicine.medical_specialtymedicine.diagnostic_testCross-sectional studybusiness.industryAudiometric testAudiologyLanguage and LinguisticsSpeech and HearingHearing disabilitySeverity of illnessotorhinolaryngologic diseasesmedicineElderly peopleAuditory functionPure tone audiometryAudiometrybusinessInternational Journal of Audiology
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Changes in hearing in 80-year-old people: a 10-year follow-up study

2004

The aims of this prospective 10-year longitudinal population study were to report changes in hearing in people aged 80 years at baseline, and to assess such changes by comparing results from both cross-sectional and longitudinal analyses. The study population comprised all residents of the city of Jyväskylä born in 1910 (n = 291). The subjects' hearing was tested on three occasions at 5-year intervals with the use of pure-tone audiometry, speech audiometry, and self-report on hearing difficulties. The results showed a significant deterioration in hearing sensitivity in both the longitudinal and cross-sectional assessments over the 10-year follow-up. However, the change in self-assessed hear…

MaleAgingLinguistics and Languagemedicine.medical_specialtyLongitudinal studyCross-sectional studyAudiologyLanguage and LinguisticsSpeech and HearingHearing AidsAcquired immunodeficiency syndrome (AIDS)Moderate hearing impairmentSurveys and Questionnairesotorhinolaryngologic diseasesmedicineHumansLongitudinal StudiesProspective StudiesHearing LossAgedAged 80 and overmedicine.diagnostic_test10 year follow upbusiness.industryAge Factorsmedicine.diseaseCross-Sectional StudiesAudiometry Pure-TonePopulation studyFemalePure tone audiometryAudiometryAudiometry SpeechbusinessBone ConductionInternational Journal of Audiology
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Speech perception outcomes after cochlear implantation in prelingually deaf infants: The Western Sicily experience

2013

Objectives: To describe audiometric characteristics and speech perception performances of prelingually deaf Sicilian children after cochlear implantation; to identify the influence of cochlear implant (CI) user and family's characteristics on speech recognition and intelligibility outcomes. Methods: Twenty-eight infants with a congenital or acquired hearing impairment and implanted before the 3rd year of life were studied; all children suffered from bilateral sensorineural hearing loss (SNHL) with evidence of lack of hearing aids benefit and no evidence of intellectual disability. The study of the main characteristics associated with CI user and family's profile was performed with a clinica…

MaleCochlear implant Deaf children Sensorineural hearing loss Speech perception Speech intelligibilitymedicine.medical_specialtySpeech perceptionHearing lossmedicine.medical_treatmentHearing Loss SensorineuralIntelligibility (communication)AudiologyDeafnessAudiometryCochlear implantSurveys and QuestionnairesIntellectual disabilityotorhinolaryngologic diseasesmedicineHumansSicilymedicine.diagnostic_testbusiness.industrySpeech IntelligibilityInfantGeneral Medicinemedicine.diseaseCochlear ImplantationCochlear ImplantsTreatment OutcomeOtorhinolaryngologyPediatrics Perinatology and Child HealthCohortSpeech PerceptionSensorineural hearing lossFemaleAudiometrymedicine.symptombusiness
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Otitis media with effusion in children: Cross-frequency correlation in pure tone audiometry.

2019

Different guidelines are adopted in clinics and countries to assess pure tone hearing sensitivity in children with otitis media with effusion (OME). Some guidelines specify a broad range of audiometric frequencies that must be tested and from which average thresholds determined, while others leave test frequencies unspecified. For guidelines that suggest specific frequencies there are various pure tone frequencies and frequency ranges given. The present study investigated whether (1) a full range of audiometric frequencies is required to evaluate hearing loss caused by OME in children, or if neighboring frequencies provide essentially the same threshold information, and (2) if different com…

MaleIntraclass correlationOtologyAudiologyDeafnessPediatricsCorrelation0302 clinical medicinePediatric SurgeryMedicine and Health SciencesPublic and Occupational Health030212 general & internal medicine030223 otorhinolaryngologyChildHearing DisordersMultidisciplinarymedicine.diagnostic_testPure toneQChild HealthRAudiologyEffusionChild PreschoolPractice Guidelines as TopicAudiometry Pure-ToneMedicineFemalePure tone audiometrymedicine.symptomAnatomyResearch Articlemedicine.medical_specialtyHearing lossScienceSurgical and Invasive Medical Procedures03 medical and health sciencesmedicineotorhinolaryngologic diseasesHumansHearing LossRetrospective Studiesbusiness.industryOtitis Media with EffusionMiddle EarBiology and Life SciencesAuditory ThresholdOtolaryngological ProceduresOtitis MediaOtitisOtorhinolaryngologyEarssense organsAudiometrybusinessHeadPLoS ONE
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High-frequency conductive hearing loss as a diagnostic test for incomplete ossicular discontinuity in non-cholesteatomatous chronic suppurative otiti…

2017

Chronic suppurative otitis media, with or without cholesteatoma, may lead to erosion of the ossicles and discontinuity of the ossicular chain. In incomplete ossicular discontinuity (IOD), partial erosion of the ossicles occurs, but some sound transmission is noted throughout the ossicular chain. High-frequency conductive hearing loss (HfCHL) has been considered a hallmark of incomplete ossicular discontinuity. This study aims to evaluate the use of HfCHL as a preoperative predictor of IOD in patients with non-cholesteatomatous chronic suppurative otitis media. The HfCHL test was defined as the preoperative air-bone gap (ABG) at 4 kHz minus the average of the ABG at 0.25 and 0.5 kHz. The tes…

MaleMedical DoctorsHealth Care ProvidersChronic Suppurative Otitis MediaHearing Loss Conductivelcsh:MedicineOtologyDeafnessOtitis Media Suppurative0302 clinical medicineMedicine and Health SciencesMedical PersonnelProspective Studieslcsh:Science030223 otorhinolaryngologyHearing DisordersEar OssiclesMultidisciplinarymedicine.diagnostic_testCholesteatomaAudiologyMiddle AgedConductive hearing lossProfessionsmedicine.anatomical_structureMiddle earAudiometry Pure-ToneFemaleRadiologymedicine.symptomAnatomyResearch ArticleAdultmedicine.medical_specialtySoft TissuesAdolescentHearing lossSurgical and Invasive Medical ProceduresSensitivity and Specificity03 medical and health sciencesYoung AdultDiagnostic MedicinePhysiciansmedicineotorhinolaryngologic diseasesHumansSurgeonsOssiclesbusiness.industrylcsh:RMiddle EarBiology and Life SciencesGold standard (test)medicine.diseaseHealth CareOtitis MediaBiological TissueOtorhinolaryngologyEarsPeople and Placeslcsh:QPopulation Groupingssense organsAudiometrybusinessHead030217 neurology & neurosurgeryPLoS ONE
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<i>GJB2</i> Mutations and Genotype-Phenotype Correlation in 335 Patients from Germany with Nonsyndromic Sensorineural Hearing Loss: Evide…

2009

We report on 335 patients (319 families) with mild-to-profound nonsyndromic sensorineural hearing loss. We identified 178 mutated <i>GJB2</i> alleles representing 29 different sequence changes (including 3 novel mutations: Q7P, N14D, H100Q), and 2 alleles with the deletion del(GJB6-D13S1830) of the <i>GJB6</i> gene. Eleven <i>GJB2</i> mutations (119 mutated alleles) were truncating (T), and 18 mutations (59 alleles) were nontruncating (NT). Biallelic <i>GJB2</i> mutations were found in 71 patients (21.2%; 67 families; 25 different genotypes). Audiograms of 62 patients (56 families) with biallelic <i>GJB2</i> mutations typically ind…

MaleMild hearing impairmentPathologymedicine.medical_specialtyGenotypePhysiologyHearing lossHearing Loss SensorineuralGenes Recessivemedicine.disease_causePolymerase Chain ReactionConnexinsSpeech and HearingAudiometryGene FrequencyGermanyGenotypeotorhinolaryngologic diseasesmedicineHumansAlleleAllele frequencyAllelesGenetic Association StudiesGeneticsMutationbiologybusiness.industrymedicine.diseaseSensory SystemsConnexin 26PhenotypeOtorhinolaryngologyMutationbiology.proteinFemaleSensorineural hearing lossmedicine.symptombusinessGJB6Audiology and Neurotology
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Otitis media with effusion with or without atopy: audiological findings on primary schoolchildren

2011

Objective: The objective of the study was to evaluate the role of atopy in otitis media with effusion (OME) in children attending primary school, focusing on the audiometric and tympanometric measurements among atopic and nonatopic subjects suffering from OME. Materials and Methods: Three hundred ten children (5-6 years old) were screened in Western Sicily by skin tests and divided into atopics (G1) and nonatopics (G2). The samples were evaluated for OME by pneumatic otoscopy, tympanogram, and acoustic reflex tests. The parameters considered were as follows: documented persistent middle ear effusion by otoscopic examination for a minimum of 3 months, presence of B or C tympanogram, absence …

MalePediatricsmedicine.medical_specialtyAudiometry/methods*OtoscopyRisk AssessmentAtopyCohort StudiesAge DistributionAudiometryotorhinolaryngologic diseasesmedicineHypersensitivityPrevalenceHumansMass ScreeningOtitis Media with Effusion/diagnosisSex DistributionAcoustic reflexChildSicilyMass screeningSchool Health ServicesAnalysis of Variancemedicine.diagnostic_testbusiness.industryOtitis Media with EffusionOdds ratiomedicine.diseaseConductive hearing lossSettore MED/32 - AudiologiaOtitisOtorhinolaryngologyEffusionChild PreschoolFemalemedicine.symptomAudiometrybusiness
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On the threshold of effective well infant nursery hearing screening in Western Sicily.

2012

Abstract Objective To determine the feasibility and effectiveness of well-infant nursery hearing screening programme for the early identification of hearing impairment, based on transient evoked otoacoustic emission (TEOAE) with a high “screen sensitivity” reducing the number of more expensive secondary level exams. Methods The newborns were screened by non-specialist health workers in well babies nursery at the twentieth day of life for 6 years consecutive. Based on PASS/FAIL criteria and presence/absence of audiological risk factors the newborns were divided into four groups each one with its personal step programme: G1 – PASS without risk factor, free to go home; G2 – PASS with risk fact…

MalePediatricsmedicine.medical_specialtyReferralHearing lossOtoacoustic Emissions SpontaneousOtoacoustic emissionAudiologyHearing screeningScreening programmeCohort StudiesNeonatal ScreeningClinical ProtocolsPredictive Value of TestsRisk FactorsWell-infant nurseryMedicineHumansRisk factorHearing LossSicilybusiness.industryIncidence (epidemiology)Infant NewbornInfantGeneral Medicinemedicine.diseaseSettore MED/32 - AudiologiaAudiometry Evoked ResponseNeonatal screening; Well-infant nursery; Sensorineural hearing loss; Otoacoustic emission;Settore MED/31 - OtorinolaringoiatriaOtorhinolaryngologySensorineural hearing loPediatrics Perinatology and Child HealthFeasibility StudiesOtoacoustic emissionSensorineural hearing lossFemalemedicine.symptombusinessInternational journal of pediatric otorhinolaryngology
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Cochlear implant users move in time to the beat of drum music.

2015

Cochlear implant users show a profile of residual, yet poorly understood, musical abilities. An ability that has received little to no attention in this population is entrainment to a musical beat. We show for the first time that a heterogeneous group of cochlear implant users is able to find the beat and move their bodies in time to Latin Merengue music, especially when the music is presented in unpitched drum tones. These findings not only reveal a hidden capacity for feeling musical rhythm through the body in the deaf and hearing impaired population, but illuminate promising avenues for designing early childhood musical training that can engage implanted children in social musical activi…

MalePeriodicityTime Factorsmedicine.medical_treatmentMusicalAudiology0302 clinical medicineCochlear implantEarly childhoodPitch Perceptionta515media_commoneducation.field_of_study05 social sciencesMiddle AgedCochlear ImplantationhumanitiesSensory SystemsFeelingta6131Audiometry Pure-ToneFemalePsychologyAdultmedicine.medical_specialtymedia_common.quotation_subjectPopulationMotor Activitybehavioral disciplines and activities050105 experimental psychology03 medical and health sciencesYoung AdultRhythmotorhinolaryngologic diseasesmedicineHumans0501 psychology and cognitive sciencesCochlear implant usersDancingeducationAgedAuditory ThresholdEntrainment (biomusicology)beat of drum musicCochlear ImplantsPersons With Hearing ImpairmentsAcoustic Stimulationhuman activitiesBeat (music)030217 neurology & neurosurgeryMusicHearing research
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Targeted next-generation sequencing of deafness genes in hearing-impaired individuals uncovers informative mutations

2014

Purpose: Targeted next-generation sequencing provides a remarkable opportunity to identify variants in known disease genes, particularly in extremely heterogeneous disorders such as nonsyndromic hearing loss. The present study attempts to shed light on the complexity of hearing impairment. Methods: Using one of two next-generation sequencing panels containing either 80 or 129 deafness genes, we screened 30 individuals with nonsyndromic hearing loss (from 23 unrelated families) and analyzed 9 normal-hearing controls. Results: Overall, we found an average of 3.7 variants (in 80 genes) with deleterious prediction outcome, including a number of novel variants, in individuals with nonsyndromic h…

MaleProbandUsher syndromeGene DosageDeafnessBioinformaticsmedicine.disease_causesensorineural hearing lossConnexinsCohort Studiestargeted next-generation sequencingOriginal Research Articlemutational loadChildGenetics (clinical)Oligonucleotide Array Sequence AnalysisGeneticsMutationmedicine.diagnostic_testHomozygoteHigh-Throughput Nucleotide SequencingPedigreeConnexin 26Treatment OutcomeChild PreschoolFemalemedicine.symptomAdultAdolescentSequence analysisHearing lossdeafness gene panelMolecular Sequence DataBiologynonsyndromic hearing lossDNA sequencingYoung AdultAudiometryGenetic variationotorhinolaryngologic diseasesmedicineHumansGenetic Predisposition to DiseaseFamily HealthBase SequenceGenetic VariationInfantDNASequence Analysis DNAmedicine.diseaseMutationAudiometryGene DeletionGenetics in Medicine
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