“many Americans don’t wash their hands after feeding or playing with their cats and dogs and aren’t aware of the risk of contracting a foodborne illness from those activities.”
“Some tips to keep pet owners from getting foodborne illness include:
–Wash hands with soap and water after preparing food for pets, petting or playing with pets, and before preparing food for people.
The active ingredients in a drug are an extremely small part of the pill, liquid, or injectable, However the inert ingredients in drugs are not just “fillers” so that a pill is easy to handle. They” can be composed of ingredients including preservatives, dyes, antimicrobials and other compounds known as excipients**. These ingredients play critical roles in making sure a drug’s active ingredient is delivered safely and effectively, as well as conferring important qualities like shelf stability and the ability to quickly distinguish pills by color.”
The excipients have been generally been classified by scientists as nontoxic and biologically inactive. Some patients have described side effects from these excipients. A USCF team decided to study if indeed certain excipients are not as biologically inactive as thought. These studies will go a long way in deducing if a person is having side effects from the drug or added ingredients.
So far the team “the researchers have now systematically screened 3,296 excipients contained in the inactive ingredient database, and identified 38 excipient molecules that interact with 134 important human enzymes and receptors.”
Future research will expand on these hypothetical findings and test using animal models.
**Excipients are crucial to drug delivery within the body. Generally, an excipient has no medicinal properties. Its standard purpose is to streamline the manufacture of the drug product and ultimately facilitate physiological absorption of the drug. Excipients might aid in lubricity, flowability, disintegration, taste and may confer some form of antimicrobial function. Selecting the appropriate excipient to support the design of your pharmaceutical formulation is an important step in the drug manufacturing process. From Pharmaceutical Excipients
About 100 years ago fashionable shoes started actually changing the shape of the foot! And a recent review concludes “wearing shoes changes the way we run and weakens the foot in a way that can contribute to many common sports injuries.” With ” between 35 and 50% of runners were injured at any one time. ” Most injuries were connected to muscles involved in movement.
Minimalist shoes may reduce injuries along with balance activities. And running barefoot will not guard against all injuries. Age, BMI, previous injuries, and a sedentary lifestyle are all injury factors no matter the shoe.
The article concludes stating “It’s likely that these factors might also make humans less conditioned to move how they did millions of years ago. This suggests a combination of getting more active, walking or running barefoot more often, and other conditioning exercises may help prevent further injuries in the future.”
So, don’t wholly blame the shoe or think a proper shoe alone is the answer!
More older adults used multiple medications and dietary supplements, and taking them together put more people at increased risk for a major drug interaction, according to a new study published online by JAMA Internal Medicine.
Most older adults in the United States use prescription and over-the-counter medications and dietary supplements. There is increased risk among older adults for adverse drug events and polypharmacy.
Dima M. Qato, Pharm. D., M.P.H., Ph.D., of the University of Illinois at Chicago, and coauthors analyzed nationally representative data to examine changes in medication use, which included concurrent use of prescription and over-the counter medications and dietary supplements, to gauge potential for major drug interactions.
The study group included 2,351 participants in 2005-2006 and 2,206 in 2010-2011 who were between the ages of 62 and 85. In-home interviews and direct medication inspection were performed.
The authors report:
Concurrent use of at least five prescription medications increased from 30.6 percent to 35.8 percent over the study period.
Concurrent use of five or more medications or supplements of any type increased from 53.4 percent to 67.1 percent.
Use of over-the-counter medications declined from 44.4 percent to 37.9 percent.
Dietary supplement use increased from 51.8 percent to 63.7 percent. Multivitamin or mineral supplements and calcium were the most commonly used supplements during the study period.
About 15.1 percent of older adults in 2010-2011 were at risk for a major drug interaction compared with an estimated 8.4 percent in 2005-2006. For example, preventive cardiovascular medications and supplements were increasingly used together in interacting drug regimens.
As many as 30 million American men have erectile dysfunction (ED). If you’re one of them and considering a so-called “herbal Viagra,” you should discuss the situation with your health care provider. Conventional treatments are available that may help you. Another important reason to see your health care provider is that ED may be a sign of an underlying health problem that needs to be treated, such as clogged blood vessels or nerve damage from diabetes. Furthermore, the U.S. Food and Drug Administration (FDA) has warned that some products marketed as dietary supplements for male sexual enhancement or ED contain prescription drug ingredients or related substances. These products may interact in dangerous ways with medicines.
Bottom Line: No complementary health approaches have been shown to be safe and effective for sexual enhancement or treating ED. Safety is a serious concern with regard to dietary supplements promoted for ED or sexual enhancement.
Safety: Many supplements promoted for ED and sexual enhancement have been found to be tainted with drug ingredients or related substances. These contaminants may interact with prescription drugs in harmful ways. For example, some of the contaminants in these supplements may interact with drugs that contain nitrates, leading to a dangerous decrease in blood pressure. People with diabetes, high blood pressure, high cholesterol, or heart disease often take drugs containing nitrates, and men with these conditions frequently have ED.
Warning signs that a dietary supplement for ED may be tainted with potentially harmful substances include:
Claims that the product is a natural alternative to prescription drugs or has effects similar to those of drugs
Promises that the product will work very rapidly or that its effects will last for a day or more
Personal testimonials about incredible benefits from the product.
From the 26 May 2015 Florida State University news release
Foam. We wear it. We sit on it. We sleep on it. We even use it to protect ourselves.
Whether it’s a football helmet, hospital bed, knee pad or body armor, the foam it contains plays a critical role in making that product both comfortable and safe. But can that foam be transformed into something significantly better, safer and more comfortable?
Changchun “Chad” Zeng with Florida State University’s High Performance Materials Institute (HPMI) says yes, and his brand new, high-performing auxetic foam is proving the point as it heads to the marketplace through a license agreement with Auxadyne LLC.
“We know what is not working with current products and technology, and what it is going to take to make it better,” said Zeng. “For example, the socks that amputees currently use to attach prosthetic devices do not adjust to limb shape and volume, creating lots of problems. My invention solves those issues.”
Part of what makes Zeng’s auxetic foam truly unique is its ability to get thicker, rather than thinner, when stretched. In practical terms, this counter-intuitive behavior, totally opposite to that of conventional foam, leads to many enhanced materials properties including a better and more comfortable fit that adjusts on the fly.
A team comprised of scientists at VIB, KU Leuven and UZ Leuven has made significant progress in uncovering the connection between psychological factors and the immune system. Their findings are based on an investigation of a massive drinking water contamination incident in Belgium in 2010, and are now published in the leading international medical journal Gut.
In December 2010, the Belgian communities of Schelle and Hemiksem in the province of Antwerp faced an outbreak of gastroenteritis, with more than 18,000 people exposed to contaminated drinking water. During the outbreak, VIB and KU Leuven set up a scientific task force to study the incident’s long-term effects, led by Guy Boeckxstaens (UZ Leuven / KU Leuven) and Adrian Liston (VIB / KU Leuven).
Seizing an unexpected opportunity
Adrian Liston (VIB/KU Leuven): “The water contamination in Schelle and Hemiksem was an ‘accidental experiment’ on a scale rarely possible in medical research. By following the patients from the initial contamination to a year after the outbreak we were able to find out what factors altered the risk of long-term complications.”
Anxiety and depression affect immune system
The scientists found that individual with higher levels of anxiety or depression prior to the water contamination developed gastrointestinal infections of increased severity. The same individuals also had an increased risk of developing the long-term complication of irritable bowel syndrome, with intermittent abdominal cramps, diarrhea or constipation a year after the initial contamination.
Guy Boeckxstaens (UZ Leuven / KU Leuven): “Irritable Bowel Syndrome is a condition of chronic abdominal pain and altered bowel movements. This is a common condition with large socio-economic costs, yet there is so much that still remains to be discovered about the causes. Our investigation found that that anxiety or depression alters the immune response towards a gastrointestinal infection, which can result in more severe symptoms and the development of chronic irritable bowel syndrome.”
Psychological factors key in preventing long-term complications
The study’s results provide valuable new insight into the cause of irritable bowel syndrome, and underscoring the connection between psychological factors and the immune system.
Adrian Liston (VIB/KU Leuven): “These results once again emphasize the importance of mental health care and social support services. We need to understand that health, society and economics are not independent, and ignoring depression and anxiety results in higher long-term medical costs.”
Agency Also to Examine Children’s Use of Cough, Cold Medications With Codeine
From the 7 July 2015 AAFP news release
On July 1, FDA officials moved to shut down the manufacture and sale of 16 unapproved prescription otic products used to relieve ear pain, inflammation and infection. Specifically, the agency notified(www.fda.gov) companies that produce and/or distribute these products that it will take enforcement action against them if they continue to make and market the ear drops.
In separate action, the agency said it also plans to scrutinize safety data pertaining to the use of codeine-containing products used to treat cough or colds in children younger than 18 years.
Prescription Ear Drops
Otic drops are frequently given to young children suffering from ear infections and other ailments that cause ear pain and swelling. A number of FDA-approved prescription otic products are available to manage these symptoms, as are legally marketed OTC ear drops. Those products are not affected by the agency’s action.
Products that have not been evaluated by the FDA for safety, quality and efficacy, on the other hand, increase patients’ risk for adverse effects, such as those due to contamination or varying dosage levels that stem from improper manufacturing practices. The unapproved products covered by this action contain the following ingredients:
benzocaine;
benzocaine and antipyrine;
benzocaine, antipyrine and zinc acetate;
benzocaine, chloroxylenol and hydrocortisone;
chloroxylenol and pramoxine; and
chloroxylenol, pramoxine and hydrocortisone.
Patients who are using these unapproved products (or their parents) are advised to consult with their physician regarding other treatment options.
Codeine-containing Cough-and-Cold Products
In a Drug Safety Communication(www.fda.gov) issued July 1, FDA officials announced that the agency is investigating the safety of using cough-and-cold medications that contain codeine in children younger than 18 years. The agency cited concerns about the potential for severe side effects associated with use of these products, including slowed or difficult breathing.
Children with existing respiratory problems, such as asthma or other breathing disorders, may be particularly susceptible to these adverse effects.
The FDA’s action comes on the heels of an April announcement(www.ema.europa.eu) from the European Medicines Agency (EMA), which declared that the use of codeine-containing cough-and-cold medications was contraindicated in children younger than 12 years because of the risk of side effects. The agency also noted at the time that use of these products was not recommended in children ages 12-18 who have breathing problems.
Furthermore, EMA officials warned, patients of any age who are considered “ultra-rapid metabolizers” of the drug, which is converted into morphine in the body, must not use codeine to treat cough or colds.
The FDA announcement states that the agency will continue to evaluate the safety of using codeine products to treat cough or colds in children and young teens — including reviewing the EMA’s action and the evidence on which it was based — and will release final conclusions when that investigation is completed.
In the meantime, agency officials recommend caution when prescribing these medications for young patients, and they urge both physicians and patients to report adverse effects(www.accessdata.fda.gov) linked to use of the drugs via MedWatch, the FDA’s Safety Information and Adverse Event reporting Program.
With summer nearly here, U.S. consumers might think they have an abundance of sunscreen products to choose from. But across the Atlantic, Europeans will be slathering on formulations that manufacturers say provide better protection against the sun’s damaging rays — and skin cancer — than what’s available stateside, according to an article in Chemical & Engineering News (C&EN), the weekly newsmagazine of the American Chemical Society.
Marc S. Reisch, a senior correspondent at C&EN, reports that sunscreens on the U.S. market do protect users from some ultraviolet-A and -B rays. But there are eight sunscreen molecules approved for use in Europe that could boost the effectiveness of products in the U.S. and also give manufacturers more flexibility in making their lotions. Some have been in line for FDA approval since 2002.
Why the hold-up? In Europe, sunscreen molecules are considered cosmetic ingredients. In the U.S., they are subject to the same scrutiny as over-the-counter drugs, which go through a more rigorous review process than cosmetics. More than 10 years ago, the FDA introduced a streamlined process to speed up the review of sunscreens from overseas to bring them to the U.S. market. But the products’ makers are still waiting for approval, and some have given up.
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The American Chemical Society is a nonprofit organization chartered by the U.S. Congress. With more than 158,000 members, ACS is the world’s largest scientific society and a global leader in providing access to chemistry-related research through its multiple databases, peer-reviewed journals and scientific conferences. Its main offices are in Washington, D.C., and Columbus, Ohio.
Health applications are enjoying a boom. There are already some 100,000 on the market on iOS (Apple) and Android platforms, generating 4.5 billion dollars’ worth (around 3.3 billion euros) of business. In Spain, a third of smartphone users will have installed at least one health application this year, according to a report from The App Date.
However, as Borja Martínez, researcher in the Telemedicine and eHealth Group at the University of Valladolid, explains to SINC: “These applications do not handle information securely and this is especially serious in apps that use clinical or medical data that are particularly critical for the user”.
These applications don’t have secure data processing and this is especially serious in apps that use clinical or medical data
Martínez is the lead author of a study that reviews these problems and proposes a series of recommendations for developers to improve the handling of information that should be confidential. The work was published in January in the ‘Journal of Medical Systems’.
This young engineer points out that “the developers, in their haste to get their applications out before the rest, neglect certain aspects that should be considered, especially privacy and security of data handled. Today the majority of health apps do not offer the user sufficient measures to protect their data”.
Risks
In their opinion, “the main risk is that someone can hack into the personal medical information of another individual or, even worse, modify it”.
A clear example, warns the researcher, “would be an app that saves electronic medical histories. If a third party unconnected with the app were to access the stored information and change any patient details, such as take away an allergy to certain medication, it could put the life of this person at risk should the case arise”.
Also, “another significant problem is that health professionals and the patients themselves are not aware of the methods that apps use with regard to the privacy and security of their data. Many take it for granted that the application is secure and others couldn’t care less. I believe that greater collaboration between countries is necessary to create international laws which are in charge of monitoring these aspects,” he says.
What can be done? According to Borja Martínez, “many things [although] it all boils down to developers analysing the type of data that their apps are going to be dealing with and applying the necessary security and privacy methods”.
Medical devices don’t get regular security updates, like smart phones and computers, because changes to their software could require recertification by regulators like the U.S. Food and Drug Administration (FDA). And FDA has focused on reliability, user safety, and ease of use—not on protecting against malicious attacks. In a Safety Communication in 2013, the agency said that it “is not aware of any patient injuries or deaths associated with these incidents nor do we have any indication that any specific devices or systems in clinical use have been purposely targeted at this time.” FDA does say that it “expects medical device manufacturers to take appropriate steps” to protect devices. Manufacturers are starting to wake up to the issue and are employing security experts to tighten up their systems. But unless such steps become compulsory, it may take a fatal attack on a prominent person for the security gap to be closed.
Snow and icy conditions affect human decisions about transportation. These decisions can ripple through other infrastructure systems, causing widespread disruptions. Shown here are points of connectivity.
Credit: Paul M. Torrens and Cheng Fu, University of Maryland, College Park; Sabya Mishra, University of Memphis; Timothy Welch, Georgia Tech.
For Paul Torrens, wintry weather is less about sledding and more about testing out models of human behavior.
Torrens, a geographer at the University of Maryland, studies how snow and icy conditions affect human decisions about transportation. He also studies how these decisions ripple through other infrastructure systems.
“After moving to the Washington, D.C., area from Arizona,” Torrens said, “I saw firsthand how snow upsets even careful plans for getting kids to school and commuting to work.”
Common disruptions such as those associated with snow, while not always catastrophic, have real economic costs, and the costs add up.
“Critical infrastructure systems are the lifelines of society,” said Dennis Wenger, program director in NSF’s Engineering Directorate. “They are complex, highly interdependent processes and systems and are subject to disruption through their normal life cycle and as a result of the impact of natural and technological hazards.”
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In real life, transportation is affected by moment-to-moment decisions by people, explained Torrens, who may adjust their transportation routines depending on their individual circumstances and activities.
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Relying on big data from social media sources, Torrens is building a dynamic, near-real-time atlas and census of a population from which motifs of human and infrastructure behavior can be extracted as rules for agents’ behavior.
“Social media data is a treasure trove for information scientists, because not only do we have the message content, but the content is stamped with a location and a time,” Torrens said. “We can study how information propagates throughout social networks and correlate that with physical situations as they unfold.”
One school system tried to open on time despite the slick conditions. Soon local Twitter users began posting photographs of snow-covered streets, car crashes and links to television news reports with the quickly viral hash-tag #closeFCPS. Information about the resulting problems seemed to spread, bottom-up, via a viral tag, rather than via official school channels.
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Crash-tested 2010 Mercedes-Benz E 350 photographed at the Insurance Institute for Highway Safety Vehicle Research Center. IIHS crash test page (Photo credit: Wikipedia)From the 30 January 2015 article by Justin Worland at Time
The chances of dying in a car crash in a new vehicle have declined dramatically in recent years to their lowest point ever, according to a new study by the Insurance Institute for Highway Safety (IIHS). Improvements to vehicle safety technology since the mid-1980s saved 7,700 lives in the United States in 2012 alone, the study found.
“There’s all the bad news about recalls, which make it sound like vehicles are getting less safe,” says IIHS president Adrian Lund. “What these results show is that motor vehicles are safer than they ever have been in the past. This is a huge reduction of people dying as occupants of motor vehicles in crashes.”
The study, which looked at data on deaths in 2011 model year vehicles, found that no one died in nine vehicle models. The death rate per million registered vehicle years, a number that represents how many people died per the number of years a car is registered to be on the road, declined to 28 for 2011 model cars. That rate was 87 for cars made a decade earlier, Lund says.
The report attributed much of that improvement to changes in technology….
Dr. Leif Salford is a neurosurgeon at Lund University Hospital (Sweden), and Chairman of the Department of Neurosurgery. Since 1988 he has led a team of researchers that have exposed thousands of laboratory rats to microwave radiation from various sources. Since the late 1990s they have used mobile telephones as the source of this radiation.
The results have been consistent and alarming: not only does radiation from a mobile phones damage the blood-brain barrier, but it does so at even when the exposure level is reduced a thousandfold.
This is presentation by Dr. Leif Salford on the effects of radio frequency radiation (RF) upon the brain. The statistics are jolting, to say the least: YouTube Link
For almost 30 years, U.S. PIRG Education Fund has conducted an annual survey of toy safety, which has led to an estimated 150 recalls and other regulatory actions over the years, and has helped educate the public and policymakers on the need for continued action to protect the health and wellbeing of children.
Among the toys surveyed this year, we found numerous choking hazards and five toys with concentrations of toxics exceeding federal standards. In addition to reporting on potentially hazardous products found in stores in 2014, this installment of the report describes the potential hazards in toys and children’s products.
The continued presence of these hazards in toys highlights the need for constant vigilance on the part of government agencies and the public to ensure that children do not end up playing with unsafe toys.
Standards for toy safety are enforced by the Consumer Product Safety Commission (CPSC). Safety standards include limits on toxics in children’s products, size requirements for toys for small children, warning labels about choking hazards, measures to keep magnets and batteries inaccessible, and noise limits.
U.S. PIRG Education Fund staff examined hundreds of toys to confirm that they are safe. We discovered that unsafe toys remain widely available. The problems we found include:
Lead. Childhood exposure to even low levels of lead can undermine development, damaging academic achievement and attentiveness. We found unsafe levels of lead in one set of play sheriff and police badges. (More details and photos of all unsafe toys can be found in Appendix A.)
Chromium. Skin contact with chromium can cause severe allergic reactions including skin redness, swelling and ulcers. Chromium compounds are also known to cause cancer. This year, lab tests revealed that a tambourine marketed to children ages two and older contained chromium at nearly 10 times the legal limit.
Phthalates. Exposure to phthalates at crucial stages of development may harm development of the male reproductive system and is linked to early puberty. Lab tests confirmed that several items purchased by our shoppers contained high levels of banned phthalates. Those items include a rubber duck, plastic-covered hairclips, and a Dora the Explorer backpack.
Small parts are pieces that might block a child’s airway. Children, especially those under age three, can choke on small parts. Our shoppers purchased a set of foam blocks marketed to children two and up that contained multiple small parts that fit into a choke test cylinder. We also identified multiple toys containing near-small parts, which are pieces that almost fit into the choke tube and can be a choking hazard.
Small balls less than 1.75 inches in diameter represent a choke hazard for children three years old and younger. We found small balls that were not labeled with the appropriate choke hazard warning. We also remain concerned about other small, rounded toys, such as toy food, that present the same choke hazard as small balls but are not labeled as a hazard.
Balloons are easily inhaled in attempts to inflate them and can become stuck in children’s throats. Balloons are responsible for more choking deaths among children than any other toy or children’s product. As in past years, we continue to find balloons on store shelves marketed to children under eight.
Magnets. When two or more powerful magnets are swallowed, they can have fatal health consequences as their attractive forces draw them together inside the body, perforating intestinal walls. Our shoppers purchased small, high-powered magnets, despite their being recalled by the CPSC.
Batteries. When batteries are ingested, chemical reactions can burn through the esophagus and blood vessels, causing fatal internal bleeding. Our shoppers purchased a toy whale that contains batteries that are accessible to small children and are nearly small enough to constitute a choke hazard. The toy has been recalled in Australia because small children can easily remove the batteries.
Excessive noise. Excessive noise exposure can lead to hearing loss. This is especially problematic for young children: Hearing loss at an early age has ramifications for speech development. This year, our shoppers found toys that are loud, though not necessarily in violation of federal limits.
Despite recent progress in making toys safer, the findings of our 2014 investigation, as well as recent recalls and legal actions against importers, highlight the need for continued attention to shortcomings in existing standards and vigilance on the part of the shopping public. To keep children safe from potentially hazardous toys, there is still more to do.
Policymakers should continue building upon recent progress in the strengthening of toy safety standards. The CPSC should:
Continue to vigorously enforce the Consumer Product Safety Improvement Act’s mandatory standards for toys, including strict limits on lead and lead paint in any toys, jewelry or other articles for children under 12 years;
Vigorously enforce the Consumer Product Safety Improvement Act’s permanent ban on the use of three specific phthalates in all toys and children’s products;
Upgrade the interim ban on three additional phthalates into a permanent prohibition and expand it to include additional phthalates;
Enlarge the small parts test tube to be more protective of children under three;
Consider extending the standard for toys with spherical ends to apply to toys intended for children under six years old instead of under four years;
Change the small-ball rule to include small round or semi-round objects, and not just “balls” in the strictest definition, since these toys pose the same hazards as small balls (this is especially true of rounded toy food, since it is “intended” to be eaten);
Enforce the use of the United States’ statutory choke hazard warning label;
Continue to enforce CPSC rules requiring online warning labels; and
Fully enforce sound and battery standards.
Parents can also take steps to protect children from potential hazards. We recommend that parents:
Shop with U.S. PIRG Education Fund’s Toy Safety Tips, available at toysafetytips.org.
Examine toys carefully for hazards before purchase – and don’t trust that they are safe just because they are on a store shelf.
Subscribe to government announcements of recalled products at www.recalls.gov.
Remember, toys on our list are presented as examples only. Other hazards may exist.
For toys you already own:
Remove small batteries if there is any question over their security or inaccessibility and keep them out of reach of children;
Remove batteries from or tape over the speakers of toys you already own that are too loud; and
Put small parts, or toys broken into small parts, out of reach. Regularly check that toys appropriate for your older children are not left within reach of children who still put things in their mouths.
Summary: Scientists are taking a closer look at aerosol formation involving an organic compound — called limonene — that provides the pleasant smell of cleaning products and air fresheners. This research will help to determine what byproducts these sweet-smelling compounds are adding to the air while we are using them to remove germs and odors.
… while researchers are still striving to fully understand the health and environmental impact of increased levels of secondary organic aerosols in the atmosphere, studies have linked exposure to outdoor aerosols generally to morbidity and mortality outcomes.”
Herbal medicines such as licorice, Indian rennet and opium poppy, are at risk of contamination with toxic mold, according to a new study. The authors of the study say it’s time for regulators to control mold contamination. An estimated 64% of people use medicinal plants to treat illnesses and relieve pain. The herbal medicine market is worth $60 billion globally, and growing fast. Despite the increasing popularity of herbal medicine, the sale of medicinal plants is mostly unregulated.
OpenFDA offers easy access to FDA public data and highlight projects using these data in both the public and private sector to further regulatory or scientific missions, educate the public, and save lives.
What does it do?
OpenFDA provides API and raw download access to a number of high-value structured datasets. The platform is currently in public beta with one featured dataset, FDA’s publically available drug adverse event reports.
In the future, openFDA will provide a platform for public challenges issued by the FDA and a place for the community to interact with each other and FDA domain experts with the goal of spurring innovation around FDA data.
We’re currently focused on working on datasets in the following areas:
Adverse Events: FDA’s publically available drug adverse event reports, a database that contains millions of adverse event and medication error reports submitted to FDA covering all regulated drugs.
Recalls(coming soon): Enforcement Report and Product Recalls Data, containing information gathered from public notices about certain recalls of FDA-regulated products
Documentation(coming soon): Structured Product Labeling Data, containing detailed product label information on many FDA-regulated product
We’ll be releasing a number of updates and additional datasets throughout the upcoming months.
Excerpts from the 26 June 2014 article at Pew Chartitable Trust
Among the state apps focused exclusively on health or public safety:
The Minnesota Air app provides real-time information about air quality conditions in 10 reporting areas across the state, as well as pollution forecasts for the Twin Cities and Rochester.
The Every Woman Counts app in California lets women know when it’s time to make an appointment for mammograms and Pap tests. Users enter information about their screening history and select a schedule for their exams, and the app sends them reminders.
The MyVaxIndiana app enables parents to keep track of their children’s vaccination records. The information comes from a state immunization system and is updated by health care workers, schools and doctors.
The NMWatch app in New Mexico uses GPS mapping to allow residents, emergency managers and responders to monitor up-to-date wildfire activity. It not only helps people who need to know whether to evacuate, but it alerts those with respiratory problems who might be affected by thick smoke in their neighborhood.
Connected Citizens
More state agencies that oversee health or emergency management have recognized that they need to embrace mobile technology to stay connected with citizens.
“It’s a natural progression,” said Theresa Pardo, director of the Center for Technology in Government at the University at Albany, a research center that focuses on innovation in government technology. “I think these new apps are really powerful. What underlies them is a massive effort to identify and integrate in sophisticated ways data that is relevant to an individual, particularly in the event of a crisis.”
Communicating critical, life-saving information during emergencies and directing the public to services after disasters is an enormous challenge for states, said Karen Cobuluis, spokeswoman for the National Emergency Management Association, the professional association for state emergency management directors.
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A Long Way to Go
While states are moving rapidly to make advances in digital technology, they still have a long way to go when it comes to overseeing their apps and mobile device projects.
In an October 2013 survey of state chief information officers, 58 percent called their state’s efforts to manage apps and mobile device projects “mostly” or “totally” fragmented and uncoordinated.
The association’s Robinson said that most states today don’t have an “enterprise-wide, well-coordinated roadmap” for investing in and deploying mobile technology. “It’s serious for the states because of the implications. There’s no shared strategic direction,” he said. “We need to address how we’re managing mobile devices.”
Robinson of NASCIO said that in many states, apps are being launched agency by agency, which creates more complexity. Plus, states often lack the in-house technical expertise to develop their own apps, so they’re forced to use outside contractors.
The proportion of marijuana-positive drivers involved in fatal motor vehicle crashes in Colorado has increased dramatically since the commercialization of medical marijuana in the middle of 2009, according to a study. The study raises important concerns about the increase in the proportion of drivers in a fatal motor vehicle crash who were marijuana-positive since the commercialization of medical marijuana in Colorado, particularly in comparison to the 34 non-medical marijuana states.
PISCATAWAY, NJ – It’s no secret that drinking and driving can be a deadly mix. But the role of alcohol in U.S. traffic deaths may be substantially underreported on death certificates, according to a study in the March issue of the Journal of Studies on Alcohol and Drugs.
Between 1999 and 2009, more than 450,000 Americans were killed in a traffic crashes. But in cases where alcohol was involved, death certificates frequently failed to list alcohol as a cause of death.
Why does that matter? One big reason is that injuries are the leading cause of death for Americans younger than 45, according to the Centers for Disease Control and Prevention. And it’s important to have a clear idea of alcohol’s role in those deaths, explained Ralph Hingson, Sc.D., of the U.S. National Institute on Alcohol Abuse and Alcoholism.
“We need to have a handle on what’s contributing to the leading cause of death among young people,” Hingson said. What’s more, he noted, researchers need reliable data to study the effects of policies aimed at reducing alcohol-related deaths.
“You want to know how big the problem is, and if we can track it,” Hingson said. “Is it going up, or going down? And what policy measures are working?”
For the new study, I-Jen Castle, Ph.D., and a team led by Hingson focused on traffic deaths because, of all types of accidental fatalities, that’s where researchers have the best data. This is partly because many U.S. states—about half right now—require that fatally injured drivers be tested for blood alcohol levels, and nationwide about 70% of those drivers are tested.
Hingson’s team used a database maintained by the National Highway Traffic Safety Administration, called the Fatality Analysis Reporting System (FARS)—which contains the blood alcohol levels of Americans killed in traffic crashes. They compared that information with deaths certificate data from all U.S. states.
Overall, they found, death certificates greatly underreported the role of alcohol in traffic deaths between 1999 and 2009: Just over 3 percent listed alcohol as a contributing cause. But based on the FARS figures, 21 percent of those deaths were legally drunk.
The picture varied widely from state to state. In some states—such as Maryland, Nevada, New Hampshire, and New Jersey—alcohol was rarely listed on death certificates. Certain other states did much better, including Delaware, Iowa, Kansas, and Minnesota. It’s not fully clear why alcohol is so often left off of death certificates. One reason could be the time it takes to get blood-alcohol test results back. Coroners or medical examiners usually have to file a death certificate within three to five days, Hingson’s team notes, but toxicology results might take longer than that.
The reasons for the wide variation among states aren’t known either. But Hingson said that’s an important question. “Some states have been pretty successful,” he noted. “What are they doing right?”
It doesn’t seem to be only a matter of passing laws: States that mandate alcohol testing for deceased drivers did not always do better when it came to reporting alcohol as a contributor on death certificates.
Whatever the reasons, Hingson said, the role of alcohol in injury deaths may be seriously underestimated on death certificates. And the situation is likely worse with other types of accidental deaths, such as falls, drug poisoning/overdoses, and drowning, for which there is no mandatory blood alcohol testing or other reporting systems.
Hingson said he thinks testing should be done in those cases as well.
“What we need,” Freudenberg said to me, “is to return to the public sector the right to set health policy and to limit corporations’ freedom to profit at the expense of public health.”
Bittman contributes to the ongoing discussion here at NobodyisFlyingthePlane about how certain industries deflect public discourse from what is best for our citizens to what makes the most profit, no matter the consequences.
The author he quotes poses a series of questions which get at the heart of the matter.
“Shouldn’t science and technology be used to improve human well-being, not to advance business goals that harm health?”
Similarly, we need to be asking not “Do junk food companies have the right to market to children?” but “Do children have the right to a healthy diet?”
Essentially its a PR game. Do we let whole industries spin how the conversation is framed or do we let the…
Women are up to 83 percent more likely to experience repeat abuse by their male partners if a weapon is used in the initial abuse incident, according to a new study that has implications for victims, counselors and police.
Women are up to 83 percent more likely to experience repeat abuse by their male partners if a weapon is used in the initial abuse incident, according to a new study that has implications for victims, counselors and police.
Michigan State University researcher Amy Bonomi and colleagues studied the domestic abuse police reports of nearly 6,000 couples in Seattle during a two-year period. An estimated one in four women in the United States experience domestic violence at least once in their lifetime.
Because previous research showed that domestic abuse is more common in poor urban neighborhoods, the researchers expected to find that repeat violence could be predicted by where the couple lived.
But that wasn’t the case. Instead, the main predictor of ongoing domestic violence was the use of a knife, gun or even a vehicle in the first incident. In those cases, women were 72 percent more likely to make follow-up calls to police for physical abuse and 83 percent more likely to call for nonphysical abuse — such as a partner threatening to kill them.
“What this is telling police is that they are likely to be called back to this particular residence if a weapon is involved the first time they are called out,” said Bonomi, chairperson and professor in MSU’s Department of Human Development and Family Studies. “It’s an indication of the danger and severity of abuse over time.”
“The presence of weapons in the home,” she added, “is also a red flag for the women themselves and the counselors who deal with domestic violence.”
The study appears online in the research journal Violence Against Women.
Research among college students found that men under the influence of alcohol are more likely to perpetrate physical, psychological or sexual aggression against their partners than men under the influence of marijuana.
Alcohol use is more likely than marijuana use to lead to violence between partners, according to studies done at the University of Tennessee, Knoxville.
Research among college students found that men under the influence of alcohol are more likely to perpetrate physical, psychological or sexual aggression against their partners than men under the influence of marijuana. Women, on the other hand, were more likely to be physically and psychologically aggressive under the influence of alcohol but, unlike men, they were also more likely to be psychologically aggressive under the influence of marijuana.
The research has implications for domestic violence intervention and prevention programs.
The studies were conducted by Ryan Shorey, a psychology doctoral student; Gregory Stuart, a psychology professor; Todd Moore, an associate psychology professor; and James McNulty, an associate professor of social psychology at Florida State University. The study of male participants is published in the journal Addictive Behaviors and the study of female participants is published in the journal Psychology of Addictive Behaviors.
The researchers’ goal was to find correlations between alcohol and marijuana use and the potential for physical, psychological and sexual violence against partners. The studies are among the first to investigate the timing of alcohol and marijuana use and intimate partner violence in college students.
Two studies included male and female college students who were at least 18 years old, had been a relationship for at least a month that involved two days a week of face-to-face contact, and had consumed alcohol in the previous month. The subjects completed an online diary once a day for 90 days.
The study of men found that odds of psychological, physical and sexual violence increased with subsequent use of alcohol. Specifically, odds of physical and sexual abuse increased on days where any alcohol was consumed and with each drink consumed. Odds of psychological abuse increased only on days when five or more drinks were consumed.
Marijuana use was unrelated to violence between intimate partners.
The study of college women found that alcohol use increased the odds of physical and psychological aggression while marijuana use increased the odds of psychological aggression.
“I think it is too early to make definitive conclusions regarding the role of marijuana and intimate partner violence perpetration, as the research in this area is quite young and, to date, studies have provided conflicting evidence regarding its role in increasing the odds for violence,” said Stuart. “However, we now have numerous studies suggesting alcohol use does increase the odds for violence between partners.”
Another study by the authors and psychology doctoral student Sara Elkins looked at women arrested for domestic violence. This study, published in the Journal of Consulting and Clinical Psychology, found that when women used marijuana they were less likely to perpetrate physical violence.
The authors say their findings provide further support for the numerous negative consequences associated with heavy alcohol consumption, particularly among college students.
“Our findings suggest that dating violence prevention and intervention programs should target reduction in alcohol use, but surprisingly, most of these programs largely ignore alcohol use,” said Shorey.
Stuart noted that their other research has shown that men arrested for domestic violence in batterer intervention programs received short-term benefits when they were given a 90-minute treatment addressing their alcohol problems…..
From the 10 January 2014 Contra Costa Times article
Assorted cosmetics and tools (Photo credit: Wikipedia)
State public health officials announced on Friday a new online database that shows which cosmetics sold in California contain certain harmful chemicals, offering the first state-run public resource to inform consumers about potentially hazardous products they use everyday on their skin and hair.
The long-awaited California State Cosmetics Program Product Database is part of a state law passed in 2005 that aims to expose products with potentially hazardous ingredients, and pressure manufacturers to reformulate makeup, soap, lotion and similar products with safer alternatives. The public can search the website by type of product, brand or ingredient, and will be shown a list of products made with chemicals that are known to cause cancer, reproductive harm or birth defects.
“It does not mean that the cosmetic product itself has been shown to cause cancer, but since most products are not extensively tested for safety, providing information on chemical components will allow consumers to make more informed choices,” said Dr. Ron Chapman, director of the state Department of Public Health.
As of November, the state had collected information from about 475 companies, which have disclosed the ingredients in roughly 30,000 products. The state is requiring only companies that sell in California and have more than $1 million per year in cosmetic sales to report the potentially harmful ingredients they use. The state is looking for about 900 chemicals that have been identified as harmful by Proposition 65 legislation and organizations such as the National Toxicology Program.
The database is part of the California Safe Cosmetics Act of 2005, legislation signed by then-Gov. Arnold Schwarzenegger. The law required the site to be up by Dec. 31, 2013, but a health department spokesman said it did not go live until Friday.
The law also gives the state some enforcement authority, such as requiring products are labeled with warnings.
“We are the one agency in the U.S. collecting this information on cosmetics,” Nerissa Wu, a state public health official who helped establish the program, told this newspaper in an interview last fall. “Our hope is that the market pressure that comes out of that … encourages manufacturers to reformulate.”
Advocates welcomed the database, but some worried that the state lacked the resources to enforce safer standards for cosmetics.
“This doesn’t ban anything. This doesn’t restrict anything,” said Gretchen Salter, senior program and policy manager at the San Francisco-based Breast Cancer Fund, an advocacy group that championed the 2005 legislation. “Ultimately our feeling is these products don’t belong in cosmetics in the first place.”
“Lasting changes will come from deep work by individuals to create systemic change.”
Reducing violence in neighborhoods enhances the community environ- ment and allows people to thrive. The prevention of violence facilitates community cohesion and participation, fosters neighborhood improve- ments, expands employment and educational opportunities, and improves overall health and well-being.
Violence influences where people live, work, and shop; whether parents let kids play outside and walk to school; and whether there is a grocery store or places for employment in the community. Violence jeopardizes health and safety directly— causing injuries, death, and emotional trauma. Witnessing or directly experiencing violence, as well as the fear of violence, are damaging, with consequences that also contribute to unhealthy behavior and a diminished community environment. Vio- lence and fear undermine attempts to improve healthy eating and active living, there- by exacerbating existing illnesses and increasing the risk for onset of disease, includ- ing chronic disease. They affect young people, low-income communities, and com- munities of color disproportionately. Violence and food- and activity-related chron- ic diseases are most pervasive in disenfranchised communities, where they occur more frequently and with greater severity, making them fundamental equity issues.
Chronic disease is a major health challenge—it contributes to premature death, lowers quality of life, and accounts for the dramatic rise in recent healthcare spend- ing. One striking example is the increasing prevalence of diabetes in the United States. Researchers predict that by 2034, the number of people suffering from dia- betes will likely double to 44.1 million, and related health care costs will triple to $336 billion.1 Improving healthy eating and active living environments and behaviors is the crucial link to preventing many forms of chronic disease. Health leaders have been making great strides in mounting a strong, effective response to chronic disease and in improving community environments to support healthy eating and activity. However, chronic disease prevention strategies—designing neighborhoods that encourage walking and bicycling to public transit, parks, and healthy food retail, or attracting grocery stores in communities that lack access to affordable fresh fruits and vegetables—are less effective when fear and violence pervade the environment. As more communities grapple with chronic disease, health practitioners and advocates are becoming increasingly aware of the need to address violence as a critical part of their efforts, and they are seeking further guidance on effective strategies.
The purpose of this paper is to provide guidance and deepen the understanding of the inter-relationship between violence and healthy eating and activity. It presents first-hand evidence based on a set of interviews Prevention Institute facilitated with community representatives—advocates and practitioners working in healthy eating and active living. Direct quotes from these interviewees appear in italics throughout this paper. In addition to the interviews, the Institute conducted a scan of peer- reviewed literature and professional reports that confirm the intersection between vio- lence and healthy eating and active living.3-12 …
**Prevention Institute was founded in 1997 to serve as a focal point for primary prevention practice—promoting policies, organizational practices, and collaborative efforts that improve health and quality of life. As a national non-profit organization, the Institute is committed to preventing illness and injury, to fostering health and social equity, and to building momentum for community prevention as an integral component of a quality health system. Publications are online and free.
Gun use in PG-13 movies has more than tripled since 1985
Researchers worry about effects on teen viewers
COLUMBUS, Ohio – The amount of gun violence shown in PG-13 films has more than tripled since 1985, the year the rating was introduced.
In fact, the most popular PG-13 movies of 2011 and 2012 showed significantly more gun violence than R-rated movies of the same time period, a new study reveals.
“It’s shocking how gun use has skyrocketed in movies that are often marketed directly at the teen audience,” said Brad Bushman, co-author of the study and professor of communication and psychology at The Ohio State University.
“You have to wonder why we are seeing this surge in gun violence in PG-13 movies, when it isn’t appearing in G, PG and R-rated films.”
Bushman conducted the research with Patrick Jamieson, Ilana Weitz and Daniel Romer of the Annenberg Public Policy Center at the University of Pennsylvania. The study was published online Nov. 11, 2013, in the journal Pediatrics.
Bushman said the results are concerning because other research has revealed the presence of a “weapons effect”: People who simply see a gun, or even a picture of a gun, are more aggressive toward others.
“Based on what researchers have found, it is not good for teens to be viewing this much gun violence in films,” he said.
PG movies suggest that “some material may not be suitable for children,” according to the Motion Picture Association of America, which creates the ratings. PG-13 movies carry a sterner warning: “Parents strongly cautioned. Some material may be inappropriate for children under 13.” The MPAA says a PG-13 movie “may go beyond the PG rating” in violence “but does not reach the restricted R cateogry.”
PG-13 movies are also the most popular among viewers – 13 of the top 25 films in release during 2012 carried that rating, including seven of the top 10, according to the MPAA.
“By the standards of the MPAA, PG-13 movies shouldn’t have as much violence as R-rated movies, but they clearly do. It appears sex scenes are more likely to result in an R rating than scenes of violence,” Bushman said.
The researchers studied a database of 915 films that were drawn from the 30 top-grossing films for each year from 1950 to 2012. Researchers identified violent sequences performed by each character for each five-minute segment of the films.
They also noted whether each violent sequence since 1985 (the first full year after the PG-13 rating was introduced) included the use of a gun.
Overall, findings showed that the rate of violent sequences nearly quadrupled from 1950 to 2010. Since 1985, 94 percent of the movies studied (367 in total) had one or more five-minute segments that included violence. Overall, the films contained 700 segments with gun violence.
Findings showed that R-rated films averaged about 1.54 segments per hour featuring gun violence, and that number didn’t fluctuate much from 1985 to 2010. Movies rated G and PG averaged 0.41 segments of gun violence per hour, which also hasn’t changed since 1985.
The story is much different for films rated PG-13, Bushman said. In 1985, PG-13 movies essentially didn’t have any scenes of gun violence, but the number rose steadily until about 2005, when it began escalating even faster.
By 2010, PG-13 films averaged as many sequences featuring gun violence per hour as R-rated films. In 2011 and 2012, PG-13 movies actually had more gun violence than R-rated movies.
“The trend of increasing gun violence in PG-13 movies is disturbing because of what we know about the weapons effect and because those are the films kids are most attracted to,” Bushman said.
The weapons effect was first shown in 1967, in a study by psychologists that showed participants who were provoked until angry acted more aggressively toward others when there was a gun on a table in front of them.
Since then, more than 50 other studies have replicated the weapons effect, even among people who weren’t angry.
“Seeing these violent gun scenes in movies may be strengthening the weapons effect among young people,” Bushman said.
“In addition, these movies essentially provide young people scripts for how to use guns in real life, as we have seen in copycat killings. It is a bad situation.”
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Data from the study were collected as part of The Coding of Media and Health Project at the Annenberg Public Policy Center. Funding for this study came from the APPC and the Robert Wood Johnson Foundation.
The emergency department entrance at Mayo Clinic’s Saint Marys Hospital. The red-and-white emergency sign is clearly visible. (Photo credit: Wikipedia)
Data from the National Hospital Ambulatory Medical Care Survey, 2009–2010
In 2009–2010, a total of 19.6 million emergency department (ED) visits in the United States were made by persons aged 65 and over. The visit rate for this age group was 511 per 1,000 persons and increased with age.
The percentage of ED visits made by nursing home residents, patients arriving by ambulance, and patients admitted to the hospital increased with age.
Twenty-nine percent of ED visits by persons aged 65 and over were related to injury, and the percentage was higher among those aged 85 and over than among those aged 65–74 or 75–84.
The percentage of ED visits caused by falls increased with age.
From 2000–2010, the number of persons in the United States aged 65 and over rose 15%, from 35.0 million to 40.3 million, and in 2010 this age group represented 13% of the population (1). It is estimated that by 2030, nearly one in five persons will be aged 65 and over (2). Given their growing proportion of the population, older individuals will comprise an increasing share of emergency department (ED) patients in the coming years. This is important because of the ED’s role in treating acute illness and injury in older adults and providing a pathway to these patients for hospital admission (3,4). This report describes ED visits made by individuals aged 65 and over and compares age groups 65–74, 75–84, and 85 and over.
Here in Toledo, Ohio my (Catholic) parish boundary includes a nearby state prison.
The bishop’s office redrew parish boundaries a few years back and decided our parish, three miles from the prison, includes the Catholics at Toledo Correctional Institution. Quite a challenge for us, we have about 100 “churchgoers” on the average Sunday, about 2/3 are over age 60. About 20 baptized Catholics (of an inmate population of 1,220) are registered within our parish.
We were encouraged to write the inmates. So I did. After about 3 letter exchanges, one asked me to visit him. So, after 3 weeks of pondering, I did. It really isn’t any big deal. Robb is very articulate and we do have some lively discussions in areas of politics, Catholic Church “hot topics”, and philosophy.
In the past year, four inmates have been murdered. at Toledo Correctional. Allegedly by other inmates. In Michigan, only one inmate was murdered in the whole state in the last year. The rise in violence is in tandem with increasing overcrowding, especially double bunking in cells designed for single occupancy.
I am including this item because overcrowding is a safety and (mental) health issue. The murders here at Toledo Correctional were in the higher security levels, Robb is in the lowest security level. Still, I cannot imagine how this is impacting Robb’s mental health.
Excerpts from the handbook
(I realize American prisons are probably better than the worst of the worst internationally, still, there is room for improvement)
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In very diverse environments and over many years, the ICRC has witnessed first- hand the consequences of overcrowding on detainees and on the authorities. Indeed, overcrowding is an increasingly widespread problem in a number of countries and places of detention. In itself, it is a very serious humanitarian concern, as it auto- matically generates substandard and often inhumane conditions of detention. Tens of thousands of people are forced to live for extended periods in congested accom- modation, with insufficient space to move, sit or sleep. This seriously compromises the ability of the administration to fulfil detainees’ basic needs in terms of living conditions, medical care, legal aid and family visits. Being squeezed into cramped living quarters, often in appalling hygiene conditions and with no privacy, makes the experience of being deprived of freedom—already stressful in normal circumstances— exponentially worse. It erodes human dignity and undermines detainees’ physical and mental health, as well as their reintegration prospects. In addition to putting excessive strain on infrastructures, it heightens the potential for tensions and conflicts among detainees and with staff. It quickly leads to difficulties in maintaining good order within the prison, resulting in potentially severe consequences in terms of safety for the detainees, as well as in terms of supervision and security.
While the consequences are particularly grave for the men, women and children deprived of their liberty, they also affect the frontline staff whose job it is to protect and meet the needs of the detainees. Overwhelmed by excessive numbers and directly exposed to the frustration of the detainees without the resources needed to guarantee security or access to the most basic services, detention staff work in difficult condi- tions and are exposed to constant pressure and risk.
ICRC knows from experience that situations of overcrowding, once established, trig- ger a downward spiral which has a negative impact on the entire criminal justice system as a result of increasing congestion, staff demotivation and the development of parallel coping mechanisms or corruption.
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3. Broader consequences of excessive imprisonment
The impact of overcrowding does not remain within the prison walls. It can have a detrimental impact on public health. The cost of the excessive use of imprisonment, which is a fundamental reason for prison overcrowding in countries worldwide (see chapter B), can be significant, increasing the poverty levels and socio-economic mar- ginalization of certain groups of people and reducing funds available for other spheres of government expenditure.
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3.1 The cost of imprisonment
Numerous studies have shown that imprisonment disproportionately affects people living in poverty. When an income generating member of the family is imprisoned, the sudden loss of income can have a severe impact on the economic status of the rest of the family—especially so in low resource countries where the state does not usually provide financial assistance to the poor and where it is not unusual for one person to financially support an extended family network. When released, often with no prospects for employment due to their criminal record, former prisoners are generally subjected to socio-economic exclusion and are vulnerable to an endless cycle of poverty, marginalization, criminality and imprisonment. Thus, imprisonment contributes directly to the impoverishment of the prisoner and his or her family. Studies have also shown that children of parents who have been imprisoned are more likely to come into conflict with the law and that once detained, they are likely to be further criminalized. Thus the cycle is expanded, creating future victims and reducing future potential economic performance
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Related articles
State report rips Toledo prison (toledoblade.com, 09/13/2013)
“A state committee on Thursday issued a harsh, lengthy inspection report of the Toledo Correctional Institution, citing significant increases in assaults, high employee-turnover rates, rampant drug trading, and three homicides reported there in the past year.The 164-page report from the Correctional Institution Inspection Committee shows that inmate-on-inmate assaults increased by nearly 113 percent and inmate-on-staff assaults increased nearly 74 percent from 2010 to 2012. The legislatively established committee monitors prison facilities, conducts unannounced inspections of prisons, and writes reports of their activities.”
“The prison has the highest staff turnover rate — 16.5 percent — of all prisons in the state, according to the report. Most staff resignations come while employees are being investigated, according to the report.
At the vanguard of innovation in the nursing home industry, the three-year-old Leonard Florence Center for Living exemplifies a new model of long-term care known as the Green House, and nothing about it seems institutional. Each of the five upper floors constitutes two separate “households” with private rooms for 10 residents. The normally dominant nurse’s station has been eliminated and instead there are common areas in each household—a living room furnished with comfortable sofas and chairs around a fireplace, an open kitchen and a communal dining table where residents often eat together. Cooking, housekeeping and even laundry are handled by two certified nursing aides known as shahbazim—derived from Persian, it means “nurturing of elders”—who also care for residents. Traditional nursing homes, in contrast, have clear demarcations separating housekeepers, kitchen workers, nurses and aides, who follow rigid schedules for serving meals or dispensing medications.
At Leonard Florence, Mehlhop can sleep, bathe, eat and roam around whenever she wants. The environment is calm and cheery, with none of the physical restraints found in most nursing homes or the alarms that sound if residents get up from a wheelchair, for example. (Instead, patients wear ankle bracelets that help the staff keep tabs on them and will disable the elevator if a patient tries to leave.)
Leonard Florence is far from the only nursing facility striving to create a homelike atmosphere and improve residents’ quality of life. Building a new Green House or undertaking a major physical renovation can be part of the strategy, but other nursing homes are primarily working to transform how they’re run, embracing a movement known simply as “culture change” that entails shifting away from the emphasis on efficiency and economies of scale that characterizes most nursing homes. Culture change typically requires an operational reorganization to give staff members more autonomy and to let residents have a say in even the smallest details of their lives. “It’s about not looking at residents as a task, but rather as who they are as individuals,”
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Yet building a new, small nursing home that can handle only a relative handful of residents is an expensive proposition. “If it weren’t for the price tag, everyone would be doing it,” says Barry Berman, chief executive officer of the Chelsea Jewish Foundation, which owns the Leonard Florence Center. The home cost $36 million to build, with some two-thirds of the money coming from private donations and government programs. Most traditional nursing homes cost less than half that much, but the Leonard Florence Center is over twice the size of a traditional nursing home and was the first Green House to be built in an urban area. Its multistory construction is also a departure from the usual single-level, ranch-style homes that are typical of Green House centers. The payoff, however, has been the residents’ lower hospitalization and readmission rates. The center has also received high scores for resident and family satisfaction, which Berman describes as “off the charts.” The foundation is now undertaking a $13 million renovation of a 30-year-old, 120-bed skilled nursing facility across town from Leonard Florence. “We’re bringing in as many elements of the Green House as we can and doing our best to retrofit a traditional nursing home,” says Adam Berman, chief operating officer of the nonprofit.
The Green House model is receiving increased academic scrutiny, and early studies have shown positive trends in quality of life for residents, greater family satisfaction, and a lower incidence of rehospitalization, bedsores, depression and other health problems. According to the Green House Project, 83% of Green Houses received a rating of four out of five stars or better on the Centers for Medicare & Medicaid Services’ five-star quality rating system, compared to 42% of nursing homes nationally. But the data are early. “The jury’s still out on whether Green Houses or other small homes achieve equal or better clinical outcomes than traditional models, and whether they’re financially sustainable—factors that may ultimately matter a lot more than the humanistic components in terms of their future growth…
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Studies of the model’s effectiveness have found a higher quality of care, reduced staff turnover and lower rates of infections for residents….
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As encouraging as such stories may be, however, there are questions about how far relatively small-scale efforts can go to reform a giant industry. In a 2010 study by Susan Miller, a professor of health services, practice and policy at Brown University School of Public Health, leadership issues, higher costs and regulatory problems were cited by long-term-care leaders as the most common barriers to implementing culture change. Yet many experts believe those obstacles can be overcome. For example, a campaign called Advancing Excellence in America’s Nursing Homes provides an array of do-it-yourself resources and networks of advisors to help improve clinical outcomes. More than 9,000 nursing homes have participated since the campaign’s launch in 2006. Meanwhile, federal regulators have adjusted some rules to encourage and reward culture change—for example, rather than checking that a nursing home has regular meal schedules, making sure that residents are well fed. And proponents point to studies showing that nursing homes committed to culture change may benefit financially. A study by Pioneer Network, for example, found that from 2004 to 2008, facilities undergoing culture change achieved higher occupancy rates and increased revenue.
Early life pain alters neural circuits in the brain that regulate stress, suggesting pain experienced by infants who often do not receive analgesics while undergoing tests and treatment in neonatal intensive care may permanently alter future responses to anxiety, stress and pain in adulthood, a research team led by Dr. Anne Murphy, associate director of the Neuroscience Institute at Georgia State University, has discovered.
n estimated 12 percent of live births in the U.S. are considered premature, researchers said. These infants often spend an average of 25 days in neonatal intensive care, where they endure 10-to-18 painful and inflammatory procedures each day, including insertion of feeding tubes and intravenous lines, intubation and repeated heel lance. Despite evidence that pain and stress circuitry in the brain are established and functional in preterm infants, about 65 percent of these procedures are performed without benefit of analgesia. Some clinical studies suggest early life pain has an immediate and long-term impact on responses to stress- and anxiety-provoking events.
The Georgia State study examined whether a single painful inflammatory procedure performed on male and female rat pups on the day of birth alters specific brain receptors that affect behavioral sensitivity to stress, anxiety and pain in adulthood. The findings demonstrated that such an experience is associated with site-specific changes in the brain that regulate how the pups responded to stressful situations. Alterations in how these receptors function have also been associated with mood disorders.
The study findings mirror what is now being reported clinically. Children who experienced unresolved pain following birth show reduced responsiveness to pain and stress.
New research from North Carolina State University and the University of Minnesota finds that people in the United States want labels on food products that use nanotechnology – whether the nanotechnology is in the food or is used in food packaging. The research also shows that many people are willing to pay more for the labeling.
Study participants supported labeling products in which nanotechnology had been added to food, as well as products in which nanotechnology had been incorporated into the packaging.
“We wanted to know whether people want nanotechnology in food to be labeled, and the vast majority of the participants in our study do,” says Dr. Jennifer Kuzma, senior author of a paper on the research and Goodnight-Glaxo Wellcome Distinguished Professor of Public Administration at NC State. “Our study is the first research in the U.S. to take an in-depth, focus group approach to understanding the public perception of nanotechnology in foods.”
The researchers convened six focus groups – three in Minnesota and three in North Carolina – and gave study participants some basic information about nanotechnology and its use in food products. Participants were then asked a series of questions addressing whether food nanotechnology should be labeled. Participants were also sent a follow-up survey within a week of their focus group meeting.
Study participants were particularly supportive of labeling for products in which nanotechnology had been added to the food itself, though they were also in favor of labeling products in which nanotechnology had only been incorporated into the food packaging.
However, the call for labeling does not indicate that people are necessarily opposed to the use of nanotechnology in food products. For example, many study participants indicated support for the use of nanotechnology to make food more nutritious or to give it a longer shelf life – but they still wanted those products to be labeled.
“People do have nuanced perspectives on this,” Kuzma says. “They want labeling, but they also want access to reliable, research-based information about the risks associated with labeled products – such as a Food and Drug Administration website offering additional information about labeled products.”
The researchers also found that about 60 percent of the study participants who responded to the follow-up survey were willing to pay an additional 5 to 25 percent of the product price for either nanotechnology-free products or for nanotechnology labeling.
The paper, “Hungry for Information: Public Attitudes Toward Food Nanotechnology and Labeling,” was published online Oct. 7 inReview of Policy Research. Lead author of the study is Jonathan Brown, a former graduate student at the University of Minnesota. The work was supported by National Science Foundation grant SES-0709056.
rom the thesis abstract: “Gun violence in America must be addressed at the highest levels of society. Newtown, Aurora, and Virginia Tech were attacks on the very fabric of America. School shootings represent attacks on our nations’ future. A public health approach to gun violence focuses on prevention. Public safety professionals, educators and community leaders are squandering opportunities to prevent horrific acts of extreme violence. Preparedness is derived by planning, which is critical to mobilizing resources when needed. Rational public policy can work. Sensible gun legislation, which is accessible through a public health approach to gun violence, neither marginalizes nor stigmatizes any one group. University administrators must fully engage the entire arsenal of resources available to confront this pernicious threat. The academic community can create powerful networks for research, collaboration and information sharing. These collective learning environments are investments in the knowledge economy. In order for the police to remain relevant, they must actively engage the community they serve by developing the operational art necessary to cultivate knowledge, relationships and expertise. Police departments must emphasize strategies that improve performance. Police officers must understand the mission and meaning of ‘To Protect and Serve’ and the consequences of public safety, which often comes at their personal peril. Gun violence in America is a public health epidemic and preventing it requires a collective responsibility.”
From the 7 October 2013 press release at Trust for America’s Health – Preventing Epidemics. Protecting People.
Prescription Drug Abuse: More than Half of States Score 6 or Less out of 10 on New Policy Report Card, While Drug Overdose Deaths Doubled in 29 States in the Last Decade
Washington, D.C. October 7, 2013 – A new report, Prescription Drug Abuse: Strategies to Stop the Epidemic, finds that 28 states and Washington, D.C. scored six or less out of 10 possible indicators of promising strategies to help curb prescription drug abuse. Two states, New Mexico and Vermont, received the highest score receiving all 10 possible indicators, while South Dakota scored the lowest with two out of 10.
According to the report by the Trust for America’s Health (TFAH), prescription drug abuse has quickly become a top public health concern, as the number of drug overdose deaths – a majority of which are from prescription drugs – doubled in 29 states since 1999. The rates quadrupled in four of these states and tripled in 10 more of these states.
Prescription drug related deaths now outnumber those from heroin and cocaine combined, and drug overdose deaths exceed motor vehicle-related deaths in 29 states and Washington, D.C. Misuse and abuse of prescription painkillers alone costs the country an estimated $53.4 billion each year in lost productivity, medical costs and criminal justice costs. Currently only one in 10 Americans with a substance abuse disorder receives treatment.
“Prescription drugs can be a miracle for many, but misuse can have dire consequences. The rapid rise of abuse requires nothing short of a full-scale response – starting with prevention and education all the way through to expanding and modernizing treatment,” said Jeffrey Levi, PhD, executive director of TFAH. “There are many promising signs that we can turn this around – but it requires urgent action.”
In the Prescription Drug Abuse report, TFAH – in consultation with a number of public health, clinical, injury prevention, law enforcement and community organization experts – reviewed a range of national recommendations and examined a set of 10 indicators of strategies being used in states to help curb the epidemic. There are indications that some of these efforts and strategies may be having a positive impact — the number of Americans abusing prescription drugs decreased from 7 million in 2010 to 6.1 in 2011, according to the National Survey on Drug Use and Health.
Some key findings from the report include:
Appalachia and Southwest Have the Highest Overdose Death Rates: West Virginia had the highest number of drug overdose deaths, at 28.9 per every 100,000 people – a 605 percent increase from 1999, when the rate was only 4.1 per every 100,000. North Dakota had the lowest rate at 3.4 per every 100,000 people. Rates are lowest in the Midwestern states.
Rescue Drug Laws: Just over one-third of states (17 and Washington, D.C.) have a law in place to expand access to, and use of naloxone – a prescription drug that can be effective in counteracting an overdose – by lay administrators.
Good Samaritan Laws: Just over one-third of states (17 and Washington, D.C.) have laws in place to provide a degree of immunity from criminal charges or mitigation of sentencing for individuals seeking to help themselves or others experiencing an overdose.
Medical Provider Education Laws: Fewer than half of states (22) have laws that require or recommend education for doctors and other healthcare providers who prescribe prescription pain medication.
Support for Substance Abuse Treatment: Nearly half of states (24 and Washington, D.C.) are participating in Medicaid Expansion – which helps expand coverage of substance abuse services and treatment.
ID Requirement: 32 states have a law requiring or permitting a pharmacist to require an ID prior to dispensing a controlled substance.
Prescription Drug Monitoring Programs: While nearly every state (49) has a Prescription Drug Monitoring Program (PDMP) to help identify “doctor shoppers,” problem prescribers and individuals in need of treatment, these programs vary dramatically in funding, use and capabilities. For instance, only 16 states require medical providers to use PMDPs.
“Fifty Americans die a day from prescription drug overdoses, and more than 6 million suffer from prescription drug abuse disorders. This is a very real epidemic – and warrants a strong public health response,” said Andrea Gielen, ScD, Director of the Johns Hopkins Center for Injury Research and Policy. “We must use the best lessons we know from other public health and injury prevention success stories to work in partnership with clinical care, law enforcement, the business community, community-based organizations, and other partners to work together to curb this crisis.”
Educate the public to understand the risks of prescription drug use to avoid misuse in the first place;
Ensure responsible prescribing practices, including increasing education of healthcare providers and prescribers to better understand how medications can be misused and to identify patients in need of treatment;
Increase understanding about safe storage of medication and proper disposal of unused medications, such as through “take back” programs;
Make sure patients do receive the pain and other medications they need, and that patients have access to safe and effective drugs;
Improve, modernize and fully-fund Prescription Drug Monitoring Programs, so they are real-time, interstate and incorporated into Electronic Health Records, to quickly identify patients in need of treatment and connect them with appropriate care and identify doctor shoppers and problem prescribers;
Make rescue medications more widely available by increasing access for at-risk individuals to naloxone and provide immunity for individuals and others seeking help; and
Expand access to and availability of effective treatment options as a key component of any strategy to combat prescription drug abuse.
According to the National Center for Injury Prevention and Control (NCIPC), nationally, sales of prescription painkillers per capita have quadrupled since 1999 – and the number of fatal poisonings due to prescription painkillers has also quadrupled. Enough prescription painkillers were prescribed in 2010 to medicate every American adult continually for a month.
“The release of the prescription drug abuse report by the Trust for America’s Health represents a significant step forward in elevating public awareness of the state of prescription drug abuse in the US”, according to Ginny Ehrlich, CEO of Clinton Health Matters Initiative (CHMI). “We are proud that the Trust has completed this important research as part of its CHMI Commitment to Action and congratulate the Trust on continuing to advocate for innovation and action towards addressing this public epidemic.”
The report was supported by a grant from the Robert Wood Johnson Foundation.
Score Summary: A full list of all of the indicators and scores, listed below, is available along with the full report on TFAH’s web site at www.healthyamericans.org and RWJF’s web site athttp://www.rwjf.org/RxReport. For the state-by-state scoring, states received one point for achieving an indicator or zero points if they did not achieve the indicator. Zero is the lowest possible overall score, 10 is the highest. Data for the indicators were drawn from a number of sources, including the National Alliance for Model State Drug Laws, NCIPC, Centers for Disease Control and Prevention, the Alliance of States with Prescription Drug Monitoring Programs, the National Conference of State Legislators, the Network for Public Health Law, the Kaiser Family Foundation and a review of current state legislation and regulations by TFAH. In August 2013, state health departments were provided with opportunity to review and revise their information.
10 out of 10: New Mexico and Vermont
9 out of 10: Kentucky, Massachusetts, New York and Washington
8 out of 10: California, Colorado, Connecticut, Delaware, Illinois, Minnesota, North Carolina, Oklahoma, Oregon, Rhode Island and West Virginia
7 out of 10: Florida, Nevada, New Jersey, Tennessee and Virginia
6 out of 10: Arkansas, District of Columbia, Georgia, Hawaii, Iowa, Louisiana, Maryland, Michigan, North Dakota, Ohio, Texas and Utah
5 out of 10: Alaska, Idaho, Indiana, Maine, Mississippi, Montana, New Hampshire and South Carolina
4 out of 10: Alabama, Arizona, Kansas, Pennsylvania, Wisconsin and Wyoming
3 out of 10: Missouri and Nebraska
2 out of 10: South Dakota
STATE-BY-STATE DRUG OVERDOSE MORTALITY RANKINGS
Note: Rates include total drug overdose mortality rates, the majority of which are from prescription drugs. 1 = Highest rate of drug overdose fatalities, 51 = lowest rate of drug overdose fatalities. Rankings are based on data from CDC’s National Center for Health Statistics, WONDER Online Database, 2010. The numbers are based on the number of people per 100,000.
1. West Virginia**** (28.9); 2. New Mexico (23.8); 3. Kentucky**** (23.6); 4. Nevada (20.7); 5. Oklahoma*** (19.4); 6. Arizona (17.5); 7. Missouri*** (17); 8. (tie) Tennessee** and Utah (16.9); 10. Delaware** (16.6); 11. Florida** (16.4); 12. Ohio*** (16.1); 13. Rhode Island** (15.5); 14. Pennsylvania (15.3); 15. Wyoming*** (15); 16. South Carolina*** (14.6); 17. Indiana**** (14.4); 18. Michigan*** (13.9); 19. Louisiana*** (13.2); 20. Washington (13.1); 21. (tie) District of Columbia and Montana** and Oregon** (12.9); 24. Colorado (12.7); 25. Arkansas** (12.5); 26. (tie) Alabama*** and Idaho** and New Hampshire** (11.8); 29. Alaska (11.6); 30. (tie) Mississippi***and North Carolina** (11.4); 32. (tie) Maryland and Massachusetts (11); 34. (tie) Hawaii and Wisconsin** (10.9); 36. Georgia*** (10.7); 37. California (10.6); 38. Maine (10.4); 39. Connecticut (10.1); 40. Illinois (10); 41. New Jersey (9.8); 42. Vermont** (9.7); 43. (tie) Kansas** and Texas (9.6); 45. Iowa**** (8.6); 46. New York (7.8); 47. Minnesota** (7.3); 48. Virginia (6.8); 49. Nebraska** (6.7); 50. South Dakota (6.3); 51. North Dakota (3.4).
** Drug Overdose Mortality Rates doubled from 1999 to 2010
*** Drug Overdose Mortality Rates tripled from 1999 to 2010
**** Drug Overdose Mortality Rates quadrupled from 1999 to 2010
Trust for America’s Health is a non-profit, non-partisan organization dedicated to saving lives by protecting the health of every community and working to make diseaseprevention a national priority. For more information, visit www.healthyamericans.org.
At least two-thirds of the perpetrators and victims of gun violence are males under the age of 30. What else do they have in common? They live in neighborhoods with high crime rates and low family incomes, they knew each other before the violence broke out, they usually aren’t employed.
But there’s another commonality these young people share which isn’t often mentioned in discussions about gun violence and crime.
It turns out that the part of the brain that controls processing of information about impulse, desire, goals, self-interest, rules and risk develops latest and probably isn’t fully formed until the mid-20s or later. And while adolescents and young men understand the concepts of ‘good’ versus ‘bad’ as well as older adults, they tend to let peer pressures rather than expected outcomes guide their behavior when choosing between risks and rewards.
Take this neurological-behavioral profile of males between ages 15 to 30 and stick a gun in their hands. The brain research clearly demonstrates that kids and young adults walking around with guns understand the risks involved. Whether it’s the NSSF’s new Project ChildSafe, the NRA’s Eddie Eagle or the grassroots gun safety programs that have expanded since Sandy Hook, nobody’s telling the kids something they don’t already know.
So what can we do to mitigate what President Obama calls this ‘epidemic’ of gun violence when the population most at risk consciously chooses to ignore the risk? I suggest that we look at what communities have done to protect themselves from other kinds of epidemics that threatened public health in the past.
And the most effective method has been to quarantine, or isolate, the area or population where the threat is most extreme. It worked in 14th-century Italy, according to Boccaccio in The Decameron. Why wouldn’t it work now?
Last month the city of Springfield, Mass., recorded its 12th gun homicide. If the killing rate continues, the city might hit 15 shooting fatalities this year, a number it actually surpassed in 2010. This gives the city a homicide rate of 10.2 per 100,000 residents, nearly three times the national rate. Virtually all the violence takes place in two specific neighborhoods bounded by Interstate 291 and State Route 83, and all the victims are between 15 and 30 years old.
This area of less than four square miles contains roughly 30,000 residents which means the homicide rate here is 45 per 100,000, more than 10 times the national rate. And the numbers haven’t really changed in the last four or five years. This isn’t an epidemic?
Don’t get me wrong. The word ‘quarantine’ evokes images of the Warsaw Ghetto and I’m not proposing anything like that. But think of police in this neighborhood behaving like public health workers; going door to door, asking people what they know about the existence of guns. There are no constitutional issues here; someone doesn’t want to answer, you go on to the next door.
Wouldn’t the city send people out to make contact with residents if, for example, the water supply suddenly couldn’t be used?
There are grassroots efforts all over the country to make neighborhoods safer from guns. But they usually consist of meetings in churches and other public places where people come together to voice and share their concerns. It’s not the folks who come out to the meeting that you need to reach; it’s the ones who remain at home.
I’m suggesting that we go block by block, again and again, to make sure that people know about the epidemic called gun violence. It’s spread by a virus called guns, and as long as young men between 15 and 30 believe they are immune to the risk of this virus, the epidemic will continue to spread.
American Journal of Public Health Provides Open Access to Articles on Gun Violence, Veterans Health, and Suicide http://ajph.aphapublications.org/topic/gunviolence
The American Journal of Public Health has compiled a collection of papers and other resources to help promote awareness and policy change surrounding gun violence, veterans health, and suicide.
According to The Illinois Environmental Protection Agency: Mercury poses a health risk to everybody but especially to young children and fetuses because they’re still developing. Prolonged low level exposure may cause learning disabilities by hurting the ability of children to think and read. Adults who have been exposed to high levels of mercury may experience trembling hands and numbness or tingling in their lips, tongues, fingers, and toes. Acute mercury poisoning especially through ingestion, can damage the brain, liver, kidneys, and even cause death.
Research published in Environmental Health and conducted in part by a scientist at the Institute for Agriculture and Trade Policy has revealed that high-fructose corn syrup (HFCS) is contaminated with the toxic heavy metal mercuryHigh-fructose corn syrup is used in almost everything, it seems. A second study conducted by David Wallinga, M.D., entitled “Not So Sweet: Missing Mercury andHigh Fructose Corn Syrup” reveals that nearly one-third of all grocery items sweetened with HFCS were contaminated with mercury
Most people don’t know how high-fructose corn syrup is really made. One of those processes is a bizarre chemical brew involving the creation of caustic soda by exposing raw materials to pools of electrified mercury in a large vat. Through this process, the caustic soda gets contaminated with mercury, and when corn kernels are exposed to this caustic soda to break them down, that contamination is passed through to the HFCS.
Another toxic chemical, glutaraldehyde, is also used in the production of HFCS. It’s so toxic that consuming even a small amount of it can burn a hole in your stomach.
WASHINGTON – The U.S. Environmental Protection Agency (EPA) has launched a web-based tool, called ChemView, to significantly improve access to chemical specific regulatory information developed by EPA and data submitted under the Toxic Substances Control Act (TSCA).
“This online tool will improve access to chemical health and safety information, increase public dialogue and awareness, and help viewers choose safer ingredients used in everyday products,” said James Jones, assistant administrator for the Office of Chemical Safety and Pollution Prevention. “The tool will make chemical information more readily available for chemical decision-makers and consumers.”
The ChemView web tool displays key health and safety data in an online format that allows comparison of chemicals by use and by health or environmental effects. The search tool combines available TSCA information and provides streamlined access to EPA assessments, hazard characterizations, and information on safer chemical ingredients. Additionally, the new web tool allows searches by chemical name or Chemical Abstracts Service (CAS) number, use, hazard effect, or regulatory action. It has the flexibility to create tailored views of the information on individual chemicals or compare multiple chemicals sorted by use, hazard effect or other criteria. The new portal will also link to information on manufacturing, processing, use, and release data reported under the Chemical Data Reporting Rule, and the Toxics Release Inventory.
In the months ahead, EPA will be continuously adding additional chemicals, functionality and links. When fully updated, the web tool will contain data for thousands of chemicals. EPA has incorporated stakeholder input into the design, and welcomes feedback on the current site.
By increasing health and safety information, as well as identifying safer chemical ingredients, manufacturers and retailers will have the information to better differentiate their products by using safer ingredients.
In 2010, EPA began a concerted effort to increase the availability of information on chemicals as part of a commitment to strengthen the existing chemicals program and improve access and usefulness of chemical data and information. This included improving access to the TSCA inventory, issuing new policies for the review of confidential business information claims for health and safety studies, and launching the Chemical Data Access Tool. Today’s launch of the ChemView provides the public with a single access point for information that has been generated on certain chemicals regulated under TSCA.
(CHICAGO) – The results of a new study by bone and joint experts at Rush University Medical Center suggest that patients with knee osteoarthritis (OA) who wear flat, flexible footwear, which allows natural foot mobility and provide sufficient support for the foot, had significant reduction in knee loading—the force placed upon the joint during daily activities.
Findings from the study were published in an issue of Arthritis & Rheumatism, a journal of the American College of Rheumatology (ACR).
The research led by Dr. Najia Shakoor, a rheumatologist at Rush, shows that long term use of the such footwear, called “mobility shoes,” helped OA patients adapt their gait or how they walk, which improved knee loading, even when the mobility shoes were no longer worn.
In previous studies, Shakoor and colleagues from Rush found that walking barefoot as well as with ‘mobility shoes,’ which are designed to mimic barefoot mechanics, was linked to reduced knee loading compared to when walking with regular footwear worn by participants. However, the authors thought the long-term effects of the specialized footwear need further studying.
“There is much interest in biomechanical interventions, such as orthotic inserts, knee braces, and footwear that aim to improve pain and delay OA progression by decreasing impact on joints,” said Shakoor, the principal investigator of the study who is also an associate professor in the department of internal medicine at Rush. “In the present study, we expand understanding of our earlier research by evaluating the impact of the mobility footwear on gait after six months of use.”
More than 27 million Americans over the age of 25 have some form of OA, which causes painful swelling and stiffness in the hand, foot, knee or hip joints. According to existing research, doctor-diagnosed arthritis will swell to 67 million U.S. adults by 2030. Furthermore, the Centers for Disease Control and Prevention (CDC) estimate that 16% of adults 45 years of age and older are burdened with symptomatic knee OA.
The Rush team recruited 16 participants with knee OA, obtaining a baseline gait with participants walking in their own shoes, mobility shoes and barefoot. Participants wore the mobility shoes for six hours each day for six days per week and patient gait was evaluated at 6, 12 and 24 weeks in all conditions.
Findings suggest that by 24 weeks, participants wearing mobility footwear saw an 18 percent reduction in knee adduction moment (KAM), which is the load on the inner or medial aspect of the knee when walking compared to baseline knee loading in their own footwear. This is where most people develop knee OA.
No significant difference in KAM was found between walking with mobility shoes and barefoot. Compared to baseline, analyses indicate an 11 percent and 10 percent reduction in KAM for OA patients walking in their own shoes and barefoot, respectively, suggesting the mobility shoes may have “re-trained” participant’s gait.
“Patients with OA who use flat, flexible footwear may experience a significant reduction in knee loading with continued use,” said Shakoor. “Our investigation provides evidence that footwear choice may be an important consideration in managing knee OA.
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The Rush research team involved in the study includes Roy H. Lidtke, Markus A. Wimmer, Rachel A. Mikolaitis, Kharma C. Foucher, Laura E. Thorp, Louis F. Fogg and Joel A. Block.
Please note: Based on the study results, a patented shoe design called X-Sole Relief Technology in Flex-OA has been developed by Dr. Comfort. The shoe has been available on the market since January 2013.
New research for the University of Guelph shows that the majority of herbal products on the market contain ingredients that are not listed on their labels.
The study, published in the journal BMC Medicine, used DNA barcoding technology to assess the components of 44 herbal products from 12 companies. They found that 60% of the products contained plant species that were not listed on the label, and 20% used fillers like rice, soybeans, and wheat which were also not divulged on the bottles.
For instance, products sold as St. John’s wort supplement, which is sometimes used to treat depression, contained Senna alexandrina, which is a plant that spurs laxative symptoms. Other products contained Parthenium hysterophorus (feverfew), which is known to cause swelling and mouth numbness. One ginkgo product contained Juglans nigra (black walnut), which should not be consumed by people with nut allergies — but this warning was not noted on the label.
“It’s common practice in natural products to use fillers such as these, which are mixed with active ingredients. But a consumer has a right to see all of the plant species used in producing a natural product on the list of ingredients,” lead author Steven Newmaster, an integrative biology professor at the Guelph-based Biodiversity Institute of Ontario said in a statement.
Ever notice that people run straight to the medicine cabinet to do harm to themselves or others? I want you to know the harder the effort is to obtain items to hurt oneself, the less likely one is to follow through on the notion. On another related note, here’s a quick not-so-fun-but-interesting fact. One of the differences between America and say, certain European countries is the oversized influence of corporations in the States. Why am I talking about that on a medical blog? Read on. If you can’t tell where I’m going with this, you’ll get it pretty quickly.
Here’s my top five items I want you to take out your medicine cabinets and lock up.
1. Any jumbo sized container of any medication. Think about two of the most common over the counter (OTC) medications used for suicide attempts: acetaminophen (Tylenol) and salicylate (aspirin). One thing they have in common is you can buy what amounts to a tub-full of it at your local superstore in the United States. They should call these things ‘suicide quantities’, because often those in the midst of a suicide attempt will grab and swallow whatever is convenient. Many different medications will hurt you if you take enough; Tylenol and aspirin certainly fit that bill. Observing that (and additional considerations after the deaths due to the lacing of Tylenol with cyanide back in 1983), the Brits decided to not only pass a law limiting quantities, but certain medications that are high-frequency and high-risk for suicide use are now mandatorily dispensed in those annoying containers that you have to pop through the plastic container. Needless to say, observed suicide rates by medication rates plummeted as a result. Wonder why that hasn’t been implemented in the good ol’ USA?
2. Have teens in your house? Lock up the Robitussin and NyQuil.
Aiming to quell heated national debate about gun control with factual answers, two UC Irvine mathematicians have designed parameters to measure how to best prevent both one-on-one killings and mass shootings in the United States. Their paper appears Friday in the journal PLOS ONE.
“It’s time to bring a scientific framework to this problem,” said lead author Dominik Wodarz, a mathematical biologist who works on disease and evolutionary dynamics. His co-author and wife, Natalia Komarova, a mathematician who studies biomedical and social trends, added: “Can we design a rational way to argue about guns?”
Both were appalled not just by the December shooting deaths of 20 youngsters and eight adults in Newtown, Conn., but also by the bitterly emotional dispute over weapons that erupted anew. They decided to put their professional expertise to work.
“This debate cannot be settled satisfactorily by verbal arguments alone, since these are often driven by opinion and lack a solid scientific backing,” the authors write. “What is under debate is essentially an epidemiological problem: How do different gun control strategies affect the rate at which people become killed by attackers, and how can this rate be minimized?”
The duo reviewed available data stretching as far back as World War I, then drew up equations to compute whether policies ranging from a total firearm ban to “arm everyone” increase or decrease homicides. After running the numbers, they found that in more common domestic and one-on-one crimes, reduced legal gun availability — if properly enforced — is likelier to lower deaths. But in rare mass shootings, armed citizens might save lives if sufficiently trained to avoid accidentally shooting fleeing bystanders.
An example of a phishing e-mail, disguised as an official e-mail from a (fictional) bank. The sender is attempting to trick the recipient into revealing confidential information by “confirming” it at the phisher’s website. Note the misspelling of the words received and discrepancy. Also note that although the URL of the bank’s webpage appears to be legitimate, the hyperlink would actually be pointed at the phisher’s webpage. (Photo credit: Wikipedia)
The author of a paper to be presented at the upcoming 2013 International Human Factors and Ergonomics Society Annual Meeting has described behavioral, cognitive, and perceptual attributes of e-mail users who are vulnerable to phishing attacks. Phishing is the use of fraudulent e-mail correspondence to obtain passwords and credit card information, or to send viruses.
In “Keeping Up With the Joneses: Assessing Phishing Susceptibility in an E-mail Task,” Kyung Wha Hong discovered that people who were overconfident, introverted, or women were less able to accurately distinguish between legitimate and phishing e-mails. She had participants complete a personality survey and then asked them to scan through both legitimate and phishing e-mails and either delete suspicious or spam e-mails, leave legitimate e-mails as is, or mark e-mails that required actions or responses as “important.”
“The results showed a disconnect between confidence and actual skill, as the majority of participants were not only susceptible to attacks but also overconfident in their ability to protect themselves,” says Hong. Although 89% of the participants indicted they were confident in their ability to identify malicious e-mails, 92% of them misclassified phishing e-mails. Almost 52% in the study misclassified more than half the phishing e-mails, and 54% deleted at least one authentic e-mail.
Gender, trust, and personality were correlated with phishing vulnerability. Women were less likely than men to correctly label phishing e-mails, and subjects who self-reported as “less trusting, introverts, or less open to new experiences” were more likely to delete legitimate e-mails.
Hong will continue to develop a user profile that can predict when and with whom phishing attacks are likely to be successful. Information gained in these studies will be used to design effective tools to prevent and combat phishing attacks.
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To receive an advance copy of the paper for media reporting purposes, or for questions about the 2013 International Annual Meeting, contact HFES Communications Director Lois Smith (310/394-1811; lois@hfes.org).
The Human Factors and Ergonomics Society is the world’s largest nonprofit individual-member, multidisciplinary scientific association for human factors/ergonomics professionals, with more than 4,600 members globally. HFES members include psychologists and other scientists, designers, and engineers, all of who have a common interest in designing systems and equipment to be safe and effective for the people who operate and maintain them.
“Human Factors and Ergonomics: People-Friendly Design Through Science and Engineering”
The 2013 World Drug Report released today in Vienna shows that, while the use of traditional drugs such as heroin and cocaine seems to be declining in some parts of the world, prescription drug abuse and new psychoactive substance [NPS]
An arrangement of psychoactive drugs (Photo credit: Wikipedia)
abuse is growing. In a special high-level event of the Commission on Narcotic Drugs, UNODC Executive Director Yury Fedotov urged concerted action to prevent the manufacture, trafficking and abuse of these substances.
Marketed as ‘legal highs’ and ‘designer drugs’, NPS are proliferating at an unprecedented rate and posing unforeseen public health challenges. The report shows that the number of NPS reported to UNODC rose from 166 at the end of 2009 to 251 by mid-2012, an increase of more than 50 per cent. For the first time, the number of NPS exceeded the total number of substances under international control (234). Since new harmful substances have been emerging with unfailing regularity on the drug scene, the international drug control system is now challenged by the speed and creativity of the NPS phenomenon.
This is an alarming drug problem – but the drugs are legal. Sold openly, including via the internet, NPS, which have not been tested for safety, can be far more dangerous than traditional drugs. Street names, such as “spice”, “meow-meow” and “bath salts” mislead young people into believing that they are indulging in low-risk fun. Given the almost infinite scope to alter the chemical structure of NPS, new formulations are outpacing efforts to impose international control. While law enforcement lags behind, criminals have been quick to tap into this lucrative market. The adverse effects and addictive potential of most of these uncontrolled substances are at best poorly understood.
The global picture for the use of traditional drugs such as heroin and cocaine shows some stability. In Europe, heroin use seems to be declining. Meanwhile, the cocaine market seems to be expanding in South America and in the emerging economies in Asia. Use of opiates (heroin and opium), on the other hand, remains stable (around 16 million people, or 0.4 per cent of the population aged 15-64), although a high prevalence of opiate use has been reported from South-West and Central Asia, Eastern and South-Eastern Europe and North America.
“Everyone has the right to a standard of living adequate for the health and well-being of himself and his family, including food, clothing, housing and medical care.”
My previous blog, adapted from the Institute of Medicine (IOM) report U.S. Health in International Perspective: Shorter Lives, Poorer Health, described how the U.S. compares in causes of mortality and years of life lost with other high income and OECD countries. Here, as outlined in the report, I explore some of the social determinants of health that may explain this. Social determinants of health, as opposed to biological determinants (biology and genetics), describe the…
The National Academies Press has published a book, Contagion of Violence: A Workshop Summary, based on a 2012 workshop.
The past 25 years have seen a major paradigm shift in the field of violence prevention, from the assumption that violence is inevitable to the recognition that violence is preventable. Part of this shift has occurred in thinking about why violence occurs, and where intervention points might lie. In exploring the occurrence of violence, researchers have recognized the tendency for violent acts to cluster, to spread from place to place, and to mutate from one type to another. Furthermore, violent acts are often preceded or followed by other violent acts.
In the field of public health, such a process has also been seen in the infectious disease model, in which an agent or vector initiates a specific biological pathway leading to symptoms of disease and infectivity. The agent transmits from individual to…
When a person is approaching the end of life, we can find no easy answers, no solution that fits every person’s or family’s situation, even when they know a lot about the options available to them.
To illustrate this you will want to read For Hospice Pioneer, Still a Tough Call, by Paula Span at the New York Times New Old Age Blog. She describes the end-of-life period for Paul Brenner, age 73, who spend years organizing and leading hospice organizations around the country. Despite all of this experience, it was still challenging for Mr. Brenner and for his family to engage with hospice.
Over and over I hear from friends and acquaintances how a loved one uses hospice for the last several days or perhaps a week at the end of life, and I am sometimes puzzled about how difficult it seems to be to decide to…
Hospitals make mistakes, sometimes deadly mistakes. A patient may get the wrong medication or even undergo surgery intended for another person. When errors like these are reported, state and federal officials inspect the hospital in question and file a detailed report.
Now, for the first time, this vital information on the quality and safety of the nation’s hospitals has been made available to the public online.
A new website, www.hospitalinspections.org, includes detailed reports of hospital violations dating back to January 2011, searchable by city, state, name of the hospital and key word. Previously, these reports were filed with the U.S. Department of Health and Human Services, Centers for Medicare and Medicaid (CMS), and released only through a Freedom of Information Act request, an arduous, time-consuming process. Even then, the reports were provided in paper format only, making them cumbersome to analyze.
Release of this critical electronic information by CMS is the result of years of advocacy by the Association of Health Care Journalists, with funding from the Ethics and Excellence in Journalism Foundation. The new database makes full inspection reports for acute care hospitals and rural critical access hospitals instantly available to journalists and consumers interested in the quality of their local hospitals.
The database also reveals national trends in hospital errors. For example, key word searches yield the incidence of certain violations across all hospitals. A search on the word “abuse,” for example, yields 862 violations at 204 hospitals since 2011. …
This blog presents a sampling of health and medical news and resources for all. Selected articles and resources will hopefully be of general interest but will also encourage further reading through posted references and other links. Currently I am focusing on public health, basic and applied research and very broadly on disease and healthy lifestyle topics.
Several times a month I will post items on international and global health issues. My Peace Corps Liberia experience (1980-81) has formed me as a global citizen in many ways and has challenged me to think of health and other topics in a more holistic manner.
Do you have an informational question in the health/medical area? Email me at jmflahiff@yahoo.com I will reply within 48 hours.
My professional work experience and education includes over 15 years experience as a medical librarian and a Master’s in Library Science. In my most recent position I enjoyed contributing to our library’s blog, performing in depth literature searches, and collaborating with faculty, staff, students, and the general public.
While I will never be be able to keep up with the universe of current health/medical news, I subscribe to the following to glean entries for this blog.