Pulmonary & Arterial hypertension
Pulmonary hypertension (PH or PHTN) is a condition of increased blood pressure within the arteries of the lungs. The most relevant mechanisms for sudden cardiac death in PAH patients seem to be related to severe dilatation of the pulmonary artery, as subsequent complications, such as left main compression syndrome, pulmonary artery dissection, pulmonary artery rupture, and massive hemoptysis, may take place.An arterial high blood pressure has the characteristic of pressure indicators, either equal of higher than 140 mm Hg for the systolic or 90 mm Hg for the diastolic pressure, after having repeatedly measured the arterial tension. Essential arterial hypertension is one of the main treatable cardiovascular risk factors. It can be well controlled and the cardiovascular risk reduced through a combination of lifestyle interventions and first-line antihypertensive drugs.
Related Conference of Pulmonary & Arterial hypertension
June 19-20, 2025
12th World Congress on Hypertension, Cardiology, Primary Health and Patient Care
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Pulmonary & Arterial hypertension Conference Speakers
Recommended Sessions
- Coronary Intervention in HTN
- Gestational Hypertension
- Heart & Cardiovascular diseases
- Hypertension
- Hypertension Diagnosis and Assessment
- Hypertension Management
- Pediatric Hypertension
- Prevalence and lifetime risk of hypertension
- Pulmonary & Arterial hypertension
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- Resistance Hypertension
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- Women’s Cardiovascular Health - CVDT 2025 (France)
- Women’s Cardiovascular Health - World Heart 2025 (Canada)
- Women’s Heart Health - Heart 2025 (Japan)