What is Idiopathic Pulmonary Arterial Hypertension (IPAH)?
Idiopathic Pulmonary Arterial Hypertension (IPAH) is a rare and progressive disease characterized by elevated blood pressure in the pulmonary arteries without a known cause. It leads to increased vascular resistance, which can result in right heart failure. In the context of gynecology, IPAH poses unique challenges due to the physiological changes that occur during pregnancy and the management of reproductive health.
