2015
DOI: 10.1093/ajcp/aqv005
|View full text |Cite
|
Sign up to set email alerts
|

The Impact of Implementation of RapidQuickFISH Testing for Detection of Coagulase-Negative Staphylococci at a Community-Based Hospital: Table 1

Abstract: The QuickFISH assay, with its ability to provide timely and actionable results nearly simultaneously with the Gram stain, in conjunction with an effective antimicrobial stewardship program, has been adopted as standard of care at our community-based hospital.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

4
10
0

Year Published

2017
2017
2021
2021

Publication Types

Select...
4
2
1

Relationship

0
7

Authors

Journals

citations
Cited by 11 publications
(14 citation statements)
references
References 17 publications
4
10
0
Order By: Relevance
“…Indeed, most of the studies that have favorable outcomes from implementing PNA FISH ® or QuickFISH ® , incorporated an AMS program. 12,19 In our study, all of the participating hospitals had active AMS programs as demonstrated by previous studies done by our group (data not published).…”
Section: Discussionsupporting
confidence: 69%
See 1 more Smart Citation
“…Indeed, most of the studies that have favorable outcomes from implementing PNA FISH ® or QuickFISH ® , incorporated an AMS program. 12,19 In our study, all of the participating hospitals had active AMS programs as demonstrated by previous studies done by our group (data not published).…”
Section: Discussionsupporting
confidence: 69%
“…Our results are in accordance to many other studies that have also reported that FISH methods provide faster results compared to conventional cultures. 6,9,12,13 Ly and colleagues' 11 also found a reduction in the duration of antibiotic treatment (-2.0 days; p = 0.01), as well as Forrest et al which evaluated the clinical utility of enterococcal PNA FISH ® , showing less time to effective therapy (1.3 vs. 3.1 days). 9 Although in our study a difference in mortality of 22% among the groups was observed (QuickFISH ® 13% versus BC 35%), it is not possible to establish a statistical association between the implementation of the QuickFISH ® and its direct impact on mortality; the study sample is a limitation as well as its design ; furthermore, part of difference in mortality between the groups could be explained in part to the higher proportion of patients with candidemia in the control group which have been shown to have significantly higher mortality compared to bacterial infections.…”
Section: Discussionmentioning
confidence: 85%
“…Together with culture and NA amplification techniques, this has potential for a ‘staging’ of biofilm infections in the future and the development of specific therapeutic strategies for the different stages. PNA FISH is becoming more widespread in diagnostic labs with the advent of validated kits designed for high‐throughput examination following blood culture. This approach may be useful in the case of specific microbial pathogens such as Staphylococcus aureus and in cases where a faster time to positivity is desirable . This approach may also help to target appropriate antimicrobial therapy .…”
Section: Diagnostic Methodsmentioning
confidence: 99%
“…• PNA FISH is becoming more widespread in diagnostic labs with the advent of validated kits designed for high-throughput examination following blood culture. This approach may be useful in the case of specific microbial pathogens such as Staphylococcus aureus and in cases where a faster time to positivity is desirable (85). This approach may also help to target appropriate antimicrobial therapy (86,87).…”
Section: Fluorescence In Situ Hybridization (Fish)mentioning
confidence: 99%
“…This technique requires prior Gram staining and subsequently the slide is viewed under a fluorescence microscope, turn-around time 1.5-3 h. Recent introduction of the next-generation test, the QuickFISH V R , the time for processing has been further reduced and the turn-around time is currently around 0.5 h. A number of different QuickFISH V R assays have been developed and validated, each capable of detecting up to a maximum of three different species per assay. Staphylococcus QuickFISH V R differentiates Staphylococcus aureus from coagulase-negative staphylococci (CoNS) [9][10][11][12], Enterococcus QuickFISH V R for identification of Gram-positive cocci in cluster differentiates Enterococcus faecalis from other Enterococcus spp., including Enterococcus faecium [12][13][14], the Gram-Negative QuickFISH V R which differentiates Escherichia coli from Pseudomonas aeruginosa and Klebsiella pneumonia [12], and finally the Candida QuickFISH V R assay differentiating Candida albicans from Candida glabrata and Candida parapsilosis [15].…”
Section: Introductionmentioning
confidence: 99%