Departamento de Emergencia, Hospital Central de las Fuerzas Armadas, Montevideo, Uruguay.
Unidad de Medicina Respiratoria, Hospital de Niños "O. Allassia" Santa Fe, Argentina.
Chest. 2012 Nov;142(5):1104-1110. doi: 10.1378/chest.11-2252.
Bronchodilators are central to the symptomatic management of patients with COPD.Previous data have shown that inhaled indacaterol improved numerous clinical outcomes over placebo.
This systematic review explored the efficacy and safety of indacaterol in comparison with tiotropium or bid long-acting β 2 -agonists (TD-LABAs) for treatment of moderate to severe COPD. Randomized controlled trials were identified after a search of different databases of published and unpublished trials.
Five trials (5,920 participants) were included. Compared with tiotropium, indacaterol showed statistically and clinically significant reductions in the use of rescue medication and dyspnea(43% greater likelihood of achieving a minimal clinically important difference [MCID] in the transitional dyspnea index [TDI]; number needed to treat for benefit [NNTB] 5 10). Additionally,the MCID in health status was more likely to be achieved with indacaterol than with tiotropium (OR = 1.43; 95% CI, 1.22–1.68; P = .00001; [NNTB ]= 10). Trough FEV 1 was significantly higher at the end of treatment with indacaterol than with TD-LABAs (80 mL, P = .00001). Similarly, indacaterol signifi cantly improved dyspnea (61% greater likelihood of achieving an MCID in TDI, P = .008) and health status (21% greater likelihood of achieving an MCID in St. George’s Respiratory Questionnaire, P 5 .04) than TD-LABA. Indacaterol showed similar levels of safety and tolerability to both comparators.
Available evidence suggests that indacaterol may prove useful as an alternative to tiotropium or TD-LABA due to its effects on health status, dyspnea, and pulmonary function.
支气管扩张剂是 COPD 患者症状管理的核心。先前的数据表明,吸入茚达特罗比安慰剂能显著改善多项临床结局。
本系统评价探讨了茚达特罗与噻托溴铵或双支长效β2 激动剂(TD-LABA)治疗中重度 COPD 的疗效和安全性。通过检索不同数据库(包括已发表和未发表的试验),确定了随机对照试验。
共纳入 5 项试验(5920 名参与者)。与噻托溴铵相比,茚达特罗在减少急救药物和呼吸困难方面显示出统计学和临床意义上的显著改善(过渡性呼吸困难指数[TDI]达到最小临床重要差异[MCID]的可能性高 43%;治疗获益所需的人数[NNTB]为 5[10])。此外,与噻托溴铵相比,健康状况达到 MCID 的可能性更大(OR=1.43;95%CI,1.22-1.68;P=0.00001;NNTB=10)。与 TD-LABA 相比,治疗结束时茚达特罗的 FEV1 谷值更高(80mL,P=0.00001)。同样,与 TD-LABA 相比,茚达特罗显著改善了呼吸困难(TDI 达到 MCID 的可能性高 61%,P=0.008)和健康状况(圣乔治呼吸问卷达到 MCID 的可能性高 21%,P=0.04)。茚达特罗的安全性和耐受性与两种对照药物相当。
现有证据表明,茚达特罗可能因其对健康状况、呼吸困难和肺功能的影响,成为噻托溴铵或 TD-LABA 的替代药物。