Exercise physiology and pulmonary arterial hypertension

Aaron B Waxman1

  • 1Pulmonary Vascular Disease Program, Dyspnea and Exercise Intolerance Center, Pulmonary Critical Care Medicine, Cardiovascular Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA. abwaxman@partners.org

Summary

Pulmonary artery hypertension (PAH) involves vascular remodeling, increasing pulmonary vascular resistance and pressure. This burdens the right ventricle, potentially causing heart failure, highlighting the need to study pressure-flow dynamics.

Related Concept Videos

Pulmonary Hypertension: Classification and Pathogenesis01:30

Pulmonary Hypertension: Classification and Pathogenesis

Pulmonary hypertension (PH) is a severe health condition in which the mean pulmonary arterial pressure increases to 25 mmHg or more, even when the body is at rest. This high pressure in the blood vessels that transport blood from the heart to the lungs can cause various symptoms, including shortness of breath, can lead to right heart failure, and significantly affect the overall quality of life.
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Treatment for Pulmonary Arterial Hypertension: Oxygen Therapy for Respiratory Failure01:16

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Treatment for Pulmonary Arterial Hypertension: Endothelin Receptor Antagonists01:18

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Treatment for Pulmonary Arterial Hypertension: Prostacyclin Receptor Agonists01:23

Treatment for Pulmonary Arterial Hypertension: Prostacyclin Receptor Agonists

Prostacyclin receptor agonists are a class of therapeutic agents integral to managing pulmonary arterial hypertension (PAH). These drugs operate by mimicking the action of prostaglandin I2, or PGI2, a naturally occurring compound in the body.
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