Kou K O, Poon C F, Kwok S L, Chan K Yk, Tang M Hy, Kan A Sy, Leung K Y
Department of Obstetrics and Gynaecology, Queen Elizabeth Hospital, Jordan, Hong Kong.
Prenatal Diagnostic Laboratory, Tsan Yuk Hospital and Department of Obstetrics and Gynaecology, Queen Mary Hospital, Hong Kong.
Hong Kong Med J. 2016 Jun;22(3):223-30. doi: 10.12809/hkmj154730. Epub 2016 May 6.
In Hong Kong, universal combined first-trimester screening for Down's syndrome was started as a 'free service' in July 2010. Non-invasive prenatal testing was available as a self-financed item in August 2011. This study aimed to determine whether the introduction of non-invasive prenatal testing as a contingent approach influenced the indications for invasive prenatal diagnosis and the consequent prenatal detection of Down's syndrome.
This historical cohort study was conducted at the Prenatal Diagnosis Clinic of Queen Elizabeth Hospital in Hong Kong. We compared the indications for invasive prenatal diagnosis and prenatal detection of Down's syndrome in singleton pregnancies 1 year before and 2 years following the availability of non-invasive prenatal testing as a contingent test after a positive aneuploidy test. All pregnant women who attended our hospital for counselling about universal Down's syndrome screening between August 2010 and July 2013 were recruited.
A total of 16 098 women were counselled. After the introduction of non-invasive prenatal testing, the invasive prenatal diagnosis rate for a positive aneuploidy screening reduced from 77.7% in 2010-11 to 68.8% in 2012-13. The new combined conventional plus non-invasive prenatal testing strategy was associated with a lower false-positive rate (6.9% in 2010-11 vs 5.2% in 2011-12 and 4.9% in 2012-13). There was no significant increase in invasive prenatal diagnosis for structural anomalies over the years. There was no significant trend in the overall prenatal detection rate of Down's syndrome (100% 1 year before vs 89.1% 2 years after introduction of non-invasive prenatal testing). Four (2.6%) of 156 women who underwent non-invasive prenatal testing for a screen-positive result had a high-risk result for trisomy 21, which was subsequently confirmed by invasive prenatal diagnosis. There were no false-negative cases.
The introduction of non-invasive prenatal testing as a contingent approach reduced the invasive prenatal diagnosis rate for a positive aneuploidy screening without affecting the invasive prenatal diagnosis rate for structural anomalies or the overall detection rate of fetal Down's syndrome.
在香港,孕早期唐氏综合征通用联合筛查于2010年7月作为一项“免费服务”启动。无创产前检测于2011年8月作为自费项目提供。本研究旨在确定将无创产前检测作为一种替代方法的引入是否会影响侵入性产前诊断的指征以及随后唐氏综合征的产前检测情况。
这项历史性队列研究在香港伊利沙伯医院产前诊断诊所进行。我们比较了在无创产前检测作为非整倍体检测阳性后的替代检测方法可用之前1年和之后2年单胎妊娠中侵入性产前诊断的指征以及唐氏综合征的产前检测情况。招募了2010年8月至2013年7月期间到我院咨询通用唐氏综合征筛查的所有孕妇。
总共为16098名女性提供了咨询。引入无创产前检测后,非整倍体筛查阳性的侵入性产前诊断率从2010 - 2011年的77.7%降至2012 - 2013年的68.8%。新的传统方法与无创产前检测相结合的策略具有较低的假阳性率(2010 - 2011年为6.9%,2011 - 2012年为5.2%,2012 - 2013年为4.9%)。多年来,因结构异常进行的侵入性产前诊断没有显著增加。唐氏综合征的总体产前检测率没有显著趋势(引入无创产前检测前1年为100%,引入后2年为89.1%)。156名因筛查阳性结果接受无创产前检测的女性中有4名(2.6%)21三体检测结果为高风险,随后经侵入性产前诊断得到证实。没有假阴性病例。
将无创产前检测作为一种替代方法的引入降低了非整倍体筛查阳性的侵入性产前诊断率,而不影响因结构异常进行的侵入性产前诊断率或胎儿唐氏综合征的总体检测率。