rv hypertension

Pulmonary arterial hypertension, also referred to as pulmonary hypertension, is a type of cardiovascular disease that can result in compromised heart and lung function. It is typically marked by an abnormal elevation in pulmonary artery pressure, which consequently increases the workload on the right ventricle of the heart.

In the initial phases of the condition, individuals might experience mild difficulty in breathing, fatigue, or a reduction in exercise capacity. As the disease advances, symptoms may intensify, manifesting as chest pain, fainting spells, or even heart failure. The etiology of pulmonary arterial hypertension is varied, encompassing common conditions such as hypertension and heart disease, as well as rare genetic disorders. Treatment approaches are generally customized based on the underlying cause, the severity of the condition, and the patient's overall health, and may involve pharmacological therapy, surgical interventions, or other treatment modalities.

For individuals diagnosed with pulmonary arterial hypertension, regular medical check-ups are advised to track the disease's progression and to adhere to the treatment regimen prescribed by a physician. Additionally, maintaining a healthy lifestyle, including moderate physical activity, abstaining from smoking, moderating alcohol intake, and adhering to a balanced diet, can significantly aid in disease management. It is crucial to remember that any medication should be taken under the supervision of a qualified healthcare professional, and self-adjustment of the medication regimen is strongly discouraged.