Multicentric Study About the Usefulness of Monitoring Plasma Levels of Colistin and Sodium Colistimethate in Patients With Infections Due to Multi-drug Resistant Gram Negative Bacilli, Treated With Colistin

Parc de Salut Mar

Status

Completed

Conditions

Multidrug Resistant Gram Negative Bacterial Infections

Treatments

Device: Prospective TDM Arm of colistin

Study type

Interventional

Funder types

Other

Identifiers

NCT01845246

PSM-COL-MC-12

Details and patient eligibility

About

Objectives: Main objective: to assess the impact of an intervention for optimizing the dosing of colistin based on its plasma levels in patients with infections due to multi-drug resistant gram negative bacilli. The impact will be evaluated in terms of clinical and microbiological outcome, and toxicity.

Secondary objectives:

To determine the percentage of patients reaching plasma levels considered adequate (Cmax / MIC 8-10) for the treatment of infections due to gram-negative bacilli susceptible to colistin, in the cohort of patients treated with standard doses of this drug without adjusting the dose.
To analyze the possible emergence of bacterial resistance to this drug and its relationship to the calculated colistin pharmacokinetic and pharmacodynamic indexes.

Methods:

Design: open controlled trial, blinded for the analyst, to be performed at thre tertiary care Hospitals in Barcelona.

Subjects: Patients attended consecutively between 2012 and 2013 infected with multi-drug resistant gram negative bacilli and treated with colistin.

Sample size: 142 cases. Intervention: Once detected the infection requiring treatment with colistin, patients will be randomized to receive the intervention or not, with a 1:1 ratio. The intervention will be performed by an Infectious Diseases physician and will consist in a recommendation on the dose of colistin based on its plasma levels 48 hours after treatment onset.

Variables: peak and through colistin levels 48 hours after treatment onset, clinical, analytical and microbiological data at baseline and during follow-up of the patients.

Outcome measures: clinical, microbiological and toxicity data. Analysis: Comparison of patient characteristics and outcome variables between patients who had received the intervention and those who had not. The analysis will be done by intention to treat, by biological effectiveness and by compliance with the protocol.

Enrollment

101 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Male or female ≥18 years of age.
Hospitalized patients with an active infection caused by MDR-BGN
Treatment with intravenous CMS for at least 3 consecutive days
Evidence of a personally signed and dated informed consent document in accordance with local regulatory and legal requirements indicating that the subject (or a legally acceptable representative) has been informed of all pertinent aspects of the study.

Exclusion criteria

Patients colonized by a MDR-BGN and no signs/symptoms of an active infection
Treatment with intravenous CMS for least than 3 days
Patients with polymicrobial infections (with an isolated microorganism different from the MDR-BGN).
Patients with a glomerular filtration rate at baseline less than 10ml/min or those requiring renal replacement therapies.
Known history of allergy, hypersensitivity or serious reaction to polymyxins.
Patients treated with nebulized CMS in addition to intravenous CMS.
Patients who have already participated in this trial.
Patients without a personally signed and dated informed consent document