新生儿筛查——促进新生儿高质量健康的一步

S. Patel, .. Ritupriya, P. Padhi, T. Naik, R. Nanda, E. Mohapatra, S. Agrawal
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摘要

新生儿筛查(NBS)被认为是新生儿高质量健康的需要。同样重要的是要了解遗传性代谢紊乱患病率的上升趋势,以及可能影响子宫内胎儿遗传变化的各种母体因素对新生儿结局的影响。目的:本研究的主要目的是确定先天性甲状腺功能减退症(CH)和葡萄糖- 6-磷酸脱氢酶(G6PD)缺乏症在最易接近的三级护理医院的频率。次要目标是查明产妇因素对疾病发生频率的影响以及疾病对新生儿健康的影响。材料与方法:对1282例48小时至8周龄的新生儿进行横断面研究。采集干血斑(DBS)标本,检测促甲状腺激素(TSH)水平和G6PD酶活性。详细记录新生儿特征和产前史。计算CH和G6PD缺乏症的患病率,并使用社会科学统计软件包(SPSS)第20版对孕产妇和新生儿变量进行关联分析。结果:CH和G6PD患病率分别为3.3/1000和6.6/1000,总体代谢性疾病患病率为9.8/1000。27.3%的新生儿低出生体重(LBW), 62%的新生儿低Ponderal指数(PI)。患病新生儿TSH升高的几率是6.62倍。低体重婴儿高TSH的概率为94%,女性新生儿为18%。TSH值较高的新生儿与母亲年龄(p=0.016)、胎龄(p=0.019)和母亲贫血(p<0.001)有显著相关性。剖腹产出生的婴儿TSH筛查呈阳性的几率是前者的两倍。结论:本研究中估计的高患病率及其与孕产妇因素的关联促使人们提出新的疑问,并建议在该地区实施强制性的NBS计划。
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Newborn Screening-A Bolstering Step towards Quality Health in Neonates
Introduction: Newborn Screening (NBS) is considered the need of the hour for quality health in neonates. It is also important to understand that the rising trend of prevalence of inherited metabolic disorders and the various maternal factors that might influence genetic changes in the foetus in- utero affecting the neonatal outcome. Aim: The primary objective of the study was to determine frequency of Congenital Hypothyroidism (CH) and Glucose- 6-Phosphate Dehydrogenase (G6PD) deficiency in a most approachable tertiary care hospital. The secondary objectives were to find out impact of maternal factors on the frequency of the disease and the impact of the disorder on the neonate’s health. Materials and Methods: The cross-sectional study was conducted on 1282 neonates of 48 hours upto eight weeks of age. The Dried Blood Spot (DBS) specimens collected were analysed for Thyroid Stimulating Hormone (TSH) level and G6PD enzyme activity. Details of neonatal characteristics and antenatal history were documented. Prevalence of CH and G6PD deficiency was calculated and maternal and neonatal variables were analysed for association using Statistical Package for the Social Sciences (SPSS) version 20. Results: The prevalence of CH and G6PD were respectively 3.3/1000 and 6.6/1000 making the overall prevalence of metabolic disorders as 9.8/1000. A 27.3% had Low Birth Weight (LBW) and 62% had low Ponderal Index (PI). The odds for raised TSH was 6.62 times in sick neonates. The probability for high TSH in LBW babies was more by 94% and in female neonates by 18%. The neonates with higher TSH values depicted significant association with maternal age (p=0.016), gestational age (p=0.019) and maternal anaemia (p<0.001). Babies born by caesarean section showed twice the chances for screening positive for TSH. Conclusion: The high prevalence estimated in this study and association with maternal factors urges new queries and recommends an obligatory need for NBS program in this region.
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