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Management of Adults With Congenital Heart Disease

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76 Specific Conditions Table 38. Patients With d-TGA and Rastelli Operation: Routine Follow-Up and Testing Intervals Type of Follow-Up or Testing Physiological Stage A* (mo) Physiological Stage B* (mo) Physiological Stage C* (mo) Physiological Stage D* (mo) Outpatient ACHD cardiologist N/A 12–24 12 3–6 Electrocardiogram N/A 12–24 12 12 Transthoracic echocardiogram N/A 12–24 12 12 For recommendations about timing of cardiac CT and CMR imaging, see supportive text for recommendation #1. * See Section 2.2 for details on the ACHD anatomic and physiological classification system. ACHD indicates adult congenital heart disease; d-TGA, dextro-transposition of the great arteries; and N/A, not applicable. 4.4.1.3. Patients With d-TGA and Rastelli Repair COR LOE Recommendation 1 B-NR 1. In adults with d-TGA and Rastelli repair, imaging is recommended to ensure timely identification of complications, including stenosis and/or regurgitation of the RV-to-PA conduit, residual VSDs, LVOT obstruction, and RV dysfunction. 4.4.2. Management of CCTGA COR LOE Recommendations Diagnostic 1 B-NR 1. In adults with congenital CCTGA, periodic* transthoracic echocardiography is recommended to assess chamber function, systemic tricuspid valve function, and associated anatomic lesions such as septal defects and LVOT stenosis. 2a B-NR 2. In adults with CCTGA, periodic cross-sectional imaging (preferably, CMR) is reasonable to assess systemic ventricular volumes and function, quantify the severity of systemic tricuspid regurgitation, and assess the severity of associated anatomic lesions. 2a B-NR 3. In adults with CCTGA without symptoms, periodic ambulatory rhythm monitoring is reasonable to screen for high-grade atrioventricular block.

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