Improved outcome with early rifampicin combination treatment in methicillin-sensitive Staphylococcus aureus bacteraemia with a deep infection focus - a retrospective cohort study

PLoS One. 2015 Apr 13;10(4):e0122824. doi: 10.1371/journal.pone.0122824. eCollection 2015.

Abstract

Introduction: Rifampicin has been used as adjunctive therapy in Staphylococcus aureus bacteraemia (SAB) with a deep infection focus. However, data for prognostic impact of rifampicin therapy is unestablished including the optimal initiation time point. We studied the impact of rifampicin therapy and the optimal initiation time for rifampicin treatment on prognosis in methicillin-sensitive S. aureus bacteraemia with a deep infection.

Methods: Retrospective, multicentre study in Finland including 357 SAB patients with a deep infection focus. Patients with alcoholism, liver disease or patients who died within 3 days were excluded. Patients were categorised according to duration of rifampicin therapy and according to whether rifampicin was initiated early (within 7 days) or late (7 days after) after the positive blood cultures. Primary end point was 90 days mortality.

Results: Twenty-seven percent of patients received no rifampicin therapy, 14% received rifampicin for 1-13 days whereas 59% received rifampicin ≥14 days. The 90 day mortality was; 26% for patients treated without rifampicin, 16% for rifampicin therapy of any length and 10% for early onset rifampicin therapy ≥14 days. Lack of rifampicin therapy increased (OR 1.89, p=0.026), rifampicin of any duration decreased (OR 0.53, p=0.026) and rifampicin therapy ≥14 days with early onset lowered the risk for a fatal outcome (OR 0.33, p<0.01) during 90 days follow-up.

Conclusion: Rifampicin adjunctive therapy for at least 14 days and initiated within 7 days of positive blood culture associated with improved outcome among SAB patients with a deep infection.

Publication types

  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Anti-Bacterial Agents / therapeutic use*
  • Bacteremia / drug therapy*
  • Bacteremia / microbiology
  • Bacteremia / mortality
  • Bacteremia / pathology
  • Ciprofloxacin / therapeutic use*
  • Cloxacillin / therapeutic use*
  • Drug Therapy, Combination
  • Female
  • Finland
  • Humans
  • Male
  • Methicillin / therapeutic use
  • Microbial Sensitivity Tests
  • Middle Aged
  • Retrospective Studies
  • Rifampin / therapeutic use*
  • Secondary Prevention*
  • Staphylococcal Infections / drug therapy*
  • Staphylococcal Infections / microbiology
  • Staphylococcal Infections / mortality
  • Staphylococcal Infections / pathology
  • Staphylococcus aureus / drug effects
  • Staphylococcus aureus / growth & development
  • Staphylococcus aureus / isolation & purification
  • Staphylococcus aureus / pathogenicity
  • Survival Analysis
  • Time-to-Treatment
  • Treatment Outcome

Substances

  • Anti-Bacterial Agents
  • Ciprofloxacin
  • Cloxacillin
  • Methicillin
  • Rifampin

Grants and funding

This study was financially supported by grants from: The Medical Society of Finland, The Medicinska Understödsföreningen Liv och Hälsa, The SSAC-foundation, The Maud Kuistila Memorial Foundation, The Suomen Infektiolääkärit r.y. foundation and The Swedish Cultural Foundation in Finland. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.