Rhodes Kirsty, Patel Deven, Duong My Linh, Haughney John, Make Barry J, Marshall Jonathan, Penz Erika, Santus Pierachille, Sethi Sanjay, Soler-Cataluña Juan Jose, Sotgiu Giovanni, Quint Jennifer K, Müllerová Hana, Vogelmeier Claus F, Nordon Clementine
Real World Science & Analytics, BioPharmaceuticals Medical, AstraZeneca, Cambridge, UK.
Respiratory Evidence Strategy, BioPharmaceuticals Medical, AstraZeneca, Gaithersburg, Maryland, USA.
BMJ Open. 2025 Jul 24;15(7):e097006. doi: 10.1136/bmjopen-2024-097006.
OBJECTIVES: Exacerbations of chronic obstructive pulmonary disease (COPD) can lead to reduced lung function and worse clinical outcomes. Previous studies have reported associations between severe exacerbations and increased risk of hospitalisation and/or mortality. This meta-analysis examined the impact of moderate exacerbations on the risk of future exacerbations and all-cause mortality. DESIGN: This meta-analysis included seven observational studies from the EXACOS (EXAcerbations of COPD and their OutcomeS)/AVOIDEX (Impact of AVOIDing EXacerbations of COPD) programme studies. DATA SOURCES: This meta-analysis used data from regional claims databases or electronic healthcare records from seven countries. ELIGIBILITY CRITERIA: The individual studies included patients with a diagnosis of COPD and ≥12 months of data availability before (regarded as baseline) and after the index (ie, the date of the first COPD diagnosis), with postindex data considered the follow-up period. DATA EXTRACTION AND SYNTHESIS: The number of COPD exacerbations experienced during the baseline period (ie, the exposure variable) was used to categorise patients into the following groups: no exacerbations, one moderate exacerbation only or two or more moderate/severe exacerbations. Outcomes assessed included risk of COPD exacerbations and all-cause mortality during follow-up as a function of baseline exacerbations. For meta-analyses, all rate ratios (RRs) were log-transformed, and associations were pooled across studies using random-effects meta-analysis models. RESULTS: Among 2 733 162 patients with COPD, one moderate exacerbation was significantly associated with a twofold increased risk of future exacerbations compared with having no exacerbations during baseline, with pooled RRs (95% CIs) of 2.47 (1.47 to 4.14) at 1 year, 2.49 (1.38 to 4.49) at 2 years and 2.38 (1.30 to 4.34) at 3 years postindex. The pooled RR (95% CI) for all-cause mortality was 1.30 (1.05 to 1.62), indicating a 30% increase in risk following one moderate exacerbation versus no exacerbations. CONCLUSIONS: Preventing moderate exacerbations in patients with COPD should be a priority that may improve patient trajectories and outcomes.
目的:慢性阻塞性肺疾病(COPD)急性加重可导致肺功能下降和更差的临床结局。既往研究报道了严重急性加重与住院和/或死亡风险增加之间的关联。本荟萃分析探讨了中度急性加重对未来急性加重风险和全因死亡率的影响。 设计:本荟萃分析纳入了EXACOS(COPD急性加重及其结局)/AVOIDEX(避免COPD急性加重的影响)项目研究中的7项观察性研究。 数据来源:本荟萃分析使用了来自7个国家的区域索赔数据库或电子医疗记录的数据。 纳入标准:个体研究纳入诊断为COPD且在索引(即首次COPD诊断日期)之前(视为基线)和之后有≥12个月可用数据的患者,索引后数据视为随访期。 数据提取与合成:使用基线期(即暴露变量)期间经历的COPD急性加重次数将患者分为以下几组:无急性加重、仅一次中度急性加重或两次或更多次中度/重度急性加重。评估的结局包括随访期间COPD急性加重风险和全因死亡率作为基线急性加重的函数。对于荟萃分析,所有率比(RRs)进行对数转换,并使用随机效应荟萃分析模型汇总各研究间的关联。 结果:在2733162例COPD患者中,与基线期无急性加重相比,一次中度急性加重与未来急性加重风险增加两倍显著相关,索引后1年、2年和3年的汇总RR(95%CI)分别为2.47(1.47至4.14)、2.49(1.38至4.49)和2.38(1.30至4.34)。全因死亡率的汇总RR(95%CI)为1.30(1.05至1.62),表明一次中度急性加重与无急性加重相比风险增加30%。 结论:预防COPD患者的中度急性加重应成为改善患者病程和结局的优先事项。
Cochrane Database Syst Rev. 2017-8-4
Cochrane Database Syst Rev. 2022-11-14
Cochrane Database Syst Rev. 2016-12-8
Cochrane Database Syst Rev. 2016-12-19
Cochrane Database Syst Rev. 2012-9-12
Cochrane Database Syst Rev. 2024-9-27
Cochrane Database Syst Rev. 2021-1-15
Cochrane Database Syst Rev. 2012-12-12
Cochrane Database Syst Rev. 2021-7-20
Int J Chron Obstruct Pulmon Dis. 2024
Int J Chron Obstruct Pulmon Dis. 2023
Int J Chron Obstruct Pulmon Dis. 2023
Int J Chron Obstruct Pulmon Dis. 2022
Int J Chron Obstruct Pulmon Dis. 2022