Impact of ILD-Specific Therapies on Perioperative Course in Patients with Progressive Interstitial Lung Disease Undergoing Lung Transplantation

Author:

Munker Dieter1,Arnold Paola1,Leuschner Gabriela1,Irlbeck Michael2,Michel Sebastian3,Kauke Teresa4,Meiser Bruno5,Behr Jürgen1,Kneidinger Nikolaus1ORCID,Veit Tobias1ORCID

Affiliation:

1. Department of Medicine V, University Hospital LMU Munich, Comprehensive Pneumology Center (CPC-M), Member of the German Center for Lung Research (DZL), 81377 Munich, Germany

2. Department of Anaesthesiology, University of Munich (LMU), 81377 Munich, Germany

3. Clinic of Cardiac Surgery, University of Munich (LMU), 81377 Munich, Germany

4. Department of Thoracic Surgery, University of Munich (LMU), 81377 Munich, Germany

5. Transplant Center, University of Munich, 81377 Munich, Germany

Abstract

Immunosuppressants and antifibrotics are currently used to treat patients with various interstitial lung diseases, which may undergo lung transplantation (LTx). The retrospective study aimed to evaluate the potential effects of therapeutic regimen on the perioperative course in patients with idiopathic pulmonary fibrosis (IPF) or progressive pulmonary fibrosis (PPF) undergoing LTx. All patients with IPF and PPF undergoing LTx between January 2014 and December 2021 were included. We retrospectively screened for previous use of immunosuppressants and antifibrotic therapy. We analyzed perioperative courses, short-term outcomes, and safety retrospectively. In total, 286 patients with diagnosis of IPF or PPF were analyzed. According to the treatment regimen before LTx, the study cohort was divided into four groups and compared. No differences between antifibrotic monotherapy, combined antifibrotic and immunosuppressive therapy with regard to postoperative complications were observed. Length of mechanical ventilation was shorter in patients with antifibrotics prior to LTx. Pretreatment with antifibrotic monotherapy and a combination of antifibrotic drugs with immunosuppressive therapy, lower body mass index (BMI) and lower blood loss, were independently associated with primary graft dysfunction grades 0–3 72 hours after LTx (p < 0.001). Finally, patients with antifibrotic monotherapy developed significantly less de novo donor-specific antibodies (DSA) (p = 0.009). Higher intraoperative blood loss, etiology of interstitial lung disease (ILD) and older age were independently associated with shorter survival after LTx. Use of antifibrotic monotherapy and a combination of antifibrotic drugs with immunosuppressive therapy in IPF/PPF patients undergoing LTx, proved to be safe and might lead to beneficial effects after LTx.

Funder

Actelion

Astra-Zeneca

Biogen

BMS

Boehringer-Ingelheim

Ferrer

Galapagos

Novartis

Roche

Sanofi-Genzyme

Publisher

MDPI AG

Subject

General Medicine

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Optimizing the prelung transplant candidate;Current Opinion in Organ Transplantation;2023-11-07

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