Collection Amniotic fluid is removed from the mother by an
amniocentesis procedure, where a long needle is inserted through the abdomen into the amniotic sac, using ultrasound guidance such that the fetus is not harmed. Amniocentesis is a low-risk procedure, with a risk of pregnancy loss between 1 in 1,500 – 1 in 700 procedures. Amniocentesis can be performed to obtain diagnostic genetic information, evaluate for intrauterine infection, or, rarely, to assess for fetal lung maturity if early delivery is required. If warranted, fluid is collected between 16 and 42 weeks of fetal development. The amount of fluid removed depends on the indication for the procedure and the testing that will be performed on the fluid.
Analysis Analysis of amniotic fluid can reveal many aspects of the baby's genetic health as well as the age and viability of the fetus. This is because the fluid contains metabolic wastes and compounds used in assessing fetal age and lung maturity, but amniotic fluid also contains fetal cells, which can be examined for genetic defects. Amniotic fluid normally has a
pH of 7.0 to 7.5. Because pH in the upper vagina is normally acidic (pH 3.8–4.5), a vaginal pH test showing a pH of more than 4.5 strengthens a suspicion of
rupture of membranes in case of clear
vaginal discharge in pregnancy. One main test that is performed on amniotic fluid is the L/S ratio test (lecithin/sphingomyelin). This test is used to determine fetal lung maturity. Both lecithin and sphingomyelin are lung surfactants that are present in increasing amounts in the maturing fetus, though past week 33, sphingomyelin levels remain relatively constant. Measuring a ratio of L/S of 2:1 or greater indicates that the fetus can be safely delivered, with functioning lungs.
Complications related to amniotic fluid Too little amniotic fluid is called
oligohydramnios. In a minority of cases, it can be a cause of problems for the mother and baby. These include contracture of the limbs,
clubbing of the feet and hands, and also a life-threatening condition called
hypoplastic lungs. The
Potter sequence refers to a constellation of findings related to insufficient amniotic fluid. On every prenatal visit, the obstetrician, gynaecologist, or midwife should measure the patient's
fundal height with a tape measure. It is important that the fundal height be measured and properly recorded to track proper fetal growth and the increasing development of amniotic fluid. The obstetrician, gynaecologist, or midwife should also routinely
ultrasound the patient—this procedure will also give an indication of proper fetal growth and amniotic fluid development. Oligohydramnios can be caused by infection, kidney dysfunction or malformation (since much of the late amniotic fluid volume is urine), procedures such as
chorionic villus sampling (CVS), and preterm premature rupture of membranes (PPROM). Oligohydramnios can sometimes be treated with
bed rest, oral and intravenous
hydration,
antibiotics,
steroids, and amnioinfusion. The opposite of oligohydramnios is
polyhydramnios, an excess volume of amniotic fluid in the amniotic sac. Too much amniotic fluid can compress nearby organs.
Amniotic fluid embolism is a rare but very often fatal condition for both mother and child.
Medical applications It is being used in some surgeries of the outside of the eye. It is also being studied for some orthopaedic conditions.
Stem cell research Recent studies show that amniotic fluid contains a considerable quantity of stem cells. These
amniotic stem cells are pluripotent and able to differentiate into various tissues, which may be useful for future human application. Some researchers have found that amniotic fluid is also a plentiful source of non-embryonic
stem cells. These cells have demonstrated the ability to differentiate into many different cell-types, including brain, liver and bone. It is possible to conserve the stem cells extracted from amniotic fluid in private stem cell banks. ==See also==