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Management of Adults With Congenital Heart Disease

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45 Table 18. Patent Ductus Arteriosus: 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 12–60 6–12 3–6 Electrocardiogram 36–60 12–60 12 12 Transthoracic echocardiogram 36–60 12–60 12 12 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. † Stage A patients who had closure of their PDA during infancy without residual shunt, chamber dilation, or complications can likely be discharged from cardiolog y care or be seen on an as-needed basis. ‡ Stage B patients with a PDA and a hemodynamically insignificant shunt who have normal chamber size without pulmonary hypertension can be seen every 36 to 60 months. Patients with ventricular dilation, dysfunction, or arrhythmia should be seen more frequently. ACHD indicates adult congenital heart disease; and PDA, patent ductus arteriosus. 4.2.1. Cor Triatriatum Sinister COR LOE Recommendations Diagnostic 2a B-NR 1. In adults with unrepaired cor triatriatum sinister, transesophageal echocardiography and/or cross-sectional imaging can be useful to identify the size and location of the membrane orifice and to assess for the presence of associated congenital cardiac defects. 2a B-NR 2. In adults with repaired cor triatriatum sinister and symptoms compatible with recurrent membrane obstruction, it is reasonable to evaluate for the presence of residual congenital cardiac defects, including pulmonary vein stenosis. 4.2. Left-Sided Lesions

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