1992
DOI: 10.1136/jcp.45.6.468
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Methods used in the United Kingdom for the culture of micro-organisms from blood.

Abstract: Clinical Microbiology

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Cited by 13 publications
(5 citation statements)
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“…Previous reports have produced sensitivities varying from 12.8%l1 to 77.3%.8 Staphaurex's previously quoted high sensitivity may explain why four UK laboratories in a 1992 survey opted to use a staphylococcal latex kit for the direct identification of positive blood cultures. 3 The design of previous clinical evaluations of commercial slide agglutination kits has been extremely variable. Some workers have used seeded blood cultures, others clinical cultures.…”
Section: Discussionmentioning
confidence: 99%
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“…Previous reports have produced sensitivities varying from 12.8%l1 to 77.3%.8 Staphaurex's previously quoted high sensitivity may explain why four UK laboratories in a 1992 survey opted to use a staphylococcal latex kit for the direct identification of positive blood cultures. 3 The design of previous clinical evaluations of commercial slide agglutination kits has been extremely variable. Some workers have used seeded blood cultures, others clinical cultures.…”
Section: Discussionmentioning
confidence: 99%
“…2 Though the early distinction between Staphylococcus aureus and coagulase negative staphylococci (CNS) may be helpful in initiating appropriate antimicrobial treatment, few laboratories in the UK proceed to rapid identification tests if staphylococci are suspected in blood culture media. 3 Those who do test directly usually prefer a tube coagulase method to detect free coagulase rather than a slide agglutination test which detects clumping factor or protein A, or both. 3 Commerical slide agglutination kits for the identification of S aureus are widely used as they are particularly convenient and technically simple.…”
mentioning
confidence: 99%
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“…Aliquot inoculation was performed in the following selective nutrient media: (i) meat-peptone agar (MPA) for aerobic and facultatively anaerobic bacteria, (ii) BAIRD-PARKER-Agar (Merck, Germany) for Staphylococcus spp., (iii) KF-Streptococcus agar (Merck, Germany) for Streptococcus spp., (iv) MRSA (MRSA, HiMedia, India) for Lactobacillus spp., (v) Bifi dum agar (HiMedia, India) for Bifi dobacterium spp., (vi) Endo (HiMedia, India) for coliform bacteria, (vii) Sabouraud agar (HiMedia, India) for microscopic fungi, and (viii) Pseudomonas agar (HiMedia, India) for Pseudomonas spp. [22][23][24]. Aft er 24 h of incubation, we recorded preliminary data, and aft er 48 h, -the fi nal ones.…”
Section: Results Th E Formation Of Bacterial Vaginitis In the Balb/c ...mentioning
confidence: 99%
“…To determine the spectrum of microbiota, aliquots from the vagina and feces were plated on eight nutrient media, namely: meat-peptone agar (MPA) -medium for cultivation of aerobic and optional anaerobic microorganisms; BAIRD-PARKER-Agar (Merck, Germany) -selective medium for staphylococci; BAIRD-PARKER-Agar with gentami-cin in concentration of 15 μg/mL -selective medium for isolation of S. aureus 8325-4 strain; KF-Streptococcus agar (Merck, Germany)selective medium for streptococci, MRSA (HiMedia, India) -selective medium for lactobacilli; BA (HiMedia, India) -selective medium for bifidobacteria; ENDO (HiMedia, India) -selective medium for coliform bacteria; Sabouraud agar (HiMedia, India) -selective medium for microscopic fungi. After cultivation at 37 °C for 24 hours, the number of colonies per petri dish was calculated, given that one such colony was grown out of one bacterium (Brown & Perry, 1992).…”
Section: Methodsmentioning
confidence: 99%