Akiyama Shoko, Oda Kenji, Mizohata Hiroko, Sasakura Natsuki, Hashimoto Kenichi, Maruoka Hiroki
Real World Data Analytics, Japan Development, GSK, Tokyo 107-0052, Japan.
Global Real-World Evidence & Health Outcomes Research Japan, GSK, Tokyo 107-0052, Japan.
J Clin Med. 2025 Jul 2;14(13):4697. doi: 10.3390/jcm14134697.
Due to limited current evidence, this post-marketing database surveillance study aimed to investigate the occurrence of hospitalization due to community-acquired pneumonia (CAP) among patients with chronic obstructive pulmonary disease in Japan who received single-inhaler triple therapy (fluticasone furoate/umeclidinium/vilanterol; FF/UMEC/VI) or multiple-inhaler triple therapy (MITT). This retrospective cohort study used health insurance claims data from the Medical Data Vision Co., Ltd. database (November 2017-April 2023) to identify overall and incident users of FF/UMEC/VI or MITT. Index date was the start of FF/UMEC/VI or MITT. Hazard ratios (HRs) for CAP hospitalization were assessed using inverse probability of treatment weighting based on propensity scores (PS). Incidence rates and time to occurrence of CAP hospitalization were also assessed. Adjustments were made to the PS model to address missing body mass index data. : In total, 8790 and 10,881 patients were included in the overall FF/UMEC/VI and MITT cohorts, and 3939 and 4017 patients were included in the incident FF/UMEC/VI and MITT cohorts, respectively. HR for CAP hospitalization among incident users ranged from 1.05 to 1.15 across all PS adjustments. Similar incidence rates of CAP hospitalization were reported among both cohorts and across all PS adjustments. The cumulative adjusted incidence rates of first CAP hospitalization at 360 days post-index among incident users was 0.060 and 0.054 in the FF/UMEC/VI and MITT cohorts, respectively. : There was no difference in the risk of CAP between patients treated with FF/UMEC/VI and MITT. This safety information may help healthcare providers select appropriate treatments.
由于目前证据有限,这项上市后数据库监测研究旨在调查在日本接受单吸入器三联疗法(糠酸氟替卡松/乌美溴铵/维兰特罗;FF/UMEC/VI)或多吸入器三联疗法(MITT)的慢性阻塞性肺疾病患者中,社区获得性肺炎(CAP)导致住院的发生率。这项回顾性队列研究使用了Medical Data Vision Co., Ltd.数据库(2017年11月 - 2023年4月)中的医疗保险理赔数据,以确定FF/UMEC/VI或MITT的总体使用者和新使用者。索引日期为FF/UMEC/VI或MITT治疗开始日期。基于倾向评分(PS)使用治疗加权的逆概率评估CAP住院的风险比(HRs)。还评估了CAP住院的发生率和发生时间。对PS模型进行了调整以处理缺失的体重指数数据。:在FF/UMEC/VI和MITT总体队列中分别纳入了8790例和10881例患者,在FF/UMEC/VI和MITT新使用者队列中分别纳入了3939例和4017例患者。在所有PS调整中,新使用者中CAP住院的HR范围为1.05至1.15。两个队列以及所有PS调整中报告的CAP住院发生率相似。在索引日期后360天,FF/UMEC/VI和MITT新使用者队列中首次CAP住院的累积调整发生率分别为0.060和0.054。:接受FF/UMEC/VI和MITT治疗的患者之间CAP风险没有差异。该安全性信息可能有助于医疗保健提供者选择合适的治疗方法。