Researcher addresses why big numbers boggle the mind – University of Miami

Linguist Caleb Everett reminds us that the mind has yet to grasp the modern worlds explosion of massive numbers and that its natural that were numbed by references to millions and billions.

As the numbersfor COVID-19, populations, net worth, jobless claims, people living in povertycreep past five, then 10, and into the hundreds, thousands, millions, and billions, our 21st-century hearts and minds begin to cloud, befuddled by quantities with a meaning that seems almost to diminish to us as the numbers increase.

Its a nature thing, an inherent bias at play, explained Caleb Everett, professor and chair of the Department of Anthropology in the University of Miami College of Arts and Sciences.

We encounter the distinctions of one vs. two vs. three frequently in nature, yet the distinction of seven to eight not that often, said Everett. Lots of languages make the singular vs. plural distinction, but languages dont make any distinction say between six vs. seven, other than with number words.

It makes sense that we as a species would evolve capacities that are naturally good at discriminating small quantities and naturally poor at discriminating large quantities, he said.

Everett pointed to research of young children in Western societies indicating that numbers are perceived in a logarithmic fashion. When prompted to place markers on a 1 to 100 number line, young children will generally misjudge the accurate distance.

Before theyre well trained in school, children will always have the one far apart from the two far apart from the three, and then it gradually declines, Everett said. Fifty and 100 could be almost as far apart on the line as one and two, since higher number differences are naturally compressed in our minds.

Everett noted that the usage of a single word for million didnt existbecause there was no need for ituntil the 14th century, when it appeared, translated from the French in Chaucers Canterbury Tales. Until then the sum was expressed, if it was at all, by combining existing word numbers, such as pusend pusendor a thousand thousand from Old English.

Yet our modern world is increasingly inundated with astronomically large numbersnumbers that, despite the human tragedy they might tell, often leave us unfazed.

The best we can do, Everett suggested, is to contextualize the numbers, i.e. break them down so that they make sense for our own experience.

Numbers dont make sense in a vacuumif we say 10,000 have died thats massive for some things, he said. Yet about 155,000 people die every day in the world under normal circumstances. Weve seen more of people talking about the figures compared to death on a normal day. If you just throw out the numbers, the numbers are massive, but theres a massive amount of people.

Everett was careful to not trivialize the number of deaths related to COVID-19 and said the tendency to associate and compareto contextualizeis an attempt to enhance meaning.

How do we make sense of those numbers of victims in the big scheme of things, in a world with seven and a half billion people? he questioned. Were just not good at that, and it makes sense that were not good at that because these are very recent distinctions that weve had to makedistinctions that were not imminently relevant to our survival over the bulk our our species history.

In his most recent book, Numbers and the Making of Us, Everett proposed that numbers shape our perceptions of the world and documented that numbers systems are learned and not inherentnot all cultures even have number systems. He used the concept of a cultural ratchet to explain how we pass learning from generation to generation.

But the scale of numbers we use todaymillions and billionshas yet to be ratcheted into our understanding.

He noted other primal and natural tendencies in the polarized reactions we are seeing currently to the COVID-19 scenario.

The tribalized camps in society and the way the culture gets transmitted in certain groups [but not in others], such as in social media, reflect the primal tendencies of our species, he said.

Faced with the persistent challenges of the pandemic landscape, he noted the natural bias that causes many to gravitate toward fearful and negative news.

Being attuned to negative things is more important for survival, Everett said. Paying a lot of attention to negative or harmful things from a survival standpoint and the reproduction of your genes makes sense.

He referenced research showing that humankind has progressed during the past few decades in areas such as medicines to cure disease, life expectancy, global wealth, new technologies, among othersprosperity which creates a new challenge for the human species.

In terms of revolutionary biases, focusing on positive things doesnt necessarily help the odds of reproduction, Everett said. The person who is fearful to some extent is going to avoid dangers and is likely to survive and reproduce.

As numbers continue to increase and if humankind does manage to generate more sustained prosperity, our natural biases will also have to adapt, he suggested.

In the same way that numbers as a cultural technology gives us the ability to be more precise with larger quantities, cultural practices of educating ourselves in the way that things are positive can help us address the natural bias that causes us to focus on negative things. If were using our biases in a constructive way, Everett said, maybe thats great.

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Researcher addresses why big numbers boggle the mind - University of Miami

Love in the time of Zoom: Why we’re in the midst of a dating revolution – Fast Company

Its nice to believe that love comes always as a magical thing, a proverbial bolt of lightning across a crowded room. Its comforting to imagine that this most human of emotions has been with us forever, ageless and unchanging.Yet the history of romance reveals something very different; something driven by the technologies that define our era as much as by the chemicals that fuel our brains.

Yes, we human beings have been falling in love since time began. Yes, we probably feel the same rush of excitement and desire that drove our ancestors to distraction, too. But how we find our loves, how we live with them and mate with them and leave them for another, has changed repeatedly over time. And now, with the future crashing into us at ever faster speeds, the ways we live and love and mate are poised to change againmore dramatically, perhaps, than ever before.

Throughout most of human history, love and marriage were only accidentally connected. Beginning with the Agricultural Revolution of around 8000 BC, when marriage as we know it first came into being, young people were paired off by their elders, matched in ways that made sense for their families, their villages, their tribes. Sex was an inherent part of the transaction, since it produced the children who would subsequently farm the fields and inherit them. Romance was not. Instead, for thousands of years, marriage was mostly a businesswitness the traditional dowry or bride priceand courtship a community sport. If there was passion, it occurred either through happenstance, or outside the bounds of marriage.

Things started to change in the 18th century, as the Industrial Revolution yanked millions of people away from the agricultural economy and into a future marked by factories, railroads, and crowded, burgeoning cities. For the first time in history, young people could imagine their lives unfolding differently from what their parents and grandparents had experienced; for the first time, masses of people could move easily from one place to another, and away from the communities that had once defined them. Land was no longer so important once industry emerged, and children no longer so crucial. And as these changes rippled through society, norms of love and marriage began to shift as well. Young people could find each other outside the confines of their village and beyond the prying eyes of their elders. They could support themselves independently and live in smaller units, what we now think of as the nuclear family. They could afford to fall in love, and to build a new narrative of marriage that included not only sex and children, but affection as well.

In the 20th century, the twin innovations of contraception and assisted reproduction transformed things again, unbundling the ancient package of marriage by enabling people to have sex without babies and babies without sexboth of which have become commonplace. Today, premarital sex has become the norm for most men and women; contraception is enthusiastically encouraged by all but the most conservative groups; and same-sex marriages have become a joyful reality across most of the world. Yes, these developments have been driven in part by changing social norms and the advocacy of dedicated activist groups. But they are also the direct result of technological change.

Fast-forward now to our own era, a time in which growing numbers of people are meeting online and a growing array of our most intimate activities are unfolding across the alien landscape of Zoom. What will happen to love and sex and romance as we increasingly live in a digital world? Its too early to know for certain, but a number of signs have already emerged.

What will happen to love and sex and romance as we increasingly live in a digital world?

To begin with, the 20th century model of meeting in person is fast being replaced by the algorithms of online dating sites. Already, nearly 40% of heterosexual couples report having met online; these numbers are even higher for same-sex couples, and for individuals pairing off for more casual encounters. Such interactions are bound to surge during the time of COVID, as closed bars and cancelled classes make online courtship the only viable kind.

Its also clear that the generation coming of age today is marrying later than their parents and grandparents did, having fewer children, and, perhaps surprisingly, less sex. Today, only about half of Americans are married by the time they turn 30. Fertility rates have plummeted to 1.7 (meaning that the average woman will give birth to 1.7 children over the course of her lifetime), well below the natural rate of replacement, and the youngest members of the millennial generation are less sexually active than any generation since those that came of age in the 1960s. According to a recent U.S. survey, more men aged 18 to 34 were living with their parents than with a romantic partner, and thats before COVID-19 pushed even more of them back to their childhood homes.

Finally, it increasingly seems that the ease and infinite variety of online dating presents its users with a double-edged deal. The good news is that nearly all people now have an almost unfathomable array of sexual and romantic choices. Rather than being confined by their parents wishes, or limited by the number of suitable prospects in a single village or community, anyone looking for love (or lust) can scroll through an endless parade of possibilities, all in the palm of their hand. Their initial encounters, therefore, are easy and risk-free. Their ability to mate and marry across social classes is vastly increased. The bad news, though, is that not everyone matches in this free-for-all, and many of those who do report being numbed over time by the sheer weight of so much choice.

Counterintuitively, perhaps, having so many options for romantic encounters is upping the bar on making these relationships work. Unless people feel an immediate attraction, and a sense that it is mutual, many are choosing to pull away from a connection that might have developed, preferring the dull thud of loneliness to the sting of rejection.

Which isnt to say that the future is bleak. On the contrary: Having the technical and societal freedom to unbundle sex from reproduction and love gives individuals an unprecedented level of control over their own lives. Its not surprising that we dont yet know precisely how to handle these choices, or how to rearrange our social structures around them. Thats what happens during revolutionary times. But even if the structures of courtship are exploding right now, even if the traditional package of heterosexual marriage is morphing into a kaleidoscope of alternative arrangements, love itselfthe pings and pangs of dopamine in our animal brainsseems likely to endure. We will find it on Tinder. On Twitter. On Zoom, if we must. And it will shake our days and break our hearts all over again.

Debora Spar is a professor of business administration at Harvard Business School whose research work is focused on issues of gender and technology, and the interplay between technological change and broader social structures. Spar explores these issues in her new book Work Mate Marry Love: How Machines Shape Our Human Destiny published by Farrar, Straus & Giroux.

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Love in the time of Zoom: Why we're in the midst of a dating revolution - Fast Company

Expert View: Five Reasons Why You Should Care About Biodiversity Loss – Swachh India NDTV

Highlights

New Delhi: Humans are not the sole occupants of this planet but the choices and demands of this one specie seem to be threatening all other species and the very existence of the planet. According to experts, our everyday choices can have an environmental impact. When humans use natural resources or invade and exploit the forests, there can be large physical, chemical and biological consequences for ecosystems. A direct consequence of human actions is loss of biodiversity. The wide variety of species whether plants, animals, birds, fish, insects or microscopic organisms, are vital to maintain the delicate balance of this only know planet with life on it, say experts.

Also Read:Significant Improvement In Air Quality During Coronavirus Lockdown: Central Pollution Control Boards Report

There are a number of issues threatening the biodiversity, from climate change to overexploitation of natural resources, asserts the environmental activist Vandana Shiva. She said,

Cultivating and conserving diversity is no luxury in our times. It is a survival imperative. Some environmental gains were made during the lockdown due to COVID-19 pandemic as it restricted human activities but those are fast slipping away. There is a need to take policy decisions focusing on the interconnectedness of the environment, forests, agriculture, and peoples health.

D. Raghunandan of Delhi Science Forum says that biodiversity loss is taking place at a very rapid rate which means that a lot of valuable resources will vanish. He said,

Biodiversity is the variety of life and fundamental to the survival of humans. Biodiversity loss affects the whole of nature because by allowing the species to go extinct unnaturally or forests to disappear upsets the balance that is required for the support system on Earth. More and more species are becoming vulnerable and habitats are being destroyed at an unprecedented rate, with forest lands being converted development. There can be unforeseen consequences- ecological and economical, of the loss of biodiversity. However, people are not concerned about the long-term effects of disappearing species and depleting natural resources because of biodiversity loss.

Mr. Raghunandan said that humans are invading forests, the habitats of various species of animals and insects in an unprecedented way and thus, resulting in an increase in human-animal interaction which escalates the probability of viruses jumping from animals to human beings. These are called zoonotic diseases. He said,

The more human beings exploit biodiversity, the more the likelihood of such pandemics like COVID-19 to occur frequently.

Ms Shiva pointed out that about 300 new pathogens that have impacted humanity in the last 50 years are a result of the loss of biodiversity. She said,

In the past, the destruction of the Western Ghats led to the monkey disease and similarly, the Ebola virus, SARS (Severe Acute Respiratory Syndrome) and MERS (Middle East Respiratory Syndrome) are all result of the invasion by humans into forests and destroying the environment. The novel coronavirus, SARS-CoV-2, is also a result of invasion into the forest ecosystem.

Also Read:Air Pollution: Nitrogen Dioxide Levels Fell By More Than 70 Per Cent During COVID-19 Lockdown In New Delhi, Says United Nations

According to Mahipal Negi, an Environmentalist based in Tehri, Uttarakhand, biodiversity conservation helps in reducing the impact of natural disasters. He said that with climate change, growing population and increasing human invasion in natural habitats and unsustainable use or resources, calamities like forest fires, floods and droughts have become frequent. The flood of June 2013 in Uttarakhand is one such example that was triggered by human lead biodiversity loss and caused a massive loss of life and economy, he said. Mr. Negi further said that after a calamity hits a region, it can recover fast from it if it has a rich indigenous biodiversity.

Mr. Negi highlighted that the loss of biodiversity is leading to food cycle changes at local and global levels. He said,

Biodiversity plays a huge role in food and nutrition for humans as it directly impacts the production of grains, vegetables, fruits, herbs, and other food items. Biodiversity is also important for the productivity of soil and impacts other food resources like livestock and marine species. Biodiversity loss that results in the loss of critical pollinators like bees and the loss of worms and other species responsible for soil quality will impact food production and disrupt the supply chain. For example, in Garhwal region of Uttarakhand, some of the indigenous vegetables that are extremely rich in iron and other nutrients have started to disappear. People are now relying more on warehouse stored unseasonal vegetables.

For example, the disappearance of bees and butterfly should be a concern because it will have a major impact on plant reproduction which will further affect the local and global food systems in the coming years. He added that the huge amount of pesticides strain over crops is one of the major reasons for the disappearance of bees apart from the loss of biodiversity.

Mr. Raghunandan highlighted that disappearance of bees and butterflies is also a stark indicator of rapid destruction of biodiversity that is happening and is visible in the Western Ghats, tropical rainforests in South India and to some extent in the North East Himalayas as well.

Also Read:Air Pollution In India Improves Amid Lockdown Due To Coronavirus

Waterman of India, Dr. Rajendra Singh highlighted that due to dumping of untreated sewage, chemical wastes and industrial pollutants, and disrupting the natural flow of the water bodies by the building of dams, major rivers like Ganga, Yamuna, Gomti, Mahi, Godavari, Damodar, Sabarmati and the Cauvery have been badly polluted. He said,

Due to human activities, there is no clean water left in our freshwater systems. The rise in pollutants is killing the rivers by harming the river biodiversity.

Mr. Raghunandan highlighted that the two species that are on the verge of disappearance from the river systems of India are the freshwater dolphins and Gharials or gavials that belong to crocodilian family and are distinguished by their long thin snouts. It is because of increased human activities like building of dams, water transportations, recreational activities, pollution from industrial activities, rise plastic particles like fishing nets in the rivers, among others. Dolphins act as indicators of river health, according to scientists, and if the dolphin population is thriving in a water body, then the overall state of that freshwater system is also likely flourishing, said Dr. Raghunandan. Dr. Singh says that the disappearance of Gharials from the river Ganga has impacted the health of the river as these reptiles act as natural cleaners of the river.

Also Read:Coronavirus Lockdown: As People Stay Home, Earth Turns Wilder And Cleaner

Mr. Negi asserted that biodiversity is very crucial for the functioning of ecosystem services essential for survival like providing oxygen, freshwater, food; moderating of climate; mitigating natural disasters like storms, droughts and floods among other. Every species in an ecosystem fulfils a role for the proper functioning of the ecosystem as a whole, said Mr. Raghunandan. Citing the example of the disappearance of vultures, he said,

Indias vultures are facing an unprecedented decline. It is estimated that over 90 per cent of the countrys vultures have already disappeared. These large birds are natures garbage men as they clean up the environment. Scientists have found that one of the reasons of their disappearance is the pesticides and chemicals laden carcasses of animals they feed on and fall prey to poisoning. It IF vultures go extinct, it will increase the amount of carrion or the decaying flesh of dead animals and humans which will in turn spread various kinds of diseases.

According to Mr. Raghunandan, extinction of some species is also a part of the functioning of the ecosystem. He said,

There is something called a background rate of extinction of species. It is a part of nature. Evolution itself dictates that some species will survive and some will disappear. Nonetheless, what we are seeing now is the direct result of human activities. For example, human activities that result in climate change, deforestation, will result in biodiversity loss. Human-driven biodiversity loss is about 20-50 times higher than the background rate. It is unnatural.

He further said that biodiversity also helps in the evolution of new species in order to compensate the functions of the ones which went extinct.

Also Read:Coronavirus Pandemic Exposes Broken System Of Bio-medical Waste Management; Experts Discuss The Issue And Solutions

According to Dr. Rajendra Singh, deforestation and urbanization are the biggest manmade factors responsible for habitat and biodiversity loss. He said that it is still not too late for the country to replenish its biodiversity and now it is high time that the central and state governments implement the Biological Diversity Act, 2002 in its true spirit. He further said,

The Act provides for the conservation of biological diversity, sustainable use of its components and fair and equitable sharing of the benefits arising out of the use of biological resources. Implementing this nicely laid down act would save the country from a number of avoidable problems and will also provide respite from air and water pollution to a great extent. However, 18 years have passed since the enactment of the Act, it is not being given its due importance as most of the local bodies across the countries have not prepared a register that records the regions biological resources and so whatever environmental clearances are being given for various public and private projects are basically invalid.

He further asserted that the Act focuses on safeguarding traditional knowledge, preservation of threatened species, which in practice, have become secondary. This is leading to human-made evils like water scarcity and animal-human conflicts.

Ms. Shiva highlighted that the Ministry of Environment, Forest and Climate Change (MoEFCC) has been giving approvals to big projects that plan to operate in forests and urged the government of India to focus on conserving the forests and preserving the biodiversity that is left in the country after years of destruction in the name of development.

Also Read:Expert Opinion: The Right To Breathe Clean Air

NDTV DettolBanega Swasth Indiacampaign is an extension of the five-year-old BanegaSwachh India initiative helmed by Campaign AmbassadorAmitabh Bachchan. Itaims to spread awareness about critical health issues facing the country.In wake of the currentCOVID-19 pandemic, the need for WASH (Water,SanitationandHygiene) is reaffirmed as handwashing is one of the ways to prevent Coronavirus infection and other diseases.The campaign highlights the importance of nutrition and healthcare for women and children to preventmaternal and child mortality,fightmalnutrition, stunting, wasting, anaemia and disease prevention throughvaccines. Importance of programmes likePublic Distribution System (PDS), Mid-day Meal Scheme, POSHAN Abhiyanand the role ofAganwadis and ASHA workersare also covered. Only a Swachh or clean India wheretoiletsare used andopen defecation free (ODF)status achieved as part of theSwachh Bharat Abhiyanlaunched byPrime Minister Narendra Modiin 2014, can eradicate diseases like diahorrea and become a Swasth or healthy India. The campaign will continue to cover issues likeair pollution,waste management,plastic ban,manual scavengingand sanitation workersandmenstrual hygiene.

3,25,60,947Cases

91,01,064Active

2,24,71,040Recovered

9,88,843Deaths

Coronavirus has spread to 188 countries. The total confirmed cases worldwide are 3,25,60,947 and 9,88,843 have died; 91,01,064 are active cases and 2,24,71,040 have recovered as on September 26, 2020 at 3:49 am.

59,03,932 85362Cases

9,60,969 -9147Active

48,49,584 93420Recovered

93,379 1089Deaths

In India, there are 59,03,932 confirmed cases including 93,379 deaths. The number of active cases is 9,60,969 and 48,49,584 have recovered as on September 26, 2020 at 2:30 am.

DistrictCases

Akola757

Aurangabad1974

Dhule228

Jalgaon1039

Mumbai45478

Mumbai Suburban5363

Nagpur692

Nashik1575

Palghar1421

Pune9920

Satara629

Solapur1291

Thane13660

Yavatmal150

Ahmednagar190

Amravati291

Beed54

Bhandara41

Buldhana88

Chandrapur32

Hingoli208

Jalna201

Kolhapur646

Latur139

Nanded176

Nandurbar42

Parbhani78

Raigad1462

Ratnagiri350

Sangli145

Gadchiroli42

gondia69

Osmanabad125

Sindhudurg114

Wardha11

Washim13

1300757 17794

273190

992806 19592

34761 416

DistrictCases

Chittoor319

Guntur511

Krishna557

Kurnool795

Sri Potti Sriramulu Nell*296

Anantapur428

East Godavari356

Prakasam104

Srikakulam183

Visakhapatnam103

West Godavari199

Y.S.R.205

Vizianagaram23

661458 7073

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Expert View: Five Reasons Why You Should Care About Biodiversity Loss - Swachh India NDTV

Halt in-person university teaching until test and trace fixed, union urges – The Guardian

Face-to-face teaching at universities should be halted until the government fixes test-and-trace failures and curbs the spread of Covid-19, the union representing academics and staff has said.

The warning from Jo Grady, general secretary of the University and College Union (UCU), comes as institutions increasingly take matters into their own hands by switching to majority online-only teaching.

Others are spending million of pounds instituting their own test-and-trace systems to identify outbreaks on campus. Strict disciplinary measures for students who flout social distancing rules are also being brought in.

Across England, one in 500 people are believed to have had Covid-19 last week, with the number of daily coronavirus infections tripling in a fortnight according to the Office for National Statistics. The R (reproduction) number was put at 1.2-1.5 for England and the UK.

More than 20 million people 30% of the UK face enhanced lockdown restrictions after extra curbs were announced in Leeds, Blackpool, Stockport, Cardiff and Swansea.

Outbreaks have hit 23 universities, forcing thousands of students into self-isolation. Hundreds of coronavirus cases were confirmed on campuses, including 172 at the University of Glasgow, 127 at Manchester Metropolitan University and 120 at Edinburghs Napier University.

In response to the Manchester outbreak, 1,700 students are being placed in quarantine for a fortnight at halls of residence at Birley and All Saints Park, in a joint move by the local authority, the university and Public Health England.

In an interview with the Guardian, Grady said the sharp rise in cases at Scottish universities which reopened earlier than those in the rest of the UK showed that test and trace was inadequate to protect staff and students. She called for in-person teaching to be abandoned where possible until the system could be fixed.

Grady urged university leaders to act now to drop face-to-face classes and potentially allow students to return home. If [vice-chancellors] dont do something now, all their efforts will be undone in a few weeks because the number of infections will be so high, or there wont be enough staff to teach, she said.

There is an urgency about this that didnt exist a month ago, because we are seeing infection rates rising and there is the danger that students are just becoming incubators.

But until there is an effective UK-wide test-and-trace programme, there are going to be cases everywhere. Even if youve got a self-contained university campus with a relatively small number of students, you are still bringing people all together from all over the UK, and staff who teach at multiple institutions moving between them.

The University of Leeds has become the latest to go online-only unless teaching is deemed safe and necessary. Six of its students tested positive for Covid-19 and the city of Leeds will go into local lockdown from midnight, meaning most students will not be able to visit their families.

It emerged that 12 universities in England and Wales are trying to combat possible shutdowns by forging ahead with testing programmes and in some cases with their own on-campus tracing teams and mechanisms.

While university leaders say publicly that their bespoke systems are to supplement the 10bn NHS test and trace programme, in private they complain that they have been forced to institute on-campus testing because it will be impossible to ensure that thousands of students can be tested.

The University of Cambridge plans to test all students living in university accommodation weekly, while the University of Exeter has invested in rapid saliva testing facilities.

Imperial College in London has gone further and set up campus-wide tracing, with a Covid-19 contact tracing hub. Students who return positive tests will be reached and asked to provide details for those they have had close contact with, including intimate physical or sexual contact or skin-to-skin contact, as well as anyone with whom they have spent at least a minute within 1 metre.

Alastair Sim, director of Universities Scotland, said the governments in England and Scotland could not provide enough tests to universities because of shortages caused by schools reopening.

There was a big peak with schools going back and I think the testing capacity got, I wouldnt say overwhelmed but certainly stretched [in a way] that wasnt really anticipated. The government, and this is both governments, could not make testing available for many students, he told the BBC.

Salford University, which has reported 20 infections among students, is among those running its own test-and-trace system, known as Sprout. But it has not yet been synchronised with class lists, meaning students were having to report to staff if they were symptomatic or living with someone who was.

At Salford, student gatherings in halls were said to have been broken up by security staff. Theyve been on hold for so long and have obviously gone a bit crazy as first-years do and now theyre faced with this, said a lecturer. Staff are really worried, none of us want to go back to face-to-face learning. Were the ones with the risk factors, rather than the 18, 19 and 20-year-olds.

The University of Southampton has developed its own rapid-response saliva test, and will test all incoming students and staff when they arrive on campus.

Universities in Liverpool and Manchester have switched to online teaching, with only clinical subjects retaining in-person classes in most cases.

Manchesters universities are preparing to clamp down on illegal gatherings with strict measures including potentially expelling students who do not comply with social distancing rules and imposing curfews on residential halls.

The University of Manchester has so far taken disciplinary action against 200 students for breaching social distancing guidelines, while several have also been issued with 100 fixed penalty notices by police.

A spokesperson for the university said it saw imposing a curfew on students living in halls as a last resort, but if residents fail to adhere to social distancing rules we will be faced with no alternative.

A government spokesperson said: Testing capacity is the highest it has ever been, but we are seeing a significant demand for tests. It is vital that staff and students only get a test if they develop coronavirus symptoms.

Our universities are home to world-leading science and innovation, but for those producing their own tests, it is important that the process works with the national system so we know what is happening and where, so we can utilise it for public safety.

In Scotland, there was intense criticism and growing confusion around new restrictions announced by universities, including a bar on going out this weekend, which the countrys commissioner for children and young people said raised concerning human rights implications.

The first minister, Nicola Sturgeon, confirmed that the ban on visiting bars, cafes or restaurants this weekend applies to all students in Scotland, even those studying part-time or living outside halls of residence.

But she hinted at a U-turn on guidance from the governments clinical director, Jason Leitch, who said students were not allowed to return to their family homes, saying there would be further guidance over the weekend. Addressing students directly at her daily briefing, Sturgeon told them: I know you might feel like you are somehow being blamed its not your fault.

Continued here:
Halt in-person university teaching until test and trace fixed, union urges - The Guardian

LETTERS: Medical school merits support; Hoping for other rallies; Questionable information; Trump good to minorities – Monitor

Medical school merits support

Although there is a need for exploratory discussion and civil debate on city budgets, it was with chagrin and incredulity that I read that during a City Council meeting, Edinburg Councilman Gilbert Enriquez entertained the idea to axe the annual contribution to the UTRGV Medical School. It was also reported that Councilman Jorge Salinas agreed and stated that these millions of contribution dollars were unnecessary.

Budgets are essential and staying within the budget is also essential, especially during our pandemic times; however, as someone who has been educated in the Rio Grande Valley as well as taught science here as a result of this education, I fear that todays dollars and cents of a balance sheet would never be able to equate to the long-term health and education of our community.

What have our contributions to UTRGV Med School through our tax money already secured? According to Veronica Gonzalez, UTRGV vice president who defended the contribution from Edinburg at a later Edinburg meeting:

More than 1,000 faculty and staff members hired and 221enrollment and graduated in its fist class.

Opened several medical clinics in Edinburg.

Set up a COVID-19 lab for testing and drive-thru sites that are still operating, and the lab can give results in 24 hours.

Contract tracers for the coronavirus have also been hired.

Nowhere will our tax money be spent better and receive higher dividends and long-term rewards than in the continued support of the UTRGV Medical School through the annual donations as promised from all the RGV cities. Our local cities as Edinburg have already contracted their support with a memorandum for 10 years, and we should stay committed as the current pandemic has proven that investment to be sound investment.

Diane Teter

Edinburg

Hoping for other rallies

I read about the area rallies in support of the guy convicted of running a fake university con; convicted of using a fake charity to pay for his legal bills and a fulllength portrait of himself; puttingterrified little Mexican kids in cages and losing track of their parents; being accused of multiple sexual assaults; stirring up racial hatred and violence nationwide; gassing peaceful protesters to create a photo op holding up a bible to dupe credulous evangelicals; asking the U.S. Supreme Court to end health care for 20 million people; being personally responsible for the deaths of tens of thousands of people by lying about the pandemic; etc. Yeah, that guy.

Hope soon to read about rallies in support of his victims.

Ed Chaney

Laguna Vista

Questionable information

The New York Times recentlyran an extensive storyexposing the state ofTexas incredibly flawedsystems in place to trackand report COVID-19 deaths.Essentially, the evidenceshows that because ofan archaic system thatvaries from one countyto another, we are notprovided accurate informationabout the number of COVID-19cases, the number of deathsand the manner in whichthe various health departmentsclassify a COVID-19death.

Original post:
LETTERS: Medical school merits support; Hoping for other rallies; Questionable information; Trump good to minorities - Monitor

Medical school ‘like All Black selection’ – focus is on what is best for the team – Stuff.co.nz

Supplied

Northland District Health Board member and Auckland University senior lecturer Mataroria Lyndon says we are generations away from worrying about Mori and Pacific students taking all the places in medical school.

Mori doctors feel unsupported and undermined as debate continues over whether Otago University medical school's admissions scheme is unfair.

The university is fighting a legal challenge to its Mirror on Society policy, which prioritises entry into first-year medical school for special category students Mori, Pasifika, rural, refugee and low socio-economic.

The legal challenge is from a man who claims the policy meant his child missed out on general entry, despite their results averaging more than 92 per cent.

Last month, a selection policy change discussion document presented to the University of Otagos medical admissions committee suggested capping the number of Mori and Pasifika special entry spaces, though the university maintains it was not a proposal for change.

Dr Mataroria Lyndon, who is a Northland District Health Board member, public health doctor, Auckland University senior lecturer and Fulbright scholar, said talk of Otago limiting progress was disappointing to say the least.

READ MORE:* Otago Uni will fight legal challenge to its med school special entry scheme* Caution urged over 'out of blue' proposal to limit special pathway for Mori, Pasifika at Otago Med School* She aspired to be a doctor at 10, to 'make a point' that Mori can

I feel for Mori medical students in these programmes who are feeling that they are being perceived negatively.As medical students, everybody sits the same assessments and comes out with the competencies expected to graduate. There is no difference there.

POOL

Prime Minister Jacinda Ardern and Director-General of Health Dr Ashley Bloomfield offer support to Otago Medical School's admissions policy. (First published September 4, 2020)

Lyndon, a graduate of Auckland Universitys counterpart scheme, said publicly funded medical schools were obliged to think beyond individuals and to serve the nation.

Getting into medical school is not a given. It is actually part of a broad strategy or plan.

Lyndon, a South Aucklander who was the first in his family to go to medical school, completed a thesis about why students pursued medicine. It showed Mori students were more motivated by serving their communities.

The same could be said about Pasifika and rural students, he said.

It is not just being Mori, for Mori, it is for everybody.

Pkeh benefited from coming from long lines of medical professionals.

Supplied

Professor Papaarangi Mary-Jane Reid, Auckland University head of Mori health, says medical school selection is like All Black selection, where you may think your child has what it takes but they may not be the best fit for the team.

University of Auckland Professor of Mori health and public health doctor Papaarangi Reid compared medical school selection to All Black selection in the September 20 edition of E-Tangata magazine.

A parent might think their child worked hard and had what it took but they might not be the best fit for the team, she wrote.

Most of the nation is ready to be benevolent towards Mori and our needs but many choke when it comes to affirming our rights and when our excellence may constrain their privilege.

The comments come after 785 female doctors signed a letter urging Otago University not to place any limits on the scheme.

Dr Janet Rhodes September 3 letter to Dean Professor Rathan Subramaniam said the scheme had begun the slow process of addressing [racial] disparity in a system designed by Pkeh for Pkeh.

Rhodes, a trainee general surgeon, told Stuff debate about the scheme was leaving her Mori colleagues feeling unsupported and undermined.

It is making them feel like their struggles are really unvalidated.

She was frustrated society was listening to people who have the resources to fight on a legal platform and ignoring Treaty of Waitangi legalities.

Supplied/Stuff

Northland District Health Board member, public health doctor, Fulbright scholar, and Auckland University senior lecturer Mataroria Lyndon says we are generations away from worrying about Mori and Pasifika taking all places in medical school.

Academic ability was not enough to make a good doctor.

Nobody should be trying to get into medical school without a back-up plan.

Of the 202 students granted entry from the 2019 first-year health science course, 120 came from special categories. Some argued the current policy allowed all places to be filled by special entry students.

Lets say there was an intake where that happened, I think that is something that should be celebrated as a real success, rather than denigrated, Rhodes said.

Opposition to that possibility showed underlying racism.

A spokeswoman said the university had received letters from a variety of people and organisations expressing views on the equity scheme.

The universitys senior leaders will meet medical students next week to discuss their concerns.

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Medical school 'like All Black selection' - focus is on what is best for the team - Stuff.co.nz

SHE Initiative Shines Light on Gender Disparities in Oncology Workforce – Targeted Oncology

The Association of Community Cancer Centers (ACCC) National Oncology Conference each year helps community oncologists approach both unique and typical challenges with innovative strategies. This year, one of the challenges addressed that has been increasingly raised throughout the year was the topic of disparities in the medical field.

To close out the ACCC 37th (Virtual) National Oncology Conference, keynote speaker Nick Smith-Stanley, MBA, addressed the topic of diversity and inclusion for women in medicine, and specifically in the field of oncology.

Smith-Stanley, associate director of finance and administration, Livestrong Cancer Institutes, Dell Medical School, associate director of administration and strategic planning, Department of Oncology, Dell Medical School, The University of Texas at Austin, explained the challenges faced by women in the oncology workplace and quantified the divide seen between the number of men and women in oncology and in positions of leadership in the medical field.

By discussing the lack of women in the field of oncology, he said, it will hopefully lead to developing strategies that address such challenges, which can then lead to real change.

He also presented how the Livestrong Cancer Institutes Dell Medical School has created a program that seeks to address this gap and give the future generation of women in medicine the tools they need to succeed.

The Growing Gender Divide Across a Medical Career Span

Oncology is known to be a male-dominated field in the healthcare space. Although the number of female students and physicians in the field has grown over the past few years, the proportion of women compared to men in medicine is still less than half. Further, the numbers get lower throughout the continuum of a medical career from medical student to physician to professor and then dean.

Smith-Stanley said that, encouragingly, for the first time in history, the number of female medical students is higher than the number of male students, but the difference is marginal. The rates decrease, however, over the course of a medical career. The number of female residents and fellows is below 50% and has not changed much in the last 10 years, and specific to oncology and hematology, the proportion of female residents and fellows is below about 45%.

Among practicing physicians, only 35% are female, and within the oncology/hematology field specifically, the rate is closer to one-third. However, this is increased from 10 years ago when the rate of female physicians was only about 28% overall and about 25% in the oncology field.

Within research in general, as of 2018, 50% of STEM (science, technology, engineering, and mathematics) positions were held by women, but specifically to science and engineering, only 28% of women hold positions in these fields.

Across all disciplines in science and oncology, we see women struggling to be considered for opportunities for promotion and leadership, Smith-Stanley said. One faculty member at Dell Medical School told us that throughout her career she has seen male colleagues with fewer accomplishments get promoted at the same time. In addition, she shared that at previous institutions, rules were not as rigid for promotion and tenure for men as they were for women, they were willing to bend the rules for men, but not for women. This shows that this is not only a personal or organizational issue, it is by far a systemic issue.

He pointed out that as a result, women hold fewer positions of leadership than men. Only 19% of department chairs were held by women in the year 2019 and only 21% of full professors are female.

This poses a greater problembecause of the lack of mentorship opportunities. If our students and junior faculty are unable to identify women in positions of leadership and mentorship to help guide their career then they are less likely to progress in their career as well, he commented.

He suggested that these rates reduce across the span of a medical career due to a lack of tools, mentorship, and support given to women in medicine.

Smith-Stanley offered some strategies to bridge the gender divide through organizational changes. Starting with culture, organizational leaders must embrace and promote an all-inclusive environment. Training on diversity and bias is one way to overcome these barriers and allow for change. Providing opportunities for professional development, including mentorship and networking, can also help to retain the women in the medical workforce.

Livestrong Cancer Institutes, he said, is one of the few cancer centers across the country that is led by a woman, S. Gail Eckhardt, MD, who is the director and associate dean of cancer programs at the company. As such, Dell Medical School is focused on addressing such healthcare disparities and leaders at the Livestrong Cancer Institutes feel that they have a responsibility to address the role that women play in cancer, research, and academics.

SHE Takes a Step Towards Overcoming Gender Disparities

The Livestrong Cancer Institute stressed the use of early education and mentorship to bridge the gender gap, which ultimately led to the development of the Summer Healthcare Experience (SHE) program in oncology. SHE is a free, immersive week-long program for introducing female-identifying high school juniors and seniors to a range of career opportunities in the cancer field. The program was launched in the summer of 2019 when 8 young women from Austin were selected with health program teachers and brought to the Dell Medical School to learn more about the various careers involved with cancer care.

The SHE program sought to empower young women to take control of their education and future careers by giving them tools to overcome challenges in the workplace. The high school students were given the opportunity to participate in research and interact with the clinical teams. Participating students also came away with a general knowledge of cancer, how it is treated, and the challenges that patients with cancer and their caregivers face. Additionally, the program promoted leadership skills and professionalism that could be used throughout their career, no matter the field.

During the week, the students worked with women in the cancer center to learn about cancer anatomy and how physicians work together for the care of patients with cancer. In the wet research lab, the students were able to see cell cultures and tumor slides and they also investigated different brain tumors in the neuro-oncology lab. The students were also able to join in on the molecular tumor boards to see the interaction between various departments for deciding on optimal care for a patient. In a survivorship session, the students were also able to meet with cancer survivors and their families and learn about their cancer journeys. Additionally, the students learned about health services research in the community and how health services researchers are investigating healthcare disparities in patients with cancer.

Throughout the week, the students were able to interact with female leaders from the cancer center, including center director Eckhardt, to hear about and learn from their experiences and the challenges they faced in their careers. They also met with a number of community organizations, from American Cancer Society to the Austin Center for Grief and Loss, to hear about how these organizations are assisting patients with cancer in the city.

Its not enough to just talk about equity and inclusion. You need to have people who are invested in the conversation and the desire to make a difference. Thats exactly what we saw in the first year of SHE, Smith-Stanley said.

The students were tasked with coming up with a comprehensive care plan for a cancer case based on all they learned during the week. These plans were then presented at the end of the week to faculty from Livestrong Cancer Institutes, Dell Medical Center, the students high school teachers, and their families.

We could not have been more thrilled with the results. They were confident, they were thoughtful, they were knowledgeable, they were compassionate. The transformation that we witnessed from Monday to Friday was remarkable, Smith-Stanley commented.

Moving forward, the Livestrong Cancer Institutes hopes to expand the SHE program to more students and extend the program to 2 weeks. The program also hopes to add in more biomedical research, entrepreneurship education, a college prep day, and even a post-program internship. Livestrong Cancer Institutes is also partnering with other organizations to spread the SHE program to 4 other cancer centers, and hopefully nationwide, although this expansion has been delayed by the coronavirus disease 2019.

Reference

Smith-Stanley N. Addressing the Disparities of Women in Oncology. Presented at: ACCC National Oncology Conference; September 14-18, 2020; Virtual.

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SHE Initiative Shines Light on Gender Disparities in Oncology Workforce - Targeted Oncology

What Women in Medicine Month means for this refugee nurse – 6 On Your Side

TWIN FALLS September marks Women in Medicine Month, and 2017 studies conducted by the Association of American Medical Colleges show that males still have a handle on the workforce in doctor and physician positions. However, these numbers also show that more women are currently enrolled in medical school, helping lessen a gender gap in the future.

The significance of Women in Medicine Month means a lot to Isabel Rutazihana, a refugee nurse who arrived in California in 2007 with her parents from the Democratic Republic of Congo to escape an ongoing conflict. The initial culture shock to the US was initially very overwhelming. Having to adapt to schooling, US customs, employment, and even driving was a lot to take in.

"The culture like as a kid, how kids viewed their parents, how parents viewed their kids, employment, everything was just totally different," said Isabel.

Despite always having the dream of becoming a doctor, she had put it aside until witnessing her mother take of a woman whose family had abandoned her. Isabel said, "I saw how much love that my mom gave to her and how much joy it brought to her. It made me feel I do want to work in something that actually brings joy to people's lives."

Isabel arrived in Twin in 2018, where she balanced school, a new family, and working as a nursing assistant at St. Luke's Magic Valley. After years of hard work, Isabel graduated from school this past December. Still, due to COVID and other personal reasons, she delayed taking her NCLEX exam, which would make her a fully registered and certified nurse. However, just recently, she finally managed to take the exam.

Isabel said, "I pushed my NCLEX a little bit farther and farther, and I finally took it about a week and a half ago, and I passed, so I'm officially a nurse!"

Isabel's long journey has been a lot, having to manage school, work, and taking care of her child. In some instances, she would miss out on helping her son with homework, tucking him in at night, and having to sacrifice quality time with her husband. However, despite her sacrifices, she attributes her success in completing school to the sacrifices her family made, and that they were the driving force to achieve her goals.

"Right now, my son can say, "Oh! My mom is a nurse, and she works at the hospital," and when he says it, I feel very proud because I accomplished something," said Isabel.

For Isabel, Women in Medicine Month means the world as it signifies women blazing their own path in a challenging field of work, "It kind of shows that as women we're not just homemakers or do secretary work and we can actually go into the field with men and can actually do."

Isabel views her becoming a nurse as just a stepping stone in her career and hopes to accomplish more in the future.

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What Women in Medicine Month means for this refugee nurse - 6 On Your Side

Confronting race in diagnosis: Medical students call for reexamining how kidney function is estimated – AAMC

Melanie Hoenig, MD, a nephrologist and associate professor at Harvard Medical School and Beth Israel Deaconess Medical Center, remembers the first time she seriously questioned the use of a patients race in the common clinical algorithm that helps doctors determine kidney function.

It was the first week of her renal pathophysiology class in 2015, and she was teaching her first-year medical students about the estimated glomerular filtration rate (GFR). She explained its a common clinical formula that incorporates a patients sex, age, and race to approximate how well the kidneys function.

Cameron Nutt, a first-year student at the time, asked why the formula adjusted for race in a way that can make kidney function appear better than it actually is for Black people, who are at greatest risk for kidney disease of any racial group. He and two other students, Danika Barry and Leo Eisenstein, wondered about the use of a formula that made biological assumptions about race, which is widely recognized as a social construct.

These questions gave Hoenig pause. Why did they correct for race? What should they do if the patient is multiracial? And why were they using a formula that assumes better kidney function in a population group that disproportionately experiences kidney failure?

I think its really important to take a step back from the way we always do things and listen to our students.

Melanie Hoenig, MD, associate professor, Harvard Medical School, and a nephrologist at Beth Israel Deaconess Medical Center

These are questions that medical students, faculty members, and clinicians at academic medical centers across the country have increasingly been asking as systemic racism has gained attention from institutional leaders.

And even as some experts have spoken out against the use of race in estimated GFR and other clinical algorithms for years, medical students have proven to be a powerful force in bringing about change recently.

I think its really important to take a step back from the way we always do things and listen to our students, Hoenig says. Having students ask probing questions makes me a better everything better clinician, human, mother, teacher, and so on.

The formula for estimating GFR now used by most laboratories was developed by a group of physicians and researchers in 1999 based on observations from a study that included 1,304 White people and 197 Black people. The researchers found that, on average, the measured GFR of study subjects who were identified as Black was higher than other groups GFR, which the researchers took to mean that the formula underestimated the level of kidney function in Black people. So, they added a race correction that assumes Black patients have a higher estimated GFR than the formula would suggest. The formula was updated a decade later in a project that looked at 10 studies that included 8,254 people, and it was further validated in 16 studies that included 3,896 people. The researchers were unable to explain the reason for the differences in kidney function between Black and non-Black people. Some researchers said the underestimation of GFR in Black people could be because they believed they have higher muscle mass.

Critics of the use of race in the formula at the University of California, San Francisco, School of Medicine argue that muscle mass can vary widely among individuals within the same race; the assumption that Black people are biologically different from people of other races is not backed by evidence and reinforces erroneous assumptions; to categorize people as either Black or not-Black fails to account for the diversity of the patient population; and the formula can lead to overestimation of kidney function for a Black patient, potentially delaying care.

The implicit acceptance of GFR race correction reinforces antiquated colonial myths that there is something fundamentally different between races, wrote four physicians in an opinion for the San Francisco Examiner. These are the same fallacious narratives that have been invoked throughout history to justify horrendous acts such as slavery and indigenous genocide, on the scientific basis that the persecuted race was biologically inferior to whites.

But some nephrologists, including the lead researcher on the development of the formula, Andrew Levey, MD, caution against removing race from the equation before more extensive research is done because it could lead to unintended consequences.

All of us should be asking what are the ultimate questions we all care about: Why are there disparities in care? How can we do a better job to make sure that every patient that is in front of us gets the best care?

Lesley Inker, MD, MS, an associate professor of medicine at Tufts University School of Medicine

Some have proposed eliminating the race coefficient, but this would induce a systematic underestimation of measured GFR in blacks, with potential unintended consequences at the individual and population levels, Levey and other physicians wrote in an article published in the Clinical Journal of the American Society of Nephrology in August. We propose a more cautious approach that maintains and improves accuracy of GFR estimates and avoids disadvantaging any racial group.

These unintended consequences could include unnecessarily discontinuing medications such as metformin, an oral diabetes medication, which could lead to prescribing more expensive interventions with potential side effects, such as insulin, says Lesley Inker, MD, MS, an associate professor of medicine at Tufts University School of Medicine in Boston and an author of the article.

She and other researchers have been working for years on developing an alternative way of estimating GFR that does not include demographics and are analyzing the implications of eliminating race from the formula.

All of us should be asking what are the ultimate questions we all care about: Why are there disparities in care? How can we do a better job to make sure that every patient that is in front of us gets the best care? Inker says.

The National Kidney Foundation (NKF) and the American Society of Nephrology (ASN) announced in July that they would form a joint task force to study and make recommendations on the use of race in GFR estimation, with initial recommendations expected later this year.

Black people are three times more likely than non-Hispanic white people to experience kidney failure and are less likely to be identified as kidney-transplant candidates, according to the NKF and ASN. They noted that the current formula is widely accepted and provides reliable and accurate information on kidney function but also that race is a social rather than a biological construct, and the inclusion of race in the formula ignores diversity within racial groups.

Because of the complexity, its a discussion thats been around for quite some time, says Tod Ibrahim, executive vice president of the ASN. In 2020, with the twin challenges of the COVID-19 pandemic and the recognition or willingness as a country to really confront systemic racism, it became clear we needed to accelerate that discussion.

Ibrahim says the task force will rely on expert testimony and will seek to learn from academic institutions that have already made the move to eliminate race from GFR estimation.

Beth Israel Deaconess Medical Center in Boston officially removed the use of race in estimation of GFR in 2017. Around this time, students at several other universities started the many-months process of lobbying for the change.

At the University of Washington (UW), questions from medical students inspired the creation of a working group that included the students and nephrologists as well as perspectives from social scientists and other interested groups. After a process that stretched over two years, the university dropped race from its estimated GFR equation on June 1, 2020.

One of the joys of working at an academic medical center is seeing generations of people that interface with the academic medical center and bring in fresh ideas bring in a fresh set of eyes to look at old problems, says Rajnish Mehrotra, MD, MS, interim head of the Division of Nephrology at UW and the editor-in-chief of the Clinical Journal of the American Society of Nephrology. It keeps us on our toes.

While many medical schools have historically been hierarchical, a culture shift seems to be occurring that has inspired medical students to challenge the status quo, according to Oluwaferanmi Okanlami, MD, MS, an assistant professor of family medicine, physical medicine and rehabilitation, and urology at the University of Michigan Medical School.

The culture and the climate of when I was a student didnt really give room for questioning, says Okanlami, who has been an advocate for diversity, equity, and inclusion. We were meant to assume what we were being taught is true [now,] people feel more empowered to assert their own truth and question others.

One of the joys of working at an academic medical center is seeing generations of people that interface with the academic medical center and bring in fresh ideas bring in a fresh set of eyes to look at old problems. It keeps us on our toes.

Rajnish Mehrotra, MD, MS, interim head of the Division of Nephrology at UW and the editor-in-chief of the Clinical Journal of the American Society of Nephrology

Karampreet Peety Kaur, now a fourth-year medical student at Vanderbilt University School of Medicine in Nashville, was one of the students who took on the initiative to create change. Kaurs effort began with doing her research. She and other students reached out to the students at Harvard who had already successfully removed race from the formula at Beth Israel Deaconess Medical Center and read up on the related literature.

We wanted to make sure we were thinking about race in the right way, Kaur says. "The scientific literature shows that race is a social construct rather than a biologic variable that reflects genetic differences ... and that fueled our questioning of the use of race.

Throughout the nearly two-year process, Kaur leaned on her own position as a student to pose questions and respectfully challenge the conventional thinking within the various departments.

The result: Vanderbilt removed race from the estimation this summer.

As medical students, our job is to be curious and to learn, Kaur says. By using that role to our advantage, we were able to have meaningful conversations with people who certainly know more about the kidney than we do.

While the use of race in the estimated GFR has gained national attention, it is not the only clinical algorithm that incorporates race.

Darshali Vyas, MD, a second-year resident at Massachusetts General Hospital in Boston, worked with two other physicians to assess more than a dozen examples of algorithms that incorporate the patients race and potentially direct health care resources away from people of color.

Vyas and the others identified potential inequities in algorithms that estimate risk for heart failure, of complications for vaginal birth after a cesarean section, and of complications and death in cardiac surgeries, among others. In each of these cases, Vyas found that the algorithms had the potential to steer people of color away from care, whether it be because their risk for heart failure was underestimated or the risk of complications from surgery were overestimated.

The article, published in the New England Journal of Medicine, garnered national attention and prompted the chairman of the U.S. House of Representatives Ways and Means Committee to call on medical professional associations to issue new guidance that corrects misuse of race in clinical algorithms. Already, the NIH Maternal Fetal Medicine Units Network, which provides the calculator to estimate the risks of vaginal birth after a cesarean section, has begun to develop a new calculator that doesnt include race.

Its important that the next steps involve policy change, Vyas says. I think that will in many cases require re-approaching the evidence and being open to creating new tools and amending tools that might have been in place for a long time.

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Confronting race in diagnosis: Medical students call for reexamining how kidney function is estimated - AAMC

Case Western Reserve University researchers to examine how COVID-19 ravaged America’s nursing homes – Newswise

Newswise Almost from the moment COVID-19 reached this nations shores, nursing homes have experienced some of its most devastating effects.

Within a few months, federal officials reported that one of every five nursing homes had experienced a death from the novel coronavirus. Not long after, several media outlets published independent analysis finding that an estimated 40% of the fatalities related to COVID-19 took place in nursing homes.

Rather than surrender to the terrifying trend, Case Western Reserve researchers saw an opportunity to help. If they could understand more about how nursing home infections spreadand even be able to identify its presence earlierthousands of families might be spared painful losses. More, stemming nursing home infections could in turn reduce COVID-19s spread across communities across the country.

Thanks to a $2.3 million National Institutes of Health (NIH) grant, they are going to try.

Well be looking at the magnitude of the problem and how long-term care residents transmit and cope with the disease, said David Canaday, a professor from the Division of Infectious Disease at the universitys School of Medicine. If we can better understand how to minimize spread in these facilities, we may also be able to optimize interventions.

The disease caused by the coronavirus is known to be particularly lethal to older adults and those with underlying conditions. According to the Centers for Disease Control (CDC), there are more than 15,000 nursing homes in the U.S. providing housing to over 1.4 million individuals.

Tens of thousands in nursing homes have died during the pandemic from COVID-19.

One of the greatest challenges in an infectious disease outbreak is determining which patients are at risk forsevereforms of illness and require additional care or hospitalization in another facility, said Mark Cameron, associate professor from the medical schools Department of Population and Quantitative Health Sciences. This is especially important with COVID-19, where the elderly and those with co-occurring diseases need more immediate and personalized treatment.

Joining Cameron and Canaday in the study is with Stefan Gravenstein, a professor of medicine at Brown University.

Their research has three main areas of focus:

As the COVID-19 pandemic continues, there are many millions more within the U.S. who are at similar risk but live in assisted living or at home in contact with their families or care providers.

Its absolutely critical to understand our vulnerabilities and develop new therapeutic strategies for our communities under care, Canaday said.

Cameron added that this population will remain most at-risk if we continue to see surges this fall, or before a vaccine comes to market.

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Case Western Reserve University researchers to examine how COVID-19 ravaged America's nursing homes - Newswise

Team assessing if dual-antibody injection prevents COVID-19 illness – Newswise

Newswise A combination antibody treatment for preventing COVID-19 illness in individuals who have had sustained exposure to someone with the virus is being studied by researchers at The University of Texas Health Science Center at Houston (UTHealth). The clinical trial is enrolling patients at Harris Health Systems Lyndon B. Johnson Hospital.

The Phase III, randomized, double-blinded, placebo-controlled trial will help researchers determine if the laboratory-made dual-antibody treatment, REGN-COV2, can prevent SARS-CoV-2 infection in individuals who share a home with someone with a confirmed infection.

If this trial demonstrates that this treatment is effective, it could be used in various settings where exposure risk is heightened, such as health care, airlines, meatpacking factories, nursing homes, and among first responders, saidRoberto C. Arduino, MD, the studys lead investigator and professor of infectious disease withMcGovern Medical Schoolat UTHealth. It is crucial that we discover treatment options that can not only prevent severe illness, but also stop the spread of COVID-19 within our communities.

The study team is seeking to enroll asymptomatic individuals who have had at least 48 hours of sustained exposure to a person with a confirmed SARS-CoV-2 infection, known as an index case. Participants must be randomized within 96 hours of the index cases diagnosis. Trial participants must live in the same household as the index case patient for 29 days during the study.

REGN-COV2 is a combination of two monoclonal (laboratory-made) antibodies that target two different sites of the spike protein found on the surface of SARS-CoV-2, the virus that causes COVID-19. Antibodies are proteins created by the immune system to fight a pathogen or infection. The targeted surface spike protein gives the virus a crown-like appearance and allows it to attach to and enter cells.

The REGN-COV2 antibody cocktail is a combination of antibodies originally isolated from patients who have recovered from COVID-19 and produced by mice that have been genetically modified to have human immune systems.

The study period will last 32 weeks. On day one of enrollment, patients will receive four subcutaneous injections of either the trial agent or a placebo. This treatment strategy is known as passive immunization, and is the current strategy used for tetanus, rabies, hepatitis B, and herpes zoster exposures. Participants will be tested for COVID-19 weekly during the first month they are enrolled.

Co-investigators from McGovern Medical School includeKaren J. Vigil, MD, an associate professor of infectious disease and medical director of infection prevention for UT Physicians outpatient operations; andSarah Duong, MD, a general internal medicine physician. Jonatan Gioia, MD, is the program manager.

Regeneron Pharmaceuticals is sponsoring the clinical trial. For more information, visitClinicalTrials.gov.

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Team assessing if dual-antibody injection prevents COVID-19 illness - Newswise

The Practice of Neurology in Mongolia – WFN News

Training has been cut from 2 years to 1 year; residents are unsalaried; exams are not standardized.

I am glad to have the great opportunity to write about the practice of neurology in my country, Mongolia. Let's begin with its interesting history. The practice of neurology got its start in Mongolia in 1939 with the establishment of 10 neurologic beds in the Central Hospital by the Russian neurologist Dr. N.Ya. Semyonova.

In 1947, a neurologist who was a faculty member of Leningrad Medical High School, Dr. G.Ya. Liberson, founded the neurology department in the medical faculty of Mongolian State University. Dr. G. Ya. Liberson's work was taken over by the first Mongolian neurologists, Dr. G. Lodon and Dr. L. Dagzmaa.

In the 1950s and 1960s, the first scientific research works were done in the field of neuroinfections (neurolues, epidemic encephalitis, polymyelitis) according to the social and ecological requirements of the country at that time (G. Lodon, D. Rawdandorj). At this time, the second adult neurology ward and the first one for children were launched, the first department of neurosurgery was founded, and the use of new diagnostic methods such as EEG and pneumoencephalography (PEG) was adopted (Tsagaankhuu G et al. 2007).

In the 1970s and 1980s, the neurologic service in the country expanded to become an independent medical branch and improved the quality of neurologic care by increasing the number of neurologists (about 100) and founding neurologic wards in all province hospitals (each with about 20 beds and two neurologists). At that time, the Mongolian neurologists were supported mostly from Ukrainian neurologists (E.P. Zagorowsky), and inherited their methods (Tsagaankhuu G et al. 2007).

The political changes in the late 1980s and early 1990s with the end of the Cold War smashed completely the old socialist social system in the country. While the loss of contact with Russian neurologists was keenly felt, one benefit was that Mongolian neurology was offered new chances to develop professional relationships with neurologists from other countries. In 2002, the Mongolian neurologic association "Monneurology" was founded, and it became a member of the WFN. Also in 2002 the first international epilepsy seminarworkshop was held with the support of the ASEAN Epilepsy Society.

In 2006, the first international neurologic INFOSeminar was held in Ulaanbaatar, with the initiation of WFN and international participation opening new opportunities in foreign relations. Today, the neurologic service in Mongolia consists of more than 20 medical doctors with PhDs and about 200 neurologists. The number of neurologists in Mongolia is 7.8 per 100,000 people, which is a very high proportion compared to most other countries of the world. About 60% of all Mongolian neurologists are working in the capital Ulaanbaatar, where more than a half of the population is concentrated (1.5 million of Mongolia's entire population of 2.5 million people live in the capital city). The number of neurologic beds is about 900 in the whole country, about 3.7 per 10,000 (Baasanjaw D et al, 2006).

In recent years, neurologic research has focused on the epidemiology of most common neurologic disorders such as stroke, epilepsy, neurodegenerative and neuroinflammatory diseases. The stroke epidemiology study revealed that there is a high percentage of the hemorrhagic type (about 50% vs. about 40% ischemic stroke and 10% subarachnoid hemorrhage), which requires special attention to prevention (Baasanjaw D et al, 1999). Also, several research studies were done on epilepsy, which is a significant cause of disability in Mongolia. But because of flaws in the design of these studies, their findings do not distinguish various exact types of epilepsy, limiting the studies' usefulness.

From 1997 to 2000, the neurogenetic group from the U.S. National Institutes of Health, which was led by Dr. Lev Goldfarb, collaborated with the Mongolian Medical Research Institute to undertake research on neurohereditary diseases in Mongolia. The investigators found a high prevalence of certain neurogenetic disorders associated with certain regions of the country. For example, Charcot Marie Tooth [CMT] type 2 disease was prevalent in Arkhangai province, where there were about 100 cases in the population of 97,000. Other disorders with a geographic prevalence included the observations of CMT type 1 disease in Khulunbuir, Dornod province; hereditary spastic spinal paralysis in the Khowd and Uws provinces; and familial oligophrenia in Dornod province. Cases of myotonic dystrophy were registered in nearly all provinces.Not all provinces were involved in the epidemiologic research, but the fact that hereditary neurologic disorders occur in high prevalence within a country that has small population deserves special clinical attention.

Despite the high number of specialists and neurology beds in Mongolia, there are many problems resulting from the difficult current socioeconomic situation in the country. There is insufficient medical and social insurance, both of which were newly founded in Mongolia only 10 years ago.

The low level of knowledge and outdated training methods of some neurologists are leading to misdiagnosis and treatment failures in many cases. Neurologic residency training lasted for 2 years during the period from 1997 to 2001 and included psychiatry training. Since 2002, the training program has been shortened to 1 year. The quality of clinical training is limited by numerous problems: Neurology residents must often pay for part or all of their training costs; they lack proper workplaces; and they are unsalaried. In most respects, neurology residency training in Mongolia lacks standards, adequate supervision, and standardized examinations.

Established neurologists require but usually do not receive training in order to bring them up to date with the massive increase in new diagnostic methods in recent years. Without such training they risk misinterpreting test results. Pharmaceutical companies are not inclined to introduce their new drugs in Mongolia because our small population means fewer sales for them. Some important medical branches in neurology, such as neurorehabilitation, are still nonexistent in the country. Instead, this type of treatment has been replaced by minimally effective traditional treatment methods.

To become familiar with the latest versions of diagnostic and treatment research, the neurologic consultant of the Ministry of Health began to implement a CME program for neurologists. The younger generation of neurologists eagerly participates in these CME opportunities. All recent information must be translated into Mongolian because knowledge of the English language is not widespread. We are also working on setting and renewing the special standards and guidelines for neurologic diseases which can be generally diagnosed and treated. Mongolia is located in the center of the Asian continent, is bordered by Russia and China, and, belongs neither among the Southeast, Pacific, nor Middle East countries.

The climate is dry and cold. Mongolia has its own culture and language, and a population with a nomadic style of life that has existed for thousands of years. We hope our geographical, cultural, and climatic conditions will not be a barrier for expanding our foreign relationships, and we continue to makes strides to improve our neurologic services in Mongolia.

At time of print, SARANGEREL JAMBAL, M.D., known to her friends as Saraa, is a neurologist at the "Reflex" Neurological Clinic in Ulaanbaatar, Mongolia.

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The Practice of Neurology in Mongolia - WFN News

COVID-19 and neurological training in Europe: from early challenges to future perspectives – DocWire News

This article was originally published here

Neurol Sci. 2020 Sep 24. doi: 10.1007/s10072-020-04723-9. Online ahead of print.

ABSTRACT

The worldwide SARS-CoV-2 pandemic is dramatically affecting health systems with consequences also for neurological residency training. Here we report early experiences and challenges that European neurologists and residents faced. The breadth of the pandemic and the social restrictions induced substantial modifications in both inpatient and outpatient clinical care and academic activities as well, adversely affecting our residency training. On the other hand we see also opportunities, such as gaining more clinical and professional skills. All these drastic and sudden changes lead us to reconsider some educational aspects of our training program that need to be improved in order to better prepare the neurologists of the future to manage unexpected and large emergency situations like the one we are living in these days. A reconsideration of the neurological training program could be beneficial to guarantee high standard level of the residency training in this period and beyond.

PMID:32970238 | DOI:10.1007/s10072-020-04723-9

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COVID-19 and neurological training in Europe: from early challenges to future perspectives - DocWire News

Oliver Sacks: His Own Life gives the celebrated neurologist and author his own documentary – The Boston Globe

Oliver Sacks (1933-2015) had a highly unusual career. The titles of some of the neurologists books tell you how unusual. Awakenings (1973), The Man Who Mistook His Wife for a Hat (1985), An Anthropologist on Mars (1995), Uncle Tungsten: Memories of a Chemical Boyhood (2001), Hallucinations (2012). Awakenings was later made into a movie (1990), with Robin Williams playing Sacks.

Those titles combine the personal and scientific, the humanistic and clinical, and that combination made Sacks famous. Or as he says in Ric Burnss Oliver Sacks: His Own Life, Im asked are you a doctor first and then a writer? The answer is I think Im equally both; and in important ways they blend together. The documentarys chief virtue, after the very considerable pleasure of getting to spend time in Sackss company, is learning how much his personal life rivaled his career in remarkableness.

Starting Sept. 25, its available for streaming via the Coolidge Corner Theatres Virtual Screening Room, at coolidge.org/films/oliver-sacks-his-own-life. In addition, the Coolidge will present a virtual Q&A with Burns and Atul Gawande, an author-physician very much in the Sacks tradition, on Sept. 30, at 8 p.m. Gawande is among the films interviewees.

The documentary was shot in 2015, shortly after Sacks learned he had terminal cancer. The diagnosis has done nothing to affect his gusto. The Falstaffian beard that readers know from Sackss author photos is matched by an equally outsize personality. He was immoderate in all possible directions, his friend the Italian writer Roberto Calasso says in the film. Nothing we see suggests otherwise.

The son of doctors, he grew up in a cultivated Jewish household in London. The most shocking moment in the documentary comes when Sacks describes his much-beloved mothers response to learning her 18-year-old son was gay. You are an abomination, she told him. The shock worsens when Sacks later says she remained the person he was closest to.

Early on, Sacks acquired passions for swimming, the periodic table of elements, mineralogy, motorcycles, and weightlifting. He came to the United States to do his medical internship in San Francisco, then residency in Los Angeles. Possessed of a serious amphetamine habit, he thought nothing of going on 36-hour rides on his bike, stopping only for gas.

In New York, Sacks began the work that would make him famous, treating patients whod been severely debilitated by encephalitis for more than four decades. Giving them the amino acid L-DOPA, Sacks helped them awaken from their near-vegetative state. We see before-and-after footage of the patients from 1969. Its both wondrous, the transformations wrought, and disturbing, the severity of the patients previous condition and seeing how some returned to it.

The documentary also includes talking-head interviews intense shyness did not keep Sacks from having many devoted friends as well as period photographs and archival films from throughout his life. These are welcome and offer a nice counterpoint to the 2015 footage. Sackss marvelous speaking voice provides a kind of voice-over throughout. Its a tribute to how articulate he was that its hard to tell when hes speaking extemporaneously and when hes reading from his just-completed memoir, On the Move.

What isnt welcome is an intrusive score and recurring bits of quite-unnecessary filmmaking flashiness: reenactments and weird, semi-abstract shots meant to represent . . . the nervous system? Sackss descriptions of neurological disorders are so compelling that trying to offer visual equivalents is superfluous as well as distracting. The movie opens with Sacks saying, Could you repeat your question more shortly? I only have an attention span of about 12 seconds. Clearly, thats not true. The filmmakers seem to think its true of the audience, though.

OLIVER SACKS: HIS OWN LIFE

Directed by Ric Burns. Available via Coolidge Corner Virtual Screening Room. 114 minutes. Unrated (as PG-13: the occasional cheerful obscenity; disturbing archival footage of neurological patients)

Mark Feeney can be reached at mark.feeney@globe.com.

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Oliver Sacks: His Own Life gives the celebrated neurologist and author his own documentary - The Boston Globe

Amicus Therapeutics Receives European Medicines Agency PRIME Designation for CLN6 Batten Disease Gene TherapyAdditional Phase 1/2 Data to be Presented…

CRANBURY, N.J., Sept. 24, 2020 (GLOBE NEWSWIRE) -- Amicus Therapeutics (Nasdaq: FOLD), a global, patient-dedicated biotechnology company focused on discovering, developing and delivering novel medicines for rare diseases, today announced the European Medicines Agency (EMA) has granted Priority Medicines (PRIME) designation to AT-GTX-501, the Companys investigational gene therapy for children living with variant late infantile neuronal ceroid lipofuscinosis 6 (vLINCL6) disease, also known as CLN6 Batten disease.

The PRIME initiative provides enhanced support and increased interaction to developers of promising medicines with the goal of optimizing development plans and speeding regulatory evaluations. The goal of EMAs PRIME is to help patients benefit as early as possible from innovative new therapies that have demonstrated the potential to significantly address an unmet medical need.

The PRIME designation is based on data from the ongoing Phase 1/2 clinical trial evaluating a single dose of AT-GTX-501 for the treatment of children with CLN6 Batten disease. Additional information about the trial is available at ClinicalTrials.gov (NCT02725580).

We are very pleased that the EMA has recognized the potential of our CLN6 gene therapy. Based on our preliminary clinical data, we believe AT-GTX-501 could potentially be a transformative treatment option for children living with CLN6 Batten disease, an ultra-rare, debilitating condition that presents in early childhood and is often associated with childhood death, said John F. Crowley, Chairman and Chief Executive Officer. We look forward to continuing to work closely with the EMA to accelerate development of this first potential treatment option for children living with CLN6 Batten disease.

Additional data from the ongoing Phase 1/2 clinical study will be presented at the Child Neurology Society Annual Meeting in October. Regulatory interactions are ongoing and the Company expects to provide feedback on the path forward in early 2021.

In the U.S., AT-GTX-501 previously was granted Rare Pediatric Disease and Orphan Drug designations by the United States Food and Drug Administration. In the EU, the Company now holds PRIME and orphan medicinal product designations.

About AT-GTX-501AT-GTX-501 is a novel gene therapy in Phase 1/2 development for CLN6 Batten disease, a rare, fatal, inherited lysosomal disorder with no approved treatment that primarily affects the nervous system. AT-GTX-501 is dosed in a one-time intrathecal infusion to deliver a functional copy of the CLN6 gene to cells of the central nervous system. The therapy is designed to address the underlying enzyme deficiency that results in progressive cell damage and neurodevelopmental and physical decline.

About Batten DiseaseBatten disease is the common name for a broad class of rare, fatal, inherited disorders of the nervous system also known as neuronal ceroid lipofuscinoses, or NCLs. In these disorders, a defect in a specific gene triggers a cascade of problems that interferes with a cells ability to recycle certain molecules. Each gene is called CLN (ceroid lipofuscinosis, neuronal) and given a different number designation as its subtype. There are 13 known forms of Batten disease often referred to as CLN1-8; 10-14. The various types of Batten disease have similar features and symptoms but vary in severity and age of onset.

Most forms of Batten disease/NCLs usually begin during childhood. The clinical course often involves progressive loss of independent adaptive skills such as mobility, feeding and communication. Patients may also experience vision loss, personality changes, behavioral problems, learning impairment and seizures. Patients typically experience progressive loss of motor function and eventually become wheelchair-bound, are then bedridden and die prematurely.

About Amicus TherapeuticsAmicus Therapeutics (Nasdaq: FOLD) is a global, patient-dedicated biotechnology company focused on discovering, developing and delivering novel high-quality medicines for people living with rare metabolic diseases. With extraordinary patient focus, Amicus Therapeutics is committed to advancing and expanding a robust pipeline of cutting-edge, first- or best-in-class medicines for rare metabolic diseases. For more information please visit the companys website at http://www.amicusrx.com, and follow on Twitter and LinkedIn.

Forward-Looking StatementsThis press release contains "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995 relating to preclinical and clinical development of our product candidates, the timing and reporting of results from preclinical studies and clinical trials and the prospects and timing of the potential regulatory approval of our product candidates. In particular, this press release relates to interim data from an ongoing Phase 1/2 study to investigate intrathecal administration of AAV-CLN6 gene therapy. The inclusion of forward-looking statements arising from this interim data, ongoing study and natural history preliminary data should not be regarded as a representation by us that any of our plans will be achieved. Any or all of the forward-looking statements in this press release may turn out to be wrong and can be affected by inaccurate assumptions we might make or by known or unknown risks and uncertainties. For example, with respect to statements regarding the goals, progress, timing, and outcomes of discussions with regulatory authorities, and in particular the potential goals, progress, timing, and results of preclinical studies and clinical trials, actual results may differ materially from those set forth in this release due to the risks and uncertainties inherent in our business, including, without limitation: the potential that results of clinical or preclinical studies indicate that the product candidates are unsafe or ineffective; the potential that it may be difficult to enroll patients in our clinical trials; the potential that regulatory authorities, including the FDA, EMA, and PMDA, may not grant or may delay approval for our product candidates; the potential that preclinical and clinical studies could be delayed because we identify serious side effects or other safety issues; and the potential that we will need additional funding to complete all of our studies. Further, the results of earlier preclinical studies and/or clinical trials may not be predictive of future results. The interim data and Phase 1/2 study discussed herein is inherently preliminary and early in the study, derived from a limited patient set, and later trial results with this patient set or others may not be consistent with these preliminary results. In addition, all forward-looking statements are subject to other risks detailed in our Annual Report on Form 10-K for the year ended December 31, 2019 and Quarterly Report on Form 10-Q for the quarter ended June 30, 2020. You are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date hereof. All forward-looking statements are qualified in their entirety by this cautionary statement, and we undertake no obligation to revise or update this news release to reflect events or circumstances after the date hereof.

CONTACTS:

Investors:Amicus TherapeuticsAndrew FaughnanDirector, Investor Relationsafaughnan@amicusrx.com(609) 662-3809

Media:Amicus TherapeuticsDiana MooreHead of Global Corporate Communicationsdmoore@amicusrx.com(609) 662-5079

FOLDG

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Amicus Therapeutics Receives European Medicines Agency PRIME Designation for CLN6 Batten Disease Gene TherapyAdditional Phase 1/2 Data to be Presented...

NIH study details self-reported experiences with post-exertional malaise in ME/CFS – National Institutes of Health

News Release

Monday, September 21, 2020

First publication from NIH ME/CFS study takes deep dive into key feature of the disease.

One of the major symptoms of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is post-exertional malaise (PEM), the worsening of symptoms after physical or mental activities. Using their own words and experiences, people with ME/CFS described how debilitating PEM can be in a study in Frontiers in Neurology. This is the first publication to come out of the National Institutes of Healths intramural post-infectious ME/CFS study.

Post-exertional malaise following normal activities is unique to ME/CFS and we do not understand the biology underlying this severe and harmful feature of the disease, said Walter Koroshetz, M.D., director of NIHs National Institute of Neurological Disorders and Stroke (NINDS). In-depth conversations with people who experienced post-exertional malaise and listening to them describe their individual experiences can provide a perspective not achieved through surveys. This study provides a window into just how much post-exertional malaise can affect a persons quality of life.

Researchers led by Avindra Nath, M.D., clinical director of NINDS, recruited 43 individuals with ME/CFS to participate in nine focus groups discussing their experiences with post-exertional malaise, including activities that led to it, how long it lasted, and techniques they used to help decrease their symptoms. Five out of the nine focus groups included participants who experienced PEM following a cardiopulmonary exercise test (CPET), which can measure how the body reacts to exercise and is often conducted using a stationary bike.

The focus groups were part of a larger study taking place at the NIH Clinical Center designed to take a comprehensive look at ME/CFS preceded by an infection. The goal of the larger study is to identify clinical and biological aspects of ME/CFS that may improve understanding of causes and how the disease changes over time. Dr. Nath and his colleagues will also examine the progression of PEM in study participants who undergo a CPET. The researchers included CPET experience in the PEM focus groups to assist in the design of the exercise challenge of the NIH ME/CFS study.

ME/CFS is a debilitating, chronic disease that may affect between 836,000 and 2.5 million people in the United States. In addition to PEM, people with ME/CFS will often experience pain, cognitive difficulties, and severe fatigue that does not improve with rest. The disease can affect all parts of the body including the immune, metabolic, cardiovascular, and neurological systems. There is no treatment for ME/CFS.

Qualitative analysis from the focus groups revealed that although the participants used a wide range of phrases to describe their experiences, many of their PEM symptoms fell into three core categories: exhaustion, cognitive difficulties, and neuromuscular complaints. Additional PEM symptoms included headaches, pain, nausea, sore throat, and sensitivity to light and sound. The onset of PEM is generally between 24 and 48 hours after exertion and can last from 24 hours to several weeks.

Almost everyone in the study indicated that complete rest, often in a dark and quiet room, was required to reduce the symptoms.

In addition, many participants described efforts to plan ahead and limit activities to avoid PEM, while also acknowledging that it can occur unexpectedly.

It was quite striking to hear the extent to which PEM can affect their quality of life, said Barbara Stussman, statistician at the NIHs National Center for Complementary and Integrative Health and lead author of the study. The widespread body symptoms, the unpredictability of PEM, and the sometimes-lengthy recovery greatly hindered individuals ability to live a normal life.

The study also identified, for the first time, differences between PEM caused by daily activities, such as grocery shopping or going to a doctors appointment, and PEM caused by the lab test CPET. The results suggest that the overall symptoms were similar, but PEM caused by the exercise test came on faster and lasted longer.

Additional research is required to learn more about the causes of PEM in people with ME/CFS. Future studies may identify sub-types of PEM, which may help guide targeted treatments.

This study was supported by the NIH Intramural Program.

The NINDS is the nations leading funder of research on the brain and nervous system.The mission of NINDS is to seek fundamental knowledge about the brain and nervous system and to use that knowledge to reduce the burden of neurological disease.

About the National Institutes of Health (NIH):NIH, the nation's medical research agency, includes 27 Institutes and Centers and is a component of the U.S. Department of Health and Human Services. NIH is the primary federal agency conducting and supporting basic, clinical, and translational medical research, and is investigating the causes, treatments, and cures for both common and rare diseases. For more information about NIH and its programs, visit http://www.nih.gov.

NIHTurning Discovery Into Health

B Stussman et al. Characterization of Post-Exertional Malaise in Patients with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome. Frontiers in Neurology, 2020.

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NIH study details self-reported experiences with post-exertional malaise in ME/CFS - National Institutes of Health

Physicians issue warning about rare neurological condition, expected to appear this fall – Newswise

Newswise Each fall, as kids go back to school and share germs with their peers and the changing seasons create environmental conditions perfect for viral growth, symptoms matching the cold and flu proliferate in classrooms and day care centers like clockwork. Sometimes these symptoms are severe enough to land patients in the emergency room. Thats where physicians started to notice a troubling trend six years ago.

A few days after presenting with symptoms like cough, congestion, and worsening asthma, these little kids will suddenly have rapid onset paralysis in one or more of their limbs, resembling polio, said pediatric neurologist Henry David, MD, the Director of Neurocritical Care at the University of Chicago Medicine Comer Childrens Hospital. Usually, this paralysis is permanent to a large degree.

Known as Acute flaccid myelitis, or AFM, this rapid onset paralysis following a viral illness is a bit of a medical mystery to physicians, with a number of quirky traits that distinguish it from other post-viral conditions. For one thing, its causes arent entirely clear though physicians agree that a viral infection is likely what triggers the condition. For another, nearly all of the patients affected are very young children, between the ages of 3 and 6, who have experienced a viral illness within the last month. Many (though not all) have a history of asthma, and many (though not all) report joint, neck, and back pain shortly before the onset of paralysis.

Perhaps strangest of all, the disease appears to follow a two-year outbreak cycle, with a rash of patients appearing every other fall. While the condition is extremely rare, affecting only a handful of children in the state of Illinois each season, its effects can be severe, causing permanent paralysis and in severe cases, respiratory failure and even death.

With an outbreak due this year and so many mysteries surrounding the condition, pediatricians are worried about what this illness means for their patients especially with potential complicating factor of the ongoing COVID-19 pandemic.

Weve been tracking this illness for about six years, but realistically, this or something like it has existed for three or four decades, said David. It seems to be an infectious and possibly immunological phenomenon, where the bodys own inflammatory response to a virus contributes to the grey matter injury of the spinal cord, damaging the patients motor neurons, which control movement. Once damaged, these neurons cant regenerate, and leaves the patient with weakened or paralyzed limbs.

Analysis of patient samples have found a connection between AFM and common enteroviruses, in particular Enterovirus D68, which typically leads to flu-like symptoms including fever, cough, congestion, vomiting, and/or diarrhea. But, as pediatric infectious disease expert Madan Kumar, DO, the Director of the Pediatric Antimicrobial Stewardship Service at Comer Childrens Hospital points out, Patients who are diagnosed with AFM dont always test positive for a virus, and about one in ten patients is completely asymptomatic for a viral illness. Diagnosis is very challenging, and we think that we may be underappreciating the number of cases.

AFM is so rare that no specific targeted treatment exists for the disease; available treatments focus on reducing the inflammatory immune response. When we see kids with limb weakness, well throw immunomodulatory therapy, plasmapheresis everything weve got at them, said David. The problem is, its not clear how much these treatments help, because often we catch the condition so late, and because there havent been enough cases to do a proper randomized clinical trial.

Once the initial illness passes, patients may receive physical therapy to aid their recovery, or seek out specialized centers that offer nerve grafting to restore some control and sensation in the paralyzed limbs.

Only an exceedingly small number of patients with enteroviruses end up with this condition, and its not clear what combination of host and viral factors trigger it, Kumar said. The thing with diseases that are this rare is that many parents and physicians have less awareness of the condition so they dont recognize the signs, and we miss the opportunity to provide early therapy for these kids."

This years predicted outbreak is especially worrisome for pediatricians because its still unclear how living in the era of COVID-19 will impact detection, diagnosis, and treatment of AFM. Given our move toward social distancing and people spending most of their time at home, weve interrupted the epidemiology of these viruses, said Kumar. This has probably delayed the onset of this years outbreak. But we know that children are a major driver in the spread of respiratory illnesses, and as kids are going back to school and businesses are reopening, its just a matter of time before these traditional seasonal viruses pick up again.

The lack of clarity in what triggers AFM also makes it uncertain whether contracting COVID-19 this fall might put kids at greater risk for the condition. It is unclear if contracting multiple respiratory viruses such as an enterovirus and a rhinovirus at the same time changes the pathophysiology of AFM. And while many children who contract COVID-19 remain asymptomatic, its unknown whether this might cause complications if they contract other respiratory illnesses.

The concerns go beyond the risk of a COVID-19 infection. Were concerned that this pandemic means that there will be less hands-on interaction between kids and many of their caregivers, David said. Parents might not notice the signs, and may be hesitant to take their children to the hospital because of fears about contracting COVID-19. People have the tendency to develop tunnel vision, and while were all so fixated on COVID-19, theres a risk of letting our guard down about other diseases.

The physicians stress that families should take all of the normal precautions to prevent viral respiratory illnesses this year, in addition to COVID-19 precautions, such as masking, social distancing and good hand hygiene. In particular, Kumar said, Get a flu vaccine. We dont know how COVID-19 will interact with other viruses. Minimize your chances if ever there was a year to be sure to get your flu vaccine, this is it.

One small silver lining to the pandemic is the increasing availability of telemedicine appointments, making it easier for patients to connect with specialists, like those at Comer Childrens Hospital, a center of excellence for managing AFM patients and a referral center for suspected cases. I often see children with AFM who had previously been to an emergency room or urgent care with early signs of weakness or partial paralysis, said David. But most providers have never seen this disease, so how would they know to look for it? Its under-reported and underdiagnosed. If we can get the word out and tell people to watch for the early signs, it might make a difference.

While its not yet clear what this seasons predicted AFM outbreak will look like, the physicians hope that with time, a greater understanding of the condition can lead to better treatments and improved outcomes. My goal is to catch more of these patients earlier in the disease course, and to share what we learn from treating them with our colleagues who are also working on this challenge, said David. Were all working to make a difference for these children.

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About the University of Chicago Medicine & Biological Sciences

The University of Chicago Medicine, with a history dating back to 1927, is one of the nations leading academic health systems. It unites the missions of the University of Chicago Medical Center, Pritzker School of Medicine and the Biological Sciences Division. Twelve Nobel Prize winners in physiology or medicine have been affiliated with the University of Chicago Medicine. Its main Hyde Park campus is home to the Center for Care and Discovery, Bernard Mitchell Hospital, Comer Childrens Hospital and the Duchossois Center for Advanced Medicine. It also has ambulatory facilities in Orland Park, South Loop and River East as well as affiliations and partnerships that create a regional network of care. UChicago Medicine offers a full range of specialty-care services for adults and children through more than 40 institutes and centers including an NCI-designated Comprehensive Cancer Center. Together with Harvey-based Ingalls Memorial, UChicago Medicine has 1,296 licensed beds, nearly 1,300 attending physicians, over 2,800 nurses and about 970 residents and fellows.

Visit UChicago Medicines health and science news blog at http://www.uchicagomedicine.org/forefront.

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Physicians issue warning about rare neurological condition, expected to appear this fall - Newswise

Neurologic function and COVID-19 | Feeling Fit – yoursun.com

Q: My family has a history of neurologic disease. My grandfather died from a stroke. An uncle was diagnosed with early-onset Alzheimer's disease at 40, and my brother recently was diagnosed with an aneurysm. I'm wondering if our family is at greater risk for COVID-19? Are there any neurologic symptoms we should be on the lookout for?

A: Being diagnosed with any neurologic disease can be difficult for patients and their families, but it can be even more concerning now. The new coronavirus, SARS-CoV-2, which causes COVID-19, has become a concern for everyone, but it is particularly concerning for older individuals and those with other health issues or decreased immune systems. Neurological disorders are among the underlying medical conditions that may increase the risk of serious COVID-19 complications for individuals of any age.

The neurological effects of COVID-19 are still being studied. What's unknown is whether these are direct effects of the virus entering the nervous system or consequences of the disease's effect on the body. There are bits of information that have come out from a number of studies looking at clinical evaluation of patients that would suggest that there is nervous system direct involvement by the virus, but the reliability of those studies is still in question.

Recent findings are indicating that stroke is one of the conditions that has been seemingly at higher incidence in patients who have involvement in the body by COVID-19. Why the strokes occur in people infected with COVID-19 is yet to be fully determined. It's thought that a lot of it might be worsening of the damaged blood vessels these individuals have, which makes them predisposed to stroke, and then their bodies are being stressed from a respiratory perspective by this intense illness.

Normally, when people are sick, particularly when their respiratory system is failing, we know there will be adverse effects on the brain because of poor oxygenation and other metabolic effects. While these effects are serious, they are not direct effects of the virus on the brain itself.

There have been reports about patients who have experienced COVID-19 and who also had some neurological signs and symptoms, such as change of taste and smell and confusion. The challenge is that there is a lot we do not know about COVID-19, including if these issues are a direct effect of the virus actually getting into the nervous system and damaging the brain, or whether it's an indirect effect as a consequence of the respiratory failure or compromise of other organs of the body. It is important to remember that COVID-19 is not the only virus that causes these symptoms of reduced smell. Influenza is well known to affect taste and smell, too, and there are other respiratory viruses that can cause similar kinds of troubles. COVID-19, however, seems to cause this at a higher frequency. But again, the challenge is whether the virus is actually directly affecting the nerves that have to do with taste and smell, or if it is the respiratory epithelium that is injured, that interacts with the nerve in the back of the nose.

The principle things that we'll see from a neurological viewpoint in relation to COVID-19 will be changes in mental awareness, cognition, troubles with difficulty of interaction or ability to interact with the environment. One of our concerns is how much of this is going to be long lasting and how much of this is just a temporary effect of metabolic disturbances. So, those are very much uncertain points at this time.

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Neurologic function and COVID-19 | Feeling Fit - yoursun.com

New treatment option brings hope to patients with neurological disease – WCVB Boston

Neurological diseases, like Parkinson's, are often devastating. The symptoms, including tremors and twisting limbs, can be painful and embarrassing, but a new treatment device is giving patients hope and doctors access to information they've never had before.At 12 years old, John Caldwell received a difficult diagnosis."They called it an essential tremor which means you have a tremor but they don't know why you have it," Caldwell said.His hands would shake and over the years, he developed dystonia, a painful twisting in his neck. He was unable to turn his head. At one point, he was taking 25 pills a day to manage his symptoms.Last fall, his wife Diane heard about a new treatment option: a deep brain stimulation implant that would allow doctors to treat his symptoms and record his brain activity after the operation."It really can provide hope to people when they reach a stage where the medicine isn't working," said Dr. Mark Richardson, director of functional neurosurgery at Massachusetts General Hospital.He said deep brain stimulation has been a successful treatment option for neurological disease for 20 years but they didn't know the effect of that stimulation on a day-to-day basis."Now we have an additional tool we can use, which is we can see the person's own brain activity and how that's responding to stimulation," Richardson said.In July, Caldwell became the first patient in New England to undergo the minimally-invasive procedure. Richardson and his team used real-time MRI guidance to insert a wire the size of a spaghetti string into his brain. It delivers electrical stimulation to treat his symptoms and connects to a pacemaker-like device to track his brain activity."This is really a whole new window into brain function. This is data, information, we've never been able to see before," said Dr. Todd Herrington, director of the deep brain stimulation program at MGH.He said that new data will help them treat each specific patient in precisely the right way."For the first time, the device can actually record activity from the brain, which we think is going to be the brain activity underlying some of these symptoms, and we think that activity may help guide us in how we adjust the stimulator for each person," Herrington said.Herrington had told Caldwell it might take two to three months to find the right setting and bring relief but at this first follow up appointment, he was amazed."Like a wave of warm just came down my body, from my head and I was sitting there like 'What is this?'" Caldwell said."Dr. Herrington asked John to hold his hands out and I looked and one hand was tremoring and one hand was not and it was absolutely amazing to me that it worked. That it was possible and it happened and it was right before my very eyes," Diane Caldwell said.His dystonia also dramatically improved. He tracks any symptoms on this device to share at his follow-up appointments but says it's a miracle to have come so far. "What they gave me more than anything is hope. I never had hope that I could ever get out of this," Caldwell said.The hope is the device could one day read brain activity and provide stimulation in real time to treat symptoms. Richardson called it "The Holy Grail" of brain modulation.

Neurological diseases, like Parkinson's, are often devastating. The symptoms, including tremors and twisting limbs, can be painful and embarrassing, but a new treatment device is giving patients hope and doctors access to information they've never had before.

At 12 years old, John Caldwell received a difficult diagnosis.

"They called it an essential tremor which means you have a tremor but they don't know why you have it," Caldwell said.

His hands would shake and over the years, he developed dystonia, a painful twisting in his neck. He was unable to turn his head. At one point, he was taking 25 pills a day to manage his symptoms.

Last fall, his wife Diane heard about a new treatment option: a deep brain stimulation implant that would allow doctors to treat his symptoms and record his brain activity after the operation.

"It really can provide hope to people when they reach a stage where the medicine isn't working," said Dr. Mark Richardson, director of functional neurosurgery at Massachusetts General Hospital.

He said deep brain stimulation has been a successful treatment option for neurological disease for 20 years but they didn't know the effect of that stimulation on a day-to-day basis.

"Now we have an additional tool we can use, which is we can see the person's own brain activity and how that's responding to stimulation," Richardson said.

In July, Caldwell became the first patient in New England to undergo the minimally-invasive procedure. Richardson and his team used real-time MRI guidance to insert a wire the size of a spaghetti string into his brain. It delivers electrical stimulation to treat his symptoms and connects to a pacemaker-like device to track his brain activity.

"This is really a whole new window into brain function. This is data, information, we've never been able to see before," said Dr. Todd Herrington, director of the deep brain stimulation program at MGH.

He said that new data will help them treat each specific patient in precisely the right way.

"For the first time, the device can actually record activity from the brain, which we think is going to be the brain activity underlying some of these symptoms, and we think that activity may help guide us in how we adjust the stimulator for each person," Herrington said.

Herrington had told Caldwell it might take two to three months to find the right setting and bring relief but at this first follow up appointment, he was amazed.

"Like a wave of warm just came down my body, from my head and I was sitting there like 'What is this?'" Caldwell said.

"Dr. Herrington asked John to hold his hands out and I looked and one hand was tremoring and one hand was not and it was absolutely amazing to me that it worked. That it was possible and it happened and it was right before my very eyes," Diane Caldwell said.

His dystonia also dramatically improved. He tracks any symptoms on this device to share at his follow-up appointments but says it's a miracle to have come so far.

"What they gave me more than anything is hope. I never had hope that I could ever get out of this," Caldwell said.

The hope is the device could one day read brain activity and provide stimulation in real time to treat symptoms. Richardson called it "The Holy Grail" of brain modulation.

Originally posted here:
New treatment option brings hope to patients with neurological disease - WCVB Boston

Evidence of an Increased Burden of Humoral Autoimmunity in the CSF and plasma of COVID-19 Patients with Comorbid Neurologic Dysfunction – Newswise

Newswise Background: Coronavirus disease 19 (COVID-19) is the most globally impactful pandemic of the past century. The causative pathogen, SARS-CoV-2, infects ACE2-expressing cells and leads to pulmonary disease and a systemic immune response. In patients with severe COVID-19, a dysregulated immune response is associated with secondary extrapulmonary dysfunction, including neurological symptoms. Neurologic complications of SARS-CoV-2 infection are increasingly recognized, yet it is unknown to what degree humoral autoimmunity is a feature of neurological impairment in COVID-19.

Objectives: To perform an unbiased survey of peripheral and central humoral autoimmunity in COVID-19 patients with neurologic dysfunction.

Methods: Paired cerebrospinal fluid (CSF) and plasma biospecimens were collected from nasopharyngeal (NP) SARS-CoV-2 PCR positive patients with comorbid neurologic impairment (n = 5). Additional unpaired CSF biospecimens were collected from neurologically impaired NP PCR positive patients (n = 3). All COVID-19 patients were PCR negative for SARS-CoV-2 in the CSF. CSF and plasma were also collected from SARS-CoV-2 uninfected healthy control volunteers. Neurologic syndromes were diverse and included myositis, seizures, and encephalopathy. Biospecimens were screened in replicate by mouse brain immunostaining, immunoprecipitation mass spectrometry (IP-MS), and human peptidome phage display immunoprecipitation sequencing (PhIP-Seq). IP-MS spectra were analyzed by both spectral counting and MS1 peak area. For PhIP-Seq, proteins with overlapping peptides that were enriched at least 10-fold above control samples, or single peptides enriched 100-fold above controls were considered candidate autoantigens. Candidate autoantigens identified by at least two of three methods (PhIP-Seq, spectral counting, and peak area) were carried forward for validation.

Results: Unexpectedly, seven of eight COVID-19 CSF samples had evidence of humoral autoimmunity by tissue staining (n = 7), and IP-MS (n = 6), PhIP-Seq (n = 7), or both (n = 6). By IP-MS, significantly more candidate autoantigens were identified in COVID-19 biospecimens than in uninfected controls. PhIP-Seq identified twice as many candidate autoantigens in COVID-19 biospecimens than in controls. Notably, COVID-19 biospecimens were enriched for clinically relevant candidate autoantigens including those associated with dermatomyositis, and myasthenia gravis (none known to be pre-existing comorbidities). Additionally, COVID-19 biospecimens were enriched for candidate autoantigens with prima facie clinical relevance as they targeted proteins enriched in skeletal muscle, endothelial cells, and at the synapse. One candidate autoantibody targeted a ciliary protein implicated in syndromic anosmia.

Conclusions: We identified evidence of an increased burden of humoral autoimmunity in COVID-19 patients with comorbid neurologic dysfunction.

Presenter:M.D., Ph.D. Christopher Bartley, University of California San Francisco, Department of Psychiatry and Behavioral Sciences, 401 Parnassus Avenue, Room LP-263, 94143, San Francisco, US

Originally posted here:
Evidence of an Increased Burden of Humoral Autoimmunity in the CSF and plasma of COVID-19 Patients with Comorbid Neurologic Dysfunction - Newswise