Can prenatal examinations detect fetal hypoxia?
In general, fetal hypoxia can be detected during prenatal examinations. If any abnormalities are found, timely medical consultation is necessary, following the doctor's guidance for appropriate treatment and management. The analysis is as follows:
Fetal hypoxia refers to a comprehensive syndrome in which the fetus suffers from acute or chronic oxygen deficiency in the uterus, threatening its health and life. It may be related to factors such as nuchal cord and meconium-stained amniotic fluid. If fetal hypoxia occurs, there may be clinical manifestations such as decreased fetal movement and abnormal fetal heart rate. At this time, prenatal examinations, such as fetal heart rate monitoring, can determine whether the fetus suffers from intrauterine hypoxia.
In addition, ultrasound can be used to observe the growth and development of the fetus, measuring indicators such as fetal head circumference, abdominal circumference, and femur length to assess the fetal growth curve. If fetal growth restriction or significantly decreased amniotic fluid volume is found, it may indicate fetal hypoxia.
However, these methods alone cannot directly confirm fetal hypoxia. Confirming fetal hypoxia requires a comprehensive evaluation by a professional doctor, integrating clinical manifestations, maternal medical history, and results from other auxiliary examinations. During pregnancy, pregnant women can appropriately change positions, such as adopting a left lateral position, to avoid uterine compression of the inferior vena cava, which may lead to insufficient uterine blood supply and worsen fetal hypoxia.