Pneumonia risk in COPD patients receiving inhaled corticosteroids alone or in combination: TORCH study results

被引:332
作者
Crim, C. [1 ]
Calverley, P. M. A. [4 ]
Anderson, J. A.
Celli, B. [2 ]
Ferguson, G. T. [3 ]
Jenkins, C. [7 ]
Jones, P. W. [5 ]
Willits, L. R.
Yates, J. C.
Vestbo, J. [6 ,8 ]
机构
[1] GlaxoSmithKline Inc, Med Dev Ctr, Global Clin Dev, Res Triangle Pk, NC 27709 USA
[2] Caritas St Elizabeths Med Ctr, Boston, MA USA
[3] Pulm Res Inst SE Michigan, Livonia, MI USA
[4] Aintree Univ Hosp NHS Fdn Trust, Liverpool L9 7AL, Merseyside, England
[5] Univ London, London, England
[6] Wythenshawe Hosp, Manchester M23 9LT, Lancs, England
[7] Woolcock Inst Med Res, Camperdown, NSW, Australia
[8] Univ Copenhagen, Hvidovre Hosp, DK-2650 Hvidovre, Denmark
关键词
Chronic obstructive pulmonary disease; fluticasone propionate; inhaled corticosteroid; pneumonia; safety; OBSTRUCTIVE PULMONARY-DISEASE; COMMUNITY-ACQUIRED PNEUMONIA; SALMETEROL/FLUTICASONE PROPIONATE; FLUTICASONE PROPIONATE; BACTERIAL-COLONIZATION; NEUTROPHIL CHEMOTAXIS; AIRWAY INFLAMMATION; EPITHELIAL-CELLS; UNITED-STATES; LUNG-DISEASE;
D O I
10.1183/09031936.00193908
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Inhaled corticosteroids (ICS) are important in reducing exacerbation frequency associated with chronic obstructive pulmonary disease (COPD). However, little is known about the risk of associated infections. In a post hoc analysis of the TOwards a Revolution in COPD Health (TORCH) study, we analysed and identified potential risk factors for adverse event reports of pneumonia in this randomised, double-blind trial comparing twice-daily inhaled salmeterol (SAL) 50 mu g, fluticasone propionate (FP) 500 mu g, and the combination (SFC) with placebo in 6,184 patients with moderate-to-severe COPD over 3 yrs. Despite a higher withdrawal rate in the placebo arm, after adjusting for time on treatment, a greater rate of pneumonia was reported in the FP and SFC treatment arms (84 and 88 per 1,000 treatment-yrs, respectively) compared with SAL and placebo (52 and 52 per 1,000 treatment-yrs, respectively). Risk factors for pneumonia were age >= 55 yrs, forced expiratory volume in 1 s <50% predicted, COPD exacerbations in the year prior to the study, worse Medical Research Council dyspnoea scores and body mass index <25 kg.m(-2). No increase in pneumonia deaths with SFC was observed; this could not be concluded for FP. Despite the benefits of ICS-containing regimens in COPD management, healthcare providers should remain vigilant regarding the possible development of pneumonia as a complication in COPD patients receiving such therapies.
引用
收藏
页码:641 / 647
页数:7
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