1University Rovira i Virgili, Primary Care Center Jaume I,c. Felip Pedrell, 45-47, Tarragona, Spain.
Am J Respir Crit Care Med. 2012 Oct 15;186(8):716-23. doi: 10.1164/rccm.201206-0996OC. Epub 2012 Aug 23.
Antimicrobial therapy remains a controversial issue in nonsevere exacerbations of chronic obstructive pulmonary disease (COPD).
To evaluate the efficacy of antibiotic therapy in moderate exacerbations of mild-to-moderate COPD.
This study involved a multicenter, parallel, double-blind, placebo-controlled, randomized clinical trial. Patients aged 40 years or older, smokers, or ex-smokers of 10 pack-years or more with spirometrically confirmed mild-to-moderate COPD (FEV(1) > 50% predicted and FEV(1)/FVC ratio < 0.7) and diagnosed with an exacerbation were enrolled in the study. The patients were randomized to receive amoxicillin/clavulanate 500/125 mg three times a day or placebo three times a day for 8 days.
The primary outcome measure was clinical cure at end of therapy visit (EOT) at Days 9 to 11. A total of 310 subjects fulfilled all the criteria for efficacy analysis. A total of 117 patients with amoxicillin/clavulanate (74.1%) and 91 with placebo (59.9%) were considered cured at EOT (difference, 14.2%; 95% confidence interval, 3.7-24.3). The median time to the next exacerbation was significantly longer in patients receiving antibiotic compared with placebo (233 d [interquartile range, 110-365] compared with 160 d [interquartile range, 66-365]; P < 0.05). The best C-reactive protein serum cut-off for predicting clinical failure with placebo was 40 mg/L, with an area under the curve of 0.732 (95% confidence interval, 0.614-0.851).
Treatment of ambulatory exacerbations of mild-to-moderate COPD with amoxicillin/clavulanate is more effective and significantly prolongs the time to the next exacerbation compared with placebo.
在慢性阻塞性肺疾病(COPD)非严重加重期,抗生素治疗仍然存在争议。
评估抗生素治疗轻中度 COPD 中度加重期的疗效。
这是一项多中心、平行、双盲、安慰剂对照、随机临床试验。纳入年龄 40 岁或以上、吸烟者或 10 包年以上的既往吸烟者,有肺量计确认的轻中度 COPD(FEV1 > 50%预测值和 FEV1/FVC 比<0.7)且诊断为加重的患者。患者随机接受阿莫西林/克拉维酸 500/125mg 每日 3 次或安慰剂每日 3 次治疗 8 天。
主要终点为治疗结束时(EOT)第 9-11 天的临床治愈率。共有 310 例患者满足所有疗效分析标准。阿莫西林/克拉维酸组 117 例(74.1%)和安慰剂组 91 例(59.9%)患者在 EOT 时被认为治愈(差异,14.2%;95%置信区间,3.7-24.3)。与安慰剂组相比,接受抗生素治疗的患者下一次加重的中位时间明显更长(233d[四分位距,110-365]比 160d[四分位距,66-365];P<0.05)。预测安慰剂临床失败的最佳 C 反应蛋白血清截断值为 40mg/L,曲线下面积为 0.732(95%置信区间,0.614-0.851)。
与安慰剂相比,阿莫西林/克拉维酸治疗轻中度 COPD 门诊加重期更有效,显著延长下一次加重的时间。