Foyt David, Carfrae Matthew
Northeast Ear Institute, Albany, New York 12203, USA.
Otol Neurotol. 2006 Feb;27(2):167-71. doi: 10.1097/01.mao.0000188340.53395.0d.
To develop a minimal access approach for implantation of the Vibrant Soundbridge middle ear hearing implant. This approach ideally uses the smallest skin incision possible, minimal or no hair shave, and the least possible amount of tissue and bone manipulation. This will facilitate the acceptability of the procedure to the general community and reduce the flap-related complication rate. The procedure is similar to the minimal access approach described for cochlear implantation.
Eight patients with various degrees of sensorineural hearing loss and one with a mixed hearing loss who met implant criteria for the Vibrant Soundbridge middle ear hearing implant received the device over a 42-month period. The first two patients underwent the traditional implant procedure with postauricular hair shave, postauricular S-shaped incision, and implant receiver suture fixation to the temporal bone. The following seven consecutive patients received a progressively smaller C-shaped postauricular skin incision, no hair shave, retrograde skull drilling for the implant seat, and no implant suture fixation until the technique closely approximated the minimal access cochlear implant procedure. Postoperative performance of the Soundbridge/Vibrant Med-El was evaluated through audiology testing and subjective patient reports.
Private neurotology clinic and tertiary care teaching hospital.
The technique was feasible in all patients. Follow-up for the minimal access group ranged from 3 years to 5 months. There were no complications related to the approach, and all patients were satisfied users of the implant. The lack of hair shave and small incision size was greatly appreciated and warmly endorsed by the patients.
The Vibrant Soundbridge/Vibrant Med-El can be safely implanted using the minimal access method that has been popularized for cochlear implant surgery. A large incision, extensive hair shave, risk of flap necrosis, and possibility of unsightly scar may deter patients from pursuing the potential benefits of implanted hearing technology. The technique may make the device more accessible to individuals who have concerns regarding cosmetics and potential flap complications.
开发一种用于植入振动声桥中耳听力植入物的微创方法。该方法理想情况下应使用尽可能小的皮肤切口,尽量少剃或不剃头发,以及尽可能少地操作组织和骨骼。这将提高该手术在普通人群中的可接受性,并降低皮瓣相关并发症的发生率。该手术类似于为人工耳蜗植入所描述的微创方法。
8例不同程度感音神经性听力损失患者和1例混合性听力损失患者,符合振动声桥中耳听力植入物的植入标准,在42个月期间接受了该装置植入。前两名患者接受了传统的植入手术,包括耳后剃发、耳后S形切口,以及将植入接收器缝合固定于颞骨。接下来的7例连续患者接受了逐渐变小的耳后C形皮肤切口,不剃头发,逆行颅骨钻孔以制作植入座,并且在该技术与微创人工耳蜗植入手术接近之前不进行植入物缝合固定。通过听力学测试和患者主观报告评估声桥/奥地利美迪耳的术后性能。
私立神经耳科诊所和三级护理教学医院。
该技术在所有患者中均可行。微创组的随访时间为3年至5个月。没有与该方法相关的并发症,所有患者对植入物的使用都很满意。患者对不剃头发和小切口尺寸非常满意并给予热情认可。
使用已在人工耳蜗植入手术中普及的微创方法,可以安全地植入振动声桥/奥地利美迪耳。大切口、大面积剃发、皮瓣坏死风险以及难看疤痕的可能性可能会阻碍患者寻求植入式听力技术的潜在益处。该技术可能会使那些担心美容和潜在皮瓣并发症的人更容易接受该装置。