Unraveling the Complexities of Hypersensitivity Pneumonitis with Autoimmune Features: A Retrospective Analysis
Within two years post-diagnosis, HPAF and HP had comparable overall outcomes. However, under immunosuppression, HPAF patients had significantly lower odds of developing PPF (adjusted OR 0.08; 95% CI 0.008-0.816; <i>p</i> = 0.033) compared to HP patients, suggesting a more favorable treatment response.
Authors
- Joana Lourenço (ORCID: https://orcid.org/0000-0002-3351-3422)
- André Carvalho (ORCID: https://orcid.org/0000-0003-2694-0909)
- David Barros Coelho (ORCID: https://orcid.org/0000-0002-0540-7200)
- Natália Melo (ORCID: https://orcid.org/0000-0001-8815-0369)
- Patrícia Caetano Mota (ORCID: https://orcid.org/0000-0002-8157-1125)
- António Morais (ORCID: https://orcid.org/0000-0001-8348-8651)
- André Terras Alexandre
- Hélder Novais Bastos (ORCID: https://orcid.org/0000-0002-1412-4202)
- S. De Castro
Institutions
- Universidade do Porto (PT)
- Hospital de São João (PT)
- Administração Regional de Saúde de Lisboa e Vale do Tejo (PT)
- University of Aveiro (PT)
Publication Details
- Journal
- Advances in respiratory medicine
- Published
- 2025-11-07
- DOI
- https://doi.org/10.3390/arm93060050
- Citations
- 1
- Primary Topic
- Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
- Type
- article
- Field-Weighted Citation Impact
- 1.52