Martinez F J, Grossman R F, Zadeikis N, Fisher A C, Walker K, Ambruzs M E, Tennenberg A M
The University of Michigan Health System, 1500 East Medical Center Drive, 3916 Taubman Center, Box 0360, Ann Arbor, MI 48109, USA.
Eur Respir J. 2005 Jun;25(6):1001-10. doi: 10.1183/09031936.05.00106404.
This is the first prospective clinical trial in which patients with acute bacterial exacerbation of chronic bronchitis have been stratified by degree of underlying illness. Uncomplicated patients were randomised to levofloxacin 750 mg once daily (q.d.) for 3 days or azithromycin q.d. for 5 days. Complicated patients were randomised to levofloxacin 750 mg q.d. for 5 days or amoxicillin 875 mg/clavulanate 125 mg twice daily for 10 days. Regardless of therapy, complicated patients demonstrated lower clinical and microbiological success than uncomplicated patients. Clinical success for clinically evaluable patients was similar for levofloxacin and azithromycin (93.0 versus 90.1%, respectively), and levofloxacin and amoxicillin/clavulanate (79.2 versus 81.7%, respectively). For microbiologically evaluable patients, clinical response to levofloxacin for 3 days was superior to azithromycin for 5 days (96.3 versus 87.4%, respectively), and levofloxacin for 5 days was similar to amoxicillin/clavulanate for 10 days (81.4 versus 80.9%, respectively). Microbiological eradication was superior for levofloxacin for 3 days compared with azithromycin for 5 days (93.8 versus 82.8%, respectively), and similar for levofloxacin and amoxicillin/clavulanate for 10 days (81.4 versus 79.8%, respectively). In conclusion, levofloxacin 750 mg for 3 days was comparable to azithromycin for 5 days for uncomplicated patients with acute bacterial exacerbation of chronic bronchitis, while 5 days of 750 mg levofloxacin was comparable to 10 days of amoxicillin/clavulanate for complicated acute bacterial exacerbation of chronic bronchitis.
这是第一项前瞻性临床试验,其中慢性支气管炎急性细菌性加重患者按基础疾病程度进行了分层。病情不复杂的患者被随机分为每日一次口服750毫克左氧氟沙星,共3天,或每日一次口服阿奇霉素,共5天。病情复杂的患者被随机分为每日一次口服750毫克左氧氟沙星,共5天,或每日两次口服875毫克阿莫西林/125毫克克拉维酸,共10天。无论采用何种治疗方法,病情复杂的患者在临床和微生物学方面的成功率均低于病情不复杂的患者。左氧氟沙星和阿奇霉素在可进行临床评估的患者中的临床成功率相似(分别为93.0%和90.1%),左氧氟沙星和阿莫西林/克拉维酸的临床成功率也相似(分别为79.2%和81.7%)。对于可进行微生物学评估的患者,3天的左氧氟沙星治疗的临床反应优于5天的阿奇霉素治疗(分别为96.