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1.
Cureus ; 11(12): e6279, 2019 Dec 03.
Artigo em Inglês | MEDLINE | ID: mdl-31911872

RESUMO

Background The selection of an appropriate imaging technique for assessment before cochlear implantation is critical for precise diagnosis and management. While magnetic resonance imaging (MRI) is used for the diagnosis of several conditions, such as labyrinthitis ossificans, cochlear nerve deficiency, and neoplasms, high-resolution computed tomography (HRCT) provides excellent details of the temporal bone. However, it remains unclear whether routine MRI provides any additional benefits over HRCT. Objectives To assess the added value of MRI as a screening tool for temporal bone abnormalities in cochlear implant candidates through comparisons of its findings with those of HRCT. Materials and method It is a retrospective analysis of preoperative HRCT and MR images in a tertiary referral center. A total of 308 patients who underwent MRI and HRCT examinations before cochlear implantation between 2013 and 2015 were included. Preoperative HRCT and MR images were screened for temporal bone abnormalities by a senior neurotologist and a neuroradiologist. Results HRCT detected inner ear deformities in 51 of the 308 (16.6%) subjects, whereas MRI revealed abnormalities in only 18 (5.8%) of subjects. HRCT detected the same inner abnormalities in 16 of the 18 (88.9%) subjects diagnosed by MRI, whereas it showed normal results for the remaining two subjects. MRI detected cochlear nerve aplasia/hypoplasia in 13 subjects, 11 of whom had associated inner ear deformities that were detected by HRCT. The MR images of nine subjects showed cochlear fibrosis, which was confirmed by HRCT in all nine subjects. Conclusion In this study, MRI did not exhibit significant additional benefits over HRCT, and its routine use for the preoperative assessment of CI candidates was not justified. However, MRI is warranted for subjects at an increased risk of cochlear nerve aplasia due to an inner ear deformity or a narrow internal auditory canal. The establishment of criteria that facilitate the performance of MRI only when absolutely needed will reduce healthcare costs, prevent unnecessary exposure to the risks associated with general anesthesia, and shorten delays before cochlear implantation.

2.
Indian J Otolaryngol Head Neck Surg ; 64(2): 142-4, 2012 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-23730574

RESUMO

The objective of this study was to report our preliminary experience with an alternative technique for cochlear implantation. Twenty patients underwent cochlear implantation via a trans-aditus ad antrum approach to the round window. The main steps involved in the surgical procedure are cortical mastoidectomy, elevation of tympanomeatal flap, incudostapedial joint dislocation, incus removal, preparation of a bed for the implant, cochleostomy via the external auditory canal, and finally insertion of the electrode into the cochlea via the aditus. Twenty-five implants were performed on 20 patients, 18 children (mean age of 3.2 years) and 2 adults. Twelve patients were males and eight were females. All the children were pre-lingual while the adults were post-lingual. Nucleus freedom cochlear implant system (Cochlear, Lane Cover, NSW, Australia) was used in four patients and a cochlear Nucleus 5 was used in six patients. A Med-el SONATA implant (MED-EL, Innsbruck, Austria) was used in 15 patients. The minimum follow-up was 5 months. Here, we describe a new alternative technique for cochlear implantation and report our preliminary results. The procedure has advantages over the existing techniques and avoids the potential complications of posterior tympanotomy, transcanal, and transmeatal techniques.

3.
Skull Base ; 16(2): 95-100, 2006 May.
Artigo em Inglês | MEDLINE | ID: mdl-17077873

RESUMO

AIM OF STUDY: To identify those patients with vestibular schwannoma (acoustic neuroma) in whom treatment becomes necessary. METHOD: Retrospective chart review. RESULT: A total of 205 patients with small tumors were followed for a mean of 40.8 months. The longest follow-up was 180 months. One hundred and ninety-seven patients had a follow-up of more than 12 months. Eight patients with a follow-up of less than 12 months were excluded from the study. In 136 patients (66.3%) the tumor did not grow. Forty-seven patients (23.9%) showed some evidence of slow growth. Eight of 197 patients (4%) had rapid growth and 6 patients (3%) had radiological evidence of tumor regression. Fifteen patients came to surgery. Five of these showed rapid growth, four developed ataxia in whom tumor growth was slow, three had ataxia without tumor growth, two patients developed brainstem compression, and one patient elected to proceed to surgery, although there were no tumor growth or symptoms. CONCLUSION: Few patients with small tumors will come to surgery in the short term. Perhaps the majority of patients with such small tumors will not need surgery. Long-term follow-up studies of 20 years or more are required to be come more confident about the natural history of these tumors. This study continues.

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