Department of Respiratory Medicine, Zhongda Hospital, Southeast University, Nanjing, Jiangsu, China (mainland).
Department of Respiratory Medicine, Jurong Hospital Affiliated to Jiangsu University, Zhenjiang, Jiangsu, China (mainland).
Med Sci Monit. 2018 Feb 15;24:944-950. doi: 10.12659/msm.907950.
BACKGROUND The aim of this study was to evaluate the therapeutic effects of tiotropium bromide on asthma. MATERIAL AND METHODS A total of 160 patients with moderate persistent asthma were randomly divided into 4 groups (n=40): the 3 control groups were given fluticasone propionate aerosol (group A), salmeterol-fluticasone propionate inhalant (group B), and tiotropium bromide inhalation powder combined with salmeterol-fluticasone propionate inhalant (group C), respectively, and the experimental group received tiotropium bromide inhalation powder combined with fluticasone propionate aerosol (group D) and salbutamol was used to relieve symptoms when necessary. RESULTS After 8 weeks of treatment, the pulmonary function of group D, which was significantly better than those of group A (P<0.05), was similar to those of groups B and C (P>0.05). Group D had significantly better asthma control test scores and nighttime symptom scores than in group A (P<0.05), without significant differences from those of group B or group C (P>0.05). The number of times salbutamol was used to alleviate symptoms was significantly different (P<0.05) between group D and group A (P<0.05), as well as between group C and group D (P<0.05). Groups D and B had similar results (P>0.05). IL-13 levels in induced sputum had significant differences (P<0.05). The levels in group D, which were higher than those of groups A and B (P<0.05), were similar to those of group C (P>0.05). CONCLUSIONS Tiotropium bromide combined with fluticasone propionate improved the respiratory function and quality of life, and is a new therapy for moderate, persistent asthma.
本研究旨在评估噻托溴铵对哮喘的治疗效果。
将 160 例中度持续哮喘患者随机分为 4 组(n=40):丙酸氟替卡松气雾剂组(A 组)、沙美特罗氟替卡松吸入剂组(B 组)、噻托溴铵粉吸入剂联合沙美特罗氟替卡松吸入剂组(C 组)和噻托溴铵粉吸入剂联合丙酸氟替卡松气雾剂组(D 组),必要时沙丁胺醇缓解症状。
治疗 8 周后,D 组患者肺功能明显优于 A 组(P<0.05),与 B 组、C 组相似(P>0.05)。D 组哮喘控制测试评分和夜间症状评分明显优于 A 组(P<0.05),与 B 组、C 组无明显差异(P>0.05)。D 组缓解症状沙丁胺醇使用次数明显少于 A 组(P<0.05),D 组与 C 组(P<0.05)也有差异。D 组和 B 组结果相似(P>0.05)。诱导痰中白细胞介素 13 水平有显著差异(P<0.05)。D 组高于 A 组和 B 组(P<0.05),与 C 组相似(P>0.05)。
噻托溴铵联合丙酸氟替卡松可改善呼吸功能和生活质量,是一种治疗中度持续性哮喘的新方法。