Duchenne Dilated Cardiomyopathy: Cardiac Management from Prevention to Advanced Cardiovascular Therapies.
Rachele AdorisioErica MencarelliNicoletta CantaruttiCamilla CalvieriLiliana AmatoMarianna CiceniaMassimo SilvettiAdele D'AmicoMaria GrandinettiFabrizio DragoAntonio AmodeoPublished in: Journal of clinical medicine (2020)
Duchenne muscular dystrophy (DMD) cardiomyopathy (DCM) is characterized by a hypokinetic, dilated phenotype progressively increasing with age. Regular cardiac care is crucial in DMD care. Early recognition and prophylactic use of angiotensin converting enzyme inhibitors (ACEi) are the main stay therapeutic strategy to delay incidence of DMD-DCM. Pharmacological treatment to improve symptoms and left ventricle (LV) systolic function, have been widely implemented in the past years. Because of lack of DMD specific drugs, actual indications for established DCM include current treatment for heart failure (HF). This review focuses on current HF strategies to identify, characterize, and treat DMD-DCM.
Keyphrases
- duchenne muscular dystrophy
- heart failure
- muscular dystrophy
- left ventricular
- angiotensin converting enzyme
- healthcare
- palliative care
- angiotensin ii
- quality improvement
- risk factors
- pulmonary hypertension
- pain management
- combination therapy
- physical activity
- chronic pain
- affordable care act
- cardiac resynchronization therapy
- congenital heart disease