Effect of Theophylline as Adjunct to Inhaled Corticosteroids on Exacerbations in Patients With COPD

医学 茶碱 慢性阻塞性肺病 安慰剂 哮喘 随机对照试验 麻醉 皮质类固醇 支气管扩张剂 内科学 病理 替代医学
作者
Graham Devereux,Seonaidh Cotton,Shona Fielding,Nicola McMeekin,Peter J. Barnes,Andrew Briggs,Graham Burns,Rekha Chaudhuri,Henry Chrystyn,Lisa Davies,Anthony De Soyza,Simon Gompertz,John Haughney,Karen Innes,Joanna Kaniewska,Amanda Lee,Alyn H. Morice,John Norrie,Anita Sullivan,Andrew M. Wilson,David Price
出处
期刊:JAMA [American Medical Association]
卷期号:320 (15): 1548-1548 被引量:67
标识
DOI:10.1001/jama.2018.14432
摘要

Importance

Chronic obstructive pulmonary disease (COPD) is a major global health issue and theophylline is used extensively. Preclinical investigations have demonstrated that low plasma concentrations (1-5 mg/L) of theophylline enhance antiinflammatory effects of corticosteroids in COPD.

Objective

To investigate the effectiveness of adding low-dose theophylline to inhaled corticosteroids in COPD.

Design, Setting, and Participants

The TWICS (theophylline with inhaled corticosteroids) trial was a pragmatic, double-blind, placebo-controlled, randomized clinical trial that enrolled patients with COPD between February 6, 2014, and August 31, 2016. Final follow-up ended on August 31, 2017. Participants had a ratio of forced expiratory volume in the first second to forced vital capacity (FEV1/FVC) of less than 0.7 with at least 2 exacerbations (treated with antibiotics, oral corticosteroids, or both) in the previous year and were using an inhaled corticosteroid. This study included 1578 participants in 121 UK primary and secondary care sites.

Interventions

Participants were randomized to receive low-dose theophylline (200 mg once or twice per day) to provide plasma concentrations of 1 to 5 mg/L (determined by ideal body weight and smoking status) (n = 791) or placebo (n = 787).

Main Outcomes and Measures

The number of participant-reported moderate or severe exacerbations treated with antibiotics, oral corticosteroids, or both over the 1-year treatment period.

Results

Of the 1567 participants analyzed, mean (SD) age was 68.4 (8.4) years and 54% (843) were men. Data for evaluation of the primary outcome were available for 1536 participants (98%) (772 in the theophylline group; 764 in the placebo group). In total, there were 3430 exacerbations: 1727 in the theophylline group (mean, 2.24 [95% CI, 2.10-2.38] exacerbations per year) vs 1703 in the placebo group (mean, 2.23 [95% CI, 2.09-2.37] exacerbations per year); unadjusted mean difference, 0.01 (95% CI, −0.19 to 0.21) and adjusted incidence rate ratio, 0.99 (95% CI, 0.91-1.08). Serious adverse events in the theophylline and placebo groups included cardiac, 2.4% vs 3.4%; gastrointestinal, 2.7% vs 1.3%; and adverse reactions such as nausea (10.9% vs 7.9%) and headaches (9.0% vs 7.9%).

Conclusions and Relevance

Among adults with COPD at high risk of exacerbation treated with inhaled corticosteroids, the addition of low-dose theophylline, compared with placebo, did not reduce the number COPD exacerbations over a 1-year period. The findings do not support the use of low-dose theophylline as adjunctive therapy to inhaled corticosteroids for the prevention of COPD exacerbations.

Trial Registration

isrctn.org Identifier:ISRCTN27066620

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