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Published on: June 24, 2020
Penicillin allergy testing in pregnancy improves maternal and neonatal clinical outcomes
Jamie L Waldron1,2, Nerlyne Desravines3, Carolina Alvarez4,5
1Department of Medicine, Division of Allergy and Immunology, Massachusetts General Hospital, Boston, Mass.
Insights
Penicillin allergy evaluation during pregnancy improves maternal and infant outcomes. This proactive approach reduces cesarean delivery rates and neonatal complications, ensuring better health for both mother and baby.
Area of Science:
- Obstetrics and Gynecology
- Allergy and Immunology
- Neonatology
Background:
- Penicillin allergy is frequently reported during pregnancy, a period of high antibiotic use.
- Unverified penicillin allergy can lead to alternative antibiotic prescriptions, increasing risks for mothers and newborns.
- These risks include higher rates of cesarean delivery, prolonged hospital stays, and increased infectious complications.
Purpose of the Study:
- To assess the impact of penicillin allergy evaluation on antibiotic use up to 30 days postpartum.
- To compare maternal and neonatal clinical outcomes between patients undergoing evaluation and a usual care group.
Main Methods:
- A prospective cohort study involving pregnant patients undergoing penicillin allergy evaluation.
- Evaluation included skin testing and supervised drug challenge with amoxicillin during the second or third trimester.
- Outcomes were compared to a control group receiving usual care using linear regression models.
Main Results:
- Patients undergoing penicillin allergy evaluation showed significantly increased perinatal beta-lactam receipt (96% vs 38%).
- These patients had reduced odds of cesarean delivery (OR=0.31) and shorter infant hospital stays (OR=0.31).
- Infants born to evaluated mothers had lower odds of high neonatal sepsis scores (OR=0.41).
Conclusions:
- Proactive penicillin allergy evaluation during pregnancy is safe and beneficial.
- This evaluation positively impacts maternal and neonatal clinical outcomes.
- It leads to improved antibiotic utilization and reduced adverse events.
Background:
Penicillin allergy is commonly reported in pregnancy, a time of high antibiotic utilization wherein β-lactam antibiotics have multiple indications. Unverified penicillin allergy leads to alternative antibiotic receipt and is associated with increased rates of cesarean delivery, prolonged maternal hospitalization, increased infectious complications, and increased number of antibiotics courses, while neonates born to those with penicillin allergy have higher infection rates, hospitalization time, and readmissions.
Objective:
Our primary aim was to evaluate the impact of penicillin allergy evaluation on antibiotic utilization through 30 days postpartum. Our secondary aim was to compare maternal and neonatal clinical outcomes to those who did not undergo penicillin allergy evaluation (usual care group).
Methods:
Participants in this prospective cohort study underwent single outpatient visit for penicillin allergy evaluation with supervised drug challenge to amoxicillin after negative skin prick and intradermal skin testing during second or third trimester. Antibiotic utilization, length of stay, and other outcomes for mother and infant were compared to a usual care group by linear regression models.
Results:
Forty-six participants completed outpatient penicillin allergy evaluation. Compared to 105 pregnant patients in the usual care group, tested individuals were more likely to be married and to have private insurance, and they had significantly increased perinatal β-lactam receipt (96% vs 38%, P < .001). Tested patients had 69% decreased odds of cesarean delivery (odds ratio = 0.31; 95% confidence interval, 0.13. 0.72), while infants of tested patients had 69% lower mean length of stay (odds ratio = 0.31; 95% confidence interval, 0.18, 0.55) and 59% lower odds of high neonatal sepsis scores (odds ratio = 0.41; 95% confidence interval, 0.19, 0.86).
Conclusions:
Proactive penicillin allergy evaluation during pregnancy benefits both maternal and neonatal clinical outcomes and is safe to perform.
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