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Short-term vs conventional glucocorticoid therapy in acute exacerbations of chronic obstructive pulmonary disease: The REDUCE randomized clinical trial

机译:慢性阻塞性肺病急性加重期短期与常规糖皮质激素治疗:REDUCE随机临床试验

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摘要

Importance: International guidelines advocate a 7- to 14-day course of systemic glucocorticoid therapyin acute exacerbations of chronic obstructive pulmonary disease (COPD). However, the optimal dose and duration are unknown. Objective: To investigate whether a short-term (5 days) systemic glucocorticoid treatment in patients with COPD exacerbation is noninferior to conventional (14 days) treatment in clinical outcome and whether it decreases the exposure to steroids. Design, Setting, and Patients: REDUCE (Reduction in the Use of Corticosteroids in Exacerbated COPD), a randomized, noninferiority multicenter trial in 5 Swiss teaching hospitals, enrolling 314 patients presenting to the emergency department with acute COPD exacerbation, past or present smokers (≥20 pack-years) without a history of asthma, from March 2006 through February 2011. Interventions: Treatment with 40 mg of prednisone daily for either 5 or 14 days in a placebo-controlled, double-blind fashion. The predefined noninferiority criterion was an absolute increase in exacerbations of at most 15%, translating to a critical hazard ratio of 1.515 for a reference event rate of 50%. Main Outcome and Measure: Time to next exacerbation within 180 days. Results: Of 314 randomized patients, 289 (92%) of whom were admitted to the hospital, 311 were included in the intention-to-treat analysis and 296 in the per-protocol analysis. Hazard ratios for the short-term vs conventional treatment group were 0.95 (90% CI, 0.70 to 1.29; P = .006 for noninferiority) in the intention-to-treat analysis and 0.93 (90% CI, 0.68 to 1.26; P = .005 for noninferiority) in the per-protocol analysis, meeting our noninferiority criterion. In the short-term group, 56 patients (35.9%) reached the primary end point; 57 (36.8%) in the conventional group. Estimates of reexacerbation rates within 180 days were 37.2% (95% CI, 29.5% to 44.9%) in the short-term; 38.4% (95% CI, 30.6% to 46.3%) in the conventional, with a difference of -1.2% (95% CI, -12.2% to 9.8%) between the short-term and the conventional. Among patients with a reexacerbation, the median time to event was 43.5 days (interquartile range [IQR], 13 to 118) in the short-term and 29 days (IQR, 16 to 85) in the conventional. There was no difference between groups in time to death, the combined end point of exacerbation, death, or both and recovery of lung function. In the conventional group, mean cumulative prednisone dose was significantly higher (793 mg [95% CI, 710 to 876 mg] vs 379 mg [95% CI, 311 to 446 mg], P <.001), but treatment-associated adverse reactions, including hyperglycemia and hypertension, did not occur more frequently. Conclusions and Relevance: In patients presenting to the emergency department with acute exacerbations of COPD, 5-day treatment with systemic glucocorticoids was noninferior to 14-day treatment with regard to reexacerbation within 6 months of follow-up but significantly reduced glucocorticoid exposure. These findings support the use of a 5-day glucocorticoid treatment in acute exacerbations of COPD. Trial Registration: isrctn.org Identifier: ISRCTN19646069 ©2013 American Medical Association. All rights reserved.
机译:重要性:国际指南主张在慢性阻塞性肺疾病(COPD)急性加重期间进行7至14天的全身糖皮质激素治疗。但是,最佳剂量和持续时间未知。目的:探讨短期(5天)全身性糖皮质激素治疗在COPD加重患者中的临床疗效是否不逊于常规(14天)治疗,并且是否能减少类固醇的暴露。设计,设置和患者:REDUCE(减少恶化的COPD中使用皮质类固醇的治疗)是一项在5所瑞士教学医院进行的随机,非劣效性多中心试验,纳入了314名因急诊COPD急性加重向急诊科就诊的吸烟者,过去或现在的吸烟者(从2006年3月至2011年2月,无哮喘病史(≥20包年)。干预措施:每天以安慰剂对照,双盲方式用40 mg泼尼松治疗5或14天。预定义的非劣效性标准是急性发作绝对增加最多15%,对于50%的参考事件发生率,危急危险比为1.515。主要结果和衡量标准:180天内再次恶化的时间。结果:在314名随机患者中,其中289名(92%)入院,意向性治疗分析中包括311名,按方案分析中包括296名。在意向性治疗分析中,短期治疗组与常规治疗组的危险比分别为0.95(90%CI,0.70至1.29; P = 0.006,为非劣势)和0.93(90%CI,0.68至1.26; P =按协议分析中的非劣效性(0.005),符合我们的非劣质性标准。在短期组中,有56名患者(35.9%)达到了主要终点。常规组为57(36.8%)。短期内180天内的恶化率估计为37.2%(95%CI,29.5%至44.9%); 38.4%(95%CI,30.6%至46.3%),常规和短期之间的差异为-1.2%(95%CI,-12.2%至9.8%)。在病情加重的患者中,事件发生的中位时间在短期内为43.5天(四分位间距[IQR],13至118),在常规情况下为29天(IQR,16至85)。死亡时间,加重,死亡或两者兼有和肺功能恢复的终点之间在两组之间没有差异。常规组中,泼尼松的平均累积剂量显着较高(793 mg [95%CI,710至876 mg]比379 mg [95%CI,311至446 mg],P <.001),但与治疗相关的不良反应包括高血糖症和高血压在内的反应并不经常发生。结论和相关性:就诊于急诊科室的COPD急性加重的患者,在随访的6个月内,全身性糖皮质激素治疗5天的疗效不劣于14天,但糖皮质激素的暴露显着降低。这些发现支持在COPD急性加重中使用5天糖皮质激素治疗。试用注册:isrctn.org标识符:ISRCTN19646069©2013 American Medical Association。版权所有。

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