Enterobacterales resistant to carbapenem are cause of severe concern in hospital-acquired infections since therapeutic options are limited. Recently approved drugs, such as bela-lactam/beta-lactamase inhibitor, have been the drug of choice. However, its use is limited in low- and middle-income countries. Thus, therapy of these infections mostly relies on polymyxins and other old drugs. The role of adjuvant carbapenem therapy in combination with polymyxins, aminoglycosides and other drugs is under investigation. From a pharmacokinetic/pharmacodynamic (PK/PD), there is an elevated probability that high-dose, extended infusion administered meropenem reach the PK/PD target of 40% above the minimal inhibitory concentration (MIC) of the pathogen when the MIC is 32mg/L or lower (non-susceptible isolates have MICs of 4mg/L or higher). However, the MIC is not routinely determined in clinical laboratories. In addition, high-level (above 32mg/L) resistance to carbapenems have been reported in many studies. This open-label, randomized clinical trial aim to assess if the addition of meropenem to the best available therapy can increase the number of days alive and free of hospitalization in patients with bloodstream infections by Enterobacterales with MIC of meropenem above 32mg/L.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
13
Meropenem 2g every 8h for patients with glomerular filtration rate (GFR) equal or higher that 50 mL/min. Dose adjustment is recommended for patients with GFR \< 50mL/min.
Hospital de Clínicas de Porto Alegre
Porto Alegre, Rio Grande do Sul, Brazil
Hospital São Lucas da Pontifícia Universidade Católica do Rio Grande do Sul
Porto Alegre, Rio Grande do Sul, Brazil
Days alive and free of hospitalization
Number of days in which patients are alive and out of the hospital
Time frame: 60 days
Overall mortality
Death for any cause
Time frame: 14, 28 and 60 days after randomization
Antimicrobial-free days
Number of days in which patients are alive and without use of antimicrobial drugs
Time frame: 60 days after randomization
Relapse of infection
Presence of infection with isolation of the same bacteria between 14 and 60 days after randomization.
Time frame: 60 days after randomization
Clostridioides difficile infection
Incidence of Clostridioides difficile infection
Time frame: 60 days after randomization
Acute Kidney Injury
Incidence of Acute Kidney Injury, according to Kidney Disease: Improving Global Outcomes (KDIGO) criteria
Time frame: 14 days after randomization
Meropenem-related adverse effects
Incidence of adverse effects related to meropenem, such as neurological toxicity and hypersensitivity reactions
Time frame: 14 days after randomization
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