Publications by authors named "J L Card"

Background: The safety of the anesthesia team model performed in oral and maxillofacial surgery (OMS) offices has been criticized by professional and mainstream media.

Purpose: This study aims to assess the incidence of adverse anesthetic events (AEs) associated with the OMS anesthesia team model and identify risk factors associated with AEs.

Study Design, Setting, Sample: This was a retrospective cohort study utilizing a patient database from Paradigm Oral Health, Lincoln, Nebraska, a managed service organization (MSO).

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Article Synopsis
  • The study evaluated an algorithmic testing approach in hematopathology to enhance cost-effectiveness in test selection at Brigham and Women's Hospital and Dana-Farber Cancer Institute, especially for expensive molecular assays.
  • Researchers developed standard ordering protocols (SOPs) for 17 disease categories, comparing data from six months of beta testing to actual testing practices, along with two years of prospective data from a community site.
  • Results showed a massive improvement in test concordance after implementing SOPs, with a decrease in overordered tests and significant potential annual savings of over $1.3 million, indicating that algorithmic testing can streamline procedures without compromising vital information.
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Our ability to understand the function of the nervous system is dependent upon defining the connections of its constituent neurons. Development of methods to define connections within neural networks has always been a growth industry in the neurosciences. Transneuronal spread of neurotropic viruses currently represents the best means of defining synaptic connections within neural networks.

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Alpha-diketones, notably diacetyl, have been used as flavoring agents. When airborne in occupational settings, exposures to diacetyl have been associated with serious respiratory disease. Other α-diketones, such as 2,3-pentanedione, and analogues such as acetoin (a reduced form of diacetyl), require evaluation, particularly, in light of recently available toxicological studies.

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Due to their role in many important signaling pathways, phosphatidylinositol 5-phosphate 4-kinases (PI5P4Ks) are attractive targets for the development of experimental therapeutics for cancer, metabolic, and immunological disorders. Recent efforts to develop small molecule inhibitors for these lipid kinases resulted in compounds with low- to sub-micromolar potencies. Here, we report the identification of CVM-05-002 using a high-throughput screen of PI5P4Kα against our in-house kinase inhibitor library.

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