The high risk of amniocentesis results suggests that the fetus has chromosomal abnormalities and may be stunted. Generally, from the perspective of eugenics, it is not recommended to continue the pregnancy, and the specifics should be in accordance with the doctor’s advice. Amniocentesis is usually performed by ultrasound-guided puncture to extract amniotic fluid, because the amniotic fluid contains cells shed by the fetus, and the genetic information of the fetus is generally obtained through technical testing, so the presence of chromosomal abnormalities can be determined through amniocentesis. If both non-invasive DNA and amniocentesis show a high risk, it mostly indicates that there is a problem with the development of the fetus, and the ultrasound may also show abnormalities. If the fetus itself has a chromosomal abnormality, even after birth, the survival rate and quality of life are not high. Therefore, if the amniocentesis is still high risk, it is recommended that the pregnancy be terminated in a timely manner, subject to medical advice.