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抗革兰阳性耐药菌的新型头孢菌素类抗生素头孢洛林酯 被引量:6

Ceftaroline:a new cephalosporin with activity against resistant Gram-positive pathogens
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摘要 头孢洛林酯是新型注射给药的广谱头孢菌素类抗生素,对革兰阳性菌,包括耐甲氧西林金黄色葡萄球菌(MRSA)和多药耐药肺炎链球菌(MDRSP)以及常见革兰阴性菌具有杀菌活性。2010年10月29日,美国FDA批准其用于治疗成人社区获得性细菌肺炎(CABP)和急性细菌皮肤和皮肤结构感染(ABSSSI),包括MRSA的感染。文中对其抗菌活性、药动学/药效学、临床疗效、不良反应等做一综述。 Ceflaroline fosamil is a novel, parenteral, broad-spectrum cephalosporin exhibiting bactericidal activity against Gram-positive organisms, including MRSA and multidrug-resistant Streptococcus pneumoniae (MDRSP), as well as common Gram-negative pathogens. On Oct. 29, 2010, the U.S. Food and Drug Adminis- tration approved ceftaroline fosamil to treat adults with community acquired bacterial pneumonia (CABP) and acute bacterial skin and skin structure infections (ABSSSI) , including methicillin-resistant Staphylococcus aureus (MR- SA). The chemistry and structure-activity relationship, antibacterial activity, pharmacokinetics, pharmacodynam- ics, therapeutic efficacy, adverse effects were reviewed in this paper.
作者 刘美
出处 《中国新药杂志》 CAS CSCD 北大核心 2012年第2期109-113,123,共6页 Chinese Journal of New Drugs
关键词 头孢洛林酯 革兰阳性耐药菌 社区获得性细菌肺炎 急性细菌皮肤和皮肤结构感染 ceflaroline fosamil resistant Gram-positive pathogens community acquired bacterial pneumo- nia (CABP) acute bacterial skin and skin structure infections (ABSSSI)
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参考文献16

  • 1IKEDA Y, BAN J, ISHIKAWA T, et al. Stability and stabiliza tion studies of TAK-599 (Ceftaroline Fosamil), a novel N-phosphono type prodrug of anti-methicillin resistant Staphylococcus aureus cephalosporin T-91825 [ J]. Chem Pharm Bull (Tokyo) , 2008, 56(10) :1406 - 1411.
  • 2FDA. Approves teflaro for bacterial infectlons[EB/OL]. [2011 - 04 - 18]. http://www, fda. gov/NewsEvents/Newsroom/PressAnnouncements/2010/ucm231594, htm.
  • 3STEED ME, RYBAK MJ. Ceftaroline: a new eephalosporin with activity against resistant gram-positive pathogens[ J ]. Pharmaco- therapy, 2010, 30(4) :375 -389.
  • 4SARAVOLATZ LD, STEIN GE, JOHNSON LB. Ceftaroline: a novel cephalosporin with activity against methicillin-resistant Staphylococcus aureus [ J]. Clin Infect Dis, 2011, 52 (9) : 1156 - 1163.
  • 5LIM L, SUTTON E, BROWN J. Ceftaroline: a new broad-spectrum cephalosporin [J]. Am J Health Syst Pharm, 2011, 68 (6) :491 -498.
  • 6KAUSHIK D, RATHI S, JAIN A. Ceftaroline: a comprehensive update [ J ]. Int J Antimicrob Agents, 2011, 37 (5) : 389 - 395.
  • 7SARAVOLATZ L, PAWLAK J, JOHNSON L. In vitro activity of ceftaroline against community-associated methicillin-resistant, vancomycin-intermediate, vancomycin-resistant, and daptomycinnonsusceptible Staphylococcus aureus isolates[ J]. Antimicrob Agents Chemother, 2010, 54(7):3027- 3030.
  • 8MORRISSEY I, GE Y, JANES R. Activity of the new cephalosporin ceftaroline against bacteraemia isolates from patients with community-acquired pneumonia [ J ].Int J Antimicrob Agents, 2009, 33(6) :515 -519.
  • 9VIDAILLAC C, LEONARD SN, RYBAK MJ. In vitro evaluation of ceftaroline alone and in combination with tobramycin against hospital-acquired meticillin-resistant Staphylococcus aureus ( HAMRSA) isolates[J].Int JAntimicrob Agents, 2010, 35 (6): 527 -530.
  • 10JACQUELINE C, CAILLON J, LE MABECQUE V, et al. In vivo efficacy of ceftaroline (PPI--0903), a new broad-spectrum cephalosporin, compared with linezolid and vancomycin against methicillin-resistant and vancomycin-intermediate Staphylococcus aureus in a rabbit endocarditis model[ J]. Antimicrob Agents Chemother, 2007,51 ( 9 ) : 3397 - 3400.

同被引文献58

  • 1李莉,刘玉华,侯安存,赵高潮,王凤莲,乌姗娜.病毒唑、蛭丹化瘀口服液联合应用对呼吸道合胞病毒抑制作用的研究[J].中国中药杂志,2004,29(9):922-923. 被引量:6
  • 2宋文辉,江文胜,黄旭升,黄进.普米克令舒雾化吸入治疗小儿喘憋性肺炎疗效观察[J].临床肺科杂志,2005,10(5):632-633. 被引量:5
  • 3张杨,李婷,李东福.小儿喘憋型肺炎加用654-2的疗效观察[J].地方病通报,2006,21(4):121-121. 被引量:1
  • 4社区获得性肺炎诊断和治疗指南[J].中华结核和呼吸杂志,2006,29(10):651-655. 被引量:3052
  • 5李娟.300例住院手术患者头孢菌素药物使用分析[J].中国新药与临床杂志,2010;10(8):915-916.
  • 6Goldstein E J C, Citron D M, Merriam C V, et al. In vitro activities of the new semisynthetic glycopeptides telavancin (TD-6424), vancomycin, daptomycin, linezolid and four comparator agents against anaerobic gram-positive species and Corynebacterium spp[J]. Antimicrob Agents Chemother, 2004, 48(6): 2149-2152.
  • 7Smith K, Gemmell C G, Lang S. Telavancin shows superior activity to vancomycin with multidrug-resistant Staphylococcus aureus in a range of in vitro biofilm models [J]. Eur J Clin MicrobiolInfectDis, 2013, 32 (10): 1327-1332.
  • 8Guskey M T, Tsuji B T. A Comparative Review of the Lipoglycopeptides: Oritavancin, Dalbavancin, and Telavanein[J]. Pharmacotherapy, 2010, 30: 80-94.
  • 9Krause K M, Renelli M, Difumorum S, et al. In vitro activity of telavancin against resistant gram-positive bacteria[J]. Antimicrob Agents Chemother, 2008, 52(7):2647-2652.
  • 10Hegde S S, Reyes N, Wiens T, et al. Pharmacodynamics of telavancin (TD-6424), a novel bactericidal agent, against gram- positive bacteria[J]. Antimicrob Agents Chemother, 2004, 48(8): 3043-3050.

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