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新生儿溶血性黄疸:病因、诊断方法及治疗

Neonatal Hemolytic Jaundice: Causes, Diagnostic Approach, and Management.

作者信息

Parastatidou Stavroula, Tsantes Andreas G, Emmanouil Chrysoula-Christina, Konstantinidi Aikaterini, Kapetanaki Anastasia, Sokou Rozeta

机构信息

Neonatal Intensive Care Unit, "Elena Venizelou" Maternity Hospital, 11521 Athens, Greece.

Laboratory of Haematology and Blood Bank Unit, "Attikon" Hospital, School of Medicine, National and Kapodistrian University of Athens, 12462 Athens, Greece.

出版信息

Children (Basel). 2025 May 23;12(6):666. doi: 10.3390/children12060666.

DOI:10.3390/children12060666
PMID:40564624
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12190970/
Abstract

Neonatal jaundice remains a common issue in daily clinical practice that needs to be distinguished in physiologic and pathologic hyperbilirubinemia. Hemolytic causes are significant, often underrecognized contributors of pathologic hyperbilirubinemia, sometimes leading to severe complications. Both immune-mediated and non-immune hemolytic conditions are included in the differential diagnosis of neonatal hemolytic jaundice. Following the detection of hemolysis, family and pregnancy history, physical examination of the neonate, and further investigations are necessary. Established and newer laboratory methods are useful in the subsequent diagnostic approach. The optimal management of hemolytic jaundice alienates the risk of permanent neurologic damage.

摘要

新生儿黄疸仍是日常临床实践中的常见问题,需要区分生理性和病理性高胆红素血症。溶血原因是病理性高胆红素血症的重要因素,往往未得到充分认识,有时会导致严重并发症。免疫介导和非免疫性溶血情况均包含在新生儿溶血性黄疸的鉴别诊断中。发现溶血后,需要了解家族史和妊娠史、对新生儿进行体格检查并进一步检查。已有的和更新的实验室方法在后续诊断中很有用。溶血性黄疸的最佳管理可消除永久性神经损伤的风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2691/12190970/bb2f41f29ff9/children-12-00666-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2691/12190970/bb2f41f29ff9/children-12-00666-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2691/12190970/bb2f41f29ff9/children-12-00666-g001.jpg

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本文引用的文献

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Patient experience and burden of haemolytic disease of the foetus and newborn: a systematic review.胎儿和新生儿溶血病的患者体验与负担:一项系统综述
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Overview on Hereditary Spherocytosis Diagnosis.遗传性球形红细胞增多症诊断概述
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Neonatal/perinatal diagnosis of hemolysis using ETCOc.使用呼气末一氧化碳(ETCOc)进行新生儿/围产期溶血诊断。
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Approach to Pregnancy Affected by Kell Alloimmunization.Kell血型同种免疫所致妊娠的处理方法
Case Rep Hematol. 2024 Jul 23;2024:1929147. doi: 10.1155/2024/1929147. eCollection 2024.
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New WHO classification of genetic variants causing G6PD deficiency.世界卫生组织关于导致葡萄糖-6-磷酸脱氢酶(G6PD)缺乏症的基因变异的新分类。
Bull World Health Organ. 2024 Aug 1;102(8):615-617. doi: 10.2471/BLT.23.291224. Epub 2024 Jun 10.
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