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Long-term Management of the Arterial Switch Patient
Jared Kirzner1, Altaf Pirmohamed1, Jonathan Ginns1
1Cornell Center for Adult Congenital Heart Disease, Departments of Medicine and Pediatrics, Division of Cardiology, New York Presbyterian Hospital, Weill Cornell Medicine, 520 East 70th Street, Starr 425, New York, NY, 10021, USA.
Insights
This review focuses on managing dextro-transposition of the great arteries (D-TGA), a cyanotic congenital heart disease. Early detection and prevention of complications like stenosis and regurgitation are crucial for long-term patient health.
Area of Science:
- Cardiology
- Pediatric Cardiology
- Congenital Heart Disease
Background:
- Dextro-transposition of the great arteries (D-TGA) accounts for approximately 3% of all congenital heart disease (CHD) and 20% of cyanotic CHD.
- The arterial switch operation (ASO) has been the standard repair for D-TGA since the late 1980s, offering superior long-term outcomes compared to the Mustard/Senning operation.
Purpose of the Study:
- To review the management of patients with D-TGA.
- To focus on identifying and preventing adverse events and long-term complications.
Main Methods:
- Review of current literature and clinical guidelines for D-TGA management.
- Emphasis on long-term follow-up strategies.
- Utilization of echocardiography and advanced imaging (CT/MRI).
Main Results:
- The arterial switch operation (ASO) is associated with superior long-term survival and complication rates.
- Common long-term complications include pulmonary stenosis, coronary artery stenosis, and neo-aortic regurgitation.
- Regular follow-up with adult congenital heart disease specialists is recommended.
Conclusions:
- Long-term surveillance is essential for all D-TGA patients.
- Prompt evaluation of new symptoms or functional decline is critical for effective management.
- Preventing and treating sequelae like stenosis and regurgitation improves patient outcomes.
Purpose Of Review:
This review paper describes the management of patients with dextro-transposition of the great arteries (D-TGA) with a focus on the complications seen and the appropriate care required to identify and prevent adverse events.
Recent Findings:
D-TGA is a form of cyanotic congenital heart disease (CHD) representing ~ 3% of all CHD and almost 20% of all cyanotic CHD. Since the late 1980s, standard of care is to repair these patients with an arterial switch operation (ASO) as opposed to a Mustard/Senning operation. The long-term survival and complication rates are superior in the ASO. Long-term follow-up is recommended for all D-TGA patients and includes management with adult congenital heart disease specialists and the use of echocardiography and advanced imaging with CT or MRI. The most common complications seen are pulmonary stenosis, coronary artery stenosis, and neo-aortic regurgitation. Careful evaluation of new symptoms or declining function is essential in preventing and treating these long-term sequelae.
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