Can Pulmonary Arterial Hypertension (PAH) be Cured?
No (manageable)
No cure; management aims to improve symptoms, slow disease progression
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What is Pulmonary Arterial Hypertension (PAH)?
PAH is a type of high blood pressure that affects the arteries in the lungs. Treatment aims to manage symptoms and improve quality of life and may include medications, oxygen therapy, and, in some cases, lung transplantation. Regular monitoring is crucial for assessing pulmonary function, managing symptoms, and adjusting treatment as needed.
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Clinical Aspects
Characteristics
High blood pressure in the arteries of the lungs
Symptoms
Shortness of breath, fatigue, chest pain
Diagnosis
Clinical evaluation, imaging
Prognosis
Variable, often progressive with significant disability
Complications
Impaired lung function, potential for complications
Etiology and Treatment
Causes
Idiopathic, genetic factors, connective tissue disorders
Treatments
Medications (vasodilators), oxygen therapy, lung transplant
Prevention
Medications (vasodilators), oxygen therapy, lung transplant
Public Health and Patient Perspectives
Epidemiology
Rare, progressive disorder affecting pulmonary arteries
Patient Perspectives
Lifelong management tailored to symptoms
For personalized advice and care, always seek the assistance of healthcare professionals. This information is meant for general understanding and not as a replacement for professional medical advice.
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