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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

Stimulant Associated Pulmonary Arterial Hypertension

January 23, 2018 By Dr. Jeremy Feldman

stimulant drugs associated with pulmonary arterial hypertension

Diet Pills and Methamphetamines Stimulants were first suspected of causing pulmonary hypertension in the late 1960’s and early 1970’s.  In Austria a diet pilled called Aminorex was marketed in the late 1960’s and shortly thereafter an epidemic of pulmonary arterial hypertension developed among users.  The pill was withdrawn in the early 1970’s and the wave of Aminorex … [Read more...]

Minimally Elevated Pulmonary Pressures

January 10, 2018 By Dr. Jeremy Feldman

Internal anatomy of the pulmonary arteries

What Do They Mean? Mild PAH? We receive many emails from our readers inquiring whether having borderline to minimally elevated echo estimated pulmonary artery pressures means that they have pulmonary arterial hypertension.  This is a very important question and many doctors unfortunately don’t understand the limits of echocardiography so patients are often left more … [Read more...]

Hereditary Hemorrhagic Telangiectasia (HHT)

December 15, 2017 By Dr. Jeremy Feldman

blood vessels

Disease Overview HHT is a rare disease that leads to abnormal blood vessel growth throughout the body.  This commonly leads to frequent nose bleeds (epistaxis), gastro-intestinal bleeding and anemia.  The more serious manifestations include abnormal blood vessels in the lungs, brain and liver.  These abnormal blood vessels can lead to infections in the brain, bleeding in the … [Read more...]

Diastolic Heart Failure vs. PAH

November 29, 2017 By Dr. Jeremy Feldman

Internal anatomy of the pulmonary arteries

The most common disease confused with pulmonary arterial hypertension is diastolic heart failure (also called heart failure with preserved ejection fraction-HeFPEF).  In my practice about 70% of patients referred to me for PAH actually have diastolic heart failure. Let’s review basic heart function.  The heart has two main actions—squeezing and relaxing.  The squeezing phase … [Read more...]

Sickle Cell and Pulmonary Hypertension

October 20, 2017 By Dr. Jeremy Feldman

Blood tests to monitor PH patients

What is Sickle Cell Disease? Sickle Cell Disease is a genetic disorder of the red blood cells. It is autosomal recessive (you need to get one defective gene copy from each of your parents). Patients with sickle cell disease have abnormal hemoglobin in their red cells. Under periods of stress the red cells become deformed and plug up the blood vessels of the lungs and other … [Read more...]

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PAH Life Expectancy

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