Ricci Giampietro, Trabalzini Franco, Faralli Mario, D'Ascanio Luca, Cristi Cristina, Molini Egisto
Department of Otolaryngology, University of Perugia, Loc. S. Andrea delle Fratte, 06156, Perugia, Italy,
Eur Arch Otorhinolaryngol. 2014 Mar;271(3):489-93. doi: 10.1007/s00405-013-2424-1. Epub 2013 Mar 24.
CHARGE syndrome is a rare, polymalformative disease, representing one of the major causes of associated blindness and deafness. Bilateral, severe-profound, sensorineural hearing loss is common in CHARGE children. Aim of this study is to present our results in children with "CHARGE syndrome" submitted to cochlear implantation (CI). The frequency of anatomic anomalies, possible variations in the surgical technique of CI, and the audiological/rehabilitative benefits attained in our patients are reported. we submitted 5 children affected by CHARGE syndrome with profound, bilateral, sensorineural hearing loss to CI. Otoacoustic emissions, auditory brainstem response, acoustic impedance testing, cranial computed tomography and magnetic resonance were carried out preoperatively in all children. CI was performed using the mastoidotomy-posterior tympanotomy approach in two cases, and the suprameatal approach in three children. Infant toddler-meaningful auditory integration scale was used to evaluate kid's audiological performance before and after CI. Intra-operatory findings and postsurgical complications were evaluated. Among our patients, intraoperative anatomical malformations were cochlear hypoplasia (100 %), ossicles malformations (100 %), semicircular canals aplasia (100 %), oval window atresia (60 %), round window atresia (40 %), widening of the aqueduct of the vestibule (20 %), and aberrant course of the facial nerve (20 %). No intra- or postoperative complication was recorded in relation to implant positioning. After a follow-up ranging from 1 to 4.5 years, only 2/5 patients used oral language as the sole mean of communication, 1 started utilizing oral language as the main mean of communication, while 2 patients did not develop any linguistic ability. In conclusion, CI in patients with CHARGE association is feasible and, despite results variability, it should be carried out in CHARGE children with severe hearing loss as soon as possible. Although the selection of a specific surgical technique does not seem to influence the audiological outcome, the suprameatal access is valuable when important surgical landmarks (i.e. lateral semicircular canal and incus) are absent.
CHARGE综合征是一种罕见的多系统发育畸形疾病,是导致相关失明和失聪的主要原因之一。双侧严重至极重度感音神经性听力损失在CHARGE综合征患儿中很常见。本研究的目的是报告我们对接受人工耳蜗植入(CI)的“CHARGE综合征”患儿的研究结果。报告了解剖异常的发生率、CI手术技术可能的变化以及我们患者所获得的听力学/康复益处。我们对5例患有CHARGE综合征且有严重双侧感音神经性听力损失的患儿进行了CI植入。所有患儿术前均进行了耳声发射、听性脑干反应、声阻抗测试、头颅计算机断层扫描和磁共振成像检查。2例患儿采用乳突切开-后鼓室切开术式进行CI植入,3例采用耳道上入路。使用婴幼儿有意义听觉整合量表评估患儿CI植入前后的听力学表现。评估术中发现和术后并发症。在我们的患者中,术中解剖畸形包括耳蜗发育不全(100%)、听小骨畸形(100%)、半规管发育不全(100%)、卵圆窗闭锁(60%)、圆窗闭锁(40%)、前庭导水管增宽(20%)以及面神经走行异常(20%)。未记录到与植入物定位相关的术中或术后并发症。随访1至4.5年,只有2/5的患者将口语作为唯一的交流方式,1例开始将口语作为主要交流方式,而2例患者未发展出任何语言能力。总之,CHARGE综合征患者的CI植入是可行的,尽管结果存在差异,但对于重度听力损失的CHARGE综合征患儿应尽早进行。虽然选择特定的手术技术似乎不影响听力学结果,但当重要的手术标志(如外侧半规管和砧骨)缺失时,耳道上入路很有价值。