Literature DB >> 8458950

Multicenter clinical evaluation of a continuous monitoring blood culture system using fluorescent-sensor technology (BACTEC 9240).

F S Nolte1, J M Williams, R C Jerris, J A Morello, C D Leitch, S Matushek, L D Schwabe, F Dorigan, F E Kocka.   

Abstract

The BACTEC 9240 (Becton Dickinson Diagnostic Instrument Systems, Sparks, Md.) is a new continuous-monitoring blood culture system that uses internal, fluorescent-CO2 sensors. In a multicenter clinical trial, organism yield and times to detection with the prototype BACTEC 9240 system were compared with those of the BACTEC NR 660 system. Equal volumes of blood were inoculated into the bottles included in the study blood culture sets (aerobic and anaerobic 9240 and NR6A and NR7A bottles). A total of 9,391 aerobic and 8,951 anaerobic bottle pairs were inoculated with 9,801 blood specimens. A total of 587 clinically significant positive blood cultures and 415 cases of sepsis were studied. The standard 9240 aerobic bottle detected significantly more Staphylococcus aureus (P < 0.05), coagulase-negative staphylococci (P < 0.01), and total microorganisms (P < 0.001) than the NR6A bottle. The standard 9240 anaerobic bottle detected significantly more coagulase-negative staphylococci (P < 0.001), members of the family Enterobacteriaceae (P < 0.01), and total microorganisms (P < 0.001) than the NR7A bottle. A total of 420 positive cultures were detected in both systems; for 284, the time to detection was equivalent with both systems (within 12 h); for 123, the 9240 system was faster; and for 13, the NR 660 system was faster (P < 0.001). The average times to detection for the 9240 and the NR 660 systems were 20.2 and 27.5 h, respectively. Ninety-nine cultures were positive only in the 9240 system, and 68 cultures were positive only in the NR 660 system (P < 0.02). The 9240 system also detected significantly more episodes of bacteremia (P < 0.001). The false-positive rates for the 9240 and NR 660 systems were 2.2 and 2.3%, respectively. The false-negative rates for the two systems after 5 days of incubation did not differ significantly. The contamination rates for the 9240 and NR 660 systems were 1.9 and 1.5%, respectively (P < 0.05). In conclusion, the prototype 9240 system detected more clinically significant positive blood cultures and did so sooner than the NR 660 system, with the additional advantages of full automation, continuous monitoring, and noninvasive sampling.

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Year:  1993        PMID: 8458950      PMCID: PMC262818          DOI: 10.1128/jcm.31.3.552-557.1993

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  5 in total

1.  Effect of blood dilution on recovery of organisms from clinical blood cultures in medium containing sodium polyanethol sulfonate.

Authors:  J F Salventi; T A Davies; E L Randall; S Whitaker; J R Waters
Journal:  J Clin Microbiol       Date:  1979-02       Impact factor: 5.948

2.  Effect of sodium polyanethol sulfonate in blood cultures.

Authors:  J Eng
Journal:  J Clin Microbiol       Date:  1975-02       Impact factor: 5.948

3.  Controlled comparison of the BacT/Alert and BACTEC 660/730 nonradiometric blood culture systems.

Authors:  M L Wilson; M P Weinstein; L G Reimer; S Mirrett; L B Reller
Journal:  J Clin Microbiol       Date:  1992-02       Impact factor: 5.948

4.  Detection of positive blood cultures by the Bactec NR660. The clinical importance of five versus seven days of testing.

Authors:  K C Masterson; J E McGowan
Journal:  Am J Clin Pathol       Date:  1988-07       Impact factor: 2.493

5.  Comparison of recovery of organisms from blood cultures diluted 10% (volume/volume) and 20% (volume/volume).

Authors:  R Auckenthaler; D M Ilstrup; J A Washington
Journal:  J Clin Microbiol       Date:  1982-05       Impact factor: 5.948

  5 in total
  51 in total

Review 1.  Detection of Brucellae in blood cultures.

Authors:  P Yagupsky
Journal:  J Clin Microbiol       Date:  1999-11       Impact factor: 5.948

2.  Validity of earlier positivity of central venous blood cultures in comparison with peripheral blood cultures for diagnosing catheter-related bacteremia in cancer patients.

Authors:  V B Malgrange; M C Escande; S Theobald
Journal:  J Clin Microbiol       Date:  2001-01       Impact factor: 5.948

3.  Direct identification of bacteria from positive blood cultures by amplification and sequencing of the 16S rRNA gene: evaluation of BACTEC 9240 instrument true-positive and false-positive results.

Authors:  Q Qian; Y W Tang; C P Kolbert; C A Torgerson; J G Hughes; E A Vetter; W S Harmsen; S O Montgomery; F R Cockerill; D H Persing
Journal:  J Clin Microbiol       Date:  2001-10       Impact factor: 5.948

Review 4.  Update on detection of bacteremia and fungemia.

Authors:  L G Reimer; M L Wilson; M P Weinstein
Journal:  Clin Microbiol Rev       Date:  1997-07       Impact factor: 26.132

5.  Surge capacity for response to bioterrorism in hospital clinical microbiology laboratories.

Authors:  Daniel S Shapiro
Journal:  J Clin Microbiol       Date:  2003-12       Impact factor: 5.948

6.  Performance of a new combination of blood culture vials in sepsis detection: a 2-year retrospective comparison.

Authors:  Paolo Bottino; Fabio Rapallo; Elisa Gamalero; Andrea Rocchetti
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2019-05-08       Impact factor: 3.267

7.  Rapid diagnosis of Brucella bacteremia by using the BACTEC 9240 system.

Authors:  R M Bannatyne; M C Jackson; Z Memish
Journal:  J Clin Microbiol       Date:  1997-10       Impact factor: 5.948

8.  Rapid, sensitive recovery of recombinant attenuated Salmonella enterica serovar Typhi vaccine strains from human blood.

Authors:  Kathleen R Lottenbach; Sandra M Kelly-Aehle; Karen E Brenneman; Roy Curtiss; Sharon E Frey
Journal:  Clin Vaccine Immunol       Date:  2013-07-24

9.  Controlled comparative evaluation of BacT/Alert FAN and ESP 80A aerobic media as means for detecting bacteremia and fungemia.

Authors:  G V Doern; A Barton; S Rao
Journal:  J Clin Microbiol       Date:  1998-09       Impact factor: 5.948

10.  Continuous quality improvement for introduction of automated blood culture instrument.

Authors:  M Alfa; S Sanche; S Roman; Y Fiola; P Lenton; G Harding
Journal:  J Clin Microbiol       Date:  1995-05       Impact factor: 5.948

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