Literature DB >> 17334306

Hearing levels in patients with microtia: correlation with temporal bone malformation.

Shin-ichi Ishimoto1, Ken Ito, Shotaro Karino, Hideki Takegoshi, Kimitaka Kaga, Tatsuya Yamasoba.   

Abstract

OBJECTIVE: To evaluate the relationship between hearing level and temporal bone abnormalities in patients with microtia. STUDY
DESIGN: Retrospective case series study between 1992 and 2004.
SETTING: Academic, tertiary care referral medical center. PATIENTS: We evaluated 115 ears of 89 patients (68 males, 21 females; mean age, 11 yr; range, 5-44 yr) with microtia. MAIN OUTCOME MEASURES: Hearing level was examined in patients with microtia. Developmental abnormalities of the temporal bone were evaluated by Jahrsdoerfer's computed tomography (CT) scoring system using high-resolution CT (HRCT) scans of the temporal bone. Temporal bone malformation scores were divided into four subgroups: ossicular development, windows connected to the cochlea, aeration of the middle ear cavity, and facial nerve aberration. Patients were divided into the stenosis and atresia groups on the basis of the appearance of the external auditory canal (EAC). We also evaluated the relationships between hearing level and four subtotal scores of the HRCT findings in the stenosis and atresia groups.
RESULTS: There was no relationship between hearing level and total points of HRCT scoring system or between hearing level and severity of microtia scored by Marx classification. With regard to subtotal points related to ossicles (4 points), the hearing level in ears with low scores (<2) (64.7 +/- 1.6 dB) was significantly different (P = .03) from that in ears with high scores (> or =2) (54.0 +/- 2.8 dB) in the stenosis group. In the atresia group, the hearing level was 64.3 +/- 2.2 dB in ears with low scores and 62.3 +/- 1.1 in ears with high scores (P > .5). As for subtotal points related to the windows connected to cochlea (2 points), the hearing level was 64.8 +/- 2.6 dB in ears with low scores (0) and 55.9 +/- 2.4 dB in ears with high scores (> = 1) in the stenosis group. In the atresia group, the hearing level was 67.7 +/- 2.3 dB in ears with low scores and 61.5 +/- 1.0 in ears with high scores. There was significant difference between ears with low and high scores in the stenosis group (P = .03) and atresia group (P = .009). There was no significant difference between ears with low and high scores with respect to the subtotal points related to aeration of the middle ear cavity and aberration of the facial nerve.
CONCLUSION: The hearing level in microtic ears correlated with the formation of oval/round windows and ossicular development but not with the degree of middle ear aeration, facial nerve aberration, or severity of microtia. The hearing level can also serve as an indictor, such as the HRCT findings, to determine whether a subject's hearing will likely improve after reconstructive surgery.

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Mesh:

Year:  2007        PMID: 17334306     DOI: 10.1097/MLG.0b013e31802ca4d4

Source DB:  PubMed          Journal:  Laryngoscope        ISSN: 0023-852X            Impact factor:   3.325


  14 in total

1.  Prognostic factors for long-term hearing preservation after canal-tympanoplasty for congenital aural atresia.

Authors:  Takashi Sakamoto; Shu Kikuta; Yayoi S Kikkawa; Makoto Kinoshita; Yuki Saito; Kenya Kobayashi; Akinobu Kakigi; Mitsuya Suzuki; Tatsuya Yamasoba
Journal:  Eur Arch Otorhinolaryngol       Date:  2014-10-17       Impact factor: 2.503

2.  Sociodemographic, health behavioral, and clinical risk factors for anotia/microtia in a population-based case-control study.

Authors:  Marisa A Ryan; Andrew F Olshan; Mark A Canfield; Adrienne T Hoyt; Angela E Scheuerle; Suzan L Carmichael; Gary M Shaw; Martha M Werler; Sarah C Fisher; Tania A Desrosiers
Journal:  Int J Pediatr Otorhinolaryngol       Date:  2019-03-23       Impact factor: 1.675

Review 3.  Microtia: epidemiology and genetics.

Authors:  Daniela V Luquetti; Carrie L Heike; Anne V Hing; Michael L Cunningham; Timothy C Cox
Journal:  Am J Med Genet A       Date:  2011-11-21       Impact factor: 2.802

Review 4.  Otologic and Audiology Concerns of Microtia Repair.

Authors:  Kausar Ali; Kriti Mohan; Yi-Chun Liu
Journal:  Semin Plast Surg       Date:  2017-08-09       Impact factor: 2.314

Review 5.  Neural crest contributions to the ear: Implications for congenital hearing disorders.

Authors:  K Elaine Ritter; Donna M Martin
Journal:  Hear Res       Date:  2018-11-14       Impact factor: 3.208

6.  Vibrant Soundbridge® in preschool children with unilateral aural atresia: acceptance and benefit.

Authors:  M Leinung; E Zaretsky; B P Lange; V Hoffmann; T Stöver; C Hey
Journal:  Eur Arch Otorhinolaryngol       Date:  2016-08-25       Impact factor: 2.503

7.  Osseointegrated implants for auricular prostheses: An alternative to autologous repair.

Authors:  Marisa A Ryan; Tawfiq Khoury; David M Kaylie; Matthew G Crowson; C Scott Brown; Jay McClennen; Eileen M Raynor
Journal:  Laryngoscope       Date:  2018-02-26       Impact factor: 3.325

Review 8.  The genetics of auricular development and malformation: new findings in model systems driving future directions for microtia research.

Authors:  Timothy C Cox; Esra D Camci; Siddharth Vora; Daniela V Luquetti; Eric E Turner
Journal:  Eur J Med Genet       Date:  2014-05-29       Impact factor: 2.708

9.  A mutation in HOXA2 is responsible for autosomal-recessive microtia in an Iranian family.

Authors:  Fatemeh Alasti; Abdorrahim Sadeghi; Mohammad Hossein Sanati; Mohammad Farhadi; Elliot Stollar; Thomas Somers; Guy Van Camp
Journal:  Am J Hum Genet       Date:  2008-04       Impact factor: 11.025

Review 10.  [Hearing rehabilitation with the Vibrant Soundbridge in patients with congenital middle ear malformation].

Authors:  J M Hempel; A Epp; V Volgger
Journal:  HNO       Date:  2021-02-18       Impact factor: 1.284

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