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

被引:1
作者
Fabyan, Kimberly D. [1 ]
Chandel, Abhimanyu [1 ]
King, Christopher S. [2 ]
机构
[1] Walter Reed Natl Mil Med Ctr, Dept Pulm & Crit Care, 8901,Rockville Pike, Bethesda, MD 20889 USA
[2] Inova Fairfax Hosp, Inova Heart & Vasc Inst, Adv Lung Dis & Transplant Program, 3330 Gallows Rd, Falls Church, VA 22003 USA
关键词
Pulmonary hypertension; Interstitial lung disease; ARTERIAL-HYPERTENSION; SILDENAFIL; FIBROSIS; SECONDARY; OUTCOMES; TRANSPLANTATION; DIAGNOSIS; BOSENTAN;
D O I
10.1007/s13665-023-00311-2
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
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.
引用
收藏
页码:105 / 112
页数:8
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