Search This Blog

Tuesday, January 21, 2020

Hospitals advised to prepare for dealing with Wuhan coronavirus

U.S. hospitals should prepare “financially and operationally” to contend with a potentially deadly outbreak of the Wuhan virus that has already killed six people and sickened hundreds more in China, a major accounting firm said Tuesday.
Although the respiratory virus is in its early stages, it has already left a mounting human and economic toll, wrote Matt Wolf, who leads RSM’s healthcare valuation consulting group. On Monday, the Centers for Disease Control and Prevention announced the first domestic case of the virus, technically called 2019 Novel Coronavirus, in a Washington state patient who had recently returned from Wuhan, China. Nearly 300 people have contracted the virus in China.
Wolf compared the outbreak to the deadly Severe Acute Respiratory Syndrome (SARS) virus in 2002 and 2003, which spooked investors and prompted Chinese markets to plunge. He also cited the Ebola virus, which spread through West Africa from 2014 to 2016, killing more than 11,000 people. Ebola also killed 11 people in the U.S.
U.S. hospitals spent more than $360 million preparing for potential Ebola cases, with those designated as frontline centers shouldering more of the costs. In the case of the Wuhan virus, the potential ripple effect is far bigger, Wolf wrote.
“An epidemic in a country like China, where foreign citizens are more likely to travel to the U.S. for leisure, only magnifies the problem,” he said.
At the height of the Ebola epidemic in 2015, more than 2.6 million tourists visited the U.S. from China, compared with slightly more than 500,000 from all of Africa, Wolf said.
Beyond China and the U.S., the Wuhan virus has spread to South Korea, Japan and Thailand, Wolf wrote. The Chinese New Year starts on Jan. 25, which means many people will take time off and travel.
Nashville’s Vanderbilt University Medical Center announced Monday it had changed its electronic prompts so that any patients entering the hospital, emergency department or clinics with a fever or respiratory symptoms will be asked whether they have been to China recently or have had contact with anyone who has. Patients at risk of having the virus will be placed in isolation, said Dr. William Schaffner, professor of infectious diseases and preventive medicine at VUMC and a member of its infection control committee.
“It should offer reassurance to people in the community that we’re aware of the events that are unfolding in China and now elsewhere, including the U.S., and that we’re bringing that sense of prevention and precaution home,” he said.
Schaffner said he would be surprised if other hospitals were not implementing similar protocols.
The CDC first warned medical providers to look out for patients with respiratory symptoms and a history of travel to Wuhan, China. The agency is developing guidance for testing and managing the illness, including at home. The CDC plans to distribute a diagnostic test soon that will speed up detection time. Currently, testing must take place at the CDC.
On Friday, the CDC implemented public health screenings at airports in San Francisco, New York and Los Angeles and plans to add them in Chicago and Atlanta this week.
Originally thought to spread only from animal-to-animal, the CDC says there is growing evidence that limited person-to-person spread is happening as well, similar to how the SARS virus spread.
“It’s unclear how easily this virus is spreading between people,” the agency said.
Given there have been six deaths in China out of hundreds of infections, Schaffner said the Wuhan virus’ mortality rate is so far much lower than that of SARS or Middle East Respiratory Syndrome (MERS), both of which were sometimes as high as 50%. On the other hand, U.S. hospitals will see thousands of flu patients and many deaths from the illness, he said.
“Familiarity, if it doesn’t breed contempt, it sometimes breeds nonchalance,” Schaffner said.

Infections Account for 13% of All Cancer Cases

An estimated 13% of all cancer cases in 2018 may be attributable to infections, concludes a new global survey.
This extrapolates to about 2.2 million cancer cases that were diagnosed worldwide, corresponding to an age-standardized incidence rate (ASIR) of 25 cases per 100,000 person-years.
The primary causes were Helicobacter pylorihuman papillomavirus (HPV), hepatitis B virus (HBV), and hepatitis C virus (HCV).
Of note, a third of all global cancer cases attributable to infection occurred in China, which accounted for 42% of cancers caused by H pylori and for 69% of those caused by HBV.
“The present work estimates for the first time incidence rates of infection-attributable cancer in 2018 at an individual country level,” write the authors, led by Catherine de Martel, MD, of the Infections and Cancer Epidemiology Group at the International Agency for Research on Cancer, France.
“Our study can help to raise awareness and inform recommendations for action against cancer, which tends to be viewed as a non-communicable disease,” they add.
The findings were published online December 17 in the Lancet Global Health.
A causal association between certain infections and human malignancies is already well established, the authors comment. Previous research by de Martel and her group found that H pylori, HBV, HCV, and HPV were responsible for 1.9 million of 12.7 million cancer cases reported in 2008. Most of these were gastric, hepatic, and cervix uteri cancers.
For the current analysis, the authors used the GLOBOCAN 2018 database of cancer incidence and mortality rates. They estimated the attributable percentages and global incidence for specific cancers that have already been associated with infectious pathogens. The absolute numbers and ASIR were calculated at the country level and were stratified by sex, age group, and country.
Their results showed that H pylori was responsible for 810,000 new cancer cases in 2018 (ASIR, 8.7 cases per 100,000 person-years), primarily underlying noncardia gastric adenocarcinoma. This was followed by HPV, responsible for 690,000 new cases (ASIR, 8.0 cases per 100,000 person-years), primarily causing cervix uteri carcinoma.
HBV contributed to 360,000 new cases (ASIR, 4.1), and HCV was responsible for 160,000 new cases (ASIR, 1.7), both primarily causing hepatocellular carcinoma.
Other infectious agents, including Epstein-Barr virus, human T-cell lymphotropic virus type 1, human herpesvirus type 8 (also known as Kaposi sarcoma herpesvirus), and parasitic infections contributed to the remaining 210,000 new cases.

Variation by Sex and Income

Overall, men and women were equally affected by cancers caused by infections, but the types of pathogens and cancers varied by sex.
There was also considerable variation by geographic region. Eastern Asia had the highest rates of infection, with 37.9 cases per 100,000 person-years, followed closely by sub-Saharan Africa (33.1). Conversely, the lowest number of cases was in northern Europe (13.6) and western Asia (13.8).
China accounted for 780,000 (35%) of the new infection-attributable cases in 2018. Of those, 340,000 were linked to H pylori, and 250,000 to HBV. South Korea also had a very high incidence of cancer caused by H pylori infection (ASIR, 35.2 cases per 100,000 person-years), as did Japan (23.8). There was also a high incidence of cancer cases related to HBV in South Korea (8.6).
Cervix uteri carcinoma accounts for approximately 80% of cancers (n = 570,000 cases) that could be attributed to HPV. Women were the most affected by HPV, accounting for 90% of the 690,000 attributed cases globally. These proportions were highest in the lowest-income countries.
In contrast, the proportions of the other types of HPV-related anogenital cancers, along with head and neck cancers, were higher in high-income countries, with a greater proportion seen in men.
“It should be emphasized that the data we present here are a snapshot of the burden of cancer attributable to infections worldwide in 2018, and comparisons with previous results are not possible because of changes in data sources, notably for cancer incidence estimates, as well as other methodological modifications,” the authors write.
The study was funded by the International Agency for Research on Cancer. The authors report no relevant financial relationships.
Lancet Glob Health. Published online December 17, 2019. Full text

Novel Approach Shows Early Promise in Boosting Memory in Alzheimer’s

Very early research suggests a novel, noninvasive brain stimulation technique guided by ultrasound may improve memory in Alzheimer’s disease (AD).
Investigators found that ultrasound-guided transcranial pulse stimulation (TPS) administered to a small number of patients with probable AD improved memory for up to 3 months and that these improvements correlated with improvements in brain networks observed on functional magnetic resonance imaging (fMRI).
However, although encouraging, Alzheimer’s experts caution the findings are highly preliminary and not near ready for prime time.
“TPS is a promising new brain therapy worthwhile to be further investigated in larger clinical studies on AD and other diseases like Parkinson’s, multiple sclerosis, and stroke,” study investigator Roland Beisteiner, MD, associated professor, Department of Neurology, Laboratory for Functional Brain Diagnostics and Therapy, Medical University of Vienna, Austria, told Medscape Medical News.
“We introduce a new add-on therapy which gives patients an additional chance [and] all established therapies may be continued,” he added.
The study was published online December 23 in Advanced Science.

Precision Medicine

Existing brain stimulation techniques have several disadvantages. In particular, established electrophysiological brain stimulation techniques are “unable to achieve focal brain activation deep in the brain,” said Beisteiner.
Transcranial magnetic stimulation (TMS) lacks precision, while deep brain stimulation (DBS) is an invasive procedure that requires surgical implantation of electrodes.
In contrast, ultrasound-guided TPS can be “spatially distinct, highly focal, and is not restricted to superficial layers of the brain,” thereby enabling a “controlled modulation of a specific brain region without unwanted costimulations of other brain areas,” the authors write.
Beisteiner noted that TPS also differs from other ultrasound-based approaches.
At present, there are three ultrasound therapies. These include tissue ablation, which is “clinically established”; blood-brain barrier opening, which is still in clinical trials; and brain activation.
The efficacy of noninvasive focal ultrasound in modulating brain function has been demonstrated in animal models and in a small clinical study of 10 health subjects who received median nerve sensory evoked potentials to target the primary somatosensory cortex. These were compared with a sham treatment that used verum stimulation.
Results showed that TPS led to increased neuromodulatory effects, which were dose-dependent as pulses increased. Similar effects were not seen in the sham condition.
TPS is delivered via a handheld ultrasound device over the skull. The device emits a stimulation pulse that is between 3 mm and 5 mm wide and roughly 3 cm long. These “ultrashort” ultrasound pulses (3 ηs) are repeated every 200 ms to 300 ms.
“In the spirit of precision medicine, the area of the brain that is to be activated is very precisely targeted [because] these areas can be situated differently in each patient,” Beisteiner said in a release.
“Thanks to a [magnetic resonance] navigation system, the treating neurologist can pinpoint on the screen where the pulse must be delivered and control everything very precisely,” he said.

Network Upregulation

The current study included 35 patients (mean age [SD], 70.37 years [8.57]; over half female) with probable AD being treated at two centers.
All participants were receiving “optimized standardized treatments.”
Subjects were treated with TPS for 2 to 4 weeks and then underwent anatomical MRIs before and after stimulation.
The first center used a “navigated approach to target AD in relevant regions of interest,” and the outcomes were compared with a “non-navigated global brain stimulation approach” at the second center.
The major global outcome parameter for patients’ cognitive state was assessed using the Consortium to Establish a Registry for Alzheimer’s Disease (CERAD) neuropsychological battery after 3 months.
In addition, fMRI was used to evaluate changes in the brain memory network related to cognitive performance.
There were no serious adverse events, and the procedure was well tolerated without even minor side effects in 93% of the patients.
The researchers found that the “memory” and “verbal” components of the CERAD score improved significantly after treatment in participants in both centers. However, the “figural” performance declined in patients of Center 1. The researchers assert that this was because the center’s protocol did not include stimulation of the occipitoparietal cortex, which is “an important area for visuospatial processing.” The finding, therefore, “supports a specific treatment effect only found for stimulated networks,” they write.
Data obtained through fMRI in 19 patients from Center 1 showed “specific upregulation of the memory network after TPS therapy,” demonstrating increased functional connectivity for hippocampus, parahippocampal cortex, parietal cortex, and precuneus.”
These increases in functional connectivity were “significantly correlated” with improvements in the CERAD scores, “indicating that upregulation of the memory network is related to cognitive performance,” the authors note.
They also note that the precise mechanism by which ultrasound affects neurons and generates neuroplastic effects is not well understood.
Nevertheless, recent laboratory studies on biological ultrasound effects suggest that TPS may “exert mechanical effects on cell membranes, affecting mechanosensitive ion channels and generating membrane pores,” the authors note. In turn, neurotransmitter and humoral factor concentrations may change.
There may also be an extra-cellular increase in levels of neurotransmitters such as serotonin and dopamine, a reduction in GABA levels, and an increase in brain-derived neurotrophic factor (BDNF) and other neurotrophic factors, which “may support cellular and network changes.”

Promising but Very Preliminary

Commenting on the study for Medscape Medical News, Ralph A. Nixon, MD, PhD, professor of psychiatry and cell biology, New York University School of Medicine, called TPS using single ultrashort ultrasound pulses “a promising novel brain stimulation technique.”
Nixon, who is also the director of the Center for Dementia Research, Nathan Kline Institute, and was not involved with the research, noted that the study was “a small pilot study without control groups,” and the findings are “too preliminary to have immediate applications for practicing clinicians.”
Nevertheless, they are consistent with “encouraging data in the literature using ultrasound-based brain stimulation techniques and justify larger-scale studies of TPS that would more definitely validate useful clinical effects on cognition in an AD population.”
Also commenting on the study for Medscape Medical News, Steven T. DeKosky, MD, deputy director, McKnight Brain Institute, and professor of neurology and neuroscience, University of Florida, called the paper “very interesting,” stating that it “appears [to be] well and carefully investigated by the research group.”
However, he also cautioned that the results in human studies are “very preliminary,” with “more direct biological findings in the animal models.”
On the other hand, “since it is a procedure available for use in humans and is noninvasive, a determination with larger numbers of people whether it really makes an extended difference in cognition over time has to be made,” said DeKosky, who was not involved with the study.
The authors acknowledge that the study was performed with an “uncontrolled design,” which is a limitation. They emphasize that further sham-controlled investigations are necessary to confirm the findings.
This work was supported by a grant from the Medical University of Vienna and University of Vienna research grant from STORZ Medical. Other aspects of funding are listed on the original paper. The authors, Nixon, and DeKosky have disclosed no relevant financial relationships.
Adv Sci. Published online December 23, 2019. Full text

Fluoroquinolones, Cancer Drugs on New FDA Watch List

The new watch list from the US Food and Drug Administration (FDA) includes 15 drugs or drug classes for which there is a potential sign of serious risk or new safety information.
The watch list, updated to cover July through September 2019, is generated from the FDA Adverse Event Reporting System and is posted on the FDA website.
Appearance on the list does not mean the FDA has found that a drug is associated with the corresponding risk, only that the agency has identified a potential safety problem. If further review shows it is associated with risk, the FDA can take actions — including requiring changes to labeling, restricting the drug’s use, or in rare cases removing it from the market.
Eight fluoroquinolones made the list this quarter with potential signs of risk for mitral and aortic regurgitation.
The FDA has issued several prior safety communications about fluoroquinolone use, including in December 2018 (aortic aneurysm), July 2018 (significant decreases in blood sugar and certain mental health side effects), July 2016 (disabling adverse effects of the tendons, muscles, joints, nerves, and central nervous system), May 2016 (restrict use for certain uncomplicated infections), August 2013 (peripheral neuropathy), and July 2008 (tendinitis and tendon rupture).
The cancer drug cisplatin is being investigated for aortic thrombosis. And two drug classes on the list, cyclin-dependent kinase 4 and 6 (CDK 4 and CDK 6) inhibitors, showed potential links with interstitial lung disease/pneumonitis. That information was updated on the drugs’ labels.
Six HIV drugs listed potential signs of risk for renal toxicity.
With baloxavir marboxil (Xofluza, Genentech), some sections of the labeling were updated this past October to include adverse reactions of erythema multiforme and rash.
This updated list includes:
Product Name: Trade (Active Ingredient) or Product ClassPotential Signal of a Serious Risk / New Safety InformationAdditional Information (as of December 20, 2019)
Cisplatin
Generic products containing cisplatin
Aortic thrombosisFDA is evaluating the need for regulatory action.
Cyclin-dependent kinase 4 and 6 (CDK 4 and CDK 6) inhibitors
  • Palbociclib  (Ibrance)
  • Ribociclib (Kisqali)
  • Letrozole and ribociclib (Kisqali Femara Co-Pack)
  • Abemaciclib (Verzenio)
Interstitial lung disease/pneumonitisThe Dosage and Administration, Warning and Precautions, and Patient Information sections of the labeling were updated September 2019 to include interstitial lung disease/pneumonitis.
Pentosan polysulfate sodium (Elmiron)Eye disordersFDA is evaluating the need for regulatory action
Bictegravir, emtricitabine and tenofovir alafenamide (Biktarvy)
Emtricitabine and tenofovir alafenamide (Descovy)
Elvitegravir, cobicistat, emtricitabine, and tenofovir alafenamide (Genvoya)
Emtricitabine, rilpivirine, and tenofovir alafenamide (Odefsey)
Darunavir, cobicistat, emtricitabine, and tenofovir alafenamide (Symtuza)
Tenofovir alafenamide (Vemlidy)
Renal toxicityFDA is evaluating the need for regulatory action.
Bosutinib monohydrate (Bosulif)
Imatinib mesylate (Gleevec)
Ponatinib (Iclusig)
Generic products containing imatinib
Thyroid dysfunctionFDA is evaluating the need for regulatory action.
Vancomycin hydrochloride (Firvanq)
Vancomycin hydrochloride (Vancocin)
Generic products containing vancomycin
Serious cutaneous adverse reactions, including drug reaction with eosinophilia and systemic symptoms (DRESS), Stevens-Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), acute generalized exanthematous pustulosis (AGEP), and Linear IgA diseaseFDA is evaluating the need for regulatory action.
Fluoroquinolones
  • Moxifloxacin hydrochloride (Avelox)
  • Delafloxacin meglumine (Bexdela)
  • Ciprofloxacin (Cipro)
  • Ciprofloxacin (Cipro XR)
  • Gemifloxacin mesylate (Factive)
  • Levofloxacin (Levaquin)
  • Moxifloxacin
  • Generic products containing fluoroquinolones
Risk of mitral and aortic regurgitationFDA is evaluating the need for regulatory action.
Glatiramer acetateDrug device usage errorsFDA is evaluating the need for regulatory action.
Deoxycholic acid (Kybella)Injection site scarringFDA is evaluating the need for regulatory action.
Baricitinib (Olumiant)Hypersensitivity reactionFDA is evaluating the need for regulatory action.
Oritavancin diphosphate (Orbactiv)Infusion-related reactionsFDA is evaluating the need for regulatory action.
Tacrolimus capsuleTherapeutic inequivalenceFDA is evaluating the need for regulatory action
Capecitabine (Xeloda),
generic products containing capecitabine
Cerebellar toxicityFDA is evaluating the need for regulatory action
Baloxavir marboxil (Xofluza)Serious skin reactionsThe Contraindications, Warnings and Precautions, Adverse Reactions and Patient Counseling Information sections of the baloxavir marboxil labeling were updated in October 2019 to include adverse reactions of erythema multiforme and rash.
Axicabtagene ciloleucel (Yescarta)DysphagiaFDA is evaluating the need for regulatory action

Chinese doctor investigating virus outbreak says he was infected

A Chinese physician who was investigating the outbreak of a deadly new virus in central China says he has himself been infected.
Wang Guangfa, who heads the Department of Pulmonary Medicine at Beijing’s Peking University First Hospital, was part of a team of experts that earlier this month visited Wuhan, where the virus emerged.
“I was diagnosed and my condition is fine,” Wang told Kong’s Cable TV on Tuesday, thanking people for their concern.

The death toll from the flu-like coronavirus strain, which officials have confirmed can be transmitted between humans, had climbed to six as of Tuesday, with the number of reported cases rising above 300. Fifteen medical personnel are among those infected.
Wang, who conducted research on Severe Acute Respiratory Syndrome (SARS) in 2003, said he was receiving treatment and would receive an injection soon. He did not give details on how he may have been infected.
“I don’t want everyone to put too much attention on my condition,” he told the channel.

Wang told state media on Jan. 10 that the outbreak appeared to be under control, with most patients showing mild symptoms and some having been discharged.

AI-powered study backs anticoagulants for heart failure patients without afib

A new study has found that blood thinning drugs improve outcomes for all heart failure patients, regardless of whether they already have atrial fibrillation (AF).
Healthcare AI company Sensyne Health analysed anonymised, routinely collected data from nearly half a million NHS patients as part of the study, then compared the data over three years of heart failure patients with no record of anticoagulant prescription with that of patients prescribed either warfarin or NOACs – the two most commonly used classes of anticoagulants.
The benefit of anticoagulants in patients with atrial fibrillation is well documented, but the data in the study also suggested a small but statistically significant survival benefit for heart failure patients without atrial fibrillation on anticoagulants.
However the company said that further analysis is required to confirm if the difference is clinically relevant, and if so which subgroups of patients would benefit the most.
The analysis also suggests that there may be relevant differences, not only between the use of warfarin compared to NOACs, but also between the NOACs currently in use.
Heart failure is a highly heterogeneous disease which affects more than one million UK adults, is one of the most common causes of hospital admission and is responsible for 10,000 deaths a year. It severely compromises a patient’s quality of life, and treating it comes with significant costs, amounting to 1-2% of the NHS’ annual budget (c. £625 million).
AI-powered study
Notably, the study used both real world data and Sensyne’s machine learning patient stratification algorithm, which identifies different subgroups of heart failure patients. This allowed the company to look at a more diverse set of patients than might traditionally be possible in a randomised controlled trial.
Explaining the benefits of their approach, Sensyne said: “In silico analysis of the real-world data in electronic patient records offers the enticing potential of a faster, more representative and cost-effective alternative.
“These findings are interesting in their own right, but the combination of these standard, statistical approaches with the application of Sensyne Health’s machine learning algorithm… is where the opportunities lie for enhanced analysis, insights and clinical understanding.”
Sensyne has a unique partnership with NHS Trusts that enables it to analyse ethically sourced, anonymised patient data to undertake such research.
Sir Bruce Keogh, interim chairman of Sensyne Health and former national medical director of the NHS Commissioning Board, said that the partnership “allows rapid and cost-effective analysis of therapeutic efficacy outside the confines of randomised clinical trials in a way that reflects the reality of routine clinical practice” and “offers the prospect of new insights leading to iterative improvements in healthcare”.

Novavax Works On Wuhan Coronavirus Vax Candidate As 1st US Case Emerges

Novavax, IncNVAX 71.08% said Tuesday afternoon it has initiated development of a vaccine candidate for the Wuhan-version of the coronavirus that has spread from China to other Asian nations and on Tuesday was confirmed to have infected at least one person in the United States.
Novavax shares surged about 60% on Tuesday following reports of the coronavirus outbreak. The company said it has extensive history working with coronaviruses and developing vaccine candidates, including its work on the MERS and SARS coronaviruses.
“Using Novavax’ recombinant nanoparticle vaccine technology, the company expects to develop a vaccine candidate from the genetic sequence of the Wuhan coronavirus,” the company said in a statement.
Novavax would also utilize its proprietary Matrix-M adjuvant to potentially provide additional immune response.

What We Know About The Coronavirus Outbreak

The newly-identified coronarvirus emerged in a seafood and poultry market in the Chinese city of Wuhan and has infected more than 300 people, including six who have died, Chinese officials said. The virus has already spread to Beijing and Shanghai, as well as a other Asian nations, including Japan and South Korea.
U.S. health officials confirmed that a man in Washington State who had recently been in the Wuhan area has the virus and is very sick.