Outcomes and Special Considerations of Cochlear Implantation in Waardenburg Syndrome

被引:22
作者
Kontorinis, Georgios [1 ]
Lenarz, Thomas [1 ]
Giourgas, Alexandros [1 ]
Durisin, Martin [1 ]
Lesinski-Schiedat, Anke [1 ]
机构
[1] Hanover Med Univ, Dept Otorhinolaryngol, D-30625 Hannover, Germany
关键词
Behavioral disorders; Cochlear implant; Hearing outcome; Inner ear malformations; Waardenburg syndrome; CHILDREN;
D O I
10.1097/MAO.0b013e31821b3ae3
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objectives: The objective of this study was a state-of-the-art analysis of cochlear implantation in patients with Waardenburg syndrome (WS). Patients: Twenty-five patients with WS treated with cochlear implants in our department from 1990 to 2010. Interventions: The 25 patients with WS underwent 35 cochlear implantations. Main Outcome Measures: Hearing outcome was evaluated using HSM sentence test in 65 dB in quiet, Freiburg Monosyllabic Test, and categories of auditory performance for children and compared with that of a control group. Anatomic abnormalities of the inner ear were examined using magnetic resonance imaging and computed tomography of the temporal bones. Results: The mean follow-up time was 8.3 years (range, 0.3-18.3 yr). The majority achieved favorable postimplantation performance with mean HSM scores of 75.3% (range, 22.6%-99%) and Freiburg Monosyllabic Test scores of 67.8% (range, 14%-95%). However, in 4 cases, the results were less satisfactory. The comparison with the control group did not reveal any statistical significance (p = 0.56). In 6 patients (24%), behavioral disorders caused temporary difficulties during the rehabilitation procedure. Except of isolated large vestibule in 1 patient, the radiological assessment of the 50 temporal bones did not reveal any temporal bone abnormalities. Conclusion: Most patients with WS performed well with cochlear implants. However, WS is related to behavioral disorders that may cause temporary rehabilitation difficulties. Finally, temporal bone malformations that could affect cochlear implantation are notcharacteristic of WS.
引用
收藏
页码:951 / 955
页数:5
相关论文
共 16 条
[1]  
ARIAS S, 1971, Birth Defects Original Article Series, V7, P87
[2]   Cochlear implants in Waardenburg syndrome [J].
Cullen, Robert D. ;
Zdanski, Carlton ;
Roush, Patricia ;
Brown, Carolyn ;
Teagle, Holly ;
Pillsbury, Harold C., III ;
Buchman, Craig .
LARYNGOSCOPE, 2006, 116 (07) :1273-1275
[3]   Cochlear implantation in children with Waardenburg syndrome [J].
Daneshi, A ;
Hassanzadeh, S ;
Farhadi, M .
JOURNAL OF LARYNGOLOGY AND OTOLOGY, 2005, 119 (09) :719-723
[4]   Cochlear implantation in Waardenburg syndrome: The Indian scenario [J].
Deka, Ramesh Chandra ;
Sikka, Kapil ;
Chaturvedy, Gaurav ;
Singh, Chirom Amit ;
Karthikeyan, C. Venkat ;
Kumar, Rakesh ;
Agarwal, Shivani .
ACTA OTO-LARYNGOLOGICA, 2010, 130 (10) :1097-1100
[5]  
FRYNS JP, 1995, GENET COUNSEL, V6, P197
[6]  
Handley Marilyn Cooper, 2006, AWHONN Lifelines, V10, P234
[7]   Dysplasia of the cerebellum in Waardenburg syndrome: Outcomes following cochlear implantation [J].
Kaufmann, Lisa ;
Sauter, Todd B. ;
Lee, Daniel J. .
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2010, 74 (01) :93-96
[8]   HISTORICAL BACKGROUND AND EVIDENCE FOR DOMINANT INHERITANCE OF THE KLEIN-WAARDENBURG SYNDROME (TYPE-III) [J].
KLEIN, D .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1983, 14 (02) :231-239
[9]   Cochlear implantation in children with internal ear malformations [J].
Loundon, N ;
Rouillon, I ;
Munier, N ;
Marlin, S ;
Roger, G ;
Garabedian, EN .
OTOLOGY & NEUROTOLOGY, 2005, 26 (04) :668-673
[10]   Temporal bone abnormalities associated with hearing loss in Waardenburg syndrome [J].
Madden, C ;
Halsted, MJ ;
Hopkin, RJ ;
Choo, DI ;
Benton, C ;
Greinwald, JH .
LARYNGOSCOPE, 2003, 113 (11) :2035-2041