Rapid detection of MRSA in screening specimens during a hospital outbreak.
Details
Serval ID
serval:BIB_46DEA102E715
Type
Inproceedings: an article in a conference proceedings.
Publication sub-type
Abstract (Abstract): shot summary in a article that contain essentials elements presented during a scientific conference, lecture or from a poster.
Collection
Publications
Institution
Title
Rapid detection of MRSA in screening specimens during a hospital outbreak.
Title of the conference
20th European Congress of Clinical Microbiology and Infectious (ECCMID)
Address
Vienna, Austria, April 10-13, 2010
ISBN
1469-0691
Publication state
Published
Issued date
04/2010
Peer-reviewed
Oui
Volume
16
Series
Clinical Microbiology and Infection
Pages
S4
Language
english
Abstract
Objectives: To compare the results of rapid PCR screening for MRSA
using the GeneXpert system with those of cultures in an outbreak setting.
Methods: GeneXpert was used for screening MRSA in nose, throat,
groin, and other clinical samples during a 6-month period. Samples were
performed using a double-swab transystem. When >1 sample was found
positive in a screening set, all second swabs of the set were analysed by
culture.
Results: From June to October 2009, 7568 rapid tests were performed,
among which 432 (5.7%) were positive (nose: 149/2090, 7.1%; throat:
98/2078, 4.7%; groin: 152/2080, 7.3%; urine: 14/1090, 1.3%; wounds:
18/150, 12%; and others:1/27, 3.7%), and 84 (1.1%) were invalid. A
total of 1517 samples were analyzed by both rapid PCR and culture.
Rapid tests had a sensitivity of 0.896 compared to cultures, a specificity
of 0.769, a PPV of 0.763, and a NPV of 0.899. The rapid test was found
to be less sensitive in throat samples (0.81) than in nose or inguinal
samples (0.93 for both). In 32/192 (16%) patients a positive rapid PCR
result was not confirmed by culture, despite several subsequent screening
samples in some patients. Cycle threshold (Ct) for SCCmec of these PCR
positive reactions were all >30.
Conclusions: GeneXpert MRSA was found to be suitable for the rapid
detection in nose, inguinal, and throat samples, however with a lower
sensitivity in the later. Negative cultures in 16% of our PCR-positive
patients raised the question of false positivity or higher sensitivity of
GeneXpert. Further work is needed to investigate these cases.
using the GeneXpert system with those of cultures in an outbreak setting.
Methods: GeneXpert was used for screening MRSA in nose, throat,
groin, and other clinical samples during a 6-month period. Samples were
performed using a double-swab transystem. When >1 sample was found
positive in a screening set, all second swabs of the set were analysed by
culture.
Results: From June to October 2009, 7568 rapid tests were performed,
among which 432 (5.7%) were positive (nose: 149/2090, 7.1%; throat:
98/2078, 4.7%; groin: 152/2080, 7.3%; urine: 14/1090, 1.3%; wounds:
18/150, 12%; and others:1/27, 3.7%), and 84 (1.1%) were invalid. A
total of 1517 samples were analyzed by both rapid PCR and culture.
Rapid tests had a sensitivity of 0.896 compared to cultures, a specificity
of 0.769, a PPV of 0.763, and a NPV of 0.899. The rapid test was found
to be less sensitive in throat samples (0.81) than in nose or inguinal
samples (0.93 for both). In 32/192 (16%) patients a positive rapid PCR
result was not confirmed by culture, despite several subsequent screening
samples in some patients. Cycle threshold (Ct) for SCCmec of these PCR
positive reactions were all >30.
Conclusions: GeneXpert MRSA was found to be suitable for the rapid
detection in nose, inguinal, and throat samples, however with a lower
sensitivity in the later. Negative cultures in 16% of our PCR-positive
patients raised the question of false positivity or higher sensitivity of
GeneXpert. Further work is needed to investigate these cases.
Create date
10/03/2011 13:52
Last modification date
20/08/2019 13:52