期刊文献+

新生儿高胆红素血症的相关影响因素分析 被引量:1

下载PDF
导出
摘要 目的探讨新生儿高胆红素血症的相关影响因素。方法收集我院2010年10月至2014年10月50例高胆红素血症患儿作为本次研究对象,定义为研究组;对照组为同期我院出生的正常新生儿,共50例。由专人记录两组间可能影响高胆红素血症发生的危险因素。结果1单因素分析提示研究组和对照组男性、羊水污染、剖宫产、母亲糖尿病史差异无统计学意义(P>0.05);研究组和对照组胎龄、出生体质量、胎膜早破、头颅血肿、母乳喂养、窒息史、开奶时间差异有统计学意义(P<0.05)。2 Logistic多因素回归分析提示胎龄、出生体质量、胎膜早破、头颅血肿、母乳喂养、窒息史、开奶时间是高胆红素血症的高危因素。结论本次研究认为胎龄、出生体质量、胎膜早破、头颅血肿、母乳喂养、窒息史、开奶时间为高胆红素血症的高危因素。
作者 马秋芹
出处 《中国医药指南》 2015年第32期54-55,共2页 Guide of China Medicine
  • 相关文献

参考文献6

二级参考文献55

  • 1兰周吉.新生儿黄疸120例临床病因分析及中西医综合防治[J].青海医药杂志,2006,36(8):69-69. 被引量:10
  • 2Am PH. Newborn screening: current status. Health Aft, 2007, 26:559-566.
  • 3Ainoon O, Boo NY, Yu YH, et al. Complete molecular characterisation of glucose-6-phosphate dehydrogenase ( G6PD ) deficiency in a group of Malaysian Chinese neonates. Malays J Pathol, 2004, 26:89-98.
  • 4Laosombat V, Sattayasevana B, Janejindamai W, et al. Molecular heterogeneity of glucose-6-phosphate dehydrogenase ( G6PD ) variants in the south of Thailand and identification of a novel variant (G6PDSongklanagarind). Blood Cells Mol Dis, 2005,34: 191-196.
  • 5Huang M J, Kua KE, Teng HC, et al. Risk factors for severe hyperbilirubinemia in neonates. Pediatr Res, 2004, 56: 682-689.
  • 6D'Apolito M, Man'one A, Servedio V, et al. Seven novel mutations of the UGT1A1 gene in patients with unconjugated hyperbilirubinemia. Haematologiea,2007, 92:133-134.
  • 7Muslu N, Turhan AB, Eskandari G, et al. The frequency of UDP-glucuronosyltransferase 1A1 promoter region ( TA ) 7 polymorphism in newborns and it's relation with jaundice. J Trop Pediatr, 2007, 53:64-68.
  • 8Wang FL, Wang MK, Boo NY, et al. Rapid detection of the UGT1A1 single nucleotide polymorphism G211A using real-time PCR with Taqman minor groove binder probes. J Clin Lab Anal, 2007, 21:167-172.
  • 9Takeuchi K, Kobayashi Y, Tamaki S, et al. Genetic polymorphisms of bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese patients with Crigler-Najjar syndrome or Gilbert's syndrome as well as in healthy Japanese subjects. J Gastroenterol Hepatol, 2004, 19 : 1023-1028.
  • 10Cebecauerova D, Jirasek T, Budisova L, et al. Dual hereditary jaundice: simultaneous occurrence of mutations causing Gilbert's and Dubin-Johnson syndrome. Gastroenterology, 2005, 129:315- 320.

共引文献320

同被引文献4

引证文献1

二级引证文献2

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