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Impact MRSA -PCR on Patient Management

Impact MRSA -PCR on Patient Management

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03096405
Enrollment
50
Registered
2017-03-30
Start date
2014-02-01
Completion date
2017-02-28
Last updated
2017-05-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

MRSA Bacteremia

Brief summary

Staphylococcus aureus represents one of the most met germs, with Escherichia coli, during bacteremia. Microbiologist distinguish at aureus S. two profiles of resistance in beta-lactamines: S. aureus sensitive to the methicillin ( SASM) and the S. aureus resistant to the methicillin ( SARM). With the implementation of the MALDI-TOF, it is now possible to identify the origin responsible of the bacteremia the day of the positivity of the hemoculture ( J0) and to set up a treatment with adapted antibiotic, which, in the case of a sepsis to aureus S., is the vancomycine. Ye it was demonstrated, that the use of the vancomycine on the SASM increased the average duration of stay and a more important rate of relapse. The PCR SARM was organized in the GHPSJ in 2014. It allows from the day of the positivity of the hemoculture ( J0), to determine the phenotype of resistance of S. aureus.

Interventions

DIAGNOSTIC_TESTPolymerase Chain Reaction of Methicillin Resistant Staphyloccus Aureus

Polymerase Chain Reaction of Methicillin Resistant Staphyloccus Aureus

Sponsors

Fondation Hôpital Saint-Joseph
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Hemoculture positive to Staphylococcus Aureus Methicillin Sensitive

Exclusion criteria

* Positive test to Staphylococcus Aureus Methicillin Sensitive but not hospitalized.

Design outcomes

Primary

MeasureTime frame
Adaptation duration of antibiotherapy24 hours

Secondary

MeasureTime frame
MortalityDay 30
average duration of hospitalizationday 30

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026