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- W2762556400 abstract "Idiopathic pulmonary fibrosis is a rare condition that affects individuals aged 60 to 70. The underlying cause of the disorder is unknown. The main symptoms are dyspnoea and cough. Auscultation of the lungs reveals early inspiratory crackles. Diagnosis is made by high-resolution computed tomography. The evolution is progressive and variable, the average survival after diagnosis being 2-3 years. Although there is no specific treatment, various different treatments seem to improve the survival. Late diagnosis is the main issue because it limits the benefits of an early treatment. The solutions are to raise the awareness of family doctors, educate patients, strengthen the support provided by the health system, and adapt legislation to improve the accessibility of patients to appropriate diagnostic and treatment." @default.
- W2762556400 created "2017-10-20" @default.
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- W2762556400 date "2017-09-18" @default.
- W2762556400 modified "2023-09-26" @default.
- W2762556400 title "Fibroza pulmonară idiopatică" @default.
- W2762556400 hasPublicationYear "2017" @default.
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