Abstract
Pulmonary arterial hypertension has a poor prognosis quoad vitam et valitudinem. Herein, we report on a middle-aged woman affected by idiopathic pulmonary arterial hypertension whose quality of life and exercise tolerance improved remarkably after a six-month course of treatment with the long-acting phosphodiesterase-5 inhibitor tadalafil.
MeSH terms
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Adult
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Carbolines / therapeutic use*
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Exercise Tolerance / drug effects*
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Female
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Hemodynamics
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Humans
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Hypertension, Pulmonary / drug therapy*
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Hypertension, Pulmonary / physiopathology
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Oxygen / blood
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Phosphodiesterase Inhibitors / therapeutic use*
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Quality of Life*
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Tadalafil
Substances
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Carbolines
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Phosphodiesterase Inhibitors
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Tadalafil
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Oxygen