COPD Center, Department of Respiratory Medicine and Allergology, Sahlgrenska University Hospital, Gothenburg, Sweden.
Department of Internal Medicine and Clinical Nutrition and.
Am J Respir Crit Care Med. 2023 Jul 15;208(2):163-175. doi: 10.1164/rccm.202209-1774OC.
Risk stratification of patients according to chronic obstructive pulmonary disease severity is clinically important and forms the basis of therapeutic recommendations. No studies have examined the association for Global Initiative for Chronic Obstructive Lung Disease (GOLD) group A and group B patients with (A1 and B1, respectively) and without (A0 and B0, respectively) an exacerbation in the past year with future exacerbations, hospitalizations, and mortality in perspective with the new GOLD ABE classification. The aim was to examine the association between GOLD A0, A1, B0, B1, and E patients and future exacerbations, respiratory and cardiovascular hospitalizations, and mortality. In this nationwide cohort study, we identified patients with a diagnosis of chronic obstructive pulmonary disease, aged ⩾30 years, and registered in the Swedish National Airway Register between January 2017 and August 2020. Patients were stratified in GOLD groups A0, A1, B0, B1, and E and were followed until January 2021 for exacerbations, hospitalizations, and mortality in national registries. The 45,350 eligible patients included 25% A0, 4% A1, 44% B0, 10% B1, and 17% E. Moderate exacerbations, all-cause and respiratory hospitalizations, and all-cause and respiratory mortality increased by GOLD group A0-A1-B0-B1-E, except for moderate exacerbations, which were higher in A1 than in B0. Group B1 had a substantially higher hazard ratio for future exacerbation (2.56; 95% confidence interval [95% CI] 2.40-2.74), all-cause hospitalization (1.28; 1.21-1.35), and respiratory hospitalization (1.44; 1.27-1.62), but not all-cause (1.04; 0.91-1.18) or respiratory (1.13; 0.79-1.64) mortality than group B0. The exacerbation rate for group B1 was 0.6 events per patient-year versus 0.2 for group B0 (rate ratio, 2.55; 95% CI, 2.36-2.76). Results were similar for group A1 versus group A0. Stratification of GOLD A and B patients with one or no exacerbation in the past year provides valuable information on future risk, which should influence treatment recommendations for preventive strategies.
根据慢性阻塞性肺疾病(COPD)的严重程度对患者进行风险分层在临床上非常重要,也是治疗建议的基础。目前尚无研究探讨全球慢性阻塞性肺疾病倡议(GOLD)A 组和 B 组(分别为 A1 和 B1)患者与过去 1 年中有无加重(分别为 A0 和 B0)与未来加重、住院和死亡之间的关系,而新的 GOLD ABE 分类则从这一角度进行了观察。目的是探讨 GOLD A0、A1、B0、B1 和 E 患者与未来加重、呼吸和心血管住院和死亡之间的关系。在这项全国性队列研究中,我们纳入了年龄 ⩾30 岁、2017 年 1 月至 2020 年 8 月在瑞典国家气道登记处登记的 COPD 诊断患者。患者被分为 GOLD A0、A1、B0、B1 和 E 组,并在全国登记处随访至 2021 年 1 月,以了解加重、住院和死亡情况。45350 名符合条件的患者中,25%为 A0 组,4%为 A1 组,44%为 B0 组,10%为 B1 组,17%为 E 组。除了中度加重的情况外,其他所有指标,包括重度加重、全因和呼吸住院和死亡,均随 GOLD A0-A1-B0-B1-E 组增加,而中度加重的情况则是 A1 组高于 B0 组。B1 组未来加重(2.56;95%置信区间[95%CI] 2.40-2.74)、全因住院(1.28;1.21-1.35)和呼吸住院(1.44;1.27-1.62)的风险比显著升高,但全因(1.04;0.91-1.18)和呼吸(1.13;0.79-1.64)死亡率则与 B0 组无显著差异。B1 组的加重发生率为 0.6 例/患者年,而 B0 组为 0.2 例/患者年(发生率比,2.55;95%CI,2.36-2.76)。A1 组与 A0 组相比,结果相似。对过去 1 年中发生或未发生 1 次加重的 GOLD A 和 B 患者进行分层,可以提供有关未来风险的有价值信息,这应影响预防策略的治疗建议。