European Respiratory Journal · 2020 · 18 citations · 8 references
MedicineGeriatric MedicineAgingPulmonologyTransplant SurgeryAge-related Chronic DiseaseFibrosisInterstitial Lung DiseaseLung TransplantationTransplant OutcomesTransplant SurvivalBiologic Antifibrotic AgentsLung Disease ProgressionMedian AgeProgressive Pulmonary FibrosisPulmonary Fibrosis ProgressionRespiratory Failure PrognosisSingle Lung TransplantationSurvival Benefit Assessment
Idiopathic pulmonary fibrosis (IPF) is a chronic lung disease that results in progressive respiratory failure and death. Antifibrotic therapy has been shown to slow disease progression [1, 2]. For many patients [3], lung transplantation is the only intervention recognised to provide significant survival benefit [4]. IPF commonly affects older patients, with a median age at diagnosis of 66 years old [5]. Without transplantation, the median survival from diagnosis is 2–4 years [5]. However, registry data indicates impaired outcomes following lung transplantation for older patients 6]. These data have prompted many centres in Europe to avoid offering transplantation to older IPF patients. This study demonstrates a clinically meaningful survival benefit of lung transplantation for IPF patients aged ≥65 years <http://bit.ly/39pwH2h>
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Efficacy and Safety of Nintedanib in Idiopathic Pulmonary Fibrosis
Luca Richeldi, Roland M. du Bois, Ganesh Raghu et al. · New England Journal of Medicine · 2014 · 4.6K citations · Full text
Joseph W. Rossano, Wida S. Cherikh, Daniel C. Chambers et al. · The Journal of Heart and Lung Transplantation · 2018 · 638 citations
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Roger D. Yusen, Jason D. Christie, Leah B. Edwards et al. · The Journal of Heart and Lung Transplantation · 2013 · 507 citations · Full text
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Daniel C. Chambers, Wida S. Cherikh, Samuel Goldfarb et al. · The Journal of Heart and Lung Transplantation · 2018 · 496 citations
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