MedPath

Seven Versus Fourteen Days of Treatment in Uncomplicated Staphylococcus Aureus Bacteremia

Phase 4
Conditions
Staphylococcus Aureus Bacteremia
Interventions
Drug: Antibiotic therapy duration for 7 days
Registration Number
NCT03514446
Lead Sponsor
Thomas Benfield
Brief Summary

Introduction: Staphylococcus aureus bacteremia (SAB) plays an important role in long-course antibiotic therapy. Current international guidelines recommend fourteen days of intravenous antibiotic treatment for SAB in order to minimize risks of secondary deep infections and complications. However, patients with simple SAB are known to have a low risk of complications. Reducing treatment length in uncomplicated SAB would reduce the total consumption of antibiotics, adverse events and duration of hospital admission. SAB7 seeks to determine if seven days of antibiotic treatment in patients with uncomplicated SAB is non-inferior to fourteen days of treatment.

Method: The study is designed as a randomized, non-blinded, non-inferiority interventional study. Primary measure of outcome will be failure to treatment or recurrence of SAB twelve weeks after termination of antibiotic treatment. As a measure of secondary outcome the prevalence of severe adverse effects will be evaluated, in particular secondary infection with Clostridium difficile, mortality as well as public health related costs. Patients identified with uncomplicated SAB, are randomized 1:1 in two parallel arms to seven or fourteen days of antimicrobial treatment, respectively. Endpoints will be tested with a statistical non-inferiority margin of 10%.

Conclusion: SAB 7 will determine if seven days of antibiotic treatment in patients with uncomplicated SAB is sufficient and safe, potentially modifying current treatment recommendations.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
284
Inclusion Criteria
  • Age > 18 years
  • Blood culture positive for Staphylococcus aureus
  • Antibiotic treatment with antimicrobial activity to S. aureus administrated within 12 hours of the first positive blood culture
  • Temperature < 37,5 degrees celsius at randomization
  • S. aureus negative follow-up blood culture obtained 48-96 hours after microbiological verified SAB.
  • Patients written consent obtained
Exclusion Criteria
  • Persistence of S. aureus bacteremia before randomization (S. aureus positive follow-up blood culture obtained 48-96 hours of the first positive blood culture)
  • Polymicrobial infection
  • Antibiotic treatment whit no antimicrobial activity to S. aureus administrated more than 12 hours of the first positive blood culture
  • Endocarditis or other intracardiac infection demonstrated with transthoracic or transesophageal echocardiography
  • Previous history of endocarditis
  • Pacemaker or other intracardiac implant
  • Failure to remove a likely focus of infection, such as central venous catheter within 72 hours of the first positive blood culture.
  • Prosthetics in joints and bones or vascular grafts
  • Pneumonia or infection involving bone or joints
  • Previously bone/join infection
  • S. aureus infection within the last 90 days
  • Pregnancy or breastfeeding
  • Neutropenia (blood neutrophils < 1,0 x 109/l)
  • Untreated cancer
  • Chemotherapy within 90 days.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Antibiotic therapy duration for 7 daysAntibiotic therapy duration for 7 days-
Primary Outcome Measures
NameTimeMethod
90-day survival without clinical or microbiological failure to treatment or relapseup to 90 days
Secondary Outcome Measures
NameTimeMethod
Acute renal injuryUp to 26 weeks

A 1.5 fold increase in creatinine or a 25% decrease of the glomerular filtration rate (GFR)

Clostridium difficile infectionUp to 26 weeks

Microbiologically verified C. difficile infection

Microbiologically failure to treatmentless than 7 days after treatment termination

Verified S. aureus infection of the same genotype as the initial infection

Microbiologically relapsemore than 7 days after treatment termination

Verified S. aureus infection of the same genotype as the initial infection

Clinical failure to treatment or relapseUp to day 90

Initiation of anti-staphylococcal therapy for more than 48 hours due to suspected recurrence.

Severe adverse eventsUp to 26 weeks

grade 3 or above adverse events

Multidrug-resistance organismUp to 26 weeks

Microbiologically verified multidrug-resistance organism

Health-associated costsUp to 26 weeks

Public health related cost estimated from a general consideration of the expenses associated with hospitalization for SAB.

MortalityDays 14, 28, 90 and 180

All-cause mortality

Trial Locations

Locations (1)

Hvidovre Hospital

馃嚛馃嚢

Hvidovre, Copenhagen, Denmark

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