Impact of immunosuppression on incidence, aetiology and outcome of ventilator-associated lower respiratory tract infections

Eur Respir J. 2018 Mar 8;51(3):1701656. doi: 10.1183/13993003.01656-2017. Print 2018 Mar.

Abstract

The aim of this planned analysis of the prospective multinational TAVeM database was to determine the incidence, aetiology and impact on outcome of ventilator-associated lower respiratory tract infections (VA-LRTI) in immunocompromised patients.All patients receiving mechanical ventilation for >48 h were included. Immunocompromised patients (n=663) were compared with non-immunocompromised patients (n=2297).The incidence of VA-LRTI was significantly lower among immunocompromised than among non-immunocompromised patients (16.6% versus 24.2%; sub-hazard ratio 0.65, 95% CI 0.53-0.80; p<0.0001). Similar results were found regarding ventilator-associated tracheobronchitis (7.3% versus 11.6%; sub-hazard ratio 0.61, 95% CI 0.45-0.84; p=0.002) and ventilator-associated pneumonia (9.3% versus 12.7%; sub-hazard ratio 0.72, 95% CI 0.54-0.95; p=0.019). Among patients with VA-LRTI, the rates of multidrug-resistant bacteria (72% versus 59%; p=0.011) and intensive care unit mortality were significantly higher among immunocompromised than among non-immunocompromised patients (54% versus 30%; OR 2.68, 95% CI 1.78-4.02; p<0.0001). In patients with ventilator-associated pneumonia, mortality rates were higher among immunocompromised than among non-immunocompromised patients (64% versus 34%; p<0.001).Incidence of VA-LRTI was significantly lower among immunocompromised patients, but it was associated with a significantly higher mortality rate. Multidrug-resistant pathogens were more frequently found in immunocompromised patients with VA-LRTI.

MeSH terms

  • Aged
  • Databases, Factual
  • Drug Resistance, Multiple, Bacterial
  • Female
  • Humans
  • Immunosuppression Therapy / adverse effects*
  • Immunosuppressive Agents / adverse effects
  • Immunosuppressive Agents / therapeutic use*
  • Incidence
  • Intensive Care Units
  • International Cooperation
  • Male
  • Middle Aged
  • Pneumonia, Ventilator-Associated / complications*
  • Pneumonia, Ventilator-Associated / drug therapy
  • Prospective Studies
  • Respiration, Artificial / adverse effects*
  • Respiratory Tract Infections / therapy*
  • Treatment Outcome

Substances

  • Immunosuppressive Agents