Hearing performance of cochlear implant patients in noise.
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Biomedical subjects
Publications and source records attributed to W D Baumgartner.
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The aim of the study was to assess the speech discrimination ability of postlingually deaf adults implanted with the Combi 40 cochlear implant and to compare the results with the postoperative data published for other devices. The postoperative open and closed set speech perception performance of 21 consecutive patients was tested using a standardized test battery comprising a number, monosyllable, sentence, consonant and vowel discrimination test as well as a rhyme test in the sound only condition. Mean values achieved for each test 1, 6 and 12 months after "switch on" were evaluated. The results demonstrate that all patients have a substantial benefit from their implant and show a continuous improvement in their speech perception abilities with increased device experience. The mean percentages of correct answers after 12 months were 93.4 for numbers, 44.6 for monosyllables, 78.5 for sentences, 67.6 for the rhyme test, 59.8 for vowel, and 67.3 for consonant discrimination. Preoperatively, the mean discrimination score for monosyllables was 0%. The speech discrimination scores of our patients were similar or higher than described for similar patient groups implanted with other devices. The high stimulation rate of the implant system using the continuous interleaved speech processing strategy as well as a deep atraumatic electrode insertion into the apicalmost regions of the scala tympani may be the reason for good performance.
The rehabilitation of profoundly deaf patients by means of cochlear implants has become a well established form of therapy. Recently, large scale studies have pointed out a variety of surgical complications. A multiplicity of new implant types are each placing more specific demands on the surgeons. Based on the experience with about 160 cochlear implantations in total, the most suitable surgical technique for the implantation of the Combi 40 cochlear implant which has been used in 41 cases is presented. An extended retroauricular incision is made and a caudally based flap is fashioned. The implant bed is drilled 0.5-1 cm behind and above the mastoid cavity. Between the implant bed and the mastoid cavity a groove for the electrodes is drilled cranial of the implant site in the right ear and caudal in the left ear. Access to the scala tympani is gained by a promontory cochleostomy via a posterior tympanotomy of 2x3 mm. Videocontrolled microendoscopes are used to inspect the scala tympani prior to electrode insertion. Electrode insertions depths of up to 30 mm are usually achieved. The electrode and the implant are secured with ionomer-based cement. The described technique has up to now been successfully performed in 30 adults and 11 children.
PURPOSE: To assess the value of a three-dimensional (3D) T2-weighted turbo spin-echo sequence (3D T2-TSE) in comparison to conventional two-dimensional (2D) T2-weighted TSE and unenhanced and enhanced T1-weighted spin-echo sequences (SE) in imaging anatomic structures and pathologic changes of the inner ear and cerebellopontine angle. PATIENTS AND METHODS: The inner ear and cerebellopontine angle were investigated by MRI in three healthy volunteers and 18 patients performing a 2D T2-weighted turbo spin-echo sequence and a 3D T2-TSE in the axial plane. In the patient study, 2D T1-weighted SE sequences both before and after the i.v. injection of gadopentetate dimeglumine in both the axial and coronal plane were performed in addition. RESULTS: Only the 3D T2-TSE enabled an accurate imaging of the anatomic structures. In cases of pathology, the 3D T2-TSE provided additional information to the performed 2D sequences. The combination of the 3D T2-TSE with unenhanced and enhanced 2D T1-weighted SE enabled the most accurate diagnosis in cases of pathology. CONCLUSIONS: Accurate depiction of anatomic structures of the inner ear and cerebellopontine angle could be obtained by 3D T2-TSE only. The most accurate diagnosis in cases of pathology was provided by the combination of the 3D T2-TSE with unenhanced and enhanced 2D T1-weighted spin-echo sequences.
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OBJECTIVE: The aims of this study were to establish a plain radiographic technique for the assessment of the postoperative appearance, position, and insertion depth of the Combi 40 cochlear implant and to correlate the radiologic findings with surgical reports. SUBJECTS AND METHODS: In an experimental study, an electrode of the Combi 40 device was inserted into the cochlea of a cadaveric skull. Digital radiographs were obtained in a modified Chausse III projection, in which the skull was placed supine on the radiography table with the infraorbitomeatal line strictly perpendicular to the film cassette. The skull was then rotated 30 degrees away from the side to be examined, and the central X-ray beam was angled 15 degrees cephalad to the infraorbitomeatal line. On these radiographs, the point of cochleostomy was marked by a needle tip and was projected inferior to the vestibule and on a line drawn through the superior semicircular canal and the vestibule. The appearance and position of the electrode was evaluated. An electrode was defined as completely inserted if all electrode contacts projected medial to the line drawn through the superior semicircular canal and the vestibule. We also studied cochlear implant insertion of the Combi 40 device in 37 patients. Postoperative digital radiographs of these patients were obtained and analyzed for the criteria as defined in the cadaveric study. In addition, the insertion depth of the electrode and the angle of insertion were measured on the radiographs. This depth was correlated with depth of insertion as estimated at surgery. RESULTS: The cadaveric study showed that the completely inserted electrode was seen on radiographs as a nonoverlapping spiral within the cochlea. All electrode contacts projected medial to the line drawn through the superior semicircular canal and the vestibule. In all 37 patients, the electrode could be seen without overlapping. According to our criteria, a completely inserted electrode was seen in 32 patients. In these patients, the insertion depth ranged from 21 to 34 mm and the angle of insertion ranged from 350 degrees to 810 degrees. In two patients, we saw a completely inserted electrode with a bend. In three patients, an incompletely inserted electrode was seen. Excellent correlation existed between the radiologic and surgical results with regard to insertion depth (r = .92). CONCLUSION: Digital radiographs obtained in the modified Chausse III projection allow clear depiction of the electrode and avoid overlapping. Such radiographs enable a reliable and accurate assessment of the position and insertion depth of the electrode of this new cochlear implant. Such images can serve as a baseline for further radiographic examinations when extrusion or slippage of the electrode is clinically suspected.
Nitric oxide synthase (NOS) isoforms I and III were localized in the guinea pig cochlea by indirect immunohistochemistry using frozen sections and paraffin sections. NOS I staining was observed in the cytoplasm of outer hair cells, in nerve cell somata and fibers of the spiral ganglion, and in axonal profiles of the spiral lamina next to the base of inner hair cells. In addition, lining cells of the inner sulcus and limbus, and cells of the spiral ligament stained for NOS I but vascular walls remained unstained. NOS III reactivity was seen in the cytoplasm of outer and inner hair cell, in lining cells of the limbus, and on the endolymphatic surface of marginal cells. Staining for NOS III of spiral ganglion perikarya showed varying intensity. Endothelial cells of cochlear glomeruli reacted for NOS III. NOS III in vascular endothelial cells implies regulatory effects of nitric oxide (NO) on vascular wall tonus and cochlear blood supply. NOS I in cochlear neurons indicates these cells as possible sources for NO during neuronal activity. Activated neurons may provide NO that adjusts cochlear perfusion to neuronal activity. Finally, NO that is liberated from hair cells or afferent synaptic terminals may act as an inhibitor on N-methyl-D-aspartate (NMDA) receptors (negative feed-back inhibition).
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The present study evaluates the short-term effect of cochlear implantation on the fundamental frequency (FO) of 13 deaf patients. All patients were provided with the Combi 40+ cochlear implant. Voice recording was made pre- and 3 months post-implantation. The FO was analysed using X-Tools software. The results showed that 38 per cent of our subjects had a statistically significant decrease of their mean F0 (p=0.001) at 3 months following implantation. It was also observed that the patients tended to have a lower F0 postoperatively approaching the normal range of F0. A large variability in F0 was noticed among the deaf subjects but no correlation with the duration of deafness was seen. There was also no correlation between speech recognition and speech production.
Cochlear implantation has been performed for almost two decades at the Vienna University Hospital. Until 1994, single-channel implants were used (Ball-Electrode, SC6/2SC6, Vienna/Epoxy, Med-E1, Innsbruck, Austria). The development of multi-channel devices (Combi 40/40+), which provide significantly improved speech recognition performance, led to the reimplantation of some patients who had previously received single-channel implants. It was of particular interest to find out if there was a deterioration of the central "learning process" by the reimplantation from the analogue single-channel device to the tonotopic pulsatile multi-channel stimulation. In this study, we attempted to demonstrate that single-channel implants have an impact on the neural organisation of the auditory system. Two groups of post-lingually deaf adult patients were tested. Group A had previously received single-channel implants and were reimplanted with the new Combi 40/40+ cochlear implant (Med-E1, Innsbruck, Austria) in the same ear. Group B was implanted only with the Combi 40/40+. Six different speech recognition tests were subsequently performed on all patients, and the two groups performed similarly. Furthermore, it was discovered that group A obtained significant speech recognition improvement (p<0.05) with monosyllabic words and number tests 1 month following reimplantation.
It is possible for most post-lingually deaf patients to attain significant open speech recognition following cochlear implantation. In contrast, many severely-profoundly sensorineural hearing-impaired patients receive no benefit from their hearing aids, especially in situations with background noise. The aim of the study was to evaluate the speech recognition ability in quiet and in noise of post-lingually deaf adults implanted with Combi 40/40+ cochlear implants versus severely-profoundly sensorineural hearing-impaired patients fitted with hearing aids. For this purpose, we tested two groups of patients: one that had received cochlear implants (n=22) and a group of subjects with severe-profound sensorineural hearing impairment, fitted with hearing aids (n = 15). All of the patients were tested using the Hochmaier, Schultz, and Moser Discrimination Test in quiet and noise. The results of the study demonstrate that most of our cochlear implant patients received a substantial benefit from their implant, achieving scores of 70 to 100 per cent (mean, 90 per cent) for the numbers test and 10 to 72 per cent (mean, 43 per cent) for the monosyllable test 1 year after implantation. Even in situations with background noise, scores of 1 to 99 per cent (mean, 45.65 per cent) for a signal to noise ratio (SNR) of +15 dB 1 year following the implantation improved to 7 to 95 per cent (mean, 50.7 per cent) at 2 years and 8 to 99 per cent (mean, 60 per cent) at 3 years after implantation. These results are significantly (p<0.04) superior to the hearing aid patients' scores of 1 to 64.2 per cent (mean, 26.7 per cent) for a SNR of 15 dB. The results of the present study may have clinical implications in regard to selection of candidates for cochlear implantation.