Clinical perspectives on new antimicrobials: Focus on fluoroquinolones

被引:20
作者
Talan, DA
机构
[1] Univ Calif Los Angeles, Dept Med, Div Emergency Med, Sylmar, CA 91342 USA
[2] Univ Calif Los Angeles, Dept Med, Div Infect Dis, Sylmar, CA 91342 USA
[3] Olive View UCLA Med Ctr, Sylmar, CA 91342 USA
关键词
D O I
10.1086/319378
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Respiratory tract infections are the most common infectious presentation in the community and hospital settings and are a major cause of morbidity and mortality worldwide. Recently, newer fluoroquinolones have been recommended for the treatment of these infections. Among them, moxifloxacin shows improved activity against gram-positive pathogens, has maintained potency against gram-negative organisms, and shows activity against atypical pathogens and anaerobes. Moxifloxacin also has excellent in vitro activity against strains resistant to penicillin, erythromycin, and other fluoroquinolones, such as levofloxacin. Moxifloxacin has demonstrated clinical efficacy rates of 90%-95% in clinical trials in community-acquired pneumonia, acute exacerbations of chronic bronchitis, and acute sinusitis. In these trials, moxifloxacin demonstrated no serious or unexpected adverse effects. Development of resistance appears to be slower for moxifloxacin than for several other fluoroquinolones, making moxifloxacin a good treatment choice. The pharmacodynamics of moxifloxacin support once-daily oral therapy of short duration, providing convenience, compliance, and safety advantages.
引用
收藏
页码:S64 / S71
页数:8
相关论文
共 64 条
  • [1] ANZUETO A, 2000, 9 INT C INF DIS BUEN, P44
  • [2] The prospects of treatment failure in the chemotherapy of infectious diseases in the 1990s
    Armstrong, D
    Neu, H
    Peterson, LR
    Tomasz, A
    [J]. MICROBIAL DRUG RESISTANCE-MECHANISMS EPIDEMIOLOGY AND DISEASE, 1995, 1 (01): : 1 - 4
  • [3] Balfour JAB, 1999, DRUGS, V57, P363
  • [4] Comparative tolerability of the newer fluoroquinolone antibacterials
    Ball, P
    Mandell, L
    Niki, Y
    Tillotson, G
    [J]. DRUG SAFETY, 1999, 21 (05) : 407 - 421
  • [5] EPIDEMIOLOGY AND TREATMENT OF CHRONIC-BRONCHITIS AND ITS EXACERBATIONS
    BALL, P
    [J]. CHEST, 1995, 108 (02) : S43 - S52
  • [6] COMMUNITY-ACQUIRED PNEUMONIA
    BARTLETT, JG
    MUNDY, LM
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (24) : 1618 - 1624
  • [7] Community-acquired pneumonia in adults: Guidelines for management
    Bartlett, JG
    Breiman, RF
    Mandell, LA
    File, TM
    [J]. CLINICAL INFECTIOUS DISEASES, 1998, 26 (04) : 811 - 838
  • [8] BAZ MN, 1999, TODAYS THER TRENDS, V17, P303
  • [9] Treatment of community-acquired pneumonia - IDSA guidelines
    Bernstein, JM
    [J]. CHEST, 1999, 115 (03) : 9S - 13S
  • [10] Comparative antimicrobial activity and kill-curve investigations of novel ketolide antimicrobial agents (HMR 3004 and HMR 3647) tested against Haemophilus influenzae and Moraxella catarrhalis strains
    Biedenbach, DJ
    Barrett, MS
    Jones, RN
    [J]. DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 1998, 31 (02) : 349 - 353