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11574例新生儿脐血G-6-PD筛查结果分析

Application and clinical value of screening with umbilical blood on the disease of glucose-6-phosphate dehydrogenate deficiency
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摘要 目的了解本地区G-6-PD缺陷的发生率及新生儿脐血筛查对诊断G-6-PD缺陷的应用价值。方法对产科出生的11574例全部活产婴作脐血G-6-PD筛查,分别于3-5岁对脐血检测G-6-PD缺陷者(320例)和G-6-PD正常者(215例)复查G-6-PD活性。结果11574例中,脐血检测G-6-PD缺陷641例,缺陷率为5.5%;男性缺陷率为7.9%,女性为3.0%,二者比较差异有统计学意义(P〈0.001),对缺陷者复查幼儿血栓测G-6-PD活性,二者符合率高达96.7%。结论G-6-PD缺陷在本地区常见,脐血筛查可作为诊断G-6-PD缺陷的有力依据,对降低其发病率有重要意义。 Objective To investigate the incidence and diagnosis of glucose-6-phosphate dehydrogenate (G-6-PD) deficiency through screening with umbilical blood or infants'peripheral blood. Methods The umbilical blood of 11574 infants delivered in our hospital was detected to screen G-6-PD deficiency. Activity of G-6-PD was also detected in 320 G-6-PD deficiency infants and 215 normal infants from 3 to 5 years old. Results Six hundred and forty-one patients in 11574 cases were screened with umbilical blood as G-6-PD deficiency and the incidence rate was 5.5%. The incidence rates in boys and girls were 7.9% and 3.0% respectively with significant difference ( P 〈 0. 01 ). The coincidence rate of detection with umbilical blood or infants peripheral blood was 96. 7%. Conclusions The G-6-PD deficiency was a common disease in this district and screening with umbilical blood may be a useful way to diagnose it.
出处 《中国医师杂志》 CAS 2006年第4期474-475,共2页 Journal of Chinese Physician
关键词 葡糖磷酸脱氢酶缺乏/血液/诊断 葡糖磷酸脱氢酶/血液 胎血 婴儿 新生 Glucosephosphate dehydrogenase deficiency/ blood / diagnosis Glucosephosphate dehydrogenase/ blood Fetal blood Infant, newborn
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