Key result
This review outlines the pathophysiology, diagnosis, and management of right ventricular failure in pulmonary arterial hypertension, a condition with an estimated median survival of 2.8 years.
Population
Patients with right ventricular failure due to pulmonary arterial hypertension (PAH)
Design
Review
Authors
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Guides RV failure assessment in PAH; leaves open optimal therapies for prospective validation.
This review outlines the pathophysiologic mechanisms, diagnostic features, and management strategies for right ventricular failure secondary to pulmonary arterial hypertension.
Marco et al. (2005) conducted a review in Pulmonary arterial hypertension with right ventricular failure. Algorithmic management approach was evaluated. This review outlines the pathophysiology, diagnosis, and management of right ventricular failure in pulmonary arterial hypertension, a condition with an estimated median survival of 2.8 years.
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