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Staphylococcus Aureus Bacteremia: Impact of an Intervention Program in Improving the Clinical Management and Review of the Clinical and Molecular Epidemiology

Staphylococcus Aureus Bacteremia: Impact of an Intervention Program in Improving the Clinical Management and Review of the Clinical and Molecular Epidemiology

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01971762
Enrollment
600
Registered
2013-10-29
Start date
2011-04-30
Completion date
2012-01-31
Last updated
2014-12-05

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

Conditions

Staphylococcus Aureus Bacteremia

Keywords

multiresistant bacteremia, bacteremia management, blood culture

Brief summary

Staphylococcus aureus bacteremia: impact of an intervention program in improving the clinical management and review of the clinical and molecular epidemiology.

Interventions

BEHAVIORALFollow recommendations based on scientific evidence to S. aureus bacteremia management
BEHAVIORALNot to follow recommendations based on scientific evidence to S. aureus bacteremia management

Sponsors

Fundación Pública Andaluza Progreso y Salud
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Patients over 14 * Clinical significant bacteremia by S. aureus * Patient hospitalized

Exclusion criteria

* Non clinical significant bacteremia * Ambulatory patient * End-of-life patients

Design outcomes

Primary

MeasureTime frameDescription
The overall target is to assess if the implementation of an active intervention program improves clinical management of the disease, according to existing recommendations.6 monthsIdentify evidence-based quality-of-care indicators (QCIs) for the management of Staphylococcus aureus bacteremia (SAB). See secondary objective for the definitions of QCIs

Secondary

MeasureTime frameDescription
Early source control6 monthsDescription: Removal of nonpermanent vascular catheter whenever the catheter was suspected or confirmed as the source of SAB, or drainage of an abscess in \<72 h. Formula: Patients in which the amenable source was removed in\<72h×100/Patients with source amenable of removal/drainage
Echocardiography in patients with clinical indications6 monthsDescription: Performance of echocardiography in patients with complicated bacteremia or predisposing conditions for endocarditis. Formula: Patients with echocardiography×100/Patients with complicated bacteremia or predisposing condition for endocarditis,alive at 96h
Follow-up blood cultures performance of control blood culture 48-96h.6 monthsDescription:Performance of control blood cultures 48-96 h after antimicrobial therapy was started regardless of clinical evolution Formula:Patients with follow-up blood culture collected×100/Patients alive at 96h.
Adjustment of vancomycin dose according to trough levels.6 monthsDescription: Measurement of trough levels of vancomycin in patients treated for at least 3 d with this antibiotic and adjustment of dose in order to achieve plasma trough levels between 15 and 20 mg/L in survivors Formula: Patients with trough level of vancomycin determined and dose adjusted×100/Patients treated with vancomycin,at 3d.
Treatment duration according to the complexity of infection.6 MonthsDescription: Duration of antimicrobial therapy of at least 14 d for uncomplicated bacteremia and 28 d for complicated bacteremia. Sequential oral treatment with fluoroquinolone plus rifampin, trimethoprim-sulfamethoxazole, or linezolid was considered accepted in selected case. Formula:Patients with appropriate duration of therapy×100/P alive at 14 or 28d in uncomplicated or complicated bacteremia
Early use of IV cloxacillin for meticillin susceptible Staphylococcus aureus as definitive therapy6 monthsDescription: Definitive therapy with intravenous cloxacillin (at least 2 g every 6 h or adjusted based on renal function in renal failure) in cases of methicillin-susceptible strains (allergic patients excluded). Treatment should be started within the first 24 h after methicillin sensitivity was available. For hemodialysis patients, cefazolin 2 g after each hemodialysis session was acceptable Formula: Definitive therapy with IV cloxacillin×100/nonallergic Patients with methicillin-susceptible isolates.

Countries

Spain

Outcome results

None listed

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