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Sonu Pawar
Sonu Pawar

How Pulmonary Arterial Hypertension Impacts Heart and Lung Health

Pulmonary Arterial Hypertension (PAH): A Serious Cardiopulmonary Condition

Pulmonary Arterial Hypertension (PAH) is a progressive, life-threatening disorder characterized by high blood pressure in the arteries that supply the lungs. This increased pressure forces the heart to work harder to pump blood, which can eventually lead to heart failure if left untreated.

Understanding Pulmonary Arterial Hypertension

PAH occurs when the small arteries in the lungs become narrowed or blocked, increasing the resistance to blood flow. Over time, this causes elevated pressure within the pulmonary arteries and places significant strain on the right side of the heart.

Causes and Risk Factors

While the exact cause of PAH is often unknown (idiopathic), several factors can contribute to its development:

  • Genetic mutations

  • Connective tissue diseases (such as scleroderma or lupus)

  • Congenital heart defects

  • Chronic liver disease

  • HIV infection

  • Use of certain drugs or toxins (including some appetite suppressants)

Symptoms of PAH

PAH symptoms are often non-specific in the early stages but worsen as the disease progresses:

  • Shortness of breath (dyspnea)

  • Fatigue

  • Chest pain

  • Dizziness or fainting (syncope)

  • Swelling in the ankles, legs, or abdomen (edema)

  • Rapid heartbeat (palpitations)

Diagnosis and Treatment

Diagnosis:PAH is typically diagnosed through a combination of physical examination, echocardiogram, right heart catheterization, pulmonary function tests, and other imaging techniques.

Treatment Options:While there is no cure, treatments can manage symptoms and slow disease progression:

  • Vasodilators (help relax blood vessels)

  • Endothelin receptor antagonists (reduce blood vessel constriction)

  • Phosphodiesterase-5 inhibitors (improve blood flow)

  • Prostacyclin analogs (dilate pulmonary arteries)

  • Oxygen therapy

  • Lifestyle modifications and supervised exercise

In severe cases, lung transplantation may be considered.

Market Overview

The Pulmonary Arterial Hypertension (PAH) market is witnessing substantial growth due to increasing awareness, advancements in targeted therapies, and growing research into gene-based and combination treatments. Major pharmaceutical companies are actively investing in new drug development to offer more effective, patient-specific solutions.

Key Market Trends

  • Rising adoption of oral PAH therapies

  • Increasing clinical trials for combination treatment regimens

  • Growing emphasis on early diagnosis and disease management

  • Expansion in emerging markets due to improved healthcare infrastructure

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