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Pulmonary Hypertension in Interstitial Lung Disease: Management Options to Move Beyond Supportive Care

PURPOSE OF REVIEW: This review delineates current diagnostic and management strategies for pulmonary hypertension due to interstitial lung disease (PH-ILD). RECENT FINDINGS: The INCREASE trial, a phase III multicenter, randomized, placebo-controlled trial demonstrated both improved 6-min walk distan...

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Detalles Bibliográficos
Autores principales: Fabyan, Kimberly D., Chandel, Abhimanyu, King, Christopher S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10200699/
https://www.ncbi.nlm.nih.gov/pubmed/37362782
http://dx.doi.org/10.1007/s13665-023-00311-2
Descripción
Sumario:PURPOSE OF REVIEW: This review delineates current diagnostic and management strategies for pulmonary hypertension due to interstitial lung disease (PH-ILD). RECENT FINDINGS: The INCREASE trial, a phase III multicenter, randomized, placebo-controlled trial demonstrated both improved 6-min walk distance and decreased disease progression with inhaled treprostinil. This pivotal trial led to inhaled treprostinil becoming the first FDA approved medication for treatment of PH-ILD. The availability of this treatment has generated subsequent recommendations for the screening for PH in patients with ILD. As a result, it is becoming increasingly important for clinicians to gain awareness and familiarity with the evolving management options for PH-ILD. SUMMARY: The management of PH-ILD has its roots in goal-directed treatment of the underlying lung disease. However, recent medication advances and ongoing clinical studies are opening opportunities for more disease-specific treatment.