Multicenter Prospective Cohort Study of Renal Failure in Patients Treated with Colistin versus Polymyxin B

Maria Helena Rigatto1, Maura S Oliveira2, Lauro V Perdigão-Neto2

  • 1Infectious Diseases Service, Hospital São Lucas da Pontifícia Universidade Católica do Rio Grande do Sul, Porto Alegre, Brazil Infectious Diseases Service, Hospital de Clinicas de Porto Alegre, Porto Alegre, Brazil.

Insights

Colistimethate sodium (CMS) is linked to higher rates of acute kidney injury compared to polymyxin B (PMB). This study found CMS significantly increased renal failure risk in patients, highlighting a critical safety difference between these antibiotics.

Area of Science:

  • Nephrology
  • Infectious Diseases
  • Pharmacology

Background:

  • Nephrotoxicity is a primary concern for colistin and polymyxin B (PMB).
  • Comparative nephrotoxicity rates between colistimethate sodium (CMS) and PMB remain unclear.
  • Understanding these differences is crucial for patient safety and effective antibiotic selection.

Purpose of the Study:

  • To compare the incidence of renal failure (RF) in patients treated with CMS versus PMB for at least 48 hours.
  • To identify risk factors associated with RF in patients receiving these antibiotics.

Main Methods:

  • A multicenter prospective cohort study involving adult patients (≥18 years).
  • Renal failure (RF) was assessed using Risk, Injury, Failure, Loss, and End-stage renal disease (RIFLE) criteria.
  • Multivariate Cox regression analysis was employed to determine independent risk factors.

Main Results:

  • The overall incidence of RF was 16.9%.
  • Patients receiving CMS had a significantly higher incidence of RF (38.3%) compared to those receiving PMB (12.7%) (P<0.001).
  • CMS therapy was an independent risk factor for RF (HR, 3.35; P<0.001), alongside ICU admission, higher weight, older age, and specific infections.

Conclusions:

  • Colistimethate sodium (CMS) is associated with significantly higher rates of renal failure compared to polymyxin B (PMB).
  • CMS is an independent risk factor for RF, irrespective of baseline creatinine clearance.
  • Further research is needed to validate these findings in diverse patient populations.

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