MedPath

Antibiotics and Gut Microbiota Among Newborn Infants

Phase 4
Completed
Conditions
Surgical Wound Infection
Infection; Cesarean Section
Complications; Cesarean Section
Interventions
Registration Number
NCT02072798
Lead Sponsor
Odense University Hospital
Brief Summary

Background Women undergoing Caesarean Section (CS) have an increased risk of postpartum infections compared to women undergoing vaginal delivery. In Denmark the incidence of post-CS infections is 7-10%. The most common infections are endometritis, Urinary tract infections (UTI) and wound infections (WI).

Prophylactic antibiotics are effective in preventing postoperative infections and national guidelines recommend that antibiotics should be administered as a single dose immediately before surgical incision. CS is an exception to this pre-incision administration approach. National guidelines recommend administration of antibiotics after umbilical cord clamping to avoid exposure of the child to antibiotics before birth. Recent studies of antibiotic prophylaxis for CS suggest that prophylactic antibiotics administered before incision compared to after umbilical cord clamping may reduce post-CS infections by up to 50%. Two Cochrane reviews from 2012 criticize these types of studies for lack of data for outcomes on the baby and on late infection in the mother.

At birth, all mammals must rapidly adapt to intake of complex milk nutrients via the gut and simultaneously tolerate the invasion of billions of microbes. This requires rapid maturation of the digestive and immune functions to avoid gut disorders and infections. Full-term, breast-fed infants normally adapt well, but factors such as caesarean birth, high hygiene levels, antibiotics treatment and formula feeding may inhibit immune development both short and long term. Birth by caesarean section in high-hygiene hospital environments, and widespread use of antibiotics, are factors that reduce gut microbiota density and diversity in the newborn for some time after birth. On the other hand, high-hygiene environments and antibiotics are essential tools to combat infections, especially for the weakest newborn infants.

This pilot study will be a feasibility study to the original study, which examines the effect of change in timing of prophylactic antibiotics on the rate of post-CS infections (endometritis, UTI and WI). The pilot study focus on antibiotic and changes in the gut microbiota of newborn infants. The feasibility study will only include pregnant women in Odense with a body mass index below 30, and planned cesarean section.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
42
Inclusion Criteria
  • Age ≥ 18 year
  • Women, who can read and understand Danish
  • A gestational age ≥ completed 28 weeks of gestation
  • Rupture of membranes and active labour (uterine contractions) is allowed.
  • BMI < 30
Exclusion Criteria
  • Hypersensitivity to cefuroxime or to any other cephalosporin antibiotics
  • Previous immediate and/or severe hypersensitivity reaction to penicillin or any other beta-lactam antibiotic.
  • Systemic exposure to any antibiotic agent within 1 week before delivery Antibiotic indicated due to PROM, fever, group B Streptococcus or other indications at the time of caesarean section.
  • Women being immunologically incompetent (e.g. HIV positive)
  • Very sick newborn infants transferred to a neonatal intensive care unit and treated with antibiotics will be excluded from the study

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
preoperative antibioticCefuroximeiv Cefuroxime 1,5g administered 15-60 minutes before incision
postoperative antibioticCefuroximeiv Cefuroxime 1,5g administered after umbilical cord clamping
Primary Outcome Measures
NameTimeMethod
Maternal: incidence of post-CS infection (endometritis, urinary tract infections and wound infection) in each study groupWithin the first 30 days after surgery
Infant: fecal microbiota at the tenth day of lifeon the tenth day of life
Secondary Outcome Measures
NameTimeMethod
Maternal: Length of hospitalizationWithin the first 30 days after Caesarean Section
Infant: concentration of cefuroxime in blood samplesduring the first 24 hours of life
Infant: immunological analyses in blood samples on day 3On the third day of life
Maternal: readmissions to hospital on suspicion of postpartum infection following cesarean sectionWithin the first 30 days after Caesarean Section
Antibiotic treatmentwithin the first 30 days after Caesarean Section

Trial Locations

Locations (1)

Odense University Hospital

🇩🇰

Odense, Fyn, Denmark

© Copyright 2025. All Rights Reserved by MedPath