TY - JOUR
T1 - Azithromycin to Prevent Sepsis or Death in Women Planning a Vaginal Birth
AU - The A-PLUS Trial Group
AU - Tita, Alan T.N.
AU - Carlo, Waldemar A.
AU - Mcclure, Elizabeth M.
AU - Mwenechanya, Musaku
AU - Chomba, Elwyn
AU - Hemingway-Foday, Jennifer J.
AU - Kavi, Avinash
AU - Metgud, Mrityunjay C.
AU - Goudar, Shivaprasad S.
AU - Derman, Richard
AU - Lokangaka, Adrien
AU - Tshefu, Antoinette
AU - Bauserman, Melissa
AU - Bose, Carl
AU - Shivkumar, Poonam
AU - Waikar, Manju
AU - Patel, Archana
AU - Hibberd, Patricia L.
AU - Nyongesa, Paul
AU - Esamai, Fabian
AU - Ekhaguere, Osayame A.
AU - Bucher, Sherri
AU - Jessani, Saleem
AU - Tikmani, Shiyam S.
AU - Saleem, Sarah
AU - Goldenberg, Robert L.
AU - Billah, Sk M.
AU - Lennox, Ruth
AU - Haque, Rashidul
AU - Petri, William
AU - Figueroa, Lester
AU - Mazariegos, Manolo
AU - Krebs, Nancy F.
AU - Moore, Janet L.
AU - Nolen, Tracy L.
AU - Koso-Thomas, Marion
N1 - Publisher Copyright:
© 2023 Massachusetts Medical Society.
PY - 2023
Y1 - 2023
N2 - Background: The use of azithromycin reduces maternal infection in women during unplanned cesarean delivery, but its effect on those with planned vaginal delivery is unknown. Data are needed on whether an intrapartum oral dose of azithromycin would reduce maternal and offspring sepsis or death. Methods: In this multicountry, placebo-controlled, randomized trial, we assigned women who were in labor at 28 weeks' gestation or more and who were planning a vaginal delivery to receive a single 2-g oral dose of azithromycin or placebo. The two primary outcomes were a composite of maternal sepsis or death and a composite of stillbirth or neonatal death or sepsis. During an interim analysis, the data and safety monitoring committee recommended stopping the trial for maternal benefit. Results: A total of 29,278 women underwent randomization. The incidence of maternal sepsis or death was lower in the azithromycin group than in the placebo group (1.6% vs. 2.4%), with a relative risk of 0.67 (95% confidence interval [CI], 0.56 to 0.79; P<0.001), but the incidence of stillbirth or neonatal death or sepsis was similar (10.5% vs. 10.3%), with a relative risk of 1.02 (95% CI, 0.95 to 1.09; P=0.56). The difference in the maternal primary outcome appeared to be driven mainly by the incidence of sepsis (1.5% in the azithromycin group and 2.3% in the placebo group), with a relative risk of 0.65 (95% CI, 0.55 to 0.77); the incidence of death from any cause was 0.1% in the two groups (relative risk, 1.23; 95% CI, 0.51 to 2.97). Neonatal sepsis occurred in 9.8% and 9.6% of the infants, respectively (relative risk, 1.03; 95% CI, 0.96 to 1.10). The incidence of stillbirth was 0.4% in the two groups (relative risk, 1.06; 95% CI, 0.74 to 1.53); neonatal death within 4 weeks after birth occurred in 1.5% in both groups (relative risk, 1.03; 95% CI, 0.86 to 1.24). Azithromycin was not associated with a higher incidence in adverse events. Conclusions: Among women planning a vaginal delivery, a single oral dose of azithromycin resulted in a significantly lower risk of maternal sepsis or death than placebo but had little effect on newborn sepsis or death.
AB - Background: The use of azithromycin reduces maternal infection in women during unplanned cesarean delivery, but its effect on those with planned vaginal delivery is unknown. Data are needed on whether an intrapartum oral dose of azithromycin would reduce maternal and offspring sepsis or death. Methods: In this multicountry, placebo-controlled, randomized trial, we assigned women who were in labor at 28 weeks' gestation or more and who were planning a vaginal delivery to receive a single 2-g oral dose of azithromycin or placebo. The two primary outcomes were a composite of maternal sepsis or death and a composite of stillbirth or neonatal death or sepsis. During an interim analysis, the data and safety monitoring committee recommended stopping the trial for maternal benefit. Results: A total of 29,278 women underwent randomization. The incidence of maternal sepsis or death was lower in the azithromycin group than in the placebo group (1.6% vs. 2.4%), with a relative risk of 0.67 (95% confidence interval [CI], 0.56 to 0.79; P<0.001), but the incidence of stillbirth or neonatal death or sepsis was similar (10.5% vs. 10.3%), with a relative risk of 1.02 (95% CI, 0.95 to 1.09; P=0.56). The difference in the maternal primary outcome appeared to be driven mainly by the incidence of sepsis (1.5% in the azithromycin group and 2.3% in the placebo group), with a relative risk of 0.65 (95% CI, 0.55 to 0.77); the incidence of death from any cause was 0.1% in the two groups (relative risk, 1.23; 95% CI, 0.51 to 2.97). Neonatal sepsis occurred in 9.8% and 9.6% of the infants, respectively (relative risk, 1.03; 95% CI, 0.96 to 1.10). The incidence of stillbirth was 0.4% in the two groups (relative risk, 1.06; 95% CI, 0.74 to 1.53); neonatal death within 4 weeks after birth occurred in 1.5% in both groups (relative risk, 1.03; 95% CI, 0.86 to 1.24). Azithromycin was not associated with a higher incidence in adverse events. Conclusions: Among women planning a vaginal delivery, a single oral dose of azithromycin resulted in a significantly lower risk of maternal sepsis or death than placebo but had little effect on newborn sepsis or death.
KW - Bacterial Infections
KW - Complications of Pregnancy
KW - Infectious Disease
KW - Neonatology
KW - Obstetrics/Gynecology
KW - Obstetrics/Gynecology General
KW - Pediatrics
UR - http://www.scopus.com/inward/record.url?scp=85151312943&partnerID=8YFLogxK
U2 - 10.1056/NEJMoa2212111
DO - 10.1056/NEJMoa2212111
M3 - Article
C2 - 36757318
AN - SCOPUS:85151312943
SN - 0028-4793
VL - 388
SP - 1161
EP - 1170
JO - New England Journal of Medicine
JF - New England Journal of Medicine
IS - 13
ER -