Key points are not available for this paper at this time.
Background Intrapartum antibiotic therapy is imperative to minimize maternal-to-fetal transmission of group B Streptococcus (GBS). Penicillin is the gold standard for treatment, but there is a paucity of data on alternate antibiotic therapies for penicillin-allergic patients. This study evaluates the effectiveness of alternate antibiotic therapies in this population. Methods This was a retrospective cohort analysis of GBS-positive pregnant patients at a single safety-net hospital from 2019 through 2022. GBS-positive penicillin-allergic patients were matched 1:2 with nonallergic controls. The primary outcomes were as follows: GBS-positive neonates, neonatal length of stay, GBS septicemia, Apgar scores, fetal demise, and 30-day neonatal complications (sepsis, deafness, pneumonia, or meningitis). χ 2 and Fisher exact analyses were performed on Stata version 16.1 (StataCorp, College Station, TX). Results Two hundred twenty-three GBS-positive pregnant patients were analyzed, including 78 penicillin-allergic (35.0%) and 145 nonallergic (65%). Patients were treated with vancomycin (n = 64, 28.7%), clindamycin (n = 7, 3.1%), cephalosporins (n = 6, 2.7%), or penicillin (n = 146, 65.5%). Rates of GBS-positive infants were low but varied by antibiotic treatment ( P < 0.01): penicillin, 0/146 (0%); vancomycin, 0/64 (0%); clindamycin, 1/7 (14.3%); and cephalosporins, 1/6 (16.7%). There was also a significant difference in 30-day neonatal complications ( P = 0.03): penicillin, 3/146 (2.1%); vancomycin, 0/64 (0%); clindamycin, 1/7 (14.3%); and cephalosporins, 1/6 (16.7%) but no difference in length of stay ( P = 0.07), 5-minute Apgar scores ( P = 0.32), or fetal demise ( P = 1.00). Conclusions Antibiotic effectiveness for GBS-positive pregnant patients varied slightly by medication, but the risk was low in all cohorts. Vancomycin appears to be effective for penicillin-allergic patients, but alternative antibiotic therapies may also provide adequate coverage with a lower risk of promoting antibiotic resistance.
Building similarity graph...
Analyzing shared references across papers
Loading...
Emma Swayze
Emily J. Liske
Lydia M. Henry
Infectious Diseases in Clinical Practice
University of Tennessee Health Science Center
Building similarity graph...
Analyzing shared references across papers
Loading...
Swayze et al. (Thu,) studied this question.
www.synapsesocial.com/papers/68e5b4f8b6db64358754e44b — DOI: https://doi.org/10.1097/ipc.0000000000001403
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: