Key result
Management of adults with congenital heart disease requires consideration of the clinical setting, surgeon expertise, and coexisting diseases associated with aging and the specific cardiac defect.
Highlights the growing population of adults with congenital heart disease and the multifaceted considerations required for their management, including transition of care and coexisting conditions.
May warrant referral to specialized ACHD centers; leaves open optimal protocols for aging-related comorbidities.
The significant decline in mortality among children and adolescents with congenital heart disease (CHD) is associated with an increasing prevalence of CHD in adults, particularly those with moderate to severe defects. As a significant percentage of adolescents and young adults are lost to follow-up in the transition from pediatric to adult care, they may present for elective procedures with substantial CHD-associated morbidity. In addition to the specific cardiac defect, the procedures performed, and the current pathophysiological status, several factors should be considered when managing the adult with CHD. These include the type of setting (adult vs pediatric institution); surgeon (pediatric vs adult cardiac surgeon); coexisting diseases associated with CHD, such as coronary artery disease, hepatic dysfunction, renal dysfunction, cerebrovascular accidents, myopathy, and coagulation disorders; acquired diseases of aging; pregnancy; and psychosocial functioning. The current status of the management of common and important congenital cardiac defects is also described.
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Nasr et al. (2014) conducted a review in Congenital heart disease. Management of adults with congenital heart disease was evaluated. Management of adults with congenital heart disease requires consideration of the clinical setting, surgeon expertise, and coexisting diseases associated with aging and the specific cardiac defect.
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