Pulmonary Hypertension

Pulmonary hypertension (PH) is high blood pressure in the arteries of the lungs, which forces the right side of the heart to work harder to pump blood. Over time, this can lead to right heart failure. PH can occur on its own (pulmonary arterial hypertension) or as a complication of lung disease, heart disease, or chronic blood clots.

Pulmonary hypertension is rare but serious, affecting an estimated 1% of the global population and up to 10% of people over age 65.

At Texas IPS, our PH program brings together pulmonologists, cardiologists, and imaging specialists to provide timely diagnosis and evidence-based treatment. Because PH symptoms—such as shortness of breath, fatigue, and chest discomfort—can mimic other conditions, accurate testing is key.

Our approach includes:

• Comprehensive evaluation with echocardiography, pulmonary function testing, and advanced imaging
• Right heart catheterization to confirm diagnosis and guide therapy
• Targeted medication management, including vasodilators and combination therapy for pulmonary arterial hypertension
• Oxygen therapy and pulmonary rehabilitation to improve functional capacity
• Long-term monitoring to track disease progression and adjust treatment as needed

Up to 90% of patients with advanced COPD may have high pulmonary arterial pressure.

Early diagnosis and intervention can improve both survival and quality of life for patients with PH. We work to identify the cause, tailor the treatment, and give patients the best chance at living well with this complex condition.