Activity of telithromycin, a new ketolide antibacterial, against atypical and intracellular respiratory tract pathogens

被引:31
作者
Hammerschlag, MR
Roblin, PM
Bébéar, CM
机构
[1] Suny Downstate Med Ctr, Div Infect Dis, Dept Pediat, Brooklyn, NY 11203 USA
[2] Univ Bordeaux 2, Bacteriol Lab, F-33076 Bordeaux, France
关键词
D O I
10.1093/jac/48.suppl_2.25
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Atypical respiratory pathogens such as Mycoplasma pneumoniae and intracellular pathogens such as Legionella spp. and Chlamydia spp. form a significant proportion of the aetiological agents underlying community-acquired pneumonia (CAP). The clinical signs or radiological features of atypical pneumonia are generally insufficient to predict accurately the pathogen involved; in addition, high costs and a considerable length of time are involved in the identification of atypical pathogens. Treatment is, therefore, most often empirical, and it is important that the activity of antibacterial agents available to treat CAP is sufficiently broad to eradicate infection with both common and atypical bacterial pathogens. Telithromycin (HMR 3647) is the first of a new family of antibacterials, the ketolides, and has been designed specifically for the treatment of community-acquired respiratory tract infections (RTIs). The excellent activity of telithromycin against the respiratory tract bacterial pathogens most commonly associated with community-acquired RTIs, including resistant strains, is well established. This review examines the considerable body of evidence showing that telithromycin also has a high level of activity against atypical and intracellular respiratory tract bacterial pathogens.
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页码:25 / 31
页数:7
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共 32 条
  • [21] Marston Barbara J., 1997, Archives of Internal Medicine, V157, P1709, DOI 10.1001/archinte.157.15.1709
  • [22] Martin R E, 1991, Infect Dis Clin North Am, V5, P585
  • [23] MAUVAIS P, 2000, 5 INT C MACR AZ STRE, P24
  • [24] RAJAGOPALANLEVA.P, 1998, 38 INT C ANT AG CHEM, P58
  • [25] In vitro activity of a new ketolide antibiotic, HMR 3647, against Chlamydia pneumoniae
    Roblin, PM
    Hammerschlag, MR
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (06) : 1515 - 1516
  • [26] Susceptibilities of Legionella spp. to newer antimicrobials in vitro
    Schülin, T
    Wennersten, CB
    Ferraro, MJ
    Moellering, RC
    Eliopoulos, GM
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (06) : 1520 - 1523
  • [27] Prospective study of community-acquired pneumonia of bacterial etiology in adults
    Sopena, N
    Sabrià, M
    Pedro-Botet, ML
    Manterola, JM
    Matas, L
    Domínguez, J
    Modol, JM
    Tudela, P
    Ausina, V
    Foz, M
    [J]. EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 1999, 18 (12) : 852 - 858
  • [28] In vitro activity of ABT 773, a new ketolide antibiotic, against Chlamydia pneumoniae
    Strigl, S
    Roblin, PM
    Reznik, T
    Hammerschlag, MR
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (04) : 1112 - 1113
  • [29] Antibiotic susceptibilities of mycoplasmas and treatment of mycoplasmal infections
    Taylor-Robinson, D
    Bébéar, C
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1997, 40 (05) : 622 - 630
  • [30] New directions for future studies of community-acquired pneumonia: Optimizing impact on patient care
    Vergis, EN
    Yu, VL
    [J]. EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 1999, 18 (12) : 847 - 851