Service d'ORL, CHU de Grenoble, 38700 La Tronche, France.
CHU de Limoges, Limoges, France.
Eur Ann Otorhinolaryngol Head Neck Dis. 2020 Sep;137 Suppl 1:S27-S35. doi: 10.1016/j.anorl.2020.07.012. Epub 2020 Aug 3.
Evaluate in France the outcomes of cochlear implantation outside the selection criteria, off-label.
This is a prospective cohort study including adults and children having received a cochlear implant (CI) in an off-label indication, that is outside the criteria established by the "Haute Autorité de santé (HAS)" in 2012. The data was collected from the "EPIIC" registry on recipients who received CIs in France between 2011 and 2014. Speech audiometry was performed at 60dB preimplantation and after one year of CI use, as well as an evaluation of the scores of the quality of life with the APHAB questionnaire, the scores for CAP and the professional/academic status in pre- and post-implantation conditions. Major and minor complications at surgery have been recorded.
In total, 590 patients (447 adults and 143 children) with an off-label indication for CIs were included in this study from the EPIIC registry (11.7% of the whole cohort of EPIIC). For adults, the median percentage of comprehension using monosyllabic word lists was 41% in preimplantation condition versus 53% after one year of CI use (P<0.001) and 60% versus 71% in dissyllabic word lists (P<0.001). The CAP scores were 5 versus 6 in pre- and post-implantation conditions respectively (P<0.001) and the APHAB scores were statistically lower after implantation (P<0.001). In the children cohort, the median percentage of comprehension using monosyllabic word lists was 51% in preimplantation condition and 65% after CI (P<0.001), and 48% versus 82% (P<0.001) for dissyllabic word lists. The CAP scores were 5 versus 7 respectively in pre- and post-CI conditions (P<0.001). Thirty-two minor complications (5.4%) and 17 major complications (2.8%) were reported in our panel of off-label indication patients.
These results suggest that a revision of the cochlear implantation candidacy criteria is necessary to allow more patients with severe or asymmetric hearing loss to benefit from a CI when there is an impact on quality of life despite the use of an optimal hearing aid.
评估法国在未列入选择标准的情况下(超适应证)进行人工耳蜗植入的结果。
这是一项前瞻性队列研究,纳入了在法国接受人工耳蜗植入(CI)的成人和儿童,这些植入均为超适应证,即不符合“法国卫生署(HAS)”于 2012 年制定的标准。该研究的数据来自 EPIIC 登记处,纳入了 2011 年至 2014 年期间在法国接受 CI 的患者。在植入前和植入后 1 年,分别在 60dB 进行言语测听,使用 APHAB 问卷、CAP 评分以及职业/学术状况评估生活质量评分。记录手术中的主要和次要并发症。
本研究共纳入了 EPIIC 登记处的 590 名(447 名成人和 143 名儿童)接受超适应证 CI 的患者(EPIIC 整个队列的 11.7%)。对于成人,植入前使用单音节词列表的理解百分比中位数为 41%,植入后 1 年为 53%(P<0.001),双音节词列表分别为 60%和 71%(P<0.001)。植入前和植入后的 CAP 评分分别为 5 分和 6 分(P<0.001),植入后 APHAB 评分明显降低(P<0.001)。在儿童队列中,植入前使用单音节词列表的理解百分比中位数为 51%,植入后为 65%(P<0.001),双音节词列表分别为 48%和 82%(P<0.001)。植入前和植入后的 CAP 评分分别为 5 分和 7 分(P<0.001)。在我们的超适应证患者组中,报告了 32 例(5.4%)轻微并发症和 17 例(2.8%)严重并发症。
这些结果表明,需要修订人工耳蜗植入候选标准,以允许更多患有严重或非对称听力损失的患者在生活质量受到影响的情况下受益于人工耳蜗,即使他们使用了最佳的助听器。