Pulmonary hypertension secondary to interstitial lung disease

被引：1
|
作者：
Shlobin, Oksana A. [1 ]
Nathan, Steven D. [1 ]
机构：
[1] Inova Heart & Vasc Inst, Adv Lung Dis & Transplant Program, Falls Church, VA 22042 USA
来源：
EXPERT REVIEW OF RESPIRATORY MEDICINE | 2011年 / 5卷 / 02期
关键词：
catheterization; histiocytosis; hypertension; interstitial; Langerhans cell; lung diseases; lymphangioleiomyomatosis; pulmonary; pulmonary fibrosis; research design; sarcoidosis; scleroderma; Swan-Ganz; systemic; VENTRICULAR DIASTOLIC DYSFUNCTION; ARTERIAL-HYPERTENSION; SYSTEMIC-SCLEROSIS; SYSTOLIC PRESSURE; CONTROLLED-TRIAL; WALK DISTANCE; SARCOIDOSIS; FIBROSIS; HISTIOCYTOSIS; SILDENAFIL;
D O I：
10.1586/ERS.11.11
中图分类号：
R56 [呼吸系及胸部疾病];
学科分类号：
摘要：
Interstitial lung diseases (ILDs) may be complicated by the development of pulmonary hypertension (PH), which is associated with worse functional impairment and a poorer prognosis. This article reviews the current state of knowledge on the prevalence, pathogenesis, diagnosis and prognosis of ILD-related PH. Whether the treatment of ILD-related PH changes clinical outcomes is currently unknown, but the current studies are summarized and the authors' perspective is offered.
引用
收藏
页码：179 / 189
页数：11
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