Audiologic Outcomes After Cochlear Implantation in Prelingually Deaf Children Who Have Combined Anomalies or Disabilities.

IF 2 3区 医学 Q3 CLINICAL NEUROLOGY Otology & Neurotology Pub Date : 2025-01-01 DOI:10.1097/MAO.0000000000004364
Yeonjoo Choi, Yun Ji Lee, Hye Ah Joo, Woo Seok Kang, Joong Ho Ahn, Jong Woo Chung, Hong Ju Park
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Abstract

Objective: To evaluate the audiologic outcomes after cochlear implantation (CI) in prelingually deaf children with comorbid disorders.

Study design: Retrospective study.

Setting: Tertiary care academic center.

Patients: We enrolled 85 deaf children (111 ears) with comorbid disorders who underwent CI surgery.

Main outcomes and measures: We selected the most common comorbid disorder and compared the categories of auditory performance (CAP) scores of each comorbidity group with those of the control group. Combined cochlear anomalies were also evaluated using temporal bone computed tomography.

Results: The most common comorbid disorder was CHARGE syndrome (n = 17), followed by developmental delay (n = 13), valvular heart disease (including septal defect) (n = 13), Waardenburg syndrome (n = 8), Down syndrome (n = 6), cerebral palsy (n = 5), and cryptorchidism (n = 5). The CAP scores differed significantly between all the groups and the control group after 6 months (p < 0.001). The differences in the CHARGE syndrome (p = 0.004), cerebral palsy (p = 0.001), and Down syndrome (p = 0.004) groups remained significant 2 years after CI. When comparing the presence or absence of anomalies within the syndromic and nonsyndromic groups, significantly poorer outcomes exist when cochlear anomalies with absent modiolus or cochlear nerve deficits were observed, regardless of the presence of syndromic disorders.

Conclusion: Compared with those in the control group, the CAP scores in the group with coexisting disabilities increased over time, but their final scores were relatively lower. Combined disabilities as well as the absent modiolus and cochlear nerve deficit may be clinical markers for poor CAP scores.

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伴有畸形或残疾的语前聋儿童人工耳蜗植入术后的听力学结果。
目的:评价伴有合并症的语前聋儿童人工耳蜗植入术后的听力学预后。研究设计:回顾性研究。环境:三级医疗学术中心。患者:我们招募了85名伴有合并症的聋儿(111耳),他们接受了CI手术。主要结果和测量:我们选择了最常见的共病障碍,并将每个共病组的听觉表现(CAP)评分类别与对照组进行比较。合并耳蜗异常也使用颞骨计算机断层扫描进行评估。结果:最常见的合并症为CHARGE综合征(n = 17),其次为发育迟缓(n = 13)、瓣膜性心脏病(n = 13)、Waardenburg综合征(n = 8)、唐氏综合征(n = 6)、脑瘫(n = 5)、隐睾(n = 5)。6个月后,两组患者CAP评分与对照组比较差异有统计学意义(p < 0.001)。在CI后2年,CHARGE综合征(p = 0.004)、脑瘫(p = 0.001)和唐氏综合征(p = 0.004)组的差异仍然显著。当比较综合征组和非综合征组中是否存在异常时,无论是否存在综合征性疾病,当观察到耳蜗异常伴有耳蜗蜗瓣缺失或耳蜗神经缺损时,结果明显较差。结论:与对照组相比,共存残疾组的CAP得分随时间推移而升高,但最终得分相对较低。综合残疾以及小毛窦缺失和耳蜗神经缺损可能是低CAP评分的临床标志。
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来源期刊
Otology & Neurotology
Otology & Neurotology 医学-耳鼻喉科学
CiteScore
3.80
自引率
14.30%
发文量
509
审稿时长
3-6 weeks
期刊介绍: ​​​​​Otology & Neurotology publishes original articles relating to both clinical and basic science aspects of otology, neurotology, and cranial base surgery. As the foremost journal in its field, it has become the favored place for publishing the best of new science relating to the human ear and its diseases. The broadly international character of its contributing authors, editorial board, and readership provides the Journal its decidedly global perspective.
期刊最新文献
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