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Health

Issues To Do At Residence

Immerse yourself in art and music with the Museum of Fine Arts, Boston’s “Art in Tune,” an event that combines works of art from the museum’s current exhibitions with music. Local musicians will perform pieces, including original compositions, that are in conversation with works by artists such as Claude Monet, Paul Cézanne and Jean-Michel Basquiat. This event is free.

When 19 o’clock

Where mfa.org/programs/music/art-in-tune?event=10078

Learn about the history, biology, and diverse uses of lichens in a workshop by Atlas Obscura. During a 90-minute workshop, Felicity Roberts, herbalist, town builder, writer and textile artist, teaches the audience about various winter mushrooms, lichens and mushrooms, from the everyday to the rare. Tickets are $ 25.

When 17:30

Where atlasobscura.com/experiences/foraging-in-a-winter-wonderland-of-lichen

Hear from Nikole Hannah-Jones and Chana Joffe-Walt, the presenters of the New York Times produced podcasts “1619” and “Nice White Parents” at the Hot Docs Podcast Festival. They will talk about audio storytelling and the impact of their series on conversations about racial justice. Tickets are $ 11.75.

When 8:30 p.m.

Where hotdocscinema.ca/podcast

Make a cup of masala chai (and even turn it into ice cream) a cooking class of Museum of Food and Drink and Malai, an ice cream parlor. Pooja Bavishi, the founder and CEO of Malai, will tell the story of the family recipe that has been handed down for generations and teach readers how to make a masala chai cake with melted ice from their blend of spices. Tickets are $ 15 and registration ends at 5 p.m.

When 19 o’clock

Where mofad.org/events/0128/masalachai

Enjoy an achievement of Beethovenis working during the last edition of the “Piano Cantabile” series at the New School’s Mannes School of Music. Three pianists, all of Mann’s students, will play the composer’s last three piano sonatas. This event is free.

When 19 o’clock

Where coparemote.com/mannessounds

Grab your popcorn and Cue up a fun selection the Sundance Film Festivalwhich runs from January 28th to February 3rd: “Playing With Sharks”, a documentary about the shark hunter and conservationist Valerie Taylor. (Mrs. Taylor filmed the real sharks that appear in “Jaws.”) Tickets are $ 15 and capacity is limited.

When 23 o’clock

Where festival.sundance.org

Collect your art materials for “Open Studio From Home: Marisol”, a Handicraft workshop for children and families from the Whitney Museum of American Art. First learn about the life and artistic practice of sculptor Marisol, then do a six-page cardboard self-portrait inspired by her work. This event is free.

When 11 clock

Where whitney.org/events/open-studio-from-home-marisol

Turn on full-day interview marathon from the Chicago Dance History Project, An organization dedicated to documenting and archiving Chicago’s dance history. Jenai Cutcher, the project’s senior / artistic director, will be interviewing some of the greats of dance, all of whom have Chicago connections, for seven hours. Respondents include Twyla Tharp, the choreographer; Mark Morris, the founder, artistic director and choreographer of the Mark Morris Dance Group; and Robert Battle, artistic director of the Alvin Ailey American Dance Theater. Tickets are $ 20.

When 12 o’clock

Where chicagodancehistory.org/events

Listen as the actor Natalie Portman discusses her new children’s book, “Natalie Portman’s Fables,” a retelling of three classic stories, with Joanna Fabicon, the senior children’s librarian at the Los Angeles Public Library. This event is free; Viewers can submit questions up until January 27 in advance.

When 6:15 pm

Where Crowdcast.io/e/skylit-portman

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Health

U.S. Virus Circumstances Prime 25 Million

Epidemiologists say the actual number of infections is likely much higher than the official numbers. Even with testing more widespread than during the first few months of the pandemic, many people who have never had symptoms may not have been tested or counted.

Ira Longini, professor of biostatistics at the University of Florida, estimates that around 20 percent of Americans had the virus – more than twice as many as reported. Statistical modeling he recently did for Florida suggests that a third of the state’s population will be infected at some point, quadrupling the reported percentage.

It would need a coordinated nationwide Study to go beyond modeling estimates and have a solid understanding of how many people actually had the virus, he said. The CDC does some serological testing, he said, but not enough to give a complete picture.

“The end result is we don’t know, but we can guess from the modeling,” said Dr. Longini.

The proportion can vary greatly from place to place. Almost one in four residents tested positive in Dewey County, SD, compared to one in 200 in San Juan County, Washington.

Many of the American metropolitan areas with the highest number of cases reported relative to their population are in the south or southwest, where the virus has spread rapidly lately, but some are in areas like the Great Plains, which got worse in the fall. The top 5 are Yuma, Ariz .; Gallup, NM; Bismarck, ND; and Lubbock and Eagle Pass, Texas.

The metropolitan areas with the most new cases per capita in the past two weeks reflect the same trend, and also highlight the virulence of the California outbreak. These areas are Laredo and Eagle Pass, Texas; Inland Empire, California; Jefferson, Ga .; and Oxnard, Calif.

More than a million people are known to have tested positive in Los Angeles County, one of the country’s hot spots in recent months. And George Rutherford, professor of epidemiology and biostatistics at the University of California at San Francisco, estimated that the actual number of infections there is twice as high as one in five Angelenos.

“It’s not enough for herd immunity, but it’s enough to blunt the curve,” he said.

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Health

Proof new UK Covid pressure could also be extra lethal

UK Prime Minister Boris Johnson speaks during a press conference on Coronavirus (COVID-19) on Downing Street on January 15, 2021 in London, England.

Dominic Lipinski | Getty Images

LONDON – There is “some evidence” that a new variant of Covid, first identified in the UK, could be more deadly than the original variety, UK Prime Minister Boris Johnson said Friday.

“We were informed today that not only is there a faster spread, but there is also evidence that the new variant – the variant first discovered in London and the south east (of England) – may be associated with a higher one Mortality rate, “Johnson told a press conference.

He added that all the evidence suggests that the vaccines from Pfizer-BioNTech and AstraZeneca-Oxford University, both of which are currently in use in the UK, will remain effective against both the old and new variants of the virus.

The evidence is still in a preliminary stage and is being assessed by the Advisory Group on New and Emerging Respiratory Virus Threats, which is advising the UK Government.

The variant known as B.1.1.7 has an unusually high number of mutations and was already associated with more efficient and faster transmission.

Scientists first discovered this mutation in September. It has since been found in at least 44 countries, including the US, which has reported its presence in 12 states.

Last week, the US Centers for Disease Control and Prevention warned that the US variant’s modeled trajectory “is growing rapidly in early 2021 and will become the predominant variant in March”.

Patrick Vallance, the UK’s chief scientific adviser, said alongside Johnson on Friday that there were early signs that the risk for those with the new variant was increased compared to the old virus.

“If you were to … take a man in his sixties, the average risk is that for every 1,000 people infected, about 10 would die from the virus. With the new variant, for 1,000 people infected, about 13 or 14 would be expected People are dying, “said Vallance.

He described the data as not yet strong and emphasized more concern about other variants of Covid in Brazil and South Africa.

– CNBC’s Sam Meredith contributed to this article.

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Health

Do Curfews Gradual the Coronavirus?

Maria Polyakova, an economist at Stanford University, has researched the impact of the pandemic on the US economy. “In general,” she said, “we expect staying at home to mechanically slow the pandemic by reducing the number of interactions between people.”

Updated

Jan. 23, 2021, 11:43 ET

“The downside is that the reduction in economic activity hurts many workers and their families in particular in the large service sector of the economy,” she added. Is the curfew worth the price?

She is at a loss to understand the logic. “Assuming nightclubs and the like are already closed anyway, prohibiting people from walking around the block with their families at night is unlikely to reduce interactions,” said Dr. Polyakova.

In addition, the virus thrives indoors, and clusters of infections are common in families and households. So a daunting question is whether forcing lengthy tampering with these settings will slow down or speed up the transmission.

“You can think of it that way,” said William Hanage, an epidemiologist at Harvard TH Chan School of Public Health. “What percentage of the transmission events occur in the time in question?” And how will the curfew stop them? “

A study recently published in Science analyzed data from the Chinese province of Hunan at the beginning of the outbreak. Curfews and lockdown measures, the researchers say, had a paradoxical effect: These restrictions reduced the spread within the community but increased the risk of infection in households, reported Kaiyuan Sun, a postdoctoral fellow at the National Institutes of Health, and his colleagues.

Dr. Longini and his colleagues have included bans and curfews in models of the pandemic in the United States and have concluded that they can be an effective way of reducing transmission.

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Pfizer to provide as much as 40 million Covid vaccine doses to Covax international program

A nurse prepares the Pfizer BioNTech Covid-19 vaccine on January 10, 2021 at a vaccination center in Sarcelles near Paris.

ALAIN JOCARD | AFP | Getty Images

Pfizer will deliver up to 40 million doses of its coronavirus vaccine to a global alliance that aims to provide coronavirus vaccines to poor nations, the head of the World Health Organization said on Friday.

The agreement will enable Covax – together with the WHO – to deliver vaccine doses to the participating countries from February, said WHO Director General Tedros Adhanom Ghebreyesus during a press conference. Tedros added that until an emergency is approved, the program expects 150 million doses of AstraZeneca’s vaccine to be available for distribution in the first quarter of this year.

The Covax program aims to provide 2 billion doses of Covid-19 vaccines to participating countries, which include low- to middle-income countries, by the end of this year. The Pfizer BioNTech vaccine requires two vaccinations spaced weeks apart, suggesting the deal would only cover 20 million people.

Tedros said the deal would allow other countries with supplies of Pfizer’s vaccine to donate them to the program. The WHO chief criticized wealthy nations for signing supply agreements with drug manufacturers for their starting doses of Covid-19 vaccines to stockpile supplies from poorer nations.

“This is not only important for COVAX, it is also an important step forward for equitable access to vaccines and an essential part of the global effort to fight this pandemic. We will only be safe everywhere if we are safe everywhere,” so Dr. Seth Berkley, CEO of Gavi, the Vaccine Alliance, said in a statement.

Albert Bourla, CEO of Pfizer, said during the press conference that the company will make the vaccine doses available to Covax and poorer countries for a fee. Pfizer was the first company to receive a global list of emergency uses for its vaccine from the WHO, allowing other countries to expedite their regulatory approval processes to begin administering the vaccine.

Bourla said the company will help ship the cans, which require ultra-cold storage and special handling, to low-income countries. UNICEF, which is helping with the dispensing of the cans, previously warned that some of the world’s poorest countries could face the challenge of storing and managing the shots upon arrival.

The program’s contract with Pfizer increases supply agreements to a total of just over 2 billion doses, but negotiations for an additional supply continue. The goal, according to Covax, is to immunize healthcare and other frontline workers as well as some high-risk individuals from the first quarter of this year.

The agreement follows the United States’ decision to remain a member of WHO under President Joe Biden. The new administration will also join the Covax program, a move the Trump administration opposed last year.

“I couldn’t escape the temptation to say that I’m very happy that this press conference is taking place on the day the United States rejoins the WHO organization. I think it’s a symbolic, great day for us,” Pfizer boss Bourla said at the meeting.

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Health

In Crises, Vaccines Can Be Stretched, however Not Simply

In desperate times, there are many ways to stretch vaccines and speed up inoculation campaigns, according to experts who have done it.

Splitting doses, delaying second shots, injecting into the skin instead of the muscle and employing roving vaccination teams have all saved lives — when the circumstances were right.

During cholera outbreaks in war zones, Doctors Without Borders has even used “takeaway” vaccination, in which the recipient is given the first dose on the spot and handed the second to self-administer later.

Unfortunately, experts said, it would be difficult to try most of those techniques in the United States right now, even though vaccines against the coronavirus are rolling out far more slowly than had been hoped.

Those novel strategies have worked with vaccines against yellow fever, polio, measles, cholera and Ebola; most of those vaccines were invented decades ago or are easier to administer because they are oral or can be stored in a typical refrigerator.

The new mRNA-based coronavirus vaccines approved thus far are too fragile, experts said, and too little is known about how much immunity they confer.

The incoming Biden administration should focus on speeding up the production of more robust vaccines “rather than playing card tricks” with current ones, said Dr. Peter J. Hotez, dean of the National School of Tropical Medicine at the Baylor College of Medicine in Houston and the inventor of a coronavirus vaccine.

There are two strategies that might work with the current vaccines, but each is controversial.

The first is being tried in Britain. In December, faced with shortages and an explosive outbreak, the country’s chief medical officers said they would roll out all of the vaccine they had, giving modest protection to as many Britons as possible. Second doses, they said, would be delayed by up to 12 weeks and might be of a different vaccine.

There is some evidence for the idea: Early data from the first 600,000 injections in Israel suggest that even one dose of the Pfizer vaccine cut the risk of infection by about 50 percent.

Nonetheless, some British virologists were outraged, saying single doses could lead to vaccine-resistant strains. The Food and Drug Administration and many American vaccinologists also oppose the idea.

Moncef Slaoui, the chief scientific adviser to Operation Warp Speed, raised a different objection to the British plan. Single doses, he warned, might inadequately “prime” the immune system; then, if those vaccine recipients were later infected, some might do worse than if they had not been vaccinated at all.

He recalled a 1960s incident in which a weak new vaccine against respiratory syncytial virus, a cause of childhood pneumonia, backfired. Some children who received it and later became infected fell sicker than unvaccinated children, and two toddlers died.

“It may be only one in 1,000 who get inadequate priming, but it’s a concern,” Dr. Slaoui said. As an alternative — the second strategy for stretching the vaccines — he proposed using half-doses of the Moderna vaccine.

There is strong evidence for doing that, he said in a telephone interview. During Moderna’s early trials, the 50-microgram vaccine dose produced an immune response virtually identical to the 100-microgram one.

Moderna chose the higher dose as its standard partly to be extra sure it would work; company scientists at the time had no idea that their product would prove 95 percent effective. The higher dose would also have a longer shelf life.

But the vaccine works better than expected, and shelf life is not an issue, so Dr. Slaoui suggested using the lower dose.

“The beauty is, you inject half and get the identical immune response,” he said. “We hope that, in a pandemic situation, the F.D.A. may simply accept it rather than asking for a new trial.”

Covid-19 Vaccines ›

Answers to Your Vaccine Questions

If I live in the U.S., when can I get the vaccine?

While the exact order of vaccine recipients may vary by state, most will likely put medical workers and residents of long-term care facilities first. If you want to understand how this decision is getting made, this article will help.

When can I return to normal life after being vaccinated?

Life will return to normal only when society as a whole gains enough protection against the coronavirus. Once countries authorize a vaccine, they’ll only be able to vaccinate a few percent of their citizens at most in the first couple months. The unvaccinated majority will still remain vulnerable to getting infected. A growing number of coronavirus vaccines are showing robust protection against becoming sick. But it’s also possible for people to spread the virus without even knowing they’re infected because they experience only mild symptoms or none at all. Scientists don’t yet know if the vaccines also block the transmission of the coronavirus. So for the time being, even vaccinated people will need to wear masks, avoid indoor crowds, and so on. Once enough people get vaccinated, it will become very difficult for the coronavirus to find vulnerable people to infect. Depending on how quickly we as a society achieve that goal, life might start approaching something like normal by the fall 2021.

If I’ve been vaccinated, do I still need to wear a mask?

Yes, but not forever. The two vaccines that will potentially get authorized this month clearly protect people from getting sick with Covid-19. But the clinical trials that delivered these results were not designed to determine whether vaccinated people could still spread the coronavirus without developing symptoms. That remains a possibility. We know that people who are naturally infected by the coronavirus can spread it while they’re not experiencing any cough or other symptoms. Researchers will be intensely studying this question as the vaccines roll out. In the meantime, even vaccinated people will need to think of themselves as possible spreaders.

Will it hurt? What are the side effects?

The Pfizer and BioNTech vaccine is delivered as a shot in the arm, like other typical vaccines. The injection won’t be any different from ones you’ve gotten before. Tens of thousands of people have already received the vaccines, and none of them have reported any serious health problems. But some of them have felt short-lived discomfort, including aches and flu-like symptoms that typically last a day. It’s possible that people may need to plan to take a day off work or school after the second shot. While these experiences aren’t pleasant, they are a good sign: they are the result of your own immune system encountering the vaccine and mounting a potent response that will provide long-lasting immunity.

Will mRNA vaccines change my genes?

No. The vaccines from Moderna and Pfizer use a genetic molecule to prime the immune system. That molecule, known as mRNA, is eventually destroyed by the body. The mRNA is packaged in an oily bubble that can fuse to a cell, allowing the molecule to slip in. The cell uses the mRNA to make proteins from the coronavirus, which can stimulate the immune system. At any moment, each of our cells may contain hundreds of thousands of mRNA molecules, which they produce in order to make proteins of their own. Once those proteins are made, our cells then shred the mRNA with special enzymes. The mRNA molecules our cells make can only survive a matter of minutes. The mRNA in vaccines is engineered to withstand the cell’s enzymes a bit longer, so that the cells can make extra virus proteins and prompt a stronger immune response. But the mRNA can only last for a few days at most before they are destroyed.

Many experts disagreed with the idea, including Dr. Walter A. Orenstein, associate director of the Emory Vaccine Center in Atlanta. “We need to know more before we can feel comfortable doing that,” he said.

“Let’s stick to the science,” added Dr. Paul A. Offit, director of the Vaccine Education Center at Children’s Hospital of Philadelphia. “There are no efficacy data on a partial dose.”

Although, like Dr. Slaoui, Dr. Offit opposed delaying second doses, he expressed doubt that doing so, as the British have, would raise the risk of worse outcomes in the partially vaccinated.

Trials in which monkeys or other animals were vaccinated and then “challenged” with a deliberate infection did not cause enhanced disease, he noted. Also, the four coronaviruses that cause common colds do not cause worse disease when people get them again. And people who have Covid-19 do not get worse when they receive antibody treatments; generally, they get better.

As is often the case, experts disagree about how and what a new vaccine will do. Some point to hard evidence that both fractional doses and delayed doses have worked when doctors have tried them out of desperation.

For example, yellow fever outbreaks in Brazil and the Democratic Republic of Congo have been stymied by campaigns using as little as 20 percent of a dose.

One shot of yellow fever vaccine, invented in the 1930s, gives lifelong protection. But a one-fifth dose can protect for a year or more, said Miriam Alia, a vaccination expert for Doctors Without Borders.

In 2018, almost 25 million Brazilians, including those in Rio de Janeiro and São Paulo, faced a fast-moving outbreak at a time when there were fewer than six million shots in the global supply. The Brazilian government switched to one-fifth doses and sent mobile teams into the slums urging everyone they met to take them, and filling out minimal paperwork. It worked: By 2019, the threat had faded.

The tactic has also been used against polio. Since 2016, there has been a global shortage of the injectable polio vaccine, which many countries use in conjunction with the live oral one. The World Health Organization has overseen trials of different ways to stretch existing supplies.

India first tried half-doses, said Deepak Kapur, chairman of Rotary International’s polio eradication efforts in that country. Later studies showed that it was possible to drop to as low as one-fifth of a dose as long as it was injected just under the skin rather than into the muscle, said Dr. Tunji Funsho, chief of polio eradication for Rotary International’s Nigeria chapter.

“That way, one vial for 10 can reach 50 people,” Dr. Funsho said.

Skin injections work better than muscle ones because the skin contains far more cells that recognize invaders and because sub-skin layers drain into lymph nodes, which are part of the immune system, said Mark R. Prausnitz, a bioengineer at Georgia Tech who specializes in intradermal injection techniques.

“The skin is our interface with the outside world,” Dr. Prausnitz said. “It’s where the body expects to find pathogens.”

Intradermal injection is used for vaccines against rabies and tuberculosis. Ten years ago, Sanofi introduced an intradermal flu vaccine, “but the public didn’t accept it,” Dr. Prausnitz said.

Intradermal injection has disadvantages, however. It takes more training to do correctly. Injectors with needle-angling devices, super-short needles or arrays of multiple needles exist, Dr. Prausnitz said, but are uncommon. Ultimately, he favors micro-needle patches infused with dissolving vaccine.

“It would really be beneficial if we could just mail these to people’s homes and let them do it themselves,” he said.

A bigger disadvantage, Dr. Slaoui, is that intradermal injection produces strong immune reactions. These can be painful, and can bleed a bit and then scab over and leave a scar, as smallpox injections often did before the United States abandoned them in 1972.

The lipid nanoparticles in the Pfizer and Moderna vaccines would be particularly prone to that effect, he said.

“It’s not dangerous,” he added. “But it’s not appealing and not practical.”

What the United States can and must do now, health experts said, is train more vaccinators, coordinate everyone delivering shots and get better at logistics.

Thanks to battles against polio, measles and Ebola, some of the world’s poorest countries routinely do better vaccination drives than the United States is now managing to do, said Emily Bancroft, president of Village Reach, a logistics and communications contractor working in Mozambique, Malawi and the Democratic Republic of Congo and also assisting Seattle’s coronavirus vaccine drive.

“You need an army of vaccinators, people who know how to run campaigns, detailed micro-plans and good data tracking,” she said. “Hospitals here don’t even know what they have on their shelves. For routine immunization, getting information once a month is OK. In an epidemic, it’s not OK.”

In 2017, the United Nations Children’s Fund recruited 190,000 vaccinators to give polio vaccines to 116 million children in one week. In the same year, Nigeria injected measles vaccine into almost five million children in a week.

In rural Africa, community health workers with little formal education delivered injectable contraceptives like Depo-Provera. The basics can be taught in one to three days, Ms. Bancroft said.

Training can be done on “injection pads” that resemble human arms. And data collection must be set up so that every team can report on a cellphone and it all flows to a national dashboard, as happens now in the poorest countries.

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Pfizer says its Covid vaccine trial for youths ages 12 to 15 is totally enrolled

Walgreens pharmacist Jessica Sahni will hold the vaccine against Pfizer BioNTech coronavirus disease (COVID-19) at the New Jewish Home in New York on December 21, 2020.

Yuki Iwamura | Reuters

Pfizer said it had fully enrolled its Covid-19 vaccine study in children ages 12-15, an important step before the vaccine could be used in that age group.

The study, an extension of the study used to support the company’s emergency approval for the vaccine in people aged 16 and over, enrolled 2,259 children between the ages of 12 and 15, Pfizer told CNBC on Friday. The entry on a government clinical trial website has been updated to determine that subjects are no longer being recruited.

The vaccine developed with German partner BioNTech was approved in December for people aged 16 and over. Studies in younger age groups are needed to ensure the correct dose as well as safety and effectiveness in these different groups, said Dr. Evan Anderson, a pediatrician at Emory University School of Medicine.

“I am very uncomfortable sending my children back to school where, despite the school’s best efforts, there is a real risk of getting Covid-19,” Anderson told CNBC in October.

While children are less affected by Covid-19 than adults, they still catch the virus and get sick. Some even died. According to a report from the American Academy of Pediatrics and the Children’s Hospital Association, more than 2.5 million cases of Covid-19 in children were reported as of Jan. 14, about 13% of all cases.

“Children can still get sick and die from Covid-19,” said Dr. Paul Offit, director of the Vaccine Education Center and an infectious disease doctor at Philadelphia Children’s Hospital. “In the past year, as many children died of Covid-19 as of influenza. And we recommend an influenza vaccine for children.”

Offit also pointed out that children can suffer from a disease related to Covid-19 called multisystem inflammatory syndrome, “which can be debilitating”.

According to the Centers for Disease Control and Prevention, as of Jan. 8, there were 1,659 cases of the syndrome in children named MIS-C and 26 related deaths. There were a total of 78 deaths from Covid-19 in children under 4 years old and 178 in children between 5 and 17 years old, according to CDC data, although those numbers do not explain all deaths from the United States

Children compete for class at PS 361 on the first day of returning to class during the coronavirus disease (COVID-19) pandemic in the Manhattan neighborhood of New York City, New York, United States, on December 7, 2020.

Carlo Allegri | Reuters

Pfizer declined to say when it expected results from the study, which would depend on the observed infection rate, to compare the rates in the placebo group with those who received the vaccine. With infection rates higher in the US since the fall – the 7-day average of daily cases now stands at 187,500, according to a CNBC analysis of the Johns Hopkins University data – vaccine effectiveness studies have shown their ads are getting faster.

However, enrollment for adolescent studies has been slower than hoped, at least for Moderna’s study in children ages 12-17, Moncef Slaoui, chief advisor to Operation Warp Speed, the Trump administration’s vaccine effort, said at their last meeting on Dec. January.

By then, around 800 children had been included in the study for over a month, of which around 3,000 were needed. Moderna’s vaccine was approved for people aged 18 and over in December, weeks after its teenage study began. Pfizer lowered the age of his trial to 12 years in October.

“While enrollment was lower during the holiday season, we expect an increase in the new year as planned,” said Moderna spokeswoman Colleen Hussey on Friday. “We are on track to provide updated data by mid-2021.”

AstraZeneca, whose vaccine developed by Oxford University is in late-stage trials in the US and approved in the UK, told CNBC Friday that it plans to continue UK trials in a new protocol for children ages 5-18 from the coming months. “”

Johnson & Johnson, whose results are expected in the third phase in adults, said it was in talks with regulators about including pediatric populations in its development plan. The same technology used for the Covid-19 vaccine was found to have been used in vaccines given to more than 200,000 people, including people over 65, infants, children, HIV-positive adults, and pregnant women .

Typically, vaccine trials are conducted in younger age groups after they have been shown to be safe and effective in older groups. The manufacturers of Covid-19 vaccines have indicated that they will follow this plan here as well.

Moderna’s chief executive Stephane Bancel said earlier this month the company is unlikely to have data on children ages 11 and younger who would include a lower dose before next year. He said he expected data for children 12 years and older could be available before September.

U.S. public health officials such as White House Chief Medical Officer Dr. Anthony Fauci, said they hope that by fall 75% to 80% of the US population could be vaccinated so life can return to some form of normal.

About 78% of the US population, or 255 million people, are over 18 years old, according to a CNBC analysis of the census data. Another 25 million people are between 12 and 17 years old.

Fauci did not immediately respond to a query about the need to include children in vaccinations in order to meet his goal of 75% to 80% coverage.

“It is important that all children are vaccinated, and manufacturers cannot conduct these trials fast enough,” Angela Rasmussen, virologist and subsidiary at the Georgetown Center for Global Health Science and Safety, told CNBC on Friday. “The more people of all ages are vaccinated, the better.”

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Pfizer Will Ship Fewer Covid-19 Vaccine Vials to Account for ‘Additional’ Doses

However, the federal health authorities that manage the government’s syringe contracts told the FDA that more than 70 percent of the sites are using more efficient syringes and that more syringes can be bought or made according to another person who is aware of the situation.

Still, Pfizer’s attempts to pressurize the FDA worried some health officials, especially since the company itself originally calculated the vials contained five doses. If an extra dose could be extracted, it would mean the vaccine supply could be stretched, protecting more Americans from the virus. On the other hand, too few specialty syringes would mean the government could pay for wasted doses.

In early January, the debate was resolved after a “standard and customary legal review process,” said an FDA spokeswoman. On January 6, in a change to the emergency approval, the FDA officially changed the vaccine datasheet to specify six doses.

“Syringes and / or needles with low dead volume can be used to extract six doses from a single vial,” says the new US bulletin. It also warned, “If standard syringes and needles are used, there may not be enough volume to extract a sixth dose from a single vial.”

In a statement, an FDA spokeswoman said the agency considered several factors in approving Pfizer’s request, including the availability of the specialty syringes, the fact that other health officials had made a similar decision, and that the change would vaccinate Americans faster.

Pfizer and the federal government have agreed to keep track of which locations receive the syringes and other equipment needed to extract the extra dose, and that the company will not bill the US for six doses per vial for locations without these devices. According to a person familiar with the negotiations who was not allowed to speak because the conversations are confidential.

Beginning next week, the number of Pfizer vaccines the federal government will allocate to each state could be based on the assumption that each vial contains six doses, according to a federal official with no legal capacity to discuss the matter. The CDC and the Department of Health and Human Services did not discuss when they could do the shift until Friday afternoon.

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New York is operating 1,000 genome checks every week to search for Covid variants

Scientists work in a laboratory testing COVID-19 samples at the New York City Health Department during the coronavirus disease (COVID-19) outbreak in New York on April 23, 2020.

Brendan McDermid | Reuters

New York State runs about 1,000 genome tests every week to look for new, contagious variants of Covid, said state health commissioner Dr. Howard Zucker, at a news conference on Friday.

“The new varieties are terrifying: the British variety, the Brazilian variety, now the South African variety,” said Governor Andrew Cuomo at the briefing. “The British variety is here.”

Zucker said the state has done about 6,000 genome tests so far and only found the strain that came from the UK. New York officials have so far identified 25 of these cases, including two new cases in Westchester County and one new case in Kings County. Said Cuomo. According to Zucker, there were no deaths in these cases.

British Prime Minister Boris Johnson told reporters on Friday that there was “some evidence” that the mutated strain could also be more deadly than the original, which hailed from Wuhan, China.

The Centers for Disease Control and Prevention previously said there was no evidence that any of the new variants were more deadly or causing more serious illness.

When asked about the potential for higher mortality associated with the British tribe, Zucker said he was in contact with the British science advisor and the evidence is still preliminary.

“The fact that it’s more communicable means there will be more cases. If there are more cases, there will be more hospitalizations, and obviously if there are more hospitalizations there is an obvious risk of more deaths,” Zucker said.

At the briefing, Cuomo said he hoped that President Joe Biden’s new administration would boost vaccine production and enable increased vaccine distribution. New York had given more than 975,000 people at least one dose of the vaccine as of Thursday, according to the state vaccine tracker.

“The British tribe is spreading. We still only have a vaccination rate of 60% to 70% of our hospital workers. This is a problem,” said Cuomo.

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Health

5 Methods Teenagers Can Get Extra Fruits and Greens Into Their Diets

Buying organic foods, which tend to cost more than traditional foods, is not strictly necessary, he added.

In 2012, the AAP published a clinical report that found that diets high in organic, dairy and meat products could reduce exposure to pesticides and potentially drug-resistant bacteria. However, there is no evidence that organic foods offer more nutritional benefits than conventional foods.

“What is most important is that children eat healthily, rich in fruits, vegetables, whole grains and low-fat or fat-free dairy products, whether they are conventional or organic,” one of the report’s lead authors said in a press release at the time.

You can also save money by buying fruits and vegetables in bulk. For example, a 3-pound bag of organic gala apples at Whole Foods in Brooklyn costs $ 4.99. If you were to buy the same amount of apples individually it would cost about $ 7.50.

Vanessa Rissetto, a registered nutritionist and acting director of the Diet Internship program at New York University, also suggested other money-saving tips: Sharing a community-supported farm membership with another family can be cheaper than owning one to buy. Or you can buy fruits and vegetables from companies that offer “ugly” organic products at high discounts.

Even if your child is not attending school in person, check to see if school lunches are still available that must include fruits and vegetables, said Diane Harris, a senior health scientist at the CDC and one of the study’s authors.

Keeping plenty of easily accessible fruit and vegetable options in your home can increase the chances of your teen choosing nutritious foods to nibble on, the experts say.

“Teens tend to be hungry and often search for food in the kitchen and pantry,” said Dr. Natalie D. Muth, a pediatrician and nutritionist in Carlsbad, California, snacking on them. This works especially when there aren’t many other processed snacks readily available. “