先天性畸形和体外受精的健康登记。

Clinical reproduction and fertility Pub Date : 1986-02-01
P A Lancaster
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引用次数: 0

摘要

生殖结果登记册可用于获取与怀孕有关的健康问题发生率的信息,并研究相关的风险因素和根本原因。在澳大利亚,一个基于多种通报来源的先天性畸形国家数据系统提供了数据,以确定3年期间(1981-1983年)主要畸形的发病率,并研究可能由环境或其他致畸物引起的发病率的区域差异。通过获得体外受精单位在1983年底前完成的妊娠报告,建立了全国体外受精妊娠登记册。这一登记册是与澳大利亚生育学会合作编制的,用于描述不育夫妇的特点和试管婴儿妊娠的管理,并确定妊娠损失和重大先天性畸形的发生率。在建立这两个数据系统时,保密问题很重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Health registers for congenital malformations and in vitro fertilization.

Registers of reproductive outcomes can be used to obtain information about the incidence of health problems related to pregnancy and to study associated risk factors and underlying causes. In Australia, a national data system for congenital malformations, based on multiple sources of notifications, has provided data to determine the incidence of major malformations over a 3-year period (1981-1983) and to study regional variations in incidence possibly due to environmental or other teratogens. A national register of pregnancies resulting from in vitro fertilization (IVF) has been established by obtaining reports from IVF units for pregnancies completed by the end of 1983. This register, developed in collaboration with the Fertility Society of Australia, has been used to describe the characteristics of infertile couples and the management of IVF pregnancies and to determine the incidence of pregnancy losses and major congenital malformations. Confidentiality issues were important in setting up both data systems.

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