期刊文献+

安庆市新生儿听力筛查5315例结果分析 被引量:2

Analysis on hearing screening results of 5 315 neonates in Anqing City
下载PDF
导出
摘要 目的通过听力筛查了解安庆市新生儿听力损失的发生情况及相关高危因素,以便早期干预和治疗。方法采用瞬态诱发耳声发射(TEOAE)对5315例新生儿听力筛查结果从性别、分娩方式、高危因素方面进行分析。结果初筛通过率为91.38%,复筛通过率为69.91%,确诊听力缺陷率为0.11%。不同性别、不同分娩方式初筛通过率比较差异均无统计学意义(X^2值分别为0.246、2.257,均P〉0.05)。正常新生儿初筛通过率与高危儿初筛通过率比较差异有统计学意义(X^2=5.445,P〈0.05)。结论开展新生儿听力筛查,加强对高危儿、复筛人群管理监测与基础信息分析利用工作具有非常重要的意义。 Objective To investigate the occurrence of neonatal hearing loss and its high-risk factors with neonatal hearing screening in Anqing City, aiming to intervene and treat early. Methods Transient evoked otoacoustic emission (TEOAE) was used to screen hearing of 5 315 neonates, and the results were analyzed from the aspects of sex, delivery mode and high-risk factors. Results The passing rate of preliminary screening was 91.38% , and that of secondary screening was 69.91%. The auditorily handicapped rate was 0. 11%. The passing rate of preliminary screening was not statistically significant between different sex and delivery mode (X^2 value was 0. 246 and 2. 257, respectively, both P 〉 0.05 ) , but it was significantly different between normal neonates and high-risk neonates (X^2 = 5. 445, P 〈 0.05 ). Conclusion It is very important to carry out hearing screening, particularly to strengthen the supervising and monitoring of high-risks neonates and secondary screening neonates, and to analyze and utilize of basic information.
出处 《中国妇幼健康研究》 2014年第1期64-65,共2页 Chinese Journal of Woman and Child Health Research
关键词 新生儿 听力筛查 高危因素 监测 neonate hearing screening high-risk factors monitoring
  • 相关文献

参考文献3

二级参考文献25

共引文献49

同被引文献21

  • 1Mahboubi H, Dwabe S, Fradldn M, et al. Genetics of hearing loss where are we standing now [J]. Eur Arch Otorhinolaryngol, 2012, 269 ( 7 ) : 1733-1745.
  • 2Papacharalampous G X, Nikolopoulos T P, Davilis D I, et al. Universal newborn heating screening, a revolutionary diagnosis of deafness : real benefits and limitations [J]. Eur Arch Otorhinolaryngol, 2011,268 (10) : 1399-1406.
  • 3Wilcken B. Screening for disease in the newborn: the evidence base for blood-spot screening[J]. Pathology,2012,44 (2) :73-79.
  • 4Fang Y, Gu M, Wang C, et al. GJB2 as Well as SLC26A4 Gene Mutations are Prominent Causes for Congenital Deafness [ J ]. Cell Biochem Biophys,2015, [ Epub ahead of print].
  • 5Song M H, Shin J W, Park H J, et al. Intrafamilial phenotypic variability in families with biallelic SLC26A4 mutations [J]. Laryngoscope,2014,124(5 ) :E194-E202.
  • 6Olusanya B O, Akinyemi O O. Community-based infant hearing screening in a developing country: parental up take of follow-up serviees F J 1. BMC Publie Health.2009.9:66.
  • 7Matsuoka K, Komori H, Nose M, et al. Simple screening method tor autoantigen proteins using the N-terminal biotinylated protein library produced by wheat eell-fi'ee synthesis [J]. J Proteome Res, 2010, 9 (8) : 4264-4273.
  • 8Shuna A, Jones Robert S, Tim S, et al. Development and model tes- ting of antemortem screening methodology to predict required drug with holds in heifers [J]. J Food Prot, 2014, 77 (2) : 292-298.
  • 9Alexandre 1, Cortes N, Justel M, et al. The value of simple microbi- ological studies for on-site screening of acute neonatal conjunctivitis in Angola [J]. J Ophthalmic Inflamm Inft, 2014, 4 ( 1 ) : 1-2.
  • 10许淑慧.580例高危儿应用婴儿20项神经运动检查法筛查分析[J].中国医师进修杂志,2013,36(z1):72-73.

引证文献2

二级引证文献12

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部