Frequency of exacerbations in patients with chronic obstructive pulmonary disease: an analysis of the SPIROMICS cohort

被引:216
|
作者
Han, MeiLan K. [1 ]
Quibrera, Pedro M. [2 ]
Carretta, Elizabeth E. [2 ]
Barr, R. Graham [3 ]
Bleecker, Eugene R. [4 ]
Bowler, Russell P. [5 ]
Cooper, Christopher B. [6 ]
Comellas, Alejandro [7 ]
Couper, David J. [2 ]
Curtis, Jeffrey L. [1 ,8 ]
Criner, Gerard [9 ]
Dransfield, Mark T. [10 ]
Hansel, Nadia N. [11 ]
Hoffman, Eric A. [12 ]
Kanner, Richard E. [13 ]
Krishnan, Jerry A. [14 ]
Martinez, Carlos H. [1 ]
Pirozzi, Cheryl B. [13 ]
O'Neal, Wanda K. [2 ]
Rennard, Stephen [15 ,16 ]
Tashkin, Donald P. [6 ]
Wedzicha, Jadwiga A. [17 ]
Woodruff, Prescott [18 ]
Paine, Robert, III [13 ,19 ]
Martinez, Fernando J. [20 ]
机构
[1] Michigan Med, Div Pulm & Crit Care, Ann Arbor, MI 48103 USA
[2] Univ N Carolina, Dept Biostat, Chapel Hill, NC USA
[3] Columbia Univ, Dept Med, New York, NY USA
[4] Wake Forest Univ, Ctr Genom & Personalized Med Res, Dept Med, Winston Salem, NC 27109 USA
[5] Natl Jewish, Div Pulm & Crit Care, Denver, CO USA
[6] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Los Angeles, CA 90095 USA
[7] Univ Iowa, Div Pulm & Crit Care, Iowa City, IA USA
[8] VA Ann Arbor Healthcare Syst, Sect Pulm & Crit Care Med, Med Serv, Ann Arbor, MI USA
[9] Temple Univ, Dept Thorac Med, Philadelphia, PA 19122 USA
[10] Univ Alabama Birmingham, Div Pulm & Crit Care, Birmingham, AL USA
[11] Johns Hopkins Sch Med, Div Pulm & Crit Care Med, Dept Med, Baltimore, MD USA
[12] Univ Iowa, Dept Radiol, Carver Coll Med, Iowa City, IA 52242 USA
[13] Univ Utah, Sch Med, Dept Med, Div Resp Crit Care & Occupat Pulm Med, Salt Lake City, UT USA
[14] Univ Illinois, Div Pulm & Crit Care, Chicago, IL USA
[15] Univ Nebraska, Med Ctr, Dept Med, Omaha, NE 68182 USA
[16] AstraZeneca, Early Clin Dev, Cambridge, England
[17] Imperial Coll, Dept Resp Med, London, England
[18] Univ Calif San Francisco, Div Pulm & Crit Care Med, Dept Med, Cardiovasc Res Inst, San Francisco, CA 94143 USA
[19] Vet Affairs Med Ctr, Salt Lake City Dept, Sect Pulm & Crit Care Med, Salt Lake City, UT 84148 USA
[20] Weill Cornell Med Coll, Dept Med, Div Pulm & Crit Care Med, New York, NY USA
来源
LANCET RESPIRATORY MEDICINE | 2017年 / 5卷 / 08期
关键词
COMPUTED-TOMOGRAPHY; COPD; DECLINE;
D O I
10.1016/S2213-2600(17)30207-2
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Background Present treatment strategies to stratify exacerbation risk in patients with chronic obstructive pulmonary disease (COPD) rely on a history of two or more events in the previous year. We aimed to understand year to year variability in exacerbations and factors associated with consistent exacerbations over time. Methods In this longitudinal, prospective analysis of exacerbations in the Subpopulations and Intermediate Outcome Measures in COPD Study (SPIROMICS) cohort, we analysed patients aged 40-80 years with COPD for whom 3 years of prospective data were available, identified through various means including care at academic and non-academic medical centres, word of mouth, and existing patient registries. Participants were enrolled in the study between Nov 12, 2010, and July 31, 2015. We classified patients according to yearly exacerbation frequency: no exacerbations in any year; one exacerbation in every year during 3 years of follow-up; and those with inconsistent exacerbations (individuals who had both years with exacerbations and years without during the 3 years of follow-up). Participants were characterised by the Global Initiative for Chronic Obstructive Lung Disease (GOLD) spirometric category (1-4) on the basis of post-bronchodilator FEV1. Stepwise logistic regression was used to compare factors associated with one or more acute exacerbations of COPD every year for 3 years versus no exacerbations in the same timeframe. Additionally, a stepwise zero-inflated negative binomial model was used to assess predictors of exacerbation count during follow-up in all patients with available data. Baseline symptom burden was assessed with the COPD assessment test. This trial is registered with ClinicalTrials.gov, number NCT01969344. Findings 2981 patients were enrolled during the study. 1843 patients had COPD, of which 1105 patients had 3 years of complete, prospective follow-up data. 538 (49%) of 1105 patients had at least one acute exacerbation during the 3 years of follow-up, whereas 567 (51%) had none. 82 (7%) of 1105 patients had at least one acute exacerbation each year, whereas only 23 (2%) had two or more acute exacerbations in each year. An inconsistent pattern (both years with and without acute exacerbations) was common (456 [41%] of the group), particularly among GOLD stages 3 and 4 patients (256 [56%] of 456). In logistic regression, consistent acute exacerbations (>= 1 event per year for 3 years) were associated with higher baseline symptom burden, previous exacerbations, greater evidence of small airway abnormality on CT, lower interleukin-15 concentrations, and higher interleukin-8 concentrations, than were no acute exacerbations. Interpretation Although acute exacerbations are common, the exacerbation status of most individuals varies markedly from year to year. Among patients who had any acute exacerbation over 3 years, very few repeatedly had two or more events per year. In addition to symptoms and history of exacerbations in the year before study enrolment, we identified several novel biomarkers associated with consistent exacerbations, including CT-defined small airway abnormality, and interleukin-15 and interleukin-8 concentrations.
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收藏
页码:619 / 626
页数:8
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