• 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

Universal newborn hearing screening--the Colorado story.

作者信息

Downs M P

出版信息

Int J Pediatr Otorhinolaryngol. 1995 Jul;32(3):257-9. doi: 10.1016/0165-5876(95)01183-c.

DOI:10.1016/0165-5876(95)01183-c
PMID:7665273
Abstract

The Colorado State Public Health Department inaugurated a state-wide program of universal newborn hearing screening in 1992. A preliminary report covers the screening of 14,494 infants. 95% passed the screening tests, 5% failed. Of the failures, 6% were found with confirmed hearing losses. The average cost per test was $25.00. Research from the University of Colorado confirms that children receiving intervention by 3 months perform significantly higher at 40 months than those identified later.

摘要

相似文献

1
Universal newborn hearing screening--the Colorado story.
Int J Pediatr Otorhinolaryngol. 1995 Jul;32(3):257-9. doi: 10.1016/0165-5876(95)01183-c.
2
Newborn hearing screening: the great omission.新生儿听力筛查:重大遗漏。
Pediatrics. 1998 Jan;101(1):E4. doi: 10.1542/peds.101.1.e4.
3
Projected cost-effectiveness of statewide universal newborn hearing screening.全州范围内新生儿普遍听力筛查的预计成本效益。
Pediatrics. 2002 Nov;110(5):855-64. doi: 10.1542/peds.110.5.855.
4
State programs for universal newborn hearing screening.国家新生儿听力普遍筛查项目。
Pediatr Clin North Am. 1999 Feb;46(1):89-94. doi: 10.1016/s0031-3955(05)70083-3.
5
Universal screening for infant hearing impairment: simple, beneficial, and presently justified.对婴儿听力障碍进行普遍筛查:简单、有益且目前具有合理性。
Int J Pediatr Otorhinolaryngol. 1995 Jul;32(3):201-11. doi: 10.1016/0165-5876(95)01165-8.
6
Universal newborn screening for hearing loss: ideal vs. reality and the role of otolaryngologists.新生儿听力损失普遍筛查:理想与现实以及耳鼻喉科医生的作用
Otolaryngol Head Neck Surg. 1996 Jul;115(1):89-93. doi: 10.1016/S0194-5998(96)70142-0.
7
[Cost analysis of a universal newborn hearing screening for clinics using the State of Hesse as an example].[以黑森州为例对诊所普遍开展新生儿听力筛查的成本分析]
HNO. 2009 Jan;57(1):21-8. doi: 10.1007/s00106-008-1879-7.
8
Cost and cost-effectiveness of universal screening for hearing loss in newborns.新生儿听力损失普遍筛查的成本及成本效益
Otolaryngol Head Neck Surg. 2001 Apr;124(4):359-67. doi: 10.1067/mhn.2001.113945.
9
Universal screening of infants for hearing loss: further justification.
J Pediatr. 1998 Sep;133(3):318-9. doi: 10.1016/s0022-3476(98)70261-6.
10
The Colorado newborn hearing screening project, 1992-1999: on the threshold of effective population-based universal newborn hearing screening.科罗拉多州新生儿听力筛查项目,1992 - 1999年:迈向基于人群的有效普遍新生儿听力筛查的开端
Pediatrics. 2002 Jan;109(1):E7. doi: 10.1542/peds.109.1.e7.

引用本文的文献

1
What Contribution Did Economic Evidence Make to the Adoption of Universal Newborn Hearing Screening Policies in the United States?经济证据对美国普遍新生儿听力筛查政策的采用有何贡献?
Int J Neonatal Screen. 2018;4(3):25. doi: 10.3390/ijns4030025. Epub 2018 Jul 20.
2
Universal Hearing Screening in Newborns Using Otoacoustic Emissions and Brainstem Evoked Response in Eastern Uttar Pradesh.在印度北方邦东部使用耳声发射和脑干听觉诱发电位对新生儿进行普遍听力筛查。
Indian J Otolaryngol Head Neck Surg. 2017 Sep;69(3):296-299. doi: 10.1007/s12070-017-1081-x. Epub 2017 Feb 3.
3
Universal neonatal hearing screening: Six years of experience in Qatar.
新生儿听力普遍筛查:卡塔尔的六年经验
Qatar Med J. 2013 Nov 1;2012(2):42-50. doi: 10.5339/qmj.2012.2.12. eCollection 2012.
4
Genetic mutations in nonsyndromic deafness patients of Chinese minority and Han ethnicities in Yunnan, China.中国云南少数民族和汉族非综合征性耳聋患者的基因突变
J Transl Med. 2013 Dec 17;11:312. doi: 10.1186/1479-5876-11-312.
5
Pathogenic substitution of IVS15 + 5G > A in SLC26A4 in patients of Okinawa Islands with enlarged vestibular aqueduct syndrome or Pendred syndrome.冲绳岛大前庭水管综合征或 Pendred 综合征患者 SLC26A4 基因 IVS15+5G>A 的致病性突变。
BMC Med Genet. 2013 May 24;14:56. doi: 10.1186/1471-2350-14-56.
6
Extremely discrepant mutation spectrum of SLC26A4 between Chinese patients with isolated Mondini deformity and enlarged vestibular aqueduct.中国孤立性Mondini 畸形和扩大的前庭水管患者 SLC26A4 基因突变谱差异极大。
J Transl Med. 2011 Sep 30;9:167. doi: 10.1186/1479-5876-9-167.
7
Prevalence of 35delG/GJB2 and del (GJB6-D13S1830) mutations in patients with non-syndromic deafness from a population of Espírito Santo-Brazil.巴西圣埃斯皮里图州非综合征性聋患者中 35delG/GJB2 和 del (GJB6-D13S1830) 突变的流行率。
Braz J Otorhinolaryngol. 2010 Jul-Aug;76(4):428-32. doi: 10.1590/S1808-86942010000400004.
8
Mutation analysis of GJB2 and GJB6 genes in Southeastern Brazilians with hereditary nonsyndromic deafness.巴西东南部遗传性非综合征型耳聋患者 GJB2 和 GJB6 基因突变分析。
Mol Biol Rep. 2011 Feb;38(2):1309-13. doi: 10.1007/s11033-010-0231-y. Epub 2010 Jun 19.
9
GJB2 mutation spectrum in 2,063 Chinese patients with nonsyndromic hearing impairment.2063例中国非综合征性听力损失患者的GJB2基因突变谱
J Transl Med. 2009 Apr 14;7:26. doi: 10.1186/1479-5876-7-26.
10
DNA sequence analysis of GJB2, encoding connexin 26: observations from a population of hearing impaired cases and variable carrier rates, complex genotypes, and ethnic stratification of alleles among controls.编码连接蛋白26的GJB2基因的DNA序列分析:来自听力受损病例群体的观察结果以及对照人群中可变的携带者频率、复杂基因型和等位基因的种族分层。
Am J Med Genet A. 2006 Nov 15;140(22):2401-15. doi: 10.1002/ajmg.a.31525.