Infectious Diseases
Poster Session 2
Emma J. Swayze, BS, MD, MS (she/her/hers)
PGY2 Resident
University of Tennessee Health Science Center
Memphis, TN, United States
Lydia M. Henry, BA
Medical Student
University of Tennessee Health Science Center
Memphis, TN, United States
Emily Liske, BS, MD
University of Tennessee Health Science Center
Memphis, TN, United States
Erin Dolvin, BS
Medical Student
University of Tennessee Health Science Center
Memphis, TN, United States
Alexa Swailes, MD
Assistant Professor
University of Tennessee Health Science Center
Memphis, TN, United States
Group B streptococcus infection is the most common cause of early-onset neonatal sepsis. Intrapartum antibiotic therapy is imperative to minimize maternal-to-fetal transmission of Group B Streptococcus (GBS). Penicillin is the agent of choice, with ampicillin or cefazolin as acceptable alternatives, but there is a paucity of data on the efficacy of alternate antibiotic therapies for penicillin-allergic patients. This study evaluates the effectiveness of alternate antibiotic therapies among pregnant patients at an urban safety net hospital.
Study Design:
This was a retrospective analysis of GBS+ pregnant patients from 2019 through 2022. Penicillin-allergic patients were matched 1:2 with non-allergic controls. Primary outcomes were GBS positive neonates, neonatal length of stay, GBS septicemia, Apgar scores, neonatal demise, and 30-day neonatal infectious complications (sepsis, deafness, pneumonia, or meningitis). Chi-square and Fischer exact analyses were performed on Stata version 16.1 (StataCorp, College Station, Texas).
Results:
229 GBS+ pregnant patients were analyzed, including 84 penicillin-allergic (36.7%) and 145 non-allergic (63.3%). Patients were treated with vancomycin (n=66, 28.8%), clindamycin if susceptibilities were performed on maternal GBS culture (n=10, 4.4 %), cephalosporins (n=6, 2.6%), or penicillin/ampicillin (n=147, 64.2%). Rates of GBS positive infants were low but varied by antibiotic treatment (p< 0.01): penicillin (0%); vancomycin (0%); clindamycin (20%); and cephalosporins(16.7%). There was a significant difference in 30-day neonatal complications (p=0.03): penicillin (2.0%); vancomycin(0%); clindamycin (10%); and cephalosporins(16.7%) but no difference in length of stay, 1 or 5-minute Apgar scores, or neonatal demise.
Conclusion:
Antibiotic effectiveness for GBS+ pregnant patients varied slightly by medication, but risk was low in all cohorts. Vancomycin appears to be most effective in reducing neonatal morbidity among penicillin-allergic patients, but alternative antibiotic therapies may also provide adequate coverage with a lower risk of promoting antibiotic resistance.