Portier H, May T, Proust A
Hôpital du Bocage, Service des maladies infectieuses, Dijon, France.
J Antimicrob Chemother. 1996 May;37 Suppl A:83-91. doi: 10.1093/jac/37.suppl_a.83.
A prospective, placebo controlled double-blind, randomised study comparing oral sparfloxacin 200 mg once daily following a 400 mg loading dose on day 1 with an oral combination of amoxycillin 1 g tid plus ofloxacin 200 mg bid was conducted in 211 hospitalised patients with community-acquired pneumonia. Patients were included in the study if they were aged > 65 years or had failed a previous course of antibacterial therapy. The duration of treatment was 10 days. The overall efficacy rates for the sparfloxacin and amoxycillin plus ofloxacin treatment groups were 91.9% and 81.5%, respectively, in evaluable patients at the end of treatment. Age or prior failure of antibacterial therapy did not affect the overall success rate of sparfloxacin. The safety profile of sparfloxacin was similar to that of the antibacterial combination. This study demonstrated that sparfloxacin given once daily is a suitable therapy for the treatment of community-acquired pneumonia in the elderly or in patients with failure of previous antibiotic therapy.
一项前瞻性、安慰剂对照双盲随机研究,将211例住院的社区获得性肺炎患者分为两组,一组在第1天给予400mg负荷剂量后,每日口服一次200mg司帕沙星;另一组口服阿莫西林1g每日三次加氧氟沙星200mg每日两次。纳入研究的患者年龄>65岁或先前抗菌治疗失败。治疗持续时间为10天。治疗结束时,司帕沙星治疗组和阿莫西林加氧氟沙星治疗组在可评估患者中的总有效率分别为91.9%和81.5%。年龄或先前抗菌治疗失败并不影响司帕沙星的总体成功率。司帕沙星的安全性与抗菌药物联合治疗相似。这项研究表明,每日一次给予司帕沙星是治疗老年人或先前抗生素治疗失败患者社区获得性肺炎的合适疗法。