Approach to pulmonary hypertension.

被引:0
|
作者
Yung G.L. [1 ]
Rubin L.J. [1 ]
机构
[1] Division of Pulmonary and Critical Care Medicine, University of California, San Diego School of Medicine, La Jolla, CA
关键词
Pulmonary Hypertension; Idiopathic Pulmonary Fibrosis; Epoprostenol; Primary Pulmonary Hypertension; Pulmonary Hypertensive Patient;
D O I
10.1007/s11926-000-0030-x
中图分类号
学科分类号
摘要
Until recently, many physicians considered pulmonary hypertension a rare and esoteric condition that is difficult to diagnose and nearly impossible to treat. However, pulmonary hypertension can complicate a variety of relatively common diseases and, with the development of new and effective therapies, there is a need for greater awareness of this condition. Pulmonary hypertension should be considered when patients present with unexplained shortness of breath, chest pain, or syncope. The usual delay of 1 to 2 years between onset of symptoms and diagnosis underscores the importance of considering pulmonary hypertension in the differential diagnosis of patients who present with atypical cardiorespiratory symptoms.
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页码:517 / 523
页数:6
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