COVID-19 Testing: PCR Swab (DTPM)
The DTPM COVID-19 RT-PCR test is intended for the qualitative detection of nucleic acid from SARS-CoV-2 in nasopharyngeal swabs, oropharyngeal swabs, nasal swabs, and mid-turbinate swab specimens.
Nasopharyngeal swabs are considered the gold standard for COVID-19 Testing. The swab collection should only be performed by trained medical professionals for the most accurate results.
Analytical Sensitivity: 99.9%
Analytical Specificity: 99.9%
Positive results are indicative of the presence of SARS-CoV-2 RNA; clinical correlation with patient history and other diagnostic information is necessary to determine patient infection status.
Negative results do not preclude SARS-CoV-2 infection and should not be used as the sole basis for patient treatment or other patient management decisions.
Frequently asked questions
What is COVID-19?
COVID-19 is caused by the SARS-CoV-2 virus. The virus can cause mild to severe respiratory illness and has spread globally, including the United States. The current information available to characterize the spectrum of clinical illness associated with COVID-19 suggests that symptoms include cough, shortness of breath or difficulty breathing, fever, chills, muscle pain, headache, sore throat or new loss of taste or smell.
What is the COVID-19-RT-PCR Test?
The test is designed to detect the virus that causes COVID-19 in respiratory specimens, for example nasal or oral swabs.
Why was my sample tested?
You live in or have recently traveled to a place where transmission of COVID-19 is known to occur, and/or
You have been in close contact with an individual suspected of or confirmed to have COVID-19.
What are the known and potential risks and benefits of the test?
Possible discomfort or other complications that can happen during sample collection.
Possible incorrect test result (see below for more information).
The results, along with other information, can help your healthcare provider make informed recommendations about your care.
The results of this test may help limit the spread of COVID-19 to your family and others in your community.
What does it mean if I have a positive test result?
What does it mean if I have a negative test result?
Is this test FDA authorized?
The EUA (Emergency Use Authorization) for this test is supported by the Secretary of Health and Human Service’s (HHS’s) declaration that circumstances exist to justify the emergency use of in vitro diagnostics for the detection and/or diagnosis of the virus that causes COVID-19. This EUA will remain in effect (meaning this test can be used) for the duration of the COVID-19 declaration justifying emergency of IVDs, unless it is terminated or revoked by FDA (after which the test may no longer be used).
Where can I go for updates and more information?
The most up-to-date information on COVID-19 is available at the CDC General webpage: https://www.cdc.gov/COVID19. In addition, please also contact your healthcare provider with any questions/concerns.
What is included in the price?
$15 Sample collecion fee