Staphylococcus aureus infective endocarditis:: diagnosis and management guidelines

被引:44
作者
Murray, RJ [1 ]
机构
[1] Royal Perth Hosp, Dept Microbiol & Infect Dis, Perth, WA 6847, Australia
关键词
Staphylococcus aureus; infective endocarditis; endocarditis; evidenced-based guidelines;
D O I
10.1111/j.1444-0903.2005.00978.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
S. aureus infective endocarditis (SAIE) is a serious infection associated with considerable morbidity and mortality. There is evidence that the incidence of SAIE is increasing. As its clinical features are non-specific, SAIE must be suspected in every case of S. aureus bacteraemia, whether it is associated with an obvious source or not. The optimal antimicrobial agent(s) and duration of treatment for SAIE are currently not known, but on the basis of present evidence, a minimum of 2 weeks of antimicrobial therapy is recommended for 'right-sided' SAIE, a minimum of 4 weeks for uncomplicated 'left-sided' SAIE, and a minimum of 6 weeks for complicated 'left-sided' or prosthetic valve SAIE. Although there is no evidence to suggest that combination therapy with a cell-wall active agent ( e. g. flucloxacillin) and an aminoglycoside decreases mortality in SAIE, combination therapy should be considered during the initial 3 - 5 days of therapy as it can shorten the duration of bacteraemia. In complicated or prosthetic valve SAIE, early and close liaison with cardiology and cardiothoracic surgery services is essential. Rapid identification and susceptibility testing of the infecting organism are important in determining the choice of definitive antimicrobial therapy.
引用
收藏
页码:S25 / S44
页数:20
相关论文
共 207 条
[31]   Efficacy of linezolid alone or in combination with vancomycin for treatment of experimental endocarditis due to methicillin-resistant Staphylococcus aureus [J].
Chiang, FY ;
Climo, M .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2003, 47 (09) :3002-3004
[32]   Prognostic factors in 61 cases of Staphylococcus aureus prosthetic valve infective endocarditis from the international collaboration on endocarditis merged database [J].
Chirouze, C ;
Cabell, CH ;
Fowler, VG ;
Khayat, N ;
Olaison, L ;
Miro, JM ;
Habib, G ;
Abrutyn, E ;
Eykyn, S ;
Corey, GR ;
Selton-Suty, C ;
Hoen, B .
CLINICAL INFECTIOUS DISEASES, 2004, 38 (09) :1323-1327
[33]   SUCCESSFUL THERAPY OF EXPERIMENTAL CHRONIC FOREIGN-BODY INFECTION DUE TO METHICILLIN-RESISTANT STAPHYLOCOCCUS-AUREUS BY ANTIMICROBIAL COMBINATIONS [J].
CHUARD, C ;
HERRMANN, M ;
VAUDAUX, P ;
WALDVOGEL, FA ;
LEW, DP .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1991, 35 (12) :2611-2616
[34]   ASSOCIATION BETWEEN SERUM INHIBITORY AND BACTERICIDAL CONCENTRATIONS AND THERAPEUTIC OUTCOME IN BACTERIAL-ENDOCARDITIS [J].
COLEMAN, DL ;
HORWITZ, RI ;
ANDRIOLE, VT .
AMERICAN JOURNAL OF MEDICINE, 1982, 73 (02) :260-267
[35]  
CORR P, 1995, AM J NEURORADIOL, V16, P745
[36]  
CRANE LR, 1986, REV INFECT DIS, V8, P364
[37]   EVALUATION OF ANTIBIOTIC DIFFUSION INTO CARDIAC VEGETATIONS BY QUANTITATIVE AUTORADIOGRAPHY [J].
CREMIEUX, AC ;
MAZIERE, B ;
VALLOIS, JM ;
OTTAVIANI, M ;
AZANCOT, A ;
RAFFOUL, H ;
BOUVET, A ;
POCIDALO, JJ ;
CARBON, C .
JOURNAL OF INFECTIOUS DISEASES, 1989, 159 (05) :938-944
[38]   ANALYSIS OF SURGICAL VERSUS MEDICAL THERAPY IN ACTIVE COMPLICATED NATIVE VALVE INFECTIVE ENDOCARDITIS [J].
CROFT, CH ;
WOODWARD, W ;
ELLIOTT, A ;
COMMERFORD, PJ ;
BARNARD, CN ;
BECK, W .
AMERICAN JOURNAL OF CARDIOLOGY, 1983, 51 (10) :1650-1655
[39]   Efficacy of linezolid plus rifampin in an experimental model of methicillin-susceptible Staphylococcus aureus endocarditis [J].
Dailey, CF ;
Pagano, PJ ;
Buchanan, LV ;
Paquette, JA ;
Haas, JV ;
Gibson, JK .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2003, 47 (08) :2655-2658
[40]   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