Outcomes of patients with COPD switching from multiple-inhaler to once-daily single-inhaler triple therapy in a real-world primary care setting in England: a retrospective pre-post cohort study.

IF 3.6 3区 医学 Q1 RESPIRATORY SYSTEM
Kieran J Rothnie, Robert P Wood, Alexandrosz Czira, Victoria L Banks, Lucinda J Camidge, Olivia K I Massey, Monica Seif, Chris Compton, Raj Sharma, David M G Halpin, Afisi S Ismaila, Claus F Vogelmeier
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引用次数: 0

Abstract

Background: Compared with multiple-inhaler triple therapy (MITT), single-inhaler triple therapy (SITT) with fluticasone furoate/umeclidinium/vilanterol (FF/UMEC/VI) demonstrated improved lung function and meaningful improvements in chronic obstructive pulmonary disease (COPD) Assessment Test score. This real-world study compared the effectiveness of switching patients with COPD in England from MITT to once-daily SITT with FF/UMEC/VI by evaluating rates of COPD exacerbation, healthcare resource use (HCRU) and associated direct medical costs.

Methods: Retrospective cohort pre-post study using linked primary care electronic health record and secondary care administrative datasets. Patients diagnosed with COPD at age ≥35 years, with smoking history, linkage to secondary care data and continuous GP registration for 12 months pre-switch and 6 months post-switch to FF/UMEC/VI were included. Index date was the first initiation of an FF/UMEC/VI prescription immediately following MITT use from 15 November 2017 to 30 September 2019. Baseline was 12 months prior to index, with outcomes assessed 6/12 months pre-switch and post-switch, and stratified by prior COPD exacerbation status.

Results: We included 2533 patients (mean [SD] age: 71.1 [9.9] years; 52.1% male). In the 6 months post-switch, there were significant decreases in the proportion of patients experiencing ≥1 moderate-to-severe (36.2%-28.9%), moderate only (24.4%-19.8%) and severe only (15.4%-11.8%) COPD exacerbation (each, p<0.0001) compared with the 6 months pre-switch. As demonstrated by rate ratios, there were significant reductions in exacerbation rates of each severity overall (p<0.01) and among patients with prior exacerbations (p<0.0001). In the same period, there were significant decreases in the rate of each COPD-related HCRU and total COPD-related costs (-24.9%; p<0.0001).

Conclusion: Patients with COPD switching from MITT to once-daily SITT with FF/UMEC/VI in a primary care setting had significantly fewer moderate and severe exacerbations, and lower COPD-related HCRU and costs, in the 6 months post-switch compared with the 6 months pre-switch.

英国基层医疗机构中慢性阻塞性肺病患者从多次吸入改为每日一次单次吸入三联疗法的疗效:一项前后回顾性队列研究。
背景:与多吸入器三联疗法(MITT)相比,使用糠酸氟替卡松/优甲乐/维兰特罗(FF/UMEC/VI)的单吸入器三联疗法(SITT)可改善肺功能,并显著提高慢性阻塞性肺病(COPD)评估测试得分。这项真实世界研究通过评估慢性阻塞性肺病加重率、医疗资源使用率(HCRU)和相关直接医疗成本,比较了英国慢性阻塞性肺病患者从MITT转为每日一次SITT使用FF/UMEC/VI的效果:使用关联的初级保健电子健康记录和二级保健行政数据集进行回顾性队列前后研究。纳入的慢性阻塞性肺病患者年龄≥35岁,有吸烟史,与二级医疗数据有关联,在转为FF/UMEC/VI前的12个月和转为FF/UMEC/VI后的6个月内连续进行全科医生登记。指数日期为 2017 年 11 月 15 日至 2019 年 9 月 30 日期间使用 MITT 后立即首次开具 FF/UMEC/VI 处方的日期。基线为指数前 12 个月,评估结果为切换前 6/12 个月和切换后 6/12 个月,并根据之前的慢性阻塞性肺疾病加重状态进行分层:我们纳入了 2533 名患者(平均 [SD] 年龄:71.1 [9.9] 岁;52.1% 为男性)。在转换后的 6 个月中,经历过≥1 次中度至重度(36.2%-28.9%)、仅中度(24.4%-19.8%)和仅重度(15.4%-11.8%)慢性阻塞性肺疾病加重的患者比例均有显著下降(每种情况的 p 均为 0.1):在初级医疗机构中,慢性阻塞性肺病患者从 MITT 转为使用 FF/UMEC/VI 的每日一次 SITT 后,与转换前 6 个月相比,转换后 6 个月的中度和重度病情加重明显减少,与慢性阻塞性肺病相关的 HCRU 和费用也明显降低。
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来源期刊
BMJ Open Respiratory Research
BMJ Open Respiratory Research RESPIRATORY SYSTEM-
CiteScore
6.60
自引率
2.40%
发文量
95
审稿时长
12 weeks
期刊介绍: BMJ Open Respiratory Research is a peer-reviewed, open access journal publishing respiratory and critical care medicine. It is the sister journal to Thorax and co-owned by the British Thoracic Society and BMJ. The journal focuses on robustness of methodology and scientific rigour with less emphasis on novelty or perceived impact. BMJ Open Respiratory Research operates a rapid review process, with continuous publication online, ensuring timely, up-to-date research is available worldwide. The journal publishes review articles and all research study types: Basic science including laboratory based experiments and animal models, Pilot studies or proof of concept, Observational studies, Study protocols, Registries, Clinical trials from phase I to multicentre randomised clinical trials, Systematic reviews and meta-analyses.
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