AI Article Synopsis
- * While there are new antifibrotic drugs that can slow the disease, their effects on the quality of life for patients still need further research.
- * Palliative care has been shown to improve symptoms, quality of life, and end-of-life care for IPF patients, suggesting that it should be integrated early into treatment plans starting from diagnosis.
Article Abstract
Idiopathic pulmonary fibrosis (IPF) is a chronic disease with an unknown etiology that causes deterioration of the structure of the lung parenchyma, resulting in a severe and progressive decline in respiratory function and early mortality. IPF is essentially an incurable disease, with a mean overall survival of 5 years in approximately 20% of patients without treatment. The combination of a poor prognosis, uncertainty about the disease's progression, and the severity of symptoms has a significant impact on the quality of life of patients and their families. New antifibrotic drugs have been shown to slow disease progression, but their impact on health-related quality of life (HRQoL) has to be proven yet. To date, studies have shown that palliative care can improve symptom management, HRQoL, and end-of-life care (EoL) in patients with IPF, reducing critical events, hospitalization, and health costs. As a result, it is essential for proper health planning and patient management to establish palliative care early and in conjunction with other therapies, beginning with the initial diagnosis of the disease.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9994447 | PMC |
| http://dx.doi.org/10.4081/mrm.2023.896 | DOI Listing |
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