Written by internationally recognized experts, Pulmonary
Hypertension bridges the gap between pulmonology and cardiology to
provide clinicians in both disciplines with knowledge of the signs,
symptoms, diagnosis, and pharmacologic and surgical treatments for
pulmonary hypertension (PH). Through the use of clinical trials,
this ground-breaking text supplies a comprehensive review of both
the primary and secondary clinical and investigative aspects of
this condition.
Discussing controversies and concepts in PH diagnosis and
management, this guide explores:
- classification and epidemiology, pathology, pathogenesis,
genetics, and diagnosis of PH
- causes of the condition, such as idiopathic pulmonary arterial
hypertension (IPAH)
- PAH-complicating connective tissue diseases (CTD), congenital
heart diseases, human immunodeficiency virus (HIV), and other
disorders
- the mechanisms, toxicities, and efficacy of therapeutic
agents
- the role of combination therapies, novel agents, and future
directions
- PH in specific patient populations such as pregnant and
critically-ill patients in the ICU
General
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