Department of Pediatrics, CSM Medical University, Lucknow, Uttar Pradesh, India.
Dev Med Child Neurol. 2013 Apr;55(4):348-56. doi: 10.1111/dmcn.12079. Epub 2013 Jan 30.
To study prevalence and risk factors for neurological disorders--epilepsy, global developmental delay, and motor, vision, and hearing defects--in children aged 6 months to 2 years in northern India.
A two-stage community survey for neurological disorders was conducted in rural and urban areas of Lucknow. After initial screening with a new instrument, the Lucknow Neurodevelopment Screen, screen positives and a random proportion of screen negatives were validated using predefined criteria. Prevalence was calculated by weighted estimates. Demographic, socio-economic, and medical risk factors were compared between validated children who were positive and negative for neurological disorders by univariate and logistic regression analysis.
Of 4801 children screened (mean age [SD] 15.32mo [5.96]; 2542 males, 2259 females), 196 were positive; 190 screen positives and 269 screen negatives were validated. Prevalence of neurological disorders was 27.92 per 1000 (weighted 95% confidence interval 12.24-43.60). Significant risk factors (p≤0.01) for neurological disorders were higher age in months (p=0.010), lower mean number of appliances in the household (p=0.001), consanguineous marriage of parents (p=0.010), family history of neurological disorder (p=0.001), and infants born exceptionally small (parental description; p=0.009). On logistic regression, the final model included age (p=0.0193), number of appliances (p=0.0161), delayed cry at birth (p=0.0270), postneonatal meningoencephalitis (p=0.0549), and consanguinity (p=0.0801).
Perinatal factors, lower socio-economic status, and consanguinity emerged as predictors of neurological disorders. These factors are largely modifiable.
研究印度北部 6 个月至 2 岁儿童的神经障碍(癫痫、全面发育迟缓、运动、视力和听力缺陷)的流行率和危险因素。
在勒克瑙的农村和城市地区进行了一项针对神经障碍的两阶段社区调查。在使用新仪器(Lucknow 神经发育筛查)进行初步筛查后,使用预定义标准对筛查阳性和随机比例的筛查阴性进行了验证。通过加权估计计算了患病率。通过单变量和逻辑回归分析,比较了验证为神经障碍阳性和阴性的儿童之间的人口统计学、社会经济和医疗危险因素。
在筛查的 4801 名儿童中(平均年龄[标准差]15.32 个月[5.96];男 2542 名,女 2259 名),有 196 名阳性;190 名筛查阳性和 269 名筛查阴性得到验证。神经障碍的患病率为 27.92/1000(加权 95%置信区间 12.24-43.60)。神经障碍的显著危险因素(p≤0.01)为月龄较大(p=0.010)、家庭用具数量较少(p=0.001)、父母近亲结婚(p=0.010)、家族神经障碍史(p=0.001)和出生时特别小的婴儿(父母描述;p=0.009)。在逻辑回归中,最终模型包括年龄(p=0.0193)、用具数量(p=0.0161)、出生后延迟哭泣(p=0.0270)、新生儿后脑膜炎(p=0.0549)和近亲结婚(p=0.0801)。
围产期因素、较低的社会经济地位和近亲结婚是神经障碍的预测因素。这些因素在很大程度上是可以改变的。