Pulmonary Hypertension in Parenchymal Lung Disease

被引：6
作者：
Ruggiero, Rosechelle M. [1 ]
Bartolome, Sonja [1 ]
Torres, Fernando [1 ,2 ]
机构：
[1] Univ Texas SW Med Ctr Dallas, Div Pulm & Crit Care Med, Dallas, TX 75390 USA
[2] Univ Texas SW Med Ctr Dallas, Lung Transplant & Pulm Hypertens Program, Dallas, TX 75390 USA
来源：
HEART FAILURE CLINICS | 2012年 / 8卷 / 03期
关键词：
Pulmonary hypertension; Interstitial lung disease; Chronic obstructive pulmonary disease; Idiopathic pulmonary fibrosis; OBSTRUCTIVE SLEEP-APNEA; POSITIVE AIRWAY PRESSURE; TERM OXYGEN-THERAPY; PLACEBO-CONTROLLED TRIAL; ARTERIAL-HYPERTENSION; COR-PULMONALE; WALK DISTANCE; COPD PATIENTS; GAS-EXCHANGE; SARCOIDOSIS;
D O I：
10.1016/j.hfc.2012.04.010
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
The pathophysiology of pulmonary hypertension (PH) in parenchymal lung diseases is partially related to hypoxic pulmonary vasoconstriction. PH treatment is controversial for these patients. This article focuses on group III PH, namely PH attributable to lung diseases and/or hypoxia. Group III includes chronic obstructive pulmonary disease and interstitial lung diseases, the most common parenchymal lung diseases associated with PH. It also includes sleep-disordered breathing and hypoventilation from any cause. Other parenchymal lung diseases associated with PH, namely sarcoidosis and systemic vasculitides (group V), are discussed. The data describing PH in specific parenchymal diseases are reviewed.
引用
收藏
页码：461 / +
页数：15
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