首页> 外文期刊>International Journal of Chronic Obstructive Pulmonary Disease >Indacaterol therapy in moderate-to-severe chronic obstructive pulmonary disease: findings from a single-center primary care cohort
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Indacaterol therapy in moderate-to-severe chronic obstructive pulmonary disease: findings from a single-center primary care cohort

机译:茚达特罗治疗中度至重度慢性阻塞性肺疾病:单中心初级保健队列的研究结果

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Background: Once-daily long-acting β2-agonists (LABAs) are an important treatment option, either alone or in combination with other inhaled long-acting bronchodilators in the management of chronic obstructive pulmonary disease (COPD).Aims/objectives: To audit the effectiveness of indacaterol as maintenance therapy in patients with moderate-to-severe COPD (Global initiative for chronic Obstructive Lung Disease [GOLD] stage II/III).Methods: This was a single-center audit of a primary care COPD cohort comprising all patients treated with indacaterol following treatment escalation (as per National Institute for Health and Care Excellence guidelines) or failure with other therapies. The sample was restricted to patients treated for a minimum of 12 months with indacaterol, for whom preswitching and follow-up spirometry as well as exacerbation frequency data were available (GOLD spirometry guidelines). Pulmonary function was assessed by spirometry (recorded as forced expiratory volume in 1 second?[FEV1]?expressed as percentage predicted). Relevant self-reported qualitative information was recorded in descriptive terms for quality of life (QoL) assessment.Results: A total of 15 patients met the audit inclusion criteria (66.6% male, mean age 64.9±7.7 years). COPD disease duration ranged from 1 to 22 years; 93% had GOLD stage II or III COPD.?Follow-up ranged in duration from 12 to 27 months. Indacaterol was associated with a significant reduction in exacerbation frequency compared with the 12 months prior to initiation (P=0.02). In those patients who experienced three or more exacerbations/year, mean exacerbation rate fell from 5.43±1.07 to 2.43±0.2 after 12 months treatment with indacaterol (P=0.02). A reduction in dyspnea was noted in 53% of patients. Similarly, improvements in exercise tolerance and well-being were self-reported in 67% and 93%, respectively.Conclusion: Indacaterol was found to be an effective LABA as an escalation or switch medication in patients with moderate-to-severe COPD. Indacaterol was effective both as monotherapy and in combination with a long-acting muscarinic antagonist. Switching to indacaterol from a LABA/inhaled corticosteroid fixed-combination inhaler significantly reduced the number of acute exacerbations and also improved self-reported QoL.
机译:背景:每天一次的长效β2-激动剂(LABAs)是单独的治疗慢性阻塞性肺疾病(COPD)或与其他吸入的长效支气管扩张药联合使用的重要治疗选择。茚达特罗在中度至重度COPD(全球慢性阻塞性肺疾病[GOLD] II / III期全球倡议)患者中作为维持治疗的有效性。方法:这是对包括所有患者在内的初级保健COPD人群的单中心审核治疗升级(根据美国国立卫生研究院的指导原则)或其他治疗失败后,使用茚达特罗治疗的患者。该样本仅限于使用茚达特罗治疗至少12个月的患者,他们可获得转换前和随访肺量测定以及加重频率数据(GOLD肺量测定指南)。通过肺活量测定法评估肺功能(记录为在1秒内的强制呼气量?[FEV1]?以预测百分比表示)。以描述性的方式记录有关自我报告的定性信息,以评估生活质量(QoL)。结果:共有15例患者符合审核纳入标准(男性为66.6%,平均年龄为64.9±7.7岁)。 COPD病程为1到22年; 93%的患者患有黄金期II或III期COPD。随访时间为12到27个月。与开始前的12个月相比,茚达特罗使发作频率显着降低(P = 0.02)。在那些每年发作三次或以上的患者中,茚达特罗治疗12个月后,平均发作率从5.43±1.07降至2.43±0.2(P = 0.02)。观察到53%的患者呼吸困难减少。同样,自我报告的运动耐受性和幸福感改善分别为67%和93%。结论:茚达特罗被发现是有效的LABA,可作为中度至重度COPD患者的递增或转换用药。茚达特罗作为单一疗法和与长效毒蕈碱拮抗剂联合均有效。从LABA /吸入皮质类固醇固定组合吸入器改用茚达特罗可显着减少急性加重次数,并改善自我报告的QoL。

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