Colletti Liliana, Colletti Giacomo, Mandalà Marco, Colletti Vittorio
ENT Department, University of Verona, Verona, Italy.
Department of Maxillo-Facial Surgery, University of Milan, Italy.
Otolaryngol Head Neck Surg. 2014 Aug;151(2):308-14. doi: 10.1177/0194599814531913. Epub 2014 Apr 23.
To compare the outcomes between 2 age-matched cohorts of children with cochlear nerve deficiency: those receiving auditory brainstem implants (group A) or cochlear implants (group B).
Retrospective cohort study.
Tertiary referral center.
Subjects were selected from a pool of 537 children fitted with cochlear implants (n = 443) or auditory brainstem implants (n = 94) over the past 14 years. Performance, examined with the Category of Auditory Performance scale, and complications were compared with a mean follow-up of 5 years.
All children had bilateral profound sensorineural hearing loss and cochlear nerve deficiency. Magnetic resonance imaging documented an absent cochlear nerve (n = 12) and a small cochlear nerve (n = 8) in group A and an absent cochlear nerve (n = 11) and a small cochlear nerve (n = 9) in group B (P = 1.000). Children with cochlear implants had Category of Auditory Performance scores spanning from 0 to 3 levels of performance, and all required manual communication mode and visual supplementation. Children with auditory brainstem implants had Category of Auditory Performance scores spanning from 2 to 7, and most patients demonstrated behavioral responses irrespective of inner ear malformations and an absent cochlear nerve or small cochlear nerve (P < .001).
In children with cochlear nerve deficiency, patients fitted with cochlear implants did not develop speech understanding and production. Those fitted with auditory brainstem implants had the opportunity to develop open-set speech perception, acquiring verbal language competence using oral communication exclusively and participating in mainstream education. The overall complication rate of auditory brainstem implants was not greater than that of cochlear implants.
比较两组年龄匹配的蜗神经缺损儿童的治疗效果:一组接受听觉脑干植入(A组),另一组接受人工耳蜗植入(B组)。
回顾性队列研究。
三级转诊中心。
研究对象选自过去14年中接受人工耳蜗植入(n = 443)或听觉脑干植入(n = 94)的537名儿童。采用听觉表现类别量表评估其表现,并比较并发症情况,平均随访时间为5年。
所有儿童均为双侧极重度感音神经性听力损失且伴有蜗神经缺损。磁共振成像显示,A组有12例蜗神经缺如、8例蜗神经细小;B组有11例蜗神经缺如、9例蜗神经细小(P = 1.000)。接受人工耳蜗植入的儿童听觉表现类别量表评分范围为0至3级,均需要使用人工交流方式并辅以视觉补充。接受听觉脑干植入的儿童听觉表现类别量表评分范围为2至7级,大多数患者无论内耳畸形情况以及蜗神经缺如或细小与否,均表现出行为反应(P < .001)。
在蜗神经缺损儿童中,接受人工耳蜗植入的患者未发展出言语理解和表达能力。接受听觉脑干植入的患者有机会发展开放式言语感知能力,仅通过口语交流获得语言能力并参与主流教育。听觉脑干植入的总体并发症发生率不高于人工耳蜗植入。