REASSESSMENT OF THE INCUBATION-TIME IN A CONTROLLED CLINICAL COMPARISON OF THE BACT ALERT AEROBIC FAN BOTTLE AND STANDARD ANAEROBIC BOTTLE USED AEROBICALLY FOR THE DETECTION OF BLOOD-STREAM INFECTIONS/
N. Cornish et al., REASSESSMENT OF THE INCUBATION-TIME IN A CONTROLLED CLINICAL COMPARISON OF THE BACT ALERT AEROBIC FAN BOTTLE AND STANDARD ANAEROBIC BOTTLE USED AEROBICALLY FOR THE DETECTION OF BLOOD-STREAM INFECTIONS/, Diagnostic microbiology and infectious disease, 32(1), 1998, pp. 1-7
This study assessed the minimum incubation time required to detect blo
odstream infections during a controlled clinical comparison of the per
formance characteristics of rite Bact/Alert aerobic FAN bottle and the
standard anaerobic bottle used aerobically except on a selective basi
s. Blood was collected from adults with suspected bloodstream infectio
ns and inoculated into each bottle, which was monitored in the BacT/Al
ert Microbial Detection System. The anaerobic bottle was vented before
incubation except when cultures were obtained from patients on the co
lorectal and gynecologic surgical and emergency services. Statistical
analysis was limited to those culture sets in which each bottle was in
oculated with greater than or equal to 8 int of blood and bacterial gr
owth was considered to be clinically significant. A total of 682 posit
ive cultures from 243 patients satisfied the inclusion criteria. Signi
ficantly more isolates of Staphylococcus aureus (p <0.001), S. epiderm
idis (p <0.001), other congulase-negative staphylococci (p <0.001), En
terococcus spp. (p = 0.04), Escherichia coli (p = 0.03), all Enterobac
teriaceae (p <0.001), Pseudomonas aeruginosa (p = 0.001), and Candida
spp. (p <0.001) were detected by the aerobic FAN bottle. Significantly
more septic episodes due to S. aureus, S. epidermidis. other coagulas
e negative staphylococci, Enterobacteriaceae, P. aeruginosa, and Candi
da spp. were detected by the aerobic FAN bottle. Significantly more ba
cterial isolates were detected by the aerobic FAN whether or not antib
iotics were being administered at the time of blood culture, whereas t
here were significantly fewer positive cultures in the vented standard
anaerobic bottle when patients were receiving antimicrobial therapy t
han when they were not. All but 5% of positive cultures were detected
within three days. Only six of the cultures requiring four or five day
s of incubation represented true misses, and only one of these six res
ulted in a change in therapy which, however, did not affect the patien
t's outcome. (C) 1998 Elsevier Science Inc.