Publications by authors named "Michael Laposata"

Objectives: Diagnostic management teams (DMT) are groups of experts with specialized knowledge to guide test selection and interpretation of results. They have been active in institutions over the past 20 years. To date, there are limited data on whether the presence of experts to advise healthcare providers on appropriate laboratory test selection and interpretation of complex test results positively impacts patient care.

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This review article summarizes the conclusions of the National Academy of Medicine committee on diagnostic error. The committee deliberated during five in-person meetings and during numerous conference calls between April 2014 and April 2015. At three of the meetings, the committee invited multiple speakers to inform its deliberations.

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  • Coagulopathy, which involves problems with blood clotting, is linked to inflammation and infections like COVID-19 caused by SARS-CoV-2, indicating a complex relationship between these conditions.
  • A protein called von Willebrand factor (vWF) is released during inflammation, and its secretion is regulated by EPAC1, an intracellular receptor that generally helps suppress inflammation.
  • Studies using EPAC1-deficient mice showed that without EPAC1, there was increased vWF release during inflammation, suggesting that targeting EPAC1 could be a new approach to managing blood clotting issues associated with inflammatory conditions.
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  • The report emphasizes the establishment of a Doctorate in Clinical Laboratory Sciences program aimed at reducing diagnostic errors in patient care by strengthening the relationship between clinical labs and healthcare professionals.
  • It provides data on the program's implementation from 2016-2020, including details about student demographics, admission rates, and effectiveness as assessed by faculty surveys.
  • Findings indicate a positive impact on clinical rounds by the students, with many expressing a desire to lead Diagnostic Management Teams after graduation, highlighting the program's potential to enhance patient safety and care quality.
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  • The study focused on evaluating diagnostic errors in test selection after a positive antinuclear antibody (ANA) test in patients suspected of having systemic autoimmune rheumatic disorder (SARD), utilizing a Diagnostic Management Team (DMT) for assessment.
  • Out of 246 patient cases reviewed, 60.6% were found to have at least one diagnostic error in test selection, with a higher number of tests ordered in the error group compared to the no error group. Male and African American/Black patients showed a higher likelihood of errors, though not statistically significant.
  • The findings revealed that errors were less frequent when tests were ordered by rheumatology specialists, indicating the potential effectiveness of DMTs in improving test selection and reducing
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  • * The exchange protein directly activated by cAMP (EPAC) is crucial for stabilizing endothelial cells and controlling inflammation; its absence leads to increased vWF release during inflammation.
  • * The study found that EPAC1's regulation of vWF secretion operates through the PI3K/eNOS pathway, indicating that targeting this pathway could be a strategy for managing thrombosis during inflammatory conditions.
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The transition to a value-based payment system offers pathologists the opportunity to play an increased role in population health by improving outcomes and safety as well as reducing costs. Although laboratory testing itself accounts for a small portion of health-care spending, laboratory data have significant downstream effects in patient management as well as diagnosis. Pathologists currently are heavily engaged in precision medicine, use of laboratory and pathology test results (including autopsy data) to reduce diagnostic errors, and play leading roles in diagnostic management teams.

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The role of laboratory medicine is essential in healthcare, since in vitro diagnostic testing represents now an unavoidable part of reasoning and clinical decision making. Laboratory tests are an essential part of most care pathways, aimed at optimizing resource utilization and improving patient outcome. The activity of laboratory professionals is interconnected with all medical disciplines, and provides a crucial support for ordering the right test, for the right patient and at the right time, but also helps interpreting and using laboratory data.

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Laboratory medicine plays an increasingly essential role in modern healthcare systems, since it is integral to most care pathways and plays an essential role for optimizing patient flow, harmonizing procedures before and after analysis, improving harmonization and containing unnecessary testing. Nevertheless, recent changes in the nature of laboratory services, promoted by innovation and introduction of more complex tests in emerging diagnostic fields, more advanced diagnostics along with other "internal" and "external" drivers, will promote a paradigmatic transformation of current scenarios. The future of laboratory professionals remains hence uncertain, and is seems obvious that the role and figure of laboratory scientists and professionals shall evolve.

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A major challenge facing most countries is the growing cost of healthcare. Laboratory testing costs constitute approximately 3% of all clinical costs, while waste of funds due to inappropriate admissions to clinical departments is reported to be as high as 15%. A frequently used approach to save money in healthcare is random reduction of laboratory budgets, focusing on decreasing the number of unnecessary laboratory tests.

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Background: The quality of healthcare in the US has been progressively addressed by 3 reports from the National Academy of Medicine, the latest of which, entitled "Improving Diagnosis in Health Care," was issued in 2015 from a 21-member panel (the author of this report was a member). The report is a review of the longstanding problem of diagnostic error. The infrastructure of healthcare delivery in the US has inadvertently made diagnostic error a major contributor to the high cost of care and preventable poor patient outcomes.

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The National Academy of Medicine (NAM) in the recently issued report Improving Diagnosis in Health Care outlined eight major recommendations to improve the quality and safety of diagnosis. The #1 recommendation was to improve teamwork in the diagnostic process. This is a major departure from the classical approach, where the physician is solely responsible for diagnosis.

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Background: Diagnostic error is extremely common in the USA and likely around the world. A major reason for the diagnostic error is both the overutilization and the underutilization of laboratory tests. Using a panel of two to four experts in coagulation, test selection was reviewed in clinical context and in real time, and consensus determinations were made to derive conclusions about the extent of overutilization and underutilization.

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Background: Airway inflammation is a significant contributor to the morbidity of cystic fibrosis (CF) disease. One feature of this inflammation is the production of oxygenated metabolites, such as prostaglandins. Individuals with CF are known to have abnormal metabolism of fatty acids, typically resulting in reduced levels of linoleic acid (LA) and docosahexaenoic acid (DHA).

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Cystic fibrosis patients and model systems exhibit consistent abnormalities in metabolism of polyunsaturated fatty acids that appear to play a role in disease pathophysiology. Recent in vitro studies have suggested that these changes are due to overexpression of fatty acid desaturases that can be reversed by supplementation with the long-chain polyunsaturated fatty acids docosahexaenoate and eicosapentaenoate. However, these findings have not been tested in vivo.

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Objective: Errors associated with laboratory testing can cause significant patient harm. Sendout testing refers to tests sent by a primary lab to a reference lab when testing is unavailable at the primary lab. Sendout testing is particularly high risk for patient harm, due to many factors including increased hand-offs, manual processes, and complexity associated with rare, low-volume tests.

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