Ceftaroline fosamil salvage therapy: an option for reduced-vancomycin-susceptible MRSA bacteraemia

被引:11
作者
Espedido, Bjoern A. [1 ,2 ,3 ]
Jensen, Slade O. [1 ,2 ,3 ]
van Hal, Sebastiaan J. [2 ,4 ]
机构
[1] Univ Western Sydney, Sch Med, Mol Med Res Grp, Sydney, NSW, Australia
[2] Ingham Inst Appl Med Res, Antibiot Resistance & Mobile Elements Grp, Sydney, NSW, Australia
[3] Univ New S Wales, South Western Sydney Clin Sch, Sydney, NSW, Australia
[4] Royal Prince Alfred Hosp, Dept Microbiol & Infect Dis, Sydney, NSW, Australia
关键词
broth microdilution; MICE strips; 'see-saw' effect; RESISTANT STAPHYLOCOCCUS-AUREUS; CASE SERIES; PHARMACODYNAMICS; INTERMEDIATE; DAPTOMYCIN; STRAINS;
D O I
10.1093/jac/dku455
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: To examine the activity of ceftaroline against reduced-vancomycin-susceptible MRSA isolates. Methods: One-hundred and three MRSA blood culture isolates (predominantly ST239-MRSA-III), with varying vancomycin phenotypes, had their ceftaroline MICs determined by broth microdilution and MIC Evaluator strip (Oxoid-Thermo Fisher). Statistical analyses were performed that examined relationships with vancomycin and daptomycin MICs. Mutations in mecA were also examined. Results: All 103 isolates (including 60 heteroresistant vancomycin-intermediate Staphylococcus aureus/vancomycin-intermediate S. aureus) were susceptible to ceftaroline, with one isolate displaying heteroresistance that may be related to a mecA mutation. Higher ceftaroline MICs were associated with vancomycin-susceptible S. aureus isolates. Conclusions: This study highlights that ceftaroline fosamil is an option for salvage therapy based on in vitro activity.
引用
收藏
页码:797 / 801
页数:5
相关论文
共 23 条
[1]   Analysis of Staphylococcus aureus clinical isolates with reduced susceptibility to ceftaroline: an epidemiological and structural perspective [J].
Alm, Richard A. ;
McLaughlin, Robert E. ;
Kos, Veronica N. ;
Sader, Helio S. ;
Iaconis, Joseph P. ;
Lahiri, Sushmita D. .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2014, 69 (08) :2065-2075
[2]  
[Anonymous], 2012, CLSI version M100-S22, V32, P1
[3]   Observation of "Seesaw Effect" with Vancomycin, Teicoplanin, Daptomycin and Ceftaroline in 150 Unique MRSA Strains [J].
Barber K.E. ;
Ireland C.E. ;
Bukavyn N. ;
Rybak M.J. .
Infectious Diseases and Therapy, 2014, 3 (1) :35-43
[4]   In Vitro Pharmacodynamics of Human Simulated Exposures of Ceftaroline and Daptomycin against MRSA, hVISA, and VISA with and without Prior Vancomycin Exposure [J].
Bhalodi, Amira A. ;
Hagihara, Mao ;
Nicolau, David P. ;
Kuti, Joseph L. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2014, 58 (02) :672-677
[5]   Large Retrospective Evaluation of the Effectiveness and Safety of Ceftaroline Fosamil Therapy [J].
Casapao, Anthony M. ;
Davis, Susan L. ;
Barr, Viktorija O. ;
Klinker, Kenneth P. ;
Goff, Debra A. ;
Barber, Katie E. ;
Kaye, Keith S. ;
Mynatt, Ryan P. ;
Molloy, Leah M. ;
Pogue, Jason M. ;
Rybak, Michael J. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2014, 58 (05) :2541-2546
[6]   LOW-AFFINITY PENICILLIN-BINDING PROTEIN ASSOCIATED WITH BETA-LACTAM RESISTANCE IN STAPHYLOCOCCUS-AUREUS [J].
HARTMAN, BJ ;
TOMASZ, A .
JOURNAL OF BACTERIOLOGY, 1984, 158 (02) :513-516
[7]   Dissemination in Japanese hospitals of strains of Staphylococcus aureus heterogeneously resistant to vancomycin [J].
Hiramatsu, K ;
Aritaka, N ;
Hanaki, H ;
Kawasaki, S ;
Hosoda, Y ;
Hori, S ;
Fukuchi, Y ;
Kobayashi, I .
LANCET, 1997, 350 (9092) :1670-1673
[8]   Reduced Vancomycin Susceptibility in Staphylococcus aureus, Including Vancomycin-Intermediate and Heterogeneous Vancomycin-Intermediate Strains: Resistance Mechanisms, Laboratory Detection, and Clinical Implications [J].
Howden, Benjamin P. ;
Davies, John K. ;
Johnson, Paul D. R. ;
Stinear, Timothy P. ;
Grayson, M. Lindsay .
CLINICAL MICROBIOLOGY REVIEWS, 2010, 23 (01) :99-+
[9]   TAK-599, a novel N-phosphono type prodrug of Anti-MRSA cephalosporin T-91825:: Synthesis, physicochemical and pharmacological properties [J].
Ishikawa, T ;
Matsunaga, N ;
Tawada, H ;
Kuroda, N ;
Nakayama, Y ;
Ishibashi, Y ;
Tomimoto, M ;
Ikeda, Y ;
Tagawa, Y ;
Iizawa, Y ;
Okonogi, K ;
Hashiguchi, S ;
Miyake, A .
BIOORGANIC & MEDICINAL CHEMISTRY, 2003, 11 (11) :2427-2437
[10]   Outcome of vancomycin treatment in patients with methicillin-susceptible Staphylococcus aureus bacteremia [J].
Kim, Sung-Han ;
Kim, Kye-Hyung ;
Kim, Hong-Bin ;
Kim, Nam-Joong ;
Kim, Eui-Chong ;
Oh, Myoung-Don ;
Choe, Kang-Won .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2008, 52 (01) :192-197