2016
DOI: 10.1080/14728214.2016.1206077
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Emerging drugs for nosocomial pneumonia

Abstract: There are several promising compounds on their way, as tedizolid-a new oxazolidone, iclaprim-a novel drug, related to trimethoprim, plazomicin-a new aminoglycoside and two combinations of ceftazidime/avibactam and ceftolozane/tazobactam against MDR bacteria, especially against MRSA and Gram-negative ESBL bacteria.

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Cited by 14 publications
(10 citation statements)
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References 72 publications
(56 reference statements)
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“…Antibiotics currently approved for MRSA nosocomial pneumonia are linezolid (an oxazolidinone), vancomycin (a glycopeptide), ceftobiprole (an extended-spectrum cephalosporin) and Telavancin (a lipoglycopeptide). Tedizolid (a second-generation oxazolidinone) is pending authorization for systemic treatment of HAP [5]. Other secondary options when these agents cannot be used include, either alone or in combination, quinolones (ciprofloxacin or levofloxacin), macrolides (erythromycin), aminoglycosides (gentamicin), tetracyclines, clindamycin (a lincosamide), and fusidic acid.…”
Section: (Continued From Previous Page)mentioning
confidence: 99%
“…Antibiotics currently approved for MRSA nosocomial pneumonia are linezolid (an oxazolidinone), vancomycin (a glycopeptide), ceftobiprole (an extended-spectrum cephalosporin) and Telavancin (a lipoglycopeptide). Tedizolid (a second-generation oxazolidinone) is pending authorization for systemic treatment of HAP [5]. Other secondary options when these agents cannot be used include, either alone or in combination, quinolones (ciprofloxacin or levofloxacin), macrolides (erythromycin), aminoglycosides (gentamicin), tetracyclines, clindamycin (a lincosamide), and fusidic acid.…”
Section: (Continued From Previous Page)mentioning
confidence: 99%
“…9,37,38 Therefore, we believe that for patients with suspected CRE HAP/VAP empirical use of carbapenem associated with colistin and/ or tigecycline may be justified. 9,37,38 Ceftazidime-avibactam could be an alternative option for empirical treatment associated with fosfomycin or gentamicin (►Fig. 1).…”
Section: Empirical Treatmentmentioning
confidence: 99%
“…[43][44][45] Carbapenems Carbapenem-containing regimens have always constituted a pivotal therapy for VAP and demonstrated a survival benefit, primarily in serious infections caused by CRE, compared with other combinations and could serve as a therapeutic backbone. 34,37,38 Real-time pharmacokinetic/pharmacodynamic optimization of high-dose continuous infusion (extension of the infusion time from 30 minutes up to 6 hours every 6 hour) meropenem may represent a valuable approach for the treatment of disseminated KPC-Kp infections even when caused by meropenem-resistant strains and has been associated with higher rate of clinical cure in VAP. 46 Some studies have ascertained the role of meropenem could be especially relevant when included in combination regimens with other active agents, if the MIC of the pathogen is < 16 mg/L.…”
Section: Targeted Treatmentmentioning
confidence: 99%
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“…A possible new indication could be the treatment of nosocomial pneumonia by MDR pathogens, especially P. aeruginosa [39]. Pending the outcomes of ongoing clinical trials, the results of off-label experiences with P. aeruginosa pneumonia are promising [40].…”
Section: Perspectivesmentioning
confidence: 99%