Malerba Mario, Radaeli Alessandro, Olivini Alessia, Ragnoli Beatrice, Ricciardolo Fabio, Montuschi Paolo
Department of Internal Medicine, University of Brescia, AOU Spedali Civili - Pzza Spedali Civili 1 - 25100 Brescia, Italy.
Curr Pharm Des. 2015;21(32):4752-62. doi: 10.2174/1871524915666150710123415.
Inhaled corticosteroids (ICS) treatment for asthma control is generally focused on lung function and symptoms, but inadequately correlated with airway inflammation.
To compare asthma control in a group of patients whose treatment was based on fraction of exhaled nitric oxide (FENO) and sputum eosinophils (intervention group) with a group in whom treatment was based on clinical score (control group). Study design and primary outcome: Randomized parallel-group longitudinal 24-month study including 5 visits every 6 months. A combination of asthma exacerbation rate and symptom score at 24 months was the primary outcome.
Fourteen patients with eosinophilic asthma per group were included.
In the intervention group, exacerbation rate/patient/year was reduced at 12 months (0.82) (-73%) and, to a greater extent at 24 months (0.5) (-84%) compared with baseline (3.21, p<0.01). In the control group, a significant reduction in exacerbation rate/patient/year was only observed between month 12 (3.0) and 24 (2.0, -33%, p<0.01). At 24 months, exacerbation rate was lower (-75%) in the intervention (0.5) than in the control group (2.0, p<0.05). Compared with baseline, mean symptom scores at 24 months were reduced in both groups (intervention group: -72%; control group: - 60%), but were lower in the intervention (8.1±1.0, p<0.05; -27%) than in the control group (11±2.6). ICS dose gradually increased in both groups throughout the study, with no between-group differences.
Compared with conventional strategy, longitudinal monitoring of FENO and sputum eosinophils improves eosinophilic asthma control in terms of reduced symptoms and exacerbations without additional increase e in ICS treatment.
吸入性糖皮质激素(ICS)用于哮喘控制的治疗通常侧重于肺功能和症状,但与气道炎症的相关性不足。
比较一组基于呼出一氧化氮分数(FENO)和痰液嗜酸性粒细胞进行治疗的患者(干预组)与一组基于临床评分进行治疗的患者(对照组)的哮喘控制情况。研究设计和主要结局:随机平行组纵向24个月研究,每6个月进行5次访视。24个月时哮喘加重率和症状评分的组合为主要结局。
每组纳入14例嗜酸性粒细胞性哮喘患者。
与基线(3.21,p<0.01)相比,干预组在12个月时(0.82)(-73%)患者/年加重率降低,在24个月时(0.5)(-84%)降低程度更大。在对照组中,仅在第12个月(3.0)至第24个月(2.0,-33%,p<0.01)观察到患者/年加重率有显著降低。在24个月时,干预组(0.5)的加重率低于对照组(2.0,p<0.05)(-75%)。与基线相比,两组在24个月时的平均症状评分均降低(干预组:-72%;对照组:-60%),但干预组(8.1±1.0,p<0.05;-27%)低于对照组(11±2.6)。在整个研究过程中,两组的ICS剂量均逐渐增加,组间无差异。
与传统策略相比,对FENO和痰液嗜酸性粒细胞进行纵向监测可改善嗜酸性粒细胞性哮喘的控制,表现为症状减轻和发作减少,且无需额外增加ICS治疗。