Olowe S A, Ransome-Kuti O
J Natl Med Assoc. 1981 Sep;73(9):811-9.
The sickle cell trait (Hgb-AS) and G-6-PD deficiency are two genetic defects which increase the hemolytic susceptibility of erythrocytes. As these two traits are common in Nigeria, blood transfusions with such defective cells are frequently given. In this study, the immediate and long-term effects of using either normal blood or blood with either or these defects for exchange transfusions in 115 neonates have been examined. Infants transfused with G-6-PD deficient blood were compared with those transfused with G-6-PD normal blood. Similarly, neonates transfused with Hgb-AS blood were compared with those who received Hgb-AA blood. There was no statistically significant difference in post-exchange serum bilirubin levels (followed for one week), hemoglobin, hematocrit, and reticulocyte counts (followed for three months). It was concluded that under normal circumstances, the use of G-6-PD deficient blood or Hgb-AS blood does not increase the risk of exchange transfusion in infants with hyperbilirubinemia.
镰状细胞性状(血红蛋白AS)和葡萄糖-6-磷酸脱氢酶(G-6-PD)缺乏是两种会增加红细胞溶血易感性的基因缺陷。由于这两种性状在尼日利亚很常见,因此经常输注带有此类缺陷细胞的血液。在本研究中,已对115例新生儿使用正常血液或带有其中任何一种缺陷的血液进行换血输血的即时和长期影响进行了检查。将输注G-6-PD缺乏血液的婴儿与输注G-6-PD正常血液的婴儿进行了比较。同样,将输注血红蛋白AS血液的新生儿与接受血红蛋白AA血液的新生儿进行了比较。换血后血清胆红素水平(随访一周)、血红蛋白、血细胞比容和网织红细胞计数(随访三个月)均无统计学上的显著差异。得出的结论是,在正常情况下,使用G-6-PD缺乏血液或血红蛋白AS血液不会增加高胆红素血症婴儿换血输血的风险。