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[捷克共和国患有特定类型出生缺陷的儿童的存活率]

[Survival of children born with selected types of birth defects in Czech Republic].

作者信息

Sípek A, Gregor V, Horácek J, Masátová D

机构信息

Ustav pro péci o matku a díte, Praha.

出版信息

Ceska Gynekol. 2004 Dec;69 Suppl 1:47-52.

Abstract

OBJECTIVE

A retrospective study of data with an analysis of the prenatal and postnatal incidence of selected types of birth defects in the Czech Republic during the period from 1994 to 2003. The objective was also to analyse the percentage of deceased children born with selected types of congenital defects from the total number of deceased children.

DATA SOURCE AND METHODS

The data on prenatal diagnostics were obtained from particular department of medical genetics in the Czech Republic. The data on the incidences of birth defects in the born children were obtained from the data of the National Health Registers, the administration of which has been entrusted to the Institute of Health Information and Statistics of the Czech Republic (IHIS CR). Specifically, the data from the National Register of Congenital Defects and the National Register of Neonates were used. The analysis of the frequencies of prenatally and postnatally diagnosed cases of twelve selected types of birth defects was carried out for the Czech Republic for the period from 1994 to 2003. For the cases of postnatally diagnosed defects, an analysis of survival and mortality of the affected individuals during the 1st year of life was carried out for selected types of birth defects.

RESULTS

In the period 1994-2003, a total of 932,153 children were born in the Czech Republic. Including the cases of successful prenatal diagnostics, we analysed 268 cases of anencephalia, 384 cases of spina bifida and 80 cases of encephalocele, 425 cases of congenital hydrocephalus, 261 cases of omphalocele and 258 cases of gastroschisis, 225 cases of congenital defects of oesophagus and 279 anorectal malformations; 232 cases of diaphragmatic hernia, 411 cases of agenesis/hypoplasia of kidneys and 438 cystic kidneys; and 1,412 cases of Down's Syndrome. The success rate of secondary prevention was high for the defects of neural tube (55-96%), for the defects of abdominal wall (55-78%) and for the Down's Syndrome (59%). As concerns the defects treatable by surgery, the survival rate in the first year of life of the born children was lowest in the case of congenital hydrocephalus (63%) and in the case of neural tube defects (75-84%). However, in the case of GIT congenital defects (the defects of abdominal wall, diaphragmatic hernia, congenital defects of oesophagus and anorectal malformations), 82 to 91% of the born children survived.

CONCLUSION

Immaturity and concurrent incidence of additional birth defects prolong the period of hospitalisation, UPV and total parenteral nutrition in the case of the affected neonates. This deteriorates the prognosis of the children born with birth defects. Possible reduction of the incidence of these cases could be achieved through improvement in prenatal diagnostics, specifically through more timely identification of mainly the serious types of defects with the presence of associated congenital defects. Another possibility to improve the survival rate of children is the development of surgical procedures and specialised neonatal and infant intensive care.

摘要

目的

对1994年至2003年期间捷克共和国特定类型出生缺陷的产前和产后发病率数据进行回顾性研究。目的还包括分析患有特定类型先天性缺陷的死亡儿童在死亡儿童总数中所占的百分比。

数据来源与方法

产前诊断数据来自捷克共和国医学遗传学的特定部门。出生儿童出生缺陷发病率数据来自国家健康登记册,其管理工作已委托给捷克共和国健康信息与统计研究所(IHIS CR)。具体而言,使用了先天性缺陷国家登记册和新生儿国家登记册的数据。对1994年至2003年期间捷克共和国12种选定类型出生缺陷的产前和产后诊断病例频率进行了分析。对于产后诊断出的缺陷病例,对选定类型的出生缺陷在出生后第一年受影响个体的生存和死亡情况进行了分析。

结果

1994年至2003年期间,捷克共和国共出生932,153名儿童。包括产前诊断成功的病例,我们分析了268例无脑儿、384例脊柱裂和80例脑膨出、425例先天性脑积水、261例脐膨出和258例腹裂、225例先天性食管缺陷和279例肛门直肠畸形;232例膈疝、411例肾发育不全/发育不良和438例多囊肾;以及1412例唐氏综合征。神经管缺陷(55 - 96%)、腹壁缺陷(55 - 78%)和唐氏综合征(59%)的二级预防成功率较高。对于可通过手术治疗的缺陷,出生儿童在出生后第一年的存活率在先天性脑积水(63%)和神经管缺陷(75 - 84%)的情况下最低。然而,对于胃肠道先天性缺陷(腹壁缺陷、膈疝、先天性食管缺陷和肛门直肠畸形),82%至91%的出生儿童存活。

结论

新生儿不成熟以及并发其他出生缺陷会延长受影响新生儿的住院时间、肠外营养支持时间和全胃肠外营养时间。这会使患有出生缺陷的儿童预后恶化。通过改善产前诊断,特别是更及时地识别主要是伴有相关先天性缺陷的严重类型缺陷,有可能降低这些病例的发病率。提高儿童存活率的另一种可能性是开发手术程序以及专门的新生儿和婴儿重症监护。

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