• Home
  • About Us
  • Blog

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

It’s November Again, Which Means Pulmonary Hypertension Awareness Month

November 9, 2015 By Dr. Jeremy Feldman

PAH AwarenessSince November is Pulmonary Hypertension Awareness month, we like to reflect on the progress made on this site and in the PAH community in general.  2014 has been an important and busy year for pulmonary hypertension.  First, we would like to thank our readers for making this website a tremendous success.  Each month, thousands of people visit this site to learn about pulmonary hypertension and our readership is constantly growing.  We launched a new section of the site—“The Doctor is In”.  Readers have been suggesting PAH topics and we have been posting blogs addressing as many of those topics as we can.  Your feedback has been wonderful.

Continuing Progress in Pulmonary Hypertension Research

Elsewhere in PAH, the FDA approved the first upfront combination therapy for PAH (Letairis combined with Adcirca) and is considering approval of a second oral prostanoid receptor agonist (Selexipag=Uptravi).  Medtronic and United Therapeutics submitted information about the Synchromed II implanted infusion system for intravenous Remodulin.  We await the FDA’s decision.  We heard from a newcomer to PAH, Reata Pharmaceuticals.  This past October they announced positive results in their interim analysis of their phase II study with bardoxylone methyl.  Gilead Sciences also completed enrollment in their phase II study of a novel compound for PAH.

Overall, this year has seen a shift in focus from medicines that relax blood vessels towards medicines that address other aspects of pulmonary hypertension such as inflammation and oxidative stress (metabolic derangements in how the pulmonary artery and heart muscle cells generate energy).

Despite all the progress, we can do more.  We need to continue to strive to increase awareness and lobby our congressional representatives to increase funding for research.  Tell your stories to a friend.  Knowledge is power.  Empower the community.

What Can We Expect From 2016 in PAH?

There are some very exciting studies that are enrolling patients.  Actelion Pharmaceuticals is set to study a combination of three medications together as upfront therapy for PAH.  Reata will launch a phase 3 study of bardoxylone methyl in connective tissue disease associated PAH.  Belleraphon will start enrolling a phase III study of inhaled nitric oxide as add-on therapy in PAH.  We hope that Gilead will announce a phase III study of their newest molecule in the second half of the year.  Many companies are also expanding their studies to include group 3 pulmonary hypertension (PH due to lung disease).  There are many other studies that will start enrolling in 2016, visit clinicaltrials.gov for a complete listing.

2016 is also likely to see more PAH medications become available as generics.  Stay tuned for more information on this topic.

We are very excited about 2016.  We look forward to providing both useful and current information about PAH to our readers.  We value your feedback and invite you to suggest topics on PAH.

Filed Under: Living with PAH

PAH Life Expectancy

PAH Research

Research, Life Expectancy & Prognosis for PH

Major Developments in Pulmonary Hypertension Affecting Prognosis 1.     Approval of

Where to Get Treatment?

CCCs for PAH

Pulmonary Hypertension Centers

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

Popular Posts

Portopulmonary hypertension

Porto-Pulmonary Syndrome

By Dr. Jeremy Feldman

An important cause of PAH is liver disease.  Up to 5% of patients with cirrhosis (scarring in the liver) or

Insurance Authorizations for PAH

Copay, Co-Insurance, Deductibles and Out of Pocket Maximum

By Dr. Jeremy Feldman

Understanding the basic terminology of your health insurance is vitally important for patients with Pulmonary

good news in pah

 

Disclaimer

Recent Blog Posts

  • Sotatercept Coming Soon January 10, 2023
  • Why Abortion Matters to PAH Patients May 3, 2022
  • Aerovate and Inhaled Imatinib February 13, 2022

Categories

Archives