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Electronic documentation. Point of care (POC) documentation is the ability for clinicians to document clinical information while interacting with and delivering care to patients. [10] The increased adoption of electronic health records (EHR) in healthcare institutions and practices creates the need for electronic POC documentation through the ...
MeSH. D000067716. Point-of-care testing ( POCT ), also called near-patient testing or bedside testing, is defined as medical diagnostic testing at or near the point of care —that is, at the time and place of patient care. [1] [2] This contrasts with the historical pattern in which testing was wholly or mostly confined to the medical ...
Multiplexed point-of-care testing (xPOCT) is a more complex form of point-of-care testing (POCT), or bedside testing. Point-of-care testing is designed to provide diagnostic tests at or near the time and place that the patient is admitted. POCT uses the concentrations of analytes to provide the user with information on the physiological state ...
Moody's Investors Service, Inc. ("Moody's") assigned first-time credit ratings to PointClickCare Technologies Inc. ("PointClickCare"), including a B1 corporate family rating ("CFR"), a B1-PD ...
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Point and click are one of the actions of a computer user moving a pointer to a certain location on a screen (pointing) and then pressing a button on a mouse or other pointing device (click). An example of point and click is in hypermedia , where users click on hyperlinks to navigate from document to document.
Point of care medical information summary. Point of care medical information summaries are defined as "web-based medical compendia specifically designed to deliver predigested, rapidly accessible, comprehensive, periodically updated, and evidence-based information" to healthcare providers. [1]
Point-of-care genetic testing identifies variations in the genetic sequence at the bedside – enabling clinicians to react and alter therapy based upon the results. [1] Traditional genetic testing involves the analysis of DNA in order to detect genotypes related to a heritable disease or phenotype of interest for clinical purposes.