Methicillin-resistant Staphylococcus aureus

被引:35
作者
Gosbell, IB [1 ]
机构
[1] S Western Area Pathol Serv, Dept Microbiol & Infect Dis, Liverpool, NSW, Australia
关键词
D O I
10.2165/00128071-200405040-00004
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Methicillin (meticillin)-resistant Staphylococcus aureus (MRSA) emerged in the 1960s and is now commonly seen in hospitals, clinics and, since the mid-1990s, the community. Risk factors for the acquisition of MRSA include chronic dermatoses, underlying medical illnesses, attending healthcare facilities, use of prescription antibacterials, surgery, intravenous lines, hospitalization in an intensive care unit, and proximity to patients colonized with MRSA. Recent community-associated strains often occur in patients without these risk factors. Staphylococci are readily spread from person to person and readily contaminate the environment. Infection control measures thus involve identifying the infected patients, separating them from other non-infected patients, cleaning of the environment and, most important of all, scrupulous attention to hand hygiene. Alcoholic antiseptic hand rubs offer an alternative to antiseptic hand washes and increase compliance. Treatment of MRSA skin infections is challenging. Topical agents such as mupirocin or fusidic acid can be used, but the organisms often become resistant. Systemic therapy involves non-beta-lactams. Parenteral treatment is generally with glycopeptides such as vancomycin; oral therapy is more complex. Monotherapy with quinolones, rifampin (rifampicin), and fusidic acid often results in the development of resistance and so, if any of these agents are chosen it should be in combination. There are no data on combination therapy, although rifampin-containing combinations are often chosen. Fourth-generation quinolones and linezolid are expensive but promising alternatives.
引用
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页码:239 / 259
页数:21
相关论文
共 240 条
[51]   Pharmacodynamics of doxycycline [J].
Cunha, BA ;
Domenico, P ;
Cunha, CB .
CLINICAL MICROBIOLOGY AND INFECTION, 2000, 6 (05) :270-273
[52]  
CUNHA BA, 2002, INFEC DIS T, V28, P247
[53]  
DACRE JE, 1983, LANCET, V2, P1036
[54]   Efficacy of linezolid in treatment of experimental endocarditis caused by methicillin-resistant Staphylococcus aureus [J].
Dailey, CF ;
Dileto-Fang, CL ;
Buchanan, LV ;
Oramas-Shirey, MP ;
Batts, DH ;
Ford, CW ;
Gibson, JK .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2001, 45 (08) :2304-2308
[55]   SIMPLIFIED TREATMENT OF ACUTE LOWER RESPIRATORY-TRACT INFECTION WITH AZITHROMYCIN - A COMPARISON WITH ERYTHROMYCIN AND AMOXICILLIN [J].
DANIEL, R .
JOURNAL OF INTERNATIONAL MEDICAL RESEARCH, 1991, 19 (05) :373-383
[56]  
den Hollander JG, 1998, ANTIMICROB AGENTS CH, V42, P377
[57]  
Dick J.R.F., 1986, Geology Today, V2, P82, DOI 10.1111/j.1365-2451.1986.tb01031.x
[58]   TOPICAL AND SYSTEMIC THERAPY FOR PYODERMAS [J].
DILLON, HC .
INTERNATIONAL JOURNAL OF DERMATOLOGY, 1980, 19 (08) :443-451
[59]   INVITRO ACTIVITY OF COMBINATIONS OF ANTIBIOTICS AGAINST STAPHYLOCOCCUS-AUREUS RESISTANT TO GENTAMICIN AND METHICILLIN [J].
DIXSON, S ;
BRUMFITT, W ;
HAMILTONMILLER, JMT .
INFECTION, 1985, 13 (01) :35-38
[60]   ORAL RIFAMPIN PLUS OFLOXACIN FOR TREATMENT OF STAPHYLOCOCCUS-INFECTED ORTHOPEDIC IMPLANTS [J].
DRANCOURT, M ;
STEIN, A ;
ARGENSON, JN ;
ZANNIER, A ;
CURVALE, G ;
RAOULT, D .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1993, 37 (06) :1214-1218