Right aortic arch anomalies occur in approximately 0.01 to 0.1 percent of the general population. In general, these anomalies do not directly cause any cardiovascular problems. However, in some patients, right aortic arches can be associated with other congenital heart defects, vascular rings, and chromosomal abnormalities such as DiGeorge syndrome. Rarely, various anatomical issues can arise, leading to complications that can require surgical intervention. This activity reviews the evaluation and management of right aortic arches and highlights the role of the interprofessional team in caring for affected patients and their families.
- Provider:StatPearls, LLC
- Activity Link: https://www.statpearls.com/ArticleLibrary/viewarticle/28590
- Start Date: 2023-09-01 05:00:00
- End Date: 2023-09-01 05:00:00
- Credit Details: AMA PRA Category 1 Credit™️: 1.5 hours
Nursing: 1.5 hours
Pharmacy: 1.5 hours - MOC Credit Details: ABS - 1.5 Point; Credit Type(s): Accredited CME (ABS)
ABPATH - 1.5 Point; Credit Type(s): Lifelong Learning (ABPATH)
ABTS - 1.5 Point; Credit Type(s): Accredited CME (ABTS)
ABIM - 1.5 Point; Credit Type(s): Medical Knowledge (ABIM)
ABS - 1.5 Point; Credit Type(s): Self-Assessment (ABS)
ABP - 1.5 Point; Credit Type(s): Lifelong Learning and Self-Assessment (ABP)
ABTS - 1.5 Point; Credit Type(s): Self-Assessment (ABTS) - Commercial Support: No
- Activity Type: Enduring Material
- CME Finder Type: Online Learning
- Fee to Participate: Variable
- Measured Outcome: Learner Knowledge, Learner/Team Competence
- Provider Ship: Directly Provided
- Registration: Open to all
- Specialty: Adolescent Medicine, Adult Congenital Heart Disease, Cardiothoracic, Cardiovascular Disease, Clinical Pathology, Congenital Cardiac, General Pediatrics, Hospital Medicine, Internal Medicine, Interventional Cardiology, Pediatric Cardiology, Pediatric Emergency Medicine, Vascular Surgery
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