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1.
Int J Pediatr Otorhinolaryngol ; 170: 111605, 2023 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-37245390

RESUMEN

OBJECTIVES: Vocal singing skills in pediatric CI users are not much known due to the limited number of studies. The principal aim of the present study was to evaluate vocal singing skills in Italian pediatric CI users. A further aim was to investigate factors that may significantly influence their performance. METHODS: The participants were twenty-two implanted children and twenty-two hearing peers. Their vocal singing skills for familiar ("Happy Birthday to You") and unfamiliar songs ("Baton Twirler" from Pam Pam 2- Tribute to Gordon) were evaluated in relation to their music perception (the Gordon test). Acoustic analysis was performed using Praat and MATLAB software. Nonparametric statistical tests and principal component analysis (PCA) were used to analyze the data. RESULTS: Hearing children outperformed implanted peers in both music perception and vocal singing tasks (all measures regarding intonation, vocal range, melody, and memory for the familiar song versus measures regarding intonation and overall melody production for the unfamiliar song). Music perception and vocal singing performances revealed strong correlations. For the familiar and unfamiliar songs, age-appropriate vocal singing was observed in 27.3% versus 45.4% of children, all implanted within 24 months of age. Age at implantation and duration of CI experience were moderately correlated with the total score obtained from the Gordon test. CONCLUSION: Implanted children show limited vocal singing skills in comparison to their hearing peers. However, some children implanted within 24 months of age seem to achieve vocal singing skills as good as their hearing peers. Future research could be useful to better understand the role of brain plasticity to implement specific training programs for both music perception and vocal singing.


Asunto(s)
Implantación Coclear , Implantes Cocleares , Música , Canto , Voz , Niño , Humanos , Percepción Auditiva
2.
Acta Otorhinolaryngol Ital ; 42(2): 169-175, 2022 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-35612509

RESUMEN

Objective: To analyse hearing attention and quality of listening in a cohort of children affected by moderate to severe unilateral hearing loss, comparing a group of hearing aid users to children with no hearing aid. Methods: Twenty-four children (12 hearing aid users, and 12 without hearing rehabilitation) underwent audiological evaluation with speech audiometry in quiet and noise, hearing attention tests, and the speech, spatial and quality of hearing questionnaire in the version for parents. Results: Concerning speech audiometry in noise, in the most difficult condition no one in the unaided group achieved a normal speech recognition threshold score (0% vs 11.6 ± 2.7% in the aided group). The selective hearing attention and shifting tests showed fewer errors in the aided group vs. the non-aided group. The questionnaire showed a significant difference between the quality of listening perceived by the parents of the two groups. The mean total scores were 152.8 ± 2.7 in the aided group and 116.1 ± 2.6 in the non-aided group (p > 0.001). Conclusions: Children with unilateral hearing loss without hearing rehabilitation show a lower quality of hearing, especially with regards to divided auditory attention. Hearing rehabilitation should be proposed as soon as possible in children with moderate to severe unilateral hearing loss.


Asunto(s)
Audífonos , Pérdida Auditiva Sensorineural , Pérdida Auditiva Unilateral , Percepción del Habla , Atención , Niño , Audición , Pérdida Auditiva Sensorineural/rehabilitación , Humanos
3.
Expert Opin Drug Saf ; 20(3): 259-264, 2021 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-33427529

RESUMEN

Introduction: The safety of subcutaneous immunotherapy (SCIT), and particularly the dramatic issue of fatal reactions, has been an obstacle that limited the implementation of a therapy with unique characteristics of action on the causes of allergy. The introduction of sublingual immunotherapy (SLIT) was aimed at solving safety problems while maintaining clinical efficacy.Areas covered: For more than 20 years, SLIT has been based on allergen extracts in drops at low average doses. As evidenced by meta-analyses, the typical adverse events (AE) have consisted of local reactions in the mouth and throat. Unlike the injection route, no correlation was observed between the administered dose and AEs. The development of SLIT products in tablets, based on higher doses than drops, has somewhat changed the concept of SLIT safety. Although large trials, performed to obtain regulatory agency approval, have shown overall high safety, rare anaphylactic reactions have been described.Expert opinion: SLIT is globally safe, and no fatal reactions have ever been reported, but with currently available high biological potency products it is necessary to follow prudential rules, such as the administration of the first dose under medical supervision and the thorough education of patients to avoid taking of higher doses than recommended.


Asunto(s)
Anafilaxia/etiología , Inmunoterapia Sublingual/efectos adversos , Alérgenos/administración & dosificación , Humanos , Inmunoterapia Sublingual/métodos , Comprimidos , Resultado del Tratamiento
4.
Artículo en Inglés | MEDLINE | ID: mdl-32349379

RESUMEN

The association between hyperacusis and developmental disorders such as autism spectrum disorders has been extensively reported in the literature; however, the specific prevalence of hyperacusis in attention deficit hyperactivity disorder (ADHD) has never been investigated. In this preliminary study, we evaluated the presence of hyperacusis in a small sample of children affected by ADHD compared to a control group of healthy children. Thirty normal hearing children with a diagnosis of ADHD and 30 children matched for sex and age were enrolled in the study. All children underwent audiological and multidisciplinary neuropsychiatric evaluation. Hearing was assessed using pure tone audiometry and immittance test; ADHD was diagnosed following the Diagnostic and Statistical Manual of Mental Disorder criteria. Hyperacusis was assessed through the administration of a questionnaire to parents and an interview with children. Hyperacusis was diagnosed in 11 children (36.7%) in the study group and in four children (13.3%) in the control group; this difference was statistically significant (p = 0.03). The preliminary results of this study suggest a higher presence of hyperacusis in children with attention deficit hyperactivity disorder compared to control children. More studies on larger samples are necessary to confirm these results.


Asunto(s)
Trastorno por Déficit de Atención con Hiperactividad , Hiperacusia , Trastorno por Déficit de Atención con Hiperactividad/complicaciones , Estudios de Casos y Controles , Niño , Manual Diagnóstico y Estadístico de los Trastornos Mentales , Humanos , Hiperacusia/complicaciones , Encuestas y Cuestionarios
5.
Ital J Pediatr ; 46(1): 3, 2020 Jan 06.
Artículo en Inglés | MEDLINE | ID: mdl-31906974

RESUMEN

BACKGROUND: Congenital cytomegalovirus (cCMV) infection is the most frequent non-genetic cause of sensorineural hearing-loss (SNHL) (i.e., hearing loss due to a cochlear and/or auditory nerve damage). It is widely accepted that SNHL at birth, when associated to cCMV symptomatic infection involving the central nervous system, benefits from antiviral therapy started in the neonatal period. Conversely, there is no consensus for antiviral treatment in congenitally infected infants diagnosed with isolated SNHL (i.e., SNHL in an otherwise asymptomatic infant) at birth. Our aim was to assess the frequency and the auditory outcome of isolated SNHL at birth due to auditory neuropathy (AN) (i.e., SNHL in a patient with normal cochlear function and auditory nerve dysfunction) in infants with cCMV infection. METHODS: We retrospectively reviewed the clinical history of 60 infants, born at term, with cCMV asymptomatic infection, without additional risk factors for SNHL, and exhibiting bilateral "pass" otoacustic emissions (OAE). None of them underwent antiviral therapy. Hearing thresholds were assessed by means of Auditory Brainstem Responses (ABR). AN affected children were followed up until possible normalization of the hearing thresholds or definitive diagnosis of AN. Each infant diagnosed with monolateral or bilateral AN was classified according to the worst ear threshold. RESULTS: In our population, the first ABR was performed at a mean age of 5.00 ± 2.79 (SD) months and AN was diagnosed in 16/60 (26.67%) infants; in 4 infants the AN was defined as mild (4/4 monolateral), moderate in 11 (5/11 bilateral), and severe in 1 (bilateral). The mean age at first ABR was 3.69 ± 2.80 (SD) months in the 16 babies with AN and 5.48 ± 2.66 (SD) months in the 44 infants with normal hearing (p = 0.007). All AN cases spontaneously recovered a normal auditory threshold over time. The mean length of the audiological follow-up was 32.44 ± 17.58 (SD) months (range 5-60 months). CONCLUSION: A delayed maturation of the auditory pathways should be considered when a mild/moderate isolated AN at birth is detected in cCMV infected infants. Prospective studies conducted on larger populations, and with a longer audiological follow-up, are needed to confirm our findings.


Asunto(s)
Infecciones por Citomegalovirus/congénito , Pérdida Auditiva Central/virología , Potenciales Evocados Auditivos del Tronco Encefálico , Femenino , Pérdida Auditiva Sensorineural/virología , Pruebas Auditivas , Humanos , Lactante , Recién Nacido , Italia , Masculino , Tamizaje Neonatal , Estudios Retrospectivos
6.
Ital J Pediatr ; 44(1): 104, 2018 Aug 24.
Artículo en Inglés | MEDLINE | ID: mdl-30143030

RESUMEN

BACKGROUND: The introduction of Universal Newborn Hearing Screening (UNHS) programs has drastically contributed to the early diagnosis of hearing loss in children, allowing prompt intervention with significant results on speech and language development in affected children. UNHS in the Lazio region has been initially deliberated in 2012; however, the program has been performed on a universal basis only from 2015. The aim of this retrospective study is to present and discuss the preliminary results of the UNHS program in the Lazio region for the year 2016, highlighting the strengths and weaknesses of the program. METHODS: Data from screening facilities in the Lazio region for year 2016 were retrospectively analyzed. Data for Level I centers were supplied by the Lazio regional offices; data for Level II and III centers were provided by units that participated to the study. RESULTS: During 2016, a total of 44,805 babies were born in the Lazio region. First stage screening was performed on 41,821 children in 37 different birth centers, with a coverage rate of 93.3%. Of these, 38.977 (93.2%) obtained a "pass" response; children with a "refer" result in at least one ear were 2844 (6.8%). Data from Level II facilities are incomplete due to missing reporting, one of the key issues in Lazio UNHS. Third stage evaluation was performed on 365 children in the three level III centers of the region, allowing identification of 70 children with unilateral (40%) or bilateral (60%) hearing loss, with a prevalence of 1.6/1000. CONCLUSIONS: The analysis of 2016 UNHS in the Lazio region allowed identification of several strengths and weaknesses of the initial phase of the program. The strengths include a correct spread and monitoring of UNHS among Level I facilities, with an adequate coverage rate, and the proper execution of audiological monitoring and diagnosis among Level III facilities. Weakness, instead, mainly consisted in lack of an efficient and automated central process for collecting, monitoring and reporting of data and information.


Asunto(s)
Diagnóstico Precoz , Pérdida Auditiva/diagnóstico , Pruebas Auditivas/métodos , Tamizaje Neonatal/métodos , Estudios de Cohortes , Femenino , Estudios de Seguimiento , Pérdida Auditiva/congénito , Pérdida Auditiva/epidemiología , Humanos , Recién Nacido , Italia/epidemiología , Masculino , Prevalencia , Estudios Retrospectivos , Medición de Riesgo , Población Rural
7.
Int J Immunopathol Pharmacol ; 31: 394632017748841, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-29251013

RESUMEN

The previous concept regarding diabetic retinopathy assigned a primary role to hyperglycemia-induced microvascular alterations, while neuronal and glial abnormalities were considered to be secondary to either ischemia or exudation. The aim of this study was to reveal the potential role of neuronal and glial cells in initial and advanced alterations of the retinopathy in human type 2 diabetes. Electron microscopy and histochemical studies were performed on 38 surgically removed human eyes (28 obtained from diabetic patients and 10 from non-diabetic patients). Morphometric analysis of basement membrane material and lipids was performed. An accumulation of metabolic by-products was found in the capillary wall with aging: this aspect was significantly more pronounced in diabetics. Müller glial cells were found to contribute to alterations of the capillary wall and to occlusion, as well as to the development of proliferative retinopathy and cystoid degeneration of the retina. Our results showed morphological evidence regarding the role of neuronal and glial cells in the pathology of diabetic retinopathy, prior and in addition to microangiopathy. These morphological findings support a neurovascular pathogenesis at the origin of diabetic retinopathy, thus the current treatment approach should be completed by neuroprotective measures.


Asunto(s)
Capilares/patología , Retinopatía Diabética/patología , Neuroglía/patología , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Membrana Basal/patología , Niño , Diabetes Mellitus Tipo 2/patología , Femenino , Humanos , Masculino , Persona de Mediana Edad , Retina/patología , Adulto Joven
8.
Int J Immunopathol Pharmacol ; 29(1): 40-53, 2016 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-26604209

RESUMEN

Normal human aging and diabetes are associated with a gradual decrease of cerebral flow in the brain with changes in vascular architecture. Thickening of the capillary basement membrane and microvascular fibrosis are evident in the central nervous system of elderly and diabetic patients. Current findings assign a primary role to endothelial dysfunction as a cause of basement membrane (BM) thickening, while retinal alterations are considered to be a secondary cause of either ischemia or exudation. The aim of this study was to reveal any initial retinal alterations and variations in the BM of retinal capillaries during diabetes and aging as compared to healthy controls. Moreover, we investigated the potential role of vascular endothelial growth factor (VEGF) and pro-inflammatory cytokines in diabetic retina.Transmission electron microscopy (TEM) was performed on 46 enucleated human eyes with particular attention to alterations of the retinal capillary wall and Müller glial cells. Inflammatory cytokines expression in the retina was investigated by immunohistochemistry.Our electron microscopy findings demonstrated that thickening of the BM begins primarily at the level of the glial side of the retina during aging and diabetes. The Müller cells showed numerous cytoplasmic endosomes and highly electron-dense lysosomes which surrounded the retinal capillaries. Our study is the first to present morphological evidence that Müller cells start to deposit excessive BM material in retinal capillaries during aging and diabetes. Our results confirm the induction of pro-inflammatory cytokines TNF-α and IL-1ß within the retina as a result of diabetes.These observations strongly suggest that inflammatory cytokines and changes in the metabolism of Müller glial cells rather than changes in of endothelial cells may play a primary role in the alteration of retinal capillaries BM during aging and diabetes.


Asunto(s)
Envejecimiento/patología , Retinopatía Diabética/patología , Retina/patología , Adulto , Anciano , Anciano de 80 o más Años , Membrana Basal/patología , Capilares/patología , Capilares/ultraestructura , Niño , Femenino , Humanos , Inmunohistoquímica , Interleucina-6/análisis , Masculino , Microscopía Electrónica de Transmisión , Persona de Mediana Edad , Retina/ultraestructura , Factor de Necrosis Tumoral alfa/análisis , Factor A de Crecimiento Endotelial Vascular/análisis
9.
Audiol Neurootol ; 21(6): 372-382, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-28099967

RESUMEN

In a subpopulation of patients, tinnitus can be modulated by movements of the jaw or head and neck due to complex somatosensory-auditory interactions. In some of these subjects, tinnitus could be related to an underlying temporomandibular (TMJ) or craniocervical (NECK) dysfunction that, if correctly identified, could streamline treatment and increase chances of tinnitus improvement. However, it is still unclear whether somatic modulation of tinnitus could be used as a screening tool for identifying such patients. In this study, we included 310 tinnitus patients with normal hearing, no psychiatric comorbidities, and a positive history of TMJ and/or NECK dysfunction and/or a positive modulation of tinnitus to evaluate the characteristics of somatic modulation, investigate the relationship between positive history and positive modulation, and identify factors most strongly associated with somatic modulation. Tinnitus modulation was present in 79.67% of the patients. We found a significant association within the same subjects between a positive history and a positive tinnitus modulation for the same region, mainly for TMJ in unilateral tinnitus patients and for TMJ + NECK in bilateral tinnitus patients. A strong correlation between history and modulation in the same somatic region within the same subgroups of subjects was also identified. Most TMJ maneuvers resulted in an increased loudness, while NECK maneuvers showed an increase in tinnitus loudness in about 59% of cases. High-pitched tinnitus and male gender were associated with a higher prevalence of modulation; no differences were found for tinnitus onset, Tinnitus Handicap Inventory score, and age. In this paper, we report a strong association between history and modulation for the same regions within the same patients; such an association should always be investigated to improve chances of a correct diagnosis of somatosensory tinnitus.


Asunto(s)
Enfermedades Musculoesqueléticas/fisiopatología , Trastornos de la Articulación Temporomandibular/fisiopatología , Acúfeno/fisiopatología , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Vértebras Cervicales/fisiopatología , Comorbilidad , Femenino , Humanos , Italia/epidemiología , Masculino , Persona de Mediana Edad , Enfermedades Musculoesqueléticas/epidemiología , Cuello/fisiopatología , Factores Sexuales , Trastornos de la Articulación Temporomandibular/epidemiología , Acúfeno/epidemiología , Adulto Joven
10.
Ann Otol Rhinol Laryngol ; 124(7): 550-60, 2015 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-25725038

RESUMEN

OBJECTIVE: One of the most debated topics in tinnitus is its standard and practical classification. The most popular classification distinguishes subjective from objective tinnitus. Other classifications are based on different features. On the whole, they seem incomplete, and the diagnostic and therapeutic algorithms are often difficult for practical purposes. The aim of this work is to develop a new diagnostic and therapeutic algorithm. METHODS: Our model is based on 10 years of experience. In particular, the starting point is the data retrieved from 212 consecutive patients in our Tinnitus Unit between May and December 2013: We found a clear auditory disorder in 74.5% of the population, muscolo-skeletal disorders and/or trigeminal disease in 57.1%, and psychiatric comorbidities in 43.8%. Different features coexisted in 59.9% of the population. RESULTS: Following such data we propose the Tinnitus Holistic Simplified Classification, which takes into account the different tinnitogenic mechanisms and the interactions between them. It differentiates tinnitus that arises from: (1) auditory alterations (Auditory Tinnitus), (2) complex auditory-somatosensory interactions (Somatosensory Tinnitus), (3) psychopathological-auditory interactions (Psychopathology-related Tinnitus), and (4) 2 or all of the previous mechanisms (Combined Tinnitus). CONCLUSIONS: In our opinion this classification provides an accurate and easy tailored path to manage tinnitus patients.


Asunto(s)
Acúfeno , Humanos , Escalas de Valoración Psiquiátrica , Reproducibilidad de los Resultados , Acúfeno/clasificación , Acúfeno/diagnóstico , Acúfeno/terapia
11.
Int J Audiol ; 51(12): 870-9, 2012 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-23013294

RESUMEN

OBJECTIVE: The aim of this study was to describe audiological and radiological characteristics, and other secondary aspects, in a family carrying a T961G mutation in the 12S rRNA mitochondrial gene. DESIGN: Case report. STUDY SAMPLE: Six members of a family participated in an audiological evaluation that included pure-tone audiometry, immittance tests, auditory brainstem responses (ABR), and otoacoustic emissions (OAE). The radiological evaluation was conducted through temporal bone CT scans using a Toshiba 16 channels Aquilon Spirale. Neuropsychiatric evaluation was also administered. RESULTS: Three participants were diagnosed with severe sensorineural hearing loss of cochlear origin and cochlear malformations visible in CT scans. One participant had a mild mixed-hearing loss and no cochlear malformations. Two participants had normal audiological and radiological findings. CONCLUSIONS: We believe our study can provide helpful insight on the clinical findings of a rare mutation, of which few data have been presented in literature.


Asunto(s)
Anomalías Múltiples , Cóclea/anomalías , Perdida Auditiva Conductiva-Sensorineural Mixta/genética , Pérdida Auditiva Sensorineural/genética , Audición/genética , Mutación , ARN Ribosómico/genética , ARN/genética , Acueducto Vestibular/anomalías , Adulto , Audiometría de Tonos Puros , Percepción Auditiva/genética , Umbral Auditivo , Niño , Preescolar , Cóclea/diagnóstico por imagen , Cóclea/fisiopatología , Potenciales Evocados Auditivos del Tronco Encefálico/genética , Femenino , Predisposición Genética a la Enfermedad , Pruebas Genéticas/métodos , Perdida Auditiva Conductiva-Sensorineural Mixta/diagnóstico , Perdida Auditiva Conductiva-Sensorineural Mixta/fisiopatología , Perdida Auditiva Conductiva-Sensorineural Mixta/psicología , Pérdida Auditiva Sensorineural/diagnóstico , Pérdida Auditiva Sensorineural/fisiopatología , Pérdida Auditiva Sensorineural/psicología , Herencia , Humanos , Lactante , Recién Nacido , Masculino , Persona de Mediana Edad , Pruebas Neuropsicológicas , Emisiones Otoacústicas Espontáneas/genética , Linaje , Fenotipo , Valor Predictivo de las Pruebas , ARN Mitocondrial , Tomografía Computarizada Espiral , Acueducto Vestibular/diagnóstico por imagen , Acueducto Vestibular/fisiopatología
12.
J Matern Fetal Neonatal Med ; 25(8): 1342-7, 2012 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-22122007

RESUMEN

OBJECTIVE: In this study, we have evaluated by means of auditory brainstem responses (ABR), in a population derived from a newborn hearing screening protocol, some aspects of maturation of the auditory pathways in the first months after birth, and the possible repercussions on early treatment. MATERIALS AND METHODS: In this retrospective study newborns were recruited through our hearing screening program, and an ABR evaluation was performed on 339 newborns, that had risk factors or had failed the screening, or both. Such population was divided in two groups for statistical analysis purposes: full-term and pre-term. The initial ABR was pathological in 70 infants. RESULTS: We observed an improvement over time of the estimated hearing threshold in follow-up ABRs in 43 newborns (26 in the full-term group, mean improvement 27.9 dB SPL, and 17 in the pre-term group, mean improvement 34.6 dB SPL); such an improvement might be related to a maturation of the auditory pathways that was not complete at birth. CONCLUSIONS: The auditory system might not be completely developed at birth, and might require some months to complete; hence any early clinical approach should consider the possibility of an overtreatment, and any therapeutic strategy should only be considered once the diagnosis is certain and definitive.


Asunto(s)
Potenciales Evocados Auditivos del Tronco Encefálico , Recien Nacido Prematuro/fisiología , Nacimiento a Término , Potenciales Evocados Auditivos del Tronco Encefálico/fisiología , Femenino , Estudios de Seguimiento , Edad Gestacional , Trastornos de la Audición/diagnóstico , Trastornos de la Audición/fisiopatología , Pruebas Auditivas/métodos , Humanos , Recién Nacido , Enfermedades del Recién Nacido/diagnóstico , Enfermedades del Recién Nacido/fisiopatología , Masculino , Tamizaje Neonatal/métodos , Observación , Estudios Retrospectivos , Nacimiento a Término/fisiología
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