一项双盲、随机、安慰剂对照研究,在慢性阻塞性肺疾病频繁加重的成年人中,使用罗红霉素和强力霉素联合、罗红霉素单独或匹配安慰剂12周。

Eskandarain Shafuddin, Graham D Mills, Mark D Holmes, Phillippa J Poole, Peter R Mullins, Peter N Black
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引用次数: 16

摘要

背景:阿奇霉素预防已被证明可减少COPD恶化,但其他抗生素的证据不足。在为期12周的治疗过程和随后的48周随访期间,我们比较了有频繁急性发作史(在过去两年中至少有三次中度或重度COPD急性发作)的COPD患者的急性发作率。结果:292例患者被随机分配到三种治疗方案中的一种,持续12周:罗红霉素300 mg /天和强力霉素100 mg /天(n = 101);罗红霉素每日300毫克(n = 97);或匹配安慰剂(n = 94)。与安慰剂(2.5(2.08-3.03))相比,罗红霉素/强力霉素治疗后的年化中重度加重率(2.83 (95% CI 2.37-3.40))或仅罗红霉素治疗后的年化中重度加重率(2.69(2.26-3.21))无差异(p = 0.352和p = 0.5832)。此外,在罗红霉素/多西环素治疗12周期间,年化恶化率无差异(1.64 (95% CI 1.17-2.30)),仅罗红霉素(1.75(1.24-2.41))或安慰剂(2.23 (1.68-3.03))(p = 0.1709和p = 0.2545)。在治疗12周或治疗后48周期间,两组之间的肺活量测量或生活质量评分也没有显著差异。两种积极治疗均与恶心有关,但其他不良事件在治疗组之间具有可比性。结论:罗红霉素/多西环素联合用药或罗红霉素单独用药12周并不能减少有频繁加重史的患者COPD加重。这些发现不支持使用这些抗生素来预防COPD患者的恶化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A double-blind, randomised, placebo-controlled study of roxithromycin and doxycycline combination, roxithromycin alone, or matching placebo for 12 weeks in adults with frequent exacerbations of chronic obstructive pulmonary disease.

A double-blind, randomised, placebo-controlled study of roxithromycin and doxycycline combination, roxithromycin alone, or matching placebo for 12 weeks in adults with frequent exacerbations of chronic obstructive pulmonary disease.

A double-blind, randomised, placebo-controlled study of roxithromycin and doxycycline combination, roxithromycin alone, or matching placebo for 12 weeks in adults with frequent exacerbations of chronic obstructive pulmonary disease.

Background: Azithromycin prophylaxis has been shown to reduce COPD exacerbations but there is poor evidence for other antibiotics. We compared exacerbation rates in COPD patients with a history of frequent exacerbations (at least three moderate or severe COPD exacerbations in the past two years) during a 12-week treatment course and over a subsequent 48-week follow up period.

Results: 292 patients were randomised to one of three treatments for 12 weeks: roxithromycin 300 mg daily and doxycycline 100 mg daily (n = 101); roxithromycin 300 mg daily (n = 97); or matching placebos (n = 94). There were no differences in the annualised moderate and severe exacerbation rates after treatment with roxithromycin/doxycycline (2.83 (95 % CI 2.37-3.40)) or roxithromycin only (2.69 (2.26-3.21)) compared to placebo (2.5 (2.08-3.03)) (p = 0.352 and p = 0.5832 respectively). Furthermore, there were no differences in the annualised exacerbation rates during 12-week treatment with roxithromycin/doxycycline (1.64 (95 % CI 1.17-2.30)), roxithromycin only (1.75 (1.24-2.41)) or placebo (2.23 (1.68-3.03)) (p = 0.1709 and p = 0.2545 respectively). There were also no significant differences between groups for spirometry or quality of life scores over either the 12-week treatment or 48-week post-treatment periods. Both active treatments were associated with nausea but otherwise adverse events were comparable among treatment groups.

Conclusions: Twelve-weeks of prophylaxis with roxithromycin/doxycycline combination or roxithromycin alone did not reduce COPD exacerbations in patients with history of frequent exacerbations. These findings do not support the use of these antibiotics to prevent exacerbations in COPD patients.

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