Prevalence of Glucose-6-Phosphate Dehydrogenase Deficiency among hospitalized Children at tertiary care Hospital in Eastern Part of Nepal

C. Jha, H. Rimal, R. Subedi, S. Parajuli
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Abstract

Introduction: Glucose 6 phosphate dehydrogenase deficiency is the most significant enzyme defect. It is X linked inherited disorder that affects males and females are rarely affected by lyonization. Severe jaundice, anemia and hemolytic crisis following ingestion of fava beans and certain drugs are known to occur in children with G6PD deficiency.  Therefore, routine neonatal and child screening programs to facilitate the identification and effective management of children with G6PD deficiency is paramount. Objective:  The main objective of this study is to find out the  hospital prevalence of G6PD deficiency in hospitalized children at Birat Medical College teaching Hospital. Methodology: This is a hospital based cross sectional study carried out in the Department of Paediatric, Birat Medical College Teaching Hospital  from30th  November 2020 to 30th May 2021. Three hundred children  upto to ten years of age admitted in department of  pediatrics were included in this study.  This study was performed on hospitalized children who were screened for G6PD deficiency. The test was carried out using the Randox G6PD quantitative in vitro test to determine the prevalence of G6PD deficiency among the admitted children upto 10 years of age.Data was analysed using SPSS version 16. Results:  This study was performed on 300 children, in which male babies (n=192; 64%) outnumbered the female babies (n=108; 36%). The majority of children were in the age group of < 1 years (n=131; 43.7%).The overall prevalence of G6PD deficiency was 9.3% of which 96.4% were moderately deficient while 3.6% was severely deficient.The highest proportion was noted in the age group of 1 to 5 years. The frequency of this disorder in males and females were 13.5% and 1.9% respectively which was statistically significant (p=0.001). Conclusion:  The present study confirms the high prevalence of G6PD deficiency in Eastern Region of Nepal. Therefore, we need to establish routine screening and educational programs in order to prevent grave complications in future.
尼泊尔东部三级医院住院儿童葡萄糖-6-磷酸脱氢酶缺乏症的患病率
葡萄糖6磷酸脱氢酶缺乏症是最显著的酶缺陷。这是一种影响男性的X连锁遗传病,女性很少受到游离化的影响。严重的黄疸,贫血和溶血危机后,摄入蚕豆和某些药物已知发生在G6PD缺乏症的儿童。因此,常规的新生儿和儿童筛查项目,以促进G6PD缺乏症儿童的识别和有效管理是至关重要的。目的:本研究的主要目的是了解Birat医学院附属医院住院儿童G6PD缺乏症的医院患病率。方法:这是一项基于医院的横断面研究,于2020年11月30日至2021年5月30日在比拉特医学院教学医院儿科进行。本研究以300名在儿科住院的10岁以下儿童为研究对象。这项研究是在G6PD缺乏症的住院儿童中进行的。试验采用Randox G6PD体外定量试验,以确定10岁以下住院儿童中G6PD缺乏症的患病率。数据分析使用SPSS version 16。结果:本研究对300名儿童进行了研究,其中男婴(n=192;64%的婴儿数量超过女婴(n=108;36%)。大多数儿童年龄< 1岁(n=131;43.7%)。G6PD总体缺乏率为9.3%,其中中度缺乏率为96.4%,重度缺乏率为3.6%。在1至5岁年龄组中所占比例最高。男性和女性的患病率分别为13.5%和1.9%,差异有统计学意义(p=0.001)。结论:目前的研究证实了G6PD缺乏症在尼泊尔东部地区的高患病率。因此,我们需要建立常规筛查和教育计划,以防止未来出现严重并发症。
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