Introduction: Nosocomial pneumonia is the second most common infection in hospital settings, resulting in substantial increases in morbidity, mortality, and length of hospital stay. The rapid increase in resistance of nosocomial pathogens to many antibiotics and the high dissemination of resistance genes highlight the need for innovative approaches to combat difficult-to-treat nosocomial respiratory infections. Areas covered: This review summarizes the synthetic antimicrobials that are currently in development for the treatment of nosocomial pneumonia, focusing on antibiotics in the final phases of clinical development and on the strategies employed by novel synthetic antimicrobial peptides. Expert opinion: Several novel synthetic antimicrobials are currently in the pipeline, and it appears that new antimicrobial peptides or mimetics will soon be made available, expanding the opportunities to treat nosocomial pneumonia. However, the approval process for use in the treatment of nosocomial pneumonia is arduous. Given that significant investments by pharmaceutical companies have ended in failure to obtain the approval of regulatory agencies, novel platforms for antimicrobial discovery are needed. The identification of new and fully synthetic chemical structures with activity against nosocomial pathogens needs to be followed by preclinical studies in large animals and by pharmacokinetic and pharmacodynamic studies in specific critically ill populations to assess lung penetration.
机构:
Univ Queensland, Univ Queensland Ctr Clin Res, Fac Med, Burns Trauma & Crit Care Res Ctr, Brisbane, Qld 4029, AustraliaUniv Queensland, Univ Queensland Ctr Clin Res, Fac Med, Burns Trauma & Crit Care Res Ctr, Brisbane, Qld 4029, Australia
Xu, Elena
Perez-Torres, David
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Hosp Univ Rio Hortega, Serv Med Intens, Valladolid 47012, SpainUniv Queensland, Univ Queensland Ctr Clin Res, Fac Med, Burns Trauma & Crit Care Res Ctr, Brisbane, Qld 4029, Australia
Perez-Torres, David
Fragkou, Paraskevi C.
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Attikon Univ Hosp, Dept Internal Med 4, Athens 12462, GreeceUniv Queensland, Univ Queensland Ctr Clin Res, Fac Med, Burns Trauma & Crit Care Res Ctr, Brisbane, Qld 4029, Australia
Fragkou, Paraskevi C.
Zahar, Jean-Ralph
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Hosp Avicenne, Microbiol Dept, Infect Control Unit, F-93000 Bobigny, FranceUniv Queensland, Univ Queensland Ctr Clin Res, Fac Med, Burns Trauma & Crit Care Res Ctr, Brisbane, Qld 4029, Australia
Zahar, Jean-Ralph
Koulenti, Despoina
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Univ Queensland, Univ Queensland Ctr Clin Res, Fac Med, Burns Trauma & Crit Care Res Ctr, Brisbane, Qld 4029, Australia
Attikon Univ Hosp, Crit Care Dept 2, Athens 12462, GreeceUniv Queensland, Univ Queensland Ctr Clin Res, Fac Med, Burns Trauma & Crit Care Res Ctr, Brisbane, Qld 4029, Australia
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Univ Buenos Aires, Hosp Clin, Dept Internal Med, Div Pulm Dis, Buenos Aires, DF, ArgentinaUniv Buenos Aires, Hosp Clin, Dept Internal Med, Div Pulm Dis, Buenos Aires, DF, Argentina
Luna, Carlos M.
Aruj, Patricia K.
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Univ Buenos Aires, Hosp Clin, Dept Internal Med, Div Pulm Dis, Buenos Aires, DF, ArgentinaUniv Buenos Aires, Hosp Clin, Dept Internal Med, Div Pulm Dis, Buenos Aires, DF, Argentina
机构:
Duke Clin Res Inst, Durham, NC USA
Duke Univ, Med Ctr, Div Infect Dis, Durham, NC USAUniv Manitoba, Fac Med, Infect Dis Sect, Winnipeg, MB R3E 0J9, Canada
Corey, G. Ralph
Stryjewski, Martin E.
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Duke Clin Res Inst, Durham, NC USA
Ctr Educ Med & Invest Clin Norberto Quirno, Dept Med, Buenos Aires, DF, Argentina
Ctr Educ Med & Invest Clin Norberto Quirno, Div Infect Dis, Buenos Aires, DF, ArgentinaUniv Manitoba, Fac Med, Infect Dis Sect, Winnipeg, MB R3E 0J9, Canada
Stryjewski, Martin E.
Kanafani, Zeina A.
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Amer Univ Beirut, Med Ctr, Div Infect Dis, Beirut, LebanonUniv Manitoba, Fac Med, Infect Dis Sect, Winnipeg, MB R3E 0J9, Canada