Time to positivity of blood cultures in paediatric patients

Catrin Kar Yee Kong1, Natalie Woon Hui Tan2, Karen Donceras Nadua2

  • 1Department of Paediatric Medicine, KK Women's and Children's Hospital, Singapore.

Insights

A 36-hour monitoring period for blood cultures (BC) in children is sufficient to detect over 97% of pathogenic bacteria. Aerobic cultures showed faster detection times than anaerobic cultures for common pediatric pathogens.

Area of Science:

  • Clinical Microbiology
  • Pediatric Infectious Diseases
  • Diagnostic Bacteriology

Background:

  • Continuous monitoring of blood culture (BC) systems aids rapid microbial detection.
  • Understanding time to positivity (TTP) variations is crucial for optimizing diagnostic protocols in pediatric care.

Purpose of the Study:

  • To analyze differences in TTP for various organisms in BACTEC blood cultures.
  • To evaluate if a 36-hour incubation period is adequate for detecting relevant pathogenic bacteria in pediatric patients.

Main Methods:

  • Retrospective audit of positive aerobic (AE) and anaerobic (AN) BC from pediatric inpatients (August 2016 - January 2019).
  • Analysis of the first positive BC per bacteraemia episode, focusing on TTP.
  • Categorization of detected organisms including Gram-negative rods (GNR), Gram-positive cocci (GPC), and contaminants.

Main Results:

  • A total of 480 first positive BC were analyzed from 372 bacteraemia episodes.
  • Median TTP was 13.20 hours for AE and 13.92 hours for AN cultures.
  • Gram-negative rods (GNR) were the most common pathogens (49.7%). Streptococcus agalactiae and Escherichia coli exhibited the fastest TTP.
  • A 36-hour cutoff detected >97.7% of pathogens in AE BC and >99.1% in AN BC, compared to 86.5% of contaminants in AE BC.

Conclusions:

  • Gram-negative rods (GNR) are the predominant pathogens in pediatric blood cultures.
  • Aerobic (AE) blood cultures demonstrate faster pathogen detection compared to anaerobic (AN) cultures.
  • A 36-hour incubation period is effective for capturing the vast majority of clinically significant bacterial pathogens in pediatric blood cultures.
Abstract