Fogarty C, Torres A, Choudhri S, Haverstock D, Herrington J, Ambler J
Lung and Chest Medical Associates, Spartanburg, SC 29303, USA.
Int J Clin Pract. 2005 Nov;59(11):1253-9. doi: 10.1111/j.1368-5031.2005.00699.x.
This pooled analysis of six prospective, multicentre trials aimed to determine the efficacy of moxifloxacin in community-acquired pneumonia (CAP) due to penicillin-, macrolide- and multidrug-resistant Streptococcus pneumoniae (MDRSP). At a central laboratory, isolates were identified and antimicrobial susceptibility determined (microbroth dilution). MDRSP was defined as resistance > or =3 drug classes. Patients received oral or sequential intravenous/oral 400 mg moxifloxacin once daily for 7-14 days. The primary endpoint was clinical success at test-of-cure for efficacy-valid patients with proven pretherapy S. pneumoniae infection. Of 140 S. pneumoniae isolated (112 respiratory, 28 blood), 23 (16.4%) were penicillin resistant, 26 (18.6%) macrolide resistant and 31 (22.1%) MDRSP. The moxifloxacin MIC90 was 0.25 microg/ml. Clinical cure with moxifloxacin was 95.4% (125/131) overall, and 100% (21/21) for penicillin-, 95.7% (22/23) for macrolide- and 96.4% (27/28) for multidrug-resistant strains. Moxifloxacin provided excellent clinical and bacteriological cure rates in CAP due to drug-resistant pneumococci.
这项对六项前瞻性多中心试验的汇总分析旨在确定莫西沙星对由青霉素、大环内酯类和多重耐药肺炎链球菌(MDRSP)引起的社区获得性肺炎(CAP)的疗效。在一个中心实验室,对分离菌株进行鉴定并测定抗菌药敏性(微量肉汤稀释法)。MDRSP被定义为对≥3类药物耐药。患者接受口服或序贯静脉/口服400mg莫西沙星,每日一次,疗程7 - 14天。主要终点是在治疗结束时,对治疗前已证实感染肺炎链球菌且疗效有效的患者的临床成功情况。在分离出的140株肺炎链球菌中(112株来自呼吸道,28株来自血液),23株(16.4%)对青霉素耐药,26株(18.6%)对大环内酯类耐药,31株(22.1%)为MDRSP。莫西沙星的MIC90为0.25μg/ml。总体而言,莫西沙星的临床治愈率为95.4%(125/131),对青霉素耐药菌株的治愈率为100%(21/21),对大环内酯类耐药菌株为95.7%(22/23),对多重耐药菌株为96.4%(27/28)。莫西沙星对耐药肺炎球菌引起的CAP提供了优异的临床和细菌学治愈率。