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Decolonization of Intestinal Carriage of MDR/XDR Gram-Negative Bacteria with Oral Colistin in Patients with Hematological Malignancies: Results of a Randomized Controlled Trial. | LitMetric

AI Article Synopsis

  • The study examined the use of oral colistin to eradicate multidrug-resistant (MDR) and extensively drug-resistant (XDR) gram-negative bacteria from the intestines of patients with blood cancers undergoing chemotherapy.
  • Patients receiving colistin showed a higher short-term success rate in decolonization compared to those not treated, and fewer developed bloodstream infections (BSI) within 30 days post-treatment.
  • However, the long-term benefits were less clear, as the colonization rates and BSI risk were similar to the control group after 90 days, indicating that while colistin may help in the short run, it does not provide lasting protection.

Article Abstract

Background: Intestinal colonization by MDR/XDR gram-negative bacteria leads to an increased risk of subsequent bloodstream infections (BSI) in patients receiving chemotherapy as a treatment for hematologic malignancies.

Objectives: The objective of this study was to evaluate the efficacy of oral colistin in eradicating the intestinal carriage of MDR/XDR Gram-negative bacteria in patients with hematological malignancies.

Methods: In a tertiary hematology center, adult patients with intestinal colonization by MDR/XDR Gram-negative bacteria were included in a randomized controlled trial (RCT) during a period from November 2016 to October 2017. Patients were treated with oral colistin for 14 days or observed with the primary outcome set as decolonization on day 21 post-treatment. Secondary outcomes included treatment safety and changes in MICs of isolated microorganisms. ClinicalTrials.gov Identifier: NCT02966457.

Results: Short-time positive effect (61.3% vs 32.3%; OR 3.32; 95% CI 1.17-9.44; p=0.0241) was demonstrated on the day 14 of colistin treatment, without any statistical difference on day 21 post-treatment. The incidence of BSI in decolonization group was lower in the first 30 days after the intervention (3.2% vs. 12.9%), but overall in the 90-day observation period, it did not show any advantages comparing to control group (log-rank test; p=0.4721). No serious adverse effects or increase in resistance to colistin was observed.

Conclusions: This study suggests that in hematological patients the strategy of selective intestinal decolonization by colistin may be beneficial to decrease the rate of MDR/XDR Gram-negative intestinal colonization and the risk of BSI in the short-term period, having no long-term sustainable effects.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5937973PMC
http://dx.doi.org/10.4084/MJHID.2018.030DOI Listing

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