Department of Respiratory Medicine, School of Medicine, Toho University, 6-11-1 Omorinishi, Ota-ku, Tokyo 143-8541, Japan.
The Second Division, Department of Internal Medicine, Hamamatsu University School of Medicine, 1-20-1 Handayama, Higashi-ku, Hamamatsu-shi, Shizuoka 431-3192, Japan.
Respir Investig. 2022 Nov;60(6):798-805. doi: 10.1016/j.resinv.2022.07.004. Epub 2022 Sep 5.
Acute exacerbation is an essential prognostic factor in idiopathic pulmonary fibrosis (IPF) and is the leading cause of death in Japanese patients with IPF. Its epidemiology, treatment status, and effect on IPF progression have been insufficiently investigated. We examined the incidence of acute exacerbation and treatment status before and after the onset of acute exacerbation in Japanese patients with IPF to provide basic information for treatment strategies.
A Japanese claims database (April 2008-March 2019) from acute-care hospitals was analyzed. Incidence of acute exacerbation, time to the next event, and percentages of patients who received each treatment by the year before and after the onset of acute exacerbation were examined in patients diagnosed with IPF at least once. Acute exacerbation was defined according to the use of steroid pulse therapy.
We identified 9961 patients with IPF and 2629 acute exacerbations (average age at the time of acute exacerbation: 74.8 years, percentage of men: 79%). The annual incidence of acute exacerbation was approximately 10% between 2010 and 2018. The time to the next acute exacerbation shortened with increasing number of these events. The percentage of patients receiving antifibrotic drugs remained constant (30%-40%) throughout the period. The percentages of patients receiving steroid therapy, immunosuppressive drugs, and oxygen therapy increased after the onset of acute exacerbation compared with before the onset.
The annual incidence of acute exacerbation was approximately 10% in recent years. It is suggested that acute exacerbation worsens respiratory function in patients with IPF.
急性加重是特发性肺纤维化(IPF)的一个重要预后因素,也是导致日本 IPF 患者死亡的主要原因。其流行病学、治疗状况及其对 IPF 进展的影响尚未得到充分研究。我们研究了日本 IPF 患者急性加重的发生率和急性加重发作前后的治疗状况,为治疗策略提供了基础信息。
分析了来自急症医院的日本理赔数据库(2008 年 4 月至 2019 年 3 月)。在至少确诊过一次 IPF 的患者中,检查了急性加重发作前和发作后每年的急性加重发作发生率、下一次事件的时间以及接受每种治疗的患者比例。急性加重根据类固醇冲击疗法的使用情况进行定义。
我们共确定了 9961 例 IPF 患者和 2629 例急性加重(急性加重时的平均年龄为 74.8 岁,男性比例为 79%)。2010 年至 2018 年期间,急性加重的年发生率约为 10%。随着急性加重次数的增加,下一次急性加重的时间缩短。在整个研究期间,接受抗纤维化药物治疗的患者比例保持在 30%至 40%之间不变。与急性加重发作前相比,接受类固醇治疗、免疫抑制剂和氧疗的患者比例在急性加重发作后增加。
近年来,急性加重的年发生率约为 10%。提示急性加重可使 IPF 患者的呼吸功能恶化。