how long can someone live with pulmonary hypertension

The life expectancy of individuals with pulmonary arterial hypertension (PAH) can vary widely due to personal differences. Generally, with timely diagnosis and appropriate treatment, patients may have a lifespan close to that of the general population. However, without intervention, survival can be significantly reduced.

The severity of PAH, which can range from mild to severe, directly impacts the prognosis. Patients with mild PAH can maintain a relatively normal lifestyle and may not experience a substantial reduction in life expectancy through medication and lifestyle modifications. As the disease progresses, more aggressive treatment options such as oxygen therapy, vasodilators, or other targeted treatments may be necessary. These interventions aim to alleviate symptoms, enhance quality of life, and extend survival as much as possible. In rare cases, heart transplantation may be considered for patients with the most severe forms of the disease.

Thus, for those with PAH, early diagnosis, regular monitoring of disease progression, and adherence to medical treatment recommendations are crucial. Additionally, maintaining a healthy lifestyle, including a balanced diet, regular exercise, smoking cessation, and moderate alcohol consumption, can help control disease progression and improve quality of life. Above all, patients should closely monitor their health and seek medical attention promptly if they experience any discomfort or worsening of symptoms.