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新生儿高胆红素血症的当前药物治疗选择及核黄疸的预防

Current drug treatment options in neonatal hyperbilirubinaemia and the prevention of kernicterus.

作者信息

Rubaltelli F F

机构信息

Department of Paediatrics, University of Florence School of Medicine, Italy.

出版信息

Drugs. 1998 Jul;56(1):23-30. doi: 10.2165/00003495-199856010-00003.

Abstract

Neonatal jaundice is a frequent problem in neonatology, but the advent of phototherapy which has simplified its treatment, it no longer represents a major concern. Early hospital discharge of neonates has now resulted in a re-emergence of kernicterus. Neonatal jaundice is principally the result of a transient deficiency of bilirubin conjugation, of a partial deficiency of hepatic bilirubin uptake and intracellular transport and of an increased enterohepatic circulation of the pigment. The fact that bilirubin production in the neonate is 2 or more times greater than in the adult per kilogram of bodyweight represents the mainstay of this condition. Prevention of kernicterus in full term infants is based on the detection of neonates at risk for developing hyperbilirubinaemia, and can be accomplished with simple tests performed on umbilical cord blood such as blood type, Rh, Coombs' test and glucose-6-phosphate dehydrogenase, in order to detect haemolytic diseases. The daily evaluation of transcutaneous bilirubin measurement gives additional information on the rise of serum bilirubin level, and can help to distinguish physiological from nonphysiological hyperbilirubinaemia. A significant hyperbilirubinaemia is more frequent in infants born before term, and in neonates who do not feed well and lose more than 10% of bodyweight. In preterm infants the typical clinical feature of kernicterus is seen very rarely, and kernicterus is now a very infrequent postmortem observation. Since it is very difficult to distinguish the effects of bilirubin from other potentially toxic factors, it is difficult to give guidelines for the treatment of jaundice in very low birthweight infants other than to keep the serum bilirubin levels to a lower level than in full term infant (e.g. 10 mg/dl lower than in full term babies). The intramuscular administration of a single dose of Sn-mesoporphyrin (6 mumol/kg bodyweight) in healthy term or near-term infants seems to be a promising treatment modality for controlling hyperbilirubinaemia.

摘要

新生儿黄疸是新生儿学中常见的问题,但光疗的出现简化了其治疗,它不再是主要的关注点。新生儿早期出院现在导致了核黄疸的再次出现。新生儿黄疸主要是由于胆红素结合的短暂缺乏、肝脏胆红素摄取和细胞内转运的部分缺乏以及色素肝肠循环增加所致。新生儿每公斤体重的胆红素生成量比成人高2倍或更多,这是这种情况的主要原因。足月婴儿核黄疸的预防基于对有发生高胆红素血症风险的新生儿的检测,可以通过对脐带血进行简单测试来完成,如血型、Rh、库姆斯试验和葡萄糖-6-磷酸脱氢酶检测,以检测溶血性疾病。经皮胆红素测量的每日评估可提供有关血清胆红素水平升高的额外信息,并有助于区分生理性和非生理性高胆红素血症。重度高胆红素血症在早产儿以及喂养不佳且体重减轻超过10%的新生儿中更为常见。在早产儿中,核黄疸的典型临床特征非常罕见,现在核黄疸是一种非常罕见的尸检观察结果。由于很难将胆红素的影响与其他潜在毒性因素区分开来,除了将血清胆红素水平保持在比足月婴儿更低的水平(例如比足月婴儿低10mg/dl)之外,很难为极低出生体重儿的黄疸治疗提供指导。在健康的足月或近足月婴儿中,肌肉注射单剂量的锡-中卟啉(6μmol/kg体重)似乎是控制高胆红素血症的一种有前景的治疗方式。

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