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Clinical outcomes and nephrotoxicity of colistin loading dose for treatment of extensively drug-resistant Acinetobacter baumannii in cancer patients

Infection and Drug Resistance Sep 16, 2017

Katip W, et al. - This study aimed at evaluating the effect of the loading dose of colistin for treatment of extensively drug-resistant Acinetobacter baumannii (XDR-AB) in cancer patients. Authors realized that administration of colistin loading resulted in no significant increase in clinical response, microbiological response or mortality rate compared to non-loading dose in cancer patients with XDR-AB-related infections. However, there appeared significantly higher nephrotoxicity when patients were administered loading dose colistin.

Methods

  • Authors conducted a retrospective cohort study of cancer patients who received either a loading or non-loading dose of colistin for treatment of XDR-AB.
  • For each group, they documented the clinical response, bacteriological eradication and serum creatinine.
  • They used logistic regression to assess the effects of therapy on each of the three aforementioned outcomes.

Results

  • Authors recruited 102 patients diagnosed with XDR-AB infections between January 2012 and December 2015.
  • A loading dose of colistin was administered to only 75 patients.
  • No marked clinical and microbiological response was evident in patients in the loading dose group or patients in the non-loading dose group.
  • However, nephrotoxicity developed in 38 (50.67%) patients in the loading dose group and 6 (22.22%) patients in the non-loading dose group according to the RIFLE criteria (p = 0.013).
  • As per multivariate logistic regression analysis, independent predictors of clinical response included Charlson score ≥4 and duration of colistin treatment ≥10 days.
  • In this study, septic shock seemed associated with both poor clinical and microbiological response.
  • Independent predictors for nephrotoxicity included loading dose colistin and patient’s age ≥60 years.

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