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Skip search results from other journals and go to results- 3 JMIR Research Protocols
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There, however, is a growing cohort of young patients with idiopathic dilated cardiomyopathy with HFr EF who are often suboptimally medically treated with minimum prospects of receiving heart transplants. In our opinion, such a group of patients would ideally benefit from ARNIs and SGLT2is. Data from key clinical trials have demonstrated the use of ARNIs as de novo therapy in patients presenting with heart failure [3,10,11].
JMIR Res Protoc 2025;14:e44027
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Disease Progression of Hypertrophic Cardiomyopathy: Modeling Using Machine Learning
Among them specifically, hypertrophic cardiomyopathy (HCM) is a genetic cardiac disease that is a cause of sudden cardiac death (SCD), especially among young adults and athletes [9]. Cardiovascular diseases represent groups of diseases that can greatly benefit from preemptive prediction, prevention, and proactive management; thus, this opens an opportunity for methods of artificial intelligence (AI) [2].
JMIR Med Inform 2022;10(2):e30483
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A review from 2016 [14] on the use of PRO instruments in HF management concluded that the Minnesota Living with Heart Failure and Kansas City Cardiomyopathy Questionnaire (KCCQ) were useful PRO instruments in clinical care. However, more studies are needed on the value and interpretability of PRO instruments in clinical settings. The aim of this study is to evaluate the changes in quality of life and well-being among patients with HF, who are participants in the FPT program over the course of 1 year [13].
JMIR Cardio 2021;5(2):e26544
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This results in infantile cardiomyopathy (including stillbirth) and lifelong severe exercise intolerance, lethargy, and fatigue [1]. Low neutrophil numbers (neutropenia), poor feeding, and growth delay are less intuitive but common features [1]. Neutropenia predisposes to serious bacterial infection and is symptomatically treated in two-thirds of UK patients with Barth syndrome via chronic subcutaneous injection therapy with granulocyte-colony stimulating factor—a distressing and expensive medication [2].
JMIR Res Protoc 2021;10(5):e22533
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Among the different types of cardiomyopathies, dilated cardiomyopathy (DCM) is by far the most common in sub-Saharan Africa [7-9].
DCM is defined as the presence of left or biventricular dilatation and contractile dysfunction in the absence of abnormal loading conditions (such as hypertension or valve disease) or coronary artery disease that is sufficient to cause global contractile impairment [10].
JMIR Res Protoc 2021;10(1):e18229
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