New option for treating upper tract urothelial cancer – Baylor College of Medicine News

Treatment of low-grade upper tract urothelial cancer usually involves radical surgery to remove the kidney and ureter, highlighting the need for improved treatments. An international team led by researchers at Baylor College of Medicine reports in the journal The Lancet Oncology that an innovative form of local chemotherapy using a mitomycin-containing reverse thermal gel offers a kidney-sparing treatment option for this rare cancer affecting 6,000 to 8,000 new patients in the United States every year.

Urothelial cancer refers to a cancer of the lining of the urinary system. While about 9 of 10 urothelial cancers arise in the bladder (lower tract), a small subset arises in the upper tract, in the lining of the kidney or the ureter, the long, thin tube that connects that kidney to the bladder, said corresponding and senior author Dr. Seth P. Lerner, professor of urology and Beth and Dave Swalm Chair in Urologic Oncology at Baylor.

To spare patients having to undergo radical kidney surgery, physicians treated the cancer with a novel formulation of mitomycin, a form of chemotherapy that urologists use to treat low-grade cancers of the bladder. Standard formulations of mitomycin are administered in a water-based solution that is washed away by the urine produced by the kidney, shortening the time the drug is in direct contact with the urothelium, which lessens the effect of the treatment. To overcome the shortcomings of standard mitomycin treatment, Lerner and his colleagues evaluated a mitomycin-containing reverse thermal gel (UGN-101, brand name Jelmyto, manufactured by UroGen Pharma).

UGN-101 is semi-solid at body temperature and becomes a viscous liquid at colder temperatures that can be injected via a catheter passed from the bladder into the renal pelvis where these tumors occur, Lerner said. The reverse thermal properties of UGN-101 allow for local administration of mitomycin as a liquid, which subsequently transforms into a semi-solid gel depot as it warms up following instillation into the urinary upper tract. Normal urine flow dissolves the gel depot, allowing tissue exposure to mitomycin over a period of 4 to 6 hours.

The researchers previously reported proof-of-concept and preliminary safety data for UGN-101 in treating 22 patients with upper tract urothelial cancer in a compassionate-use program. In the current study, Lerner and his colleagues conducted a phase 3 single-arm clinical trial to further evaluate the efficacy of the innovative reverse gel delivery of mitomycin in low-grade upper tract urothelial cancer.

Seventy-one patients received six weekly treatments with mitomycin-containing reverse thermal gel. Patients who had a complete response (complete disappearance of the tumor) were offered monthly treatments for up to 11 additional months. Efficacy of the treatment was evaluated using urine cytology (a test to look for abnormal cells in a patients urine), ureteroscopy (an examination of the upper urinary tract) and biopsy (if warranted) three months following the initiation of therapy.

The treatment was beneficial. Following the initial six weekly treatments, 59 percent of the patients had no residual tumors, including patients with cancer deemed unresectable at diagnosis, who represented 48 percent of the overall treatment population. There were side effects, including urinary tract infection, hematuria (blood in urine), flank pain and nausea, but the severity and frequency were as expected from patients who are undergoing similar interventions. The study will continue to monitor the durability of the initial response out to 12 months.

The treatment has been recently approved by the U.S. Food and Drug Administration and became the first and only approved non-surgical treatment available for patients with low-grade upper tract urothelial cancer.

The clear benefit is that patients get to keep their kidney. For people who have one kidney, this option also removes the need for dialysis, Lerner said. Other potential beneficiaries would be patients for whom, because of other conditions, it would be too risky to perform an operation to remove the kidney. Now they have an option for treatment.

Other contributors to this work include Nir Kleinmann, Surena F. Matin, Phillip M. Pierorazio, John L. Gore, Ahmad Shabsigh, Brian Hu, Karim Chamie, Guilherme Godoy, Scott Hubosky, Marcelino Rivera, Michael ODonnell, Marcus Quek, Jay D. Raman, John J. Knoedler, Douglas Scherr, Joshua Stern, Christopher Weight, Alon Weizer, Michael Woods, Hristos Kaimakliotis, Angela B. Smith, Jennifer Linehan, Jonathan Coleman, Mitchell R. Humphreys, Raymond Pak, David Lifshitz, Michael Verni, Mehrad Adibi, Mahul B. Amin, Elyse Seltzer, Ifat Klein, Marina Konorty, Dalit Strauss-Ayali, Gil Hakim and Mark Schoenberg.

For a complete list of the contributors affiliations and declaration of interests visit the publication. This trial was supported with funding from UroGen Pharma.

See the article here:

New option for treating upper tract urothelial cancer - Baylor College of Medicine News

Doctor on frontline issues warning for COVID-19 treatment: ‘This medicine … will surely kill them’ – TheBlaze

Dr. Tom Yadegar, a specialist in critical care medicine who has been treating some of the most extreme cases of the coronavirus, joined Glenn Beck on the radio program Tuesday to share some important information with the public and doctors around the world about treating COVID-19.

As the intensive care unit director at Providence Cedars-Sinai Tarzana Medical Center in California, Yadegar and has been treating patients with COVID-19 for about seven weeks and has not lost a single patient. He was recently asked to command four more regional hospitals because he and his team are performing well above other hospitals in the Los Angeles area.

Yadegar created a protocol to determine which patients with COVID-19 also have what's called "cytokine storm syndrome" -- a process by which the body's immune system rapidly releases too many cytokines into the blood.

"The immune system kind of goes awry. It doesn't act normally. The immune system gets super ramped up, and instead of attacking the virus, it attacks the patient's own vital organs," Yadegar explained. "It's actually [the patient's] own immune system that's causing the problem, not necessarily the virus.

"Don't get me wrong. This is a deadly virus. Just like the influenza virus, it can definitely cause pneumonia. It can definitely cause respiratory failure. If the patient has emphysema or heart failure, it can definitely exacerbate those," he added. "But this [coronavirus] was doing something unique. This was doing something that I really hadn't seen much in my 20 years, where it was activating the immune system. And then the immune system was causing all the destruction in the lungs."

Yadegar noted that, while a virus triggering an autoimmune disease is not necessarily an "unknown thing," the COVID-19 virus "does it at an extraordinary pace" and to a significant number of patients. He stressed the importance of recognizing that not every patient with COVID-19 will develop an autoimmune disease and that every case must be treated individually.

"One thing that I can't stress any harder to you and your listeners. There isn't necessarily one test, and there isn't one particular treatment plan. Every patient has their own kind of individual disease," he said. "You can't treat everyone with the same treatments. There isn't a one-size-fits-all for this disease. You have to do your due diligence. You have to look at the patient in front of you and then, you know, come up with a treatment for the disease that that patient is manifesting. You can't just go through the ICU, and start handing out these medicines. If you give this medicine to someone who doesn't need it, you will surely kill them."

Watch the video below for more details:

In response to the COVID-19 crisis, BlazeTV is offering our BIGGEST discount ever! Get $30 off your subscription when you use promo code GLENN. Claim your special offer at https://get.blazetv.com/glenn/.

Want more from Glenn Beck?

To enjoy more of Glenn's masterful storytelling, thought-provoking analysis and uncanny ability to make sense of the chaos, subscribe to BlazeTV the largest multi-platform network of voices who love America, defend the Constitution and live the American dream.

View post:

Doctor on frontline issues warning for COVID-19 treatment: 'This medicine ... will surely kill them' - TheBlaze

Doctors and Medicine | Health Care Mythologies – ChicagoNow

Lucky you. Just when you were at the end of your rope and about to do something insane, I have written a post to occupy your time.

Let me begin by making something very clear. I have always tried as much as possible to make my posts apolitical.

So, I am going to make a statement, which will then lead me to the heart of today's story, but it is intended simply as an example.

Why do so many people give a flying fuck about what Trump says about the science surrounding Covid-19?

Yes, he is the president. So what?

And, so I'm not accused of just picking on him, this also goes for actor, sports figures, royalty, etc.

Stay in your lane, people!

He is a lay person and should not be considered an expert on infectious disease in any sense of the word.

OK, now here is my actual point.

When it comes to learning about science or medicine, please refer to reputable doctors or scientists.

Makes sense, right?

Yet, stop and think about the anti-vaxxers. They are not doctors or scientists, for the most part, and if they are, they are not reputable.

However, until we had huge outbreaks of measles, a completely preventable illness, I might add, we went so far as to give parents waivers, so that their children wouldn't have to be vaccinated.

Because, you know, freedom.

Now, let's talk a little more about the current scenario.

Many have pointed out, and I include myself in this group, that the flu generally has far more total impact than Covid-19, yet, we don't go into lockdown every flu season.

As time has gone on, I realize now that there are differences with Covid-19 that makes the comparison invalid.

Yes, I am admitting I was proven wrong, which is pretty amazing, if you ask me.

For the flu, there is a vaccine, which, even when it's not a "good" one, still produces immunity and lessens the severity of the disease.

Also, because of the flu vaccine, the spread is not as rampant due to the "herd immunity" effect.

Finally, of those that get severely ill and die, they fall into well defined groups, the very young and very old, or those with comorbid conditions.

In contrast, Covid-19 is extremely contagious, there is no herd immunity yet and it appears to not only kill the old, or those with co-morbid conditions, but also young, healthy people.

Not as many, granted, but enough to raise concerns.

The reason for the quarantine, which I am no more happy about than you are, is simply because the disease had completely overwhelmed our medical facilities.

I am unclear how people don't realize that.

Yes, when we are allowed to venture out again, there may well be a second wave, but the hope is it will be much smaller, so that doctors, nurses and hospitals are able to handle this surge.

That's it. That is the reason we are doing what we are doing, because in the end, it will save lives.

It sucks, I grant you, but it is necessary.

One final side note.

The outpouring of support for medical personnel is heart warming.

But, how long after this crisis is over will we once again hear about that "stupid doctor" or "sadistic nurse"?

I would really hope that people come to a better understanding now about the price those in medicine pay to do their jobs and maybe, just maybe, come away with a little more respect for them.

I don't expect it from everyone, but if it changes even a few people's opinion about the medical profession, maybe this pandemic will have at least a small silver lining.

And, for the love of God, if a non physician or scientist tries to share their "theory" about Covid-19, or anything medically related, for that matter-STAY SKEPTICAL!

Please like, share and comment and above all, stay safe!

Type your email address in the box and click the "create subscription" button. My list is completely spam free, and you can opt out at any time.

Read the original here:

Doctors and Medicine | Health Care Mythologies - ChicagoNow

Schumer on Trump briefing: We have a ‘quack medicine salesman’ on TV | TheHill – The Hill

Senate Minority Leader Charles SchumerCharles (Chuck) Ellis SchumerDoes the country need a coronavirus testing czar? Not really State and local governments are going broke People over politics on PPP funding MORE (D-N.Y.) knocked President TrumpDonald John TrumpWH officials discuss HHS secretary replacement following criticism of pandemic response: WSJ Pentagon leaders at impasse about next steps for Capt. Brett Crozier: report Trump forgoes WH press briefing for the first time since Easter weekend MORE on Friday for questioning if injecting disinfectant could help cure the coronavirus, urging the administration to focus on ramping up testing.

"We seemed to have a quack medicine salesman on television. He's talking about things like disinfectant in the lungs," Schumer said during an interview withNPR.

"We need real focus in the White House on what needs to be done. Instead of talking about disinfectant the president should be talking about how he's going to implement testing. Which every expert says is the quickest path to get us moving again," he added.

After a presentation from a Department of Homeland Security official about the effects of disinfectants and sunlight on the virus, Trump questioned if the same techniques could be used as treatments inside the body.

I see the disinfectant, where it knocks it out in a minute, Trump said. One minute. And is there a way we can do something like that, by injection inside or almost a cleaning?

The remarks drew immediate pushback from doctors who warned against injecting or consuming household disinfectants to treat the disease. Lysol manufacturer Reckitt Benckiser on Friday issued a warning that under no circumstance should its products be administered into the human body or be used as a treatment for the coronavirus.

The White House on Friday argued that the media had taken Trump's remarks "out of context."

Congress included $25 billion for testing as part of the $484 billion coronavirus relief bill that passed both the House and Senate this week. A provision in the bill would require states to come up with plans for how to use the resources and for a national strategy from the administration on how to help states with testing.

Lawmakers, including Republicans, have warned that the United States is still lagging behind in testing. Public health experts say widely available tests are critical if social distancing restrictions are going to be lifted.

Schumer was asked by NPR if he had secured a promise from Trump on including additional state and local government aid in the next coronavirus bill, something the president and Treasury Secretary Steven MnuchinSteven Terner MnuchinSunday shows preview: Leaders weigh in as some states reopen economies; Biden deliberates a running mate US airlines get another .5 billion in federal payroll support IRS announces deadline for SSI, VA recipients to quickly get stimulus payments for children MORE have signaled they are open to.

"Commitments from President Trump come and go but we can force it to happen in the[next coronavirus] bill and I think there is enough bipartisan support ... to get that done," Schumer said.

Originally posted here:

Schumer on Trump briefing: We have a 'quack medicine salesman' on TV | TheHill - The Hill

We must reimagine medicine in order to protect the most vulnerable from the coronavirus – Southgate News Herald

I have heart disease and I am scared. For years, doctor's visits and medication have kept me alive. However, now I am afraid if I go to the doctor, I will catch coronavirus and die. If I dont go, my heart disease could kill me.

I have had similar conversations with seriously ill Americans nationwide who have a host of diseases. They are legitimately at greater risk of dying prematurely if they are exposed to the coronavirus (COVID-19).

Terminally ill patients at the end of their life face an even direr dilemma. They need access to quality medical care to control pain, manage symptoms, reduce suffering and extend their quality of life. A shortage of hospice care could drive them to seek pain and symptom management in already crowded, infectious emergency departments, which would increase their risk of a premature, painful death.

As the nation grapples to contain and treat patients with COVID-19, were rethinking how we care for people with other serious or terminal illnesses. Given that patients risk contracting the coronavirus at health care facilities designed to save lives, medicine must adopt accordingly, by replacing brick-and-mortar medicine with the safe, effective use of telehealth.

Fortunately, late last month the Centers for Medicare & Medicaid Services (CMS) issued regulations to implement telehealth provisions in the Coronavirus Aid, Relief, and Economic Security Act (CARES Act) that significantly expand patients access to telehealth services. They will help ensure that vulnerable populations, including terminally ill patients, can seek care in the safety of their own homes while allowing quarantined doctors the ability to safely deliver quality health care.

CMS will now pay for more than 80 additional Medicare services when furnished via telehealth. They include emergency department visits, initial nursing facility and discharge visits, and home visits, which must be provided by a clinician that is allowed to provide telehealth.

Providers can evaluate Medicare beneficiaries, who have audio phones only, a vitally important option for low-tech seniors.

Licensed clinical social worker services, clinical psychologist services, physical therapy services, occupational therapist services, and speech language pathology services can receive payment for Medicare telehealth services.

Licensed practitioners, such as nurse practitioners and physician assistants, are allowed to order Medicaid home health services during the existence of the public health emergency for the COVID-19 pandemic.

Fortunately, telehealth recently has become a rapidly growing care vehicle in the United States. According to a 2018 JAMA study, annual telehealth visits have increased at an average annual compound growth rate of 52 percent from 2005 to 2017. A 2018 study by Deloitte indicates that 9 out of 10 physicians recognize the benefits of telehealth. Furthermore, two-thirds of physicians (66 percent) note that virtual care improves patient access and the majority (52 percent) recognizes it improves patient satisfaction.

Despite these promising statistics and the new CARES Act provisions, widespread adoption of telehealth will take some time. It will require buy-in by both health care providers and patients to restructure our health system and make telehealth a first-line approach, particularly during the threat of COVID-19.

If you are a patient with a terminal or serious illness or a caregiver to one, talk with your health care providers about whether telehealth could replace an in-person office visit. While it cannot substitute all office visits, it can be used in more instances than people realize. For example, clinicians are able to furnish patients with medical equipment so that they can monitor vital health indicators remotely and more effectively.

We know from experience that doctors are more likely to take the steps necessary to learn and then implement new approaches to medicine when patients request them. Given these facts, your self-advocacy for telehealth could benefit you, others, and ultimately contribute to more widespread and appropriate adoption.

Kim Callinan is president and CEO of Compassion & Choices, which works to improve care, expand options and empower everyone to chart their own end-of-life plans.

Excerpt from:

We must reimagine medicine in order to protect the most vulnerable from the coronavirus - Southgate News Herald

New cancer treatment that tracks and zaps tumors is coming to Stanford Medicine – Stanford Medical Center Report

A new technology aims to make tumors their own worst enemy in the fightagainst cancer -- and Stanford Medicine will be the first in the world toincorporate the treatment into the clinic.

The first generation of a machine using this technology --the X1, fromthe company RefleXion Medical -- harnesses positron emission tomography to deliverradiation that tracks a tumor in real time. This PET feedback allows the systemto send beams of radiation to destroy cancerous cells with heightenedprecision.

Researchers hope that this "biology-guided radiotherapy" will increase accuracy, safety and efficacy of cancer radiation treatment. Stanford physicians plan to test the X1 later this year through clinical trials at Stanford Hospital. Their first step will be to obtain approval by the Food and Drug Administration.

"To my knowledge, this machine is the first of its kind. It combinestwo technologies - one traditionallyused in cancer diagnostics, and one in therapeutics -- into a singletechnology," said DanielChang, MD, professor of radiation oncology, who will lead the clinicaltrial. "That's what makes this really unique."

Radiation therapy is often one of the primary tools used to treat cancer.But the therapy, which bombards tumors with high-energy particles that killcancer cells, comes with a downside: The beam of destructive particles does notdiscriminate between cancerous and non-cancerous cells, and healthy cells areoften damaged in the line of fire.

With this new technology, the PET scanner provides continuous feedback aboutthe location of a tumor, based on the tumor's emissions, even if the tumormoves as a patient breathes. This PET feedback allows doctors to continuetraining beams of radiation on cancerous cells, even as the tumor's locationshifts. With less risk of targeting healthy cells, doctors would be better ableto zero in on tumors with higher doses of radiation, executing more accurateand precise radiation therapy, Chang said.

Samuel Mazin, PhD, co-founder and chief technology officer of RefleXion Medical, thought up the idea for the new technology while he was a Stanford postdoctoral scholar. Stanford Medicine will be the first to conduct clinical trials with the new machine. Both components of the machine -- PET scans and radiation -- have well-established safety profiles.

Chang and his colleagues hope that the technology will help open new avenuesof research, such as clinical trials for patients with multiple tumors who mayotherwise not be eligible for radiation therapy. The technology also could leadto studies to develop novel and more sensitive PET tracers -- molecules thatreveal where cancer is in the body -- to assess the inherent biology of tumorsand their response to treatment.

"We're excited about this technology for many reasons," Chang said. "Itopens up new possibilities for treatment by allowing us to deliver radiationthat tracks the tumor with extreme precision in real time -- something we're notcurrently able to do."

Photo courtesy of RefleXion 2020. All rights reserved.

Continue reading here:

New cancer treatment that tracks and zaps tumors is coming to Stanford Medicine - Stanford Medical Center Report

COVID-19 Crisis Highlights The Risks Of Offshoring Pharmaceutical Manufacturing : Shots – Health News – NPR

Only 28% of the factories that make active ingredients for pharmaceuticals for the domestic market are located in the U.S., according to the Food and Drug Administration. Ariana Lindquist/Bloomberg via Getty Images hide caption

Only 28% of the factories that make active ingredients for pharmaceuticals for the domestic market are located in the U.S., according to the Food and Drug Administration.

The coronavirus pandemic has renewed concerns about the dependence of the United States on other countries for supplies of prescription drugs and ingredients.

The U.S. ignored the decline of domestic medical manufacturing and waited too long to seriously invest in the federal office designed to prepare for pandemics, Sen. Chris Coons, D-Del., said in an interview.

"We are now paying both in needless exposure by our front-line health workers and needless deaths for having not been better prepared for this," he says.

Nearly three-quarters of the active ingredient manufacturing facilities for medicines sold in the U.S. are located in other countries. Only 28% are domestic, according to Food and Drug Administration figures.

"Historically, the production of medicines for the U.S. population has been domestically based," Dr. Janet Woodcock, director of the FDA's Center for Drug Evaluation and Research, said in congressional testimony last October. "However, in recent decades, drug manufacturing has gradually moved out of the United States."

John McShane, a managing partner at the health care product consulting firm Validant, says he remembers when drug companies shifted much of their manufacturing overseas. "I was actually a victim of the move of APIs [active pharmaceutical ingredients] out of the country," he says.

He was a plant manager for Abbott Laboratories in the late '90s and returned to manufacturing in 2005 after a few years directing broader quality and validation programs at the company. But his return was short-lived.

"Abbott was shutting five plants, including the plant I used to work at, and outsourcing all of the production," he says. "The plant I used to run has been demolished. It's basically green space and asphalt now."

Abbott and AbbVie, a 2013 spinoff focused on pharmaceuticals, declined to comment.

Major companies have "mown down" the U.S. plants that made the key components of their drugs, McShane says. By his count, the last major API facility constructed in the U.S. was built almost 30 years ago.

He says companies moved manufacturing to locations with tax incentives, like Ireland, or countries that had cheaper labor and more lax environmental laws at the time, like India and China. Mergers and acquisitions in the pharmaceutical industry have also contributed to plant closures.

The danger of offshore supply chains

Coons says the United States should have been "concerned about the offshoring of most of the critical components of the supply chain that keeps us healthy and safe."

Today, the biggest suppliers of active pharmaceutical ingredients are India and China. The COVID-19 pandemic has spurred fears of shortages because of work interruptions and changes in export policies.

"If we have another global pandemic that leads the world to close borders and leads global supply chains to shatter or to break down, we are distinctly vulnerable because we are now so dependent upon globally integrated supply chains," Coons says, adding that these concerns also apply to other medical products, such as masks and ventilators.

Research shows a continuing decline in domestic drug manufacturing in recent years. The number of domestic API facilities registered with the FDA fell about 10% from 2013 through 2019, according to research by health economists Rena Conti and Ernst Berndt of Boston University and the Massachusetts Institute of Technology, respectively.

Rebuilding U.S. pharmaceutical manufacturing would take substantial investments and patience.

"To even get to 50% of our drugs being made in the U.S., it will take one to two decades and billions of dollars," McShane says. It would likely take government incentives to lure pharmaceutical giants back home.

Pharmaceutical Research and Manufacturers of America, the main trade group for the brand-name drug industry, "supports efforts to invest in" U.S. manufacturing, spokeswoman Holly Campbell said in statement. But, she said, there are advantages to having a globalized supply chain when emergencies strike because companies can shift their sourcing to unaffected facilities.

BARDA funding for research and development

The government has tools to spur the development and manufacturing of treatments and vaccines for COVID-19.

In March, Congress appropriated $3.5 billion for the Biomedical Advanced Research and Development Authority as part of legislation to respond to COVID-19. BARDA is part of the Department of Health and Human Services, and it was created in 2006 to speed up the nation's response to bioterrorism, emerging diseases and nuclear threats.

BARDA found itself in the spotlight this week, when Rick Bright, its director since 2016, said in a statement that he was removed from his post because he insisted that the government fund "safe and scientifically vetted solutions" to COVID-19 and not on "drugs, vaccines and other technologies that lack scientific merit." He said he pushed back against funding "potentially dangerous drugs promoted by those with political connections."

BARDA awards grants to fund research and development of experimental products in the hopes of eventually adding them to the National Strategic Stockpile. It also established a network of four domestic manufacturing facilities able "to address every day and emergency needs."

To combat COVID-19, BARDA announced it will support Johnson & Johnson and Moderna as they develop experimental vaccines against the virus, and will help Johnson & Johnson scale up manufacturing capabilities so it can make up to 300 million vaccine doses annually in the U.S.

What Congress gave BARDA last month as part of the CARES Act was more money than the office had been granted in the past. And Sen. Coons says past low funding levels are a problem.

"If you go back and look at the budgets of the last few years, we were not robustly investing in this work," Coons says. "And we should have been investing in things like the national stockpile, innovation in vaccines and in therapeutics and in ensuring our supply chain before there was a crisis."

Interest in preparing for a pandemic can be cyclical, says Dana Goldman, director of the Schaeffer Center for Health Policy & Economics at the University of Southern California.

"We're faced by a crisis," he says. "We realize we're unprepared. We are willing to spend a lot of money dealing with the situation. And then as the risks seem to wane and we change administrations, it's natural when you're trying to find other money for other priorities that you would see this type of cycle."

Visit link:

COVID-19 Crisis Highlights The Risks Of Offshoring Pharmaceutical Manufacturing : Shots - Health News - NPR

Nuclear Medicine Market: Find Out Essential Strategies to expand The Business and Also Check Working in 2020-2027 – Bandera County Courier

Market Research Inc.proclaims a new addition of comprehensive data to its extensive repository titled as, Nuclear Medicinemarket. This informative data has been scrutinized by using effective methodologies such as primary and secondary research techniques. This research report estimates the scale of the global Nuclear Medicine market over the upcoming year. The recent trends, tools, methodologies have been examined to get a better insight into the businesses.

Request a sample copy of this report @:

https://www.marketresearchinc.com/request-sample.php?id=16624

Top key players:

Cardinal Health, GE Healthcare, Curium, Bayer

This report provides a comprehensive analysis of(Market Size & Forecast, Different Demand Market by Region, Main Consumer Profile etc

Additionally, it throws light on different dynamic aspects of the businesses, which help to understand the framework of the businesses. The competitive landscape has been elaborated on the basis of profit margin, which helps to understand the competitors at domestic as well as global level.

Get a reasonable discount on this premium report @:

https://www.marketresearchinc.com/ask-for-discount.php?id=16624

The globalNuclear Medicinemarket has been studied by considering numerous attributes such as type, size, applications, and end-users. It includes investigations on the basis of current trends, historical records, and future prospects. This statistical data helps in making informed business decisions for the progress of the industries. For an effective and stronger business outlook, some significant case studies have been mentioned in this report.

Key Objectives of Nuclear Medicine Market Report:

Study of the annual revenues and market developments of the major players that supply Nuclear Medicine Analysis of the demand for Nuclear Medicine by component Assessment of future trends and growth of architecture in the Nuclear Medicine market Assessment of the Nuclear Medicine market with respect to the type of application Study of the market trends in various regions and countries, by component, of the Nuclear Medicine market Study of contracts and developments related to the Nuclear Medicine market by key players across different regions Finalization of overall market sizes by triangulating the supply-side data, which includes product developments, supply chain, and annual revenues of companies supplying Nuclear Medicine across the globe.

Further information:

https://www.marketresearchinc.com/enquiry-before-buying.php?id=16624

In this study, the years considered to estimate the size ofNuclear Medicineare as follows:

History Year: 2013-2018

Base Year: 2018

Estimated Year: 2019

Forecast Year 2020 to 2026.

About Us

Market Research Inc is farsighted in its view and covers massive ground in global research. Local or global, we keep a close check on both markets. Trends and concurrent assessments sometimes overlap and influence the other. When we say market intelligence, we mean a deep and well-informed insight into your products, market, marketing, competitors, and customers. Market research companies are leading the way in nurturing global thought leadership. We help your product/service become the best they can with our informed approach.

Contact Us

Market Research Inc

Kevin

51 Yerba Buena Lane, Ground Suite,

Inner Sunset San Francisco, CA 94103, USA

Call Us:+1 (628) 225-1818

Write Us@sales@marketresearchinc.com

https://www.marketresearchinc.com

Read more:

Nuclear Medicine Market: Find Out Essential Strategies to expand The Business and Also Check Working in 2020-2027 - Bandera County Courier

Reasons Why Long-term Faith on Editas Medicine, Inc. (EDIT) Could Pay Off Investors – The InvestChronicle

Lets start up with the current stock price of Editas Medicine, Inc. (EDIT), which is $25.01 to be very precise. The Stock rose vividly during the last session to $25.18 after opening rate of $24.05 while the lowest price it went was recorded $23.72 before closing at $24.05.

Editas Medicine, Inc. had a pretty Dodgy run when it comes to the market performance. The 1-year high price for the companys stock is recorded $34.37 on 01/15/20, with the lowest value was $14.01 for the same time period, recorded on 03/16/20.

Price records that include history of low and high prices in the period of 52 weeks can tell a lot about the stocks existing status and the future performance. Presently, Editas Medicine, Inc. shares are logging -27.23% during the 52-week period from high price, and 78.52% higher than the lowest price point for the same timeframe. The stocks price range for the 52-week period managed to maintain the performance between $14.01 and $34.37.

The companys shares, operating in the sector of healthcare managed to top a trading volume set approximately around 511835 for the day, which was evidently lower, when compared to the average daily volumes of the shares.

When it comes to the year-to-date metrics, the Editas Medicine, Inc. (EDIT) recorded performance in the market was -15.54%, having the revenues showcasing -11.78% on a quarterly basis in comparison with the same period year before. At the time of this writing, the total market value of the company is set at 1.33B, as it employees total of 208 workers.

According to the data provided on Barchart.com, the moving average of the company in the 100-day period was set at 25.92, with a change in the price was noted -5.27. In a similar fashion, Editas Medicine, Inc. posted a movement of -17.40% for the period of last 100 days, recording 919,438 in trading volumes.

Total Debt to Equity Ratio (D/E) can also provide valuable insight into the companys financial health and market status. The debt to equity ratio can be calculated by dividing the present total liabilities of a company by shareholders equity. Debt to Equity thus makes a valuable metrics that describes the debt, company is using in order to support assets, correlating with the value of shareholders equity. The total Debt to Equity ratio for EDIT is recording 0.00 at the time of this writing. In addition, long term Debt to Equity ratio is set at 0.00.

Raw Stochastic average of Editas Medicine, Inc. in the period of last 50 days is set at 82.64%. The result represents improvement in oppose to Raw Stochastic average for the period of the last 20 days, recording 82.05%. In the last 20 days, the companys Stochastic %K was 75.42% and its Stochastic %D was recorded 72.78%.

Bearing in mind the latest performance of Editas Medicine, Inc., several moving trends are noted. Year-to-date Price performance of the companys stock appears to be encouraging, given the fact the metric is recording -15.54%. Additionally, trading for the stock in the period of the last six months notably improved by 20.04%, alongside a downfall of -7.92% for the period of the last 12 months. The shares increased approximately by 14.60% in the 7-day charts and went down by 4.21% in the period of the last 30 days. Common stock shares were lifted by -11.78% during last recorded quarter.

See original here:

Reasons Why Long-term Faith on Editas Medicine, Inc. (EDIT) Could Pay Off Investors - The InvestChronicle

Healthy food: The unexpected medicine for COVID-19 and national security | TheHill – The Hill

Many in Washington are shouting follow the science. With the novel coronavirus, while there is significant confusion over effective medical treatments to prevent or cure COVID-19, one key piece of scientific evidence is beyond dispute: Those at the highest risk of extreme illness and death have underlying conditions such as obesity, diabetes, heart disease or high blood pressure. In some studies, up to 97 percent of people dying of COVID-19 have these conditions.

So, even if youre old, but not overweight, and do not have these conditions, your chances of survival are not bad. If youre young, are significantly overweight, and have these conditions, your chances of survival are much worse. In New York City, obesity was, overwhelmingly, a key risk factor for COVID-19 hospitalizations.

In the future, America will face another serious pandemic. And weve learned from COVID-19 that waiting for medical cures or preventative medicines takes too long and follows huge losses. Further, it is clear that we cant continue to shut down our economy and parts of our military, and overwhelm our health care system. We need a strategy.

From the perspectives of science and national security, the correct strategy is clear: All Americans need to eat healthier foods, lose weight, and get into good physical shape. All of this supports immunity. It is well established that obesity, diabetes, heart disease and high blood pressure are largely preventable with healthy diet and lifestyle. But healthy living is very difficult for Americans facing relentless advertising for processed and unhealthy foods, addictive (salt and sugar) ultra-processed food, entrenched and culturally-reinforced taste preferences, limited access to healthy foods for many Americans, public policy that subsidizes disease-promoting foods, sedentary behavior, and a health care and medical education system that still largely emphasizes sick care over prevention.

In the face of this mess, it can seem like the simplest course is to give up and rely on insulin, statins, blood pressure medicine and other palliative care to moderately extend lives. But the message from COVID-19 is that chronic medications dont ensure resilience against pandemic viruses. Only good physical health appears to have helped. It is, without exaggeration, a Darwinian moment for America. Americans must build personal immunity defenses through radical changes in diet and exercise, or risk getting sick and dying.

This means reducing or eliminating the seven deadly sins from our diet: processed foods, excess industrially-raised meats, refined sugar, dairy, refined grains, vegetable oils and excess sodium a revolution in personal behavior and national policy.

The personal changes are the most difficult. Americans are seeing that personal freedom can be sharply restricted during a national crisis. Perhaps now we can appreciate how much better it might be to have personal food choices redirected to avoid future serious illness or death.

The largely preventable chronic diseases that are associated with COVID-19 mortality not only make America extremely vulnerable to pandemics, they unnecessarily add hundreds of billions of dollars a year to our national medical costs and strain our health care resources. The question is how to change food habits without drastic restrictions on personal freedoms.

America could start by cutting the subsidies in our agricultural programs, specifically massive commodity support for dairy, sugar, wheat, corn and soybeans much of which is converted into livestock feed, refined oils, white flour and high fructose corn syrup. Americans are paying billions of dollars to subsidize the foods that open the door to diseases, paying trillions of dollars to support the chronic health care costs to cover diseases, and then losing trillions more in the economy when pandemics arrive.

COVID-19 is a wake-up call: America needs to refocus its agriculture towards producing cheaper and widely available organic fruits, vegetables, nuts, seeds, beans, legumes and herbs, with a massive expansion of specialty crop support, which currently represents a mere sliver of total Farm Bill spending. Similarly, USDAs unhealthy food guidance for SNAP and school meals is a disaster and dooms kids to be the victims of the COVID-19's of the future.

Within medical training, there needs to be a greater focus on nutritional and lifestyle medicine that prevents and reverses chronic disease, rather than the increasingly robotic name it, drug it and bill it style of medicine weve been evolving toward. As COVID-19 demonstrates, we can name it, but we cant drug it, so we should try to help our bodies resist it.

The lessons for the military have been sudden and harsh. Weakened troops and a carrier group shut down by the virus. It is urgent that Americas military leaders build the immunity levels of our troops through a radical change in diet. Were already struggling to recruit a healthy military because of the obesity epidemic. Now is the time for military leadership to simply mandate reduction of disease-causing food in favor of fresh, healthy food.

Were in a war and were losing because weve been fighting with poor defenses. Ironically, COVID-19 provides the secret for Americas farmers to turn their plowshares into swords.

Casey Means, M.D., is a practicing physician with a clinical focus on nutrition, nutrigenomics and disease prevention. She is an associate editor of the International Journal of Disease Prevention and Reversal, and is chief medical officer of the metabolic health company, Levels. Follow her on Instagram at @drcaseyskitchen.

Grady Means is a writer and former corporate strategy consultant. He served in the White House as a policy assistant to Vice President Nelson Rockefeller, where he chaired the Food Stamp Reform Task Force and served as White House oversight to the National Health Insurance Experiment. Follow him on Twitter @gradymeans1.

See the article here:

Healthy food: The unexpected medicine for COVID-19 and national security | TheHill - The Hill

University Of Maryland School Of Medicine Test Experimental Therapy To Prevent COVID-19 – CBS Baltimore

BALTIMORE (WJZ) Researchers at the University of Maryland School of Medicine announced Thursday they have started testing the effectiveness of hydroxychloroquine as a therapy to prevent infection and symptoms in individuals who have been exposed to COVID-19-positive individuals.

The research is part of a national study being conducted across the COVID-19 Therapeutics Accelerator.

The goal of the research is to see if hydroxychloroquine can prevent people from becoming infected with SARS-CoV-2 and getting COVID-19/coronavirus disease when taken by people who have had recent exposure to someone with the virus.

CORONAVIRUS COVERAGE:

The research is enrolling family members and frontline workers who have been exposed to individuals who have recently tested for the virus.

The study is being conducted remotely through online video calls and by answering questions via email.

Individuals who qualify for the randomized study will take either hydroxychloroquine or a placebo daily for 14 days.

Volunteers who participate in the study will be asked to take the medication, complete an online survey to assess their symptoms and collect a sample by swabbing the inside of their nose every day for 14 days. On Day 28 a final swab will be collected and a survey completed.

This study is a randomized, multi-center study, enrolling nationwide up to 2,000 men and women who meet the eligibility criteria. For more information click right here.

For the latest information on coronavirus go to theMaryland Health Departments websiteor call 211. You can find all of WJZs coverage oncoronavirus in Maryland here.

Follow this link:

University Of Maryland School Of Medicine Test Experimental Therapy To Prevent COVID-19 - CBS Baltimore

TUESDAYS WITH JORDIE: Laughter is the best medicine – Morning Bulletin

LAUGHTER really is the best medicine. No, it may not be a universal bandaid that we apply in the hopes it will solve all of our problems or be the miracle medicine that cures all of our ailments but it sure can make life a whole lot better.

I feel that looking at the bright and funny side of life keeps us young at heart and lightens our load of stress/emotions/problems we find ourselves lugging through life.

Let me make myself perfectly clear to ensure my words are not twisted: I am not downplaying, mocking or dismissing the heartache and devastation the virus has caused, not by any means. I have had many sleepless nights worrying about the people around me, thinking about how theyre coping and checking in with my people. It is when I feel I am struggling within myself that my coping mechanism takes over. It gives me something positive to hold on to and keep me grounded through these hellish times.

Ive found my humour has been hyperactive of late, running rampant with rhymes, riddles and rib-ticklers, even latching on to, dare I say it, dad jokes. Sometimes in moments of monumental stress and times of torrential inner turmoil, when I have felt almost every draining emotion under the sun, laughter brings me comfort.

Laughter is like my default coping mechanism. Nothing beats being able to laugh like no one is watching; the throw-your-head-back, clutch-onto-your-sore-tummy, tears-streaming-down-your-face and uncontrollable-fits-of-giggles-flowing-from-deep-within kind of laughter, snorts and all. Thats the kind that seeps into the soul and makes everything okay, even just for a moment. It doesnt have to be pretty or airbrushed, it can simply take you wherever you let it and the people you can laugh like this with are the people who truly belong in your life.

Laughter brings me to a peaceful place and I love to share that with others, even if it is at my expense. It possesses the power to turn any pent-up pain or negative emotions into positive forces and it brings people together. I think humour has often been the underdog in our list of necessities to get through life because it has never been taken seriously. Maybe this is where we truly underestimate it because humour has always been there to bundle me up in a big hug and carry me through tough times.

It has been really nice to see communities all over the world band together, support each other and use humour to cheer each other up. There are some excellent examples of this over social media, one of my favourites being the Bin Isolation Outing group on Facebook. All age groups across all communities around the world have joined and have bin taking part in so many creative ways, each post carefully crafted with purpose: to make others smile and laugh, which all jokes aside, is so incredibly special!

I take my hat off to humour and the happiness it can bring to the world around us.

Continued here:

TUESDAYS WITH JORDIE: Laughter is the best medicine - Morning Bulletin

Jewish Ethics in Medicine | The Jewish – The Jewish News

By Jill Gutmann, Special to the Jewish News

Chloroquine, the anti-malarial drug, has been in the news as a possible cure for COVID-19. The efficacy of this drug is unproven. Only one promising study out of France has suggested that the drug, in combination with an antibiotic, might prove effective. Later studies have not confirmed these findings and, in fact, have shown no statistically significant change between current treatments and the drug combination. So we should not count our chickens before they hatch. In fact, there has actually been harm done through suggesting this is a cure: Two people used the drug to treat themselves, with one dying and another in serious condition. Physicians are hoarding the drugs, and people who need the pharmaceuticals for known treatments are not able to get it.

In this pandemic that is unsettling the world, all hands are on deck to find a cure and a vaccine. The question is whether Jewish people can use experimental treatments. To answer this, one must first understand the Jewish view of medicine.

Be fruitful and multiply: fill the Earth and subdue it, and rule over the fish of the sea, the birds of the sky and every living thing that moves on the Earth (Genesis 1:28). The obligation to subdue it, and rule over [it] empowers us to seek medical assistance (The Lonely Man of Faith by R. Soloveitchik).

In fact, the Talmud goes further, describing the need to seek medical intervention: In danger, one must not rely on miracle (BT, Kiddushin 39b). The implication of these warnings is clear that one must do whatever is available and possible to try to intervene with known medicine and treatments. There is an inherent duty as a Jew to seek medical attention that is preventative and curative.

Rabbinic scholars divide treatment into two categories: those that are refuah bedukah (treatment where efficacy is proven) and refuah sheeinah bedukah (treatment where efficacy is unproven). Proven treatments must always be used. For example, a person with strep throat must take appropriate medicine to cure strep throat.

On the other hand, experimental treatments are not required to be used, as there is no known efficacy. The rabbis of the Talmud and later authorities believe a person should not intentionally place himself in danger; but if a person is going to die, the calculus shifts. In this case, experimental treatments are permissible but not mandatory.

Patients must be informed of the risks and benefits in order to make an informed decision on whether to partake in experimental treatments.

In these trying times, we might hope for the miracle of a cure, but we must be careful not to cause harm through rash action. This is going to be a marathon and not a sprint for our physicians, nurses and researchers. Our Jewish values direct us to put our trust in researchers and scientists following best practices regarding experimental treatments, with the hope of finding a treatment that is refuah bedukah.

Jill Abromowitz Gutmann is a Jewish bioethicist, Rebbetzin of Temple Kol Ami and mom to four daughters.She has worked as an ethicist for the Centers for Disease Control and Prevention, the IsraeliMinistry of Health and the Jewish Hospital in Cincinnati, Ohio, and has taughtJewish Ethics for Melton International, the Florence Melton School of Metro Detroit and of Auckland, New Zealand.

More here:

Jewish Ethics in Medicine | The Jewish - The Jewish News

Strongman Medicine: The Countries That Still Claim to Have No Coronavirus Cases. – Slate

Photo illustration by Lisa Larson-Walker. Photo by KCNA/Reuters.

Welcome toStrongman Medicine, a weekly column looking at how governments around the world are taking advantage of the pandemic for censorship, surveillance, and repression. Slate is making its coronavirus coverage free for all readers. Subscribe to support our journalism.Start your free trial.

After weeks of downplaying the crisis, Russia has shifted into full lockdown mode as the number of cases in the country has exceeded 10,000. There are numerous media reports of police using their new authority to detain and harass citizens. In one egregious case, a doctor who had criticized the governments response to the crisis was detained while attempting to deliver medical supplies. Anastasia Vasilyeva of the Doctors Alliance, a group backed by opposition leader Aleksei Navalny, was arrested on April 2 along with several colleagues while bringing masks and other equipment to the Novgorod region as part of a nationwide tour to assess the preparedness of health facilities. She had previously posted videos on YouTube and given media interviews criticizing the governments response. Vasilyeva was charged with violating the governments quarantine restrictions. According to Amnesty International, she was choked and punched in the abdomen while being detained in a police station overnight.

New legislation signed by President Vladimir Putin this week punishes spreading false information with up to five years in prison and violating quarantine orders with up to sevenboth rules that are rife with opportunities for abuse.

An outspoken property tycoon and member of the ruling Communist Party has been put under investigation for publishing an essay that criticized the Chinese governments handling of COVID-19.* Ren Zhiqiang, who has not been since in public since mid-March, when he posted the essay, said the virus had revealed a crisis of government and referred to Chairman Xi Jinping as a clown with no clothes on who was still determined to play emperor. Ren, the former head of a state-owned company and son of a prominent official, has courted controversy before. His party membership was suspended for a year in 2016 after he criticized Xis handling of the state media.

Human Rights Watch this week criticized the government of Uganda for a police raid on a homeless shelter serving LGBTQ people in Kampala. Like many other countries, Uganda is currently prohibiting public gatherings of more than 10 people, but that does not apply to a residence or shelter. Nonetheless, 20 people in the shelter were sent to prison, likely putting them at greater risk for the disease and ensuring they were unable to meet with lawyers because of the lockdown. Homosexuality is illegal in Uganda, and while the infamous 2014 law that would have punished it with life in prison has been annulled, discrimination is still rampant. Police searched the shelter for evidence of homosexuality but eventually decided to charge the residents with coronavirus-related offenses.

Cambodias government passed a new emergency law that human rights groups say could allow autocratic Prime Minister Hun Sen to run the country by fiat. The law creates new crimes, punishable by multiple years of jail time, of obstructing operations during a state of emergency and not respecting measures ordered by the government to address the emergencyboth of which could easily be abused to punish government critics. The country has already arrested more than a dozen people for spreading information about the disease outbreak. Hun Sen, who even before the outbreak had been criticized for clamping down on the media under the guise of fighting fake news, is one of a number of leaders, including Hungarys Viktor Orbn and the Philippines Rodrigo Duterte, using the coronavirus as pretext to assume sweeping emergency powers.

COVID-19 has touched nearly every corner of the globe, but there are still a handful of countries reporting no cases. Most are small island nations where travel bans have been effective at keeping cases out. Other examples are more suspicious.

North Korea still says it has no cases, a claim that U.S. officials describe as impossible. The Hermit Kingdoms isolation may work to its advantage here, but given the level of cross-border trade with China, it does seem very unlikely that there are no cases at all. U.S. President Donald Trump sent a letter to Kim Jong-un in March offering assistance in fighting the disease and told reporters that North Korea is going through something, though its not clear quite what he was referring to.

Tajikistan, which borders hard-hit Iran, also claims to not have a single case, though it has quarantined more than 6,000 people who traveled abroad. The virus could wreak havoc in a poor country with a weak health system, yet dictator Emomali Rahmon has taken almost no steps to institute social distancing, and held a massive public celebration for the Nowruz holiday in late March.

Then theres Turkmenistan, where even discussing the coronavirus is banned; where President Gurbanguly Berdymukhammedov, a former dentist and health minister, has suggested that his recently published book on herbal remedies could help COVID patients; and where a 7,000-person bike ride was held on Tuesday to celebrate World Health Day.*

Maybe these countries really are just extremely lucky.

Correction, April 10, 2020: This piece originally misidentified the Chinese Communist Party as the Community Party. This piece also misstated the date when Turkmenistan held a 7,000-person bike ride to celebrate World Health Day. It was Tuesday, April 7, not April 8.

Read the original:

Strongman Medicine: The Countries That Still Claim to Have No Coronavirus Cases. - Slate

How UW Medicine, small business and Amazon combined to airlift key testing kits from China in coronavirus fight – Seattle Times

With his car keys, Geoff Baird attacked a box that had justcomefrom China to the parking lot at a UW Medicine office in Seattles Northgate neighborhood. Baird, who manages UW Medicines laboratories, ripped greedily into the cardboard.

Tubes and swabs! he called out, holding a vial with hot-pink liquid sloshing inside.

Amazon workers unloaded another 83 boxes filled with critical COVID-19 testing kits. Baird rushed to his lab to verify their quality.

Hopefully its not Q-tips and Kool Aid, he said.

The unboxing was a climactic scene in a frenzied, weekslong global logistics project involving Anita Nadelson, a Seattle businesswoman who typically imports items like dry erase boards; a mystery doctor who is a brother-in-law of the boss of Strawberry, a Chinese saleswoman and business contact of Nadelson; and Jeff Wilke, one of the most powerful executives at Amazon.

Their story and the international cast of characters brought together for this public-health mission illustrates the lengths authorities and scientistsare willing to take to increasetesting, perhaps the most important metric as officials consider lifting social- and physical-distancing restrictions.

If you loosen up before you have the ability to really ramp up your testing and case finding and contact tracing, this epidemic can rebound quite vigorously, said Dr. Jeff Duchin, health officer at Public Health Seattle & King County.

But without test kits, laboratories cant produce more results.

For weeks, Washington state has been short on testing kits containing nasopharyngeal (NP) swabs anda liquid that preserves specimens for diagnostic testing.

Baird, the interim chair of the University of Washington Department of Laboratory Medicine, said the UW Medicine Virology Lab can process some 5,000 specimens a day. On Tuesday, the lab processed just 1,953, according to the labs Twitter account.

We can do more testing than what we are doing, Baird said, adding that in recent weeks he had been barraged with requests from health officials and hospitals for testing kits. Its an important bottleneck.

The solution he sought underscores just how fragile the medical supply chain remains, how competitive the market for has become.

The nationwide shortages of testing materials fall into two main categories: the supplies needed to take a sample and transport it to the laboratory, and the items needed for analysis.

Its like everyone is trying to bake a cake at the same time, said Dr. Yvonne Maldonado, a professor of health research and policy at Stanford Medicine. There are shortages of everything in the recipes.

NP swabs thin sticks with furry tips that medical professionals stick up a persons nose until they can scrape the palate where the nasal and oral cavities meet are running low nationwide.

Once the sample is taken, its placed into a vial with a solution called viral transport media, meant to keep the specimen from drying and disintegrating.

Right now, orders for transport media are backlogged. To make up for the shortage, some labs have been producing their own solution. Nonetheless, many hospitals are still lacking.

Even though anyone can get tested, people who have test kits are essentially rationing them to patients with the most severe symptoms, said Cassie Sauer of the Washington State Hospital Association.

On the analysis side, a chemicals shortage has plagued testing nationally for about a month, said Omai Garner, the lab director of clinical microbiology for UCLA Health.

It has been a constant struggle, a constant negotiation with vendors, said Garner, whose lab performs about 800 COVID-19 tests a day.

Under the initial test procedure approved by the Centers for Disease Control and Prevention (CDC), labs needed a particular chemical to extract RNA from the virus, Garner said. Supplies quickly dwindled.

The federal governments approval of more types of tests partially closed that gap. Now, labs depend on commercial-testing manufacturers to provide kits with a proprietary assortment of solutions or chemicals, collectively known as reagents. The manufacturers themselves are now running short on reagents. Thats slowed the production of lab test kits.

If companies dont have enough manufacturing capabilities to meet the need, then that has to be addressed at the federal level, Garner said.

In Washington state, hospitals have mostly had to fend for themselves in the marketplace for testing supplies, Sauer said, although the state has been procuring some materials. Theres no central way to monitor facilities testing inventory in the state.

Shortages have been nearly constant. Less than a week after the COVID-19 outbreak was first identified at a King County nursing facility, local health officials already were asking for testing kits.

Public Health Seattle & King County on March 4 sent state officials a list of supplies it needed for the Life Care Center of Kirkland staff, asking for 200 nasal and throat swabs, and the same number of test tubes to transport the specimens,according to records reviewed by The Seattle Times.

During roughly two weeks in March, government agencies and healthcare organizations submitted at least 45 requests for swabs or testing supplies, according to a Times review of Washington state Military Department request logs.

The path toward new swab supplies began with a simple gesture from a friend.

Been asking my factories in China to try to get N95 masks, Nadelson, co-owner of a design firm, texted Baird on March 16. A supplier had offered 30. Is that worth having sent, or wait for more?

Better to wait, Baird wrote. N95 respirators are needed by the thousands.

The real shortage nationally is nasopharyngeal swabs, he told Nadelson, launching her on a quest.

Nadelson began by scrolling through Alibaba, the online Chinese commerce giant, then contacting and whittling down the factories she thought could provide equipment whiletexting Baird for technical advice.

We work with 25 factories in China, Nadelson said of her company, Three By Three Seattle. I know how to get anything made.

She soon settled on the most promising manufacturing prospect, and asked a trusted sales contact known to Nadelson as Strawberry, who works nearby in Shenzhen, to check out the plant.

Strawberry collected sample test kits, but struggled to ship the liquid. With air freight disrupted, it would take weeks for samples to arrive in Seattle.

Then, Strawberry hit on a promising lead. Her boss had a family connection to a doctor in Hubei, the Chinese province hardest hit by COVID-19. The doctor, whose identity is not known to Nadelson or Baird, could place an order for swabs with the factory, which also supplied health workers in Wuhan. Were they interested?

Geoff decided early on he was going to take this big leap of faith, Nadelson said. They put in an order for 80,000 kits for UW Medicine, hoping to distribute the kits throughout the state, and Seattle Childrens added to their order another 20,000 kits.

Nadelson fronted $125,000 later to be reimbursed by UW Medicine.

But layers of red tape, customs regulation and international shipping logistics problems complicated by COVID-19s impact on worldwide freight and supply chains remained troublesome, and Baird wanted the tests stateside, and fast.

He fired off an email to Jeff Wilke, CEO of Worldwide Consumer at Amazon, whose contact information Baird had from a mutual connection.

Amazon has made a humanitarian and a public relations push to source and deliver medical supplies in COVID-19s wake.

On the afternoon of March 30, Baird asked if we had any resources in China that could fly them here in a hurry, Wilke said in a statement to The Seattle Times. Amazon found space on a chartered flight last Saturday.

Baird obsessively tracked the flights progress to Seattle.

It could be the great Shanghai airlift of 2020, Baird said, while the supplies were airborne. Or, I could have bought 100 grand in packing peanuts.

After the jubilant unpacking and back at the UW Medicine Virology laboratory, the mood shifted. A crestfallen Baird met in the laboratory lobby with Dr. Jason Love, a pathologist for MultiCare hospitals in the Tacoma area.

Instead of NP swabs, the Chinese factory had sent nasal swabs, for use in the nostrils.

Cotton, Baird said, as if it were a dirty word, fearing the swabs contained material not suited for COVID-19 testing.

Im disappointed, Love said, trying to figure out how he could stretch strained supplies further.

But spirits for both men lifted on Monday amid new developments.

Baird determined both the nasal swabs, which were actually polyester, and the transport media were acceptable for COVID-19 testing.

Its going to work for us and help a lot of people, Baird said.

And a new preliminary preprint study of about 500 patients at the Everett Clinic, who sampled themselves inside their vehicles, showed that nasal swabs could be effective.

Sample collection for new coronavirus tests with nasal swabs were nearly as accurate as sampling as the NP swabs, according to test results from a study published Monday on the preprint server medRxiv, which has yet to be peer-reviewed. The preliminary study did not examine asymptomatic patients.

The Food and Drug Administration added the nasal swab sampling for COVID-19 to its clinical guidelines on March 23 and the CDC followedMarch 24.

Dr. Yuan-Po Tu, the lead author of the preprint, said sampling with nasal swabs could help preserve key personal protective equipment. Medical professionals must wear protective equipment when administering NP swabs because patients often cough or sneeze during the more invasive procedure.

By having the patient collect the specimen themselves, all you need is a surgical paper mask and you just stand back and you watch, Tu said.

Michael Teng, an associate professor in internal medicine at the University of South Florida who was not involved in the preliminary report, said its findings track with similar studies of other respiratory viruses, and added that nasal swabs could be less effective at detecting the virus in people without symptoms, an important consideration as public health strategies increasingly rely on broader testing.

Baird said there is no perfect sampling method. All tests have false negative rates because the virus lives in the lungs primarily.

Also on Monday, experts began to suggest COVID-19 cases may have crested in volume and started to trend downward. That eases demand on test kits.

Love on Wednesday said he was feeling more optimistic about swab supply because his lab was no longer maxing out its machinerys capability. COVID-19 testing needs have fallen off at his hospitals significantly.

Duchin said health officials would take 20,000 of the swabs procured by Baird and Nadelson, saying they would fill gaps in supply at places like shelters and long-term care facilities.

Also on Monday, a package arrived that buoyed Bairds mood. It included samples of NP swabs from one of the first factories Nadelson contacted in March.

Theyre perfect, Baird said. I think weve opened up a supply line.

Staff reporters Ryan Blethen and Daniel Gilbert contributed to this report.

Follow this link:

How UW Medicine, small business and Amazon combined to airlift key testing kits from China in coronavirus fight - Seattle Times

As India Exports Hydroxychloroquine, Punjab Faces Acute Shortage Of The Medicine Due To Panic Buying – Outlook India

Ever since rumours started floating around that Hydroxychloroquine could help improve immunity against Covid-19, Patients of joint pain and malaria diseases which it actually cures -- are not getting enough tablets of the medicine in Punjab, due to acute shortage at stores and short supply from the manufacturing companies.

Chemist associations and the drug control department have admitted that the medicine has been completely sold out at majority of medical stores as people bought it in bulk, believing that it is a magic pill to protect them against Coronavirus.

I have been getting calls from chemists from all over Punjab for its supply but I am not able to help them. Most of the shops have run out of the medicine. The lockdown has also severely hit the supply chain across the state, which is causing a lot of trouble, said Surinder Duggal, President, Punjab Chemist Association.

Duggal says that Zirakpur city, which supplies 90 per cent of the medicines in Punjab, doesnt have enough labourers to load and unload the medicines. Besides, the stock available with the whole-sellers is very limited, he added.

Pradeep Mattu, Drug Controller of Punjab, blames panic buying for the shortage. By the time government imposed restrictions on its sale, people had already hoarded it like anything. If one person buys 200 tablets without any ailment, thinking that it will improve his immunity against COVID-19, scarcity is natural, Mattu said.

The union government imposed restrictions on the sale of Hydroxychloroquine onMarch 25, 2020, when it realised that the medicine was overselling due to the misconception that it can improve immunity against Coronavirus. The government immediately regulated its sale with a provision that no chemist can sell it without a doctors prescription.

After reports that Hydroxychloroquine showed positive effects on COVID-19 infected patients in France, and a consequent tweet from the US President, calling it a game-changer, the news went viral on social media. It is a generic drug which was available over the counter, so people have gone for crazy buying it, said T.V. Narayana, National President, Indian Pharmaceutical Association.

He said that if an individual takes this medicine, thinking that it improves immunity, he or she is completely mistaken as this can cause adverse side-effects.

The Centre has already assured that India has enough raw material and manufacturing capacities to meet the domestic demand for Hydroxychloroquine. The United States has requested India to export Hydroxychloroquine to treat COVID 19 patients in the country. The Centre has reportedly decided to export the medicine to friendly countries to fulfil their needs.

Read more here:

As India Exports Hydroxychloroquine, Punjab Faces Acute Shortage Of The Medicine Due To Panic Buying - Outlook India

Clinical trial launches to evaluate antimalarial drugs for COVID-19 treatment – Washington University School of Medicine in St. Louis

Visit the News Hub

Cigna/Express Scripts provided the drugs; open to COVID-19 patients at Barnes-Jewish Hospital

Antimalarial drug, hydroxychloroquine is one of the drugs being tested in COVID-19 patients.

Washington University School of Medicine in St. Louis is launching a clinical trial for patients hospitalized with COVID-19 at Barnes-Jewish Hospital. The trial will investigate the effectiveness of different combinations of the antimalarial drugs chloroquine and hydroxychloroquine and the antibiotic azithromycin in treating ill patients infected with the novel coronavirus.

Express Scripts, a Cigna company, has donated these medications to the School of Medicine in an effort to accelerate research for a COVID-19 treatment.

The Food and Drug Administration recently gave emergency approval for hospitals across the country to use the two antimalarial drugs to treat severe cases of COVID-19. However, this treatment strategy remains unproven.

There have been only a few small studies that have evaluated chloroquine and hydroxychloroquine in patients with COVID-19 infection, and the results are unclear, said infectious disease specialist Rachel M. Presti, MD, PhD, an associate professor of medicine who is co-leading the trial. We need additional trials to understand whether the drugs are effective. We are pleased to be able to offer this clinical trial to patients with COVID-19 in the St. Louis region. Were grateful to Cigna and Express Scripts for the generous donation of these drugs. Our goal is to determine if any of these medications, alone or in combination, decrease the severity or duration of respiratory symptoms.

Respiratory symptoms of COVID-19 include dry cough and shortness of breath. According to the Centers for Disease Control and Prevention (CDC), people should seek medical attention if symptoms progress to difficulty breathing, persistent pain or pressure in the chest, confusion or inability to arouse, and bluish lips or face. This trial is only for patients who are ill enough to be admitted to the hospital. The researchers plan to enroll 500 patients over the course of the study.

To accelerate research for a COVID-19 treatment, we are supporting one of the top medical schools in the country in their efforts to quickly implement a clinical trial, said Steve Miller, MD, chief clinical officer, Cigna. This trial will help to establish whether these drugs are effective and, if so, to determine the optimal doses to help minimize the symptoms of COVID-19.

Patients with confirmed cases of COVID-19 who choose to enroll in the trial will be randomly assigned to one of four treatment groups: One group will receive chloroquine alone; a second group will receive hydroxychloroquine alone; a third group will receive chloroquine and azithromycin; and a fourth group will receive hydroxychloroquine and azithromycin.

All three medications are generic formulations long used to treat other conditions. Chloroquine and hydroxychloroquine are used for the prevention and treatment of malaria. They also are prescribed, often in combination with other medications, for autoimmune disorders, such as lupus and rheumatoid arthritis. Azithromycin is an antibiotic used to treat many types of infections caused by bacteria, including respiratory, skin, ear and eye infections.

In past research, chloroquine and hydroxychloroquine showed some effectiveness against related coronaviruses MERS and SARS. All three drugs have side effects that are well-known. Hydroxychloroquine and chloroquine in particular can cause heart rhythm problems. Presti said patients will be carefully screened for abnormal heart rhythms before being administered these drugs. These drugs also have been associated with vision loss and psychiatric side effects, but Presti said such effects are not typically seen in short-term use of the drugs.

Presti is co-leading this clinical trial with Jane OHalloran, MD, PhD, an assistant professor of medicine at Washington University. All COVID-19 related research is coordinated by the COVID task force appointed by David H. Perlmutter, MD, executive vice chancellor for medical affairs and the George and Carol Bauer Dean of the School of Medicine. The task force is led by Jeffrey Milbrandt, MD, PhD, the James S. McDonnell Professor and head of the Department of Genetics; William G. Powderly, MD, the J. William Campbell Professor of Medicine and director of the Institute for Clinical and Translational Sciences (ICTS); and Sean Whelan, PhD, the Marvin A. Brennecke Distinguished Professor and head of the Department of Molecular Microbiology.

The clinical and translational research related to COVID-19 at the School of Medicine harnesses a breadth of resources of the ICTS, which were deployed to bring this study forward in less than two weeks. Washington Universitys ICTS is part of the Clinical and Translational Science Award (CTSA) nationwide network funded by the National Center for Advancing Translational Sciences (NCATS).

This work is supported by The Foundation for Barnes-Jewish Hospital; and the National Center for Advancing Translational Sciences (NCATS) of the National Institutes of Health (NIH), grant number UL1TR002345.

Washington University School of Medicines 1,500 faculty physicians also are the medical staff of Barnes-Jewish and St. Louis Childrens hospitals. The School of Medicine is a leader in medical research, teaching and patient care, ranking among the top 10 medical schools in the nation by U.S. News & World Report. Through its affiliations with Barnes-Jewish and St. Louis Childrens hospitals, the School of Medicine is linked to BJC HealthCare.

See the original post:

Clinical trial launches to evaluate antimalarial drugs for COVID-19 treatment - Washington University School of Medicine in St. Louis

Stanford researchers devise treatment that relieved depression in 90% of participants in small study – Stanford Medical Center Report

There was a constant chattering in my brain: It was my own voice talking about depression, agony, hopelessness, she said. I told my husband, Im going down and Im heading toward suicide. There seemed to be no other option.

Lehmans psychiatrist had heard of the SAINT study and referred her to Stanford. After researchers pinpointed the spot in her brain that would benefit from stimulation, Lehman underwent the therapy.

By the third round, the chatter started to ease, she said. By lunch, I could look my husband in the eye. With each session, the chatter got less and less until it was completely quiet.

That was the most peace theres been in my brain since I was 16 and started down the path to bipolar disorder.

In transcranial magnetic stimulation, electric currents from a magnetic coil placed on the scalp excite a region of the brain implicated in depression. The treatment, as approved by the FDA, requires six weeks of once-daily sessions. Only about half of patients who undergo this treatment improve, and only about a third experience remission from depression.

Stanford researchers hypothesized that some modifications to transcranial magnetic stimulation could improve its effectiveness. Studies had suggested that a stronger dose, of 1,800 pulses per session instead of 600, would be more effective. The researchers were cautiously optimistic of the safety of the treatment, as that dose of stimulation had been used without harm in other forms of brain stimulation for neurological disorders, such as Parkinsons disease.

Other studies suggested that accelerating the treatment would help relieve patients depression more rapidly. With SAINT, study participants underwent 10 sessions per day of 10-minute treatments, with 50-minute breaks in between. After a day of therapy, Lehmans mood score indicated she was no longer depressed; it took up to five days for other participants. On average, three days of the therapy were enough for participants to have relief from depression.

The less treatment-resistant participants are, the longer the treatment lasts, said postdoctoral scholarEleanor Cole, PhD, a lead author of the study.

The researchers also conjectured that targeting the stimulation more precisely would improve the treatments effectiveness. In transcranial magnetic stimulation, the treatment is aimed at the location where most peoples dorsolateral prefrontal cortex lies. This region regulates executive functions, such as selecting appropriate memories and inhibiting inappropriate responses.

For SAINT, the researchers used magnetic-resonance imaging of brain activity to locate not only the dorsolateral prefrontal cortex, but a particular subregion within it. They pinpointed the subregion in each participant that has a relationship with the subgenual cingulate, a part of brain thatis overactive in people experiencing depression.

In people who are depressed, the connection between the two regions is weak, and the subgenual cingulate becomes overactive, said Keith Sudheimer, PhD, clinical assistant professor of psychiatry and a senior author of the study. Stimulating the subregion of the dorsolateral prefrontal cortex reduces activity in the subgenual cingulate, he said.

To test safety, the researchers evaluated the participants cognitive function before and after treatment. They found no negative side effects; in fact, they discovered that the participants ability to switch between mental tasks and to solve problems had improved a typical outcome for people who are no longer depressed.

One month after the therapy, 60% of participants were still in remission from depression. Follow-up studies are underway to determine the duration of the antidepressant effects.

The researchers plan to study the effectiveness of SAINT on other conditions, such as obsessive-compulsive disorder, addiction and autism spectrum disorders.

The depression Lehman woke up to almost two years ago was the worst episode she had ever experienced. Today, she said, she is happy and calm.

Since undergoing SAINT treatment, she has completed a bachelors degree at the University of California-Santa Barbara; she had dropped out as a young woman when her bipolar symptoms overwhelmed her studies.

I used to cry over the slightest thing, she said. But when bad things happen now, Im just resilient and stable. Im in a much more peaceful state of mind, able to enjoy the positive things in life with the energy to get things done.

Graduate student Katy Stimpson and Brandon Bentzley, MD, PhD, a medical fellow in psychiatry and behavioral sciences, are also lead authors.

Other Stanford co-authors are former lab manager MerveGulser; graduate students Kirsten Cherian, Elizabeth Choi, HaleyAaron and AustinGuerra; Flint Espil, PhD, clinical assistant professor of psychiatry and behavioral sciences; research coordinators Claudia Tischler, Romina Nejad and Heather Pankow; medical student Jaspreet Pannu; postdoctoral scholars Xiaoqian Xiao, PhD, James Bishop, PhD, John Coetzee, PhD, and Angela Phillips, PhD; Hugh Solvason, MD, PhD, clinical professor of psychiatry and behavioral sciences; research manager JessicaHawkins; BooilJo, PhD, associate professor of psychiatry and behavioral sciences; Kristin Raj, MD, clinical assistant professor of psychiatry and behavioral sciences; CharlesDeBattista, MD, professor of psychiatry and behavioral sciences; JenniferKeller, PhD, clinical associate professor of psychiatry and behavioral sciences; and AlanSchatzberg, MD, professor of psychiatry and behavioral sciences.

The research was supported byCharles R. Schwab, the Marshall and Dee Ann Payne Fund,the Lehman Family Neuromodulation Research Fund, the Still Charitable Fund,the Avy L. and Robert L. Miller Foundation, a Stanford Psychiatry Chairmans Small Grant, the Stanford CNI Innovation Award, the National Institutes of Health (grants T32035165 and UL1TR001085), the Stanford Medical Scholars Research Scholarship, the NARSAD Young Investigator Awardand the Gordie Brookstone Fund.

Go here to read the rest:

Stanford researchers devise treatment that relieved depression in 90% of participants in small study - Stanford Medical Center Report

Dr. Trump’s medicine show: Why is he pushing an unproven drug? Follow the money – Salon

Donald Trump only cares about Donald Trump. He doesn't care about you or the country.He only cares about exploiting this crisis to bail out his business and to get himself re-elected, thereby shielding himself from a series of indictments thatsurely awaithim if he loses. The sooner we embrace this easily-observable fact about Trump, the better equipped we'll be to evaluate his decisions during these overlapping health and financial calamities.

The "Trump is all about Trump" maxim goes a long way to explaining his obsessive beer-funneling of a malaria drug called hydroxychloroquine down the gullets of COVID-19 victims.

So far, there have been two public appearances by Trump that have genuinely rattled me. There was his seemingly endless and deeply disturbing CPAC address in early March of 2019: a herky-jerky, stream-of-consciousness creepshow a Willy Wonka ride into the dark, twisted world of Trump's increasingly haunted and demented brain. I've never seen a presidential speech more harrowing and unnerving than that one until the Saturday, April 4, episode of the Trump Show.

There was one particular chunk of Saturday's fact-free campaign commercial, aired across all the major networks, that rivaled anything from his CPAC remarks of more than a year ago. About an hour into Trump's delusional attempt to frame himself as competent, the president craned his head forward and, using a high-pitched whisper-voice, begged COVID-19 victims to take hydroxychloroquine as if his life depended on it.

It was one of the most bizarre moments not just in the history of this wobbly wacky-shack presidency, but in the entire history of presidential politics. Trump's pupils were dilated, punctuating his bugged-out eyesand, as usual, his hands were flapping back and forth as if to squeeze an invisible accordion to the tune of a dissonant polka played at half speed. The sound of his voice could best be compared with a greasy Aqualung weirdo in an unmarked van coaxing children into the back with the promise of candy bars if they acquiesce.

Advertisement:

"What do you have to lose?" the president rationalized in that breathless tone, "I'll say it again: What do you have to lose? Take it. I really think they should take it. But it's their choice and it's their doctor's choice, or the doctors in the hospital. But hydroxychloroquine try it, if you'd like."

There was much more to it, and the text alone doesn't do justice to the freakishness of the moment. But as I watched the president disintegrating into a cartoonish back-alley drug dealer from a 1980s after-school special, two thoughts occurred to me: 1) We're completely screwed if this shell of a man is re-elected, and 2) Why is he so obsessed with selling this malaria drug?

The corollary to the "Trump only cares about Trump" rule is that he's done nothing to earn the benefit of the doubt, so our negative assumptions about his motives ought to be considered accurate until proven otherwise. As I've said from the beginning, I absolutely hope I'm wrong about Trump, but so far, he's proved many of my worst concerns about his poseur presidency to be true. So, in this case, if Trump's pushing an unproven cure with this much vigor, then he's very likely benefiting financially somehow.

Trump is always engaged in one con or another, so he's certainly wired for a scam like this. Andthe downturn in the economy due to the pandemic has reached the books of the Trump Organization where Eric Trump and DonaldJr. are racing around like the Skipper and Gilligan struggling to guide the USSMinnow out of that freak Pacific storm. We learned the other day that the Trumps are laying off 1,500 workers, an unemployment bloodbath, while closing 17 locations mainly hotels and restaurants. Likewise, the Trumps are desperately begging their creditors to back off, creditors that includeDeutsche Bank and Palm Beach County, to whom the Trump Organization owes a pile of money.

SoTrump's businesses are under duress like everyone else's, motivating him to grab whatever cash is nearby. Apparently there's good money in pharmaceuticals.

The top manufacturer of hydroxychloroquine is Novartis. Back in early 2017, soon after the inauguration, Novartis agreed to pay Michael Cohen, Trump's former attorney-slash-fixer, $100,000 per month for lobbying access to the new president. The cash payouts were sent to Cohen's shell company, Essential Consultants, which was also a reputed slush fund for Trump. You might recall thatthe president used Essential Consultants as an intermediary foralleged hush-money payments to adult film star Stormy Daniels. Indeed, some of those checks were signed by Trump while in the White House.

Andno, this isn't somekooky conspiracy to frame Trump. Novartis executives admitted to lobbying Trump with cash payments after they, along with AT&T and several others, were exposed publicly.

All told, Novartis paid Trump more than a million dollars during the year-long agreement, paid out throughCohen's dubious company. Novartis is one of the primary manufacturers of hydroxychloroquine. Two-plus-two equals "what do you have to lose?"

All this is just for starters. The question now is whether Trump has entered into another agreement with a different pharmaceutical corporation, or whether Trump is priming the pump for a renewal of the old one with Novartis. There might be another angle we haven't considered yet. It's difficult to tell at this point, but the history is there. The players, including Cohen and Novartis, have confessed publicly and apologized.

Trump is treating this drug like he's the national spokesman, paid on commission, yet to date there isno peer-reviewed evidence that hydroxychloroquine actually works against COVID-19. In fact, it could have serious side effects contradicting Trump's whispery, "What do you have to lose?" pitch. Of course it's possible that Dr. Trump's snake oilmight work for some patients. We simply don't know. But there's a lot to lose for thosewho might experience a series of horrendous side effects taking the wrong medication for the wrong illness has a tendency to do that. Knowing all this, it's ludicrous that the U.S. government under Trump has already invested in 29 million pills, absent any clear information that they're usefulagainst the current plague.

No wonder Trump wouldn't allow Dr. Anthony Fauci, ofthe National Institute of Allergy and Infectious Diseases, to answer a reporter's question about the efficacy of hydroxychloroquine during Sunday's Trump Show. He knew that Fauci might, at the very least, contradict Trump's drug-dealer-ish rationalizations, and, as you know, coffee's for closers.

Meanwhile, we learned on Mondaythat the White HouseCOVID-19 task force erupted into an argument over the drug recently, with economic adviser Peter Navarro presenting Trump with several shoddy studies thatFauci observedwere "anecdotal" and unscientific, largely due to thelack of control groups. Who should we believe? The scientist with 40 years of experience in his current role, orTrump and Navarro, two guys with zero experience in science, one of whom hasa known history of taking money from the one of the drug's primary manufacturers? The answer is obvious to anyone outside the Trump death cult. But as Amanda Marcotte wrote on Monday, the Trump teamcould be setting up Fauci as a scapegoat for this entire pandemic, in allthis, so we shouldn't expect the actual expert to win the debate over Trump's snake oil.

In case you're wondering why the United States has the greatest number of COVID-19 victims worldwide, and nearly 11,000 deaths as of Tuesday morning, it might be because the president has prioritizedhis side hustle over actually doing the job, relentlessly pitching an unproven drug like the world's most annoying late-night infomercial host. To be clear, he's never been capable of doing the job in the first place, so his various side hustles are all he's got. Consequently, he's wedging his cumbersome bulk between doctors and patients, urging people without medical degrees to second-guess the experts.

Trump's No. 1 priority is always Trump, and he's turning hydroxychloroquine into the new "freedom fries." If you're a member of the cult, you're being commanded to take the drug. Maybe it's to own the libs, maybe it's so Trump can get paid. Either way, take it. It'll make you feel good and all the cool kids are doing it. But if it doesn't work and you die, it'll be someone else's fault. What do you have to lose?

More here:

Dr. Trump's medicine show: Why is he pushing an unproven drug? Follow the money - Salon

Preventive medicine specialists position themselves against the olgico serological passport ‘| Society – The Union Journal

The Spanish Society of Preventive Medicine, Public Health and Hygiene (Sempsph) has positioned itself this Friday against any form of ser serological passport that identifies who has passed the coronavirus infection. This can be known through a test that reveals whether the person has the antibodies that protect him against the pathogen because he has already been in contact with it.

There are several public and legal health criteria, but one of the most important is that this type of passport encourages people to become infected, summarize Sempsph sources.

The document calls on administrations not to propose measures that suppose a stratified limitation of freedoms and fundamental rights for health reasons; attending to the constitutional principles of non-discrimination, to the principles of equality, relevance and proportionality .

In a document published on its website, the society that groups Spanish preventivists recalls the confidential nature of any clinical information and that the legislation protects workers from companies when it comes to being required on whether they have past the disease.

Only in the case of healthcare employees, nursing homes and similar equipment should their serological status be taken into account and always for the purposes of better care.

The community of Castilla y Len, as well as some researchers, have advocated in recent days for the creation of this type of certificate, a safe-conduct that would allow its holders to return to normal life before the rest of the population.

The Ministry of Health, however, has been opposed to this type of initiative that is now beginning to be considered in light of the relaxation of the isolation measures that will follow the decrease in cases and deaths registered after a month of confinement.

At the moment, it is not known how long people who have recovered from infection with SARS-CoV-2, the virus that causes Covid-19, are immune to the virus. In the first SARS, which disappeared after causing nearly 800 deaths two decades ago, it would approach 10 years. MERS, another coronavirus that mainly strikes the Middle East, this period is shorter, about two years.

The Sempsph considers that the decreasing trend of new cases in Spain advises the planning of progressive de-escalation of some of the isolation measures adopted by the Government. The document avoids establishing stages and deadlines and opts for an adaptive response that allows accelerating or regressing back to normal according to the evolution of the disease and a hypothetical upswing in cases.

Regarding the use of masks by the population, the document recommends them when considering that the available evidence with SARS supports their use: The use of any type of mask reduced the transmission of infection [del SARS] in the general population. Also, the evidence seems to indicate that a use by the general population, instead of only symptomatic people, can reduce community transmission of the infection.

Among other measures in the field of care, the 54 pages of the document call on the authorities to adopt a series of measures before beginning the de-escalation of isolation, including having the capacity, including staffing, to double the number of patients treated in the ICU if necessary .

It also calls on the Government to have the ability to evaluate large numbers of symptomatic patients safely in facilities such as outdoor tents or vehicles. Likewise, to have sufficient Personal Protective Equipment (PPE) for all health workers and socio-sanitary centers and a sufficient number of surgical masks to provide all patients, in both cases even if they were duplicated the cases.

In terms of public health, preventivists consider that administrations must have the means to recover and generalize the progressive tracking of contacts of those infected and have facilities such as medicalized hotels for those infected who are not hospitalized who cannot comply with insulation measures in the home .

Society also requires administrations to organize in order to carry out rapid tests on possible cases and symptomatic contacts in the first 24 hours after the patient detects the onset of symptoms.

Information about the coronavirus

Here you can follow the last hour on the evolution of the pandemic

This is how the coronavirus curve evolves in Spain and in each autonomy

Questions and answers about coronavirus

Guide to action against the disease

In case of symptoms, these are the phones that have been enabled in each community

Click here to subscribe to the daily pandemic newsletter

Read more here:

Preventive medicine specialists position themselves against the olgico serological passport '| Society - The Union Journal