Additional clinical benefit of enoxaparin in COPD patients receiving salmeterol and fluticasone propionate in combination

被引:36
作者
Brown, Rachel A.
Allegra, Luigi
Matera, Maria G.
Page, Clive P.
Cazzola, Mario
机构
[1] Kings Coll London, Sackler Inst Pulm Pharmacol, London, England
[2] Univ Milan, Milan, Italy
[3] Univ Naples 2, Naples, Italy
[4] A Cardarelli Hosp, Naples, Italy
关键词
heparin; enoxaparin; COPD; clinical trial;
D O I
10.1016/j.pupt.2006.04.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
It is now well recognised that heparin possesses numerous anti-inflammatory properties in addition to its anticoagulant properties. Thus, the aim of this study was to investigate the effects of the low molecular weight heparin, enoxaparin (ENX), as an add-on therapy for a period of 12 weeks, to inhaled salmeterol/fluticasone propionate (SLM/FP) combination in patients with stable chronic obstructive pulmonary disease (COPD). Forty-six patients were randomised to receive 12 weeks of treatment in one of two treatment groups: (1) fixed combination of SLM 50 mu g and FP 500 mu g Diskus, one inhalation twice daily; or (2) as group 1 plus 20 mg ENX administered subcutaneously once daily for 12 weeks. Patients attended the clinic before and after 4, 8 and 12 weeks of treatment for evaluations of lung function, blood gas tensions, dyspnoea and supplemental salbutamol use. Thirty-six patients completed the 12-week treatment period, 20 from group 1 and 16 from group 2. A significant increase in forced expiratory volume in Is (FEV1) over baseline was observed after 12 weeks of treatment in group 1 (0.145 L, 95% CI: 0.994-1.406, p < 0.01), whilst significant increases in FEV1, over baseline were observed in group 2 after 4, 8 and 12 weeks of treatment with a maximum increase at 12 weeks of 0.244 L (95% CI: 1.175-1.596, p < 0.01). Both treatment groups experienced similar improvements in blood gas tensions, dyspnoea and supplemental salbutamol use. Our results suggest that addition of ENX to conventional therapy of COPD may provide additional clinical benefit and must be further investigated as a treatment for COPD. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:419 / 424
页数:6
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