Nephrotoxicity of intravenous colistin: a prospective evaluation

Int J Antimicrob Agents. 2005 Dec;26(6):504-7. doi: 10.1016/j.ijantimicag.2005.09.004. Epub 2005 Nov 8.

Abstract

Twenty-one patients who received intravenous colistimethate sodium (CMS) for at least 7 days for the treatment of multidrug-resistant Gram-negative bacterial infections were included in a prospective cohort study at 'Henry Dunant' Hospital in Athens, Greece. The mean (+/- standard deviation) and median daily doses, cumulative doses and duration of treatment of intravenous CMS were, respectively, 5.5 (+/- 1.9) and 6 million IU, 90.2 (+/- 52.0) and 72 million IU, and 17.7 (+/- 11.7) and 15 days (range 7-54 days). Three patients (14.3%) developed nephrotoxicity during treatment with CMS. The cumulative dose of administered CMS was statistically correlated with the difference in values of serum creatinine between the end and start of CMS treatment (r = 0.6, P = 0.004 by Spearman's test).

Publication types

  • Clinical Trial

MeSH terms

  • Acute Kidney Injury / blood
  • Acute Kidney Injury / chemically induced*
  • Acute Kidney Injury / urine
  • Adult
  • Aged
  • Aged, 80 and over
  • Anti-Bacterial Agents / administration & dosage
  • Anti-Bacterial Agents / adverse effects*
  • Anti-Bacterial Agents / therapeutic use
  • Cohort Studies
  • Colistin / administration & dosage
  • Colistin / adverse effects*
  • Colistin / therapeutic use
  • Creatinine / blood
  • Creatinine / urine
  • Female
  • Gram-Negative Bacterial Infections / drug therapy
  • Greece
  • Humans
  • Injections, Intravenous
  • Kidney Function Tests
  • Male
  • Middle Aged
  • Nephrotic Syndrome
  • Prospective Studies
  • Treatment Outcome

Substances

  • Anti-Bacterial Agents
  • Creatinine
  • Colistin