Cor triatriatum surgery: Difference between revisions

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==References==
==References==
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[[Category:Congenital heart disease]]
[[Category:Congenital heart disease]]

Revision as of 15:40, 4 September 2012

Cor triatriatum Microchapters

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Patient Info

Overview

Pathophysiology

Epidemiology & Demographics

Risk Factors

Natural History, Complications & Prognosis

Causes of Cor triatriatum

Differentiating Cor triatriatum from other Diseases

Diagnosis

History & Symptoms

Physical Examination

Electrocardiogram

Chest X Ray

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editors-In-Chief: Priyamvada Singh, M.B.B.S. [2]; Cafer Zorkun, M.D., Ph.D. [3]; Keri Shafer, M.D. [4]; Assistant Editor(s)-In-Chief: Kristin Feeney, B.S. [5]

Overview

In cor triatriatum, adminstration of effective surgical therapy in a timely manner can greatly impact the patient's prognosis. Considerations must made to evaluate to utilize the most appropriate surgical approach, right atrial or left atrial.

Surgical Therapy

  • The role of percutaneous balloon dilation in managing this condition remains to be determined.
  • It can be treated surgically by removing the membrane dividing the atrium.

Left atrial approach

  • Better if the patient is older, and defect is larger
  • Excise the obstructing diaphragm
  • Enlarge the left atrium as needed and close the interatrial connection

Right atrial approach

Better if the patient is younger, and defect is smaller

  • Locate the diaphragm through the ASD
  • Excise the obstructing diaphragm
  • Close the ASD

References


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