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Outcomes after extended azithromycin administration in preterm premature rupture of membranes
Alison J DiSciullo1, Marissa Hand2, Sara N Iqbal1
1Department of Obstetrics and Gynecology, MedStar Washington Hospital Center, Washington, DC (Drs DiSciullo, Iqbal, and Chornock).
Insights
Extended azithromycin administration for preterm premature rupture of membranes significantly increased gestational latency by over 3 days. This approach did not negatively impact maternal or neonatal outcomes, offering a potential improvement in expectant management.
Area of Science:
- Obstetrics and Gynecology
- Maternal-Fetal Medicine
- Pharmacology
Background:
- Preterm premature rupture of membranes (PPROM) is a leading cause of preterm birth, often linked to subclinical infection.
- Prophylactic antibiotics are standard for prolonging latency in PPROM pregnancies.
- Azithromycin is an emerging alternative to erythromycin for PPROM management.
Purpose of the Study:
- To determine if extended azithromycin administration impacts latency time in pregnancies with PPROM.
- To evaluate the effect of a 7-day azithromycin course compared to a <2-day course.
Main Methods:
- Retrospective multi-institutional cohort study of singleton pregnancies with PPROM (23 0/7–33 6/7 weeks gestation).
- Exclusion criteria included multiple gestations, allergies, labor, placental abruption, overt chorioamnionitis, or nonreassuring fetal status.
- Comparison of limited (<2 days) versus extended (7 days) azithromycin administration alongside standard ampicillin/amoxicillin treatment.
Main Results:
- Extended azithromycin administration was associated with a significantly longer median gestational latency (5.8 days vs. 2.6 days, P<.001).
- The increase in latency for the extended azithromycin group was over 3 days.
- No significant differences were observed in rates of chorioamnionitis or adverse neonatal outcomes between groups.
Conclusions:
- Extended azithromycin administration in PPROM pregnancies effectively increases latency time.
- This extended regimen appears safe, showing no adverse effects on maternal or neonatal outcomes.
- Azithromycin offers a promising therapeutic option for optimizing PPROM management.
Background:
Preterm premature rupture of membranes accounts for approximately one-quarter of all preterm deliveries and occurs in 2% to 3% of all pregnancies. With subclinical infection being a suspected cause of preterm premature rupture of membranes, the administration of prophylactic antibiotics is an accepted standard of care to extend the latency period. Historically, erythromycin was used in the antibiotic regimen recommended for women with preterm premature rupture of membranes during expectant management; however, azithromycin has recently been shown to be a suitable alternative.
Objective:
This study aimed to evaluate whether extended azithromycin administration affects the latency time in preterm premature rupture of membranes.
Study Design:
This was a retrospective multi-institutional cohort study in Washington, District of Columbia, of patients admitted from January 2012 to December 2019 with preterm premature rupture of membranes of singleton pregnancies between 23 0/7 and 33 6/7 weeks of gestation. Patients were excluded if they had multiple pregnancies, had an allergy to penicillin or macrolides, were in labor, had suspected placental abruptions, had overt chorioamnionitis, or had nonreassuring fetal status on presentation indicating the need for prompt delivery. Patients that received limited azithromycin administration (<2 days) and patients that received extended azithromycin administration (7 days) were compared. All patients otherwise received the institutional standard of 2 days of intravenous ampicillin followed by 5 days of oral amoxicillin. The primary outcome was length of gestational latency, defined as the time from membrane rupture to delivery. The selective secondary outcomes that were evaluated were rates of chorioamnionitis and adverse neonatal outcomes, including sepsis, respiratory distress, necrotizing enterocolitis, intraventricular hemorrhage, and neonatal death.
Results:
During the study period, 416 cases of preterm premature rupture of membranes were identified. Of the 287 patients who met the inclusion criteria, 165 (57.5%) received limited azithromycin administration, and 122 (42.5%) received extended azithromycin administration. Adjusted median gestational latency was significantly longer for patients who received extended azithromycin administration, extended by >3 days (2.6 days [interquartile range, 2.2-3.1] for limited azithromycin administration vs 5.8 days [interquartile range, 4.8-6.9] for extended azithromycin administration; P<.001). Neonatal secondary outcome evaluation was performed on 216 cases (76%). There was no difference in chorioamnionitis or adverse neonatal outcomes between the 2 groups.
Conclusion:
Among patients with preterm premature rupture of membranes, extended azithromycin administration was associated with increased latency, without any effect on other maternal or neonatal outcomes.
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