期刊文献+

新生儿黄疸迁延不退病因探讨 被引量:2

Etiological Study of Persistent Neonatal Jaundice
下载PDF
导出
摘要 目的探讨足月新生儿黄疸迁延不退的发生率、病因和诊断。方法总结黄疸持续2周以上的新生儿和婴儿临床资料,提出诊治要点。结果 114例中血清总胆红素(TB)均值204.123μmol/L,病因以原因不明、母乳性黄疸为主。结论黄疸迁延至2周以上者,考虑是病理性黄疸,也需要治疗。 Objective To explore the incidence,etiology and diagnosis of persistent jaundice in the full-term newborns.Methods To summarize the clinical data of newborns and infants whose jaundice lasted for 2 weeks or more,and to propose the diagnosis and treatment points.Results The mean serum total bilirubin(TB) of 114 cases was 204.123 μmol/L,the unexplained causes and breast milk jaundice were the mainly etiology.Conclusion The full-term neonatal jaundice prolongs for 2 weeks or more,that is considered pathologic jaundice,and also needs to be treated.
作者 吴衍文
出处 《临床医学工程》 2011年第9期1378-1379,共2页 Clinical Medicine & Engineering
关键词 黄疸迁延不退 病因 婴儿 新生儿 Persistent jaundice Causes Infants Newborns
  • 相关文献

参考文献9

  • 1贾德勤,金燕琼,丁艳.足月新生儿黄疸延迟临床病因分析[J].中国妇幼保健,2003,18(7):422-423. 被引量:5
  • 2徐放生,周志轩,吴婉芳,戴耀华,秦雨春,宋岚芹,曹彬.39621例住院新生儿黄疸情况调查[J].中国儿童保健杂志,2000,8(4):271-272. 被引量:12
  • 3Osborn LM, Reiff MI, Bolus R. Jaundice in the full-term neonate [J] . Pediatrics, 1984, 73 (4) : 520-525.
  • 4潘军,胡江,谢集建,李涛.药物联合蓝光治疗新生儿黄疸临床分析[J].中国现代药物应用,2010,4(13):136-137. 被引量:16
  • 5Costa E. Hematologically important mutations: bilirubin UDP-glucuronosyhransferase gene mutations in Gilbert and Crigler-Najjar syn dromes [J] . Blood Cells Mol Dis, 2006, 36 (1) : 77-80.
  • 6Chang JL, Bigler J, Schwarz Y, et al. UGT1A1 polymorphism is associated with serum bilirubin concentrations in a randomized, controlled, fruit and vegetable feeding trial [J] . JNutr, 2007, 137 (4) : 890-897.
  • 7Yamamoto A, Nishio H, Waku S, et al. Gly71Arg mutation of the bilirubin UDP-glucuronosyltransferase IA1 gene is associated with neonatal hyperbilirubinemia in the Japanese population [J] . Kobe J Med Sci, 2002, 48 (3-4) : 73-77.
  • 8田桂英,徐放生,朱凤霞,蓝常肇,韩颖.新生儿迁延性黄疸与尿苷二磷酸葡萄糖醛酸转移酶基因突变的关系[J].实用儿科临床杂志,2008,23(2):129-130. 被引量:10
  • 9Laforgia N, Faienza MF, Rinaldi A, et al. Neonatal hyperbilirubihemia and Gilbert's syndrome [J] . J Perinat Med, 2002, 30 (2) : 166-169.

二级参考文献25

  • 1华晶.经皮胆红素测定仪光疗在新生儿黄疸中的应用[J].中国中西医结合儿科学,2004(1):61-62. 被引量:23
  • 2楚爱菊,董秀华.早期干预对新生儿黄疸预防效果分析[J].中国妇幼保健,2007,22(1):69-69. 被引量:30
  • 3丁家华.苯巴比妥对新生儿高胆红素血症的预防[J].临床儿科杂志,1999,17(1):62-62.
  • 4Ribo JM. et al. proton-induced dismutation of superoxide in aprotic madia by bile pigments. Expcentia, 1990; 46(1): 63-67.
  • 5Osborn LM, et al. Jaundice in the full-term neonate. Pediatrics,1984, 73:520-525.
  • 6杨美珍.母婴同室的新生儿黄疸发病率[J].实用儿科临床杂志,1997,12(5):288-289.
  • 7Costa E. Hematologieally important mutations : Bilirubin UDP - glucuronosyltransferase gene mutations in Gilbert and Crigler - Najjar syndromes [ J]. Blood Cells Mol Dis ,2006,36( 1 ) :77 - 80.
  • 8Kaplan M, Hammerman C, Maisels MJ. Bilirubin genetics for the nongeneticist : Hereditary defects of neonatal bilirubin conjugation [ J]. Pediatrics,2003,111 (4 pt 1) :886 -893.
  • 9Yusoff S, van Rostenberghe H, Yusoff NM, et al. Frequencies of A (TA) 7TAA,G71R,and G493R mutations of the UGT1A1 gene in the Malaysian population [ J ]. Biol Neonate,2006,89 (3) : 171 - 176.
  • 10Yamamoto A, Nishio H, Waku S ,et al. Gly71Arg mutation of the bilirubin UDP- glucuronosyltransferase 1A1 gene is associated with neonatal hyperbilirubinemia in the Japanese population [ J ]. Kobe J Med Sci, 2002,48(3) :73 -77.

共引文献37

同被引文献6

引证文献2

二级引证文献3

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