Fujiki Rei, Kawayama Tomotaka, Furukawa Kyoji, Kinoshita Takashi, Matsunaga Kazuko, Hoshino Tomoaki
Fujiki Medical and Surgical Clinic, Miyazaki, Japan.
Division of Respirology, Neurology, and Rheumatology, Department of Medicine, Kurume University School of Medicine, Kurume, Japan.
J Asthma Allergy. 2023 Feb 28;16:227-237. doi: 10.2147/JAA.S401505. eCollection 2023.
The efficacy and safety of first-line triple and dual therapy remain unclear because the stepwise strategy is a worldwide standard in controller-naïve asthma. A preliminary retrospective cohort study was conducted to investigate the efficacy and safety of first-line triple and dual therapy for managing controller-naïve and symptomatic adult patients with asthma.
Patients with asthma who received first-line single-inhaler triple therapy (SITT) or dual therapy (SIDT) for at least 8 weeks were selected between December 1, 2020, and May 31, 2021, in Fujiki Medical and Surgical Clinic, Miyazaki, Japan. Data on daytime and nighttime visual analog scale (VAS) scores, lung function tests, fractional exhaled nitrogen oxide (FNO), and adverse events were compared between SITT and SIDT pre- and post-treatment.
The SITT significantly improved the nighttime, but not daytime, VAS scores better than the SIDT 2 weeks post-treatment ( = 0.0026), whereas SITT and SIDT significantly improved daytime and nighttime VAS scores after treatment compared to baseline. Both therapies also significantly improved lung functions and FNO post-treatment. The proportion of patients achieving complete control in the nighttime VAS scores after SITT was significantly higher than that four ( = 0.0186) and 8 weeks ( = 0.0061) after SIDT. Only patients with SITT experienced dry mouth.
Our study demonstrated that first-line SITT and SIDT were effective, and SITT improved disease control faster than SIDT in controller-naïve and symptomatic adult patients with asthma. The first-line SITT may contribute to faster and better control levels in symptomatic patients with asthma.
由于阶梯式治疗策略是全球初治哮喘患者的标准治疗方法,一线三联和双联疗法的疗效和安全性仍不明确。本研究进行了一项初步回顾性队列研究,以探讨一线三联和双联疗法对初治且有症状的成年哮喘患者的疗效和安全性。
2020年12月1日至2021年5月31日期间,在日本宫崎县藤木内科外科诊所,选取接受一线单吸入器三联疗法(SITT)或双联疗法(SIDT)至少8周的哮喘患者。比较SITT组和SIDT组治疗前后的日间和夜间视觉模拟量表(VAS)评分、肺功能测试、呼出一氧化氮分数(FNO)及不良事件数据。
治疗2周后,SITT组夜间VAS评分改善显著优于SIDT组(P = 0.0026),但日间VAS评分改善不显著;与基线相比,SITT组和SIDT组治疗后日间和夜间VAS评分均显著改善。两种疗法治疗后肺功能和FNO也均显著改善。SITT组夜间VAS评分达到完全控制的患者比例显著高于SIDT组治疗4周(P = 0.0186)和8周(P = 0.0061)后。只有SITT组患者出现口干。
我们的研究表明,一线SITT和SIDT均有效,且在初治且有症状的成年哮喘患者中,SITT比SIDT能更快改善疾病控制。一线SITT可能有助于更快、更好地控制有症状的哮喘患者病情。