Treatment of acute exacerbations of chronic bronchitis: Comparison of trovafloxacin and amoxicillin in a multicentre, double-blind, double-dummy study

被引:21
作者
O'Doherty B. [1 ]
Daniel R. [2 ]
机构
[1] Gorey, Co., Wexford
[2] Department of Clinical Research, Pfizer Central Research, Sandwich
关键词
Adverse Event; Treatment Group; Clinical Efficacy; Amoxicillin; Bronchitis;
D O I
10.1007/BF01691580
中图分类号
学科分类号
摘要
The efficacy and safety of trovafloxacin and amoxicillin were compared in a double-blind, double-dummy multicentre trial involving 412 patients ( ≤ 40 years of age) with acute exacerbations of chronic bronchitis (AECBs). Patients were randomized to 5 days' oral treatment with 200 or 100 mg trovafloxacin administered once daily, or 500 mg amoxicillin given three times daily. Overall clinical efficacy at the end of therapy was similar in each treatment group, with clinical success (cure + improvement) achieved in 88% and 91% of clinically evaluable patients receiving trovafloxacin 200 mg and 100 mg, respectively, and in 89% of amoxicillin-treated patients. Corresponding rates at follow-up were 77%, 85% and 79%, respectively. Similar responses were noted at the end of treatment and end of study in the intent-to-treat patients. Although all three treatments produced similar bacteriological efficacy, there was a trend towards higher eradication rates for Haemophilus influenzae among patients (both clinically evaluable and intent-to-treat populations) treated with trovafloxacin 200 mg compared with those treated with amoxicillin. Both drugs were well tolerated, with treatment-related adverse events, of which headache and gastrointestinal disturbances were the most common, occurring in 12% and 6% of patients in the trovafloxacin 200 mg and 100 mg groups, respectively, and in 9% of amoxicillin-treated patients.
引用
收藏
页码:441 / 446
页数:5
相关论文
共 11 条
[1]  
Fromtling R.A., Castaner J., Trovafloxacin mesylate, Drugs of the Future, 21, pp. 496-505, (1996)
[2]  
Gootz T.D., Brighty K.E., Fluoroquinolone antibacterials: SAR, mechanism of action, resistance, and clinical aspects, Medicinal Research Reviews, 16, pp. 433-486, (1996)
[3]  
Kp K., Wasas A., In-vitro activity of the fluoroquinolone trovafloxacin against penicillin-susceptible and -resistant Streptococcus pneumoniae, Journal of Antimicrobial Chemotherapy, 36, pp. 878-880, (1995)
[4]  
Pankuch G.A., Jacobs M.R., Appelbaum P.C., Activity of CP-99,219 compared with DU-6859a, ciprofloxacin, ofloxacin, levofloxacin, tosufloxacin, sparfloxacin and grepafloxacin against penicillin-susceptible and -resistant pneumococci, Journal of Antimicrobial Chemotherapy, 35, pp. 230-232, (1995)
[5]  
Jones R.N., In vitro antimicrobial activity of CP-99,219, a new 7-azabicylonaphthyridone, Drugs, 49, 2 SUPPL., pp. 205-207, (1995)
[6]  
Crokaert F., Aoun M., Duchateau V., Grenier P., Rossi C., Vandermies A., Klastersky J., In vitro activity of trovafloxacin (CP-99,219), sparfloxacin, ciprofloxacin, and fleroxacin against respiratory pathogens, European Journal of Clinical Microbiology & Infectious Diseases, 15, pp. 696-698, (1996)
[7]  
Teng R., Harris S.C., Nix D.E., Schentag J.J., Foulds G., Liston T.E., Pharmacokinetics and safety of trovafloxacin (CP-99,219), a new quinolone antibiotic, following administration of single oral doses to healthy male volunteers, Journal of Antimicrobial Chemotherapy, 36, pp. 385-394, (1995)
[8]  
Teng R., Liston T.E., Harris S.C., Multiple-dose pharmacokinetics and safety of trovafloxacin in healthy volunteers, Journal of Antimicrobial Chemotherapy, 37, pp. 955-963, (1996)
[9]  
Anthonisen N.R., Manfreda J., Warren C.P.W., Hershfield E.S., Harding G.K.M., Nelson N.A., Antibiotic therapy in exacerbations of chronic obstructive pulmonary disease, Annals of Internal Medicine, 106, pp. 196-204, (1987)
[10]  
Nicotra M.B., Rivera M., Awe R.J., Antibiotic therapy of acute exacerbation of chronic bronchitis, Annals of Internal Medicine, 97, pp. 18-20, (1982)