New treatments for methicillin-resistant Staphylococcus aureus
被引:40
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作者:
Stryjewski, Martin E.
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机构:
CEMIC, Dept Med, RA-1425 Buenos Aires, DF, Argentina
Duke Clin Res Inst, Div Infect Dis, Durham, NC USACEMIC, Dept Med, RA-1425 Buenos Aires, DF, Argentina
Stryjewski, Martin E.
[1
,2
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Corey, G. Ralph
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机构:
Duke Clin Res Inst, Div Infect Dis, Durham, NC USA
Duke Univ, Med Ctr, Durham, NC USACEMIC, Dept Med, RA-1425 Buenos Aires, DF, Argentina
Corey, G. Ralph
[2
,3
]
机构:
[1] CEMIC, Dept Med, RA-1425 Buenos Aires, DF, Argentina
[2] Duke Clin Res Inst, Div Infect Dis, Durham, NC USA
Purpose of review Methicillin-resistant Staphylococcus aureus (MRSA) is a dynamic pathogen. Rates of MRSA are increasing worldwide. In some centers, MRSA is becoming less susceptible to vancomycin, and these strains have been associated with worse clinical outcomes. Intermediate or fully resistant vancomycin strains of MRSA have emerged clinically, whereas MRSA acquired in the community has become epidemic. The purpose of this manuscript is to provide clinicians with an evidence-based review on new treatments for MRSA. Recent findings Linezolid, daptomycin and tigecycline have been approved during the last decade to treat infections due to MRSA. Although these agents are extremely valuable in the fight against MRSA, each one has limitations. New lypoglycopeptides (telavancin, dalbavancin and oritavancin) are in advanced phase of clinical development. Similarly, new broad-spectrum cephalosporins active against MRSA (e.g. ceftobiprole and ceftaroline) and a new dihydrofolate reductase inhibitor (iclaprim) are in or have completed phase 3 studies. Summary Here, we review the most relevant information on new drugs to treat MRSA. New studies with available agents and upcoming studies with investigational drugs will help to better understand the role of each compound in the treatment of patients infected with MRSA and assist the clinician in keeping pace with this challenging pathogen.
机构:
Univ Wisconsin, Madison Sch Pharm, Pharm Practice Div, Madison, WI 53705 USA
Univ Wisconsin Hosp & Clin, Dept Pharm, Madison, WI 53705 USAUniv Wisconsin, Madison Sch Pharm, Pharm Practice Div, Madison, WI 53705 USA
Burke, Stuart L.
Rose, Warren E.
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机构:
Univ Wisconsin, Madison Sch Pharm, Pharm Practice Div, Madison, WI 53705 USA
Univ Wisconsin Hosp & Clin, Dept Pharm, Madison, WI 53705 USAUniv Wisconsin, Madison Sch Pharm, Pharm Practice Div, Madison, WI 53705 USA
机构:
Royal Prince Alfred Hosp, Dept Infect Dis, Sydney, NSW, Australia
Royal Prince Alfred Hosp, Dept Microbiol, Sydney, NSW, Australia
Univ Sydney, Fac Med, Sydney, NSW, AustraliaRoyal Prince Alfred Hosp, Dept Infect Dis, Sydney, NSW, Australia
Lee, Andie S.
de Lencastre, Herminia
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机构:
Rockefeller Univ, Lab Microbiol & Infect Dis, 1230 York Ave, New York, NY 10021 USA
Univ Nova Lisboa, Inst Tecnol Quim & Biol Antonio Xavier, Lab Mol Genet, Oeiras, PortugalRoyal Prince Alfred Hosp, Dept Infect Dis, Sydney, NSW, Australia
de Lencastre, Herminia
Garau, Javier
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Hosp Univ Mutua Terrassa, Dept Med, Barcelona, SpainRoyal Prince Alfred Hosp, Dept Infect Dis, Sydney, NSW, Australia
Garau, Javier
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Kluytmans, Jan
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Malhotra-Kumar, Surbhi
Peschel, Andreas
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机构:
Univ Tubingen, Interfac Inst Microbiol & Infect Med, Dept Infect Biol, Tubingen, Germany
German Ctr Infect Res, Partner Site Tubingen, Tubingen, GermanyRoyal Prince Alfred Hosp, Dept Infect Dis, Sydney, NSW, Australia
Peschel, Andreas
Harbarth, Stephan
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机构:
Univ Geneva Hosp, Infect Control Programme, Geneva, Switzerland
WHO Collaborating Ctr, Fac Med, Geneva, SwitzerlandRoyal Prince Alfred Hosp, Dept Infect Dis, Sydney, NSW, Australia
机构:
S Western Area Pathol Serv, Dept Microbiol & Infect Dis, Liverpool, NSW, AustraliaS Western Area Pathol Serv, Dept Microbiol & Infect Dis, Liverpool, NSW, Australia