Pao Mritunjay, Kulkarni Anjali, Gupta Vidya, Kaul Sushma, Balan Saroja
Division of Neonatology, Apollo Center for Advanced Pediatrics, Indraprastha Apollo Hospital, New Delhi, India.
Indian J Pediatr. 2005 Oct;72(10):835-7. doi: 10.1007/BF02731109.
This study was carried out to detect the incidence of erythrocytic Glucose-6 -Phosphate dehydrogenase (G-6-PD) deficiency, to compare the incidence of hyperbilirubinemia in G-6-PD deficient neonates as compared to G-6-PD normal neonates and to asses the usefulness of neonatal screening for G-6-PD deficiency.
In a retrospective hospital based study 2,479 male and female neonates consecutively born at Indraprastha Apollo hospital between July 1998 to June 2003 who were screened for G-6-PD levels were evaluated for the incidence of G-6-PD deficiency.
Incidence of G-6-PD deficiency was found to be 2.0%. Incidence in males was 283% and female was 1.05%. The incidence of hyperbilirubinemia was found to be 32% in G-6-PD deficient neonates which was significantly higher than the incidence of hyperbilirubinemia in neonates with normal G-6-PD, which was 12.3% (P< 0.001).
Our data suggests that neonatal screening for G-6-PD deficiency is a useful test for preventing and early treatment of complications associated with it.
本研究旨在检测红细胞葡萄糖-6-磷酸脱氢酶(G-6-PD)缺乏症的发病率,比较G-6-PD缺乏的新生儿与G-6-PD正常的新生儿高胆红素血症的发病率,并评估新生儿G-6-PD缺乏症筛查的实用性。
在一项基于医院的回顾性研究中,对1998年7月至2003年6月期间在英迪拉普拉萨阿波罗医院连续出生并接受G-6-PD水平筛查的2479例男、女新生儿进行G-6-PD缺乏症发病率评估。
发现G-6-PD缺乏症的发病率为2.0%。男性发病率为2.83%,女性为1.05%。G-6-PD缺乏的新生儿中高胆红素血症的发病率为32%,显著高于G-6-PD正常的新生儿,后者为12.3%(P<0.001)。
我们的数据表明,新生儿G-6-PD缺乏症筛查是预防和早期治疗与之相关并发症的一项有用检测。