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EbookBell Team
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ISBN 10: 1282093924
ISBN 13: 9781282093928
Author: A. J. Peacock, J. A. Barberà
Pulmonary arterial hypertension (PAH) is a rare condition; yet this very rarity can be a disadvantage when it comes to treatment, making PAH difficult to diagnose, and resulting in suboptimal patient care. Furthermore, the global burden of PAH remains poorly understood and largely underestimated, as PAH commonly presents as a comorbidity with such conditions as systemic sclerosis, COPD, idiopathic pulmonary fibrosis and left-heart dysfunction. However, in recent years there has been significant investment in developing new therapies for PAH, and treatment for this previously neglected disease
Contents
Editors and Contributors
Chapter 1: Imaging of the right heart and pulmonary circulation
Chapter 2: Exercise testing and haemodynamics
Chapter 3: Epidemiology of pulmonary arterial hypertension
Chapter 4: Current treatment of PAH: prostanoids, phosphodiesterase-5 inhibitors and stimulators of soluble guanylate cyclase
Chapter 5: The future treatment of pulmonary hypertension
Chapter 6: Endothelin receptor antagonists
Chapter 7: Gene and stem cell therapy in pulmonary arterial hypertension
Abbreviations
Index
therapeutic strategies in pulmonary arterial hypertension
therapy for pulmonary arterial hypertension in adults
therapeutic strategies in pulmonary hypertension
pulmonary arterial hypertension therapies
pulmonary arterial hypertension therapeutic area
Tags: A J Peacock, J A Barbera, Therapeutic, Strategies, Pulmonary, Arterial, Hypertension
