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Objectives This document presents the fundamentals of speech audiometry in noise, general requirements for implementation and criteria for choice among the tests available in French according to the health-professional's needs. Material and methods The recommendations are based on a systematic analysis of the literature carried out by a multidisciplinary group of doctors, audiologists and audioprosthetists from all over France. They are graded A, B, C or expert opinion according to decreasing level of scientific evidence. Results Eight tests of speech audiometry in noise can be used in France. Conclusion To be complete, evaluation of hearing status requires testing understanding of speech in noise. The examination must begin with a minimum of two measurements familiarizing the subject with the test procedure. For initial diagnosis, adaptive procedures establishing the 50% speech reception threshold (SRT50) in noise are to be preferred in order to obtain a rapid and standardized measurement of perception of speech in noise. When the aim is to measure real-life speech comprehension, tests based on sentences, cocktail-party noise and free-field stimulation are to be preferred. Prosthetic gain is evaluated exclusively in free field. This is the only way to evaluate the contribution of binaurality and to measure perception in noise in an environment as close as possible to real life. In order to avoid acoustic interference in free field, at least five loudspeakers should be used, in particular for evaluating the effectiveness of directional microphones, CROS devices enabling sounds picked up in the damaged ear to be rerouted to the functional ear, or bimodal fitting (i.e., when hearing is enabled by two modalities: for example, hearing aid for one ear, cochlear implant for the other).

Objectifs Dans le contexte de l’épidémie de SARS-CoV-2, les patients présentant des pathologies relevant de l’otoneurologie médicale ont pu être dissuadés de consulter, s’exposant ainsi à un risque de perte de chance. Ce guide de conseils de bonne pratique vise à définir l’apport de la téléconsultation à l’évaluation de l’adulte ou de l’enfant vertigineux, et à préciser les éléments recueillis à distance devant conduire à une prise en charge médicale rapide. Méthodes Ces conseils de bonne pratique reposent sur l’expérience des auteurs ainsi qu’une revue de la littérature. Le recensement des solutions de télémédecine adaptées à l’otoneurologie a été effectué sur la base d’une requête par moteur de recherche datant de mars 2020. Résultats La première évaluation clinique du patient vertigineux ne peut être réussie en téléconsultation que si les conditions suivantes sont réunies : prise de contact préalable pour vérifier la faisabilité de l’évaluation à distance, présence indispensable d’un aidant auprès du patient, possibilité de réaliser des enregistrements vidéos. Que ce soit chez l’adulte ou chez l’enfant, et de façon identique à l’évaluation présentielle, l’anamnèse permet d’apprécier le type, la durée, la fréquence et les circonstances de survenue du vertige. Lors de la téléconsultation peuvent être réalisés des tests d’oculomotricité, une recherche de nystagmus, une évaluation de la posture, des tests neurologiques simplifiés, la mise en évidence d’un vertige positionnel voire son traitement. Chez l’enfant doivent être recherchés en priorité des antécédents de surdité ou ophtalmologiques, un contexte fébrile ou traumatique, une otorrhée, des signes d’irritation méningée. Conclusion La télémédecine en otoneurologie trouve sa légitimité dans la fiabilité d’un bilan clinique, basé sur l’interrogatoire et quelques tests élémentaires, incitant à proposer des algorithmes décisionnels adaptés à la téléconsultation. Cette dernière comporte néanmoins des limites lors d’un premier épisode vertigineux en urgence, si bien qu’elle ne peut se substituer, dans un certain nombre de cas, à une consultation en présentiel. Elle est souvent adaptée pour le suivi de patients vertigineux sélectionnés par une évaluation présentielle initiale.

Objectives In the context of the SARS-CoV-2 pandemic, patients may have been dissuaded from seeking consultation, thus exposing themselves to a risk of loss of chance. This guide aims to define how teleconsultation can assist in assessing vertiginous adults or children, and to gather the information needed to provide quick medical care. Methods These recommendations rely on the authors’ experience as well as on literature. A survey on otoneurologic approach via telemedicine has been conducted based on a literature search until March 2020. Results The first clinical assessment of the vertiginous patient via teleconsultation can only be successful if the following conditions are met: initial contact to verify the feasibility of the assessment at a distance, the presence of a caregiver in order to assist the patient, the possibility of making video recordings. Medical history via telemedicine, as in a face-to-face assessment, allows to assess the characteristics, duration, frequency, and potential triggering factors of the vertigo, in both children and adults. During teleconsultation, the following tests can be carried out: oculomotricity evaluation, assessment of balance, simple neurological tests, checking for positional vertigo/nystagmus and, eventually to perform canalith-repositioning procedures. In children, the following should be searched for: history of hearing or visual impairment, a context of fever or trauma, otorrhea, signs of meningeal irritation. Conclusion The neurotologic telemedicine relies on the accuracy of the clinical assessment, which is based on history taking and a few simple tests, encouraging the development of a decision-making algorithm adapted for teleconsultation. However, the latter has its limitations during an emergency examination of a new patient presenting vertigo, and, at least in some cases, cannot replace a face-to-face consultation. Teleconsultation is often adapted for follow-up consultations of previously selected vertiginous patients during face-to-face assessment.

Resume Objectifs Durant l’epidemie de Covid-19, l’acces au diagnostic et aux soins des pathologies relevant de l’audiologie medicale a regresse en France, posant un risque de perte de chance pour le patient. Ce guide de conseils de bonne pratique vise a repertorier les solutions techniques existantes permettant d’examiner a distance le patient presentant une plainte en audiologie et a decrire leurs interets et, le cas echeant, leurs limites. Methodes Les conseils ont pu etre elabores a la fois a partir de l’experience clinique des experts medicaux ayant participe a la redaction du guide, et d’une revue extensive de la litterature portant sur les recommandations de pratique clinique en tele-audiologie. Les solutions de tele-audiometrie ont ete recensees sur la base d’une requete par moteur de recherche effectuee en avril 2020, avant verification de leur disponibilite sur le marche europeen. Resultats Des solutions de video-otoscopie permettent la tele-transmission d’images compatibles avec un diagnostic de qualite soit en se connectant via internet a une plate-forme de tele-soin, soit via un smartphone ou une tablette utilisant un systeme d’exploitation iOS ou Android. Selon les memes modalites, il est possible de realiser a distance un examen audiometrique tonal dans les regles de l’art, une audiometrie vocale dans le silence ou dans le bruit ainsi que des explorations fonctionnelles objectives de l’audition. Les examens cliniques et paracliniques peuvent etre consultes par le medecin de facon differee pour etre interpretes (tele-audiologie asynchrone). Ils peuvent aussi etre realises en temps reel chez un patient, a tout âge de la vie, a condition qu’un aidant puisse etre present durant l’installation des transducteurs ou la realisation de l’acoumetrie (tele-audiologie synchrone). Les solutions de teleaudiologie trouvent egalement une application dans la formation a distance des futurs professionnels de sante engages dans la prise en charge des pathologies de l’audition. Conclusion Dans la legislation francaise, la tele-otoscopie est un acte medical qui releve soit de la tele-expertise (avis asynchrone) soit d’un acte de teleconsultation (avis synchrone). L’evaluation subjective et objective de la fonction auditive du patient est aujourd’hui possible a distance a condition de respecter les precautions listees.

International audience; Objectives: Access to diagnosis and treatments for auditory disorders and related pathologies has regressed in France during the COVID-19 pandemic, posing a risk to the patient's chance of recovery. This best practice recommendations guide aims to list the existing technological solutions for the remote examination of a patient with hearing complaint, and to outline their benefits and, where applicable, their limitations.Methods: The recommendations were developed both from the clinical experience of the medical experts who drafted the guide, and from an extensive review of the literature dealing with clinical practice recommendations for tele-audiology. Tele-audiometry solutions were identified on the basis of a search engine query carried out in April 2020, prior to verification of their availability on the European market.Results: Video otoscopy solutions allow for the teletransmission of images compatible with a high-quality diagnosis, either by connecting via internet to a tele-health platform or using a smartphone or a tablet with an iOS or Android operating system. Using the same telecommunication methods, it is possible to remotely conduct a pure-tone audiometry test in accordance with standard practice, a speech-in-quiet or a speech-in-noise audiometry test, as well as objective measures of hearing. Clinical and paraclinical examinations can be accessed by the physician to be interpreted on a deferred basis (asynchronous tele-audiology). Examinations can also be conducted in real time in a patient, at any age of life, as long as a caregiver can be present during the installation of the transducers or the acoumetry. Tele-audiology solutions also find application in the remote training of future healthcare professionals involved in the management of deafness and hearing impairment.Conclusion: Under French law, tele-otoscopy is a medical procedure that is either a tele-expertise (asynchronous adive) or a teleconsultation act (synchronous advice). Subjective and objective evaluation of the patient's hearing functions can be done remotely provided that the listed precautions are respected.

Resume Introduction Consensus de la SFORL concernant les bonnes pratiques de la realisation d’un examen audiometrique chez l’adulte et l’enfant. Methodes Un groupe de travail multidisciplinaire a effectue une revue de la litterature. Des recommandations ont ete erigees, relues par un groupe de lecture independant du groupe de travail et finalisees lors d’une reunion de synthese. Resultats Il est recommande de realiser les examens audiometriques dans un environnement sonore maitrise (

Objective To investigate the hearing performance of adult patients presenting unilateral deafness with contralateral fluctuating hearing loss who received a cochlear implant on the deaf side. Study Design Case series with chart review. Setting University tertiary referral center. Subjects and Methods Preoperatively and at 6 and 12 months postoperatively, 23 patients underwent pure tone audiometry and speech audiometry with disyllabic and monosyllabic words in a quiet environment and sentences in quiet and noisy (signal-to-noise ratio +10 dB SPL) environments under best-aided conditions. The Abbreviated Profile of Hearing Aid Benefit (APHAB) inventory was evaluated preoperatively and at 6 and 12 months postoperatively. Results No difference was found between pre- and postoperative tests for disyllabic and monosyllabic words. For sentences in quiet and noisy environments, a difference between pre- and postoperative performance was present at 1 year ( P = .002 and P = .02, respectively). In a noisy environment, a difference was present at 6 and 12 months postoperatively as compared with the preoperative value (mean ± SD: 6 months: 42% ± 7.1% vs 61% ± 6.5%, P = .016). A significant improvement in the APHAB score was found at 6 and 12 months postimplantation (Friedman's 2-way analysis of variance by ranks, P < .001). The number of years of hearing deprivation of the deaf ear was not correlated with performance. Conclusion When incapacitating fluctuating hearing loss occurs in patients presenting a contralateral deaf ear, a cochlear implant is indicated in the latter ear, significantly improving performance in noisy conditions and allowing a better quality of communication to be achieved.

The impact of hearing loss and of auditory rehabilitation (hearing aid, cochlear implant) on quality of life is a crucial issue. Commonly used questionnaires to assess quality of life in these patients (Nijmegen, APHAB, GBI) are time-consuming, difficult for patients to fill out, and show poor sensitivity to small improvements or deterioration. The objective of the present study was to validate a dedicated quality of life scale for hearing-impaired adults with or without auditory rehabilitation.ERSA (Évaluation du Retentissement de la Surdité chez l'Adulte: Evaluation of the Impact of Hearing Loss in Adults) is a self-administered questionnaire. It is divided into 4 domains, each comprising 5 questions graded from 1 to 10. The questions are simple, and formulated so patients will answer according to how they feel at the actual time of the session. Test-retest reliability was measured in 38 patients. Internal coherence and validity against the APHAB questionnaire as gold standard and in relation to hearing performance were measured in 122 patients at auditory assessment. Sensitivity to change in hearing was measured in 36 cochlear implant patients, before and 6 or 12 months after implantation.Test-retest reliability was very satisfactory (ρ=0.88). Internal coherence was good for all questions. External validity, comparing ERSA to APHAB scores in the same non-implanted hearing-impaired patients, was good (ρ=0.52). Additionally, ERSA scores correlated with hearing performance in adverse conditions (monosyllabic words: ρ=0.22; sentences in noise: ρ=0.19). In patients tested before and after cochlear implantation, improvement in hearing performance in silence and in noise correlated with an improvement in ERSA score (ρ=0.37 to 0.59, depending on the test), but not to GBI score.The ERSA questionnaire is easy and quick to use, reliable, and sensitive to change in hearing performance after cochlear implantation.

Resume Objectifs L’evaluation de l’impact de la surdite et de sa rehabilitation (aides auditives, implant cochleaire) sur la qualite de vie est fondamentale. Les questionnaires couramment utilises (Nijmegen, Aphab, GBI) sont longs, compliques a remplir et peu sensibles aux faibles ameliorations/deteriorations. L’objectif de cette etude est de valider une echelle de qualite de vie destinee aux patients adultes presentant une perte auditive qu’elle soit rehabilitee ou non. Materiel et methodes Le questionnaire d’evaluation du retentissement de la surdite chez l’adulte (Ersa) est un questionnaire auto-administre, divise en quatre sous-domaines comprenant chacun cinq questions notees de 1 a 10. Les questions sont simples et formulees de facon a ce que le patient reponde a l’instant present. La fiabilite test-retest d’Ersa a ete mesuree chez 38 patients. La coherence interne et la validite par rapport au questionnaire Aphab et aux performances auditives ont ete mesurees chez 122 patients lors du bilan de surdite. La sensibilite au changement a ete mesuree chez 36 patients avant et 6 a 12 mois apres l’implantation cochleaire. Resultats La fiabilite du questionnaire Ersa (test/retest) est tres satisfaisante (ρ = 0,88). La coherence interne est bonne pour l’ensemble des questions. La validite de structure externe, etudiee en comparant, chez les patients sourds non implantes, les scores Ersa a ceux du questionnaire Aphab, est bonne (ρ = 0,52). Le score Ersa est correle aux performances auditives dans des situations d’ecoute difficiles (mots monosyllabiques : ρ = 0,22 ; phrases dans le bruit : ρ = 0,19). Chez les patients testes avant et apres implantation, l’amelioration des performances auditives dans le silence et dans le bruit est correlee a l’amelioration du score Ersa (ρ = 0,37 a 0,59 selon les tests), mais pas au score GBI. Conclusion Le questionnaire Ersa est un outil facile, rapide d’utilisation, fiable et sensible au changement des performances auditives apres une implantation cochleaire.

Resume Objectifs Les auteurs exposent les recommandations de la Societe francaise d’oto-rhino-laryngologie et de chirurgie de la face et du cou (SFORL) concernant la strategie diagnostique et therapeutique dans la maladie de Meniere. Methodes Un groupe de travail multidisciplinaire a ete charge d’effectuer une revue de la litterature scientifique sur la thematique etudiee. Les recommandations ont ete redigees, puis relues par un groupe de lecture independant du groupe de travail. Les recommandations proposees ont ete classees en accord avec le guide d’analyse de la litterature et de gradation des recommandations, publie par l’ANAES (janvier 2000). Resultats Le diagnostic de la maladie de Meniere est pose devant l’association des quatre plaintes cliniques classiques et en l’absence d’une autre cause decelable par IRM. En cas de tableau clinique incomplet, il est recommande de realiser les tests d’explorations audio-vestibulaires objectifs. La prise en charge therapeutique comporte des traitements medicaux et chirurgicaux, conservateurs ou destructeurs de la fonction vestibulaire. La prise en charge medicale repose sur l’hygiene de vie, la betahistine, les diuretiques et l’injection transtympanique de corticoides et/ou de gentamicine. Les principaux moyens chirurgicaux disponibles sont par ordre d’agressivite la chirurgie du sac endolymphatique, la neurotomie vestibulaire et la labyrinthectomie.

Objective To evaluate the efficacy of portable Meniett low-pressure pulse generator (Medtronic Xomed, Jacksonville, FL) in Meniere disease. Study Design Randomized, double-blind, placebo-controlled, multicenter trial carried out in 17 academic medical centers. Methods One hundred twenty-nine adults presenting Meniere disease (American Academy of Otolaryngology–Head and Neck Surgery criteria) not controlled by conventional medical treatment were included. The protocol included three phases: 1) placement of a transtympanic tube and evaluation of its effect (if resolution of symptoms, the patient was excluded); 2) randomization: 6-weeks treatment with Meniett (Medtronic Xomed) or placebo device; 3) removal of the device and 6-week follow-up period. The evaluation criteria were the number of vertigo episodes (at least 20 minutes with a 12-hour free interval) and the impact on daily life as assessed by self-questionnaires. Results Ninety-seven patients passed to the second phase of the study: 49 and 48 patients received the Meniett (Medtronic Xomed) or the placebo device, respectively. In the placebo group, the number of vertigo episodes decreased from 4.3 ± 0.6 (mean ± standard error of the mean) during the first phase to 2.6 ± 0.5 after 6 weeks of treatment, and to 1.8 ± 0.8 after the removal of the device. Similar results were observed in the Meniett device (Medtronic Xomed) group: 3.2 ± 0.4 episodes during the first phase, 2.5 ± after 6 weeks of Meniett device (Medtronic Xomed) treatment, and 1.5 ± 0.2 after the third phase. Conclusion An improvement of symptoms was evidenced in all patients, with no difference between the Meniett (Medtronic Xomed) and the placebo device groups. The decrease in the number of vertigo episodes could be explained by an effect of the medical care. Level of Evidence 1b. Laryngoscope, 2016 127:470–475, 2017

Objectives The present study assessed the interest of a contralateral hearing aid (HA) in adult cochlear implant (CI) bearers. Material and methods The study recruited 10 French-speaking adult HA bearers with postlingual bilateral hearing loss, fitted for at least 2 years with a unilateral CI after loss of benefit from HA in one ear but continuing to use their contralateral HA: 4 male, 6 female; mean age, 58 years. All had regularly used bilateral HAs prior to CI. Audiometric assessment comprised: (1) individual ear hearing assessment on pure-tone audiometry and speech discrimination; and (2) free-field testing without aid, with CI only, with HA only and with CI plus HA, on pure-tone audiometry and speech discrimination with quiet background and on speech discrimination in noise. Results Speech discrimination was significantly improved in the bimodal condition (CI plus HA) as compared to CI alone, on all tests. In quiet, discrimination for disyllabic words was > 50% in 7 cases with HA alone, in 2 cases with CI alone and in 1 case in with HA + CI. Under 0 dB signal-to-noise ratio, discrimination was > 50% in 1 case with HA alone, in 3 cases with CI alone and in 6 cases with HA + CI. Conclusion The present results showed benefit in auditory perception in quiet and in noise with bimodal stimulation. When there is residual hearing in the non-implanted ear, a HA should be fitted; and in progressive bilateral hearing loss, CI should be suggested when HA benefit decreases in one ear.

Resume Objectifs L’objectif de cette etude etait de montrer l’interet et les benefices obtenus par l’utilisation d’une aide auditive controlaterale chez des adultes porteurs d’un implant cochleaire (IC). Materiel et methodes L’etude a porte sur une population d’adultes implantes cochleaires unilateraux, pour une surdite post-linguale bilaterale, avec perte du benefice prothetique d’un cote et poursuite de l’utilisation d’une aide auditive (AA) controlaterale. Il s’agissait de 10 adultes francophones, 4 hommes et 6 femmes, dont la moyenne d’âge etait de 58 ans. Ils etaient implantes depuis 2 ans au moins. Tous les patients utilisaient regulierement des AA bilaterales anterieurement a l’implantation cochleaire. L’evaluation audiometrique a comporte : (1) une evaluation de l’audition residuelle oreilles separees (tonale et vocale), (2) des tests en champ libre : « oreilles nues », IC seul, AA seule et IC et AA, en tonale, vocale dans le calme et vocale dans le bruit. Resultats Les resultats obtenus ont montre que l’intelligibilite etait significativement superieure en condition bimodale, IC et AA, par rapport a ceux obtenus avec l’IC seul, dans tous les tests realises. Dans le calme, les resultats ont montre une intelligibilite qui etait superieure a 50 % pour des mots dissyllabiques, dans 7 cas avec la seule AA, 2 cas avec l’IC et un cas en condition bimodale : IC et AA. Les tests realises avec un rapport signal/bruit a 0 dB ont montre un niveau de comprehension superieur a 50 %, pour un patient avec uniquement son AA, pour 3 d’entre eux avec l’IC et pour 6 en condition bimodale. Conclusion Les resultats obtenus ont montre l’interet du port de l’AA controlaterale a l’IC en termes d’amelioration de la perception auditive dans le calme et le bruit. En cas d’audition residuelle controlaterale a l’IC, une AA doit etre proposee ; et dans les surdites bilaterales progressives, l’IC doit etre proposee des que le patient perd le benefice de l’AA d’un des cotes.

International audience; INTRODUCTION: French Society of ENT (SFORL) good practice guidelines for audiometric examination in adults and children. METHODS: A multidisciplinary working group performed a review of the scientific literature. Guidelines were drawn up, reviewed by an independent reading group, and finalized in a consensus meeting. RESULTS: Audiometry should be performed in an acoustically controlled environment (\textless30dBA); audiometer calibration should be regularly checked; and patient-specific masking rules should be systematically applied. It should be ensured that masking is not overmasking. Adult pure-tone audiometry data should be interpreted taking account of clinical data, speech audiometry and impedancemetry. In case of discrepancies between clinical and pure-tone and speech audiometry data, objective auditory tests should be perform. In children aged 2 years or younger, subjective audiometry should be associated to behavioral audiometry adapted to the child's age. In suspected hearing impairment, behavioral audiometry should be systematically supplemented by objective hearing tests to determine and confirm the level and type of hearing impairment.

Objectives The authors present the guidelines of the French Otorhinolaryngology-Head and Neck Surgery Society ( Societe francaise d’oto-rhino-laryngologie et de chirurgie de la face et du cou : SFORL) for diagnostic and therapeutic strategy in Meniere's disease. Methods A work group was entrusted with a review of the scientific literature on the above topic. Guidelines were drawn up, then read over by an editorial group independent of the work group. The guidelines were graded according to the literature analysis and recommendations grading guide published by the French National Agency for Accreditation and Evaluation in Health (January 2000). Results Meniere's disease is diagnosed in the presence of the association of four classical clinical items and after eliminating differential diagnoses on MRI. In case of partial presentation, objective audiovestibular tests are recommended. Therapy comprises medical treatment and surgery, either conservative or sacrificing vestibular function. Medical treatment is based on lifestyle improvement, betahistine, diuretics or transtympanic injection of corticosteroids or gentamicin. The main surgical treatments, in order of increasing aggressiveness, are endolymphatic sac surgery, vestibular neurotomy and labyrinthectomy.

Aim of the study To present three pediatric cases of auditory brainstem implantation (ABI) and review literature data concerning this topic. Patients The first two children had a neurofibromatosis type II with bilateral sensorineural deafness; in both cases, the implant was inserted during the surgical removal of a vestibular schwannoma; the third patient had profound deafness due to bilateral cochlear nerve insufficiency associated with inner ear malformation. Results Two postoperative complications were observed: patient 1 had a persistent fever which required the replacement of the fat graft used to seal the translabyrinthine approach; patient 3 had a CSF leakage requiring additional surgery and lumbar external drainage. In our three patients, the numbers of active electrodes were 6/22 (Cochlear ABI 24M ABI), 11/12 (Medel Opus II ABI) and 11/12 (implant Medel), respectively. Due to additional major surgical procedures and to disappointing functional results of the ABI, patient 1 stopped wearing her implant 18 months after implantation. Nine months after surgery, patient 2 achieved open-set speech recognition and was very satisfied with the implant. Six months after implantation, patient 3 (cochlear nerve deficiency), who was 3.5 years-old at the time, clearly reacted to some environmental sounds but was not yet able to achieve speech recognition. Conclusions ABI has now entered the list of treatments that can be proposed in pediatric profound sensorineural deafness. Its major risks of complications are CSF leakage and non-auditory side effects. Its outcomes are worse and less predictable than cochlear implants. Thus, its indications must remain restricted to cases meeting the following conditions: absence of alternative option to restore hearing, patients and parents high level of motivation and realistic expectations.

Our objective is to prospectively report very early complications and outcomes of cerebellopontine angle (CPA) surgery. Between January and August 2007, 72 patients were operated on by different transpetrosal approaches in a tertiary referral center. During preoperative assessment, facial nerve function (House-Brackmann grading system), the presence of vertigo or tinnitus and caloric test results were recorded and correlated with complications and symptoms occurring daily from day (D) 1 to D 8. The overall number of complications did not differ from those of former retrospective studies; nevertheless, the prospective feature of this study prompts several comments. Even slight (grade II) preoperative facial impairments increased the risk of severe postoperative facial dysfunction. Keratitis was frequent (42%) even in patients with normal facial function. Thrombo-embolic complications only occurred after long air-travel (≥5 h). Preoperative caloric test status was predictive of postoperative vestibular disturbance occurrence. With respect to the activity recovery; younger patients (40 years old) displayed faster central compensations than the older (60 years old) patients. This study highlights several features that may be used for preoperative patient counseling and complication management. In particular, the practitioner has to pay attention to even minor preoperative clinical signs of facial dysfunction to properly inform the patient of facial outcome. Routine ophthalmologic evaluation should be practiced, even when facial function is normal or subnormal.1b.

Objective To evaluate the functional results of otosclerosis surgery using diode laser. Study design Retrospective cohort analysis. Patients One hundred seven patients operated on for otosclerosis with a diode laser (119 ears, all primary cases) and 141 patients operated on with a conventional technique (141 ears, all primary cases). Revision cases using the diode laser were also described. Methods Preoperative tomographic computed scan findings and intraoperative observations were collected. Pure-tone and vocal audiometry was performed preoperatively and postoperatively (at 3 mo and 1 yr). Results In the laser group, the air-bone gap was 29 +/- 0.8 dB (n= 112) preoperatively and 9 +/- 0.6 dB (n = 58) at 1 year. Air conduction was improved by 22 +/- 1.7 dB at 1 year (n = 58). In the conventional group, the air-bone gap was 32 +/- 0.9 dB (n=127) preoperatively and 10 +/- 0.6 dB (n = 127) at 1 year. Air conduction was improved by 25 +/- 1.1 dB (n = 127) at 1 year. No difference of hearing gain was observed between the 2 groups at 1 year. A decreased rate of footplate fracture was observed with the diode laser (3.6%) compared with the conventional technique (21.3%). Conclusion Diode laser is a reliable and safe device for otosclerosis surgery. The functional results were similar to those reported in other series.

Resume Objectifs Le but de cette etude est de presenter les principes de l'implant auditif du tronc cerebral (ITC) et d'evaluer le benefice apporte par cette technique innovante dans differentes indications. Materiel et methodes Les indications de l'ITC sont : la neurofibromatose de type 2 (NF2), les ossifications cochleaires totales bilaterales, les associations de schwannome vestibulaire a une surdite controlaterale et les malformations cochleaires majeures et aplasies du nerf auditif. Le bilan preoperatoire comporte une evaluation clinique, orthophonique, radiologique, et psychologique. La voie d'abord chirurgicale est retrosigmoide ou translabyrinthique. L'evaluation du benefice apporte en termes de perception auditive est realisee avec ou sans le support de la lecture labiale, pour des mots et phrases sans contexte. Resultats Les resultats montrent que, chez les patients NF2, le meilleur benefice fonctionnel auditif est obtenu dans les cas de schwannome vestibulaire de taille moyenne, avec une privation auditive du cote implantee breve ou nulle. Les facteurs de mauvais pronostic sont une privation auditive prolongee, un diametre cisternal superieur a 30 mm, une difficulte a la mise en place du porte-electrodes en peroperatoire et l'activation de moins de dix electrodes avec des sensations auditives. Dans les cas de surdite totale postmeningitique avec ossification cochleaire totale, le resultat obtenu est tout a fait comparable a celui des implants cochleaires dans cette indication (surdite postmeningitique sans ou avec ossification partielle). Il en est de meme pour les autres indications non tumorales (hors NF2). Conclusion Ces resultats demontrent que l'ITC apporte un benefice fonctionnel chez les patients NF2, ce d'autant que la privation auditive est breve et que le volume tumoral est limite. En cas d'ossification cochleaire postmeningitique, le resultat est comparable a celui d'un implant cochleaire, pour des cochlees non ou partiellement ossifiees.

Background. A consensus conference recommended empirical antibiotic therapy for all patients with postoperative meningitis and treatment withdrawal after 48 or 72 h if cerebrospinal fluid culture results are negative. However, this approach is not universally accepted and has not been assessed in clinical trials. Methods. We performed a cohort study of all patients who received a diagnosis of postoperative meningitis from January 1998 through May 2005 in a teaching hospital. From January 1998 through September 2003 (control period), guidelines were lacking or were not implemented. From October 2003 through May 2005 (interventional period), all patients received a predefined intravenous antibiotic therapy that was discontinued on the third day if the meningitis was considered aseptic. Clinical outcome and duration of antibiotic therapy were analyzed for each patient. Results. Seventy-five episodes of postoperative meningitis (21 cases of bacterial meningitis and 54 cases of aseptic meningitis) were investigated. Patients with aseptic meningitis received antibiotic treatment for a mean ± standard deviation duration of 11 ± 5 days during the control period and 3.5 ± 2 days during the intervention period (P = .001). The duration of antibiotic treatment for bacterial meningitis was not significantly different between the 2 periods. All episodes of bacterial and aseptic meningitis were cured, and complications were rare during both periods. Conclusions. Stopping antibiotic treatment after 3 days is effective and safe for patients with postoperative meningitis whose cerebrospinal fluid culture results are negative.

Resume Introduction Les osteomyelites de la base du crâne sont des infections rares mais severes et de diagnostic parfois difficile, compliquant habituellement une otite externe necrotique. Le but de cette etude clinique etait d'en preciser les caracteristiques cliniques et paracliniques, ainsi que les modalites therapeutiques et evolutives. Methodes Etude d'une cohorte de cinq patients evalues et suivis a l'hopital Beaujon entre 2004 et 2005. Resultats Les cinq patients etaient âges en moyenne de 75 ans (63–89). Quatre d'entre eux etaient diabetiques avec des antecedents plus ou moins recents d'otite externe. Tous presentaient des symptomes associant a des degres divers des cephalees et l'atteinte d'un ou plusieurs nerfs crâniens, en particulier, le nerf facial. Le diagnostic a ete etabli a partir des donnees de l'IRM qui montraient l'atteinte de la medullaire osseuse avec disparition de son hypersignal T1 spontane. Le germe en cause etait Pseudomonas aeruginosa. Un patient est decede de complications neurologiques liees a l'extension de l'osteomyelite. Les quatre autres ont presente une evolution clinique favorable, avec persistance d'une atteinte faciale sequellaire dans deux cas. Cette infection etait rattachee dans quatre cas au traitement inadapte de l'otite externe necrotique initiale du fait d'une antibiotherapie inefficace et/ou trop breve. Conclusions Le diagnostic d'osteomyelite de la base du crâne est evoque, chez un patient presentant une otite externe necrotique, devant l'apparition de cephalees et de l'atteinte d'un ou plusieurs nerfs crâniens. Il est etabli grâce a une evaluation IRM comportant des sequences en saturation de graisse. Cette pathologie devrait etre evitee grâce a la prise en charge adaptee des otites externes necrotiques.

International audience; IMPORTANCE: The association between hearing impairment and cognitive decline has been established; however, the effect of cochlear implantation on cognition in profoundly deaf elderly patients is not known. OBJECTIVE: To analyze the relationship between cognitive function and hearing restoration with a cochlear implant in elderly patients. DESIGN, SETTING, AND PARTICIPANTS: Prospective longitudinal study performed in 10 tertiary referral centers between September 1, 2006, and June 30, 2009. The participants included 94 patients aged 65 to 85 years with profound, postlingual hearing loss who were evaluated before, 6 months after, and 12 months after cochlear implantation. INTERVENTIONS: Cochlear implantation and aural rehabilitation program. MAIN OUTCOMES AND MEASURES: Speech perception was measured using disyllabic word recognition tests in quiet and in noise settings. Cognitive function was assessed using a battery of 6 tests evaluating attention, memory, orientation, executive function, mental flexibility, and fluency (Mini-Mental State Examination, 5-word test, clock-drawing test, verbal fluency test, d2 test of attention, and Trail Making test parts A and B). Quality of life and depression were evaluated using the Nijmegen Cochlear Implant Questionnaire and the Geriatric Depression Scale-4. RESULTS: Cochlear implantation led to improvements in speech perception in quiet and in noise (at 6 months: in quiet, 42% score increase [95% CI, 35%-49%; P \textless .001]; in noise, at signal to noise ratio [SNR] +15 dB, 44% [95% CI, 36%-52%, P \textless .001], at SNR +10 dB, 37% [95% CI 30%-44%; P \textless .001], and at SNR +5 dB, 27% [95% CI, 20%-33%; P \textless .001]), quality of life, and Geriatric Depression Scale-4 scores (76% of patients gave responses indicating no depression at 12 months after implantation vs 59% before implantation; P = .02). Before cochlear implantation, 44% of the patients (40 of 91) had abnormal scores on 2 or 3 of 6 cognition tests. One year after implant, 81% of the subgroup (30 of 37) showed improved global cognitive function (no or 1 abnormal test score). Improved mean scores in all cognitive domains were observed as early as 6 months after cochlear implantation. Cognitive performance remained stable in the remaining 19% of the participants (7 of 37). Among patients with the best cognitive performance before implantation (ie, no or 1 abnormal cognitive test score), 24% (12 of 50) displayed a slight decline in cognitive performance. Multivariate analysis to examine the association between cognitive abilities before implantation and the variability in cochlear implant outcomes demonstrated a significant effect only between long-term memory and speech perception in noise at 12 months (SNR +15 dB, P = .01; SNR +10 dB, P \textless .001; and SNR +5 dB, P = .02). CONCLUSIONS AND RELEVANCE: Rehabilitation of hearing communication through cochlear implantation in elderly patients results in improvements in speech perception and cognitive abilities and positively influences their social activity and quality of life. Further research is needed to assess the long-term effect of cochlear implantation on cognitive decline.

Objectifs Le but de cette etude etait d’analyser de facon retrospective les performances, les facteurs predictifs et les complications de l’implant cochleaire dans une population de sujets adultes presentant une surdite post-linguale. Methodes Entre 1990 et 2003, 134 patients adultes ont ete implantes, de facon unilaterale chez 129 d’entre eux et bilaterale chez 5 d’entre eux. Le benefice auditif a 6, 12, 24 et 36 mois a ete analyse ainsi que les performances a 12 mois en fonction de l’etiologie, de l’âge, de la lecture labiale et de la strategie de codage. Resultats L’implant cochleaire apporte un benefice auditif important des 6 mois postoperatoire par comparaison aux performances avant l’implantation (p Conclusion L’implant cochleaire apporte un benefice important et rapide, avec une morbidite tres faible, quels que soient l’âge des sujets, l’etiologie et la qualite de la lecture labiale.

Objective To report the first case of spontaneous intratumoral and brainstem hemorrhage in a patient with a vestibular schwannoma. Study design Case report and review of the literature. Setting University-based, tertiary referral center. Patient A 73-year-old woman with a vestibular schwannoma, anti-vitamin K overdose, and arterial hypertension experienced a rapid onset of headache, facial palsy, diplopia, and hoarseness. Interventions The patient was admitted to the intensive care unit and treated with vitamin K and corticoids. Main outcome measures Clinical and radiologic findings. Results At admission, the magnetic resonance imaging and computed tomographic scans showed an intratumoral hemorrhage. The patient entered a coma 24 hours after the onset of the symptoms. At that time, the computed tomographic scan demonstrated a massive intratumoral and brainstem hemorrhage. The patient died 3 days later. Conclusion Intratumoral, subarachnoid, and brainstem hemorrhages can occur in patients with vestibular schwannoma. Oral anticoagulant therapy is a risk factor for tumor-related hemorrhage.

Objectif Le but de ce travail est de rapporter un cas d’hemorragie labyrinthique, qui est une etiologie rare de surdite brusque, chez un patient sous traitement anticoagulant. Materiel et methode Un patient de 73 ans, traite par antivitamine K, a ete adresse dans le service pour une surdite brusque et un syndrome vertigineux. Le bilan clinique a montre une surdite totale gauche et une areflexie homolaterale non compensee. Il existait un surdosage en AVK (INR = 7,5). Resultats L’imagerie par resonance magnetique (IRM) a mis en evidence un hypersignal spontane de la cochlee et du vestibule gauches en sequence T1 sans injection de gadolinium. En sequence T2 FLAIR, il existait un hypersignal franc. Le diagnostic d’hemorragie labyrinthique a ete alors retenu. Les caracteristiques du signal T1 sans et avec injection de Gadolinium, T2 permettent d’eliminer les autres diagnostics : labyrinthite, schwannome ou lipome intra-labyrinthique. L’evolution a ete marquee par une regression des troubles de l’equilibre sans recuperation auditive. Conclusion Le diagnostic d’hemorragie labyrinthique doit etre evoque chez un patient traite par anticoagulant, presentant une surdite brusque associee a des vertiges. L’IRM permet le diagnostic.

A high rate of deterioration in hearing function and the loss of patient compliance during conservative management should be taken into account when considering hearing preservation strategies for patients with vestibular schwannoma (VS). To compare conservative management with surgery for solitary small VS. Among 693 patients followed up for VS between 1991 and 2002, 114 (16%) intracanalicular VSs (stage 1) and 302 (44%) VSs measuring15 mm in the cerebellopontine angle (stage 2) were included in this study. Initially, surgery was performed in 305 (73%) cases (50 stage 1, 255 stage 2) and 111 (27%) were managed conservatively (64 stage 1, 54 stage 2) by means of annual MRI scans and audiometry. Conservative management was chosen in patients aged60 years and in those who refused surgery. In this subgroup, the mean follow-up period was 33 months (range 6-111 months). In the conservative management group, 47% of VSs showed significant growth, 47% were stable and 6% showed regression. Seventeen patients (15%) were operated on secondarily for tumour growth and 1 (1%) was irradiated for tumour growth and because surgery was contraindicated. Deterioration of hearing function byor =1 class was observed in 56% of cases, 34% of patients were initially in hearing class D and only 10% showed stable hearing function. Of the conservative management group, 17% were lost during follow-up. After surgery, grade 1 or 2 facial function was obtained in 86% of cases. Following hearing preservation attempts (n=137), 54% of patients were in hearing classes A-C.

The aim of this study was to evaluate the functional outcome of facial nerve repair with fibrin glue in end-to-end anastomosis and intermediate nerve graft. Thirty-six patients undergoing facial nerve repair by end-to-end anastomosis or facial nerve grafting using exclusively fibrin glue between 1986 and 1999 were included in this retrospective study. The population comprised ten vestibular schwannomas (28%), nine temporal bone fractures (25%), seven facial nerve schwannomas (19%), four facial nerve hemangiomas (11%), two iatrogenic facial nerve interruptions (6%) and four miscellaneous facial nerve lesions (11%). Data were reviewed concerning etiology, location of the nerve interruption, type of repair and postoperative facial function according to the repaired facial nerve recovery scale (A: normal; B: independent movements of eyelid and mouth; C: strong closure of eyelids and mouth; D: incomplete eyelid closure; E: minimal movement; F: no movement). Eleven patients (31%) underwent end-to-end nerve anastomosis and 25 (69%) underwent intermediate facial nerve grafting. The mean follow-up period was 50 months (range: 3-95). Among patients followed-up more than 18 months (n = 20), a score of B or C was obtained in 16 patients (80%), a score D in 2 cases (10%) and a score E in 2 cases (10%). The type of repair and the site of interruption did not influence the results. Fibrin glue is a simple, rapid and efficient means of facial nerve repair. In case of intraoperative facial nerve interruption, this type of repair can be attempted in any location at the time of the tumor removal.

OBJECTIVE To assess the value of cerebrospinal fluid pressure as a decisional factor for immediate surgical revision in cerebrospinal fluid leakage after acoustic neuroma removal. STUDY DESIGN Prospective study. SETTING Tertiary referral center. PATIENTS Between 1998 and 2001, 220 patients were operated on for acoustic neuroma by different transpetrosal approaches. Among 24 patients (12%) presenting postoperative cerebrospinal fluid leakage, those with meningitis or with hydrocephalus were excluded. Fifteen patients were included in this study. METHODS Each patient had initial conservative treatment with serial depletive lumbar punctures and cerebrospinal fluid pressure measurements associated with oral acetazolamide. Surgical revision was decided on in case of persistent cerebrospinal fluid leakage. RESULTS In eight patients with high cerebrospinal fluid pressure (18+/-1.4 cm H2O; range, 14-28 cm H2O), cerebrospinal fluid leak disappeared in 3 days after conservative treatment. Seven other patients required surgical revision for persistent cerebrospinal fluid leakage. Revision surgery was efficient in six patients with low cerebrospinal fluid pressure (8+/-1.3 cm H2O, range, 3-12 cm H2O). In the remaining patient with high cerebrospinal fluid pressure (18 cm H2O), cerebrospinal fluid leakage continued despite surgical revision, requiring lumboperitoneal shunting. CONCLUSION The cerebrospinal fluid pressure value may be used as a decisional indicator for cerebrospinal fluid leakage treatment after acoustic neuroma surgery. Low cerebrospinal fluid pressure leakage would imply a revision surgery procedure without delay, whereas high cerebrospinal fluid pressure leakage would imply conservative treatment.

Objectif Evaluation de l’efficacite de l’implant cochleaire chez le sujet âge de 60 ans et plus. Materiel et methodes Les dossiers de 56 patients âges de 60 ans et plus, presentant une surdite profonde et totale bilaterale, ont ete analyses de facon retrospective. Au terme du bilan, 28 patients ont ete implantes. L’âge moyen dans ce groupe etait de 66 ans et le recul moyen etait de 22,5 mois. Les bilans orthophoniques pre et post-operatoires ont ete analyses dans le but d’evaluer le benefice apporte par l’implant cochleaire. Le bilan orthophonique pre-operatoire a ete compare a celui des patients non implantes. Resultats Le bilan orthophonique post-implantation retrouve une amelioration significative de la comprehension des mots dissyllabiques et des phrases sans contexte. Les patients âges de 60 a 70 ans et de plus de 70 ans ont des performances similaires. Les suites ont ete marquees par 1 cas de vertige secondaire a une fistule perilymphatique. Aucun retard de cicatrisation n’est survenu. Dans le groupe de patients non implantes (âge moyen : 68 ans), l’implant a ete refuse principalement en raison d’un benefice audio-prothetique juge suffisant par le patient (18 cas), mais egalement par crainte de l’intervention (5 cas). L’âge moyen, la cause et duree de la surdite ainsi que les resultats du bilan orthophonique initial etaient similaires au groupe de patients implantes. Conclusion Cette etude met en evidence le benefice apporte par l’implant cochleaire chez le sujet âge. Les resultats laissent presager qu’un benefice comparable aurait pu etre obtenu dans le groupe de patients qui a refuse l’implantation. Une implantation la plus precoce possible pourrait raccourcir la duree de la surdite et conserver une perception auditive binaurale dans le but d’optimiser les performances chez le sujet âge.

To evaluate the results of partial and total ossicular reconstruction prostheses entirely made of hydroxylapatite.A retrospective review of cases followed-up between 1997 and 2000.Tertiary referral center.One hundred adult patients (60 men and 40 women) were studied. The mean age was 55 years (range, 25 to 65 years). Fifty patients had a previous tympanoplasty. The series included 45 cholesteatomas (45%), 37 chronic otitis media without cholesteatoma (37%), 13 retraction pockets (13%), and 5 posttraumatic ossicular displacements (5%).A one-stage ossiculoplasty with a partial ossicular reconstruction prosthesis (n = 65) or a total ossicular reconstruction prosthesis (n = 35) was performed. This was associated with a simple mastoidectomy in 70 cases and a radical mastoidectomy in 10 cases.All patients were followed-up at 1 year, and 50 were reexamined 2 years after surgery. Clinical and audiometric data were collected in a database at each visit.A prosthetic extrusion was noted in two cases (2%). A prosthetic displacement occurred in 10 cases (10%). A revision surgery was carried out in 10 cases because of an ossiculoplasty failure or a disease recurrence. At 1 year, the residual air-bone gap was lower in cases with a partial ossicular reconstruction prosthesis than those with a total ossicular reconstruction prosthesis (16 +/- 9.3 versus 23 +/- 13.7 dB, p0.05). The gain in mean air conduction threshold was 21 +/- 12.8 dB in cases of partial ossicular reconstruction prosthesis and 19 +/- 11.3 dB in cases of total ossicular reconstruction prosthesis (not significant). Revision surgery, canal wall-down mastoidectomy, or cholesteatoma yielded poorer functional results.Partial ossicular reconstruction prosthesis and total ossicular reconstruction prosthesis entirely made of dense hydroxylapatite yielded high rates of air-bone gap reduction and high anatomic stability.

✓ The auditory brainstem implant (ABI) is designed to restore useful auditory sensations in patients with neurofibromatosis Type 2 (NF2). The implantation is usually performed at the time of tumor removal in patients who do not undergo radiation treatment. The authors evaluated the performance of ABIs in three patients with NF2 in whom vestibular schwannoma continued to grow after radiation treatment. These three patients with NF2 received a 21-channel ABI; a translabyrinthine approach was used for both the tumor removal and the ABI placement. The interval between radiosurgery and the tumor removal plus device implantation ranged from 2 to 11 years. In all cases, the tumor was growing and the patients presented with total deafness. The mean number of active electrodes in these three patients was equivalent to the average results reported in other patients who received ABIs. The patients in this study used the ABI regularly for everyday life and obtained useful levels of environmental sound recognition. It is concluded that hearing function can be rehabilitated using ABIs in patients with NF2, even if radiosurgery fails to control the tumor growth.

Cochlear implantation in elderly patients is a questionable subject. The purpose of this study was to evaluate the procedure and its outcome, the postoperative course, and the audiologic and social benefits of cochlear implantation in this population. Twenty-seven patients older than 60 years were compared with a control group of 15 adult patients. This retrospective study analyzed data concerning the outcome of the procedure, postoperative course, postoperative orthophonic test results, and answers of a questionnaire assessing the changes in communication, perception, and social outcomes. The procedure was uneventful in both groups. Minor complications were not more frequent in elderly patients. Orthophonic test results were comparable in both groups. At 12 months, 83% of the elderly patients had an open-set speech discrimination score above 60%. The benefits of cochlear implantation in terms of the quality of life are not statistically different with younger patients. Cost-utility analysis might support these findings.

The aim of this retrospective study was to evaluate the functional results of surgical lowering of the high jugular bulb in the treatment of patients with Ménière's disease and pulsatile tinnitus. Fifteen patients with disabling Ménière's disease associated with pulsatile tinnitus and a high and medial jugular bulb were included in this study. As treatment a complete mastoidectomy was performed, after which the jugular bulb was freed by an infralabyrinthine and subfacial approach. The bulb was then displaced downwards with surgical wax. Functional results of surgery were assessed by a questionnaire according to the 1995 guidelines of the United States American Academy Committee on Hearing and Equilibrium, audiometric and vestibular tests, and by magnetic resonance and computed tomographic imaging with vascular sequences. Surgical treatment was contraindicated in two cases: one had hypoplasia of the contralateral sigmoid sinus and the other a small petrous hemangioma located around the jugular bulb that was discovered peroperatively. Among the 13 patients treated by definitive surgery, attacks of vertigo were reported as disabling in 12 cases preoperatively (92%) versus 1 (8%) after surgical treatment. No significant change in hearing was observed after surgery. Tinnitus had been reported in all patients preoperatively and decreased in intensity in four (31%) and disappeared in three (23%) after surgery.

But de la presentation la chirurgie de l’implant cochleaire chez l’adulte est une chirurgie bien codifiee : non-mois, dans les cas plus difficiles (otite chronique, malformations, ossifications cochleaire), la voie d’abord classique par tympanotomie posterieure peut etre problematique. Objectif de l’etude Analyser les indications, resultats, complications de la chirurgie de l’implant cochleaire pour laquelle une exclusion de l’oreille moyenne a ete effectuee. Materiel et methodes Etude retrospective porte sur 30 cas (26 patients, 4 implantes bilateralement) sur 837 (3 %) chirurgie d’implantation cochleaire effectue dans le service de 2009 a 2013. Age moyenne 59 ± 19 ans (range 35/82 ans). Toutes les chirurgies ont ete effectuees avec la meme technique chirurgicale, petrectomie subtotale avec fermeture du CAE et obliteration de la cavite par greffon adipeux. Un TDM postoperatoire a ete effectue dans tous les cas pour verifier le positionnement du port-electrode. Resultats L’etiologie de la surdite etaient : otites chroniques dans 24 cas, surdite progressive dans 2 cas, meningite avec ossification cochleaire, fracture du rocher avec fuite de LCR, aplasie majeur, syndrome de l’acqueduct vestibulaire large dans 1 cas. Quatre de ces 30 cas etait de chirurgie de revision d’implant cochleaire pour malposition du port-electrode (1 cas), cholesteatome recurrent (2 cas), extrusion du port-electrode d’une cavite d’evidement (1 cas). Toutes les chirurgies se sont deroulees sans complications et effectuees en un temps. Le port-electrode a ete insere dans le tour bas de la cochlee dans 29 cas et confirme par le TDM postoperatoire. Aucun cas d’abces retro-auriculaire, infection cutanee ou pathologie recurrents a ete note (suivi moyen 21 ± 18 mois). Deux cas d’hematome sous-cutane abdominal ont ete evacues sous anesthesie locale. Un cas de panne de l’implant est survenu 5 mois apres la chirurgie. Conclusion la chirurgie de l’implant cochleaire avec exclusion de l’oreille moyenne est une technique sur et efficace dans les cas difficiles d’implantation : elle reduit les risques de pathologie recurrente, permet un fraisage extensif de la cochlee en cas d’ossification et permet une insertion du port-electrode dans l’axe du tour basal dans des conditions anatomiques difficiles.

Objective: To evaluate results of cochlear implantation in patients with far-advanced otosclerosis. Methods: Sixteen patients with far-advanced otosclerosis had undergone unilateral (n = 13) or bila

Haemangiomas involving the internal auditory meatus (IAM) are rare and can mimic other frequent lesions of the IAM such as schwannomas by their clinical and imaging aspects. The case of a patient with an atypical IAM haemangioma fluctuating in size is reported to highlight this diagnostic possibility. A 36-year-old female presented with a sudden and recurrent left sensorineural hearing loss (SNHL). Three consecutive MRIs were performed in a 10-month period of preoperative observation. They showed a fluctuation of the tumour signal and size. The surgical removal was performed via a translabyrinthine approach. Pathological findings were consistent with the diagnosis of a heamangioma. MRI and CT findings suggested the diagnosis of IAM heamangioma, but the rapid variation in size and signal was misleading. This phenomenon may be due to haemorrhage or oedema, and can be accompanied by a deterioration of the hearing function. Early surgical resection is the treatment of choice and allows to confirm the diagnosis.

Le but de cette etude est de mettre en evidence les facteurs predictifs d'une lecture labiale fonctionnelle. Les capacites en lecture labiale, et notamment en discrimination des sosies labiaux, ainsi que les capacites d'attention et de memoire visuelles ont ete evaluees aupres de 22 personnes atteintes de surdite profonde, et d'une population controle. Il en resulte que malgre un traitement visuel de la parole plus performant, les patients sourds ne discriminent pas plus les sosies labiaux que les temoins. De plus, il existe des correlations entre les capacites en lecture labiale et les capacites en memoire et attention visuelles.

Facial function and hearing preservation are the two main challenges in acoustic neuroma surgery. A retrospective study of 441 patients [192 males and 249 females; mean age; 60 years (range, 16–79)] who were operated on for a unilateral acoustic neuroma was undertaken. The mean diameter of the tumors was 26 ± 0.6 mm. One hundred four patients (14%) were operated on through conservative approaches (middle cranial fossa and retrosigmoid) and 335 (76%) through the translabyrinthine route. A cutoff value for the tumor diameter in the cerebellopontine angle (CPA) was observed at 15 mm in terms of postoperative facial and hearing function. Among lesions operated on through conservative approaches, hearing preservation was obtained in 63% and 14% of patients with tumors measuring less than 15 mm and between 16 and 20 mm in the CPA, respectively. The proportion of good facial function 1 year after surgery with tumors between 11 and 15 mm and between 16 and 20 mm was 91% and 73%, respectively. In conclusion, a classification is proposed subdividing the lesions as follows: stage 1, intracanalicular; stage 2, less than 15 mm in the CPA; stage 3, 15–30 mm in the CPA; stage 4, more than 30 mm in the CPA. This classification appears to be well correlated to facial function prognosis and the possibility of hearing function preservation.

In order to evaluate the decisional elements in the surgical strategy of deep-seated and/or extensive intratemporal lesions, a retrospective review of cases followed up between 1985 and 1996 in our department was undertaken. Eighty-one adult patients presenting temporal bone lesions located or extending beyond the middle ear limits excluding vestibular schwannomas and surgically treated were included. The population comprised 38 men and 43 women (mean age: 43 years, range: 17-81). Pre-, intra- and postoperative data were collected from medical files. The principal factors influencing the choice of the surgical approach were the location of the lesion and its presumed aggressiveness, the tumour involvement of the internal carotid artery and the labyrinth on preoperative imaging, and the preoperative hearing loss. A coherent algorithm based on these factors can be proposed for the surgical management of intratemporal lesions. High quality preoperative imaging is mandatory for the surgical planning.

The facial nerve was repaired by fibrin glue anastomosis in the cerebellopontine angle, the petrous bone and/or the parotid in 70 patients. End-to-end (n = 22) or cable graft (n = 32) anastomosis of the facial nerve or hypoglosso-facial anastomosis (n = 16) was performed for 49 cerebellopontine angle tumors (45 acoustic neuromas and four meningiomas), 13 petrous bone tumors (nine facial neuromas, two cholesteatomas, one papillary epithelial tumor, one hemangioma) five petrous bone fractures, one parotid gland tumor with petrous extension and for two patients with iatrogenic intraparotid section of the nerve trunk. Grade III facial regeneration was observed in 62% of the patients, followed for at least 1 year. End-to-end and cable graft anastomoses in the cerebellopontine angle, in the petrous bone and in the parotid led to 59% and 65% grade III regeneration, respectively. Grade III and grade IV regeneration was observed in 50% of the patients after hypoglosso-facial anastomosis. We include that fibrin glue provides a safe technique for facial nerve repair. The anastomosis should be performed without tension and vascularization of the nerve should be preserved.