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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

FAQ’s: VQ Scans & PAH Curable?

June 28, 2018 By Dr. Jeremy Feldman

VQ perfusion lung scan severe pulmonary hypertension CTEPH
Perfusion scan from a patient with severe chronic thromboembolic pulmonary hypertension. The right lung has nearly no blood flow. The left lung has multiple wedge shaped blood flow defects.

Ventilation Perfusion Lung Scans

Ventilation perfusion lung scans or VQ scans are an important test to evaluate for the possibility of chronic blood clots in your lungs.  This test is generally not performed at local imaging centers (though in some larger towns they may be).

Typically, this test is performed at regional hospitals.  Over the past 20 years, this test is not used as much to evaluate for acute blood clots in the lungs (pulmonary emboli).  However, larger hospitals should be able to perform this test. On the instructions/prescription for the test, the hospital or imaging center should be informed that chronic thromboembolic disease is being considered.

For more details about VQ scans click here.

Can PAH Be Cured?

In adults we generally don’t think of PAH as a curable disease.  However, there are some exceptions.  For example, some patients that are living at very high elevation and then move to lower elevation may have mild PAH at higher elevation and their numbers normalize at lower elevation.

Another example is if a patient has a severe pneumonia or other temporary lung problem and they are evaluated for “PAH” during that illness, the numbers may look very much like mild PAH.  Once the pneumonia or other temporary lung problem resolves then their numbers may return to normal.  Patients that are using methamphetamines can have dramatic improvement and occasionally normalization of their pulmonary artery pressures when they stop using methamphetamines.

Some patients with quite severe PAH can have their pressures return to normal while they are being treated with PAH medications.  This does not mean that they are cured of PAH.  Although it may be tempting for the patient to want to stop their medications, my practice is not to stop medications under those circumstances but to celebrate the progress.  If a patient has had a truly dramatic response to multi-agent therapy and wants to try and switch from pump therapy to an all pill regimen, I am open to this under certain circumstances.

Children with PAH who are treated with medications may also show dramatic improvement.  At times this may lead their doctors to slowly wean them off PAH medications.  These patients need to be watched very carefully for decades as their PAH may worsen and they may require restarting their PAH medications.

Filed Under: FAQ's

PAH Life Expectancy

PAH Research

Research, Life Expectancy & Prognosis for PH

Major Developments in Pulmonary Hypertension Affecting Prognosis 1.     Approval of

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Pulmonary Hypertension Centers

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