文摘
Objective: We sought to evaluate gatifloxacin in adults with acute uncomplicated bacterial rhinosinusitis. Study Design: TeqCES was an open-label, multicenter, noncomparative study of the safety and efficacy of gatifloxacin. More than 11,000 adult patients with acute uncomplicated rhinosinusitis received gatifloxacin 400 mg once daily for 10 days. Results:Moraxella catarrhalis (91 % β-lactamase producers), Haemophilus influenzae (28 % β-lactamase producers), Streptococcus pneumoniae (18 % intermediately resistant and 14 % fully resistant to penicillin), and Staphylococcus aureus were the predominant pathogens isolated from purulent nasal discharge. More than 99 % of rhinosinusitis pathogens isolated from the nasopharynx of patients meeting the clinical criteria for rhinosinusitis were susceptible to gatifloxacin. Among 10,353 patients whose clinical response could be determined, 91.6 % were cured. Clinical cure rates exceeded 90 % for the major pathogens. Gatifloxacin was well tolerated; drug-related adverse events that occurred in 1 % or more of patients were nausea (4.4 % ), dizziness (1.8 % ), diarrhea (1.4 % ), and headache (1.0 % ). Conclusion: Gatifloxacin is effective for patients with acute bacterial rhinosinusitis in the community. (Otolaryngol Head Neck Surg 2002;127:182-89.)