India should quickly adopt the rapid, inexpensive, and sensitive saliva test, On August 15, six and a half months after the first novel coronavirus case was reported in the country, India crossed another grim milestone — 50,000 deaths. The total number of cases reported as on Saturday stood at nearly 2.6 million; India has been reporting the most fresh cases in a day in the world since August 2. More than the total death toll, now 51,045, what is troubling is the shorter time taken for the death toll to double. The toll count crossed 25,000 on July 16 and doubled to over 50,000 in just 30 days. It is certain that there is some extent of underreporting of deaths across the country, especially when deaths have occurred outside the health-care system. For instance, reporting of COVID-19 cases and deaths by States such as Gujarat, West Bengal and Telangana have been suspect right from the beginning; the pandemic-defying trend seen in these States is in stark contrast to the rest of the country. No combination of factors can explain the low daily mortality figures in Gujarat and Telangana. In fact, in the last one month, the death toll on any single day in Telangana has never crossed 15 and has been in single digits on many days; the State even reported zero deaths on July 26, while in Gujarat, deaths have never crossed 30, except on one day. However, under-reporting notwithstanding, it is unlikely to be huge enough to change the death toll several-fold. Like in most Southeast Asian countries, deaths per million population have been low in India. While the case fatality rate too has been low, the continuous in the rate might be due to more cases, including,
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https://www.facebook.com/kanishksocialmediaasymptomatic ones, being detected due to increased testing with rapid antigen tests. Also, large cities that witnessed strained health-care infrastructure due to the surge in cases, leading to more deaths, seem to have passed the peak. A big shortcoming of rapid antigen tests is their low sensitivity, and despite the ICMR’s recommendation, most States have very low rates of validation of negative test results using the molecular method. Relying mostly on rapid antigen tests will result in many of the infected continuing to spread the virus. If speed, low cost and constraints of molecular testing capacity are the reasons why many States have embraced rapid antigen testing, the emergency use authorisation granted recently by the U.S’s FDA for a saliva test developed by Yale University should be good news for India. This rapid, inexpensive, non-invasive and highly sensitive test that uses saliva samples will not only help detect more cases but also reduce the need for trained care workers to collect samples. With the testing protocol made freely available, India should facilitate rapid adoption of the tests by States, after local validation. Early results of the saliva test have been encouraging and India will hugely gain by embracing it in lieu of the unreliable rapid antigen test, particularly when the virus spreads to rural areas.
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