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Management of Adults With Congenital Heart Disease

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60 Specific Conditions Table 29. Isolated Pulmonary Regurgitation After Repair of Pulmonary Stenosis: 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 36–60 24 6–12 3–6 Electrocardiogram 36–60 24 12 12 Transthoracic echocardiogram 36–60 24 12 12 For recommendations about timing of CMR imaging, see Section 4.3.2.1 supportive text for recommendation #1. Modified with permission from Stout et al. Copyright © 2018 American Heart Association, Inc. and American College of Cardiolog y Foundation. * See Section 2.2 for details on the ACHD anatomic and physiological classification system. ACHD indicates adult congenital heart disease; and CMR, cardiovascular magnetic resonance. 4.3.3. Management of Double-Chambered Right Ventricle COR LOE Recommendations Diagnostic 2a C-LD 1. In adults with RV dysfunction or symptoms attributed to DCRV, cardiac catheterization is reasonable to characterize anatomy and severity. 2a C-EO 2. In adults with DCRV and moderate or greater RVOT obstruction, diagnostic assessment with CMR (or, if contraindicated, cardiac CT) can be beneficial to characterize the anatomy.* erapeutic 1 C-LD 3. In adults with DCRV, moderate or greater RVOT obstruction, and otherwise unexplained symptoms of heart failure, cyanosis, or exercise limitation, surgical repair is recommended to improve symptoms. 2a C-LD 4. In asymptomatic adults with DCRV and severe RVOT obstruction, surgical repair is reasonable to prevent symptoms and adverse RV remodeling. * Table 27 delineates levels of severity of RVOT obstruction and their related echocardiographic parameters.

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