Quality of life in patients with hypersensitivity pneumonitis and with idiopathic pulmonary fibrosis in real-life clinical practice
Patients with fHP, especially with UIP pattern, exhibit similar clinical features and functional decline as seen in IPF patients. Cough severity, dyspnea, and exercise capacity were the strongest predictors of reduced HRQL, highlighting the need for comprehensive symptom assessment and individualized management in both IPF and HP. K-BILD and EQ-5D-5L are reliable tools for assessing HRQL and identifying significant clinical and functional factors.
Authors
- С. Н. Авдеев (ORCID: https://orcid.org/0000-0002-5999-2150)
- Baina B. Lavginova (ORCID: https://orcid.org/0000-0003-1254-6863)
- G. V. Nekludova (ORCID: https://orcid.org/0000-0002-9509-0867)
- Olga Suvorova (ORCID: https://orcid.org/0000-0001-9661-7213)
- Iuliia A. Levina (ORCID: https://orcid.org/0000-0002-0928-2900)
- S. Yu. Chikina (ORCID: https://orcid.org/0000-0002-5536-9388)
- З. М. Мержоева (ORCID: https://orcid.org/0000-0002-3174-5000)
- Н. В. Трушенко (ORCID: https://orcid.org/0000-0002-0685-4133)
Institutions
- Federal Medical-Biological Agency (RU)
Publication Details
- Journal
- Journal of Thoracic Disease
- Published
- 2025-10-01
- DOI
- https://doi.org/10.21037/jtd-2025-1042
- Primary Topic
- Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
- Type
- article
- Field-Weighted Citation Impact
- 0.00