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Ostium Secundum Atrial Septal Defects Treatment & Management

  • Author: Ira H Gessner, MD; Chief Editor: P Syamasundar Rao, MD  more...
 
Updated: Jan 07, 2016
 

Medical Care

Small-to-moderate–sized ostium secundum atrial septal defects diagnosed in the infant demonstrate significant likelihood of either spontaneous closure or reduction in size to the point that medical intervention no longer is indicated. Such patients should be followed until age 3-4 years before considering either device use or surgical closure.[5, 19]

No medications are required, except bacterial endocarditis prophylaxis for 6 months following either device or patch closure.

Consultations

Patients should be evaluated by a pediatric cardiologist. Patients with defects considered appropriate for transcatheter device closure should be evaluated by an interventional pediatric cardiologist experienced in the procedure. If surgery is contemplated, the patient should be evaluated by a cardiovascular surgeon experienced in surgery of congenital heart defects. Ideally, decisions regarding therapy should result from simultaneous evaluation of patient data at a group meeting that includes all of these physicians.

Transfer

Evaluation and treatment should be carried out at a center specializing in congenital heart disease.

Diet and activity

No special diet is required.

No activity restrictions are required except for a few weeks following either device closure or heart surgery.

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Surgical Care

Minimally invasive cardiac surgery

Minimally invasive cardiac surgery techniques allow closure without the use of blood or blood products in appropriately sized patients.[20, 21, 22]

The skin incision is short because complete vertical division of the sternum is not necessary.

If the defect is moderate in size and oval in shape, direct suture closure may be appropriate. Larger or rounder defects require patch closure. The patch can be fashioned from the patient's pericardium or made from Dacron.

Results of surgery are excellent; a 100% closure rate should be achieved. Risk of mortality does not exceed that of general anesthesia.[23, 24]

Inpatient hospital stay averages 2-3 days. Perform postoperative echocardiography to confirm closure.

Postoperative care includes bacterial endocarditis precautions for 6 months if a patch was placed.

Cardiac catheter intervention

Catheter intervention may be indicated.

Transcatheter device closure of secundum atrial septal defect now represents a standard of care for this abnormality.[25] Experience at centers throughout the world is extensive; the success rate has been high, and the risk of complications has been low.[26, 27, 28, 29, 30, 31, 32, 33] Indication for closure in the pediatric age range is a shunt of sufficient size to be clinically apparent. The reason for closure is to prevent development of complications (eg, atrial dysrhythmia, right heart dysfunction) that may appear in the adult. Small defects in children that are detectable only by echocardiography do not require closure.

In adult patients who experience a suspected thrombotic stroke and who manifest a patent foramen ovale (15-20% of all adults demonstrate a patent foramen ovale on echocardiography), concern arises that the stroke may have been caused by a paradoxical embolus.[34] In these patients, device closure of the communication is often recommended and accomplished. Studies remain controversial regarding the appropriateness of this treatment.

Transcatheter device occlusion of a secundum atrial septal defect should be accomplished only by physicians properly trained and experienced in the procedure. Proper sizing of the defect and anatomic evaluation to assure reliable seating of the device is essential.

The device is placed in the atrial septum via a catheter introduced into a femoral vein. Most operators advise monitoring the procedure with transesophageal echocardiography. Multiple studies indicate a high degree of success, with complete closure rates only slightly less than those obtained by surgery.

Studies comparing device closure with surgery establish that hospital stay is shorter in patients undergoing device closure. Total costs of the 2 techniques do not significantly differ, apparently because of the cost of the device.[35]

Complications of device occlusion include hemorrhage, vascular disruption, pain, nausea and vomiting, and arterial or venous obstruction from thrombosis or spasm. Other complications include rupture of blood vessel, tachyarrhythmias, bradyarrhythmias, and vascular occlusion. Embolization of the device during placement rarely occurs but can result in emergency surgery for removal. The most common complication is incomplete closure of the defect.[36]

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Contributor Information and Disclosures
Author

Ira H Gessner, MD Professor Emeritus, Pediatric Cardiology, University of Florida College of Medicine

Ira H Gessner, MD is a member of the following medical societies: American Academy of Pediatrics, American College of Cardiology, American Heart Association, American Pediatric Society, Society for Pediatric Research

Disclosure: Nothing to disclose.

Specialty Editor Board

Mary L Windle, PharmD Adjunct Associate Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: Nothing to disclose.

Alvin J Chin, MD Emeritus Professor of Pediatrics, University of Pennsylvania School of Medicine

Alvin J Chin, MD is a member of the following medical societies: American Association for the Advancement of Science, Society for Developmental Biology, American Heart Association

Disclosure: Nothing to disclose.

Chief Editor

P Syamasundar Rao, MD Professor of Pediatrics and Medicine, Division of Cardiology, Emeritus Chief of Pediatric Cardiology, University of Texas Medical School at Houston and Children's Memorial Hermann Hospital

P Syamasundar Rao, MD is a member of the following medical societies: American Academy of Pediatrics, American Pediatric Society, American College of Cardiology, American Heart Association, Society for Cardiovascular Angiography and Interventions, Society for Pediatric Research

Disclosure: Nothing to disclose.

Additional Contributors

Paul M Seib, MD Associate Professor of Pediatrics, University of Arkansas for Medical Sciences; Medical Director, Cardiac Catheterization Laboratory, Co-Medical Director, Cardiovascular Intensive Care Unit, Arkansas Children's Hospital

Paul M Seib, MD is a member of the following medical societies: American Academy of Pediatrics, American College of Cardiology, American Heart Association, Arkansas Medical Society, International Society for Heart and Lung Transplantation, Society for Cardiovascular Angiography and Interventions

Disclosure: Nothing to disclose.

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