Assessment of Fetal Well-Being
Olds’ Maternal-Newborn Nursing & Women’s Health: Assessment of Fetal Well-Being - Chapter 15
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Psychologic Reactions to Antenatal Testing
The need for testing often provokes feelings of fear and anxiety in patients.
Patients hold the option to refuse testing.
Ultrasound (US) is nearly routine; it is essential to provide counseling to address feelings of shock and confusion related to testing results.
Methods of Ultrasound Scanning
Transabdominal Ultrasound
Requires a full bladder for optimal assessment of fetal structures.
It is a painless procedure that typically lasts 20–30 minutes.
Transvaginal Ultrasound
Requires an empty bladder and can identify specific parameters such as:
Cervical length.
Funnel shapes.
Patient positioning is typically lithotomy for clearer images.
This method is preferred earlier in the pregnancy (2nd to 3rd trimester) for better image quality.
Ultrasound in First Trimester
Objectives include:
Confirming the location of the pregnancy.
Identifying fetal heart rate and fetal breathing movements.
Approximate gestational age determination.
Rules out a nonviable pregnancy (using measurements to estimate age).
Locates the placenta position and fetal orientation.
Ultrasound in Second & Third Trimester
Conducted to assess:
Fetal anatomy scan to screen for genetic disorders.
Diagnose fetal or congenital malformations.
Evaluate fetal growth.
Identify the sex of the fetus.
Assess Amniotic Fluid Index (AFI) for overall well-being of the fetus.
Fetal presentation and placental location.
First Trimester Combined Screening (1 of 2)
Nuchal Translucency Testing (NTT)
Performed between 11 weeks 0 days and 13 weeks 6 days.
Uses ultrasound to assess fluid accumulation in the nuchal fold behind the fetal neck.
Done in conjunction with maternal serum blood tests measuring:
Plasma-protein A analyte levels (PAPP-A).
Free beta hCG.
Important to note that this is a screening tool only, not a definitive diagnosis (diagnosis possible via amniocentesis).
First Trimester Combined Screening (2 of 2)
Cell-free Fetal DNA (cffDNA) Testing
Conducted through a maternal blood test.
Exhibits a 98% detection rate for fetal trisomy 21 (Down syndrome) and lower rates for trisomies 13 and 18.
Rh-negative mothers are advised to receive RhoGAM.
If positive for abnormalities, additional testing is recommended.
Second Trimester Assessments
Quad Screening
The most widely used screening test for:
Down syndrome (trisomy 21).
Trisomies 13 and 18.
Neural tube defects (NTDs).
Serum assessment includes:
Alpha-fetoprotein (AFP).
Human chorionic gonadotropin (hCG).
Unconjugated estriol (UE3).
Dimeric inhibin-A.
This is a noninvasive procedure, typically conducted during the 2nd trimester (optimal at 16-18 weeks).
Third Trimester Fetal Surveillance
Fetal Movement Assessment (Fetal Kick Counts)
Initiation at 28 weeks gestation; count movements at the same time each day.
Expect to feel 10 movements within 2-3 hours.
This is a noninvasive and cost-effective method that serves as an indirect measure of fetal CNS health.
Vigorous movements generally indicate fetal well-being; lack of movement or significant decreases could signify issues like chronic placental inefficiency, hypertension, diabetes, or renal disease.
Reporting Guidelines
Report to the healthcare provider if:
There are fewer than 10 movements in a 3-hour period.
There’s a significant reduction in fetal movement compared to baseline.
There is a perception of decreased fetal movement over a 24-hour period.
Nonstress Test (NST)
Purpose
A widely used method for evaluating fetal status alone or as part of a biophysical profile (BPP).
An adequately oxygenated fetus with an intact CNS should show an accelerated fetal heart rate (FHR) in response to movements.
False-positive results can occur; monitoring the baseline helps interpret results effectively.
Reactive NST
Defined by:
Accelerations of at least 15 beats/min lasting 15 seconds with each movement.
The assessment strip displays FHR (top) and uterine activity (bottom).
Advantages of NST
Quick and easy to perform.
Provides straightforward interpretation.
Inexpensive and can be conducted in various settings.
No known side effects.
Disadvantages of NST
May be challenging to obtain suitable tracings.
Requires the woman to remain still for approximately 20 minutes.
High false-positive rate can lead to unnecessary worry.
NST Results Interpretation
Reactive Results (Desired)
For pregnancies over 32 weeks:
At least two accelerations of FHR (15 beats/min lasting 15 seconds) in 20 minutes.
For preterm fetuses (under 32 weeks):
FHR should elevate 10 beats above baseline for 10 seconds in a 20-minute window.
Nonreactive NST
Occurs when there are no accelerations of FHR with fetal movement; baseline may remain stable around 130 beats/min.
Cannot rule out potential issues but indicates a need for further assessment/comparison.
Contraction Stress Test (CST)
Purpose
Evaluates placental respiratory function (oxygen and carbon dioxide exchange).
Identifies fetuses at risk for intrauterine asphyxia.
Observes the FHR response to uterine contractions.
Disadvantages of CST
Time-consuming with the potential for high false-positive results.
CST Contraindications
Instances that inhibit safe testing include:
Third-trimester bleeding from placenta previa.
Previous cesarean with classical incision.
Cervical insufficiency, premature rupture of membranes, or abnormal maternal reproductive organs.
Performing the CST
Requires contractions; spontaneous contractions are rare before labor onset.
Contractions may be induced using:
Intravenous oxytocin (Pitocin).
Breast stimulation.
Continuous monitoring of fetal heart rate and uterine contractions is critical, aiming for at least three contractions within 10 minutes.
CST Results
A Negative CST with a reactive NST is desired:
Good-quality contractions lasting over 40 seconds in 10 minutes.
No evidence of late decelerations.
A Positive CST indicates repetitive late decelerations with greater than 50% of contractions.
An Equivocal or Suspicious Result shows nonpersistent late decelerations or decelerations linked to tachysystole.
Amniotic Fluid Index (AFI)
Decreased uteroplacental perfusion leads to oligohydramnios.
AFI is determined by:
Fetal urine output.
Fetal swallowing.
An AFI of 5 cm or less requires further evaluation.
Biophysical Profile (BPP)
An assessment of five fetal biophysical variables:
Fetal heart rate acceleration (NST).
Fetal breathing (ultrasound).
Fetal movements (ultrasound).
Fetal tone (ultrasound).
Amniotic fluid volume (ultrasound).
BPP Scoring Criteria
Each normal finding scores 2 points, while each abnormal finding scores 0 points.
Maximum score is 10 points.
Score 8-10 indicates low risk.
Score 6 indicates abnormal findings, possibly acidemia (inadequate oxygenation).
Score of 4 or less indicates serious issues needing attention.
Indications for BPP
It is indicated in:
Decreased fetal movement.
Nonreactive NST.
Management of intrauterine growth restriction (IUGR).
Preterm labor.
Gestational diabetes and hypertensive disorders.
Postterm pregnancies or premature rupture of membranes (PROM).
Doppler Flow Studies
Used in high-risk pregnancies for assessing:
Placental functioning and velocity of blood flow in blood vessels.
Noninvasive techniques that focus on both maternal and fetal circulation.
Specifically measures:
Systolic/diastolic (S/D) ratio.
Reduced umbilical artery flow can signal complications.
Placental Maturity
Grading Process
Evaluated using ultrasound to observe changes in:
Basal layer.
Chorionic plate.
Placental substance.
Graded from 0 to 3, with 3 indicating maturity with extensive calcifications.
Inadequate placental function is a concern for further assessment.
Factors Influencing Placental Maturity
Factors that can cause premature placental maturity include:
Maternal smoking.
Postterm pregnancy.
Preeclampsia.
Gestational diabetes.
Amniocentesis
Utilized for detecting:
Genetic, metabolic, and DNA abnormalities.
Determining fetal lung maturity in the third trimester.
Detecting neural tube defects.
Ideally performed between 15-16 weeks, though valid at any point.
Can measure the Lecithin/Sphingomyelin (L/S) ratio for lung maturity evaluation.
Also measures alpha-fetoprotein levels.
Indications for Amniocentesis
Recommended for:
Pregnant women aged 35 or older at their due date.
Couples with a history of genetic disorders.
Pregnant women with abnormal screening results.
Procedure
Involves ultrasound guidance to locate a fluid pocket for needle insertion.
Upon entering the amniotic cavity, fluid is withdrawn.
If the mother is Rh-negative, RhoGAM is required and monitoring for potential complications is necessary.
Risks and Side Effects of Amniocentesis
Possible outcomes include:
Transient vaginal spotting or cramping.
Amniotic fluid leakage.
Chorioamnionitis.
Increased rate of loss if performed too early.
Nursing management includes assisting during the procedure and providing patient support, along with determining maternal blood type and RhoGAM needs.
Chorionic Villus Sampling (CVS)
This procedure is performed for early diagnosis (10-12 weeks) of:
Genetic, metabolic, and DNA abnormalities.
Cannot detect neural tube defects; used primarily for genetic evaluations.
Risks Associated with CVS
Possible complications include:
Spontaneous abortion.
Fetal limb reduction defects.
Failure to obtain adequate tissue.
Ruptured membranes or leakage of amniotic fluid.
Chorioamnionitis and intrauterine infections.
Benefits of CVS
Provides earlier diagnosis as compared to amniocentesis.
Can detect:
Fetal karyotype and hemoglobinopathies.
Down syndrome and Duchenne's muscular dystrophy.
Early sex determination (24 hours to 1 week post-procedure).