Results 31 to 40 of about 8,137 (207)

Transmastoid Ultrasound Detection of Middle Ear Effusion and Its Association with Clinical Audiometric Tests

open access: yesLife, 2022
Medical history taking, otoscopy, tympanometry, and audiometry are clinical methods to diagnose middle ear effusion (MEE); however, these procedures are experience-dependent and result in misdiagnosis under unfavorable conditions of the external auditory
Chin-Kuo Chen   +3 more
doaj   +1 more source

Clinical benefit of wideband-tympanometry: a pediatric audiology clinical study

open access: yes, 2019
Wideband-tympanometry (WBT) could give more informative data about the tympanic condition than the conventional tympanometry. In the actual literature, the clinical profit of wideband-tympanometry in pediatric audiological settings is not well evaluated.
Läßig, Anne   +5 more
core   +1 more source

Delayed-onset hearing loss in first-grade students who previously passed the newborn hearing screening

open access: yesFrontiers in Pediatrics
IntroductionNewborn hearing screening is essential for the early detection of hearing loss, enabling timely intervention that supports communication and academic success.
Reem Elbeltagy   +6 more
doaj   +1 more source

Wideband Tympanometry [PDF]

open access: yesAnnals of Otology and Neurotology, 2018
AbstractTraditional tympanometry done with 226 Hz probe tone frequency has some inherent defects and limitations due to which it does not give a very true picture of the middle ear status, and tympanometric findings are often very deceptive. It is not uncommon for otologists to find that on opening the middle ear, the pathology in the middle ear is ...
Nilotpal Dutta, Anirban Biswas
openaire   +1 more source

Machine Learning‐Based Risk Stratification Tool for Hearing Loss in High‐Risk Neonates

open access: yesThe Laryngoscope, EarlyView.
Machine learning models, particularly XGBoost, provide robust risk stratification for neonatal hearing loss by capturing complex interactions among clinical risk factors such as NICU stay duration and family history. To translate these predictive capabilities into routine practice, an open‐access web‐based clinical decision support tool was developed ...
Sevgi Kutlu   +4 more
wiley   +1 more source

Audiological assessment in patients with chronic obstructive pulmonary disease

open access: yesThe Egyptian Journal of Bronchology, 2017
Background Chronic obstructive pulmonary disease (COPD), as a multisystemic disease, might have an impact on the auditory function. Thus, this study was designed for the audiological assessment of COPD patients to investigate the effect of smoking, and ...
Aya M. Abdel Dayem   +3 more
doaj   +1 more source

Progressive auditory neuropathy in patients with Leber's hereditary optic neuropathy [PDF]

open access: yes, 2004
Objective: To investigate auditory neural involvement in patients with Leber's hereditary optic neuropathy (LHON).Methods: Auditory assessment was undertaken in two patients with LHON.
Luxon, LM, Ceranic, B
core  

Contribution of Treatment with Ear Popper for Hearing in Children with Middle Ear Effusion

open access: yesChildren
Objectives: we aim to assess the contribution of the EarPopper device to hearing in children with middle ear effusion (MEE). Methods: The study has three parts, including 1.
Ronit Priner, Ophir Ilan
doaj   +1 more source

The Philippine National Ear Institute: Patient and Audiologic Profiles

open access: yesPhilippine Journal of Otolaryngology Head and Neck Surgery, 2007
Background:  The Philippine National Ear Institute (PNEI) was created to promote health of hearing and balance among Filipinos.  Over the years it,  has provided audiologic services to thousands of patients annually and has published relevant hearing and
Regie Lyn P. Santos-Cortez   +9 more
doaj   +1 more source

The Audiologic and Otolaryngologic Phenotype in WHIM Syndrome

open access: yesOtolaryngology–Head and Neck Surgery, EarlyView.
Abstract Objective WHIM syndrome (warts, hypogammaglobulinemia, infections, and myelokathexis syndrome) is an ultra‐rare primary immunodeficiency disease caused by autosomal dominant hyperfunctional mutations in the chemokine receptor CXCR4. Otolaryngologists are frequently consulted to evaluate WHIM patients because of recurrent acute ear and sinus ...
Christopher K. Zalewski   +7 more
wiley   +1 more source

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