Literature DB >> 7494013

Controlled evaluation of BacT/alert standard anaerobic and FAN anaerobic blood culture bottles for the detection of bacteremia and fungemia.

M L Wilson1, M P Weinstein, S Mirrett, L G Reimer, R J Feldman, C R Chuard, L B Reller.   

Abstract

FAN medium was formulated to improve microbial recovery, particularly for fastidious microorganisms and for microorganisms causing sepsis in patients receiving antimicrobial therapy. In a controlled clinical evaluation performed at four university-affiliated hospitals, FAN anaerobic bottles were compared with standard anaerobic bottles for yield, speed of detection of microbial growth, and detection of septic episodes. A total of 10,431 blood culture sets were received; both anaerobic bottles of 7,694 blood culture sets were adequately filled with blood. Altogether, 925 isolates were recovered: 557 that were the cause of sepsis, 99 that were indeterminate as the cause of sepsis, and 269 contaminants. More Staphylococcus aureus (P < 0.001), coagulase-negative staphylococci (P < 0.001), Escherichia coli (P < 0.02), and all microorganisms combined (P < 0.005) were recovered from FAN bottles; more nonfermentative gram-negative bacilli (P < 0.05), Torulopsis glabrata (P < 0.001), and other yeasts (P < 0.01) were recovered from standard bottles. Growth of S. aureus (P < 0.001), coagulase-negative staphylococci (P < 0.001), Enterococcus faecalis (P < 0.025), streptococci other than Streptococcus pneumoniae (P < 0.01), and all microorganisms combined (P < 0.001) was detected earlier in standard bottles; growth of more isolates of E. coli (P < 0.05) and anaerobic bacteria (P < 0.01) was detected earlier in FAN bottles. The mean times to detection were 14.2 and 16.1 h for standard and FAN bottles, respectively. More septic episodes caused by S. aureus (P < 0.001), coagulase-negative staphylococci (P < 0.005), members of the family Enterobacteriaceae (P < 0.02), and all microorganisms combined (P < 0.02) were detected in FAN bottles; more septic episodes caused by nonfermentative gram-negative bacilli (P < 0.025) and yeasts (P < 0.005) were detected in standard bottles. In summary, more isolates (except for strict aerobes) were recovered from FAN bottles than from standard anaerobic bottles. Similarly, significant more septic episodes (except for those caused by strict aerobes) were detected with FAN bottles than with standard anaerobic bottles. With the exception of E. coli and anaerobic bacteria, growth of more isolates was detected earlier in standard anaerobic bottles.

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Year:  1995        PMID: 7494013      PMCID: PMC228392          DOI: 10.1128/jcm.33.9.2265-2270.1995

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


  24 in total

1.  Effects of atmosphere of incubation and of routine subcultures on detection of bacteremia in vacuum blood culture bottles.

Authors:  J L Harkness; M Hall; D M Ilstrup; J A Washington
Journal:  J Clin Microbiol       Date:  1975-10       Impact factor: 5.948

2.  Evaluation of a biphasic medium for blood cultures.

Authors:  M M Hall; C A Mueske; D M Ilstrup; J A Washington
Journal:  J Clin Microbiol       Date:  1979-11       Impact factor: 5.948

3.  Diminished growth of Pseudomonas aeruginosa in unvented blood-culture bottles.

Authors:  J G Knepper; B F Anthony
Journal:  Lancet       Date:  1973-08-11       Impact factor: 79.321

4.  Controlled evaluation of BacT/Alert standard aerobic and FAN aerobic blood culture bottles for detection of bacteremia and fungemia.

Authors:  M P Weinstein; S Mirrett; L G Reimer; M L Wilson; S Smith-Elekes; C R Chuard; K L Joho; L B Reller
Journal:  J Clin Microbiol       Date:  1995-04       Impact factor: 5.948

5.  Evaluation of the antimicrobial removal device when used with the BACTEC blood culture system.

Authors:  C L Strand
Journal:  Am J Clin Pathol       Date:  1982-12       Impact factor: 2.493

6.  The antimicrobial removal device. A microbiological and clinical evaluation.

Authors:  A J Wright; R L Thompson; C A McLimans; W R Wilson; J A Washington
Journal:  Am J Clin Pathol       Date:  1982-08       Impact factor: 2.493

7.  Evaluation of the Antibiotic Removal Device.

Authors:  M D Appleman; R S Swinney; P N Heseltine
Journal:  J Clin Microbiol       Date:  1982-02       Impact factor: 5.948

8.  Detection of yeasts and filamentous fungi in blood cultures during a 10-year period (1972 to 1981).

Authors:  J Bille; L Stockman; G D Roberts
Journal:  J Clin Microbiol       Date:  1982-11       Impact factor: 5.948

9.  The clinical significance of positive blood cultures: a comprehensive analysis of 500 episodes of bacteremia and fungemia in adults. I. Laboratory and epidemiologic observations.

Authors:  M P Weinstein; L B Reller; J R Murphy; K A Lichtenstein
Journal:  Rev Infect Dis       Date:  1983 Jan-Feb

10.  Enhanced detection of bacteremia with a new BACTEC resin blood culture medium.

Authors:  P C Appelbaum; D G Beckwith; J R Dipersio; J W Dyke; J F Salventi; L L Stone
Journal:  J Clin Microbiol       Date:  1983-01       Impact factor: 5.948

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  31 in total

1.  Fluorescent In situ hybridization allows rapid identification of microorganisms in blood cultures.

Authors:  V A Kempf; K Trebesius; I B Autenrieth
Journal:  J Clin Microbiol       Date:  2000-02       Impact factor: 5.948

2.  Controlled clinical comparison of BACTEC plus anaerobic/F to standard anaerobic/F as the anaerobic companion bottle to plus aerobic/F medium for culturing blood from adults.

Authors:  M L Wilson; S Mirrett; F T Meredith; M P Weinstein; V Scotto; L B Reller
Journal:  J Clin Microbiol       Date:  2001-03       Impact factor: 5.948

3.  Rapid detection of sepsis complicating acute necrotizing pancreatitis using polymerase chain reaction.

Authors:  W Z Zhang; T Q Han; Y Q Tang; S D Zhang
Journal:  World J Gastroenterol       Date:  2001-04       Impact factor: 5.742

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.  Evaluation of the alkaline wash/lysis procedure for the molecular diagnosis of a positive bacterial blood culture in clinical routine practice.

Authors:  Sheng-Chuan Hsi; Jun-Ren Sun; Tzong-Shi Chiueh
Journal:  J Clin Lab Anal       Date:  2010       Impact factor: 2.352

6.  Comparative recovery of microorganisms from BacT/ALERT plastic and glass FA and FN blood culture bottles.

Authors:  J A Riley; B J Heiter; P P Bourbeau
Journal:  J Clin Microbiol       Date:  2005-07       Impact factor: 5.948

7.  Differences in time to positivity can affect the negative predictive value of blood cultures drawn through a central venous catheter.

Authors:  J C Yébenes; M Serra-Prat; G Miró; G Sauca; J A Capdevila
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8.  Using the polymerase chain reaction coupled with denaturing gradient gel electrophoresis to investigate the association between bacterial translocation and systemic inflammatory response syndrome in predicted acute severe pancreatitis.

Authors:  Callum B Pearce; Vitaly Zinkevich; Iwona Beech; Viera Funjika; Ana Garcia Ruiz; Afraa Aladawi; Hamish D Duncan
Journal:  World J Gastroenterol       Date:  2005-12-07       Impact factor: 5.742

9.  Relevance of routine use of the anaerobic blood culture bottle.

Authors:  Patrick Grohs; Jean-Luc Mainardi; Isabelle Podglajen; Xavier Hanras; C Eckert; A Buu-Hoï; E Varon; Laurent Gutmann
Journal:  J Clin Microbiol       Date:  2007-06-20       Impact factor: 5.948

Review 10.  Blood culture contamination: persisting problems and partial progress.

Authors:  Melvin P Weinstein
Journal:  J Clin Microbiol       Date:  2003-06       Impact factor: 5.948

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