What is the management approach for category 2 Cardiotocography (CTG) in relation to fetal well-being and neonatal outcomes?

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Management of Category 2 Cardiotocography (CTG) and Its Relationship to Neonatal Outcomes

Category 2 CTG patterns require increased monitoring frequency and specific interventions to improve fetal outcomes, with management decisions based on the severity of abnormalities and associated risk factors.

Understanding Category 2 CTG

  • Category 2 CTG patterns are considered "indeterminate" and represent more than 50% of fetal monitoring strips that fall between normal and abnormal tracings 1
  • These patterns are concerning enough to warrant increased surveillance and interventions but do not necessarily require immediate delivery 1
  • Category 2 patterns include baseline FHR changes, minimal or absent variability, absence of accelerations, and periodic or episodic decelerations 1

Immediate Management of Category 2 CTG

  • Consider discontinuing oxytocin if being administered 1
  • Implement general measures including vaginal examination, checking maternal vital signs, administering oxygen, changing maternal position, and providing intravenous fluids 1
  • Assess fetal pH with acoustic or fetal scalp stimulation to further evaluate fetal status 1
  • Consider potential need to expedite delivery if abnormalities persist or worsen 1

Monitoring Frequency Based on CTG Category

  • For Category 2 CTG without absent/reversed end-diastolic velocity, weekly cardiotocography testing is recommended after viability 2
  • Increase frequency to twice weekly or more when Category 2 patterns are accompanied by other risk factors such as fetal growth restriction 2, 3
  • For high-risk pregnancies with normal umbilical artery Doppler, CTG monitoring is recommended every 2 weeks 3
  • For high-risk pregnancies with abnormal umbilical artery Doppler, CTG monitoring should be performed at least weekly 3

Integration with Doppler Studies

  • Serial umbilical artery Doppler assessment should be performed to assess for deterioration once fetal growth restriction is diagnosed 2
  • With decreased end-diastolic velocity or severe fetal growth restriction (estimated fetal weight less than the third percentile), weekly umbilical artery Doppler evaluation is suggested 1
  • Doppler assessment should be increased to 2-3 times per week when umbilical artery absent end-diastolic velocity is detected 1
  • In the setting of reversed end-diastolic velocity, heightened surveillance with cardiotocography at least 1-2 times per day is recommended 1

Timing of Delivery Based on CTG and Doppler Findings

  • For fetal growth restriction with normal umbilical artery Doppler and estimated fetal weight between 3rd-10th percentile: Delivery at 38-39 weeks 1, 3
  • For fetal growth restriction with decreased diastolic flow but without absent/reversed end-diastolic velocity or with severe fetal growth restriction: Delivery at 37 weeks 1, 3
  • For fetal growth restriction with absent end-diastolic velocity: Delivery at 33-34 weeks 1, 3
  • For fetal growth restriction with reversed end-diastolic velocity: Delivery at 30-32 weeks 1, 3

Mode of Delivery Considerations

  • If umbilical artery end-diastolic flow is present, induction of labor with continuous CTG monitoring is recommended 1
  • For pregnancies with fetal growth restriction complicated by absent/reversed end-diastolic velocity, cesarean delivery should be considered based on the entire clinical scenario 1, 3

Relationship to Neonatal Outcomes

  • Continuous CTG monitoring is associated with reduced rates of neonatal seizures but no clear differences in cerebral palsy or infant mortality 4
  • Infants born with severe compromise often show specific abnormalities in their first-hour CTG, including baseline fetal heart rate ≥150 bpm, non-reactive trace, reduced variability, and absence of accelerations 5
  • The positive predictive value of CTG for intrapartum fetal hypoxia is approximately only 30%, with a high false-positive rate of 60% 6
  • Despite widespread use, there is limited evidence that antenatal testing decreases the risk for fetal death in low-risk pregnancies 3

Common Pitfalls to Avoid

  • Relying solely on CTG for surveillance without integrating Doppler studies 2
  • Using CTG as the only form of surveillance in high-risk pregnancies 2
  • Failing to increase monitoring frequency when deterioration in Doppler parameters is observed 2
  • Delaying delivery when significant abnormalities are detected on CTG in the context of fetal growth restriction 2
  • Interpreting CTG based solely on pattern recognition without understanding the underlying physiology of fetal heart rate changes 6

Special Considerations for Preterm Fetuses

  • Physiological control of fetal heart rate and the resultant features observed on the CTG trace differs in the preterm fetus compared to a fetus at term, making interpretation more challenging 7
  • Antenatal corticosteroids are recommended if delivery is anticipated before 33 6/7 weeks of gestation 1
  • Intrapartum magnesium sulfate is recommended for fetal and neonatal neuroprotection for women with pregnancies that are <32 weeks of gestation 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Cardiotocography Monitoring Guidelines for Fetal Growth Restriction

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Fetal Surveillance in High-Risk Pregnancies

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Continuous cardiotocography during labour: Analysis, classification and management.

Best practice & research. Clinical obstetrics & gynaecology, 2016

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Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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