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黄疸婴儿的及时转诊:病例报告

Timely referral of infants with jaundice: case report.

作者信息

Roberts E A

机构信息

Division of Gastroenterology and Nutrition, Hospital for Sick Children, Toronto.

出版信息

Can Fam Physician. 1995 Dec;41:2137-40.

PMID:8680297
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2146456/
Abstract

Family physicians should see all infants between 2 and 4 weeks of age to exclude persistent jaundice. Early identification of infants with jaundice due to liver disease might lead to better outcomes not only for infants with extrahepatic biliary atresia but for all infants with neonatal liver diseases. The case illustrates the consequences of late identification.

摘要

家庭医生应诊治所有2至4周龄的婴儿,以排除持续性黄疸。尽早识别患有肝病引起的黄疸的婴儿,不仅可能会给患有肝外胆道闭锁的婴儿带来更好的治疗结果,而且对所有患有新生儿肝病的婴儿也是如此。该病例说明了延迟识别的后果。

相似文献

1
Timely referral of infants with jaundice: case report.黄疸婴儿的及时转诊:病例报告
Can Fam Physician. 1995 Dec;41:2137-40.
2
Diagnostic laparoscopy in prolonged jaundice.长期黄疸的诊断性腹腔镜检查
J Pediatr Surg. 2001 Mar;36(3):463-5. doi: 10.1053/jpsu.2001.21621.
3
A clinical study of obstructive jaundice among Singapore infants.新加坡婴儿阻塞性黄疸的临床研究。
J Singapore Paediatr Soc. 1992;34(3-4):205-8.
4
Prolonged neonatal jaundice and the diagnosis of biliary atresia: a single-center analysis of trends in age at diagnosis and outcomes.新生儿期黄疸迁延与胆道闭锁的诊断:单中心对诊断年龄趋势及预后的分析
Pediatrics. 2008 May;121(5):e1438-40. doi: 10.1542/peds.2007-2709. Epub 2008 Apr 28.
5
[The neonatal hepatitis syndrome].
Rev Pediatr Obstet Ginecol Pediatr. 1990 Jan-Mar;39(1):1-41.
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Quantitative analysis of ductus proliferation, proliferative activity, Kupffer cell proliferation and angiogenesis in differential diagnosis of biliary atresia and neonatal hepatitis.胆管增生、增殖活性、库普弗细胞增殖及血管生成的定量分析在胆道闭锁与新生儿肝炎鉴别诊断中的应用
Hepatogastroenterology. 2003 Nov-Dec;50(54):1811-3.
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Z Kinderchir. 1987 Aug;42(4):230-4. doi: 10.1055/s-2008-1075591.
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Pre-admission consultation and late referral in infants with neonatal cholestasis.新生儿胆汁淤积症婴儿的入院前咨询与延迟转诊
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本文引用的文献

1
Physiologic cholestasis: elevation of the primary serum bile acid concentrations in normal infants.生理性胆汁淤积:正常婴儿血清中主要胆汁酸浓度升高。
Gastroenterology. 1981 May;80(5 pt 1):1037-41.
2
Long-term prognosis for infants with intrahepatic cholestasis and patent extrahepatic biliary tract.肝内胆汁淤积且肝外胆道通畅的婴儿的长期预后
Arch Dis Child. 1981 May;56(5):373-6. doi: 10.1136/adc.56.5.373.
3
Morbidity after percutaneous liver biopsy.经皮肝穿刺活检后的发病率。
Arch Dis Child. 1987 Sep;62(9):901-4. doi: 10.1136/adc.62.9.901.
4
Prognosis of extrahepatic biliary atresia.肝外胆管闭锁的预后。
Arch Dis Child. 1989 Feb;64(2):214-8. doi: 10.1136/adc.64.2.214.
5
Late referral for biliary atresia--missed opportunities for effective surgery.胆管闭锁的延迟转诊——有效手术的错失良机。
Lancet. 1989 Feb 25;1(8635):421-3. doi: 10.1016/s0140-6736(89)90012-3.
6
Liver disease in neonatal lupus erythematosus.新生儿红斑狼疮中的肝脏疾病
J Pediatr. 1990 Feb;116(2):238-42. doi: 10.1016/s0022-3476(05)82880-x.