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Thomas L. Holland

Researcher at Duke University

Publications -  74
Citations -  5580

Thomas L. Holland is an academic researcher from Duke University. The author has contributed to research in topics: Medicine & Internal medicine. The author has an hindex of 18, co-authored 57 publications receiving 3660 citations. Previous affiliations of Thomas L. Holland include Intermountain Medical Center & Durham University.

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Staphylococcus aureus Infections: Epidemiology, Pathophysiology, Clinical Manifestations, and Management

TL;DR: This review comprehensively covers the epidemiology, pathophysiology, clinical manifestations, and management of S. aureus as a leading cause of bacteremia and infective endocarditis as well as osteoarticular, skin and soft tissue, pleuropulmonary, and device-related infections.
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Methicillin-resistant Staphylococcus aureus: an overview of basic and clinical research.

TL;DR: An overview of basic and clinical MRSA research is provided and the expansive body of literature on the epidemiology, transmission, genetic diversity, evolution, surveillance and treatment of MRSA is explored.
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Clinical management of Staphylococcus aureus bacteremia: a review.

TL;DR: In this article, the authors reviewed evidence of management strategies for Staphylococcus aureus bacteremia to determine whether transesophageal echocardiography is necessary in all adult cases and what is the optimal antibiotic therapy for methicillin-resistant S auresus (MRSA) bacterers.
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A Neutralizing Monoclonal Antibody for Hospitalized Patients with Covid-19.

J D Lundgren, +48 more
TL;DR: In this paper, the effect of neutralizing monoclonal antibody (YL-CoV555) on patients with Coronavirus disease 2019 (Covid-19) was investigated.
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The Emperor's New Clothes: PRospective Observational Evaluation of the Association Between Initial VancomycIn Exposure and Failure Rates Among ADult HospitalizEd Patients With Methicillin-resistant Staphylococcus aureus Bloodstream Infections (PROVIDE).

TL;DR: Higher vancomycin exposures did not confer a lower TF risk but were associated with more AKI, and dosing should be guided by the AUC and day-2 AUCs should be ≤515.