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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

Oxygen Saturation and Breathlessness in PAH

August 17, 2017 By Dr. Jeremy Feldman

pulse oximeter used for six minute walk

I can’t breathe! I feel short of breath all of the time. We hear these statements every day at PAH specialty centers. We take vital signs of blood pressure, heart rate, respiration rate and oxygen saturation and patients are always surprised if their oxygen saturations are within normal limits.  Read below to learn more. What is oxygen saturation? Oxygen saturation measures … [Read more...]

Is Pulmonary Arterial Hypertension a Heart Disease or a Lung Disease?

September 8, 2016 By Dr. Jeremy Feldman

Internal anatomy of the pulmonary arteries

Yes. Pulmonary Arterial Hypertension is a disease that affects both the heart and lungs. The name means high pressure in the arteries of the lungs but it has severe consequences for both the heart and the lungs. How Does PAH Affect My Lungs? Pulmonary hypertension attacks the lungs in two ways.  PAH causes vasoconstriction of the pulmonary arteries.  The pulmonary arteries … [Read more...]

What is BNP?

August 4, 2016 By Dr. Jeremy Feldman

Blood tests to monitor PH patients

BNP stands for B-type natriuretic peptide. This is a hormone that is released by the bottom two chambers of the heart (ventricles) in response to increased work. For example, increased pressure or increased stretch of the heart chambers leads to increased release of BNP.  The main physiologic role of BNP is to act on the kidneys to promote increased salt and water loss … [Read more...]

Cystatin C, A New Blood Test

April 13, 2016 By Dr. Jeremy Feldman

Blood tests to monitor PH patients

By Tabitha Moe and Jeremy Feldman For patients with congenital heart disease related PAH (PAH-CHD), a new blood test called Cystatin C is showing promise as a tool to help your doctor determine if you are at risk for problems related to PAH. Such problems might include admission to the hospital, abnormal heart rhythms and worsening heart failure. What is Cystatin C? Cystatin … [Read more...]

Eisenmenger’s Syndrome

February 9, 2016 By Dr. Jeremy Feldman

Pulmonary hypertension and pregnancy

Congenital Heart Disease & Eisenmenger's Syndrome February 4th-7th is Congenital Heart Disease Awareness week.  The incidence of congenital heart disease today is 1:100 live births.  With today’s post , I wanted to discuss a complicated problem that adults who are born with congenital heart disease may suffer from for their entire lives: Eisenmenger’s Syndrome. A … [Read more...]

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