• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

普遍新生儿听力筛查在早期识别儿童人工耳蜗植入候选者方面的局限性。

Limitations of universal newborn hearing screening in early identification of pediatric cochlear implant candidates.

作者信息

Young Nancy Melinda, Reilly Brian Kip, Burke Larisa

机构信息

Division of Pediatric Otolaryngology, Section of Otology and Neurotology, Children’s Memorial Hospital, 2300 Children's Plaza, Box 265, Chicago, IL 60614-3394, USA.

出版信息

Arch Otolaryngol Head Neck Surg. 2011 Mar;137(3):230-4. doi: 10.1001/archoto.2011.4.

DOI:10.1001/archoto.2011.4
PMID:21422305
Abstract

OBJECTIVES

To determine whether implementation of universal newborn hearing screening (UNHS) in the state of Illinois has affected the ages at diagnosis of hearing loss and implantation in children receiving cochlear implants and to determine how often children undergoing implantation had UNHS results with no indication of hearing loss (pass).

DESIGN

Retrospective case review of 417 randomly selected pediatric implant recipients born before and after UNHS was mandated by law in Illinois. Data analyzed included hearing screening status, ages at initial diagnosis of sensorineural hearing loss (SNHL) and severe to profound SNHL, and age at implantation.

SETTING

Tertiary care medical center.

PATIENTS

Children receiving implants from 1991 through 2008.

MAIN OUTCOME MEASURES

Ages at diagnosis of SNHL and implantation.

RESULTS

Children born after legally mandated UNHS had significantly younger ages at diagnosis and implantation. However, a younger age at diagnosis of SNHL was not achieved in children who had passed UNHS or who were not screened. Approximately 30% of pediatric implant recipients passed UNHS, regardless of the cause of hearing loss or the presence or absence of known risk factors.

CONCLUSIONS

Almost one-third of our pediatric implant recipients pass UNHS and are older at the time of initial diagnosis and implantation than their peers who fail UNHS. Delayed onset of SNHL limits our ability to achieve early diagnosis and implantation of a significant number of deaf children. This problem will not be solved by the current design of universal hearing screening programs.

摘要

目的

确定伊利诺伊州实施新生儿听力普遍筛查(UNHS)是否影响了接受人工耳蜗植入儿童的听力损失诊断年龄和植入年龄,并确定接受植入手术的儿童中,UNHS结果显示无听力损失迹象(通过)的频率。

设计

对伊利诺伊州依法强制实施UNHS前后出生的417名随机选择的小儿植入受者进行回顾性病例审查。分析的数据包括听力筛查状况、感音神经性听力损失(SNHL)和重度至极重度SNHL的初始诊断年龄以及植入年龄。

地点

三级医疗中心。

患者

1991年至2008年接受植入手术的儿童。

主要观察指标

SNHL诊断年龄和植入年龄。

结果

在依法强制实施UNHS后出生的儿童诊断和植入时年龄明显更小。然而,UNHS通过或未接受筛查的儿童并未实现SNHL的更早诊断。无论听力损失原因或已知风险因素是否存在,约30%的小儿植入受者UNHS通过。

结论

我们几乎三分之一的小儿植入受者UNHS通过,他们在初始诊断和植入时的年龄比UNHS未通过的同龄人更大。SNHL的延迟发作限制了我们对大量失聪儿童进行早期诊断和植入的能力。当前的听力普遍筛查计划设计无法解决这个问题。

相似文献

1
Limitations of universal newborn hearing screening in early identification of pediatric cochlear implant candidates.普遍新生儿听力筛查在早期识别儿童人工耳蜗植入候选者方面的局限性。
Arch Otolaryngol Head Neck Surg. 2011 Mar;137(3):230-4. doi: 10.1001/archoto.2011.4.
2
From hearing screening to cochlear implantation: cochlear implants in children under 3 years of age.从听力筛查到人工耳蜗植入:3岁以下儿童的人工耳蜗植入
Acta Otolaryngol. 2008 Apr;128(4):369-72. doi: 10.1080/00016480701736254.
3
Exploring factors that affect the age of cochlear implantation in children.探索影响儿童人工耳蜗植入年龄的因素。
Int J Pediatr Otorhinolaryngol. 2011 Sep;75(9):1082-7. doi: 10.1016/j.ijporl.2011.05.018. Epub 2011 Jun 23.
4
The influence of newborn hearing screening on the age at cochlear implantation in children.新生儿听力筛查对儿童人工耳蜗植入年龄的影响。
Laryngoscope. 2015 Apr;125(4):985-90. doi: 10.1002/lary.25045. Epub 2015 Feb 11.
5
Impact of newborn hearing screening: comparing outcomes in pediatric cochlear implant users.新生儿听力筛查的影响:比较小儿人工耳蜗使用者的结果
Laryngoscope. 2009 May;119(5):974-9. doi: 10.1002/lary.20188.
6
Indications for pediatric cochlear implantation at the University of Mississippi Medical Center.
J Miss State Med Assoc. 2007 Nov;48(11):331-5.
7
Impact of early hearing screening and treatment on language development and education level: evaluation of 6 years of universal newborn hearing screening (ALGO) in Flanders, Belgium.早期听力筛查与治疗对语言发育和教育水平的影响:比利时弗拉芒地区6年新生儿听力普遍筛查(ALGO)评估
Int J Pediatr Otorhinolaryngol. 2008 May;72(5):599-608. doi: 10.1016/j.ijporl.2008.01.012. Epub 2008 Mar 4.
8
[Evaluation of the Austrian Newborn Hearing Screening Program].[奥地利新生儿听力筛查项目评估]
Wien Klin Wochenschr. 2005 Sep;117(18):641-6. doi: 10.1007/s00508-005-0414-z.
9
Early language development in children with profound hearing loss fitted with a device at a young age: part II--content of the first lexicon.自幼佩戴助听设备的极重度听力损失儿童的早期语言发展:第二部分——首个词汇库的内容
Ear Hear. 2009 Oct;30(5):541-51. doi: 10.1097/AUD.0b013e3181aa00ea.
10
Evaluation of auditory development in infants and toddlers who received cochlear implants under the age of 24 months with the LittlEARS) Auditory Questionnaire.使用小耳朵(LittlEARS)听觉问卷对24个月以下接受人工耳蜗植入的婴幼儿的听觉发育进行评估。
Int J Pediatr Otorhinolaryngol. 2010 Oct;74(10):1149-55. doi: 10.1016/j.ijporl.2010.07.003. Epub 2010 Aug 4.

引用本文的文献

1
Advancing Educational Equity for Children with Hearing Loss: Celebrating the 50 Anniversary of the Individuals with Disability Education Act (IDEA).促进听力损失儿童的教育公平:庆祝《残疾人教育法》(IDEA)颁布50周年。
ORL Head Neck Nurs. 2025 Spring;43(2):40-47.
2
Newborn concurrent hearing and genetic screening for hearing impairment: A systematic review and meta‑analysis.新生儿听力与听力障碍基因联合筛查:一项系统评价与Meta分析
Exp Ther Med. 2024 Jul 16;28(3):365. doi: 10.3892/etm.2024.12654. eCollection 2024 Sep.
3
Hearing Loss: Genetic Testing, Current Advances and the Situation in Latin America.
听力损失:遗传检测、当前进展及拉丁美洲情况。
Genes (Basel). 2024 Jan 29;15(2):178. doi: 10.3390/genes15020178.
4
Validation of the LittlEARS Questionnaire in Hearing Maltese-Speaking Children.LittlEARS问卷在讲马耳他语的听力受损儿童中的验证
Audiol Res. 2022 Apr 11;12(2):191-201. doi: 10.3390/audiolres12020022.
5
Assessment of Hearing Screening Combined With Limited and Expanded Genetic Screening for Newborns in Nantong, China.中国南通新生儿听力筛查联合有限和扩展遗传筛查评估。
JAMA Netw Open. 2021 Sep 1;4(9):e2125544. doi: 10.1001/jamanetworkopen.2021.25544.
6
Neonatal Hearing Screening: Prevalence of Unilateral and Bilateral Hearing Loss and Associated Risk Factors.新生儿听力筛查:单侧和双侧听力损失的患病率及相关危险因素
Cureus. 2021 Jun 26;13(6):e15947. doi: 10.7759/cureus.15947. eCollection 2021 Jun.
7
Radixin modulates the function of outer hair cell stereocilia.根蛋白调节外毛细胞静纤毛的功能。
Commun Biol. 2020 Dec 23;3(1):792. doi: 10.1038/s42003-020-01506-y.
8
Concurrent Hearing and Genetic Screening of 180,469 Neonates with Follow-up in Beijing, China.中国北京对 180469 例新生儿进行了听力与遗传联合筛查及随访
Am J Hum Genet. 2019 Oct 3;105(4):803-812. doi: 10.1016/j.ajhg.2019.09.003. Epub 2019 Sep 26.
9
A proposal for comprehensive newborn hearing screening to improve identification of deaf and hard-of-hearing children.全面新生儿听力筛查提案,以改善聋儿和重听儿童的发现。
Genet Med. 2019 Nov;21(11):2614-2630. doi: 10.1038/s41436-019-0563-5. Epub 2019 Jun 7.
10
Hearing Impairment Among Children Referred to a Public Audiology Clinic in Gaborone, Botswana.转诊至博茨瓦纳哈博罗内一家公共听力诊所的儿童中的听力障碍情况。
Glob Pediatr Health. 2018 Apr 20;5:2333794X18770079. doi: 10.1177/2333794X18770079. eCollection 2018.