Five day moxifloxacin therapy compared with 7 day clarithromycin therapy for the treatment of acute exacerbations of chronic bronchitis

被引:118
作者
Wilson, R [1 ]
Kubin, R
Ballin, I
Deppermann, KM
Bassaris, HP
Leophonte, P
Schreurs, AJM
Torres, A
Sommerauer, B
机构
[1] Royal Brompton Hosp, London SW3 6LR, England
[2] Univ London Imperial Coll Sci Technol & Med, Host Def Unit, Natl Heart & Lung Inst, London SW3 6LR, England
[3] Bayer PLC, Div Pharmaceut, Newbury RG14 1JA, Berks, England
[4] Pendlebury Hlth Ctr, Manchester M27 2HP, Lancs, England
[5] Fachkrankenhaus Lungenheilkunde & Thoraxchirurg, Pneumol Klin, D-13125 Berlin, Germany
[6] Univ Hosp, Infect Dis Sect, Rion 26500, Greece
[7] Hop Rangueil, Pneumol Unit, F-31054 Toulouse, France
[8] Onze Lieve Vrouw Hosp, Dept Lung Dis, NL-1091 HA Amsterdam, Netherlands
[9] Hosp Clin Barcelona, Dept Pulmonol, Barcelona, Spain
[10] Bayer Pharma, F-92807 Puteaux La Defense, France
关键词
D O I
10.1093/jac/44.4.501
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
In this multinational, randomized, double-blind study, the efficacy and safety of a 5 day course of moxifloxacin 400 mg orally od was compared with that of a 7 day course of clarithromycin 500 mg orally bd in 750 patients with acute exacerbations of chronic bronchitis, characterized by at least two of the symptoms: sputum purulence, increased sputum volume or increased dyspnoea. Seven days after the end of therapy, clinical cure was achieved for 89% (287 of 322) of efficacy-evaluable patients in the moxifloxacin group and 88% (289 of 327) of patients in the clarithromycin group (95% CI, -3.9%, 5.8%). At follow-up (21-28 days post-treatment), the continued clinical cure rates were 89% (256 of 287) for moxifloxacin and 89% (257 of 289) for clarithromycin. A total of 342 pathogenic bacteria were isolated from the sputum of 287 patients. The most common pathogens were Haemophilus influenzae (37%), Streptococcus pneumoniae (31%) and Moraxella catarrhalis (18%). Seven days post-treatment, a successful bacteriological response was obtained for 77% (89 of 115) of patients in the moxifloxacin group and 62% (71 of 114) of patients in the clarithromycin group, indicating superiority of moxifloxacin (95% CI, 3.6%, 26.9%). Both treatments were well tolerated with few adverse events. This study demonstrated that for the treatment of acute exacerbations of chronic bronchitis a 5 day course of moxifloxacin 400 mg od was clinically equivalent and bacteriologically superior to a 7 day course of clarithromycin 500 mg bd.
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页码:501 / 513
页数:13
相关论文
共 38 条
[1]  
ANDREWS J, 1998, 38 INT C ANT AG CHEM, P9
[2]   ANTIBIOTIC-THERAPY IN EXACERBATIONS OF CHRONIC OBSTRUCTIVE PULMONARY-DISEASE [J].
ANTHONISEN, NR ;
MANFREDA, J ;
WARREN, CPW ;
HERSHFIELD, ES ;
HARDING, GKM ;
NELSON, NA .
ANNALS OF INTERNAL MEDICINE, 1987, 106 (02) :196-204
[4]  
BALL P, 1995, QJM-INT J MED, V88, P61
[5]   COMPARATIVE-EVALUATION OF THE CLINICAL AND MICROBIOLOGICAL EFFICACY OF CO-AMOXICLAV VS CEFIXIME OR CIPROFLOXACIN IN BACTERIAL EXACERBATION OF CHRONIC-BRONCHITIS [J].
CAZZOLA, M ;
VINCIGUERRA, A ;
BEGHI, GF ;
PAIZIS, G ;
GIURA, R ;
MADONINI, V ;
FIORENTINI, F ;
CONSIGLI, GF ;
TONNA, M ;
CASALINI, A ;
LEGNANI, D .
JOURNAL OF CHEMOTHERAPY, 1995, 7 (05) :432-441
[6]  
CELLI BR, 1995, AM J RESP CRIT CARE, V152, pS77
[7]   Efficacy and safety of a 10-day course of 400 or 600 milligrams of grepafloxacin once daily for treatment of acute bacterial exacerbations of chronic bronchitis: Comparison with a 10-day course of 500 milligrams of ciprofloxacin twice daily [J].
Chodosh, S ;
Lakshminarayan, S ;
Swarz, H ;
Breisch, S .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (01) :114-120
[8]  
CHODOSH S, 1990, NEW GENERATION QUINO, P249
[9]   In vitro activity of BAY 12-8039, a new 8-methoxyquinolone [J].
Dalhoff, A ;
Petersen, U ;
Endermann, R .
CHEMOTHERAPY, 1996, 42 (06) :410-425
[10]   Antimicrobial resistance of Streptococcus pneumoniae recovered from outpatients in the United States during the winter months of 1994 to 1995: Results of a 30-center national surveillance study [J].
Doern, GV ;
Brueggemann, A ;
Holley, HP ;
Rauch, AM .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (05) :1208-1213