In vitro evaluation of sparfloxacin activity and spectrum against 24,940 pathogens isolated in the United States and Canada, the final analysis

被引:13
作者
Jones, RN
Ballow, CH
Schentag, JJ
Johnson, DM
Deinhart, JA
机构
[1] Univ Iowa, Coll Med, Dept Pathol, Div Med Microbiol, Iowa City, IA 52242 USA
[2] Millard Fillmore Hosp, Clin Pharmacokinet Lab, Buffalo, NY 14209 USA
关键词
D O I
10.1016/S0732-8893(97)00247-2
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Sparfloxacin, a recently marketed oral fluoroquinolone, was tested against 24,940 recent clinical strains isolated from blood stream and respiratory tract cultures at 187 hospitals in the USA and Canada. Sparfloxacin activity was compared with 5 to 13 antimicrobial agents using either Etest (AB BIODISK, Solna, Sweden) and a reference broth microdilution or a standardized disk diffusion method. When applying recommended MIC breakpoint criteria of sparfloxacin susceptibility (less than or equal to 0.5 mu g/mL) for Streptococcus pneumoniae (4,410 strains) and other Streptococcus spp. (554 isolates), 93% and 88% were inhibited, respectively. Furthermore, at less than or equal to 1 mu g/mL sparfloxacin susceptibility rates for streptococci increased to 98% overall and 99.3% for S. pneumoniae. In contrast, only 46% and 68% of pneumococci were susceptible to ciprofloxacin (MIC90, 3 mu g/mL; susceptible at less than or equal to 1 mu g/mL) and penicillin (MIC90, 1.5 mu g/mL; susceptible at less than or equal to 0.06 mu g/mL), respectively. Differences between regions in the USA for rates of penicillin-resistant pneumococcal strains were observed (greatest resistances in southeast and midwest), but results indicate that the sparfloxacin potency was not adversely influenced (MIC90, 0.5 mu g/mL). Also pneumococcal isolates from the lower respiratory tract were more resistant to penicillin and other beta-lactams. Nearly all Haemophilus species and Moraxella catarrhalis strains, including those harboring beta-lactamases, were susceptible to tested fluoroquinolones (sparfloxacin, ciprofloxacin), amosicillin/clavulanic acid, and newer oral cephalosporins. Sparfloxacin was very active against oxacillin-susceptible Staphylococcus aureus (MIC90, 0.12 mu g/mL; 96-97% susceptible), Klebsiella spp. (MIC90 0.12 mu g/mL), and other tested enteric bacilli (92-95% susceptible). Comparisons between the broth microdilution MIC and disk diffusion interpretive results demonstrated excellent intermethod susceptibility category agreement (>95%) using current sparfloxacin breakpoints, but some compounds (cefpodoxime disk diffusion tests for S. aureus) may require modifications. These results demonstrate that new Gram-positive focused fluoroquinolones (sparfloxacin) possess an excellent in vitro activity and spectrum against pathogens that cause respiratory tract infections. This spectrum of activity includes strains resistant to other antimicrobial classes, including the oral cephalosporins, macrolides, amoxicillin/clavulanic acid, and earlier fluoroquinolones (ciprofloxacin, ofloxacin). Overall, sparfloxacin inhibited 89% to nearly 100% of the isolates (species variable) tested against those species against which is has Food and Drug Administration indications for clinical use. (C) 1998 Elsevier Science Inc.
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页码:313 / 325
页数:13
相关论文
共 39 条
  • [1] Safety and efficacy of sparfloxacin in the treatment of acute exacerbations of chronic obstructive pulmonary disease: A double-blind, randomised, parallel, multicentre study
    Allegra, L
    Konietzko, N
    Leophonte, P
    Hosie, J
    Pauwels, R
    Guyen, JN
    Petitpretz, P
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1996, 37 : 93 - 104
  • [2] Sparfloxacin for the treatment of community-acquired pneumonia: A pooled data analysis of two studies
    Aubier, M
    Lode, H
    GialdroniGrassi, G
    Huchon, G
    Hosie, J
    Legakis, N
    Regamey, C
    Segev, S
    Vester, R
    Wijnands, WJ
    Tolstuchow, N
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1996, 37 : 73 - 82
  • [3] Comparative in vitro assessment of sparfloxacin activity and spectrum using results from over 14,000 pathogens isolated at 190 medical centers in the USA
    Ballow, CH
    Jones, RN
    Johnson, DM
    Deinhart, JA
    Schentag, JJ
    Tritsch, M
    Ellis, S
    Burger, J
    Cole, E
    Venezia, R
    George, M
    Wolf, D
    Slifkin, M
    DePalma, J
    Rudrik, J
    Sullivan, K
    Lewis, G
    Dooley, G
    Sawicki, R
    Desiderio, D
    Louma, R
    Motyl, M
    Ruffin, L
    Torresan, J
    Dunaway, G
    Keck, G
    Truitt, L
    Brecher, S
    VanEnk, R
    Whelen, C
    Fader, R
    Whisler, G
    Jenkins, S
    Thacker, D
    DAmato, R
    Buck, R
    Buescher, S
    Lambert, K
    Tristram, D
    Kehl, S
    Lawson, C
    Washington, J
    Robertson, K
    Beall, A
    Padgett, L
    Rahman, L
    Riddle, G
    DellaLatta, P
    Marcon, M
    Northern, I
    [J]. DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 1997, 29 (03) : 173 - 186
  • [4] Baquero F, 1996, J ANTIMICROB CHEMOTH, V37, P1
  • [5] NATIONAL SURVEY OF THE IN-VITRO SPECTRUM OF PIPERACILLIN-TAZOBACTAM TESTED AGAINST MORE THAN 40,000 AEROBIC CLINICAL ISOLATES FROM 236 MEDICAL-CENTERS
    BARON, EJ
    JONES, RN
    [J]. DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 1995, 21 (03) : 141 - 151
  • [6] Canadian ciprofloxacin susceptibility study: Comparative study from 15 medical centers
    Blondeau, JM
    Yaschuk, Y
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (07) : 1729 - 1732
  • [7] RAPID DEVELOPMENT OF CIPROFLOXACIN RESISTANCE IN METHICILLIN-SUSCEPTIBLE AND METHICILLIN-RESISTANT STAPHYLOCOCCUS-AUREUS
    BLUMBERG, HM
    RIMLAND, D
    CARROLL, DJ
    TERRY, P
    WACHSMUTH, IK
    [J]. JOURNAL OF INFECTIOUS DISEASES, 1991, 163 (06) : 1279 - 1285
  • [8] Bolmstrom A., 1988, NOVEL TECHNIQUE DIRE
  • [9] EMERGENCE OF DRUG-RESISTANT PNEUMOCOCCAL INFECTIONS IN THE UNITED-STATES
    BREIMAN, RF
    BUTLER, JC
    TENOVER, FC
    ELLIOTT, JA
    FACKLAM, RR
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1994, 271 (23): : 1831 - 1835
  • [10] TETRACYCLINE AND ERYTHROMYCIN RESISTANCE AMONG CLINICAL ISOLATES OF BRANHAMELLA-CATARRHALIS
    BROWN, BA
    WALLACE, RJ
    FLANAGAN, CW
    WILSON, RW
    LUMAN, JI
    REDDITT, SD
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1989, 33 (09) : 1631 - 1633