Alternatives to vancomycin for the treatment of methicillin-resistant Staphylococcus aureus infections

被引:141
作者
Micek, Scott T. [1 ]
机构
[1] Barnes Jewish Hosp, Dept Pharm, St Louis, MO 63110 USA
关键词
D O I
10.1086/519471
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Vancomycin remains the reference standard for the treatment of systemic infection caused by methicillin-resistant Staphylococcus aureus ( MRSA). However, as a result of limited tissue distribution, as well as the emergence of isolates with reduced susceptibility and in vitro resistance to vancomycin, the need for alternative therapies that target MRSA has become apparent. New treatment options for invasive MRSA infections include linezolid, daptomycin, tigecycline, and quinupristin/ dalfopristin. Additionally, a number of new anti- MRSA compounds are in development, including novel glycopeptides ( dalbavancin, telavancin, and oritavancin), ceftobiprole, and iclaprim. The present article will review clinical issues surrounding the newly marketed and investigational agents with activity against MRSA.
引用
收藏
页码:S184 / S190
页数:7
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共 44 条
[31]   Serum, tissue and body fluid concentrations of tigecycline after a single 100 mg dose [J].
Rodvold, Keith A. ;
Gotfried, Mark H. ;
Cwik, Michael ;
Korth-Bradley, Joan M. ;
Dukart, Gary ;
Ellis-Grosse, Evelyn J. .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2006, 58 (06) :1221-1229
[32]   Tigecycline: First of a new class of antimicrobial agents [J].
Rose, Warren E. ;
Rybak, Michael J. .
PHARMACOTHERAPY, 2006, 26 (08) :1099-1110
[33]   Efficacy and safety of tigecycline monotherapy compared with vancomycin plus aztreonam in patients with complicated skin and skin structure infections: Results from a phase 3, randomized, double-blind trial [J].
Sacchidanand, S ;
Penn, RL ;
Embil, JM ;
Campos, ME ;
Curcio, D ;
Ellis-Grosse, E ;
Loh, E ;
Rose, G .
INTERNATIONAL JOURNAL OF INFECTIOUS DISEASES, 2005, 9 (05) :251-261
[34]   Adaptation of methicillin-resistant Staphylococcus aureus in the face of vancomycin therapy [J].
Sakoulas, G ;
Moellering, RC ;
Eliopoulos, GM .
CLINICAL INFECTIOUS DISEASES, 2006, 42 :S40-S50
[35]   Effectiveness and tolerability of prolonged linezolid treatment for chronic osteomyelitis: A retrospective study [J].
Senneville, Eric ;
Legout, Laurence ;
Valette, Michel ;
Yazdanpanah, Yazdan ;
Beltrand, Eric ;
Caillaux, Michle ;
Migaud, Henri ;
Mouton, Yves .
CLINICAL THERAPEUTICS, 2006, 28 (08) :1155-1163
[36]   Linezolid versus vancomycin for Staphylococcus aureus bacteraemia:: pooled analysis of randomized studies [J].
Shorr, AF ;
Kunkel, MJ ;
Kollef, M .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2005, 56 (05) :923-929
[37]   Impact of antibiotics on expression of virulence-associated exotoxin genes in methicillin-sensitive and methicillin-resistant Staphylococcus aureus [J].
Stevens, Dennis L. ;
Ma, Yongsheng ;
Salmi, Daniel B. ;
McIndoo, Eric ;
Wallace, Randi J. ;
Bryant, Amy E. .
JOURNAL OF INFECTIOUS DISEASES, 2007, 195 (02) :202-211
[38]   Telavancin versus standard therapy for treatment of complicated skin and soft-tissue infections due to Gram-positive bacteria [J].
Stryjewski, ME ;
O'Riordan, WD ;
Lau, WK ;
Pien, FD ;
Dunbar, LM ;
Vallee, M ;
Fowler, VG ;
Chu, VH ;
Spencer, E ;
Barriere, SL ;
Kitt, MM ;
Cabell, CH ;
Corey, GR .
CLINICAL INFECTIOUS DISEASES, 2005, 40 (11) :1601-1607
[39]   Telavancin versus standard therapy for treatment of complicated skin and skin structure infections caused by gram-positive bacteria:: FAST 2 study [J].
Stryjewski, ME ;
Chu, VH ;
O'Riordan, WD ;
Warren, BL ;
Dunbar, LM ;
Young, DA ;
Vallée, M ;
Fowler, VG ;
Morganroth, J ;
Barriere, SL ;
Kitt, MM ;
Corey, GR .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2006, 50 (03) :862-867
[40]   Linezolid and serotonergic drug interactions: A retrospective survey [J].
Taylor, Jeremy J. ;
Wilson, John W. ;
Estes, Lynn L. .
CLINICAL INFECTIOUS DISEASES, 2006, 43 (02) :180-187