Volume of blood required to detect common neonatal pathogens,☆☆,

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Abstract

OBJECTIVE: To determine the minimum volume of blood and the absolute number of organisms required for detection of bacteremia and fungemia by an automated colorimetric blood culture system (BacT/Alert, Organon Teknika). DESIGN: Common neonatal pathogens, Escherichia coli, Streptococcus agalactiae (group B streptococcus [GBS]: one American Type Culture Collection [ATCC] strain and one clinical isolate), Staphylococcus epidermidis, and Candida albicans, were seeded into blood to produce bacteremia or fungemia with low colony counts (1 to 3 colony-forming units [CFU] per milliliter) and ultra-low colony counts (<1 CFU/ml). For each organism, 96 culture bottles were inoculated with either 0.25, 0.5, 1.0, or 4.0 ml of the two seeded blood concentrations. Blood culture bottles were incubated in the BacT/Alert device for 5 days, and time to positivity was noted when applicable. All bottles were subcultured on plated media. DATA ANALYSIS: The Poisson statistic was used to calculate the probability of finding at least one viable CFU per inoculated culture bottle. The fraction of culture bottles with positive findings per group was divided by the probability of one or more organisms present to give the positivity index. RESULTS: Plated subculture identified no growth of organisms not detected by the colorimetric detection system. The false-positive rate for the automated device was less than 1%. The positivity index for the GBS clinical isolate was 1.13, for the GBS ATCC isolate 0.96, for S. epidermidis 0.94, for C. albicans 0.97, and for E. coli 0.95. There was a statistically significant difference with time to positivity and inocula volume (p <0.01), but the difference was not clinically important. CONCLUSIONS: If one or two viable colony-forming units are in the blood inoculated into culture media, the BacT/Alert system will detect growth rapidly. Because there appears to be a sizable subset of neonates who are at risk of sepsis with a colony count less than 4 CFU/ml, then a 0.5 ml inoculum of blood into the culture media is inadequate for sensitive and timely detection of bacteremia. One to two milliliters of blood should increase microorganism recovery in the face of low-colony-count sepsis. (J PEDIATR 1996;129:275-8)

Section snippets

Selection of microorganisms

Common neonatal pathogens, Escherichia coli (American Type Culture Collection strain 25922), Streptococcus agalactiae (group B streptococcus, ATCC strain 12386), Streptococcus agalactiae (type III, clinical isolate), Staphylococcus epidermidis (ATCC strain 35983), and Candida albicans (clinical isolate), were grown and suspended in sterile nonbacteriostatic normal saline solution.

Microbiologic quantification

Microorganisms were diluted to 108 colony-forming units per milliliter, with the turbidity measured with a

RESULTS

The automated instrument was 100% sensitive; organisms were detected on all positive plated subcultures. The instrument signaled four positive results (0.8%) that were subsequently negative on plated media. There was rare bacterial contamination. Contaminants were found in five culture bottles in the E. coli phase of the study and in two bottles of the C. albicans phase. In the case of every contaminant, the BacT/Alert device detected microbiologic growth.

The actual colony counts for the seeded

DISCUSSION

In adults, the volume of blood for culture is the most important factor influencing yield.18, 19, 20, 21, 22, 23 Numerous reports of adults indicate that more blood is better. Ilstrup and Washington20 found that the average yield for 30 ml blood is 61% greater than the yield for 10 ml blood. Mermel and Maki23 concluded that the yield of blood cultures in adults increases 3% per milliliter of blood cultured. Extrapolating data from the adult literature and applying it to children is problematic.

Acknowledgements

We thank Dr. David S. Louder for his assistance in the statistical analysis of data for this study.

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    From the Divisions of Neonatology and Pathology, Wilford Hall United States Air Force Medical Center, Lackland Air Force Base, Texas

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    Reprint requests: Robert L. Schelonka, CAPT, USAF MC, Department of Pediatrics, Wilford Hall Medical Center/PSP, 2200 Bergquist Dr., Suite 1, Lackland AFB, TX 78236-5300.

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