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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

What We Learn From Our Patients

January 20, 2016 By Dr. Jeremy Feldman

Dr. Jeremy Feldman

I recently lost a friend and patient of almost a decade.  Her battle with familial pulmonary hypertension started when she was a young girl and her mother died from the disease.  I met her in her early twenties when she already had severe PAH.  Her brother had been treated for severe PAH for several years prior. When I first met her, she had a young daughter, the light of … [Read more...]

A wish for 2016

December 29, 2015 By Dr. Jeremy Feldman

PAH resolutions

As we look back to 2015 it has been a good year for pulmonary hypertension patients.  We have made steps forward.  We have an expanding number of medications to treat PAH.  Patients are living longer and feeling better.  We have taken further steps toward understanding the genes involved in the disease. Despite our progress, we remain ineffective in answering some very basic … [Read more...]

Update: Anticoagulation (Blood Thinners) & Pulmonary Hypertension

December 22, 2015 By Dr. Jeremy Feldman

Blood tests to monitor PH patients

The question of whether anticoagulation (thinning of blood with medications) should be used in the treatment of pulmonary hypertension dates back more than 35 years.  Very early observations of small blood clots in the lungs of PAH patients propelled interest in using warfarin (our oldest blood thinner). In the 1980’s and 1990’s several small studies were completed that … [Read more...]

The Pulmonary Hypertension Team

December 11, 2015 By Dr. Jeremy Feldman

PAH Research

I would like to acknowledge the role of our PH nurse coordinators and support staff.  The care of pulmonary hypertension patients is a challenge.  A typical new patient that I see has already been to a cardiologist and at least one other pulmonologist in addition to their primary care doctor.  They have had dozens of tests and perhaps been hospitalized a few times. Intake … [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...]

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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

Where to Get Treatment?

CCCs for PAH

Pulmonary Hypertension Centers

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

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