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预测 COPD 患者再加重时间和深入了解慢性阻塞性肺疾病急性加重持续时间长的原因:一项 ECLIPSE 队列研究。

Predicting Re-Exacerbation Timing and Understanding Prolonged Exacerbations: An Analysis of Patients with COPD in the ECLIPSE Cohort.

机构信息

GlaxoSmithKline plc., Epidemiology - Value, Evidence and Outcomes, Middlesex, UK.

GlaxoSmithKline plc., Research and Development, Middlesex, UK.

出版信息

Int J Chron Obstruct Pulmon Dis. 2021 Feb 5;16:225-244. doi: 10.2147/COPD.S279315. eCollection 2021.

DOI:10.2147/COPD.S279315
PMID:33574663
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7872897/
Abstract

PURPOSE

Understanding risk factors for an acute exacerbation of chronic obstructive pulmonary disease (AECOPD) is important for optimizing patient care. We re-analyzed data from the Evaluation of COPD Longitudinally to Identify Predictive Surrogate Endpoints (ECLIPSE) study (NCT00292552) to identify factors predictive of re-exacerbations and associated with prolonged AECOPDs.

METHODS

Patients with COPD from ECLIPSE with moderate/severe AECOPDs were included. The end of the first exacerbation was the index date. Timing of re-exacerbation risk was assessed in patients with 180 days' post-index-date follow-up data. Factors predictive of early (1-90 days) vs late (91-180 days) vs no re-exacerbation were identified using a multivariable partial-proportional-odds-predictive model. Explanatory logistic-regression modeling identified factors associated with prolonged AECOPDs.

RESULTS

Of the 1,554 eligible patients from ECLIPSE, 1,420 had 180 days' follow-up data: more patients experienced early (30.9%) than late (18.7%) re-exacerbations; 50.4% had no re-exacerbation within 180 days. Lower post-bronchodilator FEV (=0.0019), a higher number of moderate/severe exacerbations on/before index date (<0.0001), higher St. George's Respiratory Questionnaire total score (=0.0036), and season of index exacerbation (autumn vs winter, =0.00164) were identified as predictors of early (vs late/none) re-exacerbation risk within 180 days. Similarly, these were all predictors of any (vs none) re-exacerbation risk within 180 days. Median moderate/severe AECOPD duration was 12 days; 22.7% of patients experienced a prolonged AECOPD. The odds of experiencing a prolonged AECOPD were greater for severe vs moderate AECOPDs (adjusted odds ratio=1.917, =0.002) and lower for spring vs winter AECOPDs (adjusted odds ratio=0.578, =0.017).

CONCLUSION

Prior exacerbation history, reduced lung function, poorer respiratory-related quality-of-life (greater disease burden), and season may help identify patients who will re-exacerbate within 90 days of an AECOPD. Severe AECOPDs and winter AECOPDs are likely to be prolonged and may require close monitoring.

摘要

目的

了解慢性阻塞性肺疾病(COPD)急性加重(AECOPD)的危险因素对于优化患者治疗非常重要。我们重新分析了来自评估 COPD 纵向以识别预测替代终点(ECLIPSE)研究(NCT00292552)的数据,以确定预测复发的因素,并与延长的 AECOPD 相关。

方法

纳入 ECLIPSE 中具有中/重度 AECOPD 的 COPD 患者。首次加重的结束日期为索引日期。在具有 180 天索引日期后随访数据的患者中评估再加重的风险时间。使用多变量部分比例优势预测模型确定预测早期(1-90 天)与晚期(91-180 天)与无再加重的因素。解释性逻辑回归模型确定与延长的 AECOPD 相关的因素。

结果

来自 ECLIPSE 的 1554 名合格患者中,有 1420 名患者有 180 天的随访数据:更多患者经历早期(30.9%)而非晚期(18.7%)再加重;50.4%在 180 天内无再加重。支气管扩张剂后 FEV 较低(=0.0019),索引日期前(<0.0001)有更多的中/重度加重,圣乔治呼吸问卷总分较高(=0.0036),以及索引加重的季节(秋季与冬季,=0.00164)均被确定为 180 天内早期(与晚期/无)再加重风险的预测因素。同样,这些都是 180 天内任何(与无)再加重风险的预测因素。中/重度 AECOPD 持续时间的中位数为 12 天;22.7%的患者经历了延长的 AECOPD。严重 AECOPD 比中度 AECOPD 发生延长 AECOPD 的可能性更大(调整后的优势比=1.917,=0.002),而春季比冬季 AECOPD 发生延长 AECOPD 的可能性更小(调整后的优势比=0.578,=0.017)。

结论

既往加重史、肺功能下降、更差的呼吸相关生活质量(疾病负担更大)和季节可能有助于识别在 AECOPD 后 90 天内再次加重的患者。严重的 AECOPD 和冬季的 AECOPD 可能会延长,需要密切监测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7872897/cfecd030193c/COPD-16-225-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7872897/852279179e83/COPD-16-225-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7872897/fce1d4633819/COPD-16-225-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7872897/816a2f41fa9f/COPD-16-225-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7872897/cb90e25bb101/COPD-16-225-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7872897/cfecd030193c/COPD-16-225-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7872897/852279179e83/COPD-16-225-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7872897/fce1d4633819/COPD-16-225-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7872897/816a2f41fa9f/COPD-16-225-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7872897/cb90e25bb101/COPD-16-225-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a723/7872897/cfecd030193c/COPD-16-225-g0005.jpg

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