Sumi Toshiyuki, Uehara Hirofumi, Tada Makoto, Keira Yoshiko, Kamada Koki, Shijubou Naoki, Yamada Yuichi, Nakata Hisashi, Mori Yuji, Chiba Hirofumi
Department of Pulmonary Medicine Hakodate Goryoukaku Hospital Hakodate Japan.
Department of Respiratory Medicine and Allergology Sapporo Medical University School of Medicine Sapporo Japan.
Respirol Case Rep. 2021 Jan 27;9(3):e00716. doi: 10.1002/rcr2.716. eCollection 2021 Mar.
Interstitial lung disease (ILD) is a common complication of systemic sclerosis (SSc). Nintedanib, an antifibrotic drug, has recently been approved for treating SSc-ILD. Although there have been no reports suggesting the development of pneumothorax with nintedanib use, its safety in patients with impaired lung function is unclear. We observed the development of refractory spontaneous pneumothorax during nintedanib therapy in two patients with SSc-ILD and impaired lung function. Nintedanib use for SSc-ILD, an extensive disease, may therefore increase the risk of pneumothorax. In addition, pneumothorax is more likely to be refractory in these cases; initiation of nintedanib treatment and follow-up should be considered carefully.
间质性肺病(ILD)是系统性硬化症(SSc)的常见并发症。抗纤维化药物尼达尼布最近已被批准用于治疗系统性硬化症相关间质性肺病(SSc-ILD)。尽管尚无报告表明使用尼达尼布会导致气胸,但它在肺功能受损患者中的安全性尚不清楚。我们观察到两名肺功能受损的SSc-ILD患者在接受尼达尼布治疗期间发生了难治性自发性气胸。因此,对于广泛病变的SSc-ILD使用尼达尼布可能会增加气胸风险。此外,这些病例中的气胸更可能是难治性的;应谨慎考虑开始尼达尼布治疗及随访。