Validation Study of Kids Hearing Game: A Self-Administered Pediatric Audiology Application.

OBJECTIVE: Conduct a comparison study between conventional audiometry and a tablet-based hearing screening application, Kids Hearing Game (KHG). If KHG measures hearing at levels comparable with conventional audiometry, it could be used to screen hearing in children. METHODS: Prospective equivalence study where measurements of pure tone hearing via KHG are compared with measurements of pure tone hearing via conventional audiometry in patients aged 6-11 years over a 4-month period. Eighteen patients completed the study. Results from 36 ears were included in the data for analysis. Decibel measurements from each frequency measured with KHG for each ear were compared with conventional audiometry. Mean measurements were calculated for each ear and frequency as well as mean differences in measurements at each ear and frequency. Tests of equivalence were used to assess mean within-subject differences in decibel measurements using a 10-dB zone of indifference. RESULTS: Mean decibel measurements using KHG for the right ear at 500, 1000, 2000, 4000, and 8000 Hz and the left ear at 1000, 2000, 4000, and 8000 Hz were found equivalent to conventional audiometry (p < 0.050). The mean decibel measurement using KHG for the left ear at 500 Hz was found not equivalent (p = 0.101). However, when left and right ear data were analyzed together, KHG was found to be equivalent to conventional audiometry across all frequencies. Eight patients having hearing loss greater than 25 dB on conventional audiometry were also identified by KHG to have hearing loss. CONCLUSION: KHG is comparable to conventional audiometry and may be used as a screening tool for children.

Aggressiveness in cholesterol granuloma of the temporal bone may be determined by the vigor of its blood source.

OBJECTIVE: Recently, it has been proposed that the aggressive behavior of cholesterol granuloma (CG) of the petrous apex is explained by its proximity to the richly vascular marrow of the petroclival junction. Most CGs of the lateral temporal bone are indolent. The purpose of the present study is to examine the factors responsible for atypical aggressive behavior in mastoid CG. STUDY DESIGN: Retrospective case series. SETTING: : Tertiary academic practice. PATIENT POPULATION: Four patients with atypically aggressive CG of the mastoid. RESULTS: In each case, the CG abutted a rich blood source: the sigmoid sinus, carotid artery, a large dural vein, or a rich deposit of vascular marrow in the mastoid tip. CONCLUSION: These observations lend further support to the theory that aggressiveness of CG is sustained by a robust source of ongoing hemorrhage.

Silicone allergy: A new cause for cochlear implant extrusion and its management.

OBJECTIVE: We introduce silicone allergy as a rare cause for cochlear implant extrusion and discuss its management. STUDY DESIGN: Retrospective case series and literature review. SETTING: Tertiary referral centers. PATIENTS: Primary eligibility criteria included patients who experienced a delayed extrusion of their cochlear implants with negative wound cultures and had a suspected or a test-proven allergy to silicone components of an implant. INTERVENTIONS: Silicone allergy testing, explantation of a cochlear implant containing allergenic silicone materials, reimplantation with a custom-made cochlear implant excluding an allergenic silicone component. OUTCOME MEASURES: Uneventful wound healing and extrusion-free long-term follow-up after the reimplantation with a custom-made cochlear implant excluding an allergenic silicone component. RESULTS: Three known cases of cochlear implant extrusion as a result of silicone allergy have been noted from 1991 through 2004 in three cochlear implant programs in the United States. All three devices extruded, resulting in explantation of the old device and reimplantation with a new custom-made device eliminating the allergenic silicone component. Wound cultures were negative in all cases. All three patients experienced a delayed extrusion of their devices. Two of these patients had a test-proven allergy to the implant's silicone components, whereas the third patient was presumed to have a hypersensitivity solely on the basis of a clinical presentation. CONCLUSION: We propose that silicone allergy is a rare cause of cochlear implant extrusion. Patients experiencing cochlear implant extrusion, particularly with a delayed onset and negative wound culture results, should be tested for silicone allergy.

Modifications of standard cochlear implantation techniques for children under 18 months of age.

Cochlear implantation is being performed in increasingly younger children. We present a retrospective cohort of 19 patients with 23 ears implanted under 18 months of age. The mean age at implantation was 11.9 months, with the youngest being 6.8 months. The facial recess was narrow in nine ears (39%), including all premature infants. An inferiorly located stapedius tendon was sectioned in seven ears (30%) to facilitate round window access. Countersinking of the receiver-stimulator required dural exposure in 22 ears (96%). The receiver-stimulator was secured with sutures in 15 ears (65%) and within a tight pocket in eight ears (35%). Tympanostomy tubes were placed in 10 ears (43%). Cochlear implantation in very young children frequently necessitates modified surgical techniques.

Malleus-to-footplate ossicular reconstruction prosthesis positioning: cochleovestibular pressure optimization.

AIMS: To determine 1) the best position for hydroxylapatite malleus-to-footplate (MFP), ossicular replacement prosthesis (ORP) in reconstructed ears, and 2) whether preserving the stapes superstructure (SS), when present, has acoustic advantages. BACKGROUND: Positioning of the MFP-ORP head beneath the neck of the malleus may produce maximal force, whereas positioning beneath the manubrium of the malleus may produce the greatest displacement. It is not clear which is the optimal placement position. In addition, we look at the effect of the SS on sound transmission to the inner ear in ossicular reconstruction. METHODS: The ear-canal air pressure and vestibular hydro-pressure were measured in human cadaver temporal bones with incus intact, removed, and replaced with the MFP-ORP; the ORP head was placed at three different positions on the malleus (head, mid-manubrium, and umbo) while keeping its base at the center of stapes footplate with intact or removed stapes SS. The vestibular pressure ratio between the ear with intact incus and MFP-ORP reconstructed ear is defined as Lmfp, the loss caused by the prosthesis in relation to the normal ossicular chain. RESULTS: The mean magnitude of Lmfp, averaged in the important speech frequency region of 0.5 to 3 kHz, is approximately 7.8 dB at the neck with stapes SS. In comparison, mean magnitude of Lmfp for mid-manubrium without stapes SS is 15 dB (p = 0.04), and with the stapes SS it is 16 dB (p = 0.05), whereas at the umbo without SS it is 15 dB (p = 0.03). In the 8 kHz region, the mean magnitude of Lmfp is approximately 1 dB with the stapes SS intact and approximately 8.5 dB when it was removed (p < 0.09). CONCLUSION: There are significant physiologic advantages to placing the hydroxylapatite MFP-ORP beneath the neck of the malleus and preserving the SS.

Minimally invasive tongue base surgery for obstructive sleep apnoea.

Moderate to severe obstructive sleep apnoea is usually associated with multiple levels of pharyngeal airway collapse, including tongue base obstruction. A new technique has recently been introduced that improves the nocturnal retro-lingual airway. This study was a prospective, non-randomized single-institution evaluation of a recently introduced surgical technique. Nineteen consecutive patients with previously untreated moderate to severe obstructive sleep apnoea underwent tongue suspension using the Respose system and concomitant palatopharyngoplasty (multilevel pharyngeal surgery). The patient demographics and treatment outcomes were prospectively collected and retrospectively analysed. There were 16 men and three women, with a mean (+/-SD) age of 44.9 years (+/- 14.2) and a mean pre-operative apnoea-hypopnoea index (AHI) of 42.8 +/- 24.8. Twelve of the 19 patients (63.2 per cent) have had post-operative polysomnography; eight of these 12 (67 per cent) met the standard criteria for surgical response. Among these eight patients, the AHI improved from 32.4 to 14.4 (p<0.01); the individual scores fell by a mean of 51.7 per cent. The apnoea index improved from 7.4 to 0.9 (p<0.01), with the individual scores falling by a mean of 81.4 per cent. There was anatomic and radiographic evidence of multilevel upper airway enlargement. Notably, the body mass index remained essentially unchanged (31.5 +/- 7.2 to 31.2 +/- 7.6, p>0.5). Subjectively, the mean Epworth sleepiness scale score fell from 11.0 +/- 5.4 to 5.4 +/- 3.8 (p<0.005). Four patients suffered transient velopharyngeal insufficiency, and two patients complained of limited anterior excursion of the tongue. There were no serious, long-term complications. The tongue suspension procedure represents a minimally invasive technique for improving the nocturnal retro-lingual airway in patients with obstructive sleep apnoea. It is easily performed by otolaryngologists, distinguishing it from other established techniques designed to address tongue base obstruction.