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北方邦新生儿筛查外展项目的可行性研究。

Feasibility study of an outreach program of newborn screening in Uttar Pradesh.

作者信息

Agarwal Meenal, Joshi Kriti, Bhatia Vijayalakshmi, Gopalakrishnan Vignesh, Dabadghao Preeti, Das Vinita, Pandey Amita, Kumar Mala, Phadke Shubha R

机构信息

Department of Medical Genetics, Sanjay Gandhi Post Graduate Institute of Medical Sciencces, Lucknow, Uttar Pradesh, 226014, India.

出版信息

Indian J Pediatr. 2015 May;82(5):427-32. doi: 10.1007/s12098-014-1557-6. Epub 2014 Nov 1.

Abstract

OBJECTIVES

To create awareness about newborn screening (NBS) in underprivileged population and establish the model of NBS as an outreach program in peripheral hospitals in and around Lucknow.

METHODS

During this project, social workers were trained in taking informed consent, demographic details of newborns, heel prick samples and transporting the filter papers to a central laboratory. These social workers were posted in seven hospitals, in and around Lucknow, catering to families with low socioeconomic strata. Assays were performed in a single laboratory and results were conveyed back to the social workers and the hospitals.

RESULTS

A total of 13,426 newborns were screened for the three conditions namely congenital hypothyroidism (CH), biotinidase deficiency and galactosemia. Over all coverage rate was 73.5 % and average time of reporting of results was 8.8 + 2.4 days. More than 85 % (86.7 %) families with positive screening test could be contacted back and out of them, 83.6 % babies could be sampled for confirmatory tests. Eleven babies were diagnosed to have CH. The study has shown positive and enthusiastic responses of the lay persons. Questionnaire based survey among lay persons showed that almost 100 % individuals understood the advantages and method of NBS.

CONCLUSIONS

This project has been successful in establishing a model of NBS as an outreach program in and around a district.

摘要

目的

提高贫困人群对新生儿筛查(NBS)的认识,并在勒克瑙及其周边地区的基层医院建立NBS外展项目模式。

方法

在该项目中,对社会工作者进行了培训,内容包括获取知情同意书、新生儿人口统计学细节、足跟采血样本以及将滤纸样本送往中央实验室。这些社会工作者被派驻到勒克瑙及其周边的七家医院,服务于社会经济阶层较低的家庭。检测在单一实验室进行,结果反馈给社会工作者和医院。

结果

共对13426名新生儿进行了先天性甲状腺功能减退症(CH)、生物素酶缺乏症和半乳糖血症这三种疾病的筛查。总体覆盖率为73.5%,结果报告的平均时间为8.8±2.4天。筛查试验呈阳性的家庭中,超过85%(86.7%)能够被回访,其中83.6%的婴儿能够接受确认检测的采样。11名婴儿被诊断为患有CH。该研究显示了普通民众积极热情的反应。对普通民众进行的问卷调查表明,几乎100%的人了解NBS的优势和方法。

结论

该项目成功地在一个地区及其周边建立了NBS外展项目模式。

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