Pandemic Canada 2020 - The response, the issues and problems

DIY-HP-LED

Well-Known Member
I wonder what American students are thinking about this, you can do stuff like this when you don't shovel as much money as you can at the 1%. They should also offer to buy their convalescent plasma and a grand a pint! :D But I figure plenty of folks will volunteer it anyway, I would anticipate no shortage of people eager to save another's life.
Trudeau announces $9B Canada Emergency Student Benefit to help university and college students
 

DIY-HP-LED

Well-Known Member
Canada's weird, left-wing, anti-American nationalism

Why do Canadians hate the United States so much? What's the deal with Canadian anti-Americanism? Let's look at the roots of Canada's national identity and talk about why Canadians are obsessed with seeing their country as "not-America."
 

DIY-HP-LED

Well-Known Member

Calling all Canadian COVID-19 survivors: A plasma trial wants you

Researchers are putting out the call for COVID-19 survivors across the country who can donate plasma to patients battling the disease, as a major clinical trial to study whether that could save lives gets Health Canada approval.

The trial, which will be overseen by doctors at several major universities and will involve 40 to 60 hospitals, cleared the hurdle at the end of last week.

Dr. Jeannie Callum, a professor at the University of Toronto and transfusion medicine specialist at Sunnybrook hospital, said they hope to have their first donor in front of them within a week.

That’s an “unbelievable” speed considering it normally takes two years just to plan a trial. “People are working every day, 12-hour days, to make this happen,” she said. “It’s amazing.”

Delphine Denis, spokesperson for Canadian Blood Services, said their approval for the collection of plasma is still “under review” and they are “expecting its approval in the next few days.” Its equivalent, Héma-Québec, will also be collecting donations.

Potential donors can fill out an online screening form at https://blood.ca/en/convalescentplasma and someone will get back to them about when and where to go.

Convalescent plasma therapy — the practice of putting the clear, straw-coloured part of blood from recovered patients into the very sick — is an old idea. It was first used to treat a German child with diphtheria in the late 1800s, and also helped save lives during the Spanish flu.

The plasma of survivors is full of antibodies that can bind to a virus and neutralize it, giving an immune boost. It’s been used successfully to treat SARS, Ebola, and many other viral infections.

But there’s not enough science to show if it works for COVID-19, because the disease is only a few months old. It has shown promise in two small Chinese studies. The Canadian one would be much bigger, and is being done in conjunction with similar studies in several countries including France, the U.K. and South Korea.

The team is looking for 800 donors and 1,200 patients. They will reassess at the halfway mark when they get to 600 recipients, to see how many they actually need, and are trying to complete the trial by year’s end.

To be eligible donors need to be under age 67, have tested positive for COVID-19, and be fully recovered with no symptoms for 28 days.

The study will start with men, Callum said, because they are “less complicated,” without the possibility of pregnancy.

“For women we have to do extra blood testing on them, and that will slow us down, so we’re ramping up just with the men, and then we’ll move to the women.”

Given the issues with access to testing, many people who’ve had coronavirus will not have a positive test result. Callum said they’d “love to include them” but just don’t have the time.

The plasma will be tested to determine the strength of the antibodies, which vary from person to person. Some plasma could be screened out if it doesn’t have strong enough antibodies.

While donors will volunteer, all patients at participating hospitals not on a ventilator will get screened for the study.

“For every three people in the trial, two will get the plasma and one will get regular care,” Callum said. Who gets what will be determined randomly.

Once all of the global trials are completed, results can be compared with other countries.

Callum said there has already been a “heartwarming” response from potential donors, including entire families who got COVID-19, and groups of friends who got it on the same vacation. “Canadians are so nice.”
 

DIY-HP-LED

Well-Known Member
An effective treatment will make a great deal of difference in mortality rates and hospital resource requirements. Convalescent plasma is one of the more promising therapies and is being studied right now, while it is being used to save lives, it is cheap, leverages an existing blood bank network and can be rapidly deployed. Some of the questions are, how effective is it, when is the best time to use it, how much and on who?

Other treatments we could see deployed this summer include artificial antibody therapy and a drug treatment. All of these treatment options might make reopening the economy and even ethically have a policy of herd immunity a possibility. With testing, limited contact tracing, proper NPI's and treatments, can give us a lot of control over this pandemic and get us out of our houses and back to work.

People don't mind getting sick, they don't want to be fucked for life or dead! Remove the fear and reopen the economy, driving mortality rates down to flu levels will do that and there is the possibility of doing that by the end of summer, in Canada at least.
----------------------------------------------------------------------------------------------------------------------------------------------------------

U of T plays leading role in effort to develop COVID-19 treatment from recovered patients' blood plasma

Researchers at the University of Toronto are playing a leading role in a national effort to study the efficacy of using blood plasma from recovered COVID-19 patients to treat those who are sick with the disease.

The joint effort with researchers at more than 40 Canadian hospitals, the Université de Montréal, University of Ottawa, McMaster University and the University of British Columbia seeks to test whether it helps to transfuse plasma – the pale yellow liquid from whole blood that is rich in antibodies – from people who have recovered from COVID-19 to patients suffering from the illness.

Antibodies in what’s known as “convalescent plasma” could give a boost to the immune system of COVID-19-infected patients to help them fight the disease, says Dr. Jeannie Callum, a professor in the department of laboratory medicine and pathobiology in the Faculty of Medicine and an associate scientist at Sunnybrook Health Sciences Centre.

“Antibodies are kind of like little forks that stick into the virus and assist your immune system,” Callum says, adding that the body’s immune system sees the virus attached to the end of the fork and tells macrophages and other immune cells to attack it. “It’s like your immune system is at war and you provided more tanks to fight the enemy.”

Doctors in China and other countries have experimented with antibody-rich convalescent plasma to treat COVID-19 patients, Callum notes. One Chinese study published last month focused on 10 “severe adult cases” and suggested that a dose of plasma from recovered patients was “well tolerated and could significantly increase or maintain the neutralizing antibodies at a high level.”

The Canadian researchers plan to recruit 1,200 adults and 100 children to participate in separate trials to get a much better idea of whether the technique works and, possibly, answer lingering questions about the novel coronavirus, including why it affects adults differently than children.

Dr. Donald Arnold, a hematologist at McMaster University, Dr. Philippe Bégin, an immuno-allergist at the Université de Montréal, and Dr. Julia Upton, an assistant professor of pediatrics at U of T and staff physician at the Hospital for Sick Children, are leading the trials.

Canada’s blood suppliers, Canadian Blood Services and Héma-Québec, will be managing donations of plasma from those who have recovered from COVID-19.

“This is the most promising thing I’ve seen in a while,” tweeted David Fisman, a professor of epidemiology in U of T’s Dalla Lana School of Public Health who is cross-appointed to the Faculty of Medicine. Rather than use convalescent serum in intensive care units, Fisman, who isn’t involved in the trial, said he could see it being used “upstream” to treat patients before their condition worsens.

Doctors have experimented with convalescent plasma as a potential treatment for other illnesses, including SARS and MERS, which belong to the same coronavirus family. The history of the approach dates back even longer – to the 1918 Spanish flu pandemic.

“We know from the use of the [plasma] product in the 1918 pandemic – it suggested that the earlier you use the product the more likely it is to change the patient’s outcome,” Callum says.

The researchers have chosen to do the trial in an “intermediate” group of patients, meaning those who have been hospitalized but aren’t so sick that they require intensive care and ventilation.

“We’re hoping to turn it around so that the person doesn’t need to go on a ventilator or go to the ICU, stays a shorter time in hospital and gets back home,” Callum says.

Dr. Rulan Parekh, a professor of pediatrics and medicine at U of T and associate chief of clinical research at the Hospital for Sick Children, is part of the SickKids group leading the pediatrics component of the trial. Although children tend to have better outcomes from COVID-19, they may have underlying conditions that put them at greater risk and that differ from those often seen in older adults, like diabetes, Parekh says.

“Even though there are few deaths [among children with COVID-19] that have been reported, it’s more likely that they will have a worsening of their clinical symptoms,” she says. “We want to see if the convalescent plasma will improve their respiratory findings.”

Because they expect to have fewer study participants in the pediatric trial, researchers will be able to follow patients over a longer period, Upton says.

Parekh – who is also a staff physician in nephrology at the University Health Network – is also leading a study, with Dr. Dana Devine of UBC and Canadian Blood Services, to follow the donors of convalescent plasma to understand factors that impact immunity.

“We want to study systematically if the virus-neutralizing antibody [concentration] is associated with outcomes in both children and adults,” Parekh says.

Even if the clinical trials support the use of blood plasma as a treatment for COVID-19, it wouldn't make the development of a vaccine any less important. The plasma treatment may help COVID-19 patients get better, but a vaccine would help prevent infection in the first place. “The vaccine is the holy grail,” Callum says, adding that the plasma treatment could help buy time until one is developed – a process that experts say may take 12 to 18 months.

For the clinical trial to go forward, Callum says Canadians who have fully recovered from COVID-19 have to be “ready to step up to the plate” and donate plasma – more than once if possible. “We’re going to be wholly dependent on their goodwill,” she says, adding that the procedure is less taxing than donating whole blood.

Richard Carl, a former COVID-19 patient who recovered at Sunnybrook, told the Globe and Mail that he already plans to donate. “The thought of asking someone to help fix this thing – I couldn’t say yes fast enough,” he said.
 

DIY-HP-LED

Well-Known Member

Reducing mortality of Covid-19 with antibody-rich plasma? Europe may have the answer if it comes together

Posted April 15, 2020 by PLOS Guest Blogger in Covid-19, General, Global Health, Immunology, Pandemic, Virus

Michel Kazatchkine (Special Advisor to the Joint United Nations Program on AIDS (UNAIDS) for Eastern Europe and Central Asia), Jean-Louis Vincent (Université Libre de Bruxelles, Brussels), Michel Goldman (Université Libre de Bruxelles, Brussels) discuss the opportunities for passive immunotherapy as a treatment option for Covid-19 patients and a greater collaboration among European nations to achieve this goal.

A few weeks ago, a small case series from China suggested that the administration of antibody-rich plasma from patients who had recovered from Covid-19, may significantly improve outcome in patients with severe forms of the disease in intensive care.

Interestingly, transfusion of convalescent plasma (so-called passive immunotherapy) has been shown to be associated with better outcomes of disease, during the SARS outbreak fifteen years ago. There is also evidence for the effectiveness of transfusion of convalescent plasma or of hyperimmune immunoglobulins in a number of viral infections, including pandemic influenza A H5N1 and H1N1, Ebola, and West Nile syndrome.

The conceptual basis for passive immunotherapy had been laid hundred years ago by European scientists, primarily Emil von Behring in Germany and Pierre-Paul Emile Roux in France, after it was established that recovery from some infections is dependent on the generation of neutralizing antibodies to the pathogen.

Within just two to three weeks after the early publication from China, clinical trials of passive immunotherapy with convalescent plasma have been initiated in the US (New York, Rochester and Baltimore), Canada, Singapore, South Korea and in Europe. European countries include Germany, Italy, France, the Netherlands and Belgium where blood transfusion centers have now started screening and collecting convalescent plasma from individuals for high titers of anti-SARS-Covid-2 antibodies.

Rapidly growing attention to this approach is based on a strong conceptual basis, evidence that recovery from Covid-19 is associated with the generation of neutralizing antibodies, lack of significant adverse reactions to plasma therapy, and the absence of any effective treatment for severely ill patients at this time.

In times of crisis, coordination at the national and global level is essential to agree on the management of the short- and mid-term public health measures that need to be implemented and on how to drive the development of specific therapies and vaccines.

Yet, looking at the response to Covid-19, the global picture is one of discord and lack of coordination. In Europe, the response has been underwhelming and chaotic, with each member state deciding public health measures to take and on the timing of their implementation unilaterally.

Scientists and clinical investigators are experienced in international cooperation particularly when responding to epidemics such as HIV/ AIDS, TB, SARS, MERS or Ebola. While researchers in the US remarkably announced their commitment to share their results on COVID-19 trials in real time (Dr Michael Joyner, Mayo Clinic) it is unfortunate that clinical investigators in Europe could not come together and conceive a joint protocol that would have given higher power to the studies and shorten time to the answer. How did the European countries that are used to actively cooperating in research and how did the European Union that is investing high amounts of funding in biomedical research, including for Covid-19, get here?

We believe it urgent and imperative that members states and the European Commission now join their efforts. A European platform should be created where data from the ongoing trials are shared, analyzed and reconciled. This move is critical at the early phase of assessment of passive immunotherapy with convalescent plasma in Covid-19. But it should not end there.

Leading scientists from Belgium, France and Switzerland will advocate for a strong coordinated research effort in Europe in a virtual conference-debate on “Mobilizing EU collective intelligence to defeat COVID-19” on Thursday, April 16 at 2:00 pm CET which can be viewed in real time. Because of its outstanding potential, a strong coordinated clinical research network in Europe is not just a nice idea. It is an immediate necessity.
 

DIY-HP-LED

Well-Known Member
Canada's economy to be particularly hard hit by COVID-19, says expert

Canada faces several economic disadvantages as it emerges from the pandemic but having the U.S. as its major trading partner could help, says Peter Hall, the chief economist for Export Development Canada.
 

DIY-HP-LED

Well-Known Member
Restrictions on COVID-19 rapid test 'part of the process,' says minister

Health Canada is putting restrictions on a made-in-Canada COVID-19 rapid testing kit, barring it from public use. Public Services and Procurement Minister Anita Anand says this kind of challenge is "part of the process of building new technology
 

DIY-HP-LED

Well-Known Member

Health Canada pauses regulatory approval for COVID-19 rapid test
The federal government had ordered 40,000 tests a month from Ottawa-based Spartan Bioscience
CBC News · Posted: May 03, 2020 11:38 AM ET | Last Updated: May 3


The rapid-testing device for COVID-19 created by Ottawa's Spartan Bioscience is now for research purposes only, says Health Canada. (Supplied by Spartan Bioscience)
Health Canada is restricting the use of a made-in-Canada, rapid COVID-19 test created by Spartan Bioscience after the National Microbiology Lab found problems with the test that made it unreliable.

"In light of the clinical results, Health Canada has placed conditions on the company's authorization to restrict the use of the product to research use only until adequate evidence of clinical performance can be provided," the federal agency said in an emailed statement sent to CBC, after the story was first reported by Le Journal de Montreal.
"The Spartan product can continue to be used for research purposes only."
The portable test was called a "game changer" by health officials because it reportedly could deliver on-location results in under 60 minutes. Further upgrades to the test made by the Ottawa-based company promised to reduce that time down to 30 minutes.
According to Spartan, Health Canada's concerns stem from the efficacy of the swabs the testing unit uses — and not with the machine itself.

Issue with swabs
The company was first informed by Health Canada about the concerns on Friday.
"The same report indicated no concerns regarding the accuracy and analytical performance of Spartan's test reagents and portable DNA analyzer device," said a statement published on the company's website.
The company said it has already shipped out 5,500 tests nationally, but said it's voluntarily recalling the product to perform more clinical tests. Most of those units were delivered to the National Microbiology Lab.
"Spartan will be working as quickly as possible to address the concerns and bring its test to market," the company said.

Prime Minister Justin Trudeau and Chief Medical Officer Dr. Theresa Tam attend a news conference in Ottawa in May. Tam said the federal government had ordered 40,000 tests per month from Spartan. (Adrian Wyld/The Canadian Press)
The federal government had ordered 40,000 tests a month from Spartan.
"While the Spartan system, the device, performed very well in a laboratory setting — along the specification the manufacturer had provided — it was in the clinical setting, the real-life setting, where it didn't perform well," Dr. Theresa Tam, Canada's chief public health officer, said during a news conference Sunday.
Canada hopes to begin testing 60,000 people for the virus daily, and Tam said the setback wouldn't affect that goal.
She also said the clinical testing done with the Spartan cube wouldn't have affected the actual diagnoses of any patients.
Dr. Howard Njoo, Canada's deputy chief of public health, said at the same news conference that he hopes the company can make the necessary adjustments so it can be used in a clinical setting in the future.

Prime Minister Justin Trudeau said on Sunday that some setbacks are expected, given that the federal government has accelerated the approval process for a number of potentially life-saving devices.
"We've said from the very beginning, that in this unprecedented crisis we needed to move very, very quickly," Trudeau said.
"When we do that quickly, there are going to be new facts that come in and situations that evolve that will require shifts in our postures.... Similarly, provinces will have to adjust to new realities and adjust to successes and challenges as they come up."

Provinces react
Several provinces were planning to use Spartan's portable testing kits.
Quebec had ordered 200,000 tests, which were expected to be delivered on May 31.
The $16-million purchase was conditional upon the approvals of Health Canada, the Public Health Agency of Canada and the National Microbiology Laboratory, the province's ministry of health and social services said in an email.
Ontario had also placed an order for more than 900,000 of the kits.

"We are actively engaging with [Health Canada] to obtain clarification," Hayley Chazan, a spokesperson for Ontario Health Minister Christine Elliott, wrote in an email.
"Despite Ontario not yet having used the Spartan tests, we are a leader in Canada in daily testing volumes per capita and rank among the top globally."
Alberta Health Services (AHS), which announced a $9.5-million contract with the company in late March, said in an email Sunday it had suspended its evaluation of the testing devices following concerns about the technology's efficacy.
AHS said it had received only a small number of devices to date, and was working to validate them before any use in clinical settings. None of the kits have been deployed for use in Alberta, AHS said.
The company said that provinces have not yet paid in full for the tests they ordered, although some have made a 10 per cent down payment. Spartan said it plans to fulfil all its contractual obligations once the issue with the swab is fixed.

Peter Lin, CBC News medical contributor and family physician, called the setback a "hiccup."
"You just have to change the swab and go through testing again," he said.
Lin said the swabs couldn't reach far enough into a person's nose to properly test for the virus.
"So what happened was that their swab is for your mouth. Therefore, it cannot fit all the way up into your nose, and you have to actually go pretty high up in the nose," the doctor said. "Their swab systems are not able to pick up everything."
 

DIY-HP-LED

Well-Known Member

Ottawa establishes COVID-19 supply council as rapid testing efforts hit a snag
Procurement process improvements come as some provinces ease into reopening Monday

The federal government says it has established a national supply council tasked with improving Canada's efforts to procure equipment and other tools to halt the spread of COVID-19 as provinces take early steps to reopen businesses shuttered by the crisis.

Procurement Minister Anita Anand said Sunday that the COVID-19 supply council is intended to strengthen the country's existing supply chains for items like masks, gloves and disinfectants.

It will also improve sourcing, production, shipping and distribution strategies for those goods.

"From start to finish — from manufacturer to arrival or production in Canada — what is it that we can be doing differently to ensure that we have proper and effective and efficient procurements within our government and across the country?" Anand said.

The news was part of a string of announcements Sunday, including a new $240-million commitment to bring mental health and primary care services online, and a one-time top-up to the Canada child benefit that will see eligible families receive an extra $300 per child as part of their regular May payment.

Prime Minister Justin Trudeau also revealed an additional $175 million for the Vancouver-based biotech firm AbCellera, a company he said has identified antibodies for use in potential drugs to treat the novel coronavirus. The funding is expected to help the company carry out human trials, which Trudeau said could begin as early as July.

"Until we have effective treatments, or better yet a vaccine, we'll still need a reliable supply of everything from masks to ventilators," he said.

'Important to have even more' equipment: Trudeau

It's the easing of those restrictions, Trudeau said, that makes it critical for Canada to improve its procurement processes.

"We recognize that as the economy starts to open in different places and in different ways, it is going to be important to have even more [personal protective equipment]," Trudeau said. "That's why we need to do everything we can to ensure we're getting the right procurement."

Doctors want Ottawa to keep them in the loop on PPE shortages, says CMA survey
Anand was able to provide some additional updates to Canada's procurement efforts Sunday.

"Our first shipment of face shields began to come in this week, with more than 740,000 received to date, half of which were produced here in Canada," the minister said.

She also announced a new contract that would see 15.5 million more face shields added to Canada's stockpile, an agreement with the Montreal-based Medicom for 20 million N95 respirators and 80 million surgical masks over the next 10 years, and a deal with another Quebec company for 11 million medical gowns.
 

DIY-HP-LED

Well-Known Member

Health Canada approves first serological test for COVID-19 immunity

Health Canada has authorized the first serological test, which will be able to detect antibodies for COVID-19.

“Serological testing will contribute to a better understanding of whether people who have been infected by COVID-19 are immune to the virus,” the statement from the government agency reads. “Further research will also help us fully understand the relationship between positive antibody tests and protection against re-infection.”

The LIAISON test from DiaSorin, an Italian-based multinational biotechnology company, was authorized for use by the U.S. Food and Drug Administration last month.


“We started to work on an immunodiagnostic test to respond to the increasing need to conduct epidemiological investigations to establish the percentage of the population exposed to the virus in the absence of a diagnosis performed with molecular tests on a swab,” Fabrizio Bonelli, chief scientific officer of DiaSorin, said in a statement in early April.
Health Canada states that under the leadership of Canada's COVID-19 Immunity Task Force, at least one million Canadian blood samples will be collected and tested over the next two years as a way to track the virus in the general population.






Researchers warn of risks with COVID-19 antibody testing
Researchers say the science still isn’t clear on how people that test positive for antibodies are protected from being reinfected.
This includes identifying specific groups that are at a “greater risk” of having been infected, particularly seniors and healthcare workers.
“This is a critical step for the work of the Immunity Task Force,” Prime Minister Justin Trudeau said on Wednesday. “These tests will help us better understand immunity against the virus and how it spreads, so we can keep Canadians safe and healthy.”
Health experts across Canada have recognized that serological testing is an important component for understanding COVID-19 immunity.
“We know that people who are infected will develop some kind of antibody response,” Dr. Theresa Tam, Canada’s chief public health officer said on Apr. 27., adding that the level of immunity and how long it will last is still in question globally.
 

DIY-HP-LED

Well-Known Member

Chinese coronavirus vaccine could be tested, manufactured in Canada

TORONTO (Reuters) - China's CanSino Biologics Inc, the company behind one of the few coronavirus vaccine candidates already in clinical trials, is collaborating with Canada's National Research Council to "pave the way" for future trials in Canada, the research council said on Tuesday.

The NRC said it would scale up a production process for CanSino's vaccine at a government facility in Montreal, and that CanSino was preparing a trial application for drug regulator Health Canada.

If CanSino's vaccine works, the collaboration could help ensure that Canadians have access to it. Local trial data could reassure Health Canada that the vaccine is safe, and local manufacturing could ensure some doses are at hand.

Asked whether the collaboration would make it possible for Health Canada to consider data gathered in China, NRC said that in general, data can be shared with the regulator's approval.

"Canadian clinical trials will expand on Chinese data and provide an enhanced understanding of the vaccine candidate's safety profile," the agency said.

A vaccine that protects people from the coronavirus could end the pandemic, but finding one that works and manufacturing enough doses is a huge challenge.

Relations between Canada and China have been strained since Canadian authorities arrested Huawei Chief Financial Officer Meng Wanzhou on Dec. 1, 2018 at the request of the United States. Her arrest infuriated the Chinese government, which subsequently detained two Canadian citizens - Michael Kovrig and Michael Spavor - on state security charges.

But in the midst of the pandemic, Canada has struggled to import protective equipment from the United States, turning in part to suppliers in China. A federal procurement website notes that Canada has "established on-the-ground support in China" to manage bulk purchases.

CanSino and the NRC have worked together since 2013, and the company's vaccine is produced using a cell line that was developed at the NRC, the agency said.

CanSino Chairman Xuefeng Yu worked in Canada from 1996 to 2009, according to the company's website, mainly for Sanofi.

Shares of Hong Kong-listed CanSino rose on April 26 after the company said Health Canada had agreed to meet to discuss a clinical trial application. [FWN2CD00V]

Separately on Tuesday, Canada promised C$600 million to replenish the GAVI vaccine alliance, to support routine vaccinations around the world. GAVI is also helping low-income countries respond to coronavirus outbreaks.
 

DIY-HP-LED

Well-Known Member
Coronavirus outbreak: WHO's reality check on COVID-19; new test approved in Canada

Health Canada has approved the country's first blood test to detect COVID-19 antibodies, to see if a person has been exposed to that virus, and if they are possibly immune. Heather Yourex-West looks at how the test works, and the questions it cannot answer. Plus, Dawna Friesen has more on the World Health Organization's hard reality check on the coronavirus.
 
Top