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Total anomalous pulmonary venous return

Definition

Total anomalous pulmonary venous return (TAPVR) is a heart disease in which the 4 veins that take blood from the lungs to the heart do not attach normally to the left atrium (left upper chamber of the heart). Instead, they attach to another blood vessel or the wrong part of the heart. It is present at birth (congenital heart disease).

Alternative Names

TAPVR; Total veins; Congenital heart defect - TAPVR; Cyanotic heart disease - TAPVR

Causes

The cause of total anomalous pulmonary venous return is unknown.

In normal circulation, blood is sent from the right ventricle to pick up oxygen in the lungs. It then returns through the pulmonary (lung) veins to the left side of the heart, which sends blood out through the aorta and around the body.

In TAPVR, oxygen-rich blood returns from the lungs to the right atrium or to a vein flowing into the right atrium, instead of the left side of heart. In other words, blood simply circles to and from the lungs and never gets out to the body.

For the infant to live, an atrial septal defect (ASD) or patent foramen ovale (passage between the left and right atria) must exist to allow oxygenated blood to flow to the left side of the heart and the rest of the body.

How severe this condition is depends on whether the pulmonary veins are blocked or obstructed as they drain. Obstructed TAPVR causes symptoms early in life and can be deadly very quickly if it is not found and corrected with surgery.

Symptoms

The infant may appear very sick and may have the following symptoms:

Note: Sometimes, no symptoms may be present in infancy or early childhood.

Exams and Tests

Tests may include:

  • Cardiac catheterization can confirm the diagnosis by showing that the blood vessels are abnormally attached
  • ECG shows enlargement of the ventricles (ventricular hypertrophy)
  • Echocardiogram may show that the pulmonary vessels are attached
  • MRI or CT scan of the heart can show the connections between the pulmonary vessels
  • X-ray of the chest shows a normal to small heart with fluid in the lungs

Treatment

Surgery to repair the problem is needed as soon as possible. In surgery, the pulmonary veins are connected to the left atrium and the defect between the right and left atrium is closed.

Outlook (Prognosis)

If this condition is not treated, the heart will get larger, leading to heart failure. Repairing the defect early provides excellent results if there is no blockage of the pulmonary veins at the new connection into the heart. Infants who have obstructed veins have worsened survival.

Possible Complications

Complications may include:

  • Breathing difficulties
  • Heart failure
  • Irregular, fast heart rhythms (arrhythmias)
  • Lung infections
  • Pulmonary hypertension

When to Contact a Medical Professional

This condition may be apparent at the time of birth. However, symptoms may not be present until later.

Call your health care provider if you notice symptoms of TAPVR. Prompt attention is required.

Prevention

There is no known way to prevent TAPVR.

Gallery

Heart - section through the middle
The interior of the heart is composed of valves, chambers, and associated vessels.
Heart - section through the middle
The interior of the heart is composed of valves, chambers, and associated vessels.
Heart - section through the middle
The interior of the heart is composed of valves, chambers, and associated vessels.
Heart - section through the middle
The interior of the heart is composed of valves, chambers, and associated vessels.

References

Valente AM, Dorfman AL, Babu-Narayan SV, Kreiger EV. Congenital heart disease in the adolescent and adult. In: Libby P, Bonow RO, Mann DL, Tomaselli GF, Bhatt DL, Solomon SD, eds. Braunwald's Heart Disease: A Textbook of Cardiovascular Medicine. 12th ed. Philadelphia, PA: Elsevier; 2022:chap 82.

Well A, Fraser CD. Congenital heart disease. In: Townsend CM Jr, Beauchamp RD, Evers BM, Mattox KL, eds. Sabiston Textbook of Surgery: The Biological Basis of Modern Surgical Practice. 21st ed. Philadelphia, PA: Elsevier; 2022:chap 59.

Last reviewed October 10, 2021 by Michael A. Chen, MD, PhD, Associate Professor of Medicine, Division of Cardiology, Harborview Medical Center, University of Washington Medical School, Seattle, WA. Also reviewed by David Zieve, MD, MHA, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team..

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