Context: The policy of storing clinical samples in a pathology laboratory is based on long-standing practice rather than on objective data regarding the actual use of the stored samples.
Objective: To determine the time after initial order that requests for add-on tests are submitted to the laboratory. These data might be useful for improving the efficiency of sample storage.
Design: Two hundred sixteen add-on requests evenly divided between inpatients and private practice patients were reviewed for types of tests added on and the time of the requests.
Results: Ninety-five percent of add-on test requests for inpatients were made by 0.75 day after the initial order (range, 0.01-4.3 days). However, the 95th percentile for private practice patients' add-on requests did not occur until 5.6 days later (range, 0.01-7.0 days). The pattern of add-on tests for hospitalized patients also differed from those for private practice patients. Most add-on tests for hospitalized patients were for routine hospital tests, and the private practice add-on requests were for assays that were not as routine, frequently for testing referred to the reference laboratory. This difference affected the rapidity of completing the add-on tests.
Conclusions: Samples for hospitalized patients can be stored for 3 days, but samples from patients in private practices should be held for 7 days. This change of "usual" storage practice would increase the efficient use of laboratory space and personnel. Screening all requests for add-on tests for hospitalized patients might reduce the frequency of unnecessary add-on requests, further increasing the efficiency of the laboratory.
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http://dx.doi.org/10.5858/2007-131-1794-POATFH | DOI Listing |
Background: The Centers for Medicare and Medicaid Services (CMS) New Technology Add-on Payment (NTAP) program supports adoption of new, costly medical technologies demonstrating substantial clinical improvement. In 2021, CMS waived the "substantial clinical improvement" criterion for devices designated under the FDA Breakthrough Devices Program (BDP). This study characterized risk-standardized payments associated with hospitalizations in which Medicare beneficiaries received calcium modification during PCI for acute myocardial infarction (AMI) following the adoption of the Shockwave C Coronary Intravascular Lithotripsy (IVL) Catheter (Shockwave Medical) with BDP designation.
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Operative Unit of Clinical Pharmacology and Pharmacovigilance, Department of Health Science, AOU Dulbecco, University Magna Graecia of Catanzaro, 88100 Catanzaro, Italy.
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Department Epidemiology & Data Science, Amsterdam University Medical Centers, University of Amsterdam, PO Box 22700, 1100 DE, Amsterdam, The Netherlands.
Like all interventions in health care, novel non-invasive tests for colorectal cancer should be properly evaluated before they can be recommended. Such evaluations should be performed in well-designed studies, of which the results can serve as the evidence base for recommendations. While the methods for evaluating novel tests have been slower to develop, there is now a solid base for developing suggestions and even strong recommendations for their assessment.
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