Principles of Fetal Physiology Underlying NST and CST Changes
The Non-Stress Test (NST) and Contraction Stress Test (CST) reflect the fetal autonomic nervous system's response to movement and uteroplacental perfusion, with heart rate accelerations indicating normal oxygenation and late decelerations signaling uteroplacental insufficiency. 1
Physiological Basis of the Non-Stress Test (NST)
Fetal Heart Rate Accelerations
- Normal fetal heart rate (FHR) ranges from 110-160 beats per minute (bpm) 1
- Acceleration mechanism: A healthy fetus increases its heart rate in response to fetal movement due to:
- Sympathetic nervous system stimulation during movement
- Intact central nervous system integration
- Adequate myocardial oxygenation allowing appropriate response 1
- Definition of acceleration:
Interpretation Criteria
- Reactive (normal) NST: Two or more FHR accelerations during 20 minutes of observation
- Nonreactive (abnormal) NST: One or no accelerations after 40 minutes of observation 2, 1
Physiological Significance
- NST provides information about immediate fetal oxygenation and acid-base balance 2
- A reactive NST indicates:
- Intact fetal central nervous system
- Functional autonomic nervous system
- Adequate myocardial oxygenation
- Normal fetal acid-base status 1
Physiological Basis of the Contraction Stress Test (CST)
Uteroplacental Perfusion During Contractions
- During uterine contractions, blood flow to the intervillous space is temporarily reduced
- In a healthy uteroplacental unit with adequate reserve, this reduction doesn't significantly affect fetal oxygenation
- In compromised uteroplacental units, contractions can trigger fetal hypoxemia 1
Late Decelerations
- Mechanism: Late decelerations occur when uterine contractions reduce uteroplacental blood flow beyond the compensatory capacity of the placenta
- Physiological sequence:
- Uterine contraction reduces intervillous blood flow
- Oxygen transfer to fetus decreases
- Fetal hypoxemia develops
- Chemoreceptors detect decreased oxygen
- Vagal stimulation occurs
- Heart rate decreases (deceleration)
- Timing: The nadir of deceleration occurs after the peak of contraction due to the time required for this physiological cascade 1
Interpretation
- Negative CST: No late decelerations observed with contractions
- Positive CST: Consistent late decelerations with contractions, indicating uteroplacental insufficiency 1
Integration of Fetal Physiological Responses
Progressive Deterioration Pattern
- Early stage: Loss of accelerations (nonreactive NST)
- Intermediate stage: Development of late decelerations with contractions (positive CST)
- Advanced stage: Baseline changes (tachycardia, bradycardia, decreased variability) 1
Factors Affecting Fetal Responses
- Gestational age: Premature fetuses (<32 weeks) have less developed autonomic nervous systems, requiring modified criteria for accelerations 2, 1
- Uteroplacental insufficiency: Primary cause of late decelerations 1
- Maternal conditions: Hypotension, cardiovascular disease, and hypertensive disorders can affect uteroplacental perfusion and alter FHR patterns 1
Clinical Implications and Pitfalls
Common Pitfalls
- Fetal sleep cycles: Can cause temporary nonreactive patterns for 20-40 minutes
- Prematurity: May show different acceleration patterns requiring adjusted criteria
- Medication effects: Some maternal medications can affect fetal heart rate patterns
- Acute events: NST and CST cannot predict sudden events like cord accidents or placental abruption 2
Key Clinical Considerations
- A reactive NST is highly predictive of good fetal outcome, comparable to a negative CST 3
- The absence of accelerations (nonreactive NST) is associated with increased rates of cesarean section for fetal distress and higher perinatal mortality 4
- Interpretation criteria significantly impact test results - using different definitions of acceleration duration can change reactivity rates 5
By understanding these physiological principles, clinicians can better interpret NST and CST results and make appropriate management decisions to optimize fetal outcomes.