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초록
Background
This study compared the growth of Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, Streptococcus pneumoniae, and Haemophilus influenzae in blood culture bottles containing anticoagulants, sodium polyanethol sulfonate (SPS) and sodium citrate.
Methods
One hundred and fifty colony forming units of five different bacterial species were inoculated into standard aerobic (SA) and standard anaerobic (SN) bottles and were combined with 5 mL of human blood in solution with SPS or sodium citrate. Time to detection (TTD) was then monitored using the BacT/ Alert 3D system (bioMerieux Inc.).
Results
Compared to the bacteria-only controls, cultures containing S. aureus, E. coli, P. aeruginosa, and S. pneumoniae plus SPS blood or citrated blood trended toward reduced TTD in both SA and SN bot-tles; however, there was no significant difference in TTD between SPS and sodium citrate anticoagulant. Although H. influenzae showed a remarkable difference in TTD between SPS (SA 14.8 h, SN 15.0 h) and sodium citrate (SA 23.5 h, SN 18.3 h), this difference was not statistically significant (P=0.10).
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Fig. 1.
Effects of blood and the anticoagulants SPS or sodium citrate on the growth (time to detection, TTD) of Staphylococcus aureus in the aerobic and anaerobic bottles by preincubation time. (A) Aerobic bottle, 25 o C. (B) Aerobic bottle, 37 o C. (C) Anaerobic bottle, 25 o C. (D) Anaerobic bottle, 37 o C.
Fig. 2.
Effects of blood and the anticoagulants SPS or sodium citrate on the growth (time to detection, TTD) of Haemophilus influenzae in the aerobic and anaerobic bottles by preincubation time. (A) Aerobic bottle, 25oC. (B) Aerobic bottle, 37oC. (C) Anaerobic bottle, 25°C. (D) Anaerobic bottle, 37 o C.
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