Rosenstein B J, Langbaum T S
Am J Dis Child. 1980 Jan;134(1):72-3. doi: 10.1001/archpedi.1980.02130130054016.
Review of the newborn nursery notes of 87 infants who had cystic fibrosis without meconium ileus (MI) indicated that 12 of them had clinical features consistent with the meconium plug syndrome (MPS). This high incidence of meconium abnormalities suggests that MI and the MPS probably represent different gradations of the same underlying pathologic abnormality. The findings further suggest that a quantitative pilocarpine iontophoresis sweat test be performed in every newborn infant with any type of meconium abnormality, including the spontaneous passage of meconium plugs.
对87例患有无胎粪性肠梗阻（MI）的囊性纤维化婴儿的新生儿护理记录进行回顾发现，其中12例具有与胎粪性栓子综合征（MPS）相符的临床特征。胎粪异常的高发生率表明，MI和MPS可能代表同一潜在病理异常的不同程度。这些发现进一步表明，应对每例有任何类型胎粪异常（包括胎粪栓子自然排出）的新生儿进行毛果芸香碱离子电渗汗液定量试验。
