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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
    • Sotatercept (Winrevair) Approved
    • 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

Uptravi (Selexipag) for PAH

June 17, 2020 By Dr. Jeremy Feldman

Uptravi was approved in 2016 to treat Pulmonary Arterial Hypertension, PAH.  We now have more than four years of experience with this medication.  There are three broad pathways that PAH medications impact.   3 Pathways PAH Medications Impact The endothelin pathway is overactive in PAH and leads to excessive blood vessel squeezing and … [Read more...]

Exciting New Clinical Trials in PAH

May 15, 2020 By Dr. Jeremy Feldman

PAH research

The wheels of progress continue to move forward in PAH research.  Two companies in particular are preparing to launch very exciting clinical trials.   Gossamer Bio Inhaled Drug Study Gossamer Bio, a biopharmaceutic company is preparing to launch a new phase 2 clinical research trial using an inhaled tyrosine kinase inhibitor.  About 10 years … [Read more...]

Pulmonary Hypertension and COVID-19

April 10, 2020 By Dr. Jeremy Feldman

PAH patient story

We are in the midst of the greatest health crisis since HIV (human immunodeficiency virus).  The last time the world saw a respiratory illness of this severity was in 1918 when a very aggressive strain of influenza swept across the world.  Today we are squarely in the middle of the COVID-19 pandemic.  Millions of Americans will be infected and many … [Read more...]

Tyrosine Kinase Inhibition and Pulmonary Arterial Hypertension

February 13, 2020 By Dr. Jeremy Feldman

PAH research

30 years ago PAH scientists and doctors believed that PAH was caused by inappropriate or excessive squeezing (vasoconstriction) of the pulmonary arteries.  The earliest medications to treat PAH focused on relaxing the pulmonary arteries.  Over the next decade we learned that PAH is a much more complex disorder than just blood vessels squeezing too … [Read more...]

Liquidia Files for Approval of Inhaled Treprostinil

February 4, 2020 By Dr. Jeremy Feldman

News about PAH

We were excited to hear that Liquidia has filed with the FDA for approval of their drug inhaled treprostinil. They had already reported exciting results with their medication, showing that it was well tolerated and maintained or improved six minute walk distance.   Currently, United Therapeutics makes Tyvaso, which is treprostinil for inhalation.  Tyvaso … [Read more...]

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PAH Life Expectancy

PAH Research

Research, Life Expectancy & Prognosis for PH

Major Developments in Pulmonary Hypertension Affecting Prognosis 1.     Approval of

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Pulmonary Hypertension Centers

Where to get treatment for pulmonary hypertension? Pulmonary arterial hypertension is a

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