3 results match your criteria: "1 Department of Surgery The Ohio State University Wexner Medical Center Columbus OH.[Affiliation]"
Liver Transpl
November 2021
Department of Internal Medicine The Ohio State University Wexner Medical Center Columbus OH Division of Gastroenterology, Hepatology and Nutrition The Ohio State University Wexner Medical Center Columbus OH Department of Surgery The Ohio State University Wexner Medical Center Columbus OH Division of Hospital Medicine The Ohio State University Wexner Medical Center Columbus OH Center for BiostatisticsDepartment of Biomedical Informatics The Ohio State University Wexner Medical Center Columbus OH.
We studied the trends and various outcomes, including the readmission rates, health care utilization, and complications among living liver donors (LLDs) in the United States. We queried the National Database for data from 2010 to 2017 for all LLDs. The primary outcomes were 30-day and 90-day readmission rates.
View Article and Find Full Text PDFJ Am Heart Assoc
October 2020
Background Atrial fibrillation (AF) driver mechanisms are obscured to clinical multielectrode mapping approaches that provide partial, surface-only visualization of unstable 3-dimensional atrial conduction. We hypothesized that transient modulation of refractoriness by pharmacologic challenge during multielectrode mapping improves visualization of hidden paths of reentrant AF drivers for targeted ablation. Methods and Results Pharmacologic challenge with adenosine was tested in ex vivo human hearts with a history of AF and cardiac diseases by multielectrode and high-resolution subsurface near-infrared optical mapping, integrated with 3-dimensional structural imaging and heart-specific computational simulations.
View Article and Find Full Text PDFBackground The aortic valve of the heart experiences constant mechanical stress under physiological conditions. Maladaptive valve injury responses contribute to the development of valvular heart disease. Here, we test the hypothesis that MG 53 (mitsugumin 53), an essential cell membrane repair protein, can protect valvular cells from injury and fibrocalcific remodeling processes associated with valvular heart disease.
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