Rates of revision and device failure in cochlear implant surgery: A 30‐year experience

医学 人工耳蜗植入 外科 植入 回顾性队列研究 人口统计学的 人工耳蜗植入术 队列 听力学 内科学 社会学 人口学
作者
Jeffrey T. Wang,Allen Y. Wang,Colleen Psarros,María de la Cruz
出处
期刊:Laryngoscope [Wiley]
卷期号:124 (10): 2393-2399 被引量:129
标识
DOI:10.1002/lary.24649
摘要

Objectives/Hypothesis To characterize revision cochlear implant surgery and quantify rates of revision and device failure. Study Design Retrospective review of 235 cases of revision cochlear implant surgery performed at the Sydney Cochlear Implant Center over a period of 30 years, between January 1982 and June 2011. Methods Patient demographics and characteristics of revision surgery were retrospectively extracted from a centralized database. Analyses of overall and cumulative rates were performed. Results During the study period, 2,827 primary cochlear implantations were performed in 2,311 patients, with 201 primary implants in 191 patients of this cohort (109 children and 82 adults) undergoing 235 revision surgeries. The most common indication for revision surgery was device failure (57.8%), followed by migration/extrusion (23.4%), infection/wound complication (17.0%), and poor outcome/secondary pathology (6.4%). The majority of revision surgeries were reimplantations. Overall revision and device failure rates were 8.3% and 4.8%, respectively. The cumulative revision rate for primary implants at all ages increased linearly by 1% per year. The cumulative revision rate was significantly higher in children, and decreased with more recently performed implantations and with newer generations of implants. Conclusions The cumulative revision rate for primary implants suggests an ongoing linear relationship between the time of postprimary implantation and the need for revision surgery. We have formed an evidence base that characterizes the nature and frequency of revision surgery in a high‐volume setting, allowing clinicians to effectively counsel prospective patients and clinics to understand the burden of revision surgery and device failure. Level of Evidence 4 Laryngoscope 124:2393–2399, 2014

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