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南非农村黑人新生儿的先天性异常——一种无声的流行病?

Congenital anomalies in rural black South African neonates--a silent epidemic?

作者信息

Venter P A, Christianson A L, Hutamo C M, Makhura M P, Gericke G S

机构信息

Department of Health Sciences, University of the North, Sovenga, Northern Transvaal.

出版信息

S Afr Med J. 1995 Jan;85(1):15-20.

PMID:7784908
Abstract

STUDY OBJECTIVE

To ascertain the incidence and spectrum of congenital anomalies in neonates born in a rural hospital.

DESIGN

This was a prospective, hospital-based study, undertaken on liveborn neonates over the period 12 June 1989 - 31 December 1992.

SETTING

Mankweng Hospital, Sovenga, Northern Transvaal.

MAIN RESULTS

Of a total of 10,380 neonates born during this period, 7,617 (73.4%) were examined within the first 24 hours of life. On the basis of published observations, only 26.2% of severe congenital anomalies diagnosable by age 5 years are diagnosable at birth. In this South African study the finding at birth of severe, externally visible congenital anomalies in 14.97 per 1,000 livebirths could mean that by age 5 years the minimum cumulative incidence of severe congenital anomalies may involve 57.14 per 1,000 children. Extrapolating from other Third-World studies, the cumulative incidence of severe congenital anomalies in such communities may affect up to 84.85 per 1,000 children by the age of 5 years. High incidences of neural tube defects (3.55 per 1,000 livebirths) and Down syndrome (2.10 per 1,000 livebirths), both conditions which can be prevented by prenatal screening, were recorded.

CONCLUSIONS

These figures indicate the necessity for inclusion of appropriate prenatal, genetic, family planning and paediatric facilities into the primary health care delivery system of rural areas, to manage such problems and to initiate programmes to reduce the incidence of selected congenital anomalies such as Down syndrome and neural tube defects.

摘要

研究目的

确定在一家乡村医院出生的新生儿先天性异常的发病率及范围。

设计

这是一项基于医院的前瞻性研究,研究对象为1989年6月12日至1992年12月31日期间出生的活产新生儿。

地点

北德兰士瓦省索文加的曼克翁医院。

主要结果

在此期间出生的10380名新生儿中,7617名(73.4%)在出生后24小时内接受了检查。根据已发表的观察结果,5岁前可诊断的严重先天性异常中,只有26.2%在出生时可诊断。在这项南非研究中,每1000例活产中有14.97例在出生时发现严重的、外部可见的先天性异常,这可能意味着到5岁时,严重先天性异常的最低累积发病率可能达到每1000名儿童中有57.14例。根据其他第三世界研究推断,此类社区中严重先天性异常的累积发病率到5岁时可能高达每1000名儿童中有84.85例。记录到神经管缺陷(每1000例活产中有3.55例)和唐氏综合征(每1000例活产中有2.10例)的高发病率,这两种情况都可通过产前筛查预防。

结论

这些数据表明,有必要将适当的产前、遗传、计划生育和儿科设施纳入农村地区的初级卫生保健系统,以处理此类问题,并启动相关项目以降低某些先天性异常(如唐氏综合征和神经管缺陷)的发病率。

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