Service de Pneumologie B et Transplantation pulmonaire, Hôpital Bichat, APHP Nord-Université Paris Cité, Paris, France.
Service de Pneumologie, Hôpital Foch, Suresnes, France.
Respirology. 2024 Jan;29(1):71-79. doi: 10.1111/resp.14605. Epub 2023 Oct 3.
Antifibrotic agents (AFAs) are now standard-of-care for idiopathic pulmonary fibrosis (IPF). Concerns have arisen about the safety of these drugs in patients undergoing lung transplantation (LTx).
We performed a multi-centre, nationwide, retrospective, observational study of French IPF patients undergoing LTx between 2011 and 2018 to determine whether maintaining AFAs in the peri-operative period leads to increased bronchial anastomoses issues, delay in skin healing and haemorrhagic complications. We compared the incidence of post-operative complications and the survival of patients according to AFA exposure.
Among 205 patients who underwent LTx for IPF during the study period, 58 (28%) had received AFAs within 4 weeks before LTx (AFA group): pirfenidone in 37 (18.0%) and nintedanib in 21 (10.2%). The median duration of AFA treatment before LTx was 13.8 (5.6-24) months. The AFA and control groups did not significantly differ in airway, bleeding or skin healing complications (p = 0.91, p = 0.12 and p = 0.70, respectively). Primary graft dysfunction was less frequent in the AFA than control group (26% vs. 43%, p = 0.02), and the 90-day mortality was lower (7% vs. 18%, p = 0.046).
AFA therapy did not increase airway, bleeding or wound post-operative complications after LTx and could be associated with reduced rates of primary graft dysfunction and 90-day mortality.
抗纤维化药物(AFAs)现在是特发性肺纤维化(IPF)的标准治疗方法。人们对这些药物在接受肺移植(LTx)的患者中的安全性产生了担忧。
我们进行了一项多中心、全国性、回顾性、观察性研究,纳入了 2011 年至 2018 年期间接受 LTx 的法国 IPF 患者,以确定围手术期维持 AFAs 是否会导致支气管吻合口问题增加、皮肤愈合延迟和出血并发症。我们根据 AFA 暴露情况比较了术后并发症的发生率和患者的生存率。
在研究期间,205 例因 IPF 接受 LTx 的患者中,有 58 例(28%)在 LTx 前 4 周内接受了 AFAs(AFA 组):吡非尼酮 37 例(18.0%),尼达尼布 21 例(10.2%)。LTx 前 AFA 治疗的中位持续时间为 13.8(5.6-24)个月。AFA 组和对照组在气道、出血或皮肤愈合并发症方面无显著差异(p=0.91,p=0.12 和 p=0.70)。AFA 组原发性移植物功能障碍的发生率低于对照组(26% vs. 43%,p=0.02),90 天死亡率也较低(7% vs. 18%,p=0.046)。
LTx 后 AFA 治疗并未增加气道、出血或伤口术后并发症,并且可能与原发性移植物功能障碍和 90 天死亡率降低相关。