Effectiveness and Toxicity of High-Dose Colistin Treatment in Patients with Multidrug-Resistant Gram-Negative

Daniela Carrasco1, Daniel Muñoz-Pichuante1, Felipe Olivares2

  • 1Instituto de Farmacia, Facultad de Ciencias, Universidad Austral de Chile, Valdivia, Chile.

Revista Medica De Chile
|April 11, 2025
PubMed

Insights

High-dose colistin showed clinical improvement for multidrug-resistant Gram-negative bacterial infections. However, effectiveness was limited in extrapulmonary infections, and acute kidney injury was common, necessitating careful benefit-risk assessment.

Area of Science:

  • Infectious Diseases
  • Pharmacology
  • Nephrology

Background:

  • Hospital-acquired infections by multidrug-resistant Gram-negative bacteria (MDRGN) pose a global health challenge.
  • Colistin, a last-resort antibiotic, faces limitations in effectiveness and adverse effects.
  • Increasing MDRGN infections and limited alternatives have led to higher colistin doses.

Purpose of the Study:

  • To evaluate the clinical effectiveness of high-dose colistin in MDRGN infections.
  • To assess the incidence of acute kidney injury (AKI) and other adverse events.
  • To identify factors influencing clinical outcomes and mortality.

Main Methods:

  • Retrospective cohort analysis of patients with MDRGN infections treated with high-dose colistin.
  • Primary outcome: clinical improvement.
  • Secondary outcomes: incidence of AKI, other adverse events, and mortality.

Main Results:

  • Clinical improvement was observed in 63.6% of treatments.
  • Extrapulmonary infections were linked to higher clinical failure rates (OR 10).
  • Acute kidney injury (AKI) occurred in 54.5% of treatments, associated with loading doses (OR 6.0).
  • Failure to control infection source significantly influenced mortality (aOR 19.6).
  • Eosinophilia (35.7%) and respiratory depression were noted adverse events.

Conclusions:

  • High-dose colistin may improve clinical outcomes in MDRGN infections but is less effective for extrapulmonary sites, especially without source control.
  • AKI is a frequent complication, limiting colistin use.
  • Eosinophilia and respiratory depression require safety monitoring; judicious use is advised.