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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

Echocardiogram

The importance of echocardiograms for pulmonary hypertension patients.

For many PH patients the first step towards being diagnosed with pulmonary arterial hypertension is undergoing an echocardiogram or echo. This is an important screening test for PAH. It is also used for routine surveillance of patients once they have been diagnosed with pulmonary hypertension. It is frequently used because it is noninvasive, relatively inexpensive, and very accessible, being available in many physician offices, outpatient settings and hospitals.

Pulmonary arterial hypertension patiemt receiving echocardiogramWhat is an echocardiogram?

The echocardiogram is a simple ultrasound of the heart performed by an ultrasound technician and read by a cardiologist. It is done with the patient lying down in a darkened room. The technician uses a computer with a transducer attachment and a clear jelly like substance. The jelly substance is wiped on the skin and helps the transducer’s accuracy. This is the same technology used to look at fetuses during pregnancy. The transducer is then pushed against the patient’s chest. It emits sound waves that “echo” back when they hit an object like a heart valve allowing a moving image to be seen on screen.

This test allows the physician to examine the chambers of the right side of the heart. They can tell if they are enlarged, if their walls are thickened, and if the septum (the wall between the right and the left side of the heart) looks like it should. This test also looks at the valves of the heart and can diagnosis congenital heart disease (like holes in the heart) or abnormal fluid around the heart (pericardial effusion). It can also estimate the pulmonary artery pressures using mathematical equations and the amount of blood being jetted back into the right atrium by the right ventricle.

Findings from an echocardiogram can suggest a diagnosis of pulmonary hypertension.

There are several findings from an echocardiogram that are suggestive of pulmonary hypertension. An enlarged right atrium, an enlarged right ventricle with a thick wall, septal shift (meaning the septum of the heart has been pushed into the left side of the heart by the enlarged chambers of the right side of the heart), and of course elevated pulmonary artery pressures are some of these results.

What to do if your echocardiogram results suggest pulmonary hypertension.

If a pulmonary hypertension specialist did not perform the echocardiogram and it shows signs of pulmonary hypertension you may be referred to a PH specialist. The pulmonary hypertension expert will investigate how the results of the echocardiogram correlate with the rest of the patient’s medical information and decide if further testing for pulmonary arterial hypertension is warranted. While the echocardiogram is a useful tool, it cannot be used to officially diagnose PAH and treatment should not be initiated based on estimated pulmonary artery pressures from the echo. A right heart catheterization is currently the only way to officially diagnose pulmonary arterial hypertension.

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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