What is the recommended diagnosis and management of chorioamnionitis in labor, including maternal and neonatal antibiotic regimens and delivery considerations?

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Last updated: February 12, 2026View editorial policy

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Chorioamnionitis: Diagnosis and Management

Immediate Action Required

Start broad-spectrum intravenous antibiotics (ampicillin 2g IV loading dose, then 1g IV every 4 hours plus gentamicin weight-based dosing) immediately upon clinical diagnosis and proceed to delivery without delay—chorioamnionitis cannot be cured by antibiotics alone and maternal sepsis can progress to death within a median of 18 hours from first signs. 1

Clinical Diagnosis

Do not wait for maternal fever to make the diagnosis. 1 Chorioamnionitis presents with maternal fever (≥100.4°F/38.0°C) plus at least one of the following: 1, 2

  • Maternal tachycardia
  • Fetal tachycardia
  • Uterine tenderness
  • Purulent or foul-smelling amniotic fluid
  • Maternal leukocytosis (>15,000 cells/mm³)

The condition can present without fever, especially at earlier gestational ages—treatment should begin as soon as any other sign of infection appears. 1 Amniocentesis results must not delay therapy; proceed based on bedside clinical assessment. 1

Maternal Antibiotic Regimen

First-line treatment: Ampicillin 2g IV initial dose, then 1g IV every 4 hours until delivery PLUS gentamicin (loading dose followed by weight-based maintenance dosing). 1, 2 This regimen covers the polymicrobial nature of intraamniotic infection. 1

For non-severe penicillin allergies: Cefazolin 2g IV initial dose, then 1g IV every 8 hours until delivery (replacing ampicillin). 1, 2

For severe penicillin allergies: Clindamycin 900mg IV every 8 hours OR vancomycin 1g IV every 12 hours until delivery. 1, 2

If cesarean delivery is performed: Add clindamycin at the time of umbilical cord clamping. 3

Timing of Antibiotics

Initiate antibiotics within 3 hours of fever recognition, or within 1 hour if septic shock is suspected. 1 Blood cultures should be obtained before antibiotic administration when feasible, but do not delay treatment. 1

Delivery Considerations

Delivery should be undertaken without delay once antibiotics are started. 1 The infection cannot be cured by antibiotics alone and requires delivery regardless of gestational age. 1, 3, 4

Route of delivery is dictated by standard obstetric indications—not by the infection itself. 1, 4 Cesarean delivery offers no fetal advantage and may increase maternal morbidity. 1 Vaginal delivery is the safer option. 3

Common pitfall: The time interval between diagnosis and delivery is not related to most adverse outcomes, but delivery should not be unnecessarily delayed. 3 Patients may require higher doses of oxytocin to achieve adequate uterine activity. 3

Postpartum Antibiotic Management

After vaginal delivery: Additional antibiotic therapy does not appear necessary. 3

After cesarean delivery: If postdelivery antibiotics are prescribed, there is support for administering one additional dose. 3

Neonatal Management

Well-Appearing Newborns

Obtain limited evaluation: Blood culture and CBC with differential. 1, 2

Start empirical antibiotics immediately: IV ampicillin (for GBS coverage) plus an aminoglycoside (gentamicin) or cefotaxime (for E. coli coverage). 1, 5

CBC timing: Sensitivity improves when sampled 6–12 hours after birth, but antibiotic therapy must not be delayed awaiting results. 1

Discontinue antibiotics once clinical course and laboratory data exclude sepsis. 1

Newborns with Any Sign of Sepsis

Perform full diagnostic work-up: 1, 5

  • Blood culture
  • CBC with differential
  • Chest radiograph if respiratory symptoms present
  • Lumbar puncture if infant is stable (critical because blood cultures can be sterile in 15-33% of newborns with meningitis) 5

Start empirical broad-spectrum antibiotics immediately with the same regimen as above (IV ampicillin plus gentamicin or cefotaxime). 1, 5

Key neonatal warning: Approximately 90% of early-onset GBS disease manifests within the first 24 hours of life. 5 Intrapartum antibiotics do not mask or delay clinical presentation—signs of sepsis will still appear rapidly. 5

Critical Prognostic Data

In women with preterm premature rupture of membranes (PPROM) managed expectantly, intraamniotic infection occurs in 58.1% of cases, reinforcing the need for high clinical suspicion. 1

Common Pitfalls to Avoid

Never withhold antibiotics pending amniocentesis results or waiting for maternal fever to develop in suspected chorioamnionitis. 1

Do not be falsely reassured by negative maternal GBS screening—more than 60% of early-onset GBS cases occur in infants born to women with negative prenatal cultures. 5

Recognize that epidural analgesia can cause fever, potentially leading to overdiagnosis, but when clinical suspicion exists, err on the side of treatment. 2

Maternal sepsis progresses rapidly—the median interval from first infection signs to death is only 18 hours. 1 This underscores the absolute necessity of immediate antibiotic administration and delivery planning.

References

Guideline

Management of Intraamniotic Infection (Chorioamnionitis)

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Oxytocin Use in Chorioamnionitis

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Management of clinical chorioamnionitis: an evidence-based approach.

American journal of obstetrics and gynecology, 2020

Guideline

Early-Onset GBS Disease in Newborns

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

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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