Antibiotics currently used in the treatment of infections caused by Staphylococcus aureus

被引:126
作者
Rayner, C
Munckhof, WJ [1 ]
机构
[1] Princess Alexandra Hosp, Infect Management Serv, Brisbane, Qld 4102, Australia
[2] Monash Univ, Victorian Coll Pharm, Facil Antiinfect Drug Dev & Innovat, Parkville, Vic, Australia
[3] Dist Hlth Serv, Brisbane, Qld, Australia
关键词
Staphylococcus aureus; antibiotics; drug selection; therapeutic drug monitoring; hospital-in-the-home;
D O I
10.1111/j.1444-0903.2005.00976.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Staphylococcal infections are a common and significant clinical problem in medical practice. Most strains of Staphylococcus aureus are now resistant to penicillin, and methicillin-resistant strains of S. aureus (MRSA) are common in hospitals and are emerging in the community. Penicillinase-resistant penicillins (flucloxacillin, dicloxacillin) remain the antibiotics of choice for the management of serious methicillin-susceptible S. aureus (MSSA) infections, but first generation cephalosporins ( cefazolin, cephalothin and cephalexin), clindamycin, lincomycin and erythromycin have important therapeutic roles in less serious MSSA infections such as skin and soft tissue infections or in patients with penicillin hypersensitivity, although cephalosporins are contra-indicated in patients with immediate penicillin hypersensitivity ( urticaria, angioedema, bronchospasm or anaphylaxis). All serious MRSA infections should be treated with parenteral vancomycin or, if the patient is vancomycin allergic, teicoplanin. Nosocomial strains of MRSA are typically multi-resistant (mrMRSA), and mrMRSA strains must always be treated with a combination of two oral antimicrobials, typically rifampicin and fusidic acid, because resistance develops rapidly if they are used as single agents. Most community-acquired strains of MRSA in Australia and New Zealand are non multiresistant (nmMRSA), and lincosamides ( clindamycin, lincomycin) or cotrimoxazole are the antibiotics of choice for less serious nmMRSA infections such as skin and soft tissue infections. New antibiotics such as linezolid and quinupristin / dalfopristin have good antistaphylococcal activity but are very expensive and should be reserved for patients who fail on or are intolerant of conventional therapy or who have highly resistant strains such as hVISA ( heterogenous vancomycin-intermediate S aureus).
引用
收藏
页码:S3 / S16
页数:14
相关论文
共 168 条
[1]   SUSCEPTIBILITY SURVEY OF PIPERACILLIN ALONE AND IN THE PRESENCE OF TAZOBACTAM [J].
ACAR, JF ;
GOLDSTEIN, FW ;
KITZIS, MD .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1993, 31 :23-28
[2]  
ADERS H, 2000, UN MED PROTECT J, V1, P5
[3]   Phenotypic and molecular characterization of community occurring, Western Samoan phage pattern methicillin-resistant Staphylococcus aureus [J].
Adhikari, RP ;
Cook, GM ;
Lamont, I ;
Lang, S ;
Heffernan, H ;
Smith, JMB .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2002, 50 (06) :825-831
[4]   Trimethoprim/sulfamethoxazole for treatment of severe Staphylococcus aureus infections [J].
Adra, M ;
Lawrence, KR .
ANNALS OF PHARMACOTHERAPY, 2004, 38 (02) :338-341
[5]  
*ADRAC, 1999, AUSTR ADVERSE DRUG R, V18, P7
[6]   Cerebrospinal fluid penetration and pharmacokinetics of vancomycin administered by continuous infusion to mechanically ventilated patients in an intensive care unit [J].
Albanèse, J ;
Léone, M ;
Bruguerolle, B ;
Ayem, ML ;
Lacarelle, B ;
Martin, C .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (05) :1356-1358
[7]   Gatifloxacin and the elderly: pharmacokinetic-pharmacodynamic rationale for a potential age-related dose reduction [J].
Ambrose, PG ;
Bhavnani, SM ;
Cirincione, BB ;
Piedmonte, M ;
Grasela, TH .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2003, 52 (03) :435-440
[8]   Development of the quinolones [J].
Andersson, MI ;
MacGowan, AP .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2003, 51 :1-11
[9]  
*ANT WRIT GROUP, 2003, THER GUID ANT VERS 1
[10]  
APELLANIZ G, 1991, J CHEMOTHERAPY, V3, P91