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用于骨传导听力的听觉骨整合植入物的稳定性、存活率和耐受性:一项随机对照试验的长期随访

Stability, Survival, and Tolerability of an Auditory Osseointegrated Implant for Bone Conduction Hearing: Long-Term Follow-Up of a Randomized Controlled Trial.

作者信息

den Besten Christine A, Stalfors Joacim, Wigren Stina, Blechert Johan Ivarsson, Flynn Mark, Eeg-Olofsson Måns, Aggarwal Rohini, Green Kevin, Nelissen Rik C, Mylanus Emmanuel A M, Hol Myrthe K S

机构信息

*Department of Otorhinolaryngology, Radboud University Medical Center, Nijmegen, The Netherlands †Department of Otorhinolaryngology, Sahlgrenska University Hospital, The Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden ‡Cochlear Bone Anchored Solutions AB, Mölnlycke, Sweden §Department of Otorhinolaryngology, Salford Royal Hospital, Salford, United Kingdom ||Department of Otorhinolaryngology, Manchester Royal Infirmary, Manchester, United Kingdom.

出版信息

Otol Neurotol. 2016 Sep;37(8):1077-83. doi: 10.1097/MAO.0000000000001111.

Abstract

OBJECTIVE

To compare implant stability, survival, and soft tissue reactions for a novel (test) and previous generation (control) percutaneous auditory osseointegrated implant for bone conduction hearing at long-term follow-up of 5 years.

STUDY DESIGN

Single follow-up visit of a previously completed multicenter, randomized, controlled trial.

PATIENTS

Fifty-seven of the 77 participants of a completed randomized controlled trial on a new auditory osseointegrated implant underwent a single follow-up visit 5 years after implantation, which comprised implant stability measurements and collection of Holgers scores. Additionally, implant survival was recorded for all 77 patients from the original trial.

RESULTS

The test implant showed significantly higher implant stability quotient (ISQ) values compared with the control implant throughout the 5-year follow-up. Mean area under the curve of ISQ high from baseline to 5 years was 71.6 (standard deviation [SD] ±2.0) and 66.7 (SD ±3.4) for the test and control implant, respectively (p < 0.0001). For both implants, the mean ISQ value recorded at 5 years was higher compared with implantation (test group +2.03 [SD ±2.55, within group p < 0.0001] and control group +2.25 [SD ±4.95, within group p = 0.12]). No difference was noticed in increase from baseline between groups (p = 0.64). Furthermore, evaluation of soft tissue reactions continued to show superiority of the test implant. At the 5-year follow-up visit, one patient (2.5%) presented with a Holgers grade 2 in the test group, compared with four patients (23.5%) in the control group (p = 0.048); no patient presented with more severe soft tissue reactions. Excluding explantations, the survival rate was 95.8% for the test group and 95.0% for the control group. The corresponding rates including explantations were 93.9 and 90.0%.

CONCLUSION

The test implant showed superiority in terms of higher mean ISQ values and less adverse soft tissue reactions, both at the single 5-year follow-up visit and during the complete follow-up. In addition, both implants showed an equally high implant survival.

摘要

目的

在一项为期5年的长期随访研究中,比较一种新型(试验性)经皮听觉骨整合植入物与上一代(对照性)经皮听觉骨整合植入物在骨传导听力方面的植入稳定性、存活率和软组织反应。

研究设计

对一项之前已完成的多中心、随机、对照试验进行单次随访。

患者

在一项关于新型听觉骨整合植入物的已完成随机对照试验的77名参与者中,有57名在植入后5年接受了单次随访,包括植入稳定性测量和收集霍尔格斯评分。此外,记录了原试验中所有77名患者的植入物存活率。

结果

在整个5年随访期间,试验性植入物的植入稳定性商数(ISQ)值显著高于对照性植入物。试验性植入物和对照性植入物从基线到5年的ISQ高值曲线下平均面积分别为71.6(标准差[SD]±2.0)和66.7(SD±3.4)(p<0.0001)。对于两种植入物,5年时记录的平均ISQ值均高于植入时(试验组+2.03[SD±2.55,组内p<0.0001],对照组+2.25[SD±4.95,组内p=0.12])。两组间从基线开始的增加量无差异(p=0.64)。此外,对软组织反应的评估继续显示试验性植入物的优越性。在5年随访时,试验组有1名患者(2.5%)出现霍尔格斯2级反应,而对照组有4名患者(23.5%)出现该反应(p=0.048);没有患者出现更严重的软组织反应。排除取出植入物的情况,试验组的存活率为95.8%,对照组为95.0%。包括取出植入物情况在内的相应存活率分别为93.9%和90.0%。

结论

在单次5年随访以及整个随访期间,试验性植入物在平均ISQ值更高和不良软组织反应更少方面显示出优越性。此外,两种植入物均显示出同样高的植入物存活率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/533e/4982756/979d346d2ca4/mao-37-1077-g001.jpg

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