Effect of antifibrotic agents on postoperative complications after lung transplantation for idiopathic pulmonary fibrosis

Author:

Moncomble Elsa1,Weisenburger Gaelle1,Picard Clément2,Dégot Tristan3,Reynaud‐Gaubert Martine4,Nieves Ana4,Mornex Jean François56,Dauriat Gaelle7,Messika Jonathan1,Godet Cendrine1,Hirschi Sandrine3,Le Pavec Jérôme7,Borie Raphael8ORCID,Mordant Pierre9,Lortat‐Jacob Brice10,Mal Hervé1ORCID,Bunel Vincent1

Affiliation:

1. Service de Pneumologie B et Transplantation pulmonaire Hôpital Bichat, APHP Nord‐Université Paris Cité Paris France

2. Service de Pneumologie Hôpital Foch Suresnes France

3. Service de Pneumologie Nouvel Hôpital Civil Strasbourg France

4. Service de Pneumologie—Maladies Pulmonaires Rares—Centre de Transplantation Pulmonaire Hôpital Nord Marseille France

5. Hospices Civils de Lyon Lyon France

6. Université de Lyon Université Lyon 1 Lyon France

7. Service de Transplantation, Chirurgie Thoracique et Vasculaire Hôpital Marie Lannelongue Le Plessis Robinson France

8. Service de Pneumologie A Hôpital Bichat Paris France

9. Service de Chirurgie Thoracique Hôpital Bichat Paris France

10. Service de Réanimation Chirurgicale Hôpital Bichat Paris France

Abstract

AbstractBackgroundAntifibrotic 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).MethodsWe 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.ResultsAmong 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).ConclusionsAFA 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.

Publisher

Wiley

Subject

Pulmonary and Respiratory Medicine

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