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1.
Sociol Health Illn ; 46(S1): 92-109, 2024 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-37329250

RESUMEN

Misophonia has gained attention in scientific circles that utilise brain imaging to validate diagnoses. The condition is promoted as not merely a symptom of other psychiatric diagnoses but as a discrete clinical entity. We illustrate the social construction of the diagnostic category of misophonia through examining prominent claims in research studies that use brain imaging to substantiate the diagnosis. We show that brain images are insufficient to establish the 'brain basis for misophonia' due to both technical and logical limitations of imaging data. Often misunderstood as providing direct access to the matter of the body, brain images are mediated and manipulated numerical data (Joyce, 2005, Social Studies of Science 35(3), p. 437). Interpretations of brain scans are further shaped by social expectations and attributes considered salient to the data. Causal inferences drawn from these studies are problematic because 'misophonics' are clinically pre-diagnosed before participating. We argue that imaging cannot replace the social process of diagnosis in the case of misophonia, nor validate diagnostic measures or otherwise substantiate the condition. More broadly, we highlight both the cultural authority and inherent limitations of brain imaging in the social construction of contested diagnoses while also illustrating its role in the disaggregation of symptoms into new diagnoses.


Asunto(s)
Trastornos de la Audición , Ciencias Sociales , Humanos , Trastornos de la Audición/diagnóstico , Neuroimagen , Encéfalo/diagnóstico por imagen
2.
Brain ; 145(3): 858-871, 2022 04 29.
Artículo en Inglés | MEDLINE | ID: mdl-35136969

RESUMEN

Susac syndrome is a disorder thought to be mediated by an autoimmune response towards endothelial cells, leading to a characteristic clinical triad of encephalopathy, visual disturbances due to branch arterial occlusions and sensorineural hearing impairment. Although it is a rare disease, three reasons make it important. First, given its variable presentation, Susac syndrome is underdiagnosed. Second, it is considered an important differential diagnosis in different neurological, psychiatric, ophthalmological and hearing disorders, and consequently is frequently misdiagnosed. Third, in many cases, Susac syndrome is diagnosed and treated late, with significant irreversible sequelae including dementia, blindness and hearing loss. Neuropathology findings derived from both Susac syndrome patient tissue and novel transgenic mouse models indicate cytotoxic CD8+ T cells adhere to microvessels, inducing endothelial cell swelling, vascular narrowing and occlusion, causing microinfarcts. Anti-endothelial cell antibodies are present in serum in 25% of Susac syndrome patients, but it is unclear whether they are aetiologically related to the disease, or an epiphenomenon. The clinical triad comprising encephalopathy, branch arterial occlusions, and sensorineural hearing impairment is considered pathognomonic, although great variability is found in presentation and natural course of disease. At first evaluation, only 13-30% of patients exhibit the full clinical triad, making diagnosis difficult. Retinal fluorescein angiography, optic coherence tomography, MRI and tonal audiometry are helpful methods for diagnosing and monitoring disease activity during treatment. By contrast, there are no reliable objective immune markers to monitor disease activity. Immunosuppression is the current treatment, with high-dose corticosteroid therapy as the mainstay, but additional therapies such as intravenous immunoglobulins, cyclophosphamide, rituximab and mycophenolate mofetil are often necessary, because the disease can be devastating, causing irreversible organ damage. Unfortunately, low rates of disease, variability in presentation and paucity of objective biomarkers make prospective controlled clinical trials for Susac syndrome treatment difficult. Current immunosuppressive treatments are therefore based on empirical evidence, mainly from retrospective case series and expert opinion. In this review, we draw attention to the need to take consider Susac syndrome in the differential diagnosis of different neurological, psychiatric, ophthalmological and hearing disorders. Furthermore, we summarize our current knowledge of this syndrome, in reference to its pathophysiology, diagnosis and management, emphasizing the need for prospective and controlled studies that allow a better therapeutic approach.


Asunto(s)
Encefalopatías , Pérdida Auditiva , Síndrome de Susac , Animales , Encefalopatías/diagnóstico , Diagnóstico Diferencial , Células Endoteliales/patología , Trastornos de la Audición/diagnóstico , Pérdida Auditiva/diagnóstico , Pérdida Auditiva/etiología , Humanos , Imagen por Resonancia Magnética , Ratones , Estudios Prospectivos , Estudios Retrospectivos , Síndrome de Susac/tratamiento farmacológico , Síndrome de Susac/terapia
3.
Z Kinder Jugendpsychiatr Psychother ; 51(3): 222-232, 2023 May.
Artículo en Alemán | MEDLINE | ID: mdl-35856746

RESUMEN

Misophonia in Childhood and Adolescence: A Narrative Review Abstract. Misophonia describes a phenomenon in which the affected children and adolescents show a strong negative physiological and emotional reaction when confronted with specific (misophonic) auditory stimuli (most commonly eating or breathing sounds). Several studies with adults yielded prevalence rates between 6 % and 20 % in various (clinical) samples, but the representativeness of samples was largely limited. More than 80 % of the first manifestation of symptoms occurs during childhood and adolescence. Regarding comorbid disorders, studies show great heterogeneity, with estimates ranging from 28-76 % of comorbid mental disorders and approximately 25 % with comorbid physical disorders. The exact etiology is currently not well studied. Initial neurophysiological explanations and imaging studies point to a specific physiological response in misophonia patients. Although many case reports are now available, and diagnostic criteria and measurement tools have been developed, misophonia currently does not represent a distinct neurological, audiological, or psychiatric disorder in the DSM-5 or ICD-11.


Asunto(s)
Trastornos de la Audición , Trastornos Mentales , Adulto , Niño , Humanos , Adolescente , Trastornos de la Audición/diagnóstico , Trastornos Mentales/diagnóstico , Trastornos Mentales/epidemiología , Trastornos Mentales/terapia , Prevalencia
4.
J Urol ; 207(1): 161-171, 2022 01.
Artículo en Inglés | MEDLINE | ID: mdl-34428922

RESUMEN

PURPOSE: The objective of this study was to investigate the presence of nonbladder sensory abnormalities in participants with overactive bladder syndrome (OAB). MATERIALS AND METHODS: Symptoms of Lower Urinary Tract Dysfunction Research Network (LURN) study participants with OAB symptoms and controls were recruited from 6 U.S. tertiary referral centers. Quantitative sensory testing (QST) was performed to determine pressure pain sensitivity at the thumbnail bed and auditory sensitivity. Fixed and mixed effect multivariable linear regressions and Weibull models were used to compare QST responses between groups. Pearson correlations were used to assess the relationship between QST measures. Associations between QST and self-reported symptoms were explored with linear regression. RESULTS: A total of 297 participants were analyzed (191 OAB, 106 controls; 76% white, 51% male). OAB cases were older than controls (57.4 vs 52.2 years, p=0.015). No significant differences in experimental thumbnail (nonbladder) pain or auditory sensitivity were detected between OAB cases and controls. Correlations between pressure and auditory derived metrics were weak to moderate overall for both groups, with some significantly stronger correlations for cases. Exploratory analyses indicated increased pressure pain and auditory sensitivity were modestly associated with greater self-reported bladder pain and pain interference with physical function. CONCLUSIONS: As a group, no significant differences between OAB cases and controls were observed in experimental nonbladder pain or auditory sensitivity during QST. Associations between QST outcomes and clinical pain raise the possibility of centrally mediated sensory amplification in some individuals with OAB.


Asunto(s)
Trastornos de la Audición/etiología , Dimensión del Dolor , Dolor/diagnóstico , Dolor/etiología , Vejiga Urinaria Hiperactiva/complicaciones , Adulto , Anciano , Estudios de Cohortes , Femenino , Trastornos de la Audición/diagnóstico , Humanos , Masculino , Persona de Mediana Edad
5.
J Med Genet ; 58(9): 619-627, 2021 09.
Artículo en Inglés | MEDLINE | ID: mdl-32820032

RESUMEN

BACKGROUND: Deafness-dystonia-optic neuronopathy (DDON) syndrome is a progressive X-linked recessive disorder characterised by deafness, dystonia, ataxia and reduced visual acuity. The causative gene deafness/dystonia protein 1 (DDP1)/translocase of the inner membrane 8A (TIMM8A) encodes a mitochondrial intermembrane space chaperon. The molecular mechanism of DDON remains unclear, and detailed information on animal models has not been reported yet. METHODS AND RESULTS: We characterized a family with DDON syndrome, in which the affected members carried a novel hemizygous variation in the DDP1 gene (NM_004085.3, c.82C>T, p.Q28X). We then generated a mouse line with the hemizygous mutation (p.I23fs49X) in the Timm8a1 gene using the clustered regularly interspaced short palindromic repeats /Cas9 technology. The deficient DDP1 protein was confirmed by western blot assay. Electron microscopic analysis of brain samples from the mutant mice indicated abnormal mitochondrial structure in several brain areas. However, Timm8a1I23fs49X/y mutation did not affect the import of mitochondria inner member protein Tim23 and outer member protein Tom40 as well as the biogenesis of the proteins in the mitochondrial oxidative phosphorylation system and the manganese superoxide dismutase (MnSOD / SOD-2). The male mice with Timm8a1I23fs49X/y mutant exhibited less weight gain, hearing impairment and cognitive deficit. CONCLUSION: Our study suggests that frameshift mutation of the Timm8a1 gene in mice leads to an abnormal mitochondrial structure in the brain, correlating with hearing and memory impairment. Taken together, we have successfully generated a mouse model bearing loss-of-function mutation in Timm8a1.


Asunto(s)
Encéfalo/metabolismo , Mutación del Sistema de Lectura , Trastornos de la Audición/genética , Trastornos de la Memoria/genética , Mitocondrias/genética , Proteínas del Complejo de Importación de Proteínas Precursoras Mitocondriales/genética , Adulto , Alelos , Animales , Encéfalo/patología , Análisis Mutacional de ADN , Modelos Animales de Enfermedad , Electroencefalografía , Estudios de Asociación Genética , Predisposición Genética a la Enfermedad , Genotipo , Trastornos de la Audición/diagnóstico , Humanos , Inmunohistoquímica , Masculino , Trastornos de la Memoria/diagnóstico , Ratones , Ratones Noqueados , Mitocondrias/ultraestructura , Linaje , Fenotipo , Superóxido Dismutasa/metabolismo
6.
Gesundheitswesen ; 84(2): 117-125, 2022 Feb.
Artículo en Alemán | MEDLINE | ID: mdl-33951738

RESUMEN

BACKGROUND: The aim of the newborn hearing screening (NHS) is to identify and treat children with bilateral hearing disorders early. The NHS is regulated in Germany by the Pediatric Directive, which recommends an evaluation after 5 years. This evaluation was performed for the first time nationwide for children born between 2011 and 2012 regarding structural, process and result quality. OBJECTIVES: Challenges in the collection of appropriate data as basis for evaluation are described and possible improvements are suggested. METHODS: All maternity and neonatology wards performing the NHS were identified and their documentations of the NHS analysed. In addition, all pediatric audiologists were identified to gather data on children with bilateral permanent congenital hearing disorder. RESULTS: The identification of relevant maternity and neonatology wards was very burdensome. More than half of them were not aware that NHS had to be documented. There was no documentation on more than 15% of the children that were to be screened. Furthermore, data concerning bilateral congenital hearing disorders was only accessible for 60% of the expected number of affected children. CONCLUSIONS: Data required for the evaluation of the NHS regarding structural, process and result quality were incomplete and missing. The database for evaluations should be defined precisely and structures needed to obtain meaningful results have to be established in advance. Nevertheless, the evaluation of the NHS provides meaningful results concerning the screening process in Germany.


Asunto(s)
Pruebas Auditivas , Tamizaje Neonatal , Niño , Femenino , Alemania/epidemiología , Audición , Trastornos de la Audición/diagnóstico , Trastornos de la Audición/epidemiología , Hospitales , Humanos , Recién Nacido , Embarazo
7.
Am J Perinatol ; 38(S 01): e231-e238, 2021 08.
Artículo en Inglés | MEDLINE | ID: mdl-32276280

RESUMEN

OBJECTIVE: Delayed maturation of auditory brainstem pathway in neonates admitted to the neonatal intensive care unit (NICU) may lead to misdiagnosis of children with normal peripheral hearing and inappropriate use of amplification devices. The aim of this study is to determine the pattern of auditory brain stem response in neonates admitted to the NICU for proper hearing assessment in this high-risk population. STUDY DESIGN: This prospective study was conducted on 1,469 infants who were admitted to the NICU, of which 1,423 had one or more risk factors for permanent congenital hearing loss and were screened with automated auditory brain stem response (AABR). A total of 60 infants were referred for diagnostic ABR analysis after failure on AABR screening. The control group comprised 60 well-baby nursery neonates with no risk factors for PCHL. RESULTS: Mean values of absolute latencies of waves III and V; interpeak latencies I-III, III-V, and I-V; amplitude of waves I, and V; and I/V amplitude ratio at 90 dBnHL measured for the right and left ears at 1 and 3 months of age show significant difference in NICU neonates compared with controls (p < 0.05). All the diagnostic ABR measurements significantly improved at the age of 3 months (p < 0.001) except wave I absolute latency of both groups (p > 0.05). Significant correlations were found between ABR readings at the age of 1 and 3 months and the gestational age of the NICU neonates (p < 0.05). CONCLUSION: Diagnostic ABR findings in NICU neonates suggested delayed maturation of the auditory brainstem pathway with a great impact of gestational age on this maturation. Auditory maturational changes were observed at 3 months of age of patient and control groups.


Asunto(s)
Tronco Encefálico/crecimiento & desarrollo , Potenciales Evocados Auditivos del Tronco Encefálico/fisiología , Trastornos de la Audición/congénito , Trastornos de la Audición/diagnóstico , Pruebas Auditivas , Egipto , Femenino , Edad Gestacional , Humanos , Lactante , Recién Nacido , Recien Nacido Prematuro , Unidades de Cuidado Intensivo Neonatal , Masculino , Tamizaje Neonatal , Estudios Prospectivos , Factores de Riesgo
8.
Int J Audiol ; 60(7): 495-506, 2021 07.
Artículo en Inglés | MEDLINE | ID: mdl-33246380

RESUMEN

OBJECTIVE: To understand the impact of face coverings on hearing and communication. DESIGN: An online survey consisting of closed-set and open-ended questions distributed within the UK to gain insights into experiences of interactions involving face coverings, and of the impact of face coverings on communication. SAMPLE: Four hundred and sixty members of the general public were recruited via snowball sampling. People with hearing loss were intentionally oversampled to more thoroughly assess the effect of face coverings in this group. RESULTS: With few exceptions, participants reported that face coverings negatively impacted hearing, understanding, engagement, and feelings of connection with the speaker. Impacts were greatest when communicating in medical situations. People with hearing loss were significantly more impacted than those without hearing loss. Face coverings impacted communication content, interpersonal connectedness, and willingness to engage in conversation; they increased anxiety and stress, and made communication fatiguing, frustrating and embarrassing - both as a speaker wearing a face covering, and when listening to someone else who is wearing one. CONCLUSIONS: Face coverings have far-reaching impacts on communication for everyone, but especially for people with hearing loss. These findings illustrate the need for communication-friendly face-coverings, and emphasise the need to be communication-aware when wearing a face covering.


Asunto(s)
Percepción Auditiva , COVID-19/prevención & control , Barreras de Comunicación , Trastornos de la Audición/psicología , Lectura de los Labios , Máscaras , Personas con Deficiencia Auditiva/psicología , COVID-19/transmisión , Señales (Psicología) , Expresión Facial , Audición , Trastornos de la Audición/diagnóstico , Trastornos de la Audición/fisiopatología , Humanos , Conducta Social , Percepción Visual
9.
Clin Otolaryngol ; 46(1): 154-160, 2021 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-32749771

RESUMEN

BACKGROUND AND OBJECTIVE: Inner ear malformations (IEMs) are common in children with hearing loss. The different types of IEMs form a unique subgroup of cochlear implant (CI) candidates. We aimed to evaluate the auditory perception outcomes of CI in children with different types of IEMs and compare them with CI users without IEMs. METHODS: The study included 274 CI users with and without IEMs as two groups (n = 137, each). Both groups' chronological age at implantation and duration of CI usage was matched (± 8 months). All subjects were evaluated pre-operatively and post-operatively by the Ling's sound test and the auditory perception test battery, which includes the Meaningful Auditory Integration Scale (MAIS), closed-set Pattern Perception Test (PPT) and open-set Sentence Recognition Test (SRT). Besides, children with IEMs were assessed for language development. RESULTS: Progress in the IEMs' group differed according to the type of ear anomaly. CI users with enlarged vestibular aqueduct had the highest scores, while users with common cavity had the lowest. Children with IEMs performed well on the closed-set test while having difficulty with the open-set test. CONCLUSION: Cochlear implantation outcomes are favourable in IEMs' patients with a cochlear nerve visible on magnetic resonance imaging. Our results indicate that it is critical to take the anatomical differences into account during follow-up and rehabilitation programmes. Each CI user should be evaluated according to his or her individual needs.


Asunto(s)
Percepción Auditiva/fisiología , Implantación Coclear , Implantes Cocleares , Oído Interno/anomalías , Trastornos de la Audición/terapia , Desarrollo del Lenguaje , Adolescente , Estudios de Casos y Controles , Niño , Preescolar , Estudios de Cohortes , Femenino , Trastornos de la Audición/diagnóstico , Trastornos de la Audición/etiología , Humanos , Masculino , Resultado del Tratamiento
10.
Psychiatr Q ; 92(2): 609-619, 2021 06.
Artículo en Inglés | MEDLINE | ID: mdl-32829440

RESUMEN

Misophonia is a condition of abnormal emotional responses to specific auditory stimuli. There is limited information available on the prevalence of this condition. This study aimed to estimate the prevalence of misophonia in an undergraduate medical student population at the University of Nottingham. A secondary aim of this study was to assess the psychometric validity of the Amsterdam Misophonia Scale (A-Miso-S) questionnaire tool in this population. The A-Miso-S was administered online to medical students at the University of Nottingham. To assess the validity of the A-Miso-S, a factor analysis was conducted. To determine prevalence and severity the results of the questionnaire were quantitatively analysed using SPSS. Actor analysis was conducted. Free text responses to one questionnaire item were analysed using a thematic approach. Responses were obtained from 336 individuals. Clinically significant misophonic symptoms appear to be common, effecting 49.1% of the sample population. This is statistically significantly higher prevalence than previous studies have found (p < 0.00001). Using the classification of the A-Miso-S, mild symptoms were seen in 37%, moderate in 12%, severe in 0.3% of participants. No extreme cases were seen. The A-Miso-S was found to be a uni-factorial tool, with good internal consistency. This study has provided new information on misophonia and validity of the A-Miso-S questionnaire in a sample population of UK undergraduate medical students. The results indicate that misophonia is a phenomenon that a significant proportion of medical students experience though only a small subset experience it severely.


Asunto(s)
Emociones , Trastornos de la Audición/epidemiología , Trastornos de la Audición/fisiopatología , Estudiantes de Medicina/estadística & datos numéricos , Estimulación Acústica , Adolescente , Femenino , Trastornos de la Audición/diagnóstico , Humanos , Masculino , Prevalencia , Reproducibilidad de los Resultados , Encuestas y Cuestionarios , Reino Unido/epidemiología , Adulto Joven
11.
Int J Audiol ; 59(4): 310-315, 2020 04.
Artículo en Inglés | MEDLINE | ID: mdl-31777297

RESUMEN

Objective: To evaluate the effects of caesarian section (CS) versus vaginal birth (VB) delivery techniques on results from neonatal hearing screening tests (NHSTs).Design: Retrospective analysis.Study sample: A total of 10,767 neonates divided into two groups according to delivery technique underwent NHSTs. Those who failed TEOAE or AABR were sent for diagnostic ABR examination.Results: A total of 5620 of 6044 (92.9%) of the neonates in the CS group passed the TEOAE test bilaterally and 424 (7.1%) failed either unilaterally or bilaterally. In the VB group, 4496 of 4723 (95.1%) neonates passed the TEOAE test bilaterally, while the remaining 227 (4.9%) failed the test either unilaterally or bilaterally. Bilateral passing rate of TEOAE test results was significantly higher in the VB group than the CS group (p < 0.05). The AABR failure rate (unilaterally or bilaterally) was 1% in the CS group, which was significantly higher than that in the VB group (0.6%). Diagnostic ABR bilateral pass rate was not statistically different between the groups.Conclusions: Delivery method was shown to affect the results of NHSTs. We found that the rates of failing the TEOAE and screening AABR examinations were higher among neonates born by CS compared to VB.


Asunto(s)
Cesárea/estadística & datos numéricos , Parto Obstétrico/estadística & datos numéricos , Trastornos de la Audición/diagnóstico , Pruebas Auditivas/estadística & datos numéricos , Tamizaje Neonatal/métodos , Parto Obstétrico/métodos , Femenino , Humanos , Recién Nacido , Masculino , Embarazo , Estudios Retrospectivos , Turquía , Vagina
12.
Adv Gerontol ; 33(3): 549-554, 2020.
Artículo en Ruso | MEDLINE | ID: mdl-33280341

RESUMEN

The aim of the study was a comparative analysis of complaints and audiological findings in patients of the audiological center depending on their age. The results of the examination of 300 firstly consulted patients (random sample) are presented. The group of young patients (19-44 years) included 40 people; middle age (45-59 years) - 62 people; elderly (60-74 years) - 100 people; senile age (75-90 years) - 98 people. The survey included the collection of complaints and anamnesis, ENT checkup, pure tone audiometry, impedancemetry, speech audiometry in headphones to detect the signs of Central Auditory Processing Disorder or in the free sound field to assess the effectiveness of hearing aids. It was found that for early diagnosis of hearing loss and prevention of age-related sensory-cognitive dysfunction, it is advisable to use not only the results of pure tone audiometry, but also the data of speech audiometry, as well as the analysis of subjective complaints. The results of the work indicate the need for hearing screening in the population over 60 years old.


Asunto(s)
Audífonos , Pérdida Auditiva , Anciano , Audiometría de Tonos Puros , Audiometría del Habla , Trastornos de la Audición/diagnóstico , Trastornos de la Audición/epidemiología , Trastornos de la Audición/etiología , Pérdida Auditiva/diagnóstico , Pérdida Auditiva/epidemiología , Pérdida Auditiva/etiología , Humanos
13.
HNO ; 68(3): 155-163, 2020 Mar.
Artículo en Alemán | MEDLINE | ID: mdl-31628531

RESUMEN

BACKGROUND: Hearing and cognition are closely related to each other. Particularly in suboptimal listening situations, cognitive abilities become important to enable speech comprehension. Besides, studies have indicated that hearing impairment is associated with a more rapid mental decline compared to persons with normal hearing. However, hearing loss also has an impact on neurocognitive testing, which is generally based on auditive stimuli. With increasing age, the risk of sensory but also of cognitive impairments increases. So far this comorbidity receives little consideration in otorhinolaryngology. MATERIALS AND METHODS: The paper presents an overview and evaluation of widely used German neurocognitive test batteries for older patients, with regard to the different test modalities and their focus. RESULTS: A multitude of different neurocognitive screening tests and detailed test batteries are available, particularly in the field of dementia. So far, sensory deficits have not been considered in neurocognitive testing, neither concerning application nor interpretation. Normative data adapted to the hearing impaired are still missing. CONCLUSION: With regard to demographic changes and the well-known bias between hearing and cognition, screening of neurocognitive functions should be implemented in basic otorhinolaryngologic diagnostics. More comprehensive test batteries might be useful for research purposes or speech therapy.


Asunto(s)
Trastornos del Conocimiento , Trastornos de la Audición , Pruebas Auditivas , Otolaringología , Cognición , Trastornos del Conocimiento/diagnóstico , Audición , Trastornos de la Audición/diagnóstico , Humanos , Pruebas de Estado Mental y Demencia
14.
Med J Malaysia ; 75(2): 136-140, 2020 03.
Artículo en Inglés | MEDLINE | ID: mdl-32281594

RESUMEN

INTRODUCTION: To correlate the score obtained using a bilingual (Malay and English) 14 points questionnaire in the detection of hearing loss at the University of Malaya, Medical Centre (UMMC), Kuala Lumpur, Malaysia over a 9 month period. METHODS: This is a prospective instrument correlation study done on 93 children aged 1-4 years of age with speech and language delay for at least 3 months. Hearing status was confirmed using otoacoustic emissions, pure tone audiometry and brainstem evoked response (BSER). Hearing status was then compared to the 14-point questionnaire final scores and is statistically correlated. RESULTS: There were 26 patients, 15 males (58%) and 11(42%) females who were diagnosed to have hearing loss. The average age of presentation was 2.49 and conductive hearing loss accounted for about 74% of cases of hearing loss. The mean questionnaire score obtained through our patients was 3.83±1.987. Discriminant analysis suggests that a questionnaire score of above 4 was indicative that the child was suffering from hearing loss. CONCLUSION: Our study suggests that the low-cost bilingual (Malay and English) questionnaire can be used to detect hearing loss in the Malaysian population and could potentially be useful in rural health centres to help detect hearing loss and to determine the urgency of referral to a tertiary health centre.


Asunto(s)
Encuestas Epidemiológicas/normas , Trastornos de la Audición/diagnóstico , Trastornos del Desarrollo del Lenguaje , Multilingüismo , Preescolar , Femenino , Humanos , Lactante , Malasia , Masculino , Padres , Estudios Prospectivos
15.
Artículo en Ruso | MEDLINE | ID: mdl-32119209

RESUMEN

Among HIV-infected patients there are individuals with masked chronic diseases that affect life quality and life-span. Their timely detection and treatment can improve life quality of HIV-infected patients. The screening examination allows to establish prevalence level, structure and features of concomitant diseases under HIV- infection to provide timely medical preventive care.


Asunto(s)
Infecciones por VIH , Trastornos de la Audición , Enfermedades Pulmonares , Tamizaje Masivo , Infecciones por VIH/complicaciones , Infecciones por VIH/diagnóstico , Trastornos de la Audición/complicaciones , Trastornos de la Audición/diagnóstico , Humanos , Enfermedades Pulmonares/complicaciones , Enfermedades Pulmonares/diagnóstico , Prevalencia , Calidad de Vida , Sistema Respiratorio
16.
Am J Perinatol ; 36(3): 296-302, 2019 02.
Artículo en Inglés | MEDLINE | ID: mdl-30081399

RESUMEN

Hearing loss is the most common congenital birth defect. In 2007, American Academy of Pediatrics updated the hearing screen guidelines to recommend hearing screen by 1 month of age, diagnostic evaluation by 3 months, and early interventions by 6 months. Early interventions have been shown to improve developmental outcome in children with hearing loss. Infants admitted to the neonatal intensive care unit (NICU) are at higher risk for hearing loss. For infants born before 34 weeks' gestation, there are no guidelines for initial hearing screen. Although auditory brain stem response can be reliably performed at 32 to 34 weeks, in most NICUs, they are screened prior to discharge per universal hearing screen guidelines. In high-risk infants, often with prolonged hospitalization, this leads to missed opportunity for early detection and implementation of early intervention services. Using quality improvement methodology, an updated hearing screen algorithm was developed and implemented in our level IV NICU along with an electronic medical record tool to improve the process of identifying infants meeting criteria for hearing screen.


Asunto(s)
Trastornos de la Audición/diagnóstico , Enfermedades del Prematuro/diagnóstico , Unidades de Cuidado Intensivo Neonatal/normas , Tamizaje Neonatal/normas , Guías de Práctica Clínica como Asunto , Mejoramiento de la Calidad , Adhesión a Directriz , Pruebas Auditivas , Humanos , Recién Nacido , Recien Nacido Prematuro , Missouri
17.
Eur Arch Otorhinolaryngol ; 276(4): 977-984, 2019 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-30671602

RESUMEN

PURPOSE: This study analyzed the late ear complications of radiotherapy for nasopharyngeal cancer (NPC) and compared the conventional and intensity-modulated radiotherapy (2D-RT and IMRT, respectively). METHODS: At 2-21 years after the end of NPC treatment, 104 ears of 52 patients were evaluated with the otoscopic examination, pure tone audiometry test, tympanometry, and subjective complaints by being blinded to the radiotherapy technique. RESULTS: There were no differences in terms of the pathology of the external, middle or inner ear, air and bone-conduction hearing thresholds, and the air-bone (A-B) gap at 500, 1000, 2000, and 4000 Hz, and tympanometry types between 2D-RT and IMRT groups (p > 0.05). There were positive correlations between the values of A500 and A1000 thresholds; gap 500, 4000, and mean cochlear RT dose (p < 0.05). There were positive correlations between the values of A500, A1000, and A4000 thresholds; gap 500, 1000, 2000, 4000, and maximum cochlear RT dose (p < 0.05). CONCLUSION: IMRT was not found to be superior to 2D-RT to prevent RT-induced ear complications. The solution of the middle ear problems must be the goal of the strategies for complications treatment.


Asunto(s)
Oído/efectos de la radiación , Trastornos de la Audición/etiología , Audición/efectos de la radiación , Neoplasias Nasofaríngeas/radioterapia , Traumatismos por Radiación/prevención & control , Radioterapia de Intensidad Modulada/efectos adversos , Radioterapia/efectos adversos , Adulto , Quimioradioterapia/efectos adversos , Oído/patología , Femenino , Trastornos de la Audición/diagnóstico , Trastornos de la Audición/prevención & control , Pruebas Auditivas , Humanos , Masculino , Persona de Mediana Edad , Neoplasias Nasofaríngeas/terapia , Radioterapia/métodos
18.
Int J Audiol ; 58(8): 468-475, 2019 08.
Artículo en Inglés | MEDLINE | ID: mdl-31012791

RESUMEN

Objective: To investigate the feasibility of using the LittlEARS® Auditory Questionnaire (LEAQ®) as part of the infant hearing screening programme in Germany. Design: LEAQ®s were distributed to 47 paediatric practices and were completed by the parents/guardians of the infants (aged between 9-14 months) involved in the study (= LEAQ® screening). The infants who failed the LEAQ® screening were invited to a LEAQ rescreening. Infants who failed the LEAQ® rescreening were sent to a paediatric ENT specialist. After 3 years, a follow-up was performed on two groups: the first group comprised infants who failed the LEAQ screening; the second group (control group) comprised 200 infants who passed the LEAQ screening. Study Sample: 5316 questionnaires were returned. Results: Six infants with permanent hearing loss were identified using the LEAQ® as a screening tool. Conclusions: An infant hearing screening using the LEAQ® is easily implementable in paediatric practices and may be a good alternative in countries where no objective screening instruments are available. The LEAQ® was suitable for monitoring hearing development in infants in general and could help to identify a late-onset or progressive hearing loss in infants.


Asunto(s)
Trastornos de la Audición/diagnóstico , Pruebas Auditivas , Audición , Tamizaje Neonatal/métodos , Encuestas y Cuestionarios , Factores de Edad , Desarrollo Infantil , Estudios de Factibilidad , Femenino , Alemania , Trastornos de la Audición/fisiopatología , Humanos , Lactante , Recién Nacido , Masculino , Valor Predictivo de las Pruebas
19.
Int J Audiol ; 58(4): 231-245, 2019 04.
Artículo en Inglés | MEDLINE | ID: mdl-30900518

RESUMEN

OBJECTIVE: As a step towards objectifying audiological rehabilitation and providing comparability between different test batteries and clinics, the Common Audiological Functional Parameters (CAFPAs) were introduced as a common and abstract representation of audiological knowledge obtained from diagnostic tests. DESIGN: Relationships between CAFPAs as an intermediate representation between diagnostic tests and audiological findings, diagnoses and treatment recommendations (summarised as "diagnostic cases") were established by means of an expert survey. Expert knowledge was collected for 14 given categories covering different diagnostic cases. For each case, the experts were asked to indicate expected ranges of diagnostic test outcomes, as well as traffic light-encoded CAFPAs. STUDY SAMPLE: Eleven German experts in the field of audiological rehabilitation from Hanover and Oldenburg participated in the survey. RESULTS: Audiological findings or treatment recommendations could be distinguished by a statistical model derived from the experts' answers for CAFPAs as well as audiological tests. CONCLUSIONS: The CAFPAs serve as an abstract, comprehensive representation of audiological knowledge. If more detailed information on certain functional aspects of the auditory system is required, the CAFPAs indicate which information is missing. The statistical graphical representations for CAFPAs and audiological tests are suitable for audiological teaching material; they are universally applicable for real clinical databases.


Asunto(s)
Audiología/estadística & datos numéricos , Corrección de Deficiencia Auditiva/estadística & datos numéricos , Sistemas Especialistas , Trastornos de la Audición/diagnóstico , Pruebas Auditivas/estadística & datos numéricos , Aprendizaje Automático , Interpretación Estadística de Datos , Trastornos de la Audición/clasificación , Trastornos de la Audición/terapia , Humanos , Valor Predictivo de las Pruebas , Probabilidad , Reproducibilidad de los Resultados
20.
Int J Audiol ; 58(8): 510-515, 2019 08.
Artículo en Inglés | MEDLINE | ID: mdl-31074295

RESUMEN

Objectives: The goal of this work was to develop and normalise an international French version of the AzBio sentence test. Design: A corpus of 1000 sentences was generated. These sentences were recorded with four talkers and processed through a four-channel cochlear implant simulation. The mean intelligibility for each sentence achieved by 16 normal-hearing listeners was computed. The consecutively ordered 165 sentences from each talker rendering an average score of 85% were sequentially assigned to 33 lists of 20 sentences. All lists were presented to 30 normal-hearing and 25 hearing-impaired listeners in order to verify their equivalency. Thirty normal-hearing adults were also recruited to assess the test's psychometrics and define norms. Results: The results of the list equivalency validation study showed no significant differences in percent correct scores for 30 sentence lists. A binomial distribution model was used to estimate the 95% critical differences for each potential percentage score. Normalization data showed an average performance between 96% and 99% with a very low standard deviation. Conclusions: With a set of 30 lists, researchers and clinicians can use the FrBio to evaluate a large number of experimental conditions; changes in performance over time or across conditions can then be tracked.


Asunto(s)
Audiometría del Habla/métodos , Trastornos de la Audición/diagnóstico , Personas con Deficiencia Auditiva/psicología , Percepción del Habla , Adolescente , Adulto , Estudios de Casos y Controles , Comprensión , Femenino , Audición , Trastornos de la Audición/fisiopatología , Trastornos de la Audición/psicología , Humanos , Masculino , Valor Predictivo de las Pruebas , Psicometría , Reproducibilidad de los Resultados , Inteligibilidad del Habla , Adulto Joven
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