Mortensen Amber, Cherrier Lauren, Walia Rajat
1Department of Pharmacy, St. Joseph's Hospital and Medical Center, Phoenix, AZ USA.
2Division of Pulmonology, Norton Thoracic Institute, St. Joseph's Hospital and Medical Center, 500 W. Thomas Rd., Ste. 500, Phoenix, AZ USA.
Multidiscip Respir Med. 2018 Jun 14;13:16. doi: 10.1186/s40248-018-0129-4. eCollection 2018.
The drug pirfenidone has been shown to slow the progression and decrease mortality of idiopathic pulmonary fibrosis (IPF). Its exact mechanism is unknown, but it likely inhibits pro-fibrotic cytokine transforming growth factor beta, a known contributor to wound healing. We evaluated whether patients taking pirfenidone until lung transplantation had increased risk of impaired wound healing post-transplant. This information could determine whether pirfenidone should be discontinued prior to listing to allow for a wash-out period.
We retrospectively reviewed patients who underwent lung transplantation for pulmonary fibrosis at Norton Thoracic Institute in Phoenix, Arizona, from January 2014 to December 2015.
We describe 18 patients who took pirfenidone up to a month before transplant. Aside from one patient who experienced sternal dehiscence due to a surgical issue, all remaining patients did well with no evidence of airway dehiscence. Each of these 17 patients had been on pirfenidone for at least 30 days; nine patients had been on pirfenidone for over 90 days. Baseline characteristics including age, sex, body mass index, renal function, liver function, glucose level, pre-transplant corticosteroid use, and post-transplant immunosuppressant therapy were similar.
In our experience, pirfenidone may be safely continued until lung transplantation. Only one patient in our series experienced impaired wound healing related to a surgical issue, even when pirfenidone was continued until lung transplantation. We found no evidence of impaired wound healing or airway complications after lung transplantation in patients who were treated with pirfenidone before lung transplantation.
已证明药物吡非尼酮可减缓特发性肺纤维化(IPF)的进展并降低死亡率。其确切机制尚不清楚,但它可能抑制促纤维化细胞因子转化生长因子β,这是伤口愈合的一个已知促成因素。我们评估了在肺移植前服用吡非尼酮的患者移植后伤口愈合受损风险是否增加。这些信息可确定在列入移植名单之前是否应停用吡非尼酮以留出洗脱期。
我们回顾性分析了2014年1月至2015年12月在亚利桑那州凤凰城诺顿胸科研究所因肺纤维化接受肺移植的患者。
我们描述了18例在移植前一个月内服用吡非尼酮的患者。除了一名因手术问题出现胸骨裂开的患者外,其余所有患者情况良好,没有气道裂开的迹象。这17名患者每人服用吡非尼酮至少30天;9名患者服用吡非尼酮超过90天。包括年龄、性别、体重指数、肾功能、肝功能、血糖水平、移植前使用皮质类固醇以及移植后免疫抑制治疗在内的基线特征相似。
根据我们的经验,吡非尼酮可安全地持续服用至肺移植。在我们的系列研究中,即使吡非尼酮持续服用至肺移植,只有一名患者因手术问题出现伤口愈合受损。我们没有发现肺移植前接受吡非尼酮治疗的患者在肺移植后有伤口愈合受损或气道并发症的证据。