• Presse Med · Jun 2020

    Review

    [Lung Transplantation for Idiopathic Pulmonary Fibrosis].

    • Jérôme Le Pavec, Gaëlle Dauriat, Pierre Gazengel, Samuel Dolidon, Amir Hanna, Séverine Feuillet, Pauline Pradere, Adrian Crutu, Valentina Florea, David Boulate, Delphine Mitilian, Dominique Fabre, Sacha Mussot, Olaf Mercier, and Elie Fadel.
    • Service de chirurgie thoracique, vasculaire et transplantation cardio-pulmonaire, hôpital Marie-Lannelongue, Le Plessis-Robinson, France; Faculté de médecine, université Paris-Sud, université Paris-Saclay, Le Kremlin Bicêtre, France; UMR_S 999, Inserm, université Paris-Sud, hôpital Marie-Lannelongue, Le Plessis-Robinson, France. Electronic address: lepavec@gmail.com.
    • Presse Med. 2020 Jun 1; 49 (2): 104026.

    AbstractIdiopathic pulmonary fibrosis (IPF) is characterized by relentlessly progressive lung function impairment that is consistently fatal in the absence of lung transplantation, as no curative pharmacological treatment exists. The pace of progression varies across patients, and acute life-threatening exacerbations occur unpredictably, causing further sharp drops in lung function. Recently introduced antifibrotic agents slow the pace of disease progression and may improve survival but fail to stop the fibrotic process. Moreover, the magnitude and kinetics of the response to these drugs cannot be predicted in the individual patient. These characteristics require that lung transplantation be considered early in the course of the disease. However, given the shortage of donor lungs, lung transplantation must be carefully targeted to those patients most likely to benefit. Current guidelines for lung transplantation listing may need reappraisal in the light of recent treatment advances. Patients with IPF often have multiple comorbidities such as coronary heart disease, frailty, and gastro-oesophageal reflux disease (GERD). Consequently, extensive screening for and effective treatment of concomitant conditions is crucial to appropriate candidate selection and outcome optimisation. A multidisciplinary approach is mandatory. Pulmonologists with expertise in IPF must work closely with lung transplant teams. Careful consideration must be given to preoperative optimisation, surgical technique, and pulmonary rehabilitation to produce the best post-transplantation outcomes.Copyright © 2020 Elsevier Masson SAS. All rights reserved.

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