Division of Pulmonary and Critical Care, University of Michigan, Ann Arbor, MI, USA.
Lancet Respir Med. 2013 Mar;1(1):43-50. doi: 10.1016/S2213-2600(12)70044-9. Epub 2012 Sep 3.
The 2011 GOLD (Global Strategy for the Diagnosis, Management, and Prevention of Chronic Obstructive Pulmonary Disease [COPD]) consensus report uses symptoms, exacerbation history, and forced expiratory volume (FEV1)% to categorise patients according to disease severity and guide treatment. We aimed to assess both the influence of symptom instrument choice on patient category assignment and prospective exacerbation risk by category.
Patients were recruited from 21 centres in the USA, as part of the COPDGene study. Eligible patients were aged 45-80 years, had smoked for 10 pack-years or more, and had an FEV1/forced vital capacity (FVC) <0·7. Categories were defined with the modified Medical Research Council (mMRC) dyspnoea scale (score 0-1 vs ≥2) and the St George's Respiratory Questionnaire (SGRQ; ≥25 vs <25 as a surrogate for the COPD Assessment Test [CAT] ≥10 vs <10) in addition to COPD exacerbations in the previous year (<2 vs ≥ 2), and lung function (FEV1% predicted ≥50 vs <50). Statistical comparisons were done with k-sample permutation tests. This study cohort is registered with ClinicalTrials.gov, number NCT00608764.
4484 patients with COPD were included in this analysis. Category assignment using the mMRC scale versus SGRQ were similar but not identical. On the basis of the mMRC scale, 1507 (33·6%) patients were assigned to category A, 919 (20·5%) to category B, 355 (7·9%) to category C, and 1703 (38·0%) to category D; on the basis of the SGRQ, 1317 (29·4%) patients were assigned to category A, 1109 (24·7%) to category B, 221 (4·9%) to category C, and 1837 (41·0%) to category D (κ coefficient for agreement, 0·77). Significant heterogeneity in prospective exacerbation rates (exacerbations/person-years) were seen, especially in the D subcategories, depending on the risk factor that determined category assignment (lung function only [0·89, 95% CI 0·78-1·00]), previous exacerbation history only [1·34, 1·0-1·6], or both [1·86, 1·6-2·1; p<0·0001]).
The GOLD classification emphasises the importance of symptoms and exacerbation risk when assessing COPD severity. The choice of symptom measure influences category assignment. The relative number of patients with low symptoms and high risk for exacerbations (category C) is low. Differences in exacerbation rates for patients in the highest risk category D were seen depending on whether risk was based on lung function, exacerbation history, or both.
National Heart, Lung, and Blood Institute, and the COPD Foundation through contributions from AstraZeneca, Boehringer Ingelheim, Novartis, and Sepracor.
2011 年 GOLD(慢性阻塞性肺疾病全球策略 [COPD] 的诊断、管理和预防)共识报告使用症状、加重史和用力呼气量(FEV1)%来根据疾病严重程度对患者进行分类,并指导治疗。我们旨在评估症状工具选择对患者类别分配的影响,以及按类别评估未来的加重风险。
在美国 21 个中心招募了符合条件的患者,作为 COPDGene 研究的一部分。合格的患者年龄在 45-80 岁之间,吸烟 10 包年或以上,FEV1/用力肺活量(FVC)<0.7。类别定义为改良的医学研究理事会(mMRC)呼吸困难量表(评分 0-1 与≥2)和圣乔治呼吸问卷(SGRQ;≥25 与<25 作为 COPD 评估测试 [CAT]≥10 与<10 的替代),加上过去一年的 COPD 加重(<2 与≥2)和肺功能(FEV1%预测值≥50 与<50)。使用 k-样本置换检验进行统计比较。这项研究队列在 ClinicalTrials.gov 注册,编号为 NCT00608764。
共有 4484 名 COPD 患者纳入本分析。使用 mMRC 量表与 SGRQ 量表进行分类的结果相似但不完全相同。基于 mMRC 量表,1507(33.6%)名患者被分配到 A 类,919(20.5%)名到 B 类,355(7.9%)名到 C 类,1703(38.0%)名到 D 类;基于 SGRQ,1317(29.4%)名患者被分配到 A 类,1109(24.7%)名到 B 类,221(4.9%)名到 C 类,1837(41.0%)名到 D 类(κ 一致性系数,0.77)。根据决定类别的危险因素(仅肺功能[0.89,95%CI 0.78-1.00]),在未来加重率(加重/人年)方面观察到显著的异质性,特别是在 D 亚组中,既往加重史[1.34,1.0-1.6]或两者[1.86,1.6-2.1;p<0.0001]。
GOLD 分类强调在评估 COPD 严重程度时要考虑症状和加重风险。症状测量工具的选择会影响类别分配。低症状和高加重风险(C 类)患者的相对数量较低。对于处于最高风险类别 D 的患者,根据风险是基于肺功能、加重史还是两者来确定,其加重率的差异是明显的。
美国国立心肺血液研究所和 COPD 基金会,通过 AstraZeneca、Boehringer Ingelheim、Novartis 和 Sepracor 的捐款。