Limitations of antibiotic options for invasive infections caused by methicillin-resistant Staphylococcus aureus: is combination therapy the answer?

被引:94
作者
Nguyen, Hien M. [1 ]
Graber, Christopher J. [1 ,2 ]
机构
[1] VA Greater Los Angeles Healthcare Syst, Infect Dis Sect, Los Angeles, CA 90073 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Los Angeles, CA 90095 USA
关键词
MRSA; combination treatment; bactericidal agents; community-acquired infections; BLOOD-STREAM INFECTIONS; VITRO PHARMACODYNAMIC MODEL; PANTON-VALENTINE LEUKOCIDIN; SKIN-STRUCTURE INFECTIONS; SIMULATED ENDOCARDIAL VEGETATIONS; VANCOMYCIN PLUS RIFAMPIN; FOREIGN-BODY INFECTION; SMALL-COLONY VARIANT; IN-VITRO; QUINUPRISTIN-DALFOPRISTIN;
D O I
10.1093/jac/dkp377
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Invasive infections caused by methicillin-resistant Staphylococcus aureus (MRSA), particularly those involving persistent bacteraemia, necrotizing pneumonia, osteomyelitis and other deep-seated sites of infections, are associated with high mortality and are often difficult to treat. The response to treatment of severe MRSA infection with currently available antibiotics active against MRSA is often unsatisfactory, leading some physicians to resort to combination antibiotic therapy. Now, with the emergence of community-associated MRSA (CA-MRSA) clones that display enhanced virulence potentially related to up-regulated toxin production, the use of adjuvant protein synthesis-inhibiting antibiotics to reduce toxin production also has been advocated by some experts. In this review, we discuss the limitations of antibiotics currently available for the treatment of serious invasive MRSA infections and review the existing literature that examines the potential role of combination therapy in these infections.
引用
收藏
页码:24 / 36
页数:13
相关论文
共 161 条
[61]   MOLECULAR-BASIS OF THE INHIBITION OF GENTAMICIN-NEPHROTOXICITY BY DAPTOMYCIN - AN INFRARED SPECTROSCOPIC INVESTIGATION [J].
GURNANI, K ;
KHOURI, H ;
COUTURE, M ;
BERGERON, MG ;
BEAUCHAMP, D ;
CARRIER, D .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1995, 1237 (01) :86-94
[62]   Management of persistent Bacteremia caused by methicillin-resistant Staphylococcus aureus:: A survey of infectious diseases consultants [J].
Hageman, Jeffrey C. ;
Liedtke, Laura A. ;
Sunenshine, Rebecca H. ;
Strausbaugh, Larry J. ;
McDonald, L. Clifford ;
Tenover, Fred C. .
CLINICAL INFECTIOUS DISEASES, 2006, 43 (05) :E42-E45
[63]  
HENRY NK, 1987, AM J MED, V82, P73
[64]   ORAL TEMAFLOXACIN VERSUS VANCOMYCIN FOR THERAPY OF EXPERIMENTAL ENDOCARDITIS CAUSED BY METHICILLIN-RESISTANT STAPHYLOCOCCUS-AUREUS [J].
HESSEN, MT ;
PITSAKIS, PG ;
KAYE, D .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1990, 34 (06) :1143-1145
[65]   High-dose vancomycin therapy for methicillin-resistant Staphylococcus aureus infections -: Efficacy and toxicity [J].
Hidayat, Levita K. ;
Hsu, Donald I. ;
Quist, Ryan ;
Shriner, Kimberly A. ;
Wong-Beringer, Annie .
ARCHIVES OF INTERNAL MEDICINE, 2006, 166 (19) :2138-2144
[66]   INVITRO EVALUATION OF CLINDAMYCIN IN COMBINATION WITH OXACILLIN, RIFAMPIN, OR VANCOMYCIN AGAINST STAPHYLOCOCCUS-AUREUS [J].
HO, JL ;
KLEMPNER, MS .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 1986, 4 (02) :133-138
[67]   Pharmacodynamics of vancomycin alone and in combination with gentamicin at various dosing intervals against methicillin-resistant Staphylococcus aureus-infected fibrin-platelet clots in an in vitro infection model [J].
Houlihan, HH ;
Mercier, RC ;
Rybak, MJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (11) :2497-2501
[68]   In vitro and in vivo synergistic activities of linezolid combined with subinhibitory concentrations of imipenem against methicillin-resistant Staphylococcus aureus [J].
Jacqueline, C ;
Navas, D ;
Batard, E ;
Miegeville, AF ;
Le Mabecque, V ;
Kergueris, MF ;
Bugnon, D ;
Potel, G ;
Caillon, J .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (01) :45-51
[69]   In vivo efficacy of linezolid in combination with gentamicin for the treatment of experimental endocarditis due to methicillin-resistant Staphylococcus aureus [J].
Jacqueline, C ;
Asseray, N ;
Batard, E ;
Le Mabecque, V ;
Kergueris, MF ;
Dube, L ;
Bugnon, D ;
Potel, G ;
Caillon, J .
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2004, 24 (04) :393-396
[70]   In vitro activity of linezolid alone and in combination with gentamicin, vancomycin or rifampicin against methicillin-resistant Staphylococcus aureus by time-kill curve methods [J].
Jacqueline, C ;
Caillon, J ;
Le Mabecque, V ;
Miègeville, AF ;
Donnio, PY ;
Bugnon, D ;
Potel, G .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2003, 51 (04) :857-864