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32 | testing to residents who wish to have such testing performed. The nasal swab test takes approximately 10 seconds to collect. You may experience some discomfort during the collection process. Once the sample is taken, it is put into a sterile container and sent for processing. A PCR analysis will be performed to determine whether you have a COVID-19 infection. Results will typically be available within 72-hours. Cost & Insurance Coverage Residents' Medicare or Medicare Advantage plan will fully cover the costs associated with the testing. Residents will have $0 out of pocket costs associated with the testing. Any follow-up care indicated by the testing will be at resident's expense subject to any applicable health insurance. Testing Consent I have read the above information about COVID-19 and have had a chance to ask questions. I understand the risks and benefits of this swab testing. I further understand that I am consenting to have my test results delivered to SRG who will inform me of the results. If I am informed of a positive result for COVID-19, I understand that I will be expected to contact my physician immediately. If I test negative for COVID-19, I understand that I was not likely infected at the time my specimen was collected. However, I understand that a negative test result does not rule out that I may get sick later or that the test could have produced a false negative, and I will continue taking all needed precautions to minimize my risk of exposure. I further understand that SRG will make the test results available to me and my physician. Furthermore, test result order profile indicates the following: 2019-nCoV Test result Disclaimer: This test, a RT-PCR nucleic acid assay, was developed at Magnolia Diagnostics following CDC instructions and therefore has FDA's Emergency Use Authorization (EUA). This test is intended for the presumptive qualitative detection of nucleic acid from the 2019-nCoV in upper and lower respiratory specimens (such as nasopharyngeal, anterior nares swabs or oropharyngeal swabs, sputum, lower respiratory tract aspirates, bronchoalveolar lavage, and nasopharyngeal wash/aspirate or nasalaspirate) collected from Individuals who meet CDC criteria for 2019-nCoV testing. Test performed indicates it was only for detection of COVID-19 virus.
Based on the information mentioned above, the Department is unable to ascertain if the allegations occurred as reported. Although the allegations may have happened or is valid, there is not a preponderance of evidence to prove or refute the alleged violations occurred; therefore, these allegations are deemed Unsubstantiated.
An exit interview was conducted with Administrator and a copy of this LIC9099 report was left at facility. |