pulmonary hypertension with rvsp

Pulmonary arterial hypertension (PAH) accompanied by elevated right ventricular systolic pressure is a type of cardiovascular disease that typically results in increased strain on the heart, impacting its function. The condition can vary in severity, with symptoms and treatment approaches differing among individuals.

In its early stages, individuals may experience only mild shortness of breath and fatigue. As the disease advances, more severe symptoms such as chest pain, fainting, and even heart failure can emerge. During diagnosis, physicians assess the severity of PAH based on patient-reported symptoms, physical examination findings, and imaging studies.

For individuals with PAH and increased right ventricular systolic pressure, it is crucial to avoid vigorous exercise and excessive fatigue in daily life and to maintain a healthy lifestyle, including smoking cessation, moderate alcohol consumption, a balanced diet, and regular physical activity. Regular check-ups and adherence to medical advice for treatment are essential; self-medicating without guidance is not advisable. Should any discomfort occur, immediate medical consultation is recommended.