Combining quinupristin/dalfopristin with other agents for resistant infections

被引:19
作者
Brown, J
Freeman, B
机构
[1] Dartmouth Hitchcock Med Ctr, Dept Infect Dis & Pharm, Lebanon, NH 03756 USA
[2] Ohio State Univ, Med Ctr, Dept Pharm, Columbus, OH 43210 USA
关键词
dalfopristin; methicillin-resistant Staphylococcus aureus; quinupristin; synergy; vancomycin-resistant Enterococcus faecium;
D O I
10.1345/aph.1D323
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
OBJECTIVE: To review the resistance mechanisms of Enterococcus and Staphylococcus spp. and summarize quinupristin/ dalfopristin's (QD's) effects on these resistant organisms when combined with other antibiotics via review of the literature and unpublished data. DATA SOURCES: Data were identified by a PubMed search (1996-May 2003) using the search terms quinupristin/dalfopristin, synergy, in vitro, in vivo, vancomycin-resistant Enterococcus faecium (VREF), methicillin-resistant Staphylococcus aureus (MRSA), and individual antibiotic names. Bibliographies of the resultant PubMed searches were reviewed and included if applicable. STUDY SELECTION AND DATA EXTRACTION: All studies reviewed were analyzed; specific drug data were included only if clinically pertinent. In vitro data from studies with adequate design were discussed, whereas all case reports and clinical trials were utilized. DATA SYNTHESIS: In the treatment of VREF, available information seems conflicting, although some clear differences have become apparent. QD-ampicillin and QD-doxycycline combinations have demonstrated beneficial activity, usually displaying synergistic or additive effects even in macrolide-, lincosamine-, and streptogramin-resistant (MLSB) isolates. Vancomycin and chloramphenicol have shown some efficacy, but antagonistic or null results also have been observed. Regarding MRSA, results from many studies of QD combinations have been ambiguous. More common combinations displayed synergy or additive effects against MRSA, but only QD-rifampin showed consistent beneficial activity against MRSA and MLSB isolates. Most other combinations displayed antagonism when tested in vitro. CONCLUSIONS: Data supporting the use of various QD-antibiotic combinations against VREF and MRSA are increasing, but further in vitro and in vivo data are needed to confirm the findings.
引用
收藏
页码:677 / 685
页数:9
相关论文
共 64 条
[1]   Treatment of vancomycin-resistant Enterococcus faecium with RP 59500 (quinupristin-dalfopristin) administered by intermittent or continuous infusion, alone or in combination with doxycycline, in an in vitro pharmacodynamic infection model with simulated endocardial vegetations [J].
Aeschlimann, JR ;
Zervos, MJ ;
Rybak, MJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (10) :2710-2717
[2]   In vitro activities of quinupristin-dalfopristin and cefepime, alone and in combination with various antimicrobials, against multidrug-resistant staphylococci and enterococci in an in vitro pharmacodynamic model [J].
Allen, GP ;
Cha, R ;
Rybak, MJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (08) :2606-2612
[3]   Antimicrobial susceptibility and molecular characterization of community-acquired methicillin-resistant Staphylococcus aureus [J].
Almer, LS ;
Shortridge, VD ;
Nilius, AM ;
Beyer, JM ;
Soni, NB ;
Bui, MH ;
Stone, GG ;
Flamm, RK .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2002, 43 (03) :225-232
[4]   Regulation of VanA- and VanB-type glycopeptide resistance in enterococci [J].
Arthur, M ;
Quintiliani, R .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2001, 45 (02) :375-381
[5]   Comparison of inhibitory and bactericidal activities and postantibiotic effects of LY333328 and ampicillin used singly and in combination against vancomycin-resistant Enterococcus faecium [J].
Baltch, AL ;
Smith, RP ;
Ritz, WJ ;
Bopp, LH .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (10) :2564-2568
[6]  
BOZIGAR PS, 2001, 41 INT C ANT AG CHEM
[7]   INVITRO ACTIVITY OF RP 59500, A NEW SEMISYNTHETIC STREPTOGRAMIN ANTIBIOTIC, AGAINST GRAM-POSITIVE BACTERIA [J].
BRUMFITT, W ;
HAMILTONMILLER, JMT ;
SHAH, S .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1992, 30 :29-37
[8]   HIGH-LEVEL PENICILLIN RESISTANCE AMONG ISOLATES OF ENTEROCOCCI - IMPLICATIONS FOR TREATMENT OF ENTEROCOCCAL INFECTIONS [J].
BUSH, LM ;
CALMON, J ;
CHERNEY, CL ;
WENDELER, M ;
PITSAKIS, P ;
POUPARD, J ;
LEVISON, ME ;
JOHNSON, CC .
ANNALS OF INTERNAL MEDICINE, 1989, 110 (07) :515-520
[9]   Aminoglycoside resistance in enterococci [J].
Chow, JW .
CLINICAL INFECTIOUS DISEASES, 2000, 31 (02) :586-589
[10]   Inhibition of protein synthesis by streptogramins and related antibiotics [J].
Cocito, C ;
DiGiambattista, M ;
Nyssen, E ;
Vannuffel, P .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1997, 39 :7-13