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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

Preventative Testing Important for PAH Patients

December 22, 2017 By Dr. Jeremy Feldman

mammogram

Many patients with PAH become very focused on caring for that specific disease, and rightly so. After all, we ask that pulmonary hypertension patients become well versed in their disease and treatments and help educate other providers on this rare disease. Sometimes providers also become hyper-focused while treating PAH patients and put preventative testing on the back burner.  … [Read more...]

Hereditary Hemorrhagic Telangiectasia (HHT) Treatment

December 18, 2017 By Dr. Jeremy Feldman

treatment laboratory

  Nose bleeding The first step in treating a nose bleed is applying pressure.  You should lean forward slightly and pinch your nose with firm pressure.  Don’t let go for ten minutes.  When you let go, don’t try and blow your nose and avoid packing your nose with tissue paper.  When you blow your nose, you will displace the clot that has stopped the bleeding. Similarly, when … [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...]

End of Year Insurance Considerations for PAH Patients

November 15, 2017 By Dr. Jeremy Feldman

insurance considerations in pah

The end of the year brings many celebrated happenings. It is a wonderful time of year to celebrate coming together with family and friends.  It also brings a much less celebrated event…open enrollment. Open Enrollment We are currently in the middle of Medicare/Medicaid open enrollment which began October 15th and will end December 7th. Coverage chosen during this time will … [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

Popular Posts

financial assistance for PAH patients

Copay Assistance from PAN Foundation Now Open

By Dr. Jeremy Feldman

The PAN Foundation announced that they have funds to help patients.  They have grants available for up to $5,300.  You

Swelling in ankles of PH patient

PAH and Diuretics

By Dr. Jeremy Feldman

Let’s Talk About Diuretics (Medicines That Make Your Kidneys Produce More Urine). One of the major problems in PAH is

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