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Autor(en) / Beteiligte
Titel
Efficacy and safety of 3-day azithromycin versus 5-day moxifloxacin for the treatment of acute bacterial exacerbations of chronic bronchitis
Ist Teil von
  • International journal of antimicrobial agents, 2007-01, Vol.29 (1), p.56-61
Ort / Verlag
London: Elsevier B.V
Erscheinungsjahr
2007
Quelle
MEDLINE
Beschreibungen/Notizen
  • Abstract Antibiotic therapy is of clinical benefit in certain patients with acute exacerbations of chronic bronchitis (AECB). In this randomised, investigator-blinded, multicentre trial, azithromycin (500 mg once a day (qd) for 3 days) was compared with moxifloxacin (400 mg qd for 5 days) for the treatment of outpatients with AECB (forced expiratory volume in 1 s (FEV1 ) >35%). Of 342 patients randomised to either treatment, 169 received azithromycin and 173 received moxifloxacin. The mean age in the azithromycin and moxifloxacin groups was 56.4 years and 55.5 years, respectively. In the intent-to-treat analysis, clinical success rates for azithromycin and moxifloxacin were comparable at Days 10–12 (90% versus 90%, respectively) and Days 22–26 (81% versus 82%, respectively). Among patients who were culture-positive at baseline for Streptococcus pneumoniae , Haemophilus influenzae , Moraxella catarrhalis or Haemophilus parainfluenzae , clinical efficacy for azithromycin versus moxifloxacin at Days 10–12 was 93% versus 84%, respectively, and at Days 22–26 it was 89% versus 73%, respectively. The incidence of at least one treatment-related adverse event (AE) in the azithromycin and moxifloxacin groups was 18.3% and 19.1%, respectively. The most common AEs were diarrhoea, nausea, abdominal pain and vaginitis. Most treatment-related AEs were of mild or moderate severity, with no serious treatment-related AEs. One subject in the moxifloxacin group discontinued treatment owing to a treatment-related AE (precordial pain and dry throat). Compliance with both regimens was >90%. Three-day azithromycin and 5-day moxifloxacin demonstrate comparable efficacy and safety for the treatment of AECB in outpatients.
Sprache
Englisch
Identifikatoren
ISSN: 0924-8579
eISSN: 1872-7913
DOI: 10.1016/j.ijantimicag.2006.08.043
Titel-ID: cdi_proquest_miscellaneous_19519770
Format
Schlagworte
Abdominal Pain - chemically induced, Acute exacerbation of chronic bronchitis, Adult, Aged, Anti-Bacterial Agents - adverse effects, Anti-Bacterial Agents - pharmacology, Anti-Bacterial Agents - therapeutic use, Antibiotic therapy, Antibiotics. Antiinfectious agents. Antiparasitic agents, Aza Compounds - adverse effects, Aza Compounds - pharmacology, Aza Compounds - therapeutic use, Azithromycin, Azithromycin - adverse effects, Azithromycin - pharmacology, Azithromycin - therapeutic use, Bacteria, Biological and medical sciences, Bronchitis, Chronic - drug therapy, Bronchitis, Chronic - microbiology, Chronic obstructive pulmonary disease, asthma, Drug Administration Schedule, Female, Fluoroquinolones, Haemophilus influenzae, Haemophilus influenzae - drug effects, Haemophilus influenzae - isolation & purification, Haemophilus parainfluenzae, Haemophilus parainfluenzae - drug effects, Haemophilus parainfluenzae - isolation & purification, Humans, Infectious Disease, Male, Medical sciences, Microbial Sensitivity Tests, Middle Aged, Moraxella (Branhamella) catarrhalis - drug effects, Moraxella (Branhamella) catarrhalis - isolation & purification, Moraxella catarrhalis, Moxifloxacin, Nausea - chemically induced, Patient Compliance, Pharmacology. Drug treatments, Pneumology, Quinolines - adverse effects, Quinolines - pharmacology, Quinolines - therapeutic use, Single-Blind Method, Streptococcus pneumoniae, Streptococcus pneumoniae - drug effects, Streptococcus pneumoniae - isolation & purification, Treatment Outcome, Vaginitis - chemically induced

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