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To: Cogito Ergo Sum who wrote (5080)4/1/2020 9:12:53 AM
From: elmatador  Read Replies (2) | Respond to of 13789
 
While TJ is stuck in Capetwon

Brazilian repatriation plane leaves OR Tambo with 321 passengers

The tourists were desperate to return home, and are now well on their way back to Brazil after a plane came to their rescue in Johannesburg.

by Dan Meyer

2020-04-01 13:40

The first group of tourists who have been left stranded in South Africa during lockdown, have taken off on a flight home.

A LATAM Airlines flight heading for Sao Paulo, Brazil, left OR Tambo International Airport on Wednesday 1 April with 321 Brazilian passengers on board.

Airport Company South Africa (Acsa) group executive for corporate affairs Refentse Shinners said that the operation to repatriate the tourists had been successful.

“We are very grateful to our staff and the various role-players who moved quickly overnight to ensure the successful facilitation of this repatriation flight,” she said

“We are especially appreciative of the work done by officials of the Brazilian Embassy who managed the process exceptionally well and ensured that the passengers were safely transferred to the airport by bus,” she added.

The crew of the LATAM aircraft did not disembark in South Africa, and a support crew of a further 16 people were on the plane ready to switch shifts.

“The 16 crew members for the flight into South Africa therefore returned to Brazil as passengers.”

Thousands more to be repatriated

This first group of foreigners getting out of South Africa, might spark an exodus, as thousands of other tourists stuck in South Africa are negotiating with their embassies to arrange similar repatriation procedures.

German tourists stuck in lockdown are desperate to return home, while there are also an undisclosed number of US citizens in South Africa looking to catch a flight. German ambassador to South Africa Martin Schäfer said that they will partner with South African Airlines (SAA) to get his compatriots home.

“We do have a strong partner in SAA, who is willing to help us with the repatriation flights and we rely now on the assistance and the help of the South African government to make sure that our people can make it to the airport and can be flown out.

“We are in discussions with the SA government. Of course, the lockdown poses some difficulties for us . People who have symptoms; people who are positive; people who are sick with the corona will have to stay in SA and will have to be treated here.”



To: Cogito Ergo Sum who wrote (5080)4/2/2020 12:16:23 AM
From: elmatador  Read Replies (1) | Respond to of 13789
 
Becton Dickinson (NYSE: BDX) yesterday announced a new point-of-care test that can detect antibodies in blood to confirm current or past exposure to COVID-19 in as little as 15 minutes.

The test has not been reviewed by the FDA but is permitted for distribution and use under the public health emergency guidance the agency issued March 16.

BD expects to begin shipping tests in April and said it will have capacity to supply more than 1 million tests over the coming months.

BD to launch point-of-care COVID-19 antibody test

APRIL 1, 2020 BY NANCY CROTTI LEAVE A COMMENT

Becton Dickinson (NYSE: BDX) yesterday announced a new point-of-care test that can detect antibodies in blood to confirm current or past exposure to COVID-19 in as little as 15 minutes.

The new test, developed and manufactured by BioMedomics (Morrisville, N.C.), will be available through BD and distributed exclusively by Henry Schein (NSDQ: HSIC) to healthcare providers throughout the United States.

The test does not require special equipment and may be used in a laboratory or at the point of care. It is designed to detects antibodies that are typically present in the middle to later stages of COVID-19 infection, but may remain present after exposure. This could help clinicians determine who has been exposed to the coronavirus, even if a person didn’t exhibit any symptoms of the COVID-19 disease, according to BD.

“Serology tests are important because they provide an additional piece of information to aid in characterizing possible prior exposure to SARS-CoV-2, especially since many infections are mild or asymptomatic in severity,” said BD integrated diagnostic solutions president Dave Hickey in a news release. “Initial evidence suggests that nearly all patients infected with SARS-CoV-2 will have developed a detectable antibody response within days of symptom onset, at which time a negative serologic test, along with molecular diagnostics, could be helpful in ruling out COVID-19. Our agreement with BioMedomics adds a rapid serology test that can augment current tests already on the market, and we are pleased to collaborate in this effort with Henry Schein, which has extensive knowledge of the point-of-care test field.”

The test analyzes blood, serum or plasma samples for the presence of immunoglobulin M (IgM) and immunoglobulin G (IgG) antibodies associated with the coronavirus (SARS-CoV-2). IgM provides the first line of defense during viral infections, followed by the generation of adaptive, high-affinity IgG responses for long-term immunity and immunological memory.

The detection of COVID-19 IgM antibodies tends to indicate a recent exposure to COVID-19, and detection of COVID-19 IgG antibodies indicates a later stage of infection, so this combined antibody test could also provide information on the stage of the disease in patients, according to BD.

Current FDA guidance recommends that results from antibody testing should not be used as the sole basis to diagnose or exclude coronavirus infection. Los Angeles-based Bodysphere today announced it has begun distributing an FDA-authorized molecular diagnostic test for COVID-19.

“BioMedomics designed the test to be easy to use and provide results in minutes, with no special equipment necessary or the need to transport the sample to a laboratory for analysis,” said

BioMedomics CEO Frank Wang. “Our test has been clinically validated at several hospitals and clinical laboratories in both the U.S. and China, and our published clinical data in the Journal of Medical Virology was one of the world’s first for a COVID-19 serology test.

It has been used widely in China during the COVID-19 outbreak and is now ready to help combat coronavirus in the U.S. through our collaboration with BD. We are committed to doing our part to battle this disease and are excited to have BD as a partner to help deliver our high-quality rapid test to those who need it most.”

“We look forward to working with such an outstanding company as BD to help make the antibody test part of the standard of care,” added Henry Schein CEO Stanley Bergman. “The test will help to identify people who have developed antibodies to the virus, which may inform future strategies regarding COVID-19.”

The test has not been reviewed by the FDA but is permitted for distribution and use under the public health emergency guidance the agency issued March 16. BD expects to begin shipping tests in April and said it will have capacity to supply more than 1 million tests over the coming months.