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GOLD 2017 治疗路径:DACCORD 观察性研究分析。

GOLD 2017 treatment pathways in 'real life': An analysis of the DACCORD observational study.

机构信息

Facharztforum Fürth, 90762 Fürth, Germany.

Pulmonary Department, Mainz University Hospital, 55131 Mainz, Germany.

出版信息

Respir Med. 2017 Oct;131:77-84. doi: 10.1016/j.rmed.2017.08.008. Epub 2017 Aug 9.

Abstract

INTRODUCTION

The 2017 update to the Global Initiative for Obstructive Lung Disease (GOLD) strategy document includes recommendations for treatment intensification or step-down in chronic obstructive pulmonary disease (COPD), although recognises that limited supporting information is available. DACCORD is an ongoing observational, non-interventional study, recruiting patients following COPD maintenance treatment change or initiation, a subset of whom were receiving a long-acting β-agonist (LABA) plus a long-acting muscarinic antagonist (LAMA) fixed-dose combination (FDC) on entry. Since there were no requirements in terms of prior medication (and no washout before commencing LABA/LAMA FDC), this provides an opportunity to generate 'real world' data to test the GOLD 2017 recommendations.

METHODS

To reduce heterogeneity, the current analyses include patients receiving indacaterol/glycopyrronium at baseline, and who, prior to the study, were receiving no COPD maintenance medication ('none'), LABA or LAMA monotherapy ('mono'), LABA plus inhaled corticosteroid (ICS; 'LABA/ICS'), or triple therapy ('triple'). At the baseline visit, data collected included: demographic and disease characteristics; COPD Assessment Test (CAT); and exacerbations in the 6 months prior to entry. At 3, 6, 9 and 12 months data on exacerbations were collected, with CAT recorded at 3 and 12 months.

RESULTS

A total of 2724 patients were included in the baseline analyses: 795, 954, 598 and 377 in the 'none', 'mono', 'LABA/ICS' and 'triple' subgroups, respectively. There were no clinically relevant differences in baseline demographics between the four groups. In terms of disease characteristics, the 'triple' group had the highest proportion of patients with a disease duration of more than 1 year since diagnosis and with severe/very severe airflow limitation, but a similar percentage of non-exacerbators compared to the 'none' group. Over the 1-year follow-up, the majority of patients in all four subgroups did not exacerbate (exacerbation rates 0.16, 0.19, 0.21, and 0.26 in the 'none', 'mono', 'LABA/ICS' and 'triple' groups, respectively). At 12 months, 61.4%, 65.0%, 71.0% and 52.4% of patients had a clinically relevant improvement in CAT score.

CONCLUSIONS

Overall, the results support the GOLD recommendations in suggesting that a switch from a mono-bronchodilator or LABA plus ICS to LABA/LAMA FDC is a valid treatment option for patients with COPD. The results also validate the use of a LABA/LAMA FDC as initial maintenance treatment for COPD, and provide first 'real world' evidence to support the newly added 'step down' recommendation (from triple to LABA/LAMA FDC).

摘要

简介

2017 年全球阻塞性肺病倡议(GOLD)策略文件的更新包括慢性阻塞性肺疾病(COPD)治疗强化或降级的建议,尽管认识到可用的支持信息有限。DACCORD 是一项正在进行的观察性、非干预性研究,招募 COPD 维持治疗改变或开始后的患者,其中一部分患者在进入时正在接受长效β-激动剂(LABA)加长效毒蕈碱拮抗剂(LAMA)固定剂量联合(FDC)。由于没有关于先前药物的要求(在开始 LABA/LAMA FDC 之前没有洗脱期),因此这为生成“真实世界”数据以检验 GOLD 2017 年建议提供了机会。

方法

为了降低异质性,目前的分析包括基线时接受茚达特罗/格隆溴铵的患者,并且在研究之前,他们没有接受 COPD 维持治疗(“无”)、LABA 或 LAMA 单药治疗(“单药”)、LABA 加吸入皮质类固醇(ICS;“LABA/ICS”)或三联疗法(“三联”)。在基线访视时,收集的数据包括:人口统计学和疾病特征;COPD 评估测试(CAT);以及进入前 6 个月的加重情况。在 3、6、9 和 12 个月时收集了加重的数据,并在 3 和 12 个月时记录了 CAT。

结果

共有 2724 名患者纳入基线分析:无、单药、LABA/ICS 和三联亚组分别为 795、954、598 和 377 例。四组之间在基线人口统计学方面没有临床相关差异。在疾病特征方面,三联组中疾病诊断后超过 1 年且有严重/非常严重气流受限的患者比例最高,但与无组相比,非加重者的比例相似。在 1 年随访期间,所有四个亚组中的大多数患者都没有加重(无、单药、LABA/ICS 和三联组的加重率分别为 0.16、0.19、0.21 和 0.26)。在 12 个月时,61.4%、65.0%、71.0%和 52.4%的患者 CAT 评分有临床相关改善。

结论

总体而言,结果支持 GOLD 建议,即从单支气管扩张剂或 LABA 加 ICS 转换为 LABA/LAMA FDC 是 COPD 患者的有效治疗选择。结果还验证了 LABA/LAMA FDC 作为 COPD 的初始维持治疗,并且提供了第一个“真实世界”证据支持新添加的“降级”建议(从三联到 LABA/LAMA FDC)。

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