Fetal Well-Being and Biophysical Profile
Assessment of Fetal Well-Being
Assuring satisfactory growth and well-being of the fetus and mother throughout pregnancy.
Screening for high-risk cases and adverse maternal or intrauterine factors that may affect fetal growth.
Detecting congenital abnormalities or inborn metabolic disorders early in pregnancy that may not be compatible with life.
Assessment Methods
Doppler flow studies
Marker screening tests
Nuchal translucency screening
Ultrasonography
Alpha-fetoprotein analysis
Amniocentesis
Chorionic villus sampling (CVS)
Percutaneous umbilical blood sampling (PUBS)
Contraction stress test
Nonstress test
Biophysical profile
Ultrasound
Non-invasive.
Useful diagnostic tool in obstetrics.
Provides a continuous picture of the fetus and allows for measurements.
Standard component of prenatal care.
Doppler Flow Studies
Non-invasive, uses sound waves to examine blood flow in blood vessels.
Monitors fetal growth, placental function, cardiac function, and central venous pressure.
Detects fetal compromise.
Nuchal Translucency Screening
Performed between 11-14 weeks.
Measures subcutaneous accumulation of fluid behind the fetal neck using ultrasound.
Screens for fetal, chromosomal, and structural abnormalities.
Alpha-Fetoprotein Analysis (AFP)
AFP is a glycoprotein and biomarker.
Increases until 14-15 weeks, then progressively falls, entering maternal circulation.
AFP elevation may indicate neural tube defects, Turner syndrome, or hydrocephaly.
Low AFP levels may indicate Down syndrome (trisomy 21).
Test is done between 15-20 weeks using a maternal blood sample.
Marker Screening Tests
Assess risk of neural tube defects and Down syndrome (second trimester).
Measures specific substances in the pregnant woman's blood originating from the fetus, placental tissue, or both.
Triple marker screening: AFP, hCG, unconjugated estriol (15-20 weeks of gestation).
Quadruple screen: AFP, hCG, unconjugated estriol, inhibin A (15-20 weeks of gestation).
Sample is obtained from maternal serum.
These tests DO NOT diagnose a problem; they only signal that further testing should be done.
Amniocentesis
Transabdominal puncture of the amniotic sac to obtain a sample of amniotic fluid for analysis (most common in the second trimester).
Used to detect chromosomal abnormalities, neural tube defects, and hereditary metabolic defects.
May be performed in late pregnancy to check fetal well-being and diagnose fetal conditions, such as infection.
May be performed to check for fetal lung maturity if early delivery is expected.
Amniocentesis Procedure
Diagnostic, outpatient office procedure performed after 15 weeks under ultrasound guidance without anesthesia.
A needle is placed into a pocket of amniotic fluid containing desquamated living fetal cells (amniocytes).
Nursing Management: Before Amniocentesis
Explain the procedure and possible complications.
Obtain informed consent.
No special restriction on diet or activity prior to the procedure.
Stop anticoagulant medications.
Empty the bladder (2nd and 3rd trimester).
Fetal monitoring before the procedure.
Administer RhoGAM to Rh-negative mothers.
Nursing Management: During and After Amniocentesis
Monitor vital signs during the procedure.
Ultrasound will be performed.
Fetal monitoring after the procedure.
Monitor maternal vital signs and fetal heart rate every 15 minutes after the procedure.
Observe the puncture site for bleeding or drainage.
Provide support after the results.
Educate on danger signs (fever, leak of amniotic fluid, vaginal bleeding).
Advise rest at home and avoidance of strenuous activities for at least 24 hours.
Fetal Lung Maturity: Lecithin-Sphingomyelin Ratio (L/S Ratio)
Test of fetal amniotic fluid to assess for fetal lung maturity.
Lecithin and sphingomyelin are part of the surfactant.
Lecithin and sphingomyelin levels are equal until 32–33 weeks gestation.
After week 33, lecithin increases and sphingomyelin remains stable.
L/S ratio of 2 or higher indicates LUNG MATURITY.
L/S ratio of 1.5 or lower indicates Respiratory Distress Syndrome
Chorionic Villus Sampling (CVS)
Diagnostic test for chromosome abnormalities and other inherited disorders.
Involves removing some chorionic villi cells (embryonic origin) from the placenta.
Performed between 10 and 13 weeks of pregnancy, earlier than amniocentesis.
Cannot detect neural tube defects.
Chorionic Villus Sampling (CVS) Management
Administer RhoGAM to Rh-negative women.
Explain the procedure and danger signs.
Potential Risks of CVS
Bleeding and hemorrhage.
Miscarriage (0.5 to 1%, similar to amniocentesis).
Infection.
Risk for either digital or limb deficiency.
Noninvasive Prenatal Testing: Harmony Test
Can be performed as early as 10 weeks.
Analyzes cell-free DNA in maternal blood.
Indicates whether the fetus is at high or low risk of having trisomy 21 (Down syndrome), trisomy 18 (Edwards syndrome), or trisomy 13 (Patau syndrome).
Nonstress Test (NST)
Noninvasive test that requires no initiation of contractions.
Indirect measure of uteroplacental function.
Recommended twice weekly after 28 weeks for clients with diabetes and other high-risk conditions.
The normal fetus produces characteristic fetal heart rate patterns in response to fetal movements, including acceleration of FHR with fetal movement.
Nonstress Test (NST) Procedure
The mother eats a meal to stimulate fetal activity and is placed in the left lateral recumbent position.
An external monitor is applied to her abdomen.
The client is handed an “Event Marker” with a button that she pushes every time she perceives fetal movement.
Obtain a baseline fetal monitor strip over 15 to 30 minutes.
Nonstress Test (NST) Interpretation
Reactive: 2 FHR accelerations from baseline of at least 15 bpm for at least 15 seconds within the 20-minute recording period.
Nonreactive: Absence of 2 FHR accelerations using the 15 by 15 criterion in a 20-minute time frame.
Contraction Stress Test (CST)
Also known as the oxytocin challenge test.
Performed at 34+ weeks of gestation.
Determines the fetal heart rate (FHR) response under stress (during contractions).
The goal is to achieve three uterine contractions in a 10-minute period without any FHR decelerations occurring.
Indicated in pregnancies in which placental insufficiency is suspected or an irregular FHR has been observed.
Risk of hyperstimulation of contractions and bradycardia.
Biophysical Profile
Screening test for utero-placental insufficiency.
Fetal biophysical activities are initiated, modulated, and regulated through the fetal nervous system.
The fetal CNS is very sensitive to diminished oxygenation.
Multiple variable assessment of fetal biophysical activities is more sensitive and reliable than the examination of a single parameter.
The profile is made up of five components:
Body movements
Fetal tone
Fetal breathing
Amniotic fluid volume
Nonstress test
Biophysical Profile - Scoring
Scored test with 5 components, each worth 2 points if present and 0 points if absent.
The duration of the test is 30 minutes.
Criteria to obtain a score (0-10 points):
Body movements: 3 or more discrete limb or trunk movements.
Fetal tone: one or more instances of full extension and flexion in the limb or trunk.
Fetal breathing: one or more fetal breathing movements of more than 30 seconds.
Amniotic fluid volume: one or more pockets of fluid measuring 2cm.
NST: Reactive= 2 points, nonreactive= 0 points.
Normal Biophysical Profile Score
3 or more body movements
One or more instances of full limb or trunk extension and flexion
Presence of at least one breathing movement
One or more pockets of amniotic fluid volume (2 cm or more)
A reactive non-stress test
Biophysical Profile - Interpretation
Score of 8 to 10 is considered normal if the amniotic fluid is adequate.
Score of 6 or 5: suspicious, probably indicating a compromised fetus, further investigation of fetal well-being is needed.
Score of 4 or less is abnormal.
Biophysical profile - Nursing Management
Explain why the test is needed
Offer support
Answer client questions