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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

CT (Computed Tomography) Scan

CT scanning is used during the evaluation process for pulmonary hypertension

CT scan severe idiopathic PAH
CT scan demonstrating severe idiopathic pulmonary arterial hypertension. Note the markedly enlarged pulmonary arteries with tiny branching smaller vessels.

A CT of the chest is commonly ordered while evaluating a patient for pulmonary hypertension as it is a useful tool for identifying other lung diseases that might be responsible for the patient’s symptoms. CT scans can be performed as an outpatient at hospitals or imaging centers. There is usually little or no preparation required for a CT scan of the chest but a patient should always check with their physician or imaging center before scheduling the test.

What is a CT scan?

CT scans use x-rays to make detailed images of structures inside the body. The pictures are taken with the patient lying on a table with the CT scanner (a large machine with a hole in the middle) hooked to it. The part of the body being imaged will be in the hole of the scanner. The scanner rotates with each rotation taking less than a second and provides a picture of a thin slice of the area being scanned. All of these pictures are then saved together and the radiologist can view them and move through them as if he is looking directly into the body. This test can be performed with or without contrast. The contrast is an iodine dye that is used to check blood flow and look for other problems. If contrast is ordered an IV will have to be placed and the dye will be injected through the patient’s vein. There is also another variation called an HRCT or high resolution CT scan. This test is the same as a standard CT but takes more pictures of smaller slices of the area of the body being scanned. An HRCT scan can be very useful in evaluating certain types of interstitial lung diseases that may be associated with pulmonary hypertension.

What CT scan results suggest pulmonary hypertension?

CT Angiogram severe pulmonary hypertension
CT Angiogram of a patient with severe idiopathic pulmonary arterial hypertension. Note the enlarged right ventricle and the smaller left ventricle. The septum is pushed towards the left ventricle due to very high pressure inside the right ventricle.

A radiologist will review the images and write a report, which will then be sent to the ordering physician. It is a good idea for the patient to ask for the images to be saved on a disk that they can take with them and show their physician. In most cases no results will be given to the patient at the time of the scan. The CT scan is most useful in diagnosing other lung diseases that may lead to increased pressures in the pulmonary arteries such as blood clots, tumors, or interstitial lung disease (disease in the tissue of the lung not the blood vessels). But findings such as enlarged pulmonary arteries and enlarged chambers of the right heart can be suggestive of pulmonary hypertension. The patient should have a follow up appointment to go over the results with the physician that ordered the test. It is important for the patient to fully understand what the results mean for their treatment plan. It is a good idea for pulmonary hypertension patients to keep a copy of the results for their records.

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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