Does CSF Antibody Testing Confirm Coronavirus in the Brain? – Medscape

Editor's note: Find the latest COVID-19 news and guidance in Medscape's Coronavirus Resource Center.

Testing for antibodies in the cerebrospinal fluid (CSF) may confirm that COVID-19 has invaded the brain.

A case series of three patients attending an inner city US hospital who had severe, laboratory-confirmed COVID-19 and encephalitis shows that while only one had abnormal white blood cells or protein present in CSF, all had evidence of immunoglobulin (IgM) antibodies.

"What was novel about our study was that we were able to show IgM, the acute phase reactant against COVID, in the spinal fluid of these patients, which is a direct indicator they had COVID in their brain," lead author Karima Benameur, MD, a neurologist and associate professor, Department of Neurology, Emory University School of Medicine, Atlanta, Georgia, told Medscape Medical News.

Benameur added that just because CSF testing indicates normal levels of inflammatory proteins, it doesn't mean the virus has not entered the brain and, therefore, to confirm this, she recommends CSF IgM testing, if possible.

The paper was published online June 2 in Emerging Infectious Diseases.

COVID-19 is typically characterized by respiratory illness and viral pneumonia with fever, cough, shortness of breath, and, in severe cases, progression to acute respiratory distress syndrome.

However, there have been few detailed investigations of neurologic complications in COVID-19 infection.

The documented cases include a 31-year-old woman with sickle cell disease who had a recent pulmonary embolus; a 34-year-old man with hypertension and signs of fever, shortness of breath, and cough; and a 64-year-old man also with hypertension and showing typical signs of the virus.

In addition to assessing CSF IgM, researchers analyzed CSF inflammatory proteins and performed molecular testing for SARS-CoV-2 using reverse transcription polymerase chain reaction (PCR).

Two of the patients had normal white blood cell counts and protein levels. "The only reason we could actually diagnose them with COVID encephalitis is because we were able to measure the IgM in their spinal fluid," said Benameur.

Neurologists ordering spinal taps on patients may incorrectly assume there's no brain involvement if the spinal fluid is normal, said Benameur.

Benameur emphasized, "just because the PCR in CSF is negative, this does not mean that the virus has not made it into the brain."

The PCR test is a good test for some viruses, including the herpes virus, but is a poor test for this new coronavirus, she said.

While all three patients had encephalitis, the female patient also developed encephalomyelitis as indicated by inflammation in her brain and spinal cord.

All patients had symptoms affecting cortical and brainstem function at the peak of neurologic illness.

It's not clear how the virus invades the brain, said Benameur. Some speculate it could be through the olfactory nerve, which might explain why some patients lose their sense of taste and/or smell.

Benameur noted that animal research shows that when the virus is injected into nose fibers, it can travel to the brain.

Experts don't know what percentage of COVID patients have the virus in the brain, said Benameur.

In addition, although all of the patients in the current case series were African American, the sample is too small to determine if neurological involvement is more prevalent in this population of COVID patients, said Benameur.

"Overall, having a poor prognosis has been reported to be more frequent in African Americans, but we don't know about neurologic complications. There are not enough subjects for us to be able to do that statistical analysis."

While the three cases were relatively young patients, again, this is not a large enough sample to determine if brain involvement is more likely in younger patients, said Benameur. She noted that she has data from additional patients and there is a wide range of ages.

The two male patients in the current series recovered and were released from hospital. The female patient died.

Her sickle cell disease may have complicated her outcome. Having hypoxia from a condition like pneumonia, in addition to sickle cell disease, may make it more difficult to get oxygen to tissues, said Benameur.

She urged all clinicians seeing COVID patients in clinics, including those without classic symptoms, to "ask them about their cognition."

Commenting for Medscape Medical News, Andrew Wilner, MD, associate professor of neurology, University of Tennessee Health Science Center, Memphis, said reports of neurological complications associated with COVID-19 "continue to multiply" as clinicians gain more experience treating these patients.

"To date, most, if not all, of the neurological complications can be explained by inflammatory changes such as thrombosis or cytokine storm as well as post-infectious causes such as antibody-related Guillain-Barre," said Wilner.

Other complications appear "nonspecific" and "related to acute, severe systemic illness such as hypoxic ischemic encephalopathy due to respiratory failure" as was the case with these three cases, he said.

"Whether unusual symptoms such as loss of olfactory sense are due to direct neuronal injury or inflammation has not been determined."

Wilner noted that although antibodies to the SARS-CoV-2 virus were present in the CSF of the current cases, SARS-CoV-2 RNA was not detected in the CSF.

"As such, this paper is consistent with prior observations that suggest the SARS-CoV-2 virus may cause neurologic injury by secondary mechanisms, but is not specifically neurotropic. Research on this important question is ongoing."

Wilner reports being medical adviser for CVS/Health and receiving royalties from "The Locum Life: A Physician's Guide to Locum Tenens."

Emerg Infect Dis. Published online June 2, 2020. Full text

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What you need to know about the COVID-19 pandemic on 13 May – World Economic Forum

A new strain of Coronavirus, COVID 19, is spreading around the world, causing deaths and major disruption to the global economy.

Responding to this crisis requires global cooperation among governments, international organizations and the business community, which is at the centre of the World Economic Forums mission as the International Organization for Public-Private Cooperation.

The Forum has created the COVID Action Platform, a global platform to convene the business community for collective action, protect peoples livelihoods and facilitate business continuity, and mobilize support for the COVID-19 response. The platform is created with the support of the World Health Organization and is open to all businesses and industry groups, as well as other stakeholders, aiming to integrate and inform joint action.

As an organization, the Forum has a track record of supporting efforts to contain epidemics. In 2017, at our Annual Meeting, the Coalition for Epidemic Preparedness Innovations (CEPI) was launched bringing together experts from government, business, health, academia and civil society to accelerate the development of vaccines. CEPI is currently supporting the race to develop a vaccine against this strand of the coronavirus.

1. How COVID-19 is impacting the globe

COVID-19 is a serious disease and causes a wide range of problems from gastrointestinal disease (diarrhoea and nausea) to heart damage and blood clotting disorders. As one virologist pointed out for Agenda this week, it can also cause neurological symptoms in some patients.

Some patients have experienced brain inflammation or even stroke. According to other reports, COVID-19 patients have suffered from GuillainBarr syndrome, a neurological disorder where the immune system mistakenly attacks nerve cells, resulting in muscle weakness and eventual paralysis.

While more research is needed, these symptoms drive home the importance of taking this disease and its long-term effects seriously. Virologist Jeremy Rossman said this information also "highlights the continued importance of preventing viral transmission and identifying those who are, and have been, infected."

Public areas and urban environments could be transformed by coronavirus, according to a Reuters article. Social distancing could create green mazes in public parks while cities could be designed to be more compact to ensure that residents can access goods and services more easily.

"We are in a very experimental stage," said architect Harm Timmermans. "There will be a lot of trial and error, but the notion of the local will definitely be very important."

Parc de la Distance, a new design for a public park by Austrian architecture firm Studio Precht.

Image: Studio Precht, VIA Reuters

Baseball and soccer have returned to South Korea and the measures taken there can provide a glimpse into what might be needed to resume other sports in the months ahead. These might include barely-filled stadiums, crowd noise pumped in through loud speakers, and athletes that trade handshakes for fist bumps.

Truly safe mass events will need something else: a contained virus. South Korea is one of the first countries to contain COVID-19 and other countries will need to follow suit or risk future outbreaks.

Local league baseball has restarted in South Korea, but live audiences arent permitted.

Image: REUTERS/Kim Hong-Ji

Has working from home left you exhausted? You're not alone, explained one expert for the Conversation this week. The self-control needed to manage the demands of working from home can deplete both your mental and physical energies. Finding ways to detach yourself from work can help you you get back on track.

License and Republishing

World Economic Forum articles may be republished in accordance with our Terms of Use.

Written by

Linda Lacina, Digital Editor, World Economic Forum

The views expressed in this article are those of the author alone and not the World Economic Forum.

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What you need to know about the COVID-19 pandemic on 13 May - World Economic Forum

Aeglea BioTherapeutics Announces 1-Year Data for Pegzilarginase in Patients with Arginase 1 Deficiency at the 6th Congress of the European Academy of…

Pegzilarginase Showed Durable Clinical Response at 56 Week Analysis

All Patients Demonstrated a Marked and Sustained Reduction in Plasma Arginine

Favorable Safety Profile, Consistent with Previously Reported Results

AUSTIN, Texas, May 26, 2020 (GLOBE NEWSWIRE) -- Aeglea Biotherapeutics, Inc. (NASDAQ:AGLE), a clinical-stage biotechnology company developing a new generation of human enzyme therapeutics as innovative solutions for rare and other high-burden diseases, today announced a new 56 week analysis on Arginase 1 Deficiency (ARG1-D) patients who have been treated with pegzilarginase from the Companys completed Phase 1/2 clinical trial and the ongoing Phase 2 open-label extension study. The data were shared yesterday in a virtual, late-breaking oral presentation at the 6th Congress of the European Academy of Neurology.

Arginase 1 Deficiency is a devastating disease that is frequently under diagnosed or misdiagnosed as more common neurological conditions, such as cerebral palsy, due to lack of awareness of this rare condition, said George Diaz, M.D., Ph.D., division chief of medical genetics in theDivision of Medical Genetics and Genomics and Department of Genetics and Genomic Sciences at theIcahn School of MedicineatMount Sinai, New York, NY. Because of the conditions progressive nature, it is essential that patients be diagnosed early, and there is an urgent need for a therapy that addresses the underlying cause of the disease and improves clinical manifestations.

The results of this long-term data demonstrate that treatment with pegzilarginase resulted in a durable clinical response, which is a critical factor in effectively treating a life-long, progressive condition, said Ravi M. Rao, M.B Ch.B PhD, chief medical officer of Aeglea. We are also pleased to see that the lowering of arginine levels observed in the 20 week analysis were maintained through the 56 week analysis. These results align with the primary endpoint of PEACE, our ongoing pivotal Phase 3 clinical trial, and together with the durable clinical response bolsters our belief that pegzilarginase has the potential to be an impactful treatment for people living with Arginase 1 Deficiency.

The presentation, titled 1 Year Data from First in Human Study of Pegzilarginase for the Treatment of Arginase 1 Deficiency (ARG1-D), includes data on 13 patients treated with pegzilarginase who completed the 56 week treatment period (8 weeks Part 2 repeat dosing + 48 weeks open-label extension).

Highlights from the 56 week analysis include:

The presentation is available for download on the Presentations & Events section of the Companys website.

About the Phase 1/2 and Open-Label Extension Trial

The Phase 1/2, multicenter, single arm, open-label extension study of pegzilarginase enrolled patients aged 2 years and older with Arginase 1 Deficiency in the United States, Canada, and Europe. The trial investigates single ascending doses (Part 1), repeated weekly dosing for eight weeks (Part 2). The trial enrolled 16 adult and pediatric patients and 14 patients rolled over to the open-label extension. The primary endpoint of the trial is safety and tolerability of intravenous administration of pegzilarginase in patients with Arginase 1 Deficiency. The trial also evaluated the pharmacokinetic and pharmacodynamic effects of repeated doses of pegzilarginase on plasma arginine levels, and evaluation of clinical outcomes using several mobility assessments.

Please visit http://www.clinicaltrials.gov for more information.

About Pegzilarginase in Arginase 1 Deficiency

Pegzilarginase is an enhanced human arginase that enzymatically lowers levels of the amino acid arginine. Aeglea is developing pegzilarginase for the treatment of patients with Arginase 1 Deficiency (ARG1-D), a rare debilitating disease presenting in childhood with persistent hyperargininemia, severe progressive neurological abnormalities and early mortality. Pegzilarginase is intended for use as an enzyme therapy to reduce elevated blood arginine levels in patients with ARG1-D. Aegleas Phase 1/2 and Phase 2 open-label extension data for pegzilarginase in patients with ARG1-D demonstrated clinical improvements and sustained lowering of plasma arginine. The Companys single, global pivotal Phase 3 PEACE trial is designed to assess the effects of treatment with pegzilarginase versus placebo over 24 weeks with a primary endpoint of plasma arginine reduction.

About Aeglea BioTherapeutics

Aeglea BioTherapeutics is a clinical-stage biotechnology company redefining the potential of human enzyme therapeutics to benefit people with rare and other high burden diseases. Aeglea's lead product candidate, pegzilarginase, is in a pivotal Phase 3 trial for the treatment of Arginase 1 Deficiency and has received both Rare Pediatric Disease and Breakthrough Therapy Designation. The Company received approval of its Clinical Trial Application (CTA) for ACN00177 for the treatment of Homocystinuria by the United Kingdoms Medicines and Healthcare Products Regulatory Agency (MHRA). Aeglea has an active discovery platform, with the most advanced program for Cystinuria. For more information, please visit http://aegleabio.com.

Safe Harbor / Forward Looking Statements

This press release contains "forward-looking" statements within the meaning of the safe harbor provisions of the U.S. Private Securities Litigation Reform Act of 1995. Forward-looking statements can be identified by words such as: "anticipate," "intend," "plan," "goal," "seek," "believe," "project," "estimate," "expect," "strategy," "future," "likely," "may," "should," "will" and similar references to future periods. These statements are subject to numerous risks and uncertainties that could cause actual results to differ materially from what we expect. Examples of forward-looking statements include, among others, statements we make regarding our cash forecasts, the timing and success of our clinical trials and related data, the timing and expectations for regulatory submissions and approvals, timing and results of meetings with regulators, the timing of announcements and updates relating to our clinical trials and related data, our ability to enroll patients into our clinical trials, the expected impact of the COVID-19 pandemic on our operations and clinical trials, success in our collaborations, the potential addressable markets of the our product candidates and the potential therapeutic benefits and economic value of our lead product candidate or other product candidates. Further information on potential risk factors that could affect our business and its financial results are detailed in our most recent Quarterly Report on Form 10-Q for the quarter ended March 31, 2020 filed with the Securities and Exchange Commission (SEC), and other reports as filed with the SEC. We undertake no obligation to publicly update any forward-looking statement, whether written or oral, that may be made from time to time, whether as a result of new information, future developments or otherwise.

Media Contact:Kelly Boothe, Ph.D.Director, Corporate CommunicationsAeglea BioTherapeutics512.399.5458media@aegleabio.com

Investor Contact:Joey PerroneSenior Director, Finance & Investor RelationsAeglea BioTherapeuticsinvestors@aegleabio.com

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The Effects of Puberty and Menstrual Cycle on Migraine in Girls – Neurology Advisor

Migraine attacks were more frequent in post-pubertal compared to pre-pubertal girls, while the headache characteristics did not differ between the groups, according to study results published in the European Journal of Paediatric Neurology. Findings also suggest that more attacks occur during the follicular vs the luteal phase.

The goal of the current study was to explore the association between migraine attacks and the menstrual cycle in adolescent girls, while taking into account clinical pubertal status and ovulatory cycles. In addition, the study aimed to describe headache characteristics in prepubertal, peri-pubertal and post-pubertal girls with migraine.

The researchers combined 2 different tools to determine the cycle phase and to detect anovulatory cycles: menstrual diary and progesterone saliva measurements.

The prospective study included 47 girls (mean age 12.5 years), including 16 pre-pubertal (mean age 9.8 years), 19 peri-pubertal (mean age 12.6 years) and 12 post-pubertal (mean age 16 years) girls according to Tanner stage and/or menstrual bleeding.

The most important result of the present study is a significant increase in migraine attacks after puberty. Migraine attacks were significantly more common in post-pubertal girls (2820.9 attacks), compared to pre-pubertal (8.89.3 attacks, P =.005) and peri-pubertal (109.8 attacks, P =.012) girls. There were no significant differences between the groups in accompanying symptoms or duration of pain.

Migraine attacks were significantly more common in follicular vs. luteal phase in peri-pubertal and post-pubertal girls (P =.030), but there were no differences in accompanying symptoms, duration of pain and aura between follicular and luteal phase.

There were significant differences in body mass index (BMI) between the groups, as the highest BMI was evident in post-pubertal girls (25.05.5 kg/m2), followed by peri-pubertal (19.52.9 kg/m2) and pre-pubertal (17.12.4 kg/m2) girls. In accordance with previous studies, increased BMI correlated with an increase of migraine attacks.

The study had several limitations, according to the researchers, including the potential limitations of progesterone assays in saliva, inclusion of a well characterized group of girls, and a limited sample size.

Puberty seems to modulate frequency and onset of migraine in girls but not the headache characteristics as a first step towards an adult pattern of migraine, concluded the researchers.

Reference

Bttcher B, Kyprianou A, Lechner C, et al. Manifestation of migraine in adolescents: Does it change in puberty? [published online ahead of print, 2020 Feb 20]. Eur J Paediatr Neurol. 2020;S1090-3798(20)30037-4. doi:10.1016/j.ejpn.2020.02.006

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Announcing the American Academy of Neurology 2020 Research Program Recipients – Newswise

Newswise MINNEAPOLIS The American Academy of Neurology (AAN), the worlds largest association of neurologists, is pleased to announce the recipients of the 2020 AAN Research Program. This years program has awarded more than $3 million toward neuroscience research and training.

Funding will support the following 2020 AAN Research Program recipients and projects:

Career Development Award Funded by the American Academy of Neurology Oluwole Awosika, MD, Cincinnati, Ohio Hugo Aparicio, MD, Boston, Mass.

Clinical Research Training Scholarship Funded by the American Academy of NeurologyMark Etherton, MD, PhD, Boston, Mass.Carlyn Patterson Gentile, MD, PhD, Philadelphia, Pa. David Lin, MD, Boston, Mass.

Clinical Research Training Scholarship in ALSFunded by The ALS Association and American Brain Foundation, in collaboration with the American Academy of NeurologySarah Berth, MD, PhD, Baltimore, Md.

Clinical Research Training Scholarships in Lewy Body DiseasesFunded by The Mary E. Groff Charitable Trust, the Alzheimers Association, and the American Brain Foundation, in collaboration with the American Academy of NeurologyLenora Higginbotham, MD, Atlanta, Ga.

Clinical Research Training Scholarship in Neuromuscular DiseaseFunded by the Muscle Study Group and the American Brain Foundation, in collaboration with the American Academy of NeurologyPaloma Gonzalez-Perez, MD, PhD, Boston, Mass.

Clinical Research Training Scholarship in Parkinson's DiseaseFunded by the Parkinsons Foundation and American Brain Foundation, in collaboration with the American Academy of NeurologyJames Curtis, MS, CCC-SLP, BCS-S, New York, N.Y.

Clinical Research Training Scholarship in Tourette SyndromeFunded by the Tourette Association of America and American Brain Foundation, in collaboration with the American Academy of NeurologyAlonso Zea Vera, MD, Cincinnati, Ohio

McKnight Clinical Translational Research Scholarship in Cognitive Aging and Age-Related Memory LossFunded by the McKnight Brain Research Foundation through the American Brain Foundation and the American Academy of NeurologyBryan Baxter, PhD, Boston, Mass.Sarah Getz, PhD, Miami, Fla.

Neuroscience Research Training ScholarshipFunded by the American Academy of NeurologyWilliam Zeiger, MD, PhD, Los Angeles, Calif.Richard Krolewski, MD, PhD, Boston, Mass.

Practice Research Training ScholarshipFunded by the American Academy of NeurologyDeanna Saylor, MD, Baltimore, Md.

Richard Olney Clinician Scientist Development Award in ALSFunded by The ALS Association and American Brain Foundation, in collaboration with the American Academy of NeurologyCollin Kreple, MD, PhD, Saint Louis, Mo.

Robert W. Katzman, MD Clinical Research Training Scholarship in Alzheimer's or Related DisordersFunded by the Alzheimers Association and the American Brain Foundation, in collaboration with the American Academy of NeurologyLawren VandeVrede, MD, PhD, San Francisco, Calif.

Susan Spencer, MD Clinical Research Training Scholarship in EpilepsyFunded by the American Epilepsy Society, the Epilepsy Foundation, and American Brain Foundation, in collaboration with the American Academy of NeurologyColin Ellis, MD, Philadelphia, Pa.

Clinician Scientist Development Award in Multiple SclerosisFunded by the National Multiple Sclerosis Society and American Brain FoundationFarinaz Safavi, MD, PhD, Bethesda, Md.

The American Academy of Neurology is the worlds largest association of neurologists and neuroscience professionals, with over 36,000 members. The AAN is dedicated to promoting the highest quality patient-centered neurologic care. A neurologist is a doctor with specialized training in diagnosing, treating and managing disorders of the brain and nervous system such as Alzheimers disease, stroke, migraine, multiple sclerosis, concussion, Parkinsons disease and epilepsy.

For more information about the American Academy of Neurology, visit AAN.com or find us on Facebook, Twitter, Instagram, LinkedIn and YouTube.

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The Second Neurologist President of the AHA: His Vision,… : Neurology Today – LWW Journals

By Dawn Fallik May 7, 2020

Mitchell Elkind, MD, MS, FAAN, the president-elect of the American Heart Association (AHA), discusses his career, his vision for AHA, and how COVID-19 will change the field of neurology.

Mitchell Elkind, MD, MS, FAAN, was always fascinated by the mind and brain, and now he's connecting both to matters of the heart. As the president-elect of the American Heart Association (AHA), Dr. Elkind, professor of neurology and epidemiology at Columbia University Vagelos College of Physicians, is the second neurologist to head the organization. The first was former AAN president Ralph L. Sacco, MD, MS, FAHA, FAAN, chairman of neurology at University of Miami Miller School of Medicine

But Dr. Elkind wasn't always focused on biology and physiology. Before going to Harvard Medical School, he earned his undergraduate degree in philosophy at Harvard and his master's degree in the history and philosophy of science at Cambridge University in England. Neurology Today spoke to Dr. Elkind about his plans for the AHA, his thoughts on medical and residency challenges in the time of COVID-19, and why he's grateful for his Peloton bike.

When I was in medical school, I saw the brain as the next frontier of medicine and science, and that's largely been borne out. When I started training, there was maybe one medication for multiple sclerosis; now there are many. I was a resident when IV tPA was approved for stroke and now it's a reality, part of regular treatment for strokes, and that's exciting to see.

I was fortunate to have several great mentors. As a resident, C. Miller Fisher, one of the giants of vascular neurology, was still conducting weekly conferences, and I learned much of the approach to neurological patients, and especially stroke medicine, from him. Other mentors, including Walter Koroshetz, then at Massachusetts General Hospital and J. P. Mohr at Columbia also paved my path. Perhaps the greatest influence on my career, though, has been Dr. Ralph Sacco, now chair at the University of Miami, with whom I continue to collaborate and learn, not just about stroke, but about leadership and commitment. He was also the first neurologist president of the AHA.

In training, during the rotations, you spend a lot of time with patients. They always say you learn neurology stroke by stroke, and it's true. Every patient is different, and neurology is not just about the brain, but the personality and experience of the individual.

You start as a doctor with a lot of intense focus on the patients. But as you choose a specialty and transition from learning to teaching, that shifts, and then you throw research into the mix. So now I'm still seeing patients, but I'm also doing administration, writing grants, teaching...I didn't think about those aspects initially.

I miss some parts of it. Personally, I spend the bulk of my time doing research, so in some ways I'm not primarily a clinician. But if you woke me up in the middle of the night and asked What do you do? I'd say I'm a doctor.' I never wanted to do just one thing, so it's very gratifying to be involved in multiple areas. If I were just seeing patients or I were only in the lab, I think I'd feel like I was missing out. I like to remain open-minded to different experiences - although some people will think that being involved in the American Heart Association is a bit of a left turn for someone in neurology.

I think people don't understand that the AHA is different from the AAN or even the American College of Cardiology. Those are essentially professional organizations, and they are focused on the lives and well-being of those practitioners. The AHA is more of a public health organization focused on prevention and treatment of cardiovascular disease, and that includes strokes. It's got a wide range of activities, and it even began to include brain health a few years ago.

Part of what I hope to do during my tenure is not only to incorporate stroke and other vascular disease of the brain into the message of the AHA, but also brain health and brain science. We just announced our impact goals for 2030, and the mission is to extend the healthy lifespan, free of disability, by two years in the US. There are a lot of neurological diseases that we don't think of as vascular disease, but we have learned that blood vessel disease contributes to dementia and cognitive decline as well. Inflammation of the blood vessels, for example, can lead to blood supply issues to the brain, potentially leading to Alzheimer's and other degenerative diseases.

The AHA has tremendous resources and provides some of the highest levels of grant funding outside of the NIH. I hope members of the neurology community start looking more to AHA for funding.

The treatment of inflammation is an important developing area. It started with cardiology and moved into stroke and it's playing a bigger role in neurology as well. There's a lot of promise there, and we need to continue developing better biomarkers of different diseases as well, both imaging biomarkers and blood biomarkers.

Many have to do with long-term illnesses, like Alzheimer's, where the pathology begins 20 years before people have symptoms. It's hard to know when it's early enough for us to intervene and make a difference. When a disease goes on for so long, when is it right to start treating someone at a young age to prevent something that might happen in old age. We have to think deeply about how we conduct those clinical trials.

Although it's thought of as mainly a respiratory illness, there are implications for cardiology and neurology as well. There is evidence that the virus can enter cells through the ACE2 receptors in heart cells, and these may also be found in neurons. There was some evidence of brain involvement with the original SARS virus, which was also a coronavirus, since it was found in the brainstem in some patients after they died.

People with pre-existing conditions, such as heart disease and stroke, also have a higher mortality from COVID-19.

All of which is to say that we may find there are neurological aspects that people may not be aware of yet. This is a disease that started at the end of December. Now it's March and more than 400 papers have been published about it already. It's amazing how much work has been done.

Trainees are working incredibly hard. It's a challenging situation. They are having to shift from a primarily educational mode to a service mode. We're even bringing people back from retirement. It's an all-hands-on-deck approach. I think resident education might suffer in the short term, and the neurological community will need to consider how best to make up for this. There will be a lot to unpack once we get to the other side. In the meantime, our residents and fellows are doing heroic work, and I am in awe of this generation.

We've been doing telestroke for a long time, and it's filtered out to other areas of medicine. Now our practice has shifted largely to doing outpatient visits by telehealth and we're even doing visits within the hospital that way to minimize contact with COVID-19 patients and preserve personal protective equipment. As a nation, we're fortunate in the sense that telehealth technology started 20 years ago, so it wasn't too hard to fall back on that. We've got to ramp up the internet infrastructure, though, as telehealth may be increasingly used in the future.

I like to cook, and I like to eat. I really like to make pizza, that's my favorite thing. But I'm also trying to stay fit, so I'm glad I recently got the Peloton bike.

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The Second Neurologist President of the AHA: His Vision,... : Neurology Today - LWW Journals

The History of the World Federation of Neurology – WFN News

The World Federation of Neurology (WFN) was founded in 1957 in Brussels. Although there had been international medical congresses before it, the London Congress of Medicine 1913 was a landmark in the general acceptance of neurology.

The First International Neurological Congress was held in 1931 in Berne. Subsequent meetings took place in London, Copenhagen, Paris and Lisbon. The plurality of several international congresses of neurosciences was one of the reasons the Brussels Congress in 1957 was named The First International Congress of Neurological Sciences.

The movers were two Americans and one European: Houston Merritt, Pearce Bailey Jr. and Ludo van Bogaert, respectively. In 1956, Merritt and Bailey proposed a world neurological federation at a meeting of the AmericanAcademy of Neurology. The National Institute of Neurological Diseases and Blindness (NINDB), National Institutes of Health, U.S., offered an annual grant of $126,190 (U.S.) for five years in order to get the federation started. By the end of 1962, the WFN Secretariat had received more than $500,000 from the original NINDB grant. Thirty-eight national delegates met in Brussels in 1957.

Van Bogaert from Antwerp, Belgium, was a respected neurologist, and the leading neuropathologist of his time. He was elected WFN president, Macdonald Critchley and Auguste Tournay were elected vice presidents and Pearce Bailey was elected secretary-treasurer general.

Van Bogaert established the first Project Commissions (later renamed Research Groups) consisting of international leaders of various sectors of neurology. A series of commissions were established, such as the Research Group on Extrapyramidal Disease organized by Melvin Yahr.

Van Bogaert believed that it was time to create a new and separate organization of the Research Groups. The name of the association would be the World Association of Neurological Commissions (WANC).

There was agreement that Adolphe Franceschetti should become the WANC president and David Klein vice president and secretary-treasurer general. Van Bogaert's successor as president, Macdonald Critchley, thought this was wrong, and that the research arm was essential for WFN in order to survive. Van Bogaert's presidency was successful, but ended in a financial crisis. He had described the three elements of his WFN rescue plan: the increase in annual dues, a decentralization plan and the new organization for the Problem Commissions. The differences of opinion had been dramatic, and John Walton's proposal was to create a new organizational unit of the WFN the Research Committee. The Problem Commissions were renamed Research Groups and organized in the new Research Committee.

Critchley became the next president. During his presidency, WANC became an integral part of the WFN. How could WFN now survive? Critchley was able to see that every cloud had a silver lining. He instilled a feeling of pioneer optimism in the organization. The work of the WFN not only continued, it flourished in spite of a miserable economy. The orientation of the federation remained truly international, harmonious and stimulating.

The reason lay in the vitality of the organization. No new administrative initiatives could be taken, but the activity that had been introduced in the Research Groups was high. How to balance the budget of the WFN?

Were the annual WFN dues too high? Since they had remained unchanged at $2 for 20 years despite inflation, the Finance Committee recommended the dues be raised to $5 on the basis of the WFN's state of bankruptcy. The WFN accountants had to audit all financial statements of the WFN, including those of all Research Groups, and had to urge the national societies that were delinquent in paying their dues.

The Finance Committee also suggested that a Publications Subcommittee of WFN be formed and chaired by Professor Robert Daroff. The subcommittee was charged with development of resources from WFN-sponsored journals, starting with the contracts of the Journal of the Neurological Sciences, Journal of Neuroimmunology, Acta Neuropathologica and the WFN's World Neurology newsletter. It also was decided to have the WFN accountants shift from a cash to an accrual method of accounting commencing Jan. 1, 1987. Any further increase in the number of WFN officers, which would progressively jeopardize WFN's finances, was strongly discouraged.

The WFN Finance Committee recommended that a Fundraising Subcommittee be formed, chaired by Professor Helmut Lechner to investigate. Registration fees, advertisements, exhibit hall rentals and sponsorships were new sources of income.

John Walton took over as the new WFN president in 1998. One of the most central steps of the subsequent WFN re-organization was to establish a corporate status for the association. The impending appointment of officers based in different countries and continents made the creation of a new secretariat pressing. The committee structure had to be reviewed. Financial planning systems, including itemized annual budgets, were introduced and expenditure monitored by the treasurer and reported to the Finance Committee.

It was recommended to separate the offices of secretary-general and treasurer. Following the World Congress in Vancouver, Canada, in 1993, 50 percent of the profits were retained by the host society and 50 percent were transferred to the funds of the WFN, in return for the WFN administrative costs involved in planning the congress and program.

The WFN income increased because of the increase in annual dues and the royalties from its scientific journals. Developments in neurosciences had increased, and effective new drugs were available.

James Toole was the WFN secretary-treasurer general in Richard Masland's administration. They managed to have the new WFN newsletter, World Neurology, survive, and it became an important communication medium for the federation. In 1989, Toole became the editor-in-chief of the Journal of Neurological Sciences.

The U.S. Congress in concert with President George H.W. Bush, declared the 1990s the "Decade of the Brain." In response to a request by the Congress, the Advisory Council of the National Institute of Neurological Disorders and Stroke produced an implementation plan, focusing on 14 major disease categories in which neurological research gives promise of rapid progress for the coming decade. The plan called for increased allocations for basic and clinical neurosciences of $190 million in the first year, rising to $385 million per year in the latter part of the decade.

Jun Kimura was the first vice president in James Toole's administration. He also chaired the Constitution and Bylaws Committee during the critical transition period from the "old" organization to the incorporated WFN. Many of these important projects stemmed from the Strategic Planning Meeting held in St. Albans in 2000, making steady progress in achieving some of the missions agreed upon during those intense discussions.

Johan Aarli had two main initiatives as president of the WFN. He articulated the need to study and develop creative methods to implement improved delivery and increased rural distribution of neurological health, "The Africa Initiative." Second, he was determined to bring into the WFN the 1.2 billion people within The People's Republic of China. This took place at the WFN's Silver Jubilee in 2007.

The Council of Delegates remains the ruling body of the federation. WFN must hold an annual general meeting which all member societies are entitled to attend. It consists of the national delegates of the national neurologic associations. There is a quorum of a meeting of the Council of Delegates if the number of authorized delegates personally present is at least 15.

From 1993, the president, the secretary treasurer general, the first vice president and the chairman of the research committee constituted the WFN Management Committee. Their function was to advise the Council of Delegates and the various committees of the issues of policy and day-to-day management. The WFN Steering Committee was disbanded when the new WFN was organized in 2001.

One major element of the new WFN is the appointment of trustees: the president, the first vice president, the secretary-treasurer general, and three who are elected in accordance with the articles of association, and up to two co-opted individuals. The trustees are charity trustees who have control of the federation and its property and funds.

Two WFN members have contributed to this account of WFN's history: Noshir Wadia: In Service of the WFN, and Jun Kimura: Internal Struggle in Kyoto.

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The History of the World Federation of Neurology - WFN News

Cannabidiol Is Safe and Effective for Patients With Lennox Gastaut Syndrome – Neurology Advisor

The following article is part of coverage from the American Academy of Neurologys Annual Meeting (AAN 2020). Due to the global COVID-19 pandemic, the Academy made the necessary decision to cancel the meeting originally scheduled for April 25May 1, 2020, in Toronto. While live events will not proceed as planned, readers can click here catch up on the latest research intended to be presented at the meeting.

Add-on cannabidiol (CBD) was found to be safe and effective for patients with Lennox Gastaut Syndrome (LGS), according to study results intended to be presented at the annual meeting of the American Academy of Neurology (AAN 2020).

Previous studies have suggested that CBD is a safe and effective treatment option for patients with LGS. The goal of the current study was to investigate the long-term profile of add-on CBD in the third analysis of the open label extension (GWPCARE5) of two phase 3, randomized controlled trials (GWPCARE3 and GWPCARE4).

The study cohort included 366 of 368 eligible patients (mean age, 16 years; 54% men; median follow-up, 150 weeks) who completed 1 of the 2 randomized-controlled trials; however, 119 participants withdrew from the study. The participants received plant-derived highly purified CBD (Epidiolex; 100 mg/mL oral solution).

The primary outcome of the study was the safety of CBD treatment; the secondary outcome was the efficacy, based on median percentage change in drop and total seizure frequency.

Treatment with CBD was associated with median percentage reductions in seizure frequency of 48 to 71% for drop seizures and 48 to 68% for total seizures.

During the extended follow-up, adverse events were documented in 96% of the participants, including serious adverse events in 42% of participants and events that led to discontinuation in 12% of participants. The most common adverse events (20%) included diarrhea, convulsion, pyrexia, somnolence, vomiting, upper respiratory tract infection, and decreased appetite.

Although there were 11 deaths during the follow-up period, none were deemed to be treatment-related.

Long-term treatment with add-on CBD in patients with LGS produced sustained seizure reductions, with no new safety concerns, concluded the researchers.

Reference

Patel A, Chin R, Mitchell W, et al. Long-term safety and efficacy of cannabidiol (CBD) treatment in patients with Lennox-Gastaut Syndrome (LGS): 3-year results of an open-label extension (OLE) trial (GWPCARE5). Intended to be presented at the 2020 annual meeting of the American Academy of Neurology. Abstract S25.004.

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Cannabidiol Is Safe and Effective for Patients With Lennox Gastaut Syndrome - Neurology Advisor

Robots, iPads, and Teamwork – Duke Today

As the COVID-19 epidemic is making neurological emergencies harder to treat--and potentially more dangerous for the patient--neurology providers at Dukes three hospitals are rising to the challenge with robots, iPads, and an unprecedented level of collaboration.

The patient in Durham Regional Hospital was unresponsive to questions. The ambulance had brought him into the emergency room with meningitis, or inflammation around the brain--as well as symptoms that could have been caused by COVID-19.

Now, with the patients condition worsening, neurologist Matthew Ehrlich, MD, MPH, had to weigh the risks and benefits of examining him in person.

Were the benefits of confirming the patients earlier signs of seizure with an EEG worth the risk of possibly exposing an EEG technician (and possibly the rest of the hospital) to infection with the coronavirus? Could Ehrlich assess the patients condition using a virtual consult via an iPad or telestroke robot without exposing himself, or should he enter the room to give an in-person evaluation, opening an avenue for infection for himself, his colleagues, his wife, and family? And were the mans symptoms due to COVID-19, or to any number of unrelated conditions, making all of these concerns irrelevant?

Like he had done many other times in the past few weeks, Ehrlich evaluated his limited information as best he could. An EEG was unlikely to alter the course of treatment for the patient, so that test could be postponed. On the other hand, an in-person neurological assessment would probably help Ehrlich decide on the next steps more effectively than a virtual consult. Ehrlich put on his mask and protective gear, and entered the room to see the patient.

Matt Ehrlich, MD, MHS

Neurological emergencies were dangerous before the COVID-19 pandemic. Stroke, traumatic brain injury, severe seizures, and other conditions require a rapid, coordinated response by a team of experts. Emergency medical technicians, neurologists, advanced practice providers, emergency medicine doctors, imaging technicians, physical and speech therapists, and others all play a role in transporting patients, deciding on the proper form of treatment, and in beginning the long rehabilitation process.

The constant potential for COVID-19 transmission has disrupted the way hospitals respond to these emergencies. It may also be making these conditions more dangerous. Now, providers like Ehrlich have to decide how to provide treatment while also keeping our providers (and the hospital system) safe from infection. Theyre making these decisions in close quarters, with limited supplies, without established procedures or guidebooks, and with our intensive care units more crowded than ever.

(Note: Do not hesitate to call 911 if you or someone you know is experiencing a heart attack or stroke. These emergencies require prompt medical care, and our hospitals are taking steps to make sure all of our providers and patients are safe. Delaying treatment increases the likelihood of early death or a permanent disability.)

Teams at Dukes three hospitals have turned to a combination of technology and an unprecedented level of teamwork to rise to this challenge. Technology in the form of iPads and robots originally designed for telestroke visits, allow providers to interact with patients without ever having to come in close physical contact. And teamwork and communication, both within and across the hospital systems, allow the hospital neurology teams to share information and coordinate strategies in a situation that is evolving and changing on a daily basis.

The robot sitting in a corner

Over the past two months, office workers across the country have come to rely on teleconferences to connect with their colleagues. DukeHealth and other health systems have also accelerated their ability to provide virtual clinic visits. Hospital providers, however, cant just Zoom in to a meeting with their patients.

To start, there arent enough desktop or laptop computers to go around. And in order to function and be safe, any teleconferencing device would have to be easily transportable, user friendly, and capable of being sterilized between users.

As it turns out, Duke Raleigh and Duke Regional Hospitals had been using equipment that fit all of those requirements for years. Both hospitals were already equipped with telestroke robots, or remote-controlled machines with two-way cameras. During night hours when a neurologist is not present, these machines allowed off-site neurologists to evaluate and treat patients who are having strokes.

Now, nurse practitioner Stacey Bennett, MSN, can give lessons about risk reduction, and answer questions about life after stroke without having to enter the same room as a potential COVID-19 patient. We had previously only used the robots during off hours. During the day it just sat there in a corner. We took the initiative to use it to start talking to people.

Stacey Bennett, MSN

Other providers such as neurologists like Ehrlich, advanced practice providers, or speech or physical therapists, also use the robot interact with patients without potentially exposing themselves, their colleagues, or other patients to infection (a nurse or other caregiver who is already in the same room as the patient can help guide the robot and facilitate any provider-patient interactions).

The robots were especially useful during the earliest days of the pandemic, when masks and other protective equipment were in short supply, but they continue to be in use in both Duke Regional and Duke Raleigh Hospitals.

These machines have made things safer for everyone while still allowing patients to get the care they need, said Bennett. We all feel really fortunate that we have it. The Neurology team at Duke Regional has since supplemented their telestroke robot with eight modified iPads that allow provider-patient interaction via Facetime.

One of Duke Regional Hospital's eight modified iPads, nicknamed "Dr. K. Rona," allows patients and providers to interact without increasing the risk of spreading the coronavirus.

Working together, within and across Duke hospitals

More important than any technological advance, however, is the teamwork and communication that have allowed Dukes providers to work in teams within and across hospitals to respond to this crisis.

Within Duke Regional, teamwork across service lines enabled the telestroke robots success. At first, every surface of the robot had to be thoroughly scrubbed and disinfected every time it went in and out of a room. This laborious process took nearly 10 minutes and potentially exposed a health-care worker to infection with every scrubbing.

Using draping equipment borrowed from Regionals Surgery Department and under guidelines from their Infectious Disease colleagues, Bennetts team were able to obtain sheeting that covered the robots and could be quickly replaced between uses.

The COVID-19 pandemic has also accelerated group trainings, communication, and shared standards of care for neurology care in Duke University Hospital, Duke Regional Hospital, and Duke Raleigh Hospital. This January, providers from all three hospitals held a hospital neurology summit to work together to identify problems, build on strengths, and find ways to help patients. This group was made of an inclusive group of providers, with advanced practice providers, stroke managers, and other experts as well as neurologists all taking part in the discussion.

The summit really allowed us to put a face to a name and identify as one team of neurohospitalists. We made a pledge to have each other's back and choose to work on things together. said Bennett. The goal became helping each other actually improve patient care instead of trying to get each other to be the same.

Members of this summit from all three hospitals have stayed in touch throughout the COVID-19 pandemic, discussing how to protect themselves, how to deliver care at a distance, and ways that COVID-19 might influence what happens during a stroke or other neurological emergency. Theyve also undergone group trainings so that providers at one Duke hospital can cover colleagues at another if needed.

We try new things together. We keep one another in the loop and let each other know how things are going. We are encouraging to each other. We respect our team members opinions and ideas. I have never felt more supported by my community as a healthcare worker, Bennett said.

Ehrlichs patient eventually tested negative for COVID-19. The patient did, however, have bacterial meningitis, an acute medical emergency, as well as a related infection in his bloodstream. Thanks to his prompt treatment, the patient was able to recover and has since returned home.

The steps Ehrlich takes to return home every day have evolved into a routine. He enters his house through the garage to prevent his dog or two-year-old daughter from jumping on him before he can strip, bag his work clothes and shoes, scrub his phone, keys, and wallet with Lysol, and hop straight into the shower. It takes a while before I can go back to feeling like a human being again, Ehrlich said.

Still, Ehrlich remains confident about his and his colleagues ability to provide care throughout the rest of the pandemic.

"The coronavirus pandemic has really shone a spotlight on the innovative, collegial, and collaborative nature of our stroke and neurohospitalist teams. Though we've sailed into largely uncharted waters over the past couple months, the incredible response from our Duke teams shows we can weather the storm, and continue to provide top-notch care to our patients during these difficult times," Ehrlich said.

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Robots, iPads, and Teamwork - Duke Today

COVID-19 on the brain: BBC News at the National Hospital for Neurology and Neurosurgery – University College London Hospitals

BBC medical correspondent Fergus Walsh met with NHNN patient Paul Mylrea, 64, who is making a remarkable recovery after suffering two major strokes triggered by COVID-19 infection.

Im very lucky in physical terms but it has been tough, said Paul who had previously been very healthy and active and had a passion for diving.

After my second stroke, my wife and daughters thought that was it, they would never see me again. The doctors told them there was not much they could do except wait. Then I somehow survived.

Pauls first stroke was caused by a blood clot in his brain and happened while he was recovering from COVID-19 at University College Hospital. The clinical team also found blood clots in his lungs and legs so prescribed powerful blood-thinning drugs.

A couple of days later, however, he suffered a second, even bigger stroke and was transferred to the NHNN for specialist care.

Pauls consultant neurologist, Dr Arvind Chandratheva, said: I immediately assumed the blood-thinning drugs had caused a bleed in the brain but what we discovered was unlike anything we have seen before.

Despite the blood-thinning treatment, Pauls second stroke had been caused by another clot in his brain and blood tests showed that he had extraordinarily high levels of a clotting marker called D-dimer. Normally these levels are less than 300 and can rise to 1,000 in stroke patients but in Pauls case they were 80,000.

"I've never seen that level of clotting before something about his body's response to the COVID-19 infection had caused his blood to become incredibly sticky," said Dr Chandratheva.

It puzzled us why a fit and healthy man had experienced so many blood clots in rapid succession, despite blood-thinning treatment. But in just two weeks in April 2020, our team saw six people with COVID-19 who had similar strokes caused by a blocked, large artery in the brain.

We were witnessing the unfolding of a distinctive pattern of stroke associated with the pandemic.

Specialists at the NHNN have also seen an increase in COVID-19 patients with extensive inflammation in the brain. They do not think this is caused by COVID-19 itself but by the bodys immune system overreacting to the disease.

Consultant neurologist Dr Michael Zandi said: We are starting to see a number of effects of COVID-19 on the brain which are very concerning. For some people it could be devastating and life-altering.

We need to be prepared for decades of impact on peoples brains and mental health. The closest comparison we have is the 1918 flu pandemic when a lot of brain disease and problems emerged over the following 10 to 20 years."

Paul, who is a leading communications professional and speaks six languages, spent five weeks in hospital but is now recovering extremely well at home.

In the BBC report, we see Paul having online neurorehabilitation with clinical psychologist Dr Catherine Doogan and occupational therapist Kate Kelly as part of the N-ROL programme. The programme is led by Professor Nick Ward and supported by fundraising efforts by the charity SameYou to allow people to continue with their rehabilitation at home during the pandemic.

Paul said: I have been getting progressively stronger thanks to the ongoing care of the NHNN.

Here is the full news report, online articleand podcast(at 22m 20s).

For further information also see an article featuring Dr Chandratheva in The Conversation.

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COVID-19 on the brain: BBC News at the National Hospital for Neurology and Neurosurgery - University College London Hospitals

How a Rural Hospital Developed and Launched its Telehealth Platform – mHealthIntelligence.com

August 11, 2020 -Small hospitals across the country are turning to telehealth to expand their treatment options and give patients access to specialists they might otherwise have to travel long distances to see. These services not only improve care for patients, but help the hospital to keep that care in the community.

Such is the case with the Beauregard Health System, an acute care hospital in rural DeRidder, LA. This past June, the 49-bed not-for-profit hospital launched a platform, through a partnership with SOC Telemed, to provide critical care, psychiatry, in-patient and emergency neurology and cardiology services via telemedicine.

The need for cardiology services was especially important. The hospitals only full-time cardiologist had left the previous April, and the hospital was transferring, on average, 30 patients each month to other hospitals.

Our community was vulnerable without a full-time local cardiologist, Traci Thibodeaux, MHA, CMPE, Beauregards chief operating officer, said in a press release. We wanted to partner with a cardiology group in Lake Charles, but knew they couldnt meet our needs for an onsite full-time physician.

In a recent Q&A with mHealthIntelligence, Thibodeaux explains how Beauregard planned out and launched its connected health strategy.

READ MORE: Telehealth Is The Best Tool in the Healthcare Toolbox for FQHCs

Q. What was the thinking behind deciding to partner with a telehealth company to offer these services on a telemedicine platform?

A. Beauregard Health System decided to partner with a telehealth provider because we needed to evolve from our grass roots approach and expand to include additional specialists - on one platform, using one process and the same equipment - to make it as seamless as possible for patients, nursing, and physicians.Since we are small rural acute care hospital, there are some specialties that we know well never offer locally.

Q. How were these 5 specialties psychiatry, critical care, inpatient neurology, emergency neurology and cardiology chosen? Were there specific arguments that these particular specialties need to be included in a telehealth strategy?

A. The specialties are critical for various reasons.

With psychiatry, our Emergency Department can get overwhelmed with trying to care for the sensitivities and complexities that this patient population presents.We have to consider patient safety, staff safety, and the safety of other patients and families, which includes children.We want all of our patients and families to feel safe and well cared for in our facility.

READ MORE: Telecritical Care Expands Telehealth From the ICU to Where Its Needed

Tele-psych consultation allows us to expeditiously determine the best and safest course and place of treatment, which often requires a transfer to a more appropriate care setting.

Cardiology and Neurology are important because, without these consultations, patients were automatically transferred to other facilities for a higher level of care, whether or not they truly needed it, since we werent able to offer on-site cardiology and neurology evaluations.

Telemedicine creates an opportunity to keep patients local when it is safe to do so.Our team on the ground, in consultation with a specialist who has assessed the patient, effectively care for many patients using this approach.This prevents unnecessary disruption for patients and families (and) prevents adding unnecessary direct and indirect cost of care for families, which includes transportation, travel, lodging, insurance, child care and missed work.

When we launched Tele-Critical Care in December of 2019, we had no way of knowing what a profound impact this would have on our patients, nurses, physicians and community.We were perfectly positioned to effectively care for every wave of COVID 19 that we first started seeing in March of this year at our hospital and through our current peak.This has allowed us to provide excellent care and weve undoubtedly gained a tremendous amount of community trust and support.

Q. What are the biggest challenges in launching a telehealth platform to address these services?

READ MORE: Senators Propose $50M Program to Fund RPM Pilots in Rural Areas

A. The biggest challenges were uncertainty of utilization and success.We questioned whether we would have a return on our investment with insurance plans reimbursing the service.We hoped that nursing would support the technology and see it as value-add for patient care.We prayed that the patient and family would have a great experience.We worried that we would have the WiFi and audio/video quality to support the interaction without interruption. We questioned whether the patient and family would have a good experience without the face to face interaction.

Q. How were clinicians and other staff brought on board? Was there any pushback or concerns about moving to telehealth?

A. The medical staff and board members were supportive of the project, but I might generalize that they were all cautiously optimistic going into this. Before COVID 19, the support of specialists were nice to have, but not essential, as we would transfer higher risk patients out for higher level of care.

Mid-pandemic, the medical staff and board have been so supportive that the telemedicine project has evolved and expanded into an organizational strategy.Tenured physicians who have practiced traditional medicine and bedside care are extremely supportive and accept that telemedicine is here to stay.

Ive (also) gotten additional feedback from nurses in the units who have learned from the online physician, as theyve had to be the hands of these virtual physicians.Nursing has to be on point in communicating vitals, assisting with the evaluation and assessment as directed by the on-screen physician and reporting pertinent details and changes in status.As one of our seasoned ICU nurses stated, I have to be prepared and on my game.Its made me a better nurse.

Q. Had you looked at other health systems/hospitals to see how they adopted telehealth? If so, what lessons were learned in how they did this?

A. At the time we were gearing up to launch telemedicine, our organization was also shopping for a new electronic health record. While we were checking references and networking with users of the various systems, we would ask about telemedicine and virtual visit capabilities.Most facilities had Tele-Stroke programs (as did we) but were not yet offering robust inpatient telemedicine services.

We had a need to stop unnecessary transfers; we realized that telemedicine was more of a sure thing than our ability to successfully recruit for the needed specialties. We decided to forge ahead with telemedicine and were determined to make the technical and logistics side work.At that point, the biggest wild card was whether the patient and family would have a positive experience and the service would add-value to our hospitalists and community physicians.

Q. What advice would you give a similar-sized hospital about launching a telehealth strategy?

A. Design your implementation strategy with a multi-disciplinary team. While medical staff and board support are certainly foundational to the strategic plan and investment, youve got to have champions -namely, physician (such as hospitalist leader or CMO), executive sponsor, IT, nurse leader, nurse educator, clinical workflow and documentation, heath information, contracting and revenue cycle.This team will have to collaborate on workflow, logistics and the what-ifs.

It is best to have folks involved on the front-end so that they buy in, remain engaged and have enough knowledge and familiarity to help trouble-shoot the workflow at go-live. If you have the right folks, a sense of pride and ownership develops, and failure is not an option.

Q. How will you measure success for these services? What benchmarks are being used to note whether a particular program is improving care or reducing workload stress?

A. We expect to see the number of patients we are transferring out by service line decrease, as compared to the baseline data prior to our telemedicine launch.We expect to find our case mix index trend up a little, as we are caring for slightly more complex patients relative to neurologic, cardiovascular and critical care. We expect a corresponding uptick in revenue relative to the level of care provided.

We expect to see physician satisfaction improve, since they will be better supported by specialists that we didnt previously have access to. We expect our patient experience to be impacted since the engagement between the patient and family and on-screen physician has been remarkable from a patient experience perspective.

For example, over the weekend we were able to keep and care for two neurology patients who we might have otherwise transferred out prior to telemedicine.Weve effectively cared for critically ill patients.Weve also been able to survive the challenges of the COVID 19 pandemic, while so many other hospitals have had to lay off staff or close their doors.In addition, weve provided our medical staff with access to specialists that we would not have otherwise had.

The most surprising aspect of our telemedicine program is how the nursing staff appreciates being able to provide more comprehensive care for their patients, how the nursing staff is able to learn from the on-screen physician, and how well-received the service has been with our patients who had mostly only been exposed to face-to-face care.

Q. How will you scale up or expand your telehealth strategy in the future?

A. We look forward to launching virtual visits in conjunction with our patient portal and the new EHR, which goes live January 1, 2021. We are exploring other specialties and virtual services (and) are open to any virtual opportunity that is affordable, sustainable, and adds value to our patients and medical staff.

Q. What can or could state and federal officials do to help hospitals like yours use more telehealth?

A. The loosening of some regulations related to telemedicine has been a great start, but it is in response to COVID 19, and were not certain what the new regulatory normal looks like.Especially burdensome for providers is the ongoing battle with insurance plans to figure out which hoops they require to approve services and then, even more challenging, is how to get reimbursement.There are very few standard rules of engagement. Every plan has its own requirements and nuances, which is frustrating, discouraging, labor intensive and costly.

Especially for rural communities, we need more planning and investment in infrastructure to support access to care, such as fiber networks, affordable internet and device availability for home monitoring systems for elderly and other at risk populations.Additionally, shifting focus to programs that support more population health initiatives and comprehensive and sustainable programs to close the gap on disparities in health care is crucial.

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How a Rural Hospital Developed and Launched its Telehealth Platform - mHealthIntelligence.com

Could the keto diet’s benefits be linked to changes in the gut microbiota? – Gut Microbiota for Health

Although the ketogenic (or keto) diet was initially used for treating childhood refractory epilepsy in the 1920s, fasting has been used to treat epilepsy since 500 BC. Later on, variations of the ketogenic diet (such as the Atkins diet) have appeared and its use has extended into adults for purposes other than reducing seizure frequency. They include treating weight loss, metabolic syndrome, certain cancers and psychiatric disorders such as Alzheimers disease.

This high-fat diet resembles the physiological effects of fasting by restricting carbohydrate intake to between 20g and 50g non-fiber carbohydrate per day (an average person in an industrialized country consumes 200g carbohydrate per day). This means replacing grains, fruit, starchy vegetables, legumes and sweets with carb-free or very low-carb foods such as non-starchy vegetables, cheese, avocados, nuts and seeds, eggs, meat, seafood and olive or coconut oil for cooking and dressing. That fat is then turned into ketone bodies in the liver, which can be taken up and used to fuel the bodys cells.

While scientists still struggle with figuring out which mechanisms underlie the keto diets therapeutic benefits, the gut microbiota, epigenetic changes and metabolic reprogramming appear to be involved in the response to diet.

Elaine Hsiao and her colleagues found that the microbiome is required for the anti-seizure effects of the keto diet. When germ-free mice received stool from mice on a keto diet, seizures were reduced, with Akkermansia muciniphila and Parabacteroides being involved in reducing electrical activity in the brain.

This has led scientists to explore whether the keto diet might be worth considering in gastrointestinal disease.

A new study in mice and humans, led by Peter J. Turnbaugh from UC San Francisco, breaks down the effects of the keto diet on the gut microbiome involving a reduction in bifidobacteria levels and pro-inflammatory Th17 immune cells.

First, Ang and colleagues assigned 17 men who were overweight or obese (but non-diabetic) to a control diet for 4 weeks, followed by the keto diet for 4 weeks. Metagenomic sequencing revealed bifidobacteria speciesin particular Bifidobacterium adolescentisdecreased the most on the keto diet.

The authors were also interested in exploring whether these changes were specific to the keto diet or were also observed in the high-fat and high-carbohydrate diet that is known to promote metabolic disease in mice by inducing shifts in the gut microbiome. To this end, Ang and colleagues fed groups of mice with high-fat diets formulated with graded levels of carbohydrates. It turned out that Bifidobacterium levels decreased with increasing carbohydrate restriction, thus highlighting that carbohydrate restriction, rather than high-fat intake, is the main contributor to the keto diets impact on the gut microbiome.

The mucus layer was maintained in the absence of dietary carbohydrates and bile acid metabolism was not affected. This led the authors to test whether ketone bodies themselves could be directly responsible for the progressive decreasing of Bifidobacterium as carbohydrates decreased.

Feeding mice with the high-fat diet and high-carbohydrate diet or the keto diet supplemented with a synthetic ketone esterdeveloped for mimicking ketosis without modifying dietled to increased levels of beta-hydroxybutyrate ketone bodies in the intestinal lumen and less adiposity. That can be explained by the fact that, beyond the liver, intestinal epithelial cells are also a source of ketone bodies.

Interestingly, in vitro experiments in human stool samples and work in rodents showed that ketone bodies selectively inhibited bifidobacterial growth in a dose- and pH-dependent mechanism. While other members of the gut microbiota were also affected to a lesser extent, the selective inhibitory effects of ketone bodies on Bifidobacterium may involve changes at the gut ecosystems ecological level and warrants further research.

Finally, both mono-colonization of germ-free mice with B. adolescentisthe most abundant species in the baseline diet that experienced the most marked decrease after going on the keto diet and human microbiome transplantations into germ-free mice showed that the keto diet mediates the lack of intestinal pro-inflammatory Th17 induction by reducing colonization levels of B. adolescentis. The observed differences in the gut were also detected on Th17 cells in the visceral adipose tissue.

To sum up, this study shows that the keto diet induces changes in the gut microbiome characterized by marked suppression of bifidobacteria coupled with a decrease in intestinal Th17. Said reduction would be worth considering in the context of improving obesity and immune-related diseases with increased Th17 activation.

The results reported here regarding changes in beneficial bifidobacteria, together with gut-related side effects and the nutritional safety of the keto diet due to the exclusion of major food groups, warrants caution on the use of this diet for managing gut symptoms or gastrointestinal disease progression.

References:

Kossoff EH, Zupec-Kania BA, Auvin S, et al. Optimal clinical management of children receiving dietary therapies for epilepsy: updated recommendations of the international ketogenic diet study group. Epilepsia Open. 2018; 3(2):175-92. doi: 10.1002/epi4.12225.

Wheless JW. History of the ketogenic diet. Epilepsia. 2008; 49(Suppl. 8):3-5. doi: 10.1111/j.1528-1167.2008.01821.x.

Tuck CJ, Staudacher HM. The keto diet and the gut: cause for concern? Lancet Gastroenterol Hepatol. 2019; 4(12):908-9. doi: 10.1016/S2468-1253(19)30353-X.

Cabrera-Mulero A, Tinahones A, Bandera B, et al. Keto microbiota: a powerful contributor to host disease recovery. Rev Endocr Metab Disord. 2019; 20(4):415-25. doi: 10.1007/s11154-019-09518-8.

Olson CA, Vuong HE, Yano JM, et al. The gut microbiota mediates the anti-seizure effects of the ketogenic diet. Cell. 2018; 173(7):1728-41. doi: 10.1016/j.cell.2018.04.027.

Ang QY, Alexander M, Newman JC, et al. Ketogenic diets alter the gut microbiome resulting in decreased intestinal Th17 cells. Cell. 2020. doi: 10.1016/j.cell.2020.04.027.

Turnbaugh PJ, Backhed F, Fulton L, et al. Diet-induced obesity is linked to marked but reversible alterations in the mouse distal gut microbiome. Cell Host Microbe. 2008; 3:213-23. doi: 10.1016/j.chom.2008.02.015.

Newport MT, Vanltallie TB, Kashiwaya Y, et al. A new way to produce hyperketonemia: use of ketone ester in a case of Alzheimers disease. Alzheimers Dement. 2015; 11(1):99-103. doi: 10.1016/j.jalz.2014.01.006.

Reddel S, Putignani L, Del Chierico F. The impact of low-FODMAPs, gluten-free, and ketogenic diets on gut microbiota modulation in pathological conditions. Nutrients. 2019; 11(2):373. doi: 10.3390/nu11020373.

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Could the keto diet's benefits be linked to changes in the gut microbiota? - Gut Microbiota for Health

Association between the high risk for obstructive sleep apnea and intracranial carotid artery calcification in patients with acute ischemic stroke. -…

Obstructive sleep apnea (OSA) is an independent risk factor for stroke. Furthermore, intracranial carotid artery calcification (ICAC) is a marker for subclinical atherosclerosis and future cardiovascular events. We investigated the association between the high risk for OSA and ICAC in patients with acute ischemic stroke.We retrospectively investigated 73 patients who were admitted to the hospital with acute ischemic stroke in the internal carotid artery (ICA) territory due to large-artery atherosclerosis. The risk for OSA was assessed using the Berlin Questionnaire, and patients were classified into low-risk (LR-OSA) and high-risk groups (HR-OSA). We compared the burden of ICAC between the two groups. Univariable and multivariable analyses were conducted to investigate the association of high risk for OSA with the presence of calcium in intracranial ICA.The HR-OSA group of 35 patients (48%) was significantly older and had a higher rate of hypertension and diabetes mellitus than the LR-OSA group. The HR-OSA group had more frequent ICAC (92% vs. 63%, p<0.001), higher Agatston score (162.0 vs. 8.5, p<0.001), and greater total volume of ICAC (261.2 mm vs. 20.1 mm, p<0.001) in the intracranial ICA. Presence of calcium in symptomatic intracranial ICA was positively correlated with age (odds ratio, OR, 1.432; 95% confidence interval, CI, 1.098-1.868) and HR-OSA (OR, 18.272; 95% CI, 0.500-668.401) in multivariable logistic regression analysis.This study showed that the presence of calcium in symptomatic intracranial ICA was related to high risk for OSA in patients with acute ischemic stroke.

PubMed

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Association between the high risk for obstructive sleep apnea and intracranial carotid artery calcification in patients with acute ischemic stroke. -...

Annovis Bio Files Patent Application for Method of Inhibiting, Preventing, or Treating Neurological Injuries Due to Viral and Other Infections…

BERWYN, Pa., May 27, 2020 (GLOBE NEWSWIRE) -- Annovis Bio Inc. (NYSE American: ANVS), a clinical-stage drug platform company addressing Alzheimers disease (AD), Parkinsons disease (PD) and other neurodegenerative diseases, announced todaythat it filed a patent application with the U.S. Patent & Trademark Office (USPTO) concerning a method of inhibiting, preventing, or treating neurological injuries due to viral, bacterial, fungal, protozoan, or parasitic infections in humans and in animals via administration of ANVS401 or related compounds.

Researchers have noted the similarities between many types of infections of the brain, including infections resulting from COVID-19, commented Maria Maccecchini, Ph.D., CEO of Annovis Bio. In fact, autopsies conducted in China have shown the coronavirus to be present in the brain and some people infected with the virus have developed encephalitis and other neurological problems. In addition to our own studies, a number of universities and companies are looking at how viral and bacterial infections (e.g., herpes, HIV, Zika, Lyme disease, gingivitis) cause neurological disorders and neurodegeneration. These short- and long-term neurological problems arecaused becauseinvasion of the brain by a virus or bacterium causes levels of neurotoxic proteins to rise, which consequently impairs axonal transport, induces inflammation, and leads to nerve cell death. Because ANVS401 has been shown to protect nerve cells against the ill effects of an increase of neurotoxic proteins in the brain, we believe our compound could help with the treatment of neurological diseases associated with COVID-19 and other infections.

A brain infection is a bacterial, viral, fungal, protozoan, or parasitic infection of the tissue of the brain itself or the membranes surrounding the brain andspinal cord. Bacteria andvirusesare the most common causes of brain infections.

About Annovis Bio

Headquartered in Berwyn, Pennsylvania, Annovis Bio, Inc. (Annovis) is a clinical-stage, drug platform company addressing neurodegeneration, such as Alzheimers disease (AD), Parkinsons disease (PD) and Alzheimers in Down Syndrome (AD-DS). We believe that we are the only company developing a drug for AD, PD and AD-DS that inhibits more than one neurotoxic protein and, thereby, improves the information highway of the nerve cell, known as axonal transport. When this information flow is impaired, the nerve cell gets sick and dies. We expect our treatment to improve memory loss and dementia associated with AD and AD-DS, as well as body and brain function in PD. We have an ongoing Phase 2a study in AD patients and plan to commence a second Phase 2a study in PD patients and AD patients. For more information on Annovis, please visit the companys website:www.annovisbio.com.

Forward-Looking Statements

Statements in this press release contain forward-looking statements that are subject to substantial risks and uncertainties. Forward-looking statements contained in this press release may be identified by the use of words such as anticipate, expect, believe, will, may, should, estimate, project, outlook, forecast or other similar words, and include, without limitation, statements regarding the timing, effectiveness and anticipated results of ANVS401 clinical trials. Forward-looking statements are based on Annovis Bio, Inc.s current expectations and are subject to inherent uncertainties, risks and assumptions that are difficult to predict. Further, certain forward-looking statements are based on assumptions as to future events that may not prove to be accurate. Such risks include the possibility that the patent application referenced in this release may not be approved, the timing of any decision by the USPTO, and that ANVS401 is subject to further clinical trials and may not be an effective treatment of infections. These and other risks and uncertainties are described more fully in the section titled Risk Factors in the Annual Report on Form 10-K for the year ended December 31, 2019 filed with the Securities and Exchange Commission. Forward-looking statements contained in this announcement are made as of this date, and Annovis Bio, Inc. undertakes no duty to update such information except as required under applicable law.

Investor Relations:

Dave Gentry, CEORedChip Companies Inc.407-491-4498Dave@redchip.com

SOURCE: Annovis Bio Inc.

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Annovis Bio Files Patent Application for Method of Inhibiting, Preventing, or Treating Neurological Injuries Due to Viral and Other Infections...

Alterity Therapeutics presents data on ATH434 to the American Academy of Neurology – Yahoo Finance

MELBOURNE, Austriliaand SAN FRANCISCO, May 21, 2020 /PRNewswire/ -- Alterity Therapeutics (ASX: ATH, NASDAQ: ATHE) ("Alterity" or "the Company") has presented data on ATH434 (formerly PBT434) for the treatment of Multiple System Atrophy at the American Academy of Neurology (AAN) virtual meeting.

Chief Medical Officer & Senior VP Clinical Development, Dr David Stamler had been invited to make an oral presentation at the Parkinson's Disease Interventions and Clinical Trials session at the AAN Annual meeting in Toronto in April 2020 but the meeting was cancelled due to the COVID-19 pandemic. This was replaced with the opportunity to make a virtual presentation which is currently live on the 2020 AAN Science Highlights Virtual Platform available here.

The presentation was based on an abstract entitled A Phase 1 Study of PBT434, a Novel Small Molecule Inhibitor of a-Synuclein Aggregation, in Adult and Older Adult Volunteers published in the journal Neurology.

In addition, Dr Stamler was interviewed by Neurology Today. The article is available here.

The abstract, presentation and article share findings from Alterity's completed Phase 1 trial of leading drug candidate ATH434, which evaluated the safety, tolerability, and pharmacokinetics in healthy adult and older adult volunteers.

Importantly, the abstract provides detailed data demonstrating that ATH434 not only crosses the blood brain barrier in humans, but that clinically tested doses achieved concentrations in the brain that were comparable to or exceeded those associated with efficacy in animal models of disease. Safety data were presented indicating that ATH434 was well tolerated and demonstrated a similar adverse event profile in adults and older ( 65 years) adults.

The data support Alterity's plans to proceed with clinical testing of ATH434 for the treatment of Multiple System Atrophy, a form of atypical Parkinsonism.

Dr David Stamler told Neurology Today: "Because we're treating the underlying cause of disease by targeting alpha synuclein, I think we have potential to affect all aspects of disease the motor symptoms, the blood pressure problems, gait and balance, and even bowel and bladder dysfunction."

END

Authorisation & Additional informationThis announcement was authorised by Geoffrey Kempler, CEO and Chairman of Alterity Therapeutics Limited.

Contact:

Investor RelationsRebecca Wilson, WE CommunicationsE: WE-AUAlterity@we-worldwide.com Tp: +61 3 8866 1216

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SOURCE Alterity Therapeutics Limited

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Alterity Therapeutics presents data on ATH434 to the American Academy of Neurology - Yahoo Finance

Enteral Feeding Device Used for Neurology Market to 2025: Growth Analysis by Manufacturers, Regions, Types and Applications – 3rd Watch News

A recent research on Enteral Feeding Device Used for Neurology market, now available with Market Study Report, LLC, is a thorough study on the latest market trends prevailing in the global business sphere. The report also offers important details pertaining to market share, market size, profit estimations, applications and statistics of this industry. The report further presents a detailed competitive analysis including growth strategies adopted by key players of the industry.

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Enteral Feeding Device Used for Neurology Market to 2025: Growth Analysis by Manufacturers, Regions, Types and Applications - 3rd Watch News

Ipsen: New Surveys Show Over 80% of Patients with Spasticity and Cervical Dystonia Treated with Botulinum Toxin-A Experience Debilitating Symptom…

PARIS--(BUSINESS WIRE)--Regulatory News:

Ipsen (Euronext: IPN; ADR: IPSEY) today presents the results of two patient surveys. The surveys involved over 400 respondents from five countries, living with spasticity or cervical dystonia and receiving botulinum neurotoxin type A (BoNT-A) injections. The results show that over 80% of respondents experienced debilitating symptom recurrence, and revealed that a lack of long-lasting symptom control between injections has a profound impact on the personal and professional lives of patients.1-4

The results from these two important patient surveys provide significant insight into the real-life burden of the two conditions; however, they also highlight a worrying disconnect between patients treatment expectations and their actual experience. The findings, which build on our growing understanding of spasticity and cervical dystonia, provide us with the potential to unlock meaningful changes in clinical practice, said Dr Alberto Esquenazi, Department of Physical Medicine and Rehabilitation, Gait and Motion Analysis Laboratory, MossRehab and Albert Einstein Medical Centre, U.S. and lead investigator on the spasticity survey.

The first survey1,2 investigated the burden of spasticity on patients lives. Of the 210 respondents from France, Germany, Italy, the U.K., and the U.S., 83% reported that symptoms of spasticity returned between two sessions of BoNT-A, with 59% of these patients experiencing that return within three months of their last treatment. Symptom recurrence significantly impacted patients quality of life, including sleep, relationships, performance of daily tasks and working lives. In addition, 47% of working patients reported being unable to work when symptoms re-emerge and 45% of working patients felt less efficient at work than before.1,2

The second survey3,4 adopted a similar approach, analyzing data from 209 respondents with cervical dystonia from across France, Germany, Italy, the U.K., and the U.S. Of the respondents, 88% reported the reappearance of pre-existing symptoms between BoNT-A injections. The majority of working respondents reported a significant impact on their professional life, with 66% stating that they did not feel comfortable at work and 66% did not feel as efficient at work as usual. Patients personal lives were also significantly compromised by their symptom recurrence, with an impact on their ability to socialize, sleep well, drive, or perform daily tasks.3,4

In both surveys, over 70% of patients said they would like longer lasting benefits from their treatment.1-4

The Carenity 2 surveys reveal the debilitating impact that symptom recurrence can have across every aspect of life for patients with spasticity and cervical dystonia, indicating that more needs to be done to relieve the burden of symptoms for patients suffering from these neurological conditions.1-4

Full results of the Carenity 2 survey in spasticity were published in Frontiers in Neurology on 07 May 2020.1

Antony Fulford-Smith, Vice President, Global Medical Affairs, Ipsen, commented: Spasticity and cervical dystonia have a devastating effect on patients lives, seriously affecting their mobility, employment and quality of life. At Ipsen, we are constantly searching for ways to improve disease management and comprehensive care with a patient-centered approach. Its clear from these surveys that more can be done to relieve the burden of these challenging diseases on patients day-to-day lives.

Spasticity and cervical dystonia are distinct neurological conditions, though they share the characteristics of poor muscle control and spasms and are routinely treated with BoNT-A injections.3,5,6 Spasticity affects more than 12 million people worldwide7 and is generally caused by damage to the area of the brain and spinal cord responsible for controlling muscle and stretch reflexes due to stroke, traumatic brain and spinal cord injury, multiple sclerosis and cerebral palsy.5 Cervical dystonia is a rare disorder of unknown origin in most of the primary cases, characterized by involuntary contractions of the neck muscles.6

About the Carenity 2 surveys

The two patient surveys, commissioned by Ipsen, were conducted between May to September 2019 by Carenity, an online patient community. A total of 419 respondents from France, Germany, Italy, the U.K and the U.S responded to the surveys via the online platform Carenity. Eligible participants were over 18 years old and had (or cared for someone with) spasticity or cervical dystonia (CD) treated with BoNT-A for at least one year. To assess burden of spasticity or CD for patients and their caregivers, the Carenity 2 surveys explored the impact of symptom re-emergence on quality of life.1-4

Ipsen has an ongoing partnership with Carenity, a social media platform for people living with chronic diseases and presented findings from the first Carenity international survey which focused on spasticity at TOXINS 2019.8

About spasticity

Spasticity is estimated to affect more than 12 million people worldwide.7 It is a condition in which certain muscles are continuously contracted causing stiffness or tightness of the muscles, which can interfere with normal movement, gait and speech.5 Spasticity is usually caused by damage to the parts of the brain or spinal cord that control voluntary movement,5,9 leading to a change in the balance of signals between the nervous system and the muscles which leads to increased activity in the muscles.5 Spinal cord injury, multiple sclerosis, cerebral palsy, stroke, brain or head trauma and metabolic diseases can all cause spasticity.9 Spasticity is experienced by 34% of stroke survivors within 18 months following a stroke.10

About cervical dystonia

Cervical dystonia (CD), also known as spasmodic torticollis, is a movement disorder in which involuntary muscular contractions occur primarily in the neck muscles.6,11 This can cause the head to turn to one side or to be pulled backward or forward.6,12 CD is relatively uncommon, affecting 57 to 280 people per million.13 It can occur at any age, although symptoms generally appear in middle age, often beginning slowly and usually reaching a plateau over a few months or years.14 The degeneration of the spine, irritation of nerve roots or frequent headaches can make CD particularly painful.14 In most cases the cause is unknown and no cure exists.13

About Ipsen

Ipsen is a global specialty-driven biopharmaceutical group focused on innovation and Specialty Care. The Group develops and commercializes innovative medicines in three key therapeutic areas Oncology, Neuroscience and Rare Diseases. Its commitment to oncology is exemplified through its growing portfolio of key therapies for prostate cancer, neuroendocrine tumors, renal cell carcinoma and pancreatic cancer. Ipsen also has a well-established Consumer Healthcare business. With total sales over 2.5 billion in 2019, Ipsen sells more than 20 drugs in over 115 countries, with a direct commercial presence in more than 30 countries. Ipsens R&D is focused on its innovative and differentiated technological platforms located in the heart of the leading biotechnological and life sciences hubs (Paris-Saclay, France; Oxford, UK; Cambridge, US). The Group has about 5,800 employees worldwide. Ipsen is listed in Paris (Euronext: IPN) and in the United States through a Sponsored Level I American Depositary Receipt program (ADR: IPSEY). For more information on Ipsen, visit http://www.ipsen.com.

IpsenCautionary Note Regarding Forward-Looking Statements

The forward-looking statements, objectives and targets contained herein are based on the Groups management strategy, current views and assumptions. Such statements involve known and unknown risks and uncertainties that may cause actual results, performance or events to differ materially from those anticipated herein. All of the above risks could affect the Groups future ability to achieve its financial targets, which were set assuming reasonable macroeconomic conditions based on the information available today. Use of the words "believes", "anticipates" and "expects" and similar expressions are intended to identify forward-looking statements, including the Groups expectations regarding future events, including regulatory filings and determinations. Moreover, the targets described in this document were prepared without taking into account external growth assumptions and potential future acquisitions, which may alter these parameters. These objectives are based on data and assumptions regarded as reasonable by the Group. These targets depend on conditions or facts likely to happen in the future, and not exclusively on historical data. Actual results may depart significantly from these targets given the occurrence of certain risks and uncertainties, notably the fact that a promising product in early development phase or clinical trial may end up never being launched on the market or reaching its commercial targets, notably for regulatory or competition reasons and also taking into consideration assessment delays of certain clinical trials in light of the ongoing COVID-19 pandemic. The Group must face or might face competition from generic products that might translate into a loss of market share. Furthermore, the Research and Development process involves several stages each of which involves the substantial risk that the Group may fail to achieve its objectives and be forced to abandon its efforts with regards to a product in which it has invested significant sums. Therefore, the Group cannot be certain that favorable results obtained during pre-clinical trials will be confirmed subsequently during clinical trials, or that the results of clinical trials will be sufficient to demonstrate the safe and effective nature of the product concerned. There can be no guarantees a product will receive the necessary regulatory approvals or that the product will prove to be commercially successful. If underlying assumptions prove inaccurate or risks or uncertainties materialize, actual results may differ materially from those set forth in the forward-looking statements. Other risks and uncertainties include but are not limited to, general industry conditions and competition; general economic factors, including interest rate and currency exchange rate fluctuations; the impact of pharmaceutical industry regulation and health care legislation; global trends toward health care cost containment; technological advances, new products and patents attained by competitors; challenges inherent in new product development, including obtaining regulatory approval; the Group's ability to accurately predict future market conditions; manufacturing difficulties or delays; financial instability of international economies and sovereign risk; dependence on the effectiveness of the Groups patents and other protections for innovative products; and the exposure to litigation, including patent litigation, and/or regulatory actions. The Group also depends on third parties to develop and market some of its products which could potentially generate substantial royalties; these partners could behave in such ways which could cause damage to the Groups activities and financial results. The Group cannot be certain that its partners will fulfil their obligations. It might be unable to obtain any benefit from those agreements. A default by any of the Groups partners could generate lower revenues than expected. Such situations could have a negative impact on the Groups business, financial position or performance. The Group expressly disclaims any obligation or undertaking to update or revise any forward-looking statements, targets or estimates contained in this press release to reflect any change in events, conditions, assumptions or circumstances on which any such statements are based, unless so required by applicable law. The Groups business is subject to the risk factors outlined in its registration documents filed with the French Autorit des Marchs Financiers. The risks and uncertainties set out are not exhaustive and the reader is advised to refer to the Groups 2018 Registration Document available on its website (www.ipsen.com).

References

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Ipsen: New Surveys Show Over 80% of Patients with Spasticity and Cervical Dystonia Treated with Botulinum Toxin-A Experience Debilitating Symptom...

Novartis study reveals that migraine support in the workspace can significantly decrease the impact of the disease on affected employees -…

Basel, May 26, 2020 Novartis announces data from its Migraine Care pilot program which was created in collaboration with patient groups and leading experts in neurology, telemedicine and digital medicine, to provide a complementary, independent, third-party service for all Swiss-based Novartis associates living with migraine to improve their quality of life. These data have been published in the European Journal of Neurology after the 6th Congress of the European Academy of Neurology was held virtually due to COVID-19.

The study confirms the high burden of people living and working with migraine but also demonstrates that empowering individuals can significantly increase quality of life and productivity, said Dr. Gantenbein, Head of the Swiss Headache Society. This further emphasizes the notion that employer-led well-being programs can benefit individuals, companies and society as a whole.

About Migraine Care

Migraine Care is a pilot program created by Novartis, in collaboration with patient groups and leading experts in neurology, telemedicine and digital medicine, to provide a complementary, independent, third-party service for all Swiss-based Novartis associates living with migraine to improve their quality of life. The program, endorsed by the Swiss Headache Society, aims to raise awareness of migraine in the workplace and provide free coaching to Novartis associates living with migraine. It also aims to empower associates in the management of the disease by leveraging both medical and lifestyle options.

339 Novartis employees registered to the program, out of which 141 consented to their data being analyzed and 79 completed the program at six months. Participants received monthly sessions of individualized telecoaching comprised of educational modules and action plans from a specialized nurse by phone and through a specially developed module on the Migraine Buddy smartphone application. The mean age of participants at baseline was 41.5 years with 70.0% being females. 64.1% of participants had a confirmed diagnosis of migraine. Out of which, 56.8% were not being treated by a physician despite 74.0% having migraine disability assessment (MIDAS) grade 2. At the end of six months, participants reported 54.0% decrease in migraine-related disability and a 9.0% increase in the patient activation measure (PAM), a measure which assesses patient knowledge, skill, and confidence for self-management. Loss of productivity through both, absenteism and presenteism, were reduced by more than 50.0% and in addition participants report their private life being significantly less impaired by migraine.

Novartis is exploring opportunities to work with other employers who are interested in supporting their employees and family members living with migraine.

About Migraine

Migraine is a distinct neurological disease1. It involves recurrent attacks of moderate to severe head pain that is typically pulsating, often unilateral and associated with nausea, vomiting and sensitivity to light, sound and odors2. Migraine is associated with personal pain, disability and reduced quality of life, and financial cost to society3. It has a profound and limiting impact on an individual's abilities to carry out everyday tasks; the World Health Organization reported migraine to be one of the top 10 causes of years lived with disability for men and women4. It remains under-recognized and under-treated3,5.

Disclaimer

This media update contains forward-looking statements within the meaning of the United States Private Securities Litigation Reform Act of 1995. Forward-looking statements can generally be identified by words such as potential, can, will, plan, may, could, would, expect, anticipate, seek, look forward, believe, committed, investigational, pipeline, launch, or similar terms, or by express or implied discussions regarding potential marketing approvals, new indications or labeling for the investigational or approved products described in this media update, or regarding potential future revenues from such products. You should not place undue reliance on these statements. Such forward-looking statements are based on our current beliefs and expectations regarding future events, and are subject to significant known and unknown risks and uncertainties. Should one or more of these risks or uncertainties materialize, or should underlying assumptions prove incorrect, actual results may vary materially from those set forth in the forward-looking statements. There can be no guarantee that the investigational or approved products described in this media update will be submitted or approved for sale or for any additional indications or labeling in any market, or at any particular time. Nor can there be any guarantee that such products will be commercially successful in the future. In particular, our expectations regarding such products could be affected by, among other things, the uncertainties inherent in research and development, including clinical trial results and additional analysis of existing clinical data; regulatory actions or delays or government regulation generally; global trends toward health care cost containment, including government, payor and general public pricing and reimbursement pressures and requirements for increased pricing transparency; our ability to obtain or maintain proprietary intellectual property protection; the particular prescribing preferences of physicians and patients; general political, economic and business conditions, including the effects of and efforts to mitigate pandemic diseases such as COVID-19; safety, quality, data integrity or manufacturing issues; potential or actual data security and data privacy breaches, or disruptions of our information technology systems, and other risks and factors referred to in Novartis AGs current Form 20-F on file with the US Securities and Exchange Commission. Novartis is providing the information in this media update as of this date and does not undertake any obligation to update any forward-looking statements contained in this media update as a result of new information, future events or otherwise.

About Novartis

Novartis is reimagining medicine to improve and extend peoples lives. As a leading global medicines company, we use innovative science and digital technologies to create transformative treatments in areas of great medical need. In our quest to find new medicines, we consistently rank among the worlds top companies investing in research and development. Novartis products reach nearly 800 million people globally and we are finding innovative ways to expand access to our latest treatments. About 109,000 people of more than 145 nationalities work at Novartis around the world. Find out more athttps://www.novartis.com.

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Novartis study reveals that migraine support in the workspace can significantly decrease the impact of the disease on affected employees -...

Early consultation with a neurologist can go a long way in mitigating the effects of Parkinsons disease – Express Healthcare

Dr (Lt Gen) CS Narayanan, HOD, Department of Neurology, Manipal Hospitals, Dwarka discusses how Parkinsons disease varies from person to person and how it can be managed with proper medication and following a healthy lifestyle

Early consultation with a neurologist can go a long way in mitigating the effects of Parkinsons disease which is a chronic neurological illness caused by damage to brain cells that produce a chemical messenger called dopamine. Early detection and timely medical intervention are the keys to the effective management of the disease.

The effects and severity of Parkinsons disease vary person to person from various advanced age groups and for those, who led a very active disease or distress free so far, it comes as trauma. When Parkinsons hit persons may develop an unfamiliar pain and stiffness in the right shoulder and notice that they are taking longer than usual to shave, wear their clothes and get ready for work. Over time they may develop a tremor in their hands. It is evident that a general sense of fatigue overpowers the patients.

Sometimes people feel depressed also. These are clear signs and symptoms of Parkinsons and at this point in time, people should consult a neurologist for the management of the disease as there is no cure for it as such.

The neurologists normally see all the symptoms and decide about the stage. After a thorough examination, experts point out whether it is an early-stage case or a severe one. While there are no conclusive tests, we need to depend on the combination of symptoms and findings on physical examination.

Combating Parkinsons is not difficult and patients, with proper consultation, come to terms with it. Taking prescribed medicine regularly along with a regimen of exercise and also modified lifestyle help a lot in managing the disease.

While Parkinsons disease is more common in those who are above 50 years of age, it can also sometimes affect younger persons. It may also be inherited sometimes. Typically people with Parkinsons disease experience tremor, slowness of movements, limb rigidity, along with gait and balance problems. These are called motor symptoms. Patients may also have several non-motor symptoms such as mood disorders, difficulty in planning and organising, sleep difficulty, constipation, lack of ability to smell, and sexual dysfunction. The severity of symptoms and pace of progression of symptoms often varies from one person to another.

A combination of medications, some designed to replenish the amount of dopamine in the brain and others to arrest the progression of the disease are often prescribed. They are very effective in the early stages but the neurologist may adjust the doses and introduce new drugs as the disease progresses. If the medications become less effective over time or if side-effects become bothersome, advanced approaches to management such as deep brain stimulation (DBS) and surgery are considered. With DBS, electrodes are surgically implanted in the brain. They send electrical impulses to stimulate the parts of the brain that control movement. Evidence suggests that patients with Parkinsons disease also benefit from a multidisciplinary approach to care.

Parkinsons disease can be managed with proper attention and medical consultation. It is proven that early consultation and close interaction with a neurologist thereafter can go a long way in mitigating the effects of Parkinsons disease. By knowing the nature of the disease and the various effective ways of managing it, patients with Parkinsons disease can pursue their work, hobbies, and go on to lead a life full of joy.

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Early consultation with a neurologist can go a long way in mitigating the effects of Parkinsons disease - Express Healthcare

May is American Stroke Month; Baystate Health neurologist says know the signs for this brain attack – masslive.com

SPRINGFIELD Dr. Rajiv Padmanabhan doesnt need a calendar to remind him that May is American Stroke Month.

However, the Baystate Medical Center neurologist notes that many people remain unaware of the symptoms of stroke and the importance of getting immediate medical attention to avoid disability and even death.

He adds that the coronavirus pandemic further underscores the importance of calling 9-1-1 when this cerebrovascular accident that impacts blood and oxygen flow to the brain is suspected.

Though not common, Padmanabhan said stroke can be a complication in severe cases of COVID-19, the disease caused by the new coronavirus.

He adds anyone experiencing a life-threatening event like a stroke should not let fear of exposure to COVID-19 prevent them from seeking immediate medical care. He said Baystate is among those in the medical community that has taken extensive steps" to reduce such exposure.

It is very important not to delay care in stroke as the outcome can be worse. It is very important now more than ever to call 9-1-1 right away, Padmanabhan said.

It is important to know that time is brain. The phrase time is brain emphasizes that human nervous tissue is rapidly lost as stroke progresses and emergent evaluation and therapy are required.

Sometimes referred to as a brain attack," a stroke is caused by blockage of blood flow or bleeding into the brain and its symptoms include numbness, confusion and severe headache.

A ruptured brain aneurysm a weakened area of a blood vessel that begins to bleed can also cause stroke.

Interruption in the flow of blood, which carries oxygen and other nutrients to the brain, can cause cells to die and impair function. The act F.A.S.T. evaluation helps with awareness of stroke and the need for quick treatment.

A healthy lifestyle can help reduce stroke risk and other preventative measures include discussions with a medical provider about maintaining the desired blood pressure and whether there is a family history for cardiovascular disease.

Padmanabhan was asked to explain further about stroke, which is the leading cause of disability among adults and one of the top causes of death in the United States.

Q. A stroke can be quite disabling. Why is that?

A. The part of the brain that controls that part of body is unique in its purpose and function and, usually after a stroke, that part of the brain ceases to function resulting in loss of that modality. That being said, each part of brain works in unison with other areas and stroke in one area can affect the connections other parts of the brain rely on.

Thus, strokes can be disabling not only in the loss of function but also by the way of the downstream effects.

Q. What is the difference between ischemic and hemorrhagic stroke?

A. A hemorrhagic stroke is due to rupture in an artery due to weakening of the arterial wall. This results in blood seeping into the brain affecting that part of the body where the bleed occurred.

An ischemic stroke is a clotting type of stroke that occurs when a clot forms within an artery due to plaque, that is, hardening of artery, or due to a clot arising from elsewhere. A clotting stroke and a bleeding stroke affect the body similarly and so to tell the difference urgent scans are needed and treatments change according to the type of stroke.

Q. The death rate from stroke has dropped considerably since the drug tPA, tissue plasminogen activator, was approved by the FDA in the 1990s to treat acute ischemic stroke. How does it work and how are patients evaluated for this treatment?

A. TPA breaks up the clot in a clogged artery in an ischemic stroke and tries to restore flow back to brain. This reduces the number of nerve cells, that is, neurons, to survive, improving the chances of good outcome or recovery and minimizing the severity and consequently decreasing complications from a severe stroke, including death.

Q. Thrombectomy therapy can also be used to treat acute ischemic stroke. Would you explain this and when is it applicable and is it used in combination with tPA?

A. Thrombectomy is most useful when we can actually see a large clot in the artery that can be removed by the way of a catheter device that is threaded up an artery in the groin under anesthesia.

This offers the best hope for patients who otherwise would have worse outcomes. It can be done in some cases until 24 hours of stroke. To identify and treat as quickly as possible, we incorporate scans looking not only at the brain but also the arteries that go the brain in a very rapid manner so we can effectuate treatment much faster.

Q. What success has Baystate seen in treating acute ischemic stroke patients with this therapy?

A. We have had tremendous success in the approaches we have taken both by decreasing the time to treatment by the way of clot busting treatment but also having the ability to quickly get the patient to the catheter lab to remove the clot and restore blood flow in a timely manner.

This has led to more discharges to home rather than to nursing home.

Q. How is hemorrhagic stroke treated?

A. We usually control the blood pressure to minimize further damage to the brain, and in addition if the patient is on a blood thinner, we have medications to reverse the effects of blood thinner as well.

Q. What are some of the cardiovascular risks for stroke that people should be aware and possibly address to avoid stroke?

There are modifiable risk factors: such as hypertension, that is, high blood pressure, diabetes, smoking, sedentary lifestyle, obesity, high cholesterol.

There is also a correlation with sleep apnea.

Atrial fibrillation can pose a risk for clotting stroke.

Cutting salt, exercising more and checking your numbers with your primary care doctor is important.

Q. How are health care providers better managing these risks in their patients?

A. Primary care providers are on the frontline of these risk factor assessments and management.

It is very important to follow up with your primary care doctor and the ask the question: what are my risk factors, and what are my numbers?

It is also important to tell your primary care doctor of any medical conditions that run in the family, and that may increase the risk for stroke and heart attack.

Q. Signs of stroke can differ by gender. Would you explain?

A. In the Atherosclerosis Risk in Communities Study it was found that men were more likely to experience walking issues with stroke compared to women.

The National Institutes of Health recommends improved education for women and their caregivers to seek care early, especially with mild symptoms, and not wait to call 9-1-1.

Q. Most strokes occur in people over 65, but it is estimated that about 10 percent of strokes occur in those 45 and younger in the U.S. What are some of the causes of this, and is vaping considered a potential risk factor?

A. Stroke in age less than 45, often described as stroke in young, may not only be due to traditional risk factors. There can be additional factors for example, certain rare clotting disorders, tear in the arteries, and due to effects of vaping, smoking and illicit drugs.

One study found vaping increasing the stroke risk by three-fold compared to those who did not.

Adding cigarette smoking to vaping can further increase stroke risk by another two-fold.

Q. What success has Baystate seen in terms of lower morbidity and mortality rates around strokes in the last decade with improved treatment and awareness?

A. There has been a significant improvement in not only the deaths, but also disability following the implementation of specialized stroke systems of care in the last 10 years, thus cutting treatment times, significant improvement in window for treatment of thrombectomy for clot removal especially over the last several years.

Q. Are most of your patients aware of the signs of stroke and the importance of calling 9-1-1 quickly?

A. Many of the patients are not aware of all the stroke signs and symptoms. And in one survey many of the patients did not know their risk factors and importance of controlling them after a stroke had already occurred.

It is important for family and caregivers to be aware of stroke symptoms to be able to act quickly by calling 9-1-1.

Q. What is the No. 1 thing you would like people to know in terms of lowering their risk for stroke?

A. It is important to see your primary care doctor and make sure you ask the risk questions. Majority of strokes are preventable.

Q. Is it too late for older people, especially those with underlying conditions, to reduce their risk for stroke?

A. Not at all, older patients may have several underlying conditions, but with the help of their primary care doctor, it is possible to have a tailored approach to management of risk factors.

Additionally, with the new blood thinners we prescribe for atrial fibrillation to prevent the bleeding, complications have decreased over the years; it is important to know to ask about the newer agents when you visit your doctor.

Q. What more do you want younger people to know in terms of preventing their risk for stroke as they age?

A. It is good to have a healthy routine of diet and exercise and to continue to follow up with your primary care doctor. If you are smoking then quitting smoking now can be very important in preventing stroke and heart problems.

Q. Do brain aneurysms affect stroke risk?

A. Yes, a ruptured brain aneurysm can cause stroke in a manner different from the traditional stroke and can occur in the first 14 to 21 days of aneurysm bleed.

To help prevent and manage such complications we have dedicated staff and protocols in the neurointensive care unit at Baystate.

If an aneurysm is found incidentally and has not ruptured, we do have neurointervenitional clinic expertise that your doctor can refer to to help address this by the way of catheter-guided coiling of the aneurysm to prevent a bleeding from occurring in the first place.

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May is American Stroke Month; Baystate Health neurologist says know the signs for this brain attack - masslive.com