Pulmonary hypertension (high blood pressure in the lungs)


Description

High blood pressure in the pulmonary arteries. This elevation in the pressure makes the right side of the heart work harder, and can cause the heart to fail. It can result from a problem in the pulmonary vessels themselves (Primary Pulmonary Hypertension), or from a problem outside the vessels (Secondary Pulmonary Hypertension). Secondary causes include: pulmonary embolus, COPD, autoimmune diseases, CHF, and sleep apnea.

Symptoms

Shortness of breath during activity, chest pain, weakness, fatigue, fainting, light-headedness during exercise, dizziness, leg swelling.

Tests

Common tests used for diagnosis and treatment

Workup:
A history and physical exam will be performed. This problem is usually first detected by echocardiogram (ultrasound of the heart). Tests to establish the diagnosis and reveal a secondary cause of the pulmonary hypertension include: right heart catheterization, echocardiogram, lung biopsy, and/or pulmonary function test.

Tests:
Complete blood count (CBC), Comprehensive metabolic panel (CMP), CT Scan, D-Dimer, Electrocardiogram (EKG), Magnetic resonance imaging (MRI), Urinalysis (UA), X-ray

Other Specific Tests: Right heart catheterization, echocardiogram, lung biopsy, pulmonary function test

Specialists:
Internal Medicine, Cardiology, Pulmonology, Pediatric Cardiology, Pediatric Pulmonology

Treatment

There is no known cure. The goal of treatment is to reduce symptoms. Medicines used include: ambrisentan (Letairis), bosentan/Tracleer, calcium channel blockers, diuretics, sildenafil (Viagra), and/or prostacyclin. Patients with low oxygen levels will receive oxygen. Severe cases may need a lung or heart/lung transplant.  
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