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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

Acceleron Launches a Phase 2 Study of Sotatercept for PAH

May 4, 2018 By Dr. Jeremy Feldman

acceleron Sotatercept drug for PAH

All of our existing therapies for Pulmonary Arterial Hypertension act by vasodilation or relaxing blood vessels.  The current medications fall into one of three basic classes: 1.    PDE5 inhibitor a. Sildenafil (Revatio/Viagra) b. Tadalafil (Adcirca/Cialiis) c. Riociguat (Adempas—not truly a PDE5inhibitor but similar action) 2.    ERA a. Ambrisentan (Letairis) b. … [Read more...]

Liquidia: Exciting New Clinical Trial in Pulmonary Arterial Hypertension

April 19, 2018 By Dr. Jeremy Feldman

PAH research

Clinical trials are essential to improving the care of PAH patients. These clinical trials allow us to determine if new medicines are safe and effective. Clinical trials also allow us to make improvements to existing treatments. For example, we are eagerly awaiting the approval of the implanted pump for intravenous Remodulin. Another example of a company that is trying to … [Read more...]

Pulmonary Arterial Hypertension Research

March 21, 2018 By Dr. Jeremy Feldman

pulmonary hypertension research laboratory

FDA Approval Process for PAH Drugs The past decade has seen many new drugs approved to treat PAH.  The development of a new drug is a long and expensive process.  Candidate new drugs are identified and then enter the clinical research pathway.  Before a medication is ever tested in humans, the medication is tested in a variety of laboratory settings and then in animal models.  … [Read more...]

Pulmonary Arterial Hypertension Life Expectancy & Survival Rates

March 16, 2018 By Dr. Jeremy Feldman

high risk vs. low risk life expectancy in Pulmonary Hypertension

The treatment for Pulmonary Arterial Hypertension has come a long way since the mid 1990’s when Flolan was first approved.  There has been an explosion of new medications that have dramatically altered how we treat patients.  We no longer sequentially add therapies to most of our patients.  Rather, we often start two or even three different therapies as part of an initial … [Read more...]

Help Arrives for Some PAH Patients Who Can’t Afford Their Medication

February 23, 2018 By Dr. Jeremy Feldman

News about PAH

Thousands of Pulmonary Arterial Hypertension patients across America are now experiencing a crisis.  They previously received support from Caring Voices Coalition. With the closing of Caring Voices, many of these patients have been unable to find foundation support, leaving them responsible for many thousands of dollars per month to receive their PAH medications. The PHA and … [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

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