Actively Recruiting
Piperacillin-tazobactam and Temocillin as Carbapenem-alternatives for the Treatment of Severe Infections Due to Extended-spectrum Beta-lactamase-Producing Gram-negative Enterobacteriaceae in the Intensive Care Unit
Led by Assistance Publique - Hôpitaux de Paris · Updated on 2023-04-18
600
Participants Needed
2
Research Sites
168 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Infections due to extended-spectrum beta-lactamase (ESBL)-producing Enterobacteriaceae are a major public health concern, in particular in the intensive care unit (ICU), due to the increase in their incidence. Carbapenems are the treatment of choice of these infections, but their increased use may select for carbapenem resistance in Gram-negative bacilli, which currently represents the greatest threat in terms of antibiotic resistance. Several retrospective studies have shown that the use of non-carbapenem antibiotics (mainly the association of piperacillin/tazobactam, but also cefepime and temocillin) may be safe alternatives to carbapenems to treat these pathogens when the strain is susceptible to the corresponding antibiotic. However, one recent randomized controlled study, the Merino trial, failed to demonstrate the non-inferiority of piperacillin/tazobactam, as compared to meropenem, in patients with Gram-negative bacilli bacteremia resistant to third generation cephalosporins (mainly ESBL producers). However, the patients included in that study were not ICU patients, dosing and modalities of piperacillin/tazobactam administration were not optimal (30-min infusion whereas 4-hours infusion may be associated with better outcome), and cause of death of patients in the piperacillin/tazobactam arm were not due to antimicrobial treatment failure (mostly death due to care withdrawal in cancer patients). Recently, a retrospective bicenter study performed in ICU patients showed that outcome of patients with severe infection (i.e. sepsis and septic shock according to the Sepsis-3 definition) due to ESBL-producing Enterobacteriaceae susceptible to non-carbapenem agents treated with a non-carbapenem agent was similar to that of patients treated with carbapenems. Given the scarcity of data in ICU patients, the disputable results of the Merino trial, we will therefore conduct a multicenter, randomized, open-label trial of non-carbapenem beta-lactam (piperacillin/tazobactam or temocillin) treatment vs. meropenem treatment for ESBL-producing Enterobaceriaceae severe infection in ICU patients. Our hypothesis is that a non-carbapenem beta-lactam treatment is non-inferior to carbapenem treatment in patients with ESBL-producing Enterobacteriaceae severe infection in the ICU.
CONDITIONS
Official Title
Piperacillin-tazobactam and Temocillin as Carbapenem-alternatives for the Treatment of Severe Infections Due to Extended-spectrum Beta-lactamase-Producing Gram-negative Enterobacteriaceae in the Intensive Care Unit
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients 18 years or older
- Hospitalized in the intensive care unit (ICU)
- Severe infection such as sepsis or septic shock according to Sepsis-3 definition, within 24 hours of infection diagnosis
- Infection caused by ESBL-producing Enterobacteriaceae susceptible to meropenem and either piperacillin/tazobactam (MIC <8 mg/L) or temocillin (MIC 64;8 mg/L)
- Signed informed consent from patient or legal representative or close relative
- Affiliated with social security (excluding AME)
You will not qualify if you...
- Pregnancy or breastfeeding
- Known allergy to beta-lactam antibiotics
- Severe neutropenia (absolute neutrophil count <0.5 x 10^9/L)
- Infections requiring prolonged antimicrobial treatment such as endocarditis, mediastinitis, osteomyelitis/septic arthritis, undrained abscess, or prosthetic-associated infection
- Moribund patients with SAPS II score >75 at inclusion
- Decision to withhold or withdraw care
- Concomitant infection requiring antibiotics active against Gram-negative bacilli or polymicrobial infection resistant to study drugs
- Participation in another interventional drug study or exclusion period after a previous drug study
- Hypersensitivity to any components of the study drug formulations
AI-Screening
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Trial Site Locations
Total: 2 locations
1
LUYT Charles -Edouard
Paris, France, 75013
Actively Recruiting
2
MAYAUX Julien
Paris, France, 75013
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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