New evidence in severe pneumonia: imipenem/ cilastatin/relebactam.

R M Girón, A Ibáñez, R M Gómez-Punter,T Alarcón

Revista espanola de quimioterapia : publicacion oficial de la Sociedad Espanola de Quimioterapia(2022)

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摘要
Imipenem combined with beta-lactamase inhibitor relebactam (IMI/REL) has an extensive bactericidal activity against Gram-negative pathogens producing class A or class C beta-lactamases, not active against class B and class D. The phase 3 clinical trial (RESTORE-IMI-2), double-blind, randomized, evaluated IMI/REL vs. piperacillin-tazobactam (PIP/TAZ) for treatment of hospital-acquired pneumonia (HAP) and ventilator-associated pneumonia (VAP), demonstrated non-inferiority at all-cause mortality at 28 days (15.9% vs 21.3%), favorable clinical response at 7-14 days end of treatment (61% vs 59.8%) and with minor serious adverse effects (26.7% vs 32%). IMI/REL is a therapeutic option in HAP and VAP at approved dosage imipenem 500 mg, cilastatin 500 mg and relebactam 250 mg once every 6h, by an IV infusion over 30 min.
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关键词
Carbapenem resistant, Hospital acquired pneumonia, ventilator-associated bacterial pneumonia, nosocomial pneumonia
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