Study of Effectiveness and Safety of Azithromycin-based Extended-spectrum Prophylaxis to Prevent Post Cesarean Infection

Inclusion criteria

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Pregnant Women aged 14 years and over at ≥ 24 weeks' viable gestation who will undergo unscheduled/non-elective cesareans with either:

• Labor (spontaneous or induced): active labor (ongoing contractions and at least 4cm dilated or contractions for at least 4 hours with documented cervical change of ≥1cm dilatation or ≥50% effacement), or
• Membrane rupture (standardized to duration of at least 4 hours prior to randomization).

Exclusion criteria

• Patient unwilling or unable to provide consent
• Multiple pregnancy
• Known azithromycin (or other macrolide) allergy
• Vaginal delivery
• Elective or scheduled cesarean prior to labor or membrane rupture.
• Azithromycin, erythromycin or other macrolide antibiotic use within 7 days of enrollment.
• Clinical chorioamnionitis or any other active bacterial infection (e.g. pyelonephritis, pneumonia, abscess) at time of randomization.
• Patient is unable or unlikely to follow-up after delivery (e.g. no prenatal care or a non-resident patient)
• Fetal demise or major congenital anomaly
• Significant liver disease defined as known cirrhosis or elevated transaminases of at least 3-fold upper limit of normal
• Significant renal disease defined as serum creatinine known to be >2.0 mg/dl or on dialysis.
• Active congestive heart failure (EF<45%) or pulmonary edema
• Active diarrhea at time of delivery
• Any patient with significant electrolyte abnormalities such as hypokalemia or hypocalcemia
• Any patient with structural heart disease or arrhythmias, or taking any medications known to prolong the QT interval
• Patient currently being treated with efavirenz, nelfinavir or fluconazole