Trial for the Treatment of Extensively Drug-Resistant Gram-negative Bacilli (OVERCOME)
- Conditions
- PneumoniaBlood Stream Infection
- Interventions
- Registration Number
- NCT01597973
- Lead Sponsor
- University of Michigan
- Brief Summary
Approximately 444 subjects who are greater than or equal to 18 to 95 years of age, are non-pregnant, and are in the inpatient setting of one of the study sites will be evaluated to treatment efficacy. Analysis will include subjects with bloodstream infection (BSI) or pneumonia due to at least one of the following gram-negative bacilli organisms: Acinetobacter baumannii, Klebsiella spp, Escherichia coli, Enterobacter spp. and/or Pseudomonas aeruginosa that demonstrates in vitro non-susceptibility defined as extensively drug-resistant Gram-negative bacilli (XDR-GNB) which includes XDR-AB, XDR-PA and CRE. If a subject has both BSI and pneumonia at the time of study enrollment, they will be included as a subject with pneumonia.
Objectives:
Primary:
•Determine whether the treatment regimen of Colistimethate sodium (colistin) combined with a carbapenem (imipenem or meropenem) is associated with a decreased risk for mortality compared to colistin alone for subjects with bloodstream infection (BSI) and/or pneumonia due to XDR-GNB.
Secondary:
•Determine what treatment regimen (colistin monotherapy or colistin combined with a carbapenem (imipenem or meropenem) is more likely to reduce the emergence of colistin resistance among XDR-GNB isolates during therapy.
- Detailed Description
The Gram-negative bacilli organisms Acinetobacter baumannii, Klebsiella spp., Escherichia coli, Enterobacter spp. and Pseudomonas aeruginosa have become a frequent cause of bloodstream infection and pneumonia in the hospital and other healthcare settings. Among these pathogens, antimicrobial resistance has emerged to many classes of antimicrobial agents. Most concerning, has been the emergence of resistance to group 2 carbapenems (such as imipenem). In several regions of the world, including Southeastern Michigan, strains of extensively-drug resistant Gram-negative bacilli (XDR-GNB) that exhibit resistance to most, and in some cases all types of available antimicrobial agents, including group 2 carbapenems, have emerged and disseminated. Treatment options for XDR-GNB typically include Colistimethate sodium (referred to as colistin in this study), used alone (monotherapy) or in combination with other agents. Unfortunately, resistance to colistin has begun to emerge in some strains of XDR-GNB, which is a truly concerning development, since colistin is one of the last remaining treatment options for XDR-GNB. No prospective, randomized controlled trials have been conducted to evaluate the clinical efficacy of colistin monotherapy versus colistin-containing combination therapy or the impact of these therapeutic modalities on the emergence of colistin resistance among XDR-GNB. We plan to conduct a double-blind randomized controlled trial including patients with pneumonia and bloodstream infection due to XDR-GNB. After enrollment, subjects will be randomized to receive 14 days of either colistin monotherapy or colistin plus meropenem.
In the Detroit metro area, infections due to XDR-GNB have developed into a regional challenge and common problem. We have assembled a multi-disciplinary team that includes Infectious Diseases researchers, clinicians, infectious diseases pharmacists, microbiologists, epidemiologists and statistical experts to address critically important questions and challenges regarding the management of bloodstream infection and pneumonia due to XDR-GNB. Specifically, we hypothesize that the combination of colistin and imipenem will provide superior efficacy in the treatment of XDR-GNB pneumonia and bloodstream infection and will prevent the emergence of decreased susceptibility to colistin among XDR-GNB strains. We also aim to analyze tools that could be used in "real time" to aid clinicians treating patients with infection due to XDR-GNB. For example, we aim to analyze the association between the presence of in vitro synergy of the colistin and carbapenem (imipenem or meropenem) combination (as determined by E-test) and clinical outcomes; and the association between colistin plasma levels and clinical outcomes and the development of nephrotoxicity.
Due to the growing threat of XDR-GNB around the world, several international sites were subsequently added including sites in Asia, Israel, and Europe.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 467
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Hospitalized Adults (> 18 years to 95 years of age), at one of the study sites.
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Diagnosis of BSI and/or pneumonia due to a preliminary result of gram-negative non-lactose fermenter that is oxidase negative; or a final results of XDR-A. baumannii; carbapenem-resistant Enterobacteriaceae; or XDR- P. aeruginosa and/or patients with suspected BSI and/or HAP (hospital acquired pneumonia) and who have had a prior history (within last 6 months) of XDR-GNB that was susceptible to colistin.
o If final results do not indicate that the pathogen is an XDR-GNB, and identifies alternative treatment options, the patient would be eligible for the study if the subject is allergic to all the alternative treatment options.
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Patients with polymicrobial respiratory or blood infections, including XDR-GNB and one or more pathogens, will be included in the study, as long as the XDR-GNB is determined to be a true pathogen (AB, CRE or PA). Other pathogens will be treated with antimicrobial agents as determined by the treating physician.
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If more than one XDR-GNB study pathogens is identified as a study pathogen causing BSI and/or pneumonia, then the first study pathogen recovered will be considered as the primary study pathogen. If more than one study pathogen is recovered from the same culture, then the infection will be categorized as being caused by multiple study pathogens.
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Patients with a life expectancy of > 24 hours
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Signed written informed consent and HIPAA Authorization form (US sites)
- Female patients who are pregnant
- Female patients who are nursing
- Patients who are prisoners
- Patients who are less than 18 years of age or greater than or equal to 96 years of age
- Patients with neutropenia (WBC < 500 cells/mm3)
- The presence of any of the following known clinical syndromes involving XDR-GNB as a pathogen which necessitate durations of antimicrobial therapies greater than 14 days: endocarditis, osteomyelitis, prosthetic joint infections, meningitis and/or other central nervous system infections.
- Patients receiving valproic acid (with or without a known seizure disorder).
- Patients who received 72 hours or more of polymyxin treatment (intravenous or inhaled [pneumonia]) within 96 hours of enrollment.
- Patients who have end-stage renal disease requiring hemodialysis, will be excluded from evaluation pertaining to nephrotoxicity in the per protocol population.
- Patients with known Type 1 or other severe drug allergy to either of the study drugs or to β-lactams.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description colistin and meropenem colistin and meropenem - colistin and placebo colistin and placebo -
- Primary Outcome Measures
Name Time Method Mortality participants will be followed daily for the duration of hospital stay, an expected average of 4 weeks Determine whether the treatment regimen of colistin combined with a carbapenem (imipenem or meropenem) is associated with a decreased risk for all-cause mortality during the 30 day post-enrollment period compared to colistin combined with a placebo for subjects with bloodstream infection (BSI) and/or pneumonia due to extensively drug-resistant Gram-negative bacilli (XDR-GNB).
- Secondary Outcome Measures
Name Time Method Number of Participants Who Develop Colistin Resistance patients' resistance data will be collected up to 30 days Determine what treatment regimen (colistin monotherapy (combined with placebo)) or colistin combined a carbapenem (imipenem or meropenem) is more likely to reduce the frequency of emergence of colistin resistance among XDR-GNB isolates during therapy. Measurements of Minimum Inhibitory Concentration of colistin to XDR-GNB. This is shown below as numbers of those subjects who develop colistin resistance and their percentages of the total completed population.
Clinical Failure at the End of Therapy 48 hours after end of treatment, that is up to 16 days Clinical failure as defined by either Blood Stream Infection (BSI) or Pneumonia; based on death between 48 hours and end of treatment, medication change from protocol, a positive blood culture after 5 days of blood stream infection treatment, or no improvements in PaO2/FiO2 at end of treatment.
Microbiologic Cure at the End of Therapy From 5 days after enrollment up to 14 days following enrollment (i.e. end of treatment) Microbiologic cure at the end of therapy as defined by the number of participants who no longer have the causative XDR-GNB pathogens for their BSI or pneumonia identified based on microbiologic testing
Number of Participants With Toxicities Related to Treatment Medications Up to 16 days Frequency is shown for each of the following: Nephrotoxicity, Hepatotoxicity, Seizures, Neurotoxicity, Hypersensitivity reaction
Trial Locations
- Locations (19)
The Ohio State University Wexner Medical Center
🇺🇸Columbus, Ohio, United States
Jackson Memorial Hospital-Jackson Health System
🇺🇸Miami, Florida, United States
Beaumont Health System
🇺🇸Royal Oak, Michigan, United States
Universita della Campania 'Luigi Vanvitelli'
🇮🇹Naples, Italy
University Hospital of Heraklion
🇬🇷Crete, Greece
Rambam Health Care Campus
🇮🇱Haifa, Israel
University Multiprofile Hospital for Active Treatment and Emergency Medicine "N.I. Pirogov"
🇧🇬Sofia, Bulgaria
Chang Gung Memorial Hospital
🇨🇳Tao-Yuan, Kwei-San, Taiwan
Evangelismos General Hospital of Athens
🇬🇷Athens, Greece
Attikon University General Hospital of Athens
🇬🇷Athens, Greece
General Hospital of Athens "Laiko" 1st Department of Medicine
🇬🇷Athens, Greece
Tel-Aviv Sourasky Medical Center
🇮🇱Tel Aviv, Israel
Siriraj Hospital
🇹🇭Bangkoknoi, Bangkok, Thailand
Rabin Medical Centre, Beilinson Campus
🇮🇱Petach Tikva, Central District, Israel
Hippokration General Hospital of Thessaloniki
🇬🇷Thessaloníki, Greece
Wayne State University
🇺🇸Detroit, Michigan, United States
Mount Sinai Hospital
🇺🇸New York, New York, United States
Henry Ford Health System
🇺🇸Detroit, Michigan, United States
Assaf Harofeh Medical Center
🇮🇱Zerifin, Beer Yaakov, Israel