Tag Archives: coronavirus

A Third of COVID Survivors Suffer Mental or Neurological Problems

A third of coronavirus patients were found to suffer from psychiatric or brain problems within six months of their COVID-19 diagnosis, according to a study published recently.

Researchers analyzed the health records of 236,379 COVID patients, mostly from the US, and found that 34 percent had been diagnosed with neurological or psychiatric disorders six months on.

About one in eight of the patients, or 12.8 percent, were diagnosed for the first time with such an illness, the study showed.

Anxiety, at 17 percent, and depression or mood disorders, at 14 percent, were the most common diagnoses, according to the research.

Instances of post-COVID cases of stroke, dementia and other neurological disorders were rarer, but still significant — especially in people who had been seriously ill with the virus, the scientists said.

https://www.thelancet.com/

Summer Sunlight Could Inactivate 90% of Coronavirus Particles in 30 minutes

A team of scientists is calling for greater research into how sunlight inactivates SARS-CoV-2 after realizing there’s a glaring discrepancy between the most recent theory and experimental results. UC Santa Barbara mechanical engineer Paolo Luzzatto-Fegiz and colleagues noticed the virus was inactivated as much as eight times faster in experiments than the most recent theoretical model predicted.

The theory assumes that inactivation works by having UVB hit the RNA of the virus, damaging it,” explained Luzzatto-Fegiz.

But the discrepancy suggests there’s something more going on than that, and figuring out what this is may be helpful for managing the virus.

UV light, or the ultraviolet part of the spectrum, is easily absorbed by certain nucleic acid bases in DNA and RNA, which can cause them to bond in ways that are hard to fix.

But not all UV light is the sameLonger UV waves, called UVA, don’t have quite enough energy to cause problems. It’s the mid-range UVB waves in sunlight that are primarily responsible for killing microbes and putting our own cells at risk of Sun damage.

Short-wave UVC radiation has been shown to be effective against viruses such as SARS-CoV-2, even while it’s still safely enveloped in human fluids.

But this type of UV doesn’t usually come into contact with Earth’s surface, thanks to the ozone layer.

UVC is great for hospitals,” said co-author and Oregon State University toxicologist Julie McMurry. “But in other environments – for instance, kitchens or subways – UVC would interact with the particulates to produce harmful ozone.”

In July 2020, an experimental study tested the effects of UV light on SARS-CoV-2 in simulated saliva. They recorded the virus was inactivated when exposed to simulated sunlight for between 10-20 minutes.

Natural sunlight may be effective as a disinfectant for contaminated nonporous materials,” Wood and colleagues concluded in the paper.

Luzzatto-Feigiz and team compared those results with a theory about how sunlight achieved this, which was published just a month later, and saw the math didn’t add up. his study found the SARS-CoV-2 virus was three times more sensitive to the UV in sunlight than influenza A, with 90 percent of the coronavirus‘s particles being inactivated after just half an hour of exposure to midday sunlight in summer.

By comparison, in winter light infectious particles could remain intact for days.

Source: https://www.news.ucsb.edu/
AND
https://www.sciencealert.com/

COVID-19: Single vaccine jab linked to 85% and 94% drop in risk of coronavirus hospital admissions

The COVID-19  vaccines being used in the UK could reduce a person’s risk of being admitted to hospital by as much as 94% four weeks after the first dose, new data suggests. Experts examined coronavirus hospital admissions in Scotland among people who have had their first jab and compared them to those who had not yet received a vaccine.

Four weeks after receiving the initial dose, the Oxford/Astrazeneca  jab appeared to reduce a person’s risk of hospital admission by 94%. Those who received the Pfizer jab had a reduction in risk of 85% between 28 and 34 days after the first dose. Data for the two jabs combined showed that among people over the age of 80 – who are at high risk of severe disease – the reduction in risk of hospital admission was 81% four weeks after the first dose.

https://news.sky.com/

The Vaccination against Covid-19 Prevents the Transmission of the Virus

A growing body of evidence suggests that the Covid-19 vaccine can slow the spread of the coronavirus, Dr. Anthony Fauci said Wednesday. Whether vaccination can prevent transmission of the virus is “the looming question,” Fauci, director of the National Institute of Allergy and Infectious Diseases, said during a White House coronavirus response team briefing.

If a person gets infected despite being vaccinated — we refer to that as a ‘breakthrough’ infection — does that person have the capability of transmitting to another person?” “There have been some studies that are pointing in a very favorable direction,” he said, adding that these studies will have to be corroborated by additional research.

Fauci highlighted two recent studies that looked at a person’s viral load — that is, how much virus he or she has in the body — and transmissibility. One study from Spain, published Feb. 2 in The Lancet, found a direct correlation between viral load and transmissibility. The higher the viral load, the greater the transmissibility of the virus.

That’s in line with what years of research on HIV have shown: there’s a direct link between the viral load in someone’s blood and the likelihood that individual will transmit HIV to a sexual partner, Fauci said.

For SARS-CoV-2, the virus that causes Covid-19, researchers are focused on how much virus is found the nasopharynx, the upper part of the throat behind the nose that’s reached with a long, skinny swab.

https://www.nbcnews.com/

New Drug Reduces Risk Of Death By 24% For Critically Ill COVID Patients

Patients across the UK who are admitted to intensive care units due to COVID-19 are set to receive new life-saving treatments which can reduce the time spent in hospital by up to 10 days, the government has announced today (Thursday 7 January).

Results from the government-funded REMAP-CAP clinical trial published today showed tocilizumab and sarilumab reduced the relative risk of death by 24%, when administered to patients within 24 hours of entering intensive care.

Most of the data came from when the drugs were administered in addition to a corticosteroid, such as dexamethasone – also discovered through government-backed research through the RECOVERY clinical trial – which is already provided as standard of care to the NHS.

Patients receiving these drugs, typically used to treat rheumatoid arthritis, left intensive care between 7 to 10 days earlier on average. The rollout of these treatments could therefore contribute significantly towards reducing pressures on hospitals over the coming weeks and months.

Source: https://www.gov.uk/

New Variant Of Coronavirus Identified In England

Health Secretary Matt Hancock said at least 60 different local authorities had recorded Covid infections caused by the new variantHe said the World Health Organization had been notified and UK scientists were doing detailed studies.“Nothing to suggest” it caused worse disease or that vaccines would no longer work, he added. Over the last week, there had been sharp, exponential rises in coronavirus infections across London, Kent, parts of Essex and Hertfordshire.

We’ve currently identified over 1,000 cases with this variant predominantly in the South of England although cases have been identified in nearly 60 different local authority areas.“We do not know the extent to which this is because of the new variant but no matter its cause we have to take swift and decisive action which unfortunately is absolutely essential to control this deadly disease while the vaccine is rolled out”, he explained.

England’s Chief Medical Officer Prof Chris Whitty said current coronavirus swab tests would detect the new variant that has been found predominantly in Kent and neighbouring areas in recent weeks. The changes or mutations involve the spike protein of the virus – the part that helps it infect cells, and the target Covid vaccines are designed around.

It is too soon to know exactly what this will do to the behaviour of the virus.

Source: https://www.bbc.com/

New Oxford/AstraZeneca’s Coronavirus Vaccine To Cost Just £2 Per Dose

Britain could have 19million doses of Oxford and AstraZeneca‘s coronavirus vaccine by the end of the year after clinical trials showed it is up to 90 per cent effective at preventing infection and can be stored cheaply in a fridge. President of AstraZeneca, Tom Keith-Roach said today that, on top of the four million doses on standby for the UK, a further 15million could be ready to roll out by the end of next month. They will be given to healthcare workers and the elderly first, subject to approval by regulators.

The vaccine is expected to cost just £2 per dose and can be stored in ordinary equipment, unlike other jabs made by Pfizer and Moderna that showed similarly promising results last week but need to be kept in ultra-cold temperatures using expensive equipment.  It’s also a fraction of the price, with Pfizer‘s costing around £15 per dose and Moderna‘s priced at about £26 a shot.

Oxford‘s trials found the jab has a nine in ten chance of working when administered as a half dose first and then a full dose a month later. Efficacy drops to 62 per cent when someone is given two full doses a month apart.

https://www.dailymail.co.uk/

Pfizer Says Its COVID-19 Vaccine Is 95% Effective

Pfizer and BioNTech said Wednesday that a final data analysis found their coronavirus vaccine was 95% effective in preventing COVID-19 and, in addition, appeared to fend off severe disease.

Vaccine, called BNT162b2, was highly effective against the virus 28 days after the first dose, and its effectiveness was consistent across all ages, races and ethnicities, the drugmakers said. Additionally, the elderly, who are seen as at high risk of severe illness from COVID-19, saw vaccine effectiveness of more than 94%, they added.

The final analysis underlines the results of the positive interim efficacy analysis announced on November 9,” BioNTech CEO Ugur Sahin said in a statement. “The data indicates that our vaccine … is able to induce a high rate of protection against COVID-19 only 29 days after the first dose. In addition, the vaccine was observed to be well-tolerated in all age groups with mostly mild to moderate side effects, which may be due in part to the relatively low dose.”

The vaccine also appeared to prevent severe disease in volunteers. There were 10 cases of severe cases of COVID-19 observed in the phase three trial, with nine of the cases occurring in the placebo group, the companies said. There were also no “serious” safety concerns, they said, with most adverse events resolving shortly after vaccination. The company’s shares jumped 3% in premarket trading.

The final analysis evaluated 170 confirmed COVID-19 infections among the late-stage trial’s more than 43,000 participants. The companies said 162 cases of COVID-19 were observed in the placebo group versus eight cases observed in the group that received its two-dose vaccine. That resulted in an estimated vaccine efficacy of 95%, they said.

The news comes more than a week after the companies announced that their vaccine was more than 90% effective and two days after Moderna said preliminary phase three trial data showed its vaccine was 94.5%. Both vaccines use messenger RNA, or mRNA, technology. It’s a new approach to vaccines that uses genetic material to provoke an immune response.

A safe and effective vaccine is seen by investors and policymakers as a solution to get the global economy back on track after the pandemic wreaked havoc on nearly every country across the globe and upended businesses. The virus continues to spread rapidly, with more than 55.6 million cases worldwide and at least 1.33 million deaths as of Wednesday, according to data compiled by Johns Hopkins University.

Pfizer and BioNTech‘s initial results on Nov. 9 were based on the first interim efficacy analysis conducted by an external and independent Data Monitoring Committee from the phase three clinical trial. The independent group of experts oversees U.S. clinical trials to ensure the safety of participants. Medical experts note it remains unclear how long the vaccines will provide immunity and whether or how often people may need periodic booster shots.

These vaccines are going to be approved and then rolled out with basically a few months’ worth of data. You’re not going to do a two-year study to see whether it’s effective for two years with more than 200,000 people dying this year” in the U.S., Paul Offit, director of the Vaccine Education Center at Children’s Hospital of Philadelphia, said in a recent interview.

Pfizer said it plans to submit an application for emergency use authorization to the Food and Drug Administrationwithin days.” Pfizer CEO Albert Bourla said at Tuesday’s New York Times Dealbook conference that the company had accumulated enough safety data needed to submit the vaccine for review.

The companies reiterated that they expect to produce up to 50 million doses this year and up to 1.3 billion doses in 2021. They also said they are “confident” in their ability to distribute the vaccine, which requires a storage temperature of minus 94 degrees Fahrenheit. By comparison, Moderna‘s vaccine can be stored for up to six months at negative 4 degrees Fahrenheit.

Source: https://www.nbcdfw.com/

Moderna’s coronavirus vaccine is 94.5% effective

The Moderna vaccine is 94.5% effective against coronavirus, according to early data released Monday by the company, making it the second vaccine in the United States to have a stunningly high success rate.”These are obviously very exciting results,” said Dr. Anthony Fauci, the nation’s top infectious disease doctor. “It’s just as good as it gets — 94.5% is truly outstanding.”

Moderna heard its results on a call Sunday afternoon with members of the Data Safety and Monitoring Board, an independent panel analyzing Moderna‘s clinical trial data.
It was one of the greatest moments in my life and my career. It is absolutely amazing to be able to develop this vaccine and see the ability to prevent symptomatic disease with such high efficacy,” said Dr. Tal Zacks, Moderna‘s chief medical officer.

Vaccinations could begin in the second half of December, Fauci said. Vaccinations are expected to begin with high-risk groups and to be available for the rest of the population next spring.

The company says its vaccine did not have any serious side effects. A small percentage of those who received it experienced symptoms such as body aches and headaches.
Moderna plans to apply to the US Food and Drug Administration for authorization of its vaccine soon after it accumulates more safety data later this month.

Fauci says he expects the first Covid-19 vaccinations to begin “towards the latter part of December, rather than the early part of December.”

Pfizer And Biontech Announce Vaccine Against COVID-19

Pfizer Inc. (NYSE: PFE) and BioNTech SE (Nasdaq: BNTX) today announced their mRNA-based vaccine candidate, BNT162b2, against SARS-CoV-2 has demonstrated evidence of efficacy against COVID-19 in participants without prior evidence of SARS-CoV-2 infection, based on the first interim efficacy analysis conducted on November 8, 2020 by an external, independent Data Monitoring Committee (DMC) from the Phase 3 clinical study.

After discussion with the Food and Drug Administration (FDA), the companies recently elected to drop the 32-case interim analysis and conduct the first interim analysis at a minimum of 62 cases. Upon the conclusion of those discussions, the evaluable case count reached 94 and the DMC performed its first analysis on all cases. The case split between vaccinated individuals and those who received the placebo indicates a vaccine efficacy rate above 90%, at 7 days after thed second dose. This means that protection is achieved 28 days after the initiation of the vaccination, which consists of a 2-dose schedule. As the study continues, the final vaccine efficacy percentage may vary. The DMC has not reported any serious safety concerns. 

Today is a great day for science and humanity. The first set of results from our Phase 3 COVID-19 vaccine trial provides the initial evidence of our vaccine’s ability to prevent COVID-19,” said Dr. Albert Bourla, Pfizer Chairman and CEO. “We are reaching this critical milestone in our vaccine development program at a time when the world needs it most with infection rates setting new records, hospitals nearing over-capacity and economies struggling to reopen. With today’s news, we are a significant step closer to providing people around the world with a much-needed breakthrough to help bring an end to this global health crisis. We look forward to sharing additional efficacy and safety data generated from thousands of participants in the coming weeks.”

Source: https://www.pfizer.com/