| Literature DB >> 25857869 |
Geert M Verleden1,2, Robin Vos1,2, Bart Vanaudenaerde1, Lieven Dupont1,2, Jonas Yserbyt2, Dirk Van Raemdonck3, Stijn Verleden1.
Abstract
Chronic lung allograft dysfunction (CLAD) was recently introduced as an overarching term mainly to classify patients with chronic rejection after lung transplantation, although other conditions may also qualify for CLAD. Initially, only the development of a persistent and obstructive pulmonary function defect, clinically identified as bronchiolitis obliterans syndrome (BOS), was considered as chronic rejection, if no other cause could be identified. It became clear in recent years that some patients do not qualify for this definition, although they developed a chronic and persistent decrease in FEV1 , without another identifiable cause. As the pulmonary function decline in these patients was rather restrictive, this was called restrictive allograft syndrome (RAS). In the present review, we will further elaborate on these two CLAD phenotypes, with specific attention to the diagnostic criteria, the role of pathology and imaging, the risk factors, outcome, and the possible treatment options.Entities:
Keywords: azithromycin-responsive allograft dysfunction; bronchiolitis obliterans syndrome; chronic lung allograft dysfunction; chronic rejection; lung transplantation; restrictive allograft syndrome
Mesh:
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Year: 2015 PMID: 25857869 DOI: 10.1111/tri.12579
Source DB: PubMed Journal: Transpl Int ISSN: 0934-0874 Impact factor: 3.782