TY - JOUR
T1 - Meropenem/ vaborbactam: a next generation β-lactam β-lactamase inhibitor combination
AU - Novelli, Andrea
AU - Del Giacomo, Paola
AU - Rossolini, Gian Maria
AU - Tumbarello, Mario
PY - 2020
Y1 - 2020
N2 - Introduction: infections due to carbapenem-resistant Enterobacterales (CRE) constitute a worldwide threat and are associated with significant mortality, especially in fragile patients, and costs. Meropenem-vaborbactam (M/V) is a combination of a group 2 carbapenem with a novel cyclic boronic acid-based β-lactamase inhibitor which has shown good efficacy against KPC carbapenemase-producing Klebsiella pneumoniae, which are amongst the most prevalent types of CRE.Areas covered: This article reviews the microbiological and pharmacological profile and current clinical experience and safety of M/V in the treatment of infections caused by CRE.Expert opinion: M/V is a promising drug for the treatment of infections due to KPC-producing CRE (KPC-CRE). It exhibited an almost complete coverage of KPC-CRE isolates from large surveillance studies and a low propensity for resistance selection, retaining activity also against strains producing KPC mutants resistant to ceftazidime-avibactam. Both meropenem and vaborbactam have a favorable pharmacokinetic profile, with similar kinetic properties, a good intrapulmonary penetration and are efficiently cleared during continuous veno-venous hemofiltration (CVVH). According to available data, M/V monotherapy is associated with higher clinical cure rates and lower rates of adverse events, especially in terms of nephrotoxicity, if compared to "older" combination therapies.
AB - Introduction: infections due to carbapenem-resistant Enterobacterales (CRE) constitute a worldwide threat and are associated with significant mortality, especially in fragile patients, and costs. Meropenem-vaborbactam (M/V) is a combination of a group 2 carbapenem with a novel cyclic boronic acid-based β-lactamase inhibitor which has shown good efficacy against KPC carbapenemase-producing Klebsiella pneumoniae, which are amongst the most prevalent types of CRE.Areas covered: This article reviews the microbiological and pharmacological profile and current clinical experience and safety of M/V in the treatment of infections caused by CRE.Expert opinion: M/V is a promising drug for the treatment of infections due to KPC-producing CRE (KPC-CRE). It exhibited an almost complete coverage of KPC-CRE isolates from large surveillance studies and a low propensity for resistance selection, retaining activity also against strains producing KPC mutants resistant to ceftazidime-avibactam. Both meropenem and vaborbactam have a favorable pharmacokinetic profile, with similar kinetic properties, a good intrapulmonary penetration and are efficiently cleared during continuous veno-venous hemofiltration (CVVH). According to available data, M/V monotherapy is associated with higher clinical cure rates and lower rates of adverse events, especially in terms of nephrotoxicity, if compared to "older" combination therapies.
KW - KPC carbapenemase
KW - KPC-producing Klebsiella pneumoniae
KW - carbapenem-resistant Enterobacterales (CRE)
KW - meropenem-vaborbactam (M/V)
KW - KPC carbapenemase
KW - KPC-producing Klebsiella pneumoniae
KW - carbapenem-resistant Enterobacterales (CRE)
KW - meropenem-vaborbactam (M/V)
UR - http://hdl.handle.net/10807/151598
U2 - 10.1080/14787210.2020.1756775
DO - 10.1080/14787210.2020.1756775
M3 - Article
SN - 1478-7210
SP - N/A-N/A
JO - Expert Review of Anti-Infective Therapy
JF - Expert Review of Anti-Infective Therapy
ER -