期刊文献+

新生儿甲状腺功能低下筛查有利于早发现与早诊断的体会 被引量:5

新生儿甲状腺功能低下筛查有利于早发现与早诊断的体会
下载PDF
导出
摘要 目的探讨新生儿甲状腺功能低下筛查对早发现和早诊断的作用。方法对2009~2011年的134604例新生儿甲状腺水平进行检测,再检测召回的可疑患儿的血清甲状腺功能,对其进行确诊,将确诊的74例患儿作为观察组,再随机选取正常健康的74例新生儿作为健康对照组,对筛查的基本情况和两组研究对象的早期临床症状进行观察。结果检出可疑甲状腺功能低下患儿共666例,召回397例患儿,总召回率为60.04%,确诊为甲状腺功能低下的患儿74例,总发病率为5.5/10000;观察组新生儿患者脐疝、黄疸延迟、皮肤毛发干燥和粘液性水肿的发生率分别为45.95%、55.41%、17.57%和18.92%,均明显高于健康对照组(14.86%、28.37%、0和0),差异具有统计学意义(P<0.05)。结论在人群中开展新生儿甲状腺功能低下筛查,可以帮助早期发现和诊断疾病,有效提高新生儿的健康素质。 Objective To investigate the neonatal hypothyroid screening on early detection and early diagnosis in the presence of role. Methods From 2009 to 2011 of 134604 cases of neonatal thyroid levels were detected, and detection recall suspicious patients serum thyroid function, carries on the diagnosis to be confirmed, 74 cases as the observation group, and then randomLy selected normal healthy 74 newborns as healthy control group, the screening and the basic situation of the two group study early clinical symptom observation. Results The detection of suspected hypothyroidism in all 666 cases, 397 cases of total recall, recall rate of 60.04%, diagnosed with hypothyroidism in 74 cases, the total incidence of 5.5/10000; observationgroup, jaundice, neonatal umbilical hernia in patients with delayed skin and hair drying and mucinous edema rate were 45.95%, 55.41%, in 17.57% and 18.92%, were significantly higher than those in the control group ( 14.86%, 28.37%, 0 and 0), the difference was statistically significant(P〈0.05). Conclusion In a population of neonatal screening for congenital hypothyroidism, can help in the early detection and diagnosis of the disease, effectively improve the health quality of newborn.
出处 《当代医学》 2012年第36期5-6,共2页 Contemporary Medicine
关键词 新生儿 甲状腺功能低下筛查 早发现 早诊断 Newborn Screening for congenital hypothyroidism Early detection Early diagnosis
  • 相关文献

参考文献3

二级参考文献5

  • 1Guthrie R. Screening for "inborn errors of metabolism" in the newborn infant: a multiple test program[J]. Birth Defects Original Article Series IV, 1962 = 92-98.
  • 2Guthrie R, Susi A. A simple phenylalanine method for detecting phenylketonuria in large populations of newborn infants[J]. Pediatrics, 1963,32:338-343.
  • 3Guthrie R. The origin of newborn screening[J]. Screening, 1992,1:5- 15.
  • 4Bradford LT, Alissa J, Donna W. Status of Newborn Screening Programs in the United States[J]. Diatrics,2006, 117(5 ):212 -252.
  • 5我国八大城市新生儿筛查五年回顾[J].中华儿科杂志,1997,35(12):655-656. 被引量:141

共引文献77

同被引文献42

引证文献5

二级引证文献18

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