Requena Gema, Wood Robert, Ito Risako, Wild Rosie, Mita Chifuku, Payne Poppy, Mukai Isao, Castillo Catherine M, Gelwicks Steven, Siddiqui Rad, Noorduyn Stephen G, Oga Toru
Value Evidence and Outcomes, GSK, Brentford, Middlesex, UK.
Real-world Evidence, Adelphi Real World, Bollington, Cheshire, UK.
J Asthma. 2025 Feb;62(2):216-225. doi: 10.1080/02770903.2024.2394152. Epub 2024 Aug 30.
In Japan, the optimal initiation timing and efficacy of single-inhaler triple therapy (SITT) in asthma management remain unexplored. This study investigated SITT initiation timing following an asthma exacerbation, and examined patient demographics and clinical characteristics.
Observational, retrospective cohort study in patients with asthma aged ≥15 years who initiated SITT following their earliest observed asthma exacerbation (February-November 2021), using data from Japanese health insurance claims databases (JMDC and Medical Data Vision [MDV]). The study period ended May 2022 for JMDC and September 2022 for MDV. Descriptive analyses were performed independently by database. Variables evaluated included timing of SITT initiation post exacerbation (prompt, delayed and late, ≤30, 31-180 and >180 days post index, respectively), patient demographics, clinical characteristics, and pre-index treatment.
Of patients in the JMDC and MDV databases, most initiated SITT promptly after an asthma exacerbation, 60.8% ( = 951/1565) and 44.4% ( = 241/543), respectively. Delayed initiation occurred in 22.6% ( = 354/1565) and 26.3% ( = 143/543) of patients, and late initiation occurred in 16.6% ( = 260/1565) and 29.3% ( = 159/543), respectively. Most patients were indexed on a moderate asthma-related exacerbation, 97.1% ( = 1519/1565) and 68.7% ( = 373/543), respectively.
Most patients with asthma initiated SITT promptly following a moderate exacerbation, with delayed and late initiation more common among patients with complex clinical profiles. The findings underscore the necessity for future research to examine the interaction between patient characteristics, clinical outcomes, and the timing of SITT initiation to optimize treatment strategies, as clinical practice may vary by exacerbation severity.
在日本,单吸入器三联疗法(SITT)在哮喘管理中的最佳起始时机和疗效仍未得到探索。本研究调查了哮喘急性加重后SITT的起始时机,并分析了患者的人口统计学特征和临床特征。
对年龄≥15岁、在最早观察到的哮喘急性加重(2021年2月至11月)后开始使用SITT的哮喘患者进行观察性、回顾性队列研究,数据来自日本医疗保险理赔数据库(JMDC和医疗数据视野[MDV])。JMDC的研究期于2022年5月结束,MDV的研究期于2022年9月结束。各数据库独立进行描述性分析。评估的变量包括急性加重后SITT起始的时间(及时、延迟和晚期,分别为指数日后≤30天、31 - 180天和>180天)、患者人口统计学特征、临床特征以及指数前治疗。
在JMDC和MDV数据库的患者中,大多数在哮喘急性加重后及时开始使用SITT,分别为60.8%(n = 951/1565)和44.4%(n = 241/543)。22.6%(n = 354/1565)和26.3%(n = 143/543)的患者起始延迟,16.6%(n = 260/1565)和29.3%(n = 159/543)的患者起始较晚。大多数患者因中度哮喘相关急性加重被纳入研究,分别为97.1%(n = 1519/1565)和68.7%(n = 373/543)。
大多数哮喘患者在中度急性加重后及时开始使用SITT,临床情况复杂的患者中起始延迟和较晚的情况更为常见。研究结果强调了未来研究的必要性,即研究患者特征、临床结局与SITT起始时间之间的相互作用,以优化治疗策略,因为临床实践可能因急性加重的严重程度而异。