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WHO says plasma therapy still ‘experimental’ --plus other developments

GENEVA — The World Health Organization says using plasma from the recovered to treat COVID-19 is still considered an “experimental” therapy and that the preliminary results showing it may work are still “inconclusive.”

President Donald Trump on Sunday approved an emergency authorization of convalescent plasma for COVID-19 patients.

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How does coronavirus spread at a concert? Germans do a test

BERLIN (AP) — Germany held a pop concert Saturday to see how those attending could spread coronavirus if they had it.

German researchers studying COVID-19 packed part of a Leipzig arena with volunteers, collecting data in a “real life” simulation of a pop concert but one with strict health and safety controls.

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Why Antibody Tests Won’t Help You Much

Getting an antibody test to see if you had Covid-19 months ago is pointless, according to guidelines issued this week by a major medical society.

Many tests are inaccurate, some look for the wrong antibodies and even the right antibodies fade away, said experts at the Infectious Diseases Society of America, which issued the new guidelines.

Because current tests cannot determine if someone is immune, the society said, they “cannot inform decisions to discontinue physical distancing or lessen the use of personal protective equipment.”

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How Feds Decide On Remdesivir Shipments To States Remains Mysterious

By the second week in July, COVID-19 cases in North Carolina were climbing fast.

With nearly 19,000 diagnoses over the previous two weeks, only five states recorded more new coronavirus cases than North Carolina did.

"Today is our highest day of hospitalizations and our second-highest day of cases," Gov. Roy Cooper, a Democrat, announced on July 9, standing behind a podium in the state's Emergency Operations Center. "Please continue to treat the virus like the deadly threat that it is."

One of the few treatment options for patients seriously ill with COVID-19 is the antiviral drug remdesivir. Authorized by the Food and Drug Administration in May for emergency use in the pandemic, remdesivir is in short supply. The federal government has taken on the responsibility for deciding where vials of the medicine should go.

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