McDermott Ann-Louise, Williams Jo, Kuo Michael J, Reid Andrew P, Proops David W
Department of Otolaryngology, The Birmingham Children's Hospital, Steelhouse Lane, Birmingham B4 6NH, UK.
Int J Pediatr Otorhinolaryngol. 2008 Jun;72(6):751-7. doi: 10.1016/j.ijporl.2008.01.035. Epub 2008 Apr 22.
To evaluate complication rates and outcomes of children with Down syndrome fitted with a Bone Anchored Hearing Aid (Baha). To evaluate whether the Bone Anchored Hearing Aid is a successful form of aural rehabilitation in children with Down syndrome from a patients' perspective.
Retrospective case analysis and postal questionnaire study.
The Birmingham Children's Hospital, UK.
A total of 15 children were fitted with a Baha between February 1992 and February 2007. The age range was 2-15 years. A postal questionnaire was sent to each family. The Glasgow Children's Benefit Inventory (GCBI) was used in this study.
Implantation results, skin reactions and other complications were recorded. Quality of life after receiving a Baha was assessed with the GCBI.
All 15 patients are using their Baha 7 days a week for more than 8h a day after a follow-up of 14 months with continuing audiological benefit. No fixtures were lost, and skin problems were encountered in 3 (20%). Regarding quality of life, all 15 patients had improved social and physical functioning as a result of better hearing.
Baha has an important role in the overall management of individuals with Down syndrome after conventional hearing aids and/or ventilation tubes have been considered or already failed. This study has shown a 20% rate of soft tissue reaction and there were no fixture losses in this group. No significant increase in complication rates was identified in children with Down syndrome. Finally, there was a significantly improved quality of life in children with Down syndrome after receiving their Baha. There was a high patient/carer satisfaction with Baha. Two of our series had bilateral two stage fixture procedures without any complications. More consideration should be given to bilateral bone anchored hearing aids in this group.
评估佩戴骨锚式助听器(Baha)的唐氏综合征患儿的并发症发生率及治疗效果。从患者角度评估骨锚式助听器是否是唐氏综合征患儿成功的听力康复方式。
回顾性病例分析及邮寄问卷调查研究。
英国伯明翰儿童医院。
1992年2月至2007年2月期间,共有15名儿童佩戴了Baha。年龄范围为2至15岁。向每个家庭发送了邮寄问卷。本研究使用了格拉斯哥儿童受益量表(GCBI)。
记录植入结果、皮肤反应及其他并发症。使用GCBI评估佩戴Baha后的生活质量。
在随访14个月后,所有15名患者每周7天、每天使用Baha超过8小时,听力持续受益。未出现固定装置丢失的情况,3例(20%)出现皮肤问题。在生活质量方面,所有15名患者因听力改善,社交和身体功能均有所提高。
在考虑或已使用传统助听器和/或通气管失败后,Baha在唐氏综合征患者的整体治疗中具有重要作用。本研究显示软组织反应率为20%,该组未出现固定装置丢失的情况。未发现唐氏综合征患儿的并发症发生率显著增加。最后,唐氏综合征患儿佩戴Baha后生活质量显著提高。患者/护理人员对Baha的满意度很高。我们系列中的2例患者进行了双侧两阶段固定装置手术,未出现任何并发症。该组应更多考虑双侧骨锚式助听器。