Within seven weeks of the first reported case of the COVID-19 virus on December 31, 2019, 76,769 people were infected, and 2,249 had died. By January 30, WHO declared SARS-2-CoV, the virus that causes the Covid-19 disease, a public health emergency of international concern. That was just the beginning of the disaster pandemic would leave in its wake. A year has passed, and finally, there is progress. The WHO states that we are on the brink of a WHO EUL/PQ authorized vaccine, but it will take time before global inoculation. Meanwhile, breakthrough self-tests for Covid 19 infection are available and an essential part of preventing the disease’s further spread.
What is a covid 19 test home kit?
The U.S. Food and Drug Administration (FDA) describes the COVID-19 RT-PCR test as “a real-time reverse transcription-polymerase chain reaction (rRT-PCR) test for the qualitative detection of nucleic acid from SARS-CoV-2 in upper and lower respiratory specimens.”
What does this all mean? The Coronavirus Study Group (CSG) of the International Committee on Taxonomy of Viruses designates the Coronavirus virus as Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2). So, Covid-19 is connected to severe acute respiratory syndrome coronaviruses (SARS-CoVs), which hails from the SARS-related coronavirus (SARS-CoVs) species. We are well familiar with the SARS virus when it was first identified during an outbreak in China and spread to four other countries in early 2003.
Without delving into the viruses’ complex genetics, as of August 2020, the FDA has authorized three types of COVID-19 detection tests. One of these is molecular tests, also known as nucleic acid amplification, genetic, RNA, or PCR tests. Testing is essential because while infection by SARS-CoV-2 can cause fever, fatigue, and respiratory symptoms, in acute cases, particularly people with compromised immune systems, the outcome be organ failure, severe SARS, or death.
How is a covid 19 test taken?
When a Covid 19 test is required, a patient must have a respiratory sample taken. Administrating it is painless and straightforward, and using an Anterior Nasal Q-tip swab collection procedure is most common. Samples are then processed and tested. Results reveal whether the patient is actively infected or suggest that the virus might be present.
Are covid 19 tests accurate?
Molecular tests can give a false-negative result if the viral RNA level in a specific sample is too low to be detected, and findings can be skewed if no steps are taken to guarantee that the tests are performed correctly. The American Society for Microbiology established verification measures to help laboratories develop effective verification procedures for commercial U.S. EUA COVID-19 molecular tests to ensure data accuracy.
What is the OmeCare Covid 19 test?
Currently, there are test kits on the market, so a Covid 19 test can be done at home, such as the one developed by OmeCare. The OmeCare COVID-19 assay is an rRT-PCR test, as described above. It is used for the qualitative detection of nucleic acid from the SARS-CoV-2 (COVID-19) virus during the active infection stage.
OmeCare’s PCR Covid-19 Self-Administered Testing Kits offer employers, state agencies, colleges, and schools a ready-to-use, out of box Covid-19 testing solution to ensure the safety and wellbeing of employees, students, and faculty. The kit doesn’t require health care provider supervision for test swab collection. It provides individualized supplies, easy-to-use instructions, and a video tutorial for users to do a Covid 19 test at home or on-site via self-collection.
Meticulous testing; fast, credible results
The OmeCare test is implemented using cutting-edge microfluidic technology, such as the Fluidigm Juno, Fluidigm Biomark HD, and standard thermocyclers. It was FDA Emergency Use Authorized (EUA) by Fluidigm on 05/25/2020.
Moreover, just one Biomark system can examine as many as 6,000 tests a day, with a turnaround time of 24-48 hours once a sample is received. The OmeCare test is also highly accurate, with a 98-100% sensitivity and specificity profile. The company runs tests at its clinical-grade, state-of-the-art College of Pathologists (CAP) and Clinical Laboratory Improvements Amendment (CLIA) accredited laboratory. No aspect of testing is outsourced.
Available in all states, tests are conducted with the highest scientific standards, and all healthcare data and genetic data are stored in a HIPAA-compliant cloud and on designated servers with filesystem-level and client-server encryption guaranteeing maximum security. While the test is available in both a healthcare and a home-testing kit format, it is currently being offered through doctors, but an at-home version will be available soon!
Meanwhile, one test is available for $150, 10 tests for $750 ($75 per test), and 50 tests for $2999 ($60 per test). Packages come with no commitment and can be purchased once or every week for you students, family, or colleagues.