14 November 2017
A literature review entitled Has non-invasive prenatal testing impacted termination of pregnancy and live birth rates of infants with Down syndrome? written by Hill, Barrett, Choolani, Lewis, Fisher & Chitty has been published.
While the DSA acknowledges that the offer of prenatal testing for Down’s syndrome is a routine part of antenatal care, we are committed to ensuring that the prenatal testing process informs all potential parents and professionals of the joys and challenges of having a child with Down’s syndrome.
Before and during testing, easily understood and up-to-date information MUST be provided in an unbiased way by well trained professionals concerning:
- The accuracy of tests and associated risks of further tests;
- The life prospects of people with Down’s syndrome;
- The impact on families;
- The support available in the community;
- Broad and non-directive counselling services for those who may need it.
- We expect respect and support for parents making choices about antenatal tests and their outcomes – whatever they decide to do.
The DSA continues to work with professionals at all levels to educate them about Down’s syndrome and the lives of those with the condition so that parent’s who choose to undergo testing have the best possible experience.