Literature DB >> 3170719

Clinical evaluation of diagnostic hemoperfusion for in vivo enrichment of bacteria and fungi in comparison with a conventional blood culture technique.

E Kühnen1, K P Schaal, F Keller, F Bartels.   

Abstract

The hemoperfusion module, a newly developed technique for recovering pathogenic microorganisms from patients suffering from septicemia, was compared with conventional blood cultures. The module was interconnected with the extracorporeal circulation of 92 predominantly hemodialyzed patients. Nearly 12 liters of flowing blood (up to 200 ml min-1; mean running time, 60 min) came in contact with the coated charcoal. Of 99 modules examined, 44 (44.7%) yielded positive cultures and contained 54 potentially pathogenic bacteria or fungi (22 species). Only 32 of 190 (16.8%) conventional blood cultures were positive and contained 37 microorganisms (10 species). Even when patients were receiving antibiotic treatment, the frequency of isolation was significantly higher in hemoperfusion (21 of 44 modules positive, 47.7%) than in conventional blood cultures (10 of 88 cultures positive, 11.4%). In contrast, 23 of 55 modules (41.8%) and 22 of 102 conventional blood cultures (21.6%) were positive when patients were not treated with antibiotics prior to blood sampling. Altogether, hemoperfusion modules appeared to be superior to and more sensitive than the conventional blood cultures used and seemed to be a valuable tool for detecting septicemia.

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Year:  1988        PMID: 3170719      PMCID: PMC266675          DOI: 10.1128/jcm.26.8.1609-1613.1988

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


  25 in total

1.  Practical aerobic membrane filtration blood culture technique: development of procedure.

Authors:  N M Sullivan; V L Sutter; S M Finegold
Journal:  J Clin Microbiol       Date:  1975-01       Impact factor: 5.948

2.  Early detection of Chlamydia trachomatis using fluorescent, DNA binding dyes.

Authors:  S H Salari; M E Ward
Journal:  J Clin Pathol       Date:  1979-11       Impact factor: 3.411

3.  Evaluation of acridine orange stain for detection of microorganisms in blood cultures.

Authors:  L R McCarthy; J E Senne
Journal:  J Clin Microbiol       Date:  1980-03       Impact factor: 5.948

4.  Effect of volume of blood cultured on detection of bacteremia.

Authors:  M M Hall; D M Ilstrup; J A Washington
Journal:  J Clin Microbiol       Date:  1976-06       Impact factor: 5.948

5.  Bacterial growth studied by flow cytometry.

Authors:  H B Steen; E Boye
Journal:  Cytometry       Date:  1980-07

6.  The importance of blood volume cultured on detection of bacteraemia.

Authors:  P Sandven; E A Høiby
Journal:  Acta Pathol Microbiol Scand B       Date:  1981-06

7.  Gas-liquid chromatography in routine processing of blood cultures for detecting anaerobic bacteraemia.

Authors:  M Reig; D Molina; E Loza; M A Ledesma; M A Meseguer
Journal:  J Clin Pathol       Date:  1981-02       Impact factor: 3.411

8.  [Investigation of the viability of radioactively labelled bacteria after adsorption on activated charcoal (author's transl)].

Authors:  F Keller; K Feldmann; B Gaugler; E Besenfelder
Journal:  Zentralbl Bakteriol Mikrobiol Hyg A       Date:  1981

9.  Automated detection of microbial growth in blood cultures by using stainless-steel electrodes.

Authors:  R L Holland; B H Cooper; N G Helgeson; A W McCracken
Journal:  J Clin Microbiol       Date:  1980-08       Impact factor: 5.948

10.  Combined use of phage typing, enterococcinotyping and species differentiation of group D streptococci as an effective epidemiological tool.

Authors:  E Kühnen; K Rommelsheim; L Andries
Journal:  Zentralbl Bakteriol Mikrobiol Hyg A       Date:  1987-10
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