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.
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。
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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.
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