| Literature DB >> 31636088 |
Davide Elia1, Antonella Caminati2, Maurizio Zompatori3,4, Roberto Cassandro1, Chiara Lonati5, Francesca Luisi1, Giuseppe Pelosi6, Steeve Provencher7, Sergio Harari1,5.
Abstract
Pulmonary hypertension related to chronic lung disease, mainly represented by COPD and idiopathic pulmonary fibrosis, is associated with a worse outcome when compared with patients only affected by parenchymal lung disease. At present, no therapies are available to reverse or slow down the pathological process of this condition and most of the clinical trials conducted to date have had no clinically significant impact. Nevertheless, the importance of chronic lung diseases is always more widely recognised and, along with its increasing incidence, associated pulmonary hypertension is also expected to be growing in frequency and as a health burden worldwide. Therefore, it is desirable to develop useful and reliable tools to obtain an early diagnosis and to monitor and follow-up this condition, while new insights in the therapeutic approach are explored.Entities:
Mesh:
Year: 2019 PMID: 31636088 DOI: 10.1183/16000617.0065-2019
Source DB: PubMed Journal: Eur Respir Rev ISSN: 0905-9180