Study of the Nasal Intracellular Reservoir of Staphylococcus Aureus in Patients With S. Aureus Bacteremia

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCentre Hospitalier Universitaire de Saint Etienne

About this trial

Staphylococcus aureus bacteremia is a serious infection associated with a high mortality rate (with or without associated infective endocarditis (IE)), long hospital stays and multiple complications, due to the terrain in which it occurs and its secondary localization. They may be community-acquired or healthcare-associated infections. Being a carrier of S. aureus is a known risk factor for S. aureus bacteremia. Although several mucosal sites of carriage have been described, screening for carriage is most often carried out at the nasal level, both for reasons of simplicity and because it is the predominant site of carriage of this bacterium. However, S. aureus carriage is a frequent occurrence, affecting around 1/3 of the general population.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Bacteremia

Patient affiliated or entitled to a social security plan

Patient who has signed a consent form to participate in the study.

Disqualifiers

Antibiotic therapy in place for more than 5 days at the time of inclusion

Nasal decolonization of S. aureus within 12 months

Pregnant or breast-feeding women

Patients under guardianship

Trial population

Patients treated at St-Etienne University Hospital with bacteremia with or without IE. Patients will be assigned to the experimental group in the case of S. aureus bacteremia (whether or not associated with an IE), or to the control group in the case of bacteremia caused by a pathogenic bacterium other than S. aureus (whether or not associated with an IE).

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Nasal swab

    Diagnostic test

    Nasal swab to detect nasal carriage of S. aureus

  • Venous sampling

    Biological/Vaccine

    Peripheral venous sampling to collect peripheral blood mononuclear cells.

  • Antibiotic treatment

    Biological/Vaccine

    Antibiotic treatment for bacteremia (+/- 1 month), in all patients with S. aureus

  • Nasal swab

    Device

    A new nasal swab will be taken using the same technique, to see whether or not the carriage persists

  • Intracellular reservoir test

    Biological/Vaccine

    In the event of positive carriage, a new intracellular reservoir test will be performed. A search for relapse (new S. aureus infection) or recurrence (S. aureus bacteremia if the 1st bacteremia was due to another pathogen) will be carried out.

Treatment groups

405 Participants
are divided into 2 treatment groups
Group A: Experimental group5 interventions
Group B: Control group5 interventions

Trial outcomes

Primary outcomes

1

Number of intracellular S. aureus carriers at nasal level research

Number of intracellular S. aureus carriers at nasal level research in patients with S. aureus bacteremia associated or not

Time frame
At inclusion

Secondary outcomes

1

Number of intracellular S. aureus carriers at nasal level research

Time frame
Day 7
2

In-hospital mortality rate (%)

In-hospital mortality rate directly related to infection (septic shock, multivisceral failure, death during surgical management related to infection) during bacteremia

Time frame
Month 1
3

Mean duration of S. aureus bacteremia (Day)

Time frame
Month 1
4

Average number of secondary localizations of S. aureus bacteremia

Clinically diagnosed, or on examination carried out as part of the extension work-up performed as part patient management (Scan, echocardiography, scintigraphy, etc.)

Time frame
Month 2

Other outcomes

Sponsors and contacts

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