Intrapartum Fetal Surveillance
Module 5 Overview
Instructor: Kathryn Zeigler, DNP, FNP-C
Chapter 17: Intrapartum Fetal Surveillance
Fetal Oxygenation
Requirements for Adequate Fetal Oxygenation:
Normal maternal blood flow and volume to the placenta
Normal oxygen saturation of maternal blood
Normal fetal circulatory and oxygen-carrying functions
An open circulatory path between the placenta and fetus through vessels in the umbilical cord
Adequate exchange of oxygen and carbon dioxide in the placenta
Maternal Arterial System and Placental Function
Components Involved in Fetal Oxygenation:
Maternal arterial system
Intervillous space where the exchange of O2/CO2 and nutrients/waste occurs
Chorionic villi enable nutrient exchange
Umbilical vein via spiral arteries connects to the placenta
Fetal Heart Rate (FHR) Regulation
Conversion of increased cardiac output in the fetus:
Achieved primarily through an increase in heart rate.
Conversely, a marked decrease in FHR decreases cardiac output.
Influencing Systems:
Sympathetic Nervous System:
Catecholamines (epinephrine and norepinephrine) increase heart rate and consequently cardiac output.
Parasympathetic Nervous System (PNS):
Vagus nerve: Reduces FHR and maintains variability; greater influence is seen starting at 28-32 weeks.
Autonomic Nervous System Response:
Baroreceptors located in major arteries respond to stretching with increased blood pressure.
May stimulate the vagus nerve to decrease FHR and BP, leading to decreased cardiac output.
**Central Nervous System Components:
Cerebral cortex causes FHR to increase with fetal movement and decrease with sleep.
Hypothalamus coordinates the two branches of the autonomic nervous system.
Medulla oblongata maintains a balance between the two opposing forces that adjust FHR.
Adrenal Glands:
Secrete epinephrine and norepinephrine in response to sympathetic nervous stimulation.
Effects: Increases FHR, decreases BP leading to the release of aldosterone and sodium retention, resulting in increased fetal blood volume.
Chemoreceptors:
Respond to changes in oxygen, carbon dioxide, and pH.
Sighting Locations for Chemoreceptors:
Located in the medulla oblongata and at aortic and carotid bodies.
Notable role in the response to low O2 by increasing cardiac output.
Pathological Influences on Fetal Oxygenation
Factors affecting fetal oxygenation:
Alterations in the placenta or issues related to either fetal factors or the mother.
Maternal Influences:
Hypotension: Decreases perfusion to the placenta.
Hypertension: Compromises blood flow.
Maternal acid-base alterations: Affect fetal condition.
Lower maternal O2 tension: Leads to fetal distress.
Uterine Activity:
Tachysystole may lead to fetal compromise even with weak uterine contractions.
Umbilical Flow Interruptions:
Causes:
Abruption and infarction of the placenta.
Antepartum and Intrapartum Considerations
Maternal History and Risk Factors for Fetal Compromise
Risk Factors:
Previous stillbirth (unexplained or possibly recurring causes)
Previous cesarean section
Poor nutrition, low pre-pregnancy weight, inadequate weight gain
Multiple pregnancies with close spacing
Presence of chronic diseases (cardiac, anemia, hypertension, diabetes, asthma, autoimmune diseases)
Acute infections (urinary tract, pneumonia, gastrointestinal)
Hematologic issues (anemia, deep vein thrombosis)
Use of drugs (prescription, OTC, herbal, illicit)
Psychosocial stressors (domestic violence)
Identified Problems During Pregnancy:
Intrauterine growth restriction (IUGR)
Gestation >42 weeks
Marked decrease in fetal movement
Multifetal gestation
Preeclampsia or eclampsia
Gestational diabetes
Placental abnormalities (placenta previa, abruptio placentae)
Severe maternal anemia
Maternal infection and trauma
Hypotension or hypertension
Hypertonic uterine contractions
Abnormal labor (preterm or dysfunctional)
Prolonged rupture of membranes
Chorioamnionitis
Fever
Fetal and Placental Problems:
Fetal anemia
Persistent abnormal or nonreassuring fetal heart rates/patterns
Meconium-stained amniotic fluid
Abnormal fetal presentation or position
Prolapsed cord
Abruptio placentae
Intermittent Auscultation and Fetal Heart Rate Assessment
Steps for Procedure: Intermittent Auscultation
Preparation Steps:
Explain the procedure and perform hand hygiene.
Use Leopold maneuvers to identify the fetal back (FHTs usually heard loudest over the fetal back).
Assessing FHR:
If normal, document findings; if abnormal, apply Continuous Electronic Fetal Monitoring (CEFM).
Assess fetal heart rate (FHR) using a Doppler transducer or fetoscope.
Verify the heartbeat is fetal by comparing with the mother’s radial pulse rate.
Count the baseline for 30-60 seconds between contractions (ctx).
Reassuring Findings:
FHR of 110-160 bpm
Regular rhythm
Accelerations present
No decelerations
Electronic Fetal Monitoring (EFM) Considerations
Benefits and Limitations:
Continuous or intermittent:
Reduced mobility.
Adjustment with position changes may be needed; belts may be uncomfortable.
Medicalizes labor; however, provides more data.
Offers a permanent record and trends over time and includes ctx information, along with fetal reactions.
Baseline Variance Conditions:
Baseline: 110-160 bpm
Variability: Moderate (6-25 bpm)
Accelerations defined as 15 x 15 or (10 x 10 for ≤ 32w)
Decelerations: absent OR variable decelerations lasting < 60 seconds with a rapid return to baseline, with normal baseline and moderate variability.
Equipment for EFM
Devices for External Monitoring:
Ultrasound transducer (measures FHR)
Tocotransducer (measures ctx)
Devices for Internal Fetal Monitoring:
Fetal scalp electrode (FSE)
Intrauterine pressure catheter (IUPC)
Evaluating Electronic Fetal Monitoring Strips
Normal FHR:
110-160 bpm
Variability:
Fluctuations in baseline FHR reflecting fetal autonomic nervous system function requiring adequate oxygenation.
Variability definitions:
Absent: undetectable
Minimal: ≤ 5 bpm
Moderate: 6-25 bpm
Marked: > 25 bpm
Accelerations:
Represent temporary increases in FHR noted as 15 x 15 or 10 x 10 in preterm.
Reassuring indicators reflecting responsiveness of the CNS and absence of acidosis.
Decelerations:
Represent periodic decrease in fetal heart rate.
Types:
Early Decelerations: Gradual decrease in FHR, nadir occurs with peak of ctx (result of head compression).
Late Decelerations: Subtle appearance; nadir occurs after ctx peaks (caused by placental insufficiency).
Variable Decelerations: Abrupt decreases and increases in FHR (caused by cord compression).
Uterine activity should be assessed for frequency, duration, intensity, and resting tone to mitigate risks and ensure adequate monitoring.
Nonreassuring Fetal Heart Rate Assessment
Categorization of FHR Assessments
Normal (Reassuring):
Normal baseline, moderate variability, absence of decelerations besides early decels, acceleration presence = CATEGORY 1
Indeterminate:
All tracings not categorized as Category 1 or 2 = CATEGORY 2
Nonreassuring:
Absent variability, recurrent late decelerations, recurrent variable decelerations, bradycardia, sinusoidal pattern = CATEGORY 3
Nursing Responses to Nonreassuring Fetal Heart Rate Patterns
Identify the cause:
Evaluate FHR patterns and assess maternal vital signs.
If indicated, perform SVE (sterile vaginal exam).
Medications and Procedures:
Stop oxytocin or other uterine stimulants as needed.
Terbutaline may be ordered for tocolysis.
Reposition the patient and increase IV fluids to enhance placental perfusion.
Administer 8-10 L/min of oxygen via facemask.
Consider using internal monitors depending on the situation.
Documentation Responsibilities:
Keep provider updated on FHR patterns, interventions taken, fetal and maternal responses, and orders received.
Be prepared for urgent delivery if signs of severe nonreassuring patterns occur.
Preterm Labor Management
Definition:
Labor occurring between 20 weeks and 37 weeks gestation.
Conditions Increasing Risks:
Maternal conditions such as infection, diabetes, chronic hypertension, drug use, connective tissue disorders, and previous preterm births.
Symptoms of Preterm Labor:
Cramping, low back pain, increased discharge, pelvic pressure, changes felt in the abdomen, and a sense of pressure in the vulva/thighs.
Medications and Treatments:
Betamethasone or Dexamethasone given to enhance fetal lung maturity reduc signifying respiratory distress syndrome.
Tocolytic Medications:
Magnesium sulfate for neuroprotection, Nifedipine and Indomethacin for tocolysis, and Terbutaline as an adjunct when indicated.
Drug Guidelines for Preterm Labor
Betamethasone:
12 mg IM for two doses 24 hours apart to accelerate fetal lung maturity.
Dexamethasone:
6 mg IM every 12 hours for four doses for similar effects.
Magnesium Sulfate:
Used for neuroprotection and can be given for tocolysis, regular monitoring of serum levels is essential.
Terbutaline:
Administered subcutaneously or via IV with strict evaluation for maternal heart rate and blood pressure responses.