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Pulmonary Hypertension RN

  • What is Pulmonary Hypertension?
    • What is Pulmonary Hypertension?
    • Pulmonary Hypertension Symptoms
    • Types of Pulmonary Hypertension
    • Causes of Pulmonary Hypertension
    • PH vs. PAH
    • Diastolic Heart Failure vs. PAH
    • WHO Group 3 Pulmonary Hypertension, IPF & COPD
    • Pulmonary Veno-Occlusive Disease
    • Hereditary Hemorrhagic Telangiectasia (HHT)
      • Hereditary Hemorrhagic Telangiectasia (HHT) Treatment
    • Functional Classification of Pulmonary Hypertension
    • Congenital Heart Disease
      • Eisenmenger’s Syndrome
      • Update on Management of PAH-CHD
      • Congenital Heart Disease & Sleep Apnea
      • Complex Congenital Heart Disease
      • Atrial Septal Defect and Pulmonary Arterial Hypertension
    • Pediatric Pulmonary Arterial Hypertension
    • Sickle Cell and Pulmonary Hypertension
    • Stimulant Associated Pulmonary Arterial Hypertension
    • Porto-Pulmonary Syndrome
    • Research, Life Expectancy & Prognosis for PH
  • Diagnosing & Monitoring PAH
    • Pulmonary Arterial Hypertension Diagnosis
    • How Am I Doing? Assessing Your PAH.
    • Blood Tests
    • Cardiopulmonary Exercise Test (CPET)
    • CT (Computed Tomography) Scan
    • Echocardiogram: An Overview
    • Echocardiogram: A Detailed Look
    • Pulmonary Function Tests (PFTs)
    • Right Heart Catheterization
    • Six Minute Walk
    • Ventilation Perfusion Scan (VQ Scan)
    • CTEPH
      • CTEPH: WHO Group 4 Pulmonary Hypertension
      • PTE (Pulmonary Thromboendarterectomy) Surgery
      • Adempas used to Treat PAH and CTEPH
  • PAH Treatment
    • Pulmonary Hypertension Centers
    • Pulmonary Hypertension Treatments
    • Continuously Infused Therapies Used to Treat PH
    • Prostanoids for Treatment of PH
    • Adcirca and Revatio Used to Treat Pulmonary Arterial Hypertension (PAH)
    • Adempas used to Treat PAH and CTEPH
    • Tracleer, Letairis, and Opsumit Treatments
    • Oxygen Therapy for Pulmonary Hypertension
    • Salt and Water Restrictions
    • Exercise & PAH
    • Diuretics
    • Blood Thinners
    • Getting the Most Out of PAH Therapy
      • Letairis
      • Opsumit
      • Sildenafil (Revatio)
  • Research
  • FAQ’s
    • Implanted Remodulin Pump, Right Heart Catheterization, PAH & Pregnancy
    • Oral Treatments, Care Centers & Hole in Heart
    • FAQ’s: Altitude, Cold & Allergy Medications
    • FAQ’s: Psoriasis, Idiopathic PAH, Contraceptives & PAH
    • FAQ’s: Causes of Pulmonary Hypertension, Symptom Frequency & Care Centers
    • FAQ: PAH Experts, Pregnancy, Mild PAH & Vacationing
    • FAQ’s: CTEPH, Blood Clots, Corrective Surgery & PAH Care Centers
    • FAQ’s: VQ Scans & PAH Curable?
    • FAQ’s: Mild Pulmonary Hypertension?
    • FAQ’s: Boating, Swimming & Eating with PAH
    • FAQ’s: Borderline Pulmonary Hypertension, Hand Swelling, Children with PAH, Costs

Congenital Heart Disease: An Overview

January 22, 2016 By Dr. Jeremy Feldman

Dr. Tabitha Moe

What is Congenital Heart Disease? As we are developing from a single egg fertilized by a single sperm, cells divide and begin to develop into the different tissues of our adult bodies.  This is a very complex process that is like a kind of perfectly choreographed ballet.  A special cluster of cells slowly differentiates into the cardiovascular system.  Cells that become the … [Read more...]

Sarcoidosis and Pulmonary Hypertension

December 9, 2015 By Dr. Jeremy Feldman

Dr. Jeremy Feldman PAH Specialist

What is Sarcoidosis? Sarcoidosis is an uncommon and poorly understood multisystem disease that commonly affects the lungs and lymph nodes.  However, it may affect any organ of the body.  Despite decades of research, the exact cause remains unknown.  The most common manifestation of the disease is enlarged lymph nodes in the chest and nodules and scarring in the lungs.  The … [Read more...]

What Does the Pulmonary Artery Pressure Really Tell Us?

October 29, 2015 By Dr. Jeremy Feldman

Internal anatomy of the pulmonary arteries

I received a great question from a reader this week.  The reader asked why some patients are quite disabled from Pulmonary Arterial Hypertension when they have only moderately elevated pulmonary artery pressures and other patients can have very high pulmonary artery pressures and yet remain very functional, even working full time. This question gets at a key concept of PAH.  … [Read more...]

Do I Need a Right Heart Catheterization?

September 25, 2015 By Dr. Jeremy Feldman

It is important to assess the right ventricle of the heart of PH patients

This question comes up all the time in the evaluation and care of pulmonary hypertension patients.  We have received a number of questions from readers asking about whether a heart catheterization is needed.  I thought it might be useful to review some basics about right heart catheterization.  Below are some commonly asked questions about the procedure. 1.      Do I need to … [Read more...]

Echocardiography and Pulmonary Arterial Hypertension: A Detailed Look

July 22, 2015 By Dr. Jeremy Feldman

Internal anatomy of the pulmonary arteries

An echocardiogram (or echo) is an ultrasound-based test that can tell us a great deal about your heart.  By bouncing and receiving ultrasound waves off your heart and adjacent structures, we can generate images of your heart.  We can learn about the size and function of the right and left side of your heart and the valves. We can estimate pressures but not directly measure … [Read more...]

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PAH Life Expectancy

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Major Developments in Pulmonary Hypertension Affecting Prognosis 1.     Approval of

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