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病因和诊断评估:巴西严重至极重度感音神经性听力损失的算法。

Etiologic and diagnostic evaluation: algorithm for severe to profound sensorineural hearing loss in Brazil.

机构信息

* Human Molecular Genetics Laboratory, Molecular Biology and Genetic Engineering Center (CBMEG), University of Campinas (Unicamp) , Campinas, São Paulo , Brazil.

出版信息

Int J Audiol. 2013 Nov;52(11):746-52. doi: 10.3109/14992027.2013.817689. Epub 2013 Aug 3.

Abstract

OBJECTIVE

Evaluation of the effectiveness of imaging and genetic testing, and establishment of a cost-effective diagnostic protocol for the etiologic diagnosis of sensorineural hearing loss (SNHL) in Brazil.

DESIGN

Prospective cohort study.

STUDY SAMPLE

Analysis of 100 unrelated Brazilian patients with severe to profound bilateral SNHL submitted to cochlear implant (CI) between 2002 and 2010 at the University of Campinas hospital. The study was based upon three groups: individuals with congenital, progressive, and sudden SNHL.

RESULTS

After the diagnostic investigation, the number of cases with unknown etiology was reduced from 72 to 42 (a 42% reduction); 25% of cases were due to environmental factors, 19% to genetic causes, and 14% to inner-ear abnormalities or other clinical features. The genetic and imaging findings contributed to the diagnosis of SNHL in 19% and 20% of the cases analysed, respectively. Molecular testing mainly contributed to the diagnosis of patients with congenital SNHL, while the contribution of radiologic examination was higher for individuals with progressive or sudden SNHL. A sequential diagnostic protocol was proposed based on these data.

CONCLUSIONS

The proposed diagnostic workup algorithm could provide better optimization of etiologic diagnosis, as well as reduced costs, compared to a simultaneous testing approach.

摘要

目的

评估影像学检查和基因检测的有效性,为巴西感音神经性听力损失(SNHL)的病因诊断建立一种经济有效的诊断方案。

设计

前瞻性队列研究。

研究样本

对 2002 年至 2010 年间在坎皮纳斯大学医院接受人工耳蜗植入(CI)的 100 例无亲缘关系的巴西严重至极重度双侧 SNHL 患者进行分析。该研究基于以下三个组:先天性、进行性和突发性 SNHL 患者。

结果

在进行诊断性检查后,病因不明的病例数从 72 例减少到 42 例(减少 42%);25%的病例是由环境因素引起的,19%是由遗传原因引起的,14%是由内耳异常或其他临床特征引起的。遗传和影像学发现分别有助于诊断 19%和 20%分析病例的 SNHL。分子检测主要有助于先天性 SNHL 患者的诊断,而对于进行性或突发性 SNHL 患者,放射学检查的贡献更高。根据这些数据提出了一种序贯诊断方案。

结论

与同时进行测试的方法相比,所提出的诊断性检查算法可以更好地优化病因诊断,并降低成本。

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