加强遗传筛选的知情选择:一项试点研究

C. Skelly, S. Ulrich
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引用次数: 1

摘要

出生缺陷是婴儿死亡的主要原因。新的测试提供了对许多胎儿非整倍体的筛查。这些测试在怀孕早期就提供,客户面临许多选择。这使得对客户的教育更具挑战性,并威胁到客户做出知情选择的能力。该项目的目的是衡量妇女在决定是否进行许多可选的产前基因筛查测试后报告的知情选择水平。在中西部的一家私人妇产科诊所,使用多维知情选择测量(MMIC)来测量知情选择的水平。这个顶点项目是一个小型试点研究,包括26名产前客户。75%的产前客户有良好的知识,57%的人做出了知情的选择。未来的研究和方法将集中于提高这一报告水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enhancing Informed Choice for Genetic Screening: A Pilot Study
Birth defects are the leading cause of infant mortality. New tests offer screening for many fetal aneuploidies. These tests are offered very early in pregnancy and clients are faced with many options. This has made the education of the client more challenging and threatens the ability of the client to make an informed choice. The purpose of this project was to measure the level of informed choice women reported after making a decision on whether or not to have the many optional prenatal genetic screening tests. The level of informed choice was measured using the Multi-dimensional Measure of Informed Choice (MMIC), at a Midwestern private OB-GYN office. This capstone project was a small pilot study which included 26 prenatal clients. Seventy-five percent of the prenatal clients had good knowledge and 57 percent made an informed choice. Future studies and methods will focus on improving this reported level.
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