how long can you live with pulmonary arterial hypertension

Survival rates for patients with pulmonary arterial hypertension (PAH) can vary significantly among individuals. Generally speaking, those who receive an early diagnosis and appropriate treatment tend to have a more favorable prognosis.

PAH is a chronic and progressive condition that can impose a substantial burden on the heart, potentially leading to heart failure. Patient survival spans can range from a few years to over a decade, contingent on the severity of the disease and the efficacy of treatment. Patients with mild PAH may maintain a relatively normal lifestyle and enjoy a longer lifespan by adopting lifestyle changes, managing blood pressure, and adhering to specific pharmacological therapies. Conversely, those with severe PAH may have a shorter survival span, even with aggressive treatment interventions.

Hence, early diagnosis, proactive treatment, and regular follow-ups are crucial for individuals with PAH. Additionally, it is imperative for patients to adhere to their healthcare provider's recommendations for a healthy lifestyle, including smoking cessation, salt restriction, maintaining an appropriate weight, and engaging in moderate physical activity. Should any symptoms worsen or new symptoms emerge, immediate medical attention is advised. Throughout the treatment journey, patients must strictly comply with their prescribed medication regimens and avoid making unilateral adjustments or discontinuing medication without professional guidance.