Urushiyama Hirokazu, Jo Taisuke, Hasegawa Wakae, Yokoyama Akira, Ando Takahiro, Sakamoto Yukiyo, Kumazawa Ryosuke, Uda Kazuaki, Michihata Nobuaki, Awano Nobuyasu, Hiroki Matsui, Fushimi Kiyohide, Yasunaga Hideo, Nagase Takahide
Department of Respiratory Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Department of Health Services Research, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
ERJ Open Res. 2022 Nov 28;8(4). doi: 10.1183/23120541.00209-2022. eCollection 2022 Oct.
Acute exacerbation is a life-threatening event in patients with fibrosing interstitial lung diseases (ILDs). Although nintedanib reduces acute exacerbation incidence, its effectiveness during acute exacerbation is unclear.
Using data from the Diagnosis Procedure Combination database (September 2015-March 2020) in Japan, we identified patients with fibrosing ILDs who received intravenous injection of high-dose corticosteroid within 3 days post-admission and analysed their first hospitalisation. We performed overlap propensity score weighting to compare in-hospital outcomes between patients who received nintedanib within 14 days post-admission and those who did not. The primary and secondary outcomes were in-hospital mortality and length of hospitalisation in the patients discharged alive, respectively.
Among the 6235 identified patients, 353 patients received nintedanib within 14 days post-admission. In-hospital mortality occurred in 13.7% and 6.0% patients in the control (n=5882) and nintedanib-treated (n=353) patients, respectively. The mean length of hospitalisation was 39.9 and 30.4 days in the control and nintedanib-treated patients, respectively. After overlap propensity score weighting, nintedanib treatment was significantly associated with lower in-hospital mortality in the adjusted cohort (OR 0.43, 95% CI 0.27-0.70; p=0.001). The mean length of hospitalisation in nintedanib-treated patients (30.7 days) was significantly shorter than that in the control group (37.5 days; p<0.001).
Nintedanib initiation during acute exacerbation was significantly associated with a lower risk of in-hospital death and shorter length of hospitalisation in patients with fibrosing ILDs. Our results elucidate the potential role of nintedanib in the treatment of acute exacerbation in patients with fibrosing ILDs. Further prospective studies are warranted.
急性加重是纤维化间质性肺疾病(ILDs)患者的一种危及生命的事件。尽管尼达尼布可降低急性加重的发生率,但其在急性加重期间的有效性尚不清楚。
利用日本诊断程序组合数据库(2015年9月至2020年3月)的数据,我们确定了在入院后3天内接受静脉注射大剂量皮质类固醇的纤维化ILDs患者,并分析了他们的首次住院情况。我们进行了重叠倾向评分加权,以比较入院后14天内接受尼达尼布治疗的患者与未接受治疗的患者的住院结局。主要和次要结局分别是住院死亡率和存活出院患者的住院时间。
在6235名确定的患者中,353名患者在入院后14天内接受了尼达尼布治疗。对照组(n = 5882)和尼达尼布治疗组(n = 353)的住院死亡率分别为13.7%和6.0%。对照组和尼达尼布治疗组的平均住院时间分别为39.9天和30.4天。经过重叠倾向评分加权后,在调整后的队列中,尼达尼布治疗与较低的住院死亡率显著相关(OR 0.43,95%CI 0.27 - 0.70;p = 0.001)。尼达尼布治疗组的平均住院时间(30.7天)显著短于对照组(37.5天;p < 0.001)。
在急性加重期间开始使用尼达尼布与纤维化ILDs患者较低的住院死亡风险和较短的住院时间显著相关。我们的结果阐明了尼达尼布在纤维化ILDs患者急性加重治疗中的潜在作用。有必要进行进一步的前瞻性研究。