在巴基斯坦开展新生儿代谢紊乱筛查:早期挑战和机遇的定性研究

Rare Pub Date : 2023-01-01 DOI:10.1016/j.rare.2023.100011
Muhammad Wasim , Haq Nawaz Khan , Hina Ayesha , Fazli Rabbi Awan
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引用次数: 0

摘要

在许多国家,新生儿筛查(NBS)举措提供了关于先天性代谢错误(IEM)患病率的见解,但巴基斯坦缺乏此类数据。巴基斯坦关于肠病的报告很少,也没有报告提供全面的基于人群的流行情况信息。针对这一不足,我们的研究调查了巴基斯坦旁遮普省(拉合尔费萨拉巴德)的特殊学校和护理中心,重点关注智力残疾儿童。收集了疑似IEM的409名ID儿童(费萨拉巴德212名,拉合尔197名)的信息。我们的目标是揭示生物化学和分子基础,最终揭示巴基斯坦旁遮普省的患病率。本报告详细介绍了我们在与受影响儿童、家长和学校工作人员接触方面所面临的挑战,强调了尽管资源有限,但在巴基斯坦建立IEM新生儿筛查项目方面所做的努力的潜力。通过在巴基斯坦开展NBS项目,将有助于减少社会对此类IEM的负担。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Initiating newborn screening for metabolic disorders in Pakistan: A qualitative study of the early challenges and opportunities

In multiple countries, newborn screening (NBS) initiatives have provided prevalence insights for inborn errors of metabolism (IEM), but Pakistan lacks such data. Few reports exist on IEM in Pakistan, and none offer comprehensive population-based prevalence information. In response to this deficiency, our study surveyed specialized schools and care centers in Punjab (Faisalabad, Lahore), Pakistan, focused on children with intellectual disabilities (ID). Information from 409 ID children (n = 212 from Faisalabad and n = 197 from Lahore) suspected of IEM was collected. Our objective was to uncover biochemical and molecular underpinnings, ultimately revealing prevalence rates for Punjab, Pakistan. This report details our challenges engaging with affected children, parents, and school staff, emphasizing the potential of such efforts, despite resource limitations, to establish an IEM newborn screening program in Pakistan. By developing NBS program in Pakistan, it will help to minimize the burden of such IEM from the society.

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