| Literature DB >> 28050216 |
Juan Carlos Cisneros Lesser1, Rubens Vuono de Brito Neto2, Graziela de Souza Queiroz Martins2, Ricardo Ferreira Bento2.
Abstract
Introduction Middle fossa approach has been suggested as an alternative for patients in whom other routes of electrode insertion are contraindicated. Even though there are temporal bone studies about the feasibility of introducing the cochlear implant through the middle fossa, until now, very few studies have described results when cochlear implant surgery is done through this approach. Objective The objective of this study is to review a series of temporal bone studies related to cochlear implantation through the middle fossa and the results obtained by different surgical groups after cochlear implantation through this approach. Data Sources PubMed, MD consult and Ovid-SP databases. Data Synthesis A total of 8 human cadaveric temporal bone studies and 6 studies reporting cochlear implant surgery through the middle fossa approach met the inclusion criteria. Temporal bone studies show that it is feasible to perform cochlear implantation through this route. So far, only two surgical groups have performed cochlear implantation through the middle fossa with a total of 15 implanted patients. One group entered the cochlea in the most upper part of the basal turn, inserting the implant in the direction of the middle and apical turns; meanwhile, the other group inserted the implant in the apical turn directed in a retrograde fashion to the middle and basal turns. Results obtained in both groups were similar. Conclusions The middle fossa approach is a good alternative for cochlear implantation when other routes of electrode insertion are contraindicated.Entities:
Keywords: cochlear implants; deafness; middle fossa approach; sensorineural hearing loss
Year: 2016 PMID: 28050216 PMCID: PMC5205528 DOI: 10.1055/s-0036-1582266
Source DB: PubMed Journal: Int Arch Otorhinolaryngol ISSN: 1809-4864
Patient description and results obtained with cochlear implantation through the middle fossa by two surgical groups
| Patient description and results obtained | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| # | Author | Gen | Age | Cause of deafness | Dur | Implant / side | Follow-up | Free-field hearing threshold average | Open set sentence recognition (%) |
| 1 | Colleti et al | M | 58 | Fibro-adhesive otitis media | 3 R 6 L | Laura-Flex / L | 9 months | N/A** | 90% |
| 2 | M | 39 | Head trauma | 18 R 10 L | Laura-Flex / L | 6 months | N/A** | 75% | |
| 3 | M | 20 | Genetic (prelingual) | 20 R 20 L | Laura-Flex / R | 6 months | N/A** | 50% | |
| 4 | M | 66 | Chronic ear disease | 12 R 40 L | Nucleus CI24M / R | 9 months | N/A** | 85% | |
| 5 | F | 19 | Cogan syndrome | 2 R 2 L | Nucleus CI24M / R | 6 months | N/A** | 75% | |
| 6 | M | 18 | Genetic (prelingual) | 18 R 18 L | Nucleus CI24M / L | 6 months | N/A** | 70% | |
| 7 | M | 23 | Genetic (prelingual) | 23 R 23 L | Nucleus CI24M / R | 1 month | N/A** | 40% | |
| 8 | M | 57 | Otosclerosis | 4 R 4 L | Nucleus CI24M / L | 3 months | N/A** | 60% | |
| 9 | M | 24 | Cogan syndrome | 0.5 R 0.5 L | Combi 40+ double array / R | 6 months | N/A** | 75% | |
| 10 | F | 9 | Genetic (prelingual) | 9 R 9 L | Combi 40+ double array / L | 3 months | N/A** | 30% | |
| 11 | M | 13 | Genetic (prelingual) | 13 R 13 L | Combi 40+ double array / L | 1 month | N/A** | 35% | |
| 12 | Bento et al | M | 38 | Chronic ear disease | 4 R 4 L | Nucleus 24 R (ST) / L | *mean 23 months | 36.25 dB | 100% |
| 13 | F | 61 | Chronic ear disease | 6 R 5 L | Nucleus 24 RE (ST) / L | *mean 23 months | 37.5 dB | 30% | |
| 14 | F | 46 | Ototoxicity and chronic ear disease secondary to radiotherapy | 6 R 6 L | Nucleus 24 RE (ST) / R | *mean 23 months | 38.3 dB | 90% | |
| 15 | F | 46 | Chronic ear disease | 26 R 26 L | Med-El Sonata Medium / L | *mean 23 months | 47.5 dB | 50% | |
Abbreviations: F, female; M, male; Gen, gender; y, years; Dur, duration of deafness before implantation; L, left ear; R, right ear.
Note: The cause of deafness is described as well as the time of deafness before implantation. The implanted side and implant model used are described.
*In the article by Bento et al,13 there is no specific description of the follow-up time, only the mean for the 4 patients.
**Colleti et al9 10 11 12 do not describe free field hearing thresholds.