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
March 23-24, 2026
13th International Conference on Hypertension and Cardiovascular Diseases
London, UK
May 21-22, 2026
13th World Congress on Hypertension, Cardiology, Primary Health and Patient Care
Paris, France
July 23-24, 2026
13th International Conference on Geriatric Cardiology, Cardiovascular Diseases and Palliative Care
Paris, France
Pulmonary & Arterial hypertension Conference Speakers
Recommended Sessions
- Coronary Intervention in HTN
- Gestational Hypertension
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- Hypertension
- Hypertension Diagnosis and Assessment
- Hypertension Management
- Pediatric Hypertension
- Prevalence and lifetime risk of hypertension
- Pulmonary & Arterial hypertension
- Renal/ Renovascular Hypertension
- Resistance Hypertension
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