Division of Pulmonary, Critical Care, and Sleep Medicine, Department of Medicine, University of Washington, Seattle, WA.
Division of Pulmonary, Critical Care, and Sleep Medicine, Department of Medicine, University of Washington, Seattle, WA; Health Services Research & Development Center of Innovation for Veteran-centered and Value-driven Care, VA Puget Sound Healthcare System, Seattle, WA.
Chest. 2020 Aug;158(2):529-538. doi: 10.1016/j.chest.2020.02.073. Epub 2020 Apr 9.
Although inhaled therapy reduces exacerbations among patients with COPD, the effectiveness of providing inhaled treatment per risk stratification models remains unclear.
Are inhaled regimens that align with the 2017 Global Initiative for Chronic Obstructive Lung Disease (GOLD) strategy associated with clinically important outcomes?
We conducted secondary analyses of Long-term Oxygen Treatment Trial (LOTT) data. The trial enrolled patients with COPD with moderate resting or exertional hypoxemia between 2009 and 2015. Our exposure was the patient-reported inhaled regimen at enrollment, categorized as either aligning with, undertreating, or potentially overtreating per the 2017 GOLD strategy. Our primary composite outcome was time to death or first hospitalization for COPD. Additional outcomes included individual components of the composite outcome and time to first exacerbation. We generated multivariable Cox proportional hazard models across strata of GOLD-predicted exacerbation risk (high vs low) to estimate between-group hazard ratios for time to event outcomes. We adjusted models a priori for potential confounders, clustered by site.
The trial enrolled 738 patients (73.4% men; mean age, 68.8 years). Of the patients, 571 (77.4%) were low risk for future exacerbations. Of the patients, 233 (31.6%) reported regimens aligning with GOLD recommendations; most regimens (54.1%) potentially overtreated. During a 2.3-year median follow-up, 332 patients (44.9%) experienced the composite outcome. We found no difference in time to composite outcome or death among patients reporting regimens aligning with recommendations compared with undertreated patients. Among patients at low risk, potential overtreatment was associated with higher exacerbation risk (hazard ratio, 1.42; 95% CI, 1.09-1.87), whereas inhaled corticosteroid treatment was associated with 64% higher risk of pneumonia (incidence rate ratio, 1.64; 95% CI, 1.01-2.66).
Among patients with COPD with moderate hypoxemia, we found no difference in clinical outcomes between inhaled regimens aligning with the 2017 GOLD strategy compared with those that were undertreated. These findings suggest the need to reevaluate the effectiveness of risk stratification model-based inhaled treatment strategies.
尽管吸入疗法可减少 COPD 患者的恶化,但根据风险分层模型提供吸入治疗的效果仍不清楚。
与 2017 年全球慢性阻塞性肺疾病倡议 (GOLD) 策略一致的吸入方案是否与临床重要结局相关?
我们对长期氧疗试验 (LOTT) 数据进行了二次分析。该试验招募了 2009 年至 2015 年间患有中度静息或运动性低氧血症的 COPD 患者。我们的暴露因素是患者在入组时报告的吸入方案,根据 2017 年 GOLD 策略分为与方案一致、治疗不足或潜在过度治疗。我们的主要复合结局是死亡或首次因 COPD 住院的时间。其他结局包括复合结局的单个组成部分和首次恶化的时间。我们根据 GOLD 预测的恶化风险(高 vs 低)生成了多变量 Cox 比例风险模型,以估计事件时间结局的组间风险比。我们预先根据地点进行了模型调整,以对潜在混杂因素进行分层。
该试验共纳入 738 名患者(73.4%为男性;平均年龄 68.8 岁)。其中 571 名(77.4%)患者未来恶化的风险较低。其中 233 名(31.6%)患者报告的方案与 GOLD 建议一致;大多数方案(54.1%)潜在过度治疗。在中位随访 2.3 年期间,332 名患者(44.9%)发生了复合结局。我们发现,与治疗不足的患者相比,报告与建议一致的方案的患者在复合结局或死亡时间方面没有差异。在低风险患者中,潜在过度治疗与更高的恶化风险相关(风险比,1.42;95%CI,1.09-1.87),而吸入皮质类固醇治疗与肺炎风险增加 64%相关(发病率比,1.64;95%CI,1.01-2.66)。
在患有中度低氧血症的 COPD 患者中,我们发现与 2017 年 GOLD 策略一致的吸入方案与治疗不足的方案相比,临床结局没有差异。这些发现表明需要重新评估基于风险分层模型的吸入治疗策略的有效性。