Hoey Andrew Wesley, Pai Irumee, Driver Sandra, Connor Steve, Wraige Elizabeth, Jiang Dan
a Department of Paediatric Otolaryngology , Evelina London Children's Hospital , London , UK.
b Department of Head and Neck Imaging , Guy's and St Thomas' NHS Foundation Trust , London , UK.
Cochlear Implants Int. 2017 Jul;18(4):216-225. doi: 10.1080/14670100.2017.1315510. Epub 2017 May 9.
Congenital Cytomegalovirus (cCMV) is a well-defined cause for neonatal mortality and morbidity, particularly sensorineural hearing loss and other neurodevelopmental disruption. We present a retrospective study which provides an overview of the assessment and preoperative work-up for patients diagnosed with cCMV and their cochlear implant (CI) outcomes.
This was a retrospective case series study of all children with a confirmed diagnosis of cCMV who underwent cochlear implantation at St Thomas' Hospital from 2003 to 2015. Data were collected on the preoperative audiology, imaging findings, and neurological assessment. CI outcomes were measured using the Speech Intelligibility Rating (SIR), Category of Auditory Performance (CAP), and Infant-Toddler Meaningful Auditory Integration Scale (IT-MAIS).
Eleven patients underwent cochlear implantation, 45% had severe-to-profound hearing loss, and 55% had bilateral profound hearing loss. The mean age at initial assessment was 2.1 years (median 1.7, range 0.6-7.5) and the mean age of implantation was 4.0 years (median 2.5, range 0.9-11.8). The mean length of follow-up was 4.8 years (median 2.3, range 1.5-14). Six patients had bilateral simultaneous implantation (55%), four bilateral sequential (36%), and one unilateral (9%). Nine patients had white matter changes on magnetic resonance imaging, largely in the periventricular and cortical regions. Of the 11 patients, 4 (36%) had associated neurological comorbidities and 3 (27%) had additional neurocognitive developmental delay of varying severity. The majority of patients showed improvement in auditory outcomes. No statistically significant correlation was found between age of implantation, neurocognitive, and neurological comorbidities or length of follow-up and hearing outcomes.
While the overall outcomes were mixed, most children in our cohort were found to benefit from cochlear implantation. Our data also highlight the significant neurodevelopmental comorbidities associated with cCMV and their negative impact on CI outcomes. With the recent advances in medical treatment, this underlines the importance of multidisciplinary management of these patients.
先天性巨细胞病毒(cCMV)是新生儿死亡和发病的明确病因,尤其是感音神经性听力损失和其他神经发育障碍。我们开展了一项回顾性研究,概述了被诊断为cCMV的患者的评估和术前检查及其人工耳蜗(CI)植入结果。
这是一项对2003年至2015年在圣托马斯医院接受人工耳蜗植入的所有确诊为cCMV的儿童进行的回顾性病例系列研究。收集了术前听力学、影像学检查结果和神经学评估的数据。使用言语可懂度评分(SIR)、听觉表现类别(CAP)和婴幼儿有意义听觉整合量表(IT-MAIS)来衡量人工耳蜗植入结果。
11例患者接受了人工耳蜗植入,45%有重度至极重度听力损失,55%有双侧极重度听力损失。初次评估时的平均年龄为2.1岁(中位数1.7岁,范围0.6 - 7.5岁),植入时的平均年龄为4.0岁(中位数2.5岁,范围0.9 - 11.8岁)。平均随访时间为4.8年(中位数2.3年,范围1.5 - 14年)。6例患者双侧同时植入(55%),4例双侧序贯植入(36%),1例单侧植入(9%)。9例患者在磁共振成像上有白质改变,主要位于脑室周围和皮质区域。11例患者中,4例(36%)有相关神经合并症,3例(27%)有不同程度的额外神经认知发育迟缓。大多数患者的听觉结果有所改善。在植入年龄、神经认知和神经合并症或随访时间与听力结果之间未发现统计学上的显著相关性。
虽然总体结果不一,但我们队列中的大多数儿童从人工耳蜗植入中受益。我们的数据还突出了与cCMV相关的显著神经发育合并症及其对人工耳蜗植入结果的负面影响。随着近期医学治疗的进展,这凸显了对这些患者进行多学科管理的重要性。