Department of Respiratory and Critical Care Medicine, First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Scottish Centre for Respiratory Medicine, University of Dundee, Dundee, United Kingdom.
Am J Respir Crit Care Med. 2020 Jun 15;201(12):1499-1507. doi: 10.1164/rccm.201910-1972OC.
Bronchiectasis guidelines regard treatment to prevent exacerbation and treatment of daily symptoms as separate objectives. We hypothesized that patients with greater symptoms would be at higher risk of exacerbations and therefore that a treatment aimed at reducing daily symptoms would also reduce exacerbations in highly symptomatic patients. Our study comprised an observational cohort of 333 patients from the East of Scotland (2012-2016). Either symptoms were modeled as a continuous variable or patients were classified as having high, moderate, or low symptom burden (>70, 40-70, and <40 using the St. George's Respiratory Questionnaire symptom score). The hypothesis that exacerbation reductions would only be evident in highly symptomatic patients was tested in a analysis of a randomized trial of inhaled dry powder mannitol ( = 461 patients). In the observational cohort, daily symptoms were a significant predictor of future exacerbations (rate ratio [RR], 1.10; 95% confidence interval [CI], 1.03-1.17; = 0.005). Patients with higher symptom scores had higher exacerbation rates (RR, 1.74; 95% CI, 1.12-2.72; = 0.01) over 12-month follow-up than those with lower symptoms. Inhaled mannitol treatment improved the time to first exacerbation (hazard ratio, 0.56; 95% CI, 0.40-0.77; < 0.001), and the proportion of patients remaining exacerbation free for 12 months of treatment was higher in the mannitol group (32.7% vs. 14.6%; RR, 2.84; 95% CI, 1.40-5.76; = 0.003), but only in highly symptomatic patients. In contrast, no benefit was evident in patients with lower symptom burden. Highly symptomatic patients have increased risk of exacerbations, and exacerbation benefit with inhaled mannitol was only evident in patients with high symptom burden.
支气管扩张症指南将预防加重和治疗日常症状视为两个独立的目标。我们假设症状更严重的患者发生加重的风险更高,因此,旨在减轻日常症状的治疗也会降低高症状负担患者的加重风险。我们的研究包括了来自苏格兰东部的 333 名患者的观察性队列(2012-2016 年)。要么将症状建模为连续变量,要么将患者分为高、中或低症状负担(使用圣乔治呼吸问卷症状评分,>70、40-70 和 <40)。在一项吸入干粉甘露醇的随机试验( = 461 名患者)的分析中,检验了只有高症状负担患者才会出现加重减少的假设。在观察性队列中,日常症状是未来加重的显著预测因素(风险比 [RR],1.10;95%置信区间 [CI],1.03-1.17; = 0.005)。在 12 个月的随访中,高症状评分的患者比低症状评分的患者有更高的加重率(RR,1.74;95% CI,1.12-2.72; = 0.01)。吸入甘露醇治疗改善了首次加重的时间(风险比,0.56;95% CI,0.40-0.77; < 0.001),并且甘露醇组在治疗 12 个月时无加重的患者比例更高(32.7%比 14.6%;RR,2.84;95% CI,1.40-5.76; = 0.003),但仅在高症状负担的患者中。相比之下,低症状负担的患者没有获益的迹象。高症状负担的患者加重风险增加,吸入甘露醇的加重获益仅在高症状负担的患者中显现。