Long-Term Outcomes of Cochlear Implantation in Usher Syndrome

被引:2
作者
Fehrmann, Mirthe L. A. [1 ,2 ]
Lanting, Cris P. [1 ,2 ]
Haer-Wigman, Lonneke [3 ]
Yntema, Helger G. [3 ]
Mylanus, Emmanuel A. M. [1 ,2 ]
Huinck, Wendy J. [1 ,2 ]
Pennings, Ronald J. E. [1 ,2 ]
机构
[1] Radboud Univ Nijmegen Med Ctr, Dept Otorhinolaryngol, Geert Grootepl Zuid 10, NL-6525 GA Nijmegen, Netherlands
[2] Donders Inst Brain Cognit & Behav, Nijmegen, Netherlands
[3] Radboud Univ Nijmegen Med Ctr, Dept Clin Genet, Nijmegen, Netherlands
关键词
Clinical decision-making; Cochlear implantation outcomes; Disease management; Usher syndrome type 1; Usher syndrome type 2; Usher syndrome type 3; Usher syndrome; SPEECH RECOGNITION; NERVE DEFICIENCY; PERFORMANCE; CHILDREN; HEARING; HISTOPATHOLOGY; LOCALIZATION; RESTORATION; EXPRESSION; GENETICS;
D O I
10.1097/AUD.0000000000001544
中图分类号
R36 [病理学]; R76 [耳鼻咽喉科学];
学科分类号
100104 ; 100213 ;
摘要
Objectives:Usher syndrome (USH), characterized by bilateral sensorineural hearing loss (SNHL) and retinitis pigmentosa (RP), prompts increased reliance on hearing due to progressive visual deterioration. It can be categorized into three subtypes: USH type 1 (USH1), characterized by severe to profound congenital SNHL, childhood-onset RP, and vestibular areflexia; USH type 2 (USH2), presenting with moderate to severe progressive SNHL and RP onset in the second decade, with or without vestibular dysfunction; and USH type 3 (USH3), featuring variable progressive SNHL beginning in childhood, variable RP onset, and diverse vestibular function. Previous studies evaluating cochlear implant (CI) outcomes in individuals with USH used varying or short follow-up durations, while others did not evaluate outcomes for each subtype separately. This study evaluates long-term CI performance in subjects with USH, at both short-term and long-term, considering each subtype separately.Design:This retrospective, observational cohort study identified 36 CI recipients (53 ears) who were categorized into four different groups: early-implanted USH1 (first CI at <= 7 years of age), late-implanted USH1 (first CI at >= 8 years of age), USH2 and USH3. Phoneme scores at 65 dB SPL with CI were evaluated at 1 year, >= 2 years (mid-term), and >= 5 years postimplantation (long-term). Each subtype was analyzed separately due to the significant variability in phenotype observed among the three subtypes.Results:Early-implanted USH1-subjects (N = 23 ears) achieved excellent long-term phoneme scores (100% [interquartile ranges {IQR} = 95 to 100]), with younger age at implantation significantly correlating with better CI outcomes. Simultaneously implanted subjects had significantly better outcomes than sequentially implanted subjects (p = 0.028). Late-implanted USH1 subjects (N = 3 ears) used CI solely for sound detection and showed a mean phoneme discrimination score of 12% (IQR = 0 to 12), while still expressing satisfaction with ambient sound detection. In the USH2 group (N = 23 ears), a long-term mean phoneme score of 85% (IQR = 81 to 95) was found. Better outcomes were associated with younger age at implantation and higher preimplantation speech perception scores. USH3-subjects (N = 7 ears) achieved a mean postimplantation phoneme score of 71% (IQR = 45 to 91).Conclusions:This study is currently one of the largest and most comprehensive studies evaluating CI outcomes in individuals with USH, demonstrating that overall, individuals with USH benefit from CI at both short- and long-term follow-up. Due to the considerable variability in phenotype observed among the three subtypes, each subtype was analyzed separately, resulting in smaller sample sizes. For USH1 subjects, optimal CI outcomes are expected with early simultaneous bilateral implantation. Late implantation in USH1 provides signaling function, but achieved speech recognition is insufficient for oral communication. In USH2 and USH3, favorable CI outcomes are expected, especially if individuals exhibit sufficient speech recognition with hearing aids and receive ample auditory stimulation preimplantation. Early implantation is recommended for USH2, given the progressive nature of hearing loss and concomitant severe visual impairment. In comparison with USH2, predicting outcomes in USH3 remains challenging due to the variability found. Counseling for USH2 and USH3 should highlight early implantation benefits and encourage hearing aid use.
引用
收藏
页码:1542 / 1553
页数:12
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共 50 条
[41]   Outcomes of cochlear implantation in children with Usher syndrome: a long-term observation [J].
Remjasz-Jurek, Agnieszka ;
Claroes, Pedro ;
Claroes-Pujol, Astrid ;
Pujol, Carmen ;
Claroes, Andres .
EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY, 2023, 280 (05) :2119-2132
[42]   Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology [J].
Richards, Sue ;
Aziz, Nazneen ;
Bale, Sherri ;
Bick, David ;
Das, Soma ;
Gastier-Foster, Julie ;
Grody, Wayne W. ;
Hegde, Madhuri ;
Lyon, Elaine ;
Spector, Elaine ;
Voelkerding, Karl ;
Rehm, Heidi L. .
GENETICS IN MEDICINE, 2015, 17 (05) :405-424
[43]  
Sharma Anu, 2002, Ear and Hearing, V23, P532, DOI 10.1097/00003446-200212000-00004
[44]   HISTOPATHOLOGY OF THE INNER-EAR IN USHERS SYNDROME AS OBSERVED BY LIGHT AND ELECTRON-MICROSCOPY [J].
SHINKAWA, H ;
NADOL, JB .
ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY, 1986, 95 (03) :313-318
[45]   CLINICAL-DIAGNOSIS OF THE USHER SYNDROMES [J].
SMITH, RJH ;
BERLIN, CI ;
HEJTMANCIK, JF ;
KEATS, BJB ;
KIMBERLING, WJ ;
LEWIS, RA ;
MOLLER, CG ;
PELIAS, MZ ;
TRANEBJAERG, L .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1994, 50 (01) :32-38
[46]   Plastic changes in the central auditory system after hearing loss, restoration of function, and during learning [J].
Syka, J .
PHYSIOLOGICAL REVIEWS, 2002, 82 (03) :601-636
[47]   Usher syndrome type IV: clinically and molecularly confirmed by novel ARSG variants [J].
Velde, Hedwig M. ;
Reurink, Janine ;
Held, Sebastian ;
Li, Catherina H. Z. ;
Yzer, Suzanne ;
Oostrik, Jaap ;
Weeda, Jack ;
Haer-Wigman, Lonneke ;
Yntema, Helger G. ;
Roosing, Susanne ;
Pauleikhoff, Laurenz ;
Lange, Clemens ;
Whelan, Laura ;
Dockery, Adrian ;
Zhu, Julia ;
Keegan, David J. ;
Farrar, G. Jane ;
Kremer, Hannie ;
Lanting, Cornelis P. ;
Damme, Markus ;
Pennings, Ronald J. E. .
HUMAN GENETICS, 2022, 141 (11) :1723-1738
[48]   Hearing Restoration in Cochlear Nerve Deficiency: the Choice Between Cochlear Implant or Auditory Brainstem Implant, a Meta-analysis [J].
Vesseur, Annemarie ;
Free, Rolien ;
Snels, Chantal ;
Dekker, Friedo ;
Mylanus, Emmanuel ;
Verbist, Berit ;
Frijns, Johan .
OTOLOGY & NEUROTOLOGY, 2018, 39 (04) :428-437
[49]   Genetics and pathological mechanisms of Usher syndrome [J].
Yan, Denise ;
Liu, Xue Z. .
JOURNAL OF HUMAN GENETICS, 2010, 55 (06) :327-335
[50]   Localization and expression of clarin-1, the Clrn1 gene product, in auditory hair cells and photoreceptors [J].
Zallocchi, Marisa ;
Meehan, Daniel T. ;
Delimont, Duane ;
Askew, Charles ;
Garige, Suneetha ;
Gratton, Michael Anne ;
Rothermund-Franklin, Christie A. ;
Cosgrove, Dominic .
HEARING RESEARCH, 2009, 255 (1-2) :109-120