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1.
Clin Pract ; 12(4): 557-564, 2022 Jul 15.
Article in English | MEDLINE | ID: mdl-35892445

ABSTRACT

Empagliflozin, a sodium-glucose transporter 2 inhibitor, has been shown to bind to late sodium channels in mice cardiomyocytes. We sought to investigate the electrocardiographic (ECG) features associated with empagliflozin use in patients with diabetes mellitus. We compared ECG features of 101 patients before and after initiation of empagliflozin and found that empagliflozin was associated with a significant increase in QRS duration among diabetes patients with heart failure.

2.
Article in English | MEDLINE | ID: mdl-31083298

ABSTRACT

African Americans, other minorities and underserved populations are consistently under- represented in clinical trials. Such underrepresentation results in a gap in the evidence base, and health disparities. The ABC Cardiovascular Implementation Study (CVIS) is a comprehensive prospective cohort registry that integrates social determinants of health. ABC CVIS uses real world clinical practice data to address critical gaps in care by facilitating robust participation of African Americans and other minorities in clinical trials. ABC CVIS will include diverse patients from collaborating ABC member private practices, as well as patients from academic health centers and Federally Qualified Health Centers (FQHCs). This paper describes the rationale and design of the ABC CVIS Registry. The registry will: (1) prospectively collect socio-demographic, clinical and biospecimen data from enrolled adults, adolescents and children with prioritized cardiovascular diseases; (2) Evaluate the safety and clinical outcomes of new therapeutic agents, including post marketing surveillance and pharmacovigilance; (3) Support National Institutes of Health (NIH) and industry sponsored research; (4) Support Quality Measures standards from the Center for Medicare and Medicaid Services (CMS) and Commercial Health Plans. The registry will utilize novel data and technology tools to facilitate mobile health technology application programming interface (API) to health system or practice electronic health records (EHR). Long term, CVIS will become the most comprehensive patient registry for underserved diverse patients with cardiovascular disease (CVD) and co morbid conditions, providing real world data to address health disparities. At least 10,000 patients will be enrolled from 50 sites across the United States.


Subject(s)
Black or African American/statistics & numerical data , Social Determinants of Health/statistics & numerical data , Vulnerable Populations/statistics & numerical data , Georgia , Humans , Prospective Studies , Registries
3.
Circ Heart Fail ; 9(6): e002558, 2016 06.
Article in English | MEDLINE | ID: mdl-27188913

ABSTRACT

Transthyretin-related cardiac amyloidosis is a progressive infiltrative cardiomyopathy that mimics hypertensive and hypertrophic heart disease and often goes undiagnosed. In the United States, the hereditary form disproportionately afflicts black Americans, who when compared with whites with wild-type transthyretin amyloidosis, a phenotypically similar condition, present with more advanced disease despite having a noninvasive method for early identification (genetic testing). Although reasons for this are unclear, this begs to consider the inadequate access to care, societal factors, or a biological basis. In an effort to improve awareness and explore unique characteristics, we review the pathophysiology, epidemiology, and therapeutic strategies for transthyretin amyloidosis and highlight diagnostic pitfalls and clinical pearls for identifying patients with amyloid heart disease.


Subject(s)
Amyloid Neuropathies, Familial/ethnology , Amyloid Neuropathies, Familial/genetics , Black or African American/genetics , Cardiomyopathies/ethnology , Cardiomyopathies/genetics , Mutation , Prealbumin/genetics , Amyloid Neuropathies, Familial/physiopathology , Amyloid Neuropathies, Familial/therapy , Cardiomyopathies/physiopathology , Cardiomyopathies/therapy , Genetic Predisposition to Disease , Heredity , Humans , Phenotype , Predictive Value of Tests , Prognosis
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