Literature DB >> 8659454

Clinical evaluation of the BacT/Alert and isolator aerobic blood culture systems.

H D Engler1, G A Fahle, V J Gill.   

Abstract

The BacT/Alert (BTA) (Organon Teknika, Durham, NC) and Isolator 10 (ISO) (Wampole Laboratories, Cranbury, NJ) blood culture systems were evaluated for their ability to detect aerobic and facultatively anaerobic microorganisms in blood of adult patients. For each culture 8 mL of blood was inoculated into both the aerobic standard BTA bottle and the ISO tube. Of 7,259 paired culture sets, 1,168 organisms were recovered, and 667 (57.1%) of these were considered clinically significant. This represented 540 clinically significant positive cultures from 266 patients. Of the significant isolates, 410 were recovered by both systems, 108 by BTA only and 149 by ISO only (P <.025). Overall, the BTA detected 77.7% of the significant isolates, whereas ISO detected 83.8%. The ISO recovered significantly more isolates of Staphylococcus aureus (P = .0001), coagulase-negative Staphylococcus spp (P <.01), and non-Enterobacteriaceae gram-negative rod species (P <.0025), whereas the BTA detected significantly more isolates of Streptococcus spp (P <.0025). Growth of S aureus (P <.0025), Enterococcus spp (P <.0025), and Streptococcus spp (P <.0075) was detected earlier by the BTA when laboratory coverage was available during the first shift only (7:30 AM to 4:00 PM), and additionally of Enterobacteriaceae (P <.0005) and other gram-negative rod species (P <.0001) if coverage was extended to 12:00 AM. Yeasts were detected more rapidly by the ISO (P <.0025). The ISO contamination rate (5.9%) was six times that of the BTA. Taking into account its ability to rapidly detect most organisms, its automated and thus labor-saving features, and the minimal contamination rate associated with its use, the BTA appears to be a reliable alternative to the ISO as a blood culturing system, although improvement in detection of staphylococci and non-Enterobacteriaceae gram-negative rods would be desirable.

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Year:  1996        PMID: 8659454     DOI: 10.1093/ajcp/105.6.774

Source DB:  PubMed          Journal:  Am J Clin Pathol        ISSN: 0002-9173            Impact factor:   2.493


  5 in total

1.  Performance of five agar media for recovery of fungi from isolator blood cultures.

Authors:  G W Procop; F R Cockerill; E A Vetter; W S Harmsen; J G Hughes; G D Roberts
Journal:  J Clin Microbiol       Date:  2000-10       Impact factor: 5.948

Review 2.  Developments for improved diagnosis of bacterial bloodstream infections.

Authors:  A J M Loonen; P F G Wolffs; C A Bruggeman; A J C van den Brule
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2014-05-22       Impact factor: 3.267

3.  Rapid Detection and Identification of Candidemia by Direct Blood Culturing on Solid Medium by Use of Lysis-Centrifugation Method Combined with Matrix-Assisted Laser Desorption Ionization-Time of Flight Mass Spectrometry (MALDI-TOF MS).

Authors:  Evgeny A Idelevich; Barbara Grünastel; Karsten Becker
Journal:  J Clin Microbiol       Date:  2016-12-28       Impact factor: 5.948

4.  Direct blood culturing on solid medium outperforms an automated continuously monitored broth-based blood culture system in terms of time to identification and susceptibility testing.

Authors:  E A Idelevich; B Grünastel; G Peters; K Becker
Journal:  New Microbes New Infect       Date:  2015-12-23

5.  Direct Blood Culturing of Candida spp. on Solid Medium by a Rapid Enrichment Method with Magnetic Beads Coated with Recombinant Human Mannan-Binding Lectin.

Authors:  Xiao-Ping Chen; Jin-Xing Lu; Xiao-Li Chen; Hao Zheng; Wen-Ge Li; You-Hong Zhong
Journal:  J Clin Microbiol       Date:  2020-03-25       Impact factor: 5.948

  5 in total

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