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Published on: November 16, 2016
Benzylpenicillin Concentrations in Intrapartum Group B Streptococcus Prevention Guidelines; A Systematic Review of
Brian Deegan1, Ashley Gourlay1, Lars Eriksson2
1Women's and Newborn Services, Royal Brisbane and Women's Hospital, Herston, Queensland, Australia.
Insights
Intrapartum antibiotics like benzylpenicillin are used to prevent Group B Streptococcus (GBS) disease. Current evidence is insufficient to confirm if fetal drug concentrations meet the minimum inhibitory concentration (MIC) for GBS.
Area of Science:
- Obstetrics and Gynecology
- Neonatal Medicine
- Pharmacology
Background:
- Intrapartum antibiotics are administered to reduce neonatal risk of early-onset Group B Streptococcus (GBS) disease.
- Protocols aim to achieve fetal serum and amniotic fluid concentrations above the GBS minimum inhibitory concentration (MIC) at birth.
Purpose of the Study:
- To summarize evidence on intrapartum benzylpenicillin dosing.
- To compare fetal serum and amniotic fluid concentrations with GBS MICs.
Main Methods:
- Systematic review of PubMed, CINAHL, Cochrane Library, and Embase.
- Included studies examining benzylpenicillin concentrations in umbilical cord blood and/or amniotic fluid.
Main Results:
- Seven studies were included with varied doses and methods.
- Benzylpenicillin concentrations were often higher than the target MIC (0.125 mcg/mL).
- Methodological limitations included reporting total concentrations and protocol violations.
Conclusions:
- Lack of high-quality evidence supports current intrapartum antibiotic dosing for achieving adequate fetal MICs.
- Rigorous studies accounting for drug protein binding are needed to optimize dosing regimens.
Introduction:
Intrapartum antibiotics are often used to reduce neonatal risk of early-onset Group B Streptococcus (GBS) disease. Protocols aim to achieve a fetal serum and amniotic fluid concentration above the minimum inhibitory concentration (MIC) of GBS at the time of birth.
Aims:
We aimed to summarise the evidence for currently recommended doses of benzylpenicillin by comparing intrapartum fetal serum and amniotic fluid concentrations of benzylpenicillin with the associated MIC of GBS at the time of birth.
Methods:
We systematically reviewed PubMed, the Cumulative Index to Nursing and Allied Health Literature (CINAHL), the Cochrane Library, and Embase databases. We sought studies in which umbilical cord blood and/or amniotic fluid were examined for Benzylpenicillin concentrations after intrapartum intravenous administration.
Results:
Seven studies were included, using a variety of doses, applying different assay techniques, and reporting a wide range of concentrations reported in the umbilical cord serum and amniotic fluid. Concentrations were often significantly higher than the target MIC of 0.125 mcg/mL. Significant methodological limitations included reporting of total concentrations of antibiotic only and substantial protocol violations.
Discussion:
There is a lack of high-quality evidence to support the current dosing of intrapartum antibiotics, with regards to whether appropriate MICs are achieved in the fetus. Studies applying rigorous methodology and accounting for drug protein binding are required to determine the dosing regimens required to achieve these concentrations in the umbilical cord serum and amniotic fluid.
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