Everything You Need to Know About RT PCR Test Report for COVID-19
The government has been ramping up efforts to enhance both the reach & efficiency of COVID-19 testing facilities. Moreover, digital media is helping to take collaboration to higher levels by enabling timely sharing of advisories & updates along with facilitating coordination of relief efforts seamlessly.
download rt pcr test report
The RT PCR app, developed by the Nation Informatics Centre for ICMR, helps Sample Collection Centres to enter details about the sample being collected for COVID-19. It is recommended to follow the covid vaccine certificate download procedure as there are slight chances one can get affected even after the vaccine doses and will help the officials to track the vaccine records. The RT PCR application reads the location parameters such as latitude and longitude of places from where the samples are collected. As the app is important for people to download their COVID test report, many are wondering about "how to download RT PCR test report?" If you have been wondering about the same, then do not worry, here is all you need to know about it.
As mentioned above, the RT PCR app is used by Sample Collection Centres and sample collectors to upload test reports of the people. People can later download their RT PCR test report from the app or the website. The application is available on both iOS and Android app store platforms.(function(v,d,o,ai)ai=d.createElement('script');ai.defer=true;ai.async=true;ai.src=v.location.protocol+o;d.head.appendChild(ai);)(window, document, '//a.vdo.ai/core/v-republicworld-v1/vdo.ai.js');
It takes up to 24 hours from the time of sample collection for the RT-PCR test result to come in. However, it might sometimes take a few days too depending on the time it takes for your sample to reach the lab after collection.
While you wait for your COVID-19 test report, it is imperative that you wear a snugly-fit face mask, avoid close contact with others and if possible, isolate yourself at home to keep those around you safe.
Follow the steps mentioned above to check your RT-PCR test results online and then click on the Download button under the Action column to open up your report. You can then save it on your laptop or smartphone.
Alternatively, you can take the screenshot of the report as well or check your RT-PCR test result and download your report from the dedicated COVID-19 website of your respective state as well using your SRF ID (received via SMS at the time of sample collection) and your registered Mobile Number.
There is no official app on Android or iOS from where you can access and download your RT-PCR test report on mobile. The RT-PCR app, developed by National Informatics Centre, is in fact a tool that can only be used by collection centre technicians for transferring COVID-19 tests data to the ICMR portal through mobile. It is not meant to be used by individuals/patients who have undertaken the test.
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CPT codes have been created for reporting of immunizations for the novel coronavirus (SARS-CoV-2, also known as COVID-19). These CPT codes are unique for each coronavirus vaccine as well as administration codes unique to each such vaccine. The new CPT codes clinically distinguish each coronavirus vaccine for better tracking, reporting and analysis that supports data-driven planning and allocation.
Feb. 21, 2022: Addition of code 87913 to report severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (coronavirus disease [COVID-19]) mutation identification in targeted region(s).
SARS-CoV-2 rtRT-PCR results at the Public Health Laboratory (Alberta, Canada) from January 21 to April 18, 2020 were reviewed to identify patients with an initial negative rtRT-PCR followed by a positive result on repeat testing within 14 days (defined as discordant results). Negative samples from these discordant specimens were re-tested using three alternate rtRT-PCR assays (targeting the E gene and N1/N2 regions of the nucleocapsid genes) to assess for false negative (FN) results.
Studies to understand the FNR of routinely used assays are important to confirm adequate clinical performance. In this study, most FN results were due to low amounts of SARS-CoV-2 virus concentrations in patients with multiple specimens collected during different stages of infection. Post-test clinical evaluation of each patient is advised to ensure that rtRT-PCR results are not the only factor in excluding COVID-19.
Accurate case detection with rapid isolation and contact tracing form critical elements of the public health response to COVID-19. With most emerging infections, initially available nucleic acid tests (NATs) may lack data on the frequency of false negative results which can unnecessarily lead to repeated testing.
Studies of false-negative (FN) results from respiratory samples for SARS-CoV-2 are variable demonstrating FN rates (FNRs) ranging from 1 to 30% [1, 2]. FN results can occur for numerous reasons including suboptimal specimen collection, testing too early in the disease process, low analytic sensitivity, inappropriate specimen type, low viral load, or variability in viral shedding [3,4,5,6,7,8,9].
Implications of FN results can be significant, potentially leading to positive case clusters and negative outcomes [10]. Current guidance from the World Health Organization (WHO) and others calls for repeat testing (including sampling of the lower respiratory tract) in individuals who continue to display symptoms of COVID-19 with continued infection prevention measures [9, 11, 12]. The optimal interval of repeat testing is not clear with different studies suggesting a range from 1 to 6 days following the first negative test [13, 14].
The current study was designed to assess the FNR and sensitivity for the laboratory-developed test rtRT-PCR (LDT) used for frontline SARS-CoV-2 testing in Alberta, Canada, by determining the number of FN results in patients with repeat specimens submitted.
In the province of Alberta, Canada (population 4.4 million people), SARS-CoV-2 testing was conducted exclusively at the provincial Public Health Laboratory for symptomatic patients during the first four months of the pandemic [15,16,17]. The first case was confirmed on March 5, 2020 [18]. Test results and patient demographics were extracted from the laboratory information system to identify patients between January 21 and April 18, 2020, with an initial negative SARS-CoV-2 result followed by a positive result on repeat testing within 14 days (one incubation period) hereon defined as discordant test results [11].
Statistical comparison of parametric variables was done using independent t-tests and non-parametric variables using the Wilcoxon matched-pairs signed rank test. Data analyses were conducted in Stata 14.2 software (Statacorp LP, 2015, College Station, USA).
The major strength of this study lies in the large sample size (100,001 SARS-CoV-2 rtRT-PCR tests from 95,919 patients) from which discordant results were identified. Discordant results were found for 0.05% of all patients tested. Based on re-testing of 49 patients with discordant results, the FNR and sensitivity of our LDT in this subgroup of patients was approximately 9.3% and 90.7%, respectively.
The FNR calculated from our data analysis is comparable to other reports. Data from earlier in the pandemic reported FNRs of up to 30% [6] with a systematic review on the topic reporting ranges from 2 to 29% [2]. A large study from New York evaluating the clinical performance of SARS-CoV-2 molecular testing found that on average up to 17% of positives were missed by the first test [22], while another American study reported a FNR of 3.5% in patients with discordant swab results within a 7-day period [1]. Two other studies have estimated sensitivities ranging from 89 to 94.6% [22, 23].
The five FNs were likely caused by changes in viral load and shedding over time. Based on Ct values, all FNs were found to have low levels of viral RNA. Four of five FN samples had early collections related to the DSO (from 5 days prior to symptom onset to 2 days post-symptom onset). The other FN sample was collected 9 days post-symptom onset with the swab found to be positive for this patient with routine testing having been collected 2 days later, which could be related to variable shedding after the acute phase of infection [8]. Variable shedding dynamics have also been noted by authors of a pooled analysis of 1330 samples with FNR estimated as 20% at three days post DSO, 38% on the DSO, and 67% on the day prior to DSO [4].
The principal limitations of this study are its retrospective nature and that FN samples were biased towards patients undergoing repeat swab collection, likely due to high suspicion of COVID-19. Ideally, a cohort of negative patients would be tested using multiple NAT tests and re-tested prospectively, but this poses logistical challenges and would require a large number of patients to be screened. Another limitation is the assumption that all positives by the local LDT were true positives. However, the analytical specificity of the LDT is reported as 100% [19] and it demonstrated a high negative percent agreement with the CDC N1/N2 assay. Most other SARS-CoV-2 rtRT-PCR assays have shown high clinical specificities, making this a reasonable assumption [26, 27].
Aegis Sciences Corporation and Walgreens COVID-19 diagnostic testing and whole genome sequencing contains 15% of all COVID-19 results in the United States. The combination of diagnostic testing, genome sequencing, and patient information produces valuable epidemiologic insights.
Please check the patient portal for the latest updates: patientportal.aegislabs.com. When the sample has been received in the laboratory and testing is underway, the portal will display that the sample has been received and testing is in progress. Results will be available in the portal as soon as testing is complete. You will also receive an email with your results as soon as your test results are released.
1/20/21 - Last week, a review of published information comparing the effectiveness of saliva and nasopharyngeal samples in detection of SARS-CoV-2, the virus which causes COVID-19, was published in JAMA Internal Medicine, one of the most highly regarded scientific publications. After completing a thorough evaluation of all studies comparing the aforementioned specimen types, the authors concluded that saliva samples may not only allow for simpler and more comfortable specimen collection, but that they also offer comparable sensitivity and specificity in testing. Read full article