Maisels M J, Newman T B
Department of Pediatrics, William Beaumont Hospital, Royal Oak, MI 48073-6769, USA.
Pediatrics. 1995 Oct;96(4 Pt 1):730-3.
To document the occurrence of classical kernicterus in full-term, otherwise healthy, breast-fed infants.
We reviewed the files of 22 cases referred to us by attorneys throughout the United States during a period of 18 years, in which neonatal hyperbilirubinemia was alleged to be responsible for brain damage in apparently healthy, nonimmunized, full-term infants. To qualify for inclusion, these infants had to be born at 37 or more weeks' gestation, manifest the classic signs of acute bilirubin encephalopathy, and have the typical neurologic sequelae.
Six infants, born between 1979 and 1991, met the criteria for inclusion. Their peak recorded bilirubin levels occurred 4 to 10 days after birth and ranged from 39.0 to 49.7 mg/dL. All had one or more exchange transfusions. One infant had an elevated reticulocyte count (9%) but no other evidence of hemolysis. The other infants had no evidence of hemolysis, and no cause was found for the hyperbilirubinemia (other than breast-feeding).
Although very rare, classic kernicterus can occur in apparently healthy, full-term, breast-fed newborns who do not have hemolytic disease or any other discernible cause for their jaundice. Such extreme elevations of bilirubin are rare, and we do not know how often infants with similar serum bilirubin levels escape harm. We also have no reliable method for identifying these infants early in the neonatal period. Closer follow-up after birth and discharge from the hospital might have prevented some of these outcomes, but rare, sporadic cases of kernicterus might not be preventable unless we adopt an approach to follow-up and surveillance of the newborn that is significantly more rigorous than has been practiced. The feasibility, risks, costs, and benefits of this type of intervention need to be determined.
记录足月、健康的母乳喂养婴儿中经典型核黄疸的发生情况。
我们回顾了18年间美国各地律师转交给我们的22例病例档案,这些病例中,新生儿高胆红素血症被认为是导致明显健康、未接种疫苗的足月婴儿脑损伤的原因。为符合纳入标准,这些婴儿必须在妊娠37周或更晚出生,表现出急性胆红素脑病的典型症状,并具有典型的神经后遗症。
1979年至1991年间出生的6名婴儿符合纳入标准。他们记录的胆红素峰值水平出现在出生后4至10天,范围为39.0至49.7mg/dL。所有婴儿都接受了一次或多次换血治疗。一名婴儿网织红细胞计数升高(9%),但没有其他溶血证据。其他婴儿没有溶血证据,且未发现高胆红素血症的原因(除母乳喂养外)。
尽管非常罕见,但经典型核黄疸可发生在无溶血病或其他明显黄疸原因的看似健康的足月母乳喂养新生儿中。如此极端的胆红素升高很少见,我们不知道血清胆红素水平相似的婴儿有多少能逃过伤害。我们也没有可靠的方法在新生儿期早期识别这些婴儿。出生后和出院后更密切的随访可能会避免一些这样的结果,但除非我们采用比以往更为严格的新生儿随访和监测方法,否则罕见的散发性核黄疸病例可能无法预防。需要确定这种干预措施的可行性、风险、成本和益处。