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May 24-28, 2010
NY man's kidney transplant gave him woman's cancer Illnesses among workers highlight concerns about health risks of oil cleanup FDA weighs penalties in JNJ drug recall Dirty laundry? How nasty germs survive in your washer Swallowing batteries: a powerful new danger to kids
Stanley InnerSpace introduces a new intelligent locking system for small storage carts AAMI soliciting auction items from individuals for their scholarship fund Have a safe and happy holiday! Statement by APIC in response to release of the “First State-Specific Healthcare-Associated Infections Summary Data Report” The Centers for Disease Control and Prevention (CDC) released a report Thursday showing that U.S. healthcare facilities have reduced the rate of central-line associated bloodstream infections by 18 percent. The report compares national and state data from January to June 2009 with national data from 2006 to 2008. Central-line associated bloodstream infections (CLABSIs) are estimated to claim the lives of 30,000 U.S. patients each year and contribute significantly to healthcare costs. The Association for Professionals in Infection Control and Epidemiology (APIC) is encouraged by this report, which shows significant progress in preventing healthcare-associated infections (HAIs) in many of our nation’s hospitals. The new report is based on epidemiologically sound, surveillance data collected through the CDC’s healthcare-associated infection monitoring system, the National Healthcare Safety Network (NHSN). Collected in a standardized fashion, using standardized definitions, these data provide a solid benchmark against which future efforts can be measured and represent the quality of data that are needed for the prevention HAIs. APIC believes the NHSN surveillance network is the best currently available method for ensuring the establishment of a scientifically meaningful reporting and monitoring system for HAIs. While not all healthcare-associated infections are preventable, APIC believes that every healthcare institution should be working toward a goal of HAI elimination. Many of our member facilities have seen that central-line associated bloodstream infections can be reduced to zero, and that in many instances “zero” can be maintained. Reducing infections also conserves healthcare resources by decreasing excess length-of-stay and associated costs. While many healthcare institutions have made progress, some still lag behind. Preventing infections requires the full commitment of hospital leadership to ensure adequate resources and to instill a culture of patient safety within the institution. Adequately resourced programs include a sufficient number of trained staff to interpret the data and lead interventions. Infection prevention programs also require automated surveillance technologies that streamline the review and collection of infection data, allowing infection preventionists to focus on the activities that protect patients. Eliminating preventable infections is the right thing to do for our patients and for our healthcare institutions. APIC’s mission is to improve health and patient safety by reducing risks of infection and other adverse outcomes. The association’s more than 13,000 members direct infection prevention programs that save lives and improve the bottom line for hospitals and other healthcare facilities around the globe. APIC advances its mission through education, research, collaboration, practice guidance, public policy and credentialing. Visit APIC online at www.apic.org.
The First
State-Specific Healthcare-Associated Infections Summary Data Report is
available at
www.cdc.gov/hai/statesummary.html.
NY man's kidney transplant gave him woman's cancer The scenario was unique, as far as doctors could tell: A man had gotten a transplanted kidney from a woman who had uterine cancer and didn't know it. Vincent Liew decided to keep the kidney after his transplant surgeon concluded there was only a slim chance he could be sickened by the feminine cancer — advice that gambled with Liew's life and lost, a lawyer for his widow told jurors Thursday in what experts say may be the only known case of uterine cancer being transmitted by transplant. Jurors began deliberating the case against NYU Langone Medical Center Thursday afternoon and were to return on Friday. Langone should be held responsible "for taking a huge risk with Vincent Liew's life" by not urging him to have the kidney removed at once, Daniel Buttafuoco said during closing arguments in the medical-malpractice case, which is refreshing longstanding questions about organ transplant risks and rewards. NYU Langone Medical Center says it advised Liew of the risk, honored his choice and aggressively monitored the kidney for signs of cancer. Though tests found nothing, Liew suffered back pain and ultimately had the kidney removed about six months after the 2002 transplant. He died about three weeks later of cancer that came from his donor, his autopsy said, without specifying the type of cancer. He was 37. "This should not have happened, but it's not NYU Medical Center's fault. It's not (transplant surgeon Dr. Thomas) Diflo's fault. It's not Mr. Liew's fault," the hospital's lawyer, Robert Elliott, said in his summation. "The best care that could have been provided was." Liew's widow, Kimberly, is seeking more than $3 million in damages in her lawsuit against the hospital. Liew, originally from Singapore, worked in the Hong Kong Economic and Trade Office in New York. A diabetic since his teens who was on three-times-a-week dialysis, he had been awaiting a kidney for about five years when he got the transplant Feb. 25, 2002. The donor, Sandy Cabrera, 50, had died of a stroke about a day earlier in Newburgh, N.Y. An autopsy in the days after her death found that she had uterine cancer that had begun to spread to her lungs. The news didn't reach Diflo until mid-April 2002, according to trial testimony. The hospital that treated Cabrera, St. Luke's Cornwall, declined to comment. With no medical literature available on uterine cancer being transmitted by transplant, Diflo testified that he told Liew the safest plan was removing the kidney, but that the odds of Liew developing the cancer were slight.
In dueling
testimony from cancer specialists, the two sides have disputed whether it
was indeed uterine cancer that killed Liew, though both acknowledge the
malignancy derived from the transplant and caused his death. The federal
Centers for Disease Control and Prevention estimate that 1 percent of U.S.
organ transplants are suspected of transmitting illnesses, though data are
sparse. (Associated Press)
Visit here for the article.
Illnesses among workers highlight concerns about health risks of oil cleanup Scattered reports of illnesses among workers helping to clean up oil in the Gulf of Mexico have highlighted concerns about possible health risks posed by the disaster and cleanup efforts. In the latest incident, seven workers were hospitalized Wednesday after complaining of nausea, dizziness and headaches, prompting the Coast Guard to order all 125 boats working in the Breton Sound area to return to port as a precaution. Five of the workers were released Thursday, but two remained hospitalized and an investigation was underway to try to determine the cause. Local, state and federal officials, along with independent experts, have been monitoring for any signs that the oil or chemicals being used to try to clean it up are making workers or residents sick. Air monitoring has not found any alarmingly high levels of toxic chemicals, officials said. But at least one senior official at the Environmental Protection Agency questioned the official reassurances, noting that none of the monitoring data had been released publicly. He likened the response to previous toxic waste disasters and the World Trade Center cleanup, which left workers with long-term respiratory problems despite repeated official claims that workers did not need respirators because the working conditions were safe. Assessing the health risks is also complicated by several unknowns, including how the chemicals being used to disperse the oil might affect the toxicity of the oil, several experts said. The most worrisome chemicals are substances known as volatile organic compounds, such as benzene and toluene, which can cause cancer at high levels and long exposures. Although such substances have been detected in air sampling, the levels have been within the range considered safe, officials said. But those and other substances, such as hydrogen sulfide, can cause acute symptoms including severe skin irritation, headaches, dizziness, nausea and burning sensations, as well as breathing problems and neurological complications including memory problems, confusion and disorientation. Most acute symptoms from the chemical exposure disappear after the exposure ends, but long-term complications can occur. Some fishermen involved in cleaning up the Exxon Valdez oil spill in Alaska suffered long-lasting neurological problems. The National Institute of Environmental Health Sciences designed a worker safety training course in English, Spanish and Vietnamese that all gulf oil spill cleanup workers are supposed to complete before they can be hired. They are also supposed to be equipped with protective gear, such as gloves and boots. Nevertheless, anecdotal reports have emerged of workers doing cleanup in street clothes and bare hands, raising questions about how well trained and equipped they are.
Some
critics are calling for workers to be equipped with full-body hazardous
waste suits and respirators -- a move officials said they have not taken
because most do not appear to be being exposed to dangerous levels of fumes
that would make that necessary. Respirators and heavy suits could pose risks
in the heat and difficult working conditions, they said.
Visit the Washington Post for the article.
FDA weighs penalties in JNJ drug recall The Johnson & Johnson unit that recalled millions of bottles of liquid children’s Tylenol and other pediatric medicines last month may face criminal penalties, product seizures or other sanctions, an official from the Food and Drug Administration said Thursday. The agency is considering further actions against McNeil Consumer Healthcare, the Johnson & Johnson unit, after a pattern of violations in manufacturing and quality control practices led to a number of recent recalls, Dr. Joshua M. Sharfstein, the FDA’s principal deputy commissioner, said at a Congressional hearing on Thursday. On April 30, McNeil voluntarily recalled more than 136 million bottles of liquid pediatric Tylenol, Motrin, Benadryl and Zyrtec because they may have contained too much of the active ingredient of the drug, metal specks or inactive ingredients that failed testing requirements, the agency said. But McNeil’s problems go beyond those related to last month’s recall, including other forms of contamination, dating back two years. During a session in which some committee members questioned McNeil’s integrity, Dr. Sharfstein noted lengthy delays by the company in reporting problems to the agency. And in one case, in 2008, Dr. Sharfstein said, McNeil hired a contractor to quietly remove packages of Motrin from retailers for suspected quality problems — which he suggested was essentially an unannounced recall that was not reported to the FDA. He said the FDA was “considering additional enforcement actions against the company for its pattern of noncompliance, which may include seizures, injunction or criminal penalties.” Another agency official, Deborah M. Autor, the director of the F.D.A. Office of Compliance at the Center for Drug Evaluation and Research, told the panel that officials had referred the McNeil case to the office of criminal investigation, the agency’s law enforcement arm, which works with the Justice Department to prosecute companies accused of violating the laws governing drug manufacturing and marketing. The House Committee on Oversight and Government Reform called Thursday’s hearing to examine the circumstances surrounding last month’s recall and whether the F.D.A. had responded adequately. But the evidence presented indicated long-running problems. For example, Dr. Sharfstein said, in 2008, McNeil notified the F.D.A. that it had hired an outside contractor to buy samples of Motrin from retailers to determine whether problems with the drug’s ability to dissolve warranted a recall. In 2009, however, the agency received information that the contractor had been buying up inventories of the product in what seemed to be an unannounced recall, he said. McNeil later initiated a formal recall of the products after the agency questioned the company about the contractor’s conduct, he said.
Some
committee members said that if Congress wanted to prevent delayed actions by
drug makers on defective medicines, it should give the F.D.A. the authority
to recall such products and levy civil penalties on companies. Now, the
agency cannot require a recall, but pharmaceutical companies may voluntarily
recall problem drugs.
Visit the New York Times for the article.
Dirty laundry? How nasty germs survive in your washer Your dirty laundry may actually be even dirtier after you wash it. That's because experts say washing machines are teeming with bacteria that find their way onto your clothes -- and then onto you. Our smallest items -- our undergarments -- are the biggest culprits because of the presence of fecal matter and the different types of bacteria it can carry. Charles Gerba, a professor of microbiology at the University of Arizona, has done extensive research on the germs that fester in our washing machines. "If you wash a load of just underwear, there will be about 100 million E. coli in the wash water, and they can be transmitted to the next load of laundry," Gerba said. "There's about a tenth of a gram of poop in the average pair of underwear," he added. Fecal matter can carry a number of different germs, including the hepatitis A virus, norovirus, rotavirus, salmonella and E. coli. Philip Tierno, a professor of microbiology and pathology at the New York University School of Medicine and author of the book, "The Secret Life of Germs," said bacteria from the skin, such as staphylococcus, can be found on clothing and towels. You may have been relying on your detergent to get rid of all the dirt and germs, but if you're not using bleach or very hot water, you're not killing the bacteria -- they're getting on your hands and staying in the washing machine. "Most of the hot water people use is not hot enough. You need water that's between 140 and 150 degrees to kill germs," said Tierno. If you're using cold water, Gerba recommends washing your hands after you handle wet clothes, especially if you're washing children's clothes. Using the right concentration of bleach will kill the bacteria, but using bleach isn't always appropriate, such as when you wash lingerie or colored clothing. "If you can't use chlorine bleach, you may want to resort to something like Clorox 2 because it has peroxide," said Tierno. Another option is to periodically clean your washing machine with bleach and water without any clothing in it -- just let the machine go through its regular cycle. One of the most effective germ-killers is the sun, so scientists say avoid the dryer altogether and let your clothes dry in the sun. "The ultraviolet radiation kills germs," said Tierno. "It's just as effective as bleach," he added. But a washing machine is just one of many germ-laden objects that you may encounter in a given day. Handrails, ATM's, refrigerator handles and telephone handsets are among the others. Gerba added that day care centers and young children's classrooms are also full of germs, as are airplane toilets.
Airplane
water also got a thumbs-down from Gerba and Tierno. "Plane water is very
contaminated," said Tierno. "Things aren't cleaned properly, so there's a
biofilm on the water."
Visit ABC News for the article.
Swallowing batteries: a powerful new danger to kids In the world as seen through the eyes of a child, one of those tiny hearing-aid batteries might look like an "Iron Man" pill. Or swallowing a lithium cell or two might make you run like the Energizer Bunny. So, a lot of batteries -- particularly the "button batteries" used to power calculators, hearing aids and a host of handheld digital devices-- are going down the hatch. Between 2007 and 2009, the American Assn. of Poison Control Centers received reports of 3,461 to 3,758 button-battery ingestion incidents yearly. A new study published in the journal Pediatrics says that lithium cell batteries -- especially those that are 20-millimeters (about three-quarters of an inch) or larger -- have become a particularly common danger to children. Far from creating indefatigable bunnies or comic-strip characters, the ingestion of these batteries can have very bad consequences indeed: vocal cord paralysis, esophageal narrowing, and destruction or perforation of the trachea or gastric wall, causing bleeding that can be -- and has been -- fatal to some children. A total of 13 children died between 1985-2009 and 73 had "major outcomes" that caused an acute health crisis or ongoing health problems for the child. And in the past decade, roughly, 92.1% of the fatal and major cases involved 20-mm lithium cell batteries. The Pediatrics study notes that from 1985-2009, there was a 6.7-fold increase in the incidence of button-battery ingestions with serious or fatal outcomes. More than 90% of those who experienced a major injury were under 4 years of age. Like coins, grapes and hot dogs, button batteries can cause a choking hazard by lodging in the throat and sitting atop the windpipe. But unlike coins, grapes and hotdogs, lithium cell batteries generate an external electrolytic current (while weakened, this current even flows from a largely expended battery). When it's in contact with fluid-filled tissue such as a child's esophagus, the battery's current causes a chemical reaction that creates hydroxide at its negative pole. The hydroxide burns and causes ulcers and perforations in that tissue. As it burns through the walls of the esophagus or the gastro-intestinal canal, it can cause internal bleeding that can be catastrophic.
In three of
the most serious cases reviewed, the battery had been lodged in a child's
throat for only two-to-two-and-a-half hours--long enough for severe burns.
"The window of opportunity for injury free removal of an esophageal battery
is [less than] 2 hours, considerably shorter than previously reported,"
wrote the authors, who hail from the National Capitol Poison Center.
Visit the Los Angeles Times for the article.
Premier awards Kimberly-Clark national and ASCEND agreements for KimVent Oral Care products Kimberly-Clark Health Care announced that it has received a new national agreement for its KIMVENT Oral Care products from Premier Purchasing Partners, L.P., the group purchasing unit of Premier, Inc. Kimberly-Clark was also selected as the sole source provider of oral care products for Premier's ASCEND program. ASCEND (Accelerated Supply Chain Endeavor) is designed to help healthcare providers achieve and sustain rapid improvements in supply chain performance. With easy-to-use components, the KimVent 24-Hour Oral Care Kits are designed to help critical care nurses reach protocol compliance and specifically address the risk factors associated with ventilator-associated pneumonia (VAP). Oral aspiration of pathogenic bacteria and contaminated secretions has been identified as a major cause of VAP.
The KimVent
Oral Care products now feature new, smaller packages from previous design
that require less space and generate less package waste. Kimberly-Clark
Health Care showcased its oral care products last week along with the
Kimberly-Clark HAI Education Bus at the 2010 National Teaching Institute &
Critical Care Exposition (NTI-2010). To learn more about the Kimberly-Clark
KimVent 24-Hour Oral Care products visit
www.kchealthcare.com/kimvent.
Stanley InnerSpace introduces a new intelligent locking system for small storage carts
Offering an
unparalleled level of cart security, Stanley InnerSpace is now taking orders
for small carts with its new Intelligent Locking System (ILS). Managed
wirelessly through a web-based software application that includes “drag and
drop” administrative features, ILS intuitively tracks and communicates
remotely with carts. Other main features of the ILS Carts include user
access with either a prox card or keypad code; the flexibility to
incorporate computer monitors to the cart without losing stability; and the
ability to program different access rights for different users. To learn
more visit
www.StanleyInnerSpace.com/ILS
AAMI soliciting auction items from individuals for their scholarship fund
The AAMI
Foundation is conducting a silent auction to help benefit the new
scholarship program, which provides critically important scholarships to
students seeking a career in the medical technology profession. The auction
includes numerous vacation packages to Las Vegas, Disney World, Washington,
D.C., and other popular destinations. Other items that will be auctioned off
include hand-crafted work from AAMI members such as beautiful photography,
hand-knitted scarves, baby clothing, and jewelry. All proceeds from the
auction will benefit the Michael J. Miller Scholarship Program. If you have
an item that you would like to donate, please contact Steve Campbell at
scampbell@aami.org
by next Friday, June 4. To view and/or bid on the items, visit
www.aami.org/auction
Have a safe and happy holiday!
HPN wishes you and yours a happy and healthy Memorial Day! We’ll be
back again on Tuesday, June 1 with more of the latest healthcare news.
Heart tests at hospital went unread Study of healthcare law rebuts state protests on Medicaid costs Hundreds of EMTs, paramedics said to be working with fake credentials Proton Pump Inhibitors (PPI): Class labeling change due to fracture risk Sisters of Charity of Leavenworth Health System renews agreement with Broadlane Rising maternal mortality rate causes alarm, calls for action Weight-loss drugs and risk of liver failure Heart tests at hospital went unread Nearly 4,000 tests for heart disease performed over the last three years at Harlem Hospital Center — more than half of all such tests performed — were never read by doctors charged with making a diagnosis, hospital officials acknowledged Tuesday. The echocardiogram tests, a type of ultrasound used to evaluate heart muscle and valve functions, were ordered by doctors at the hospital. The tests were stored on a computer and basically forgotten, officials said. The lapse occurred because the cardiology service at the hospital had developed a system by which technicians were given the responsibility to scan all tests and flag any that looked abnormal, so that they would be given priority when doctors read them. It appears, officials said, that the tests that were not flagged were put aside and forgotten. The city’s Health and Hospitals Corporation, which runs the public hospital system, including Harlem Hospital, and Columbia University, whose medical school supplies the cardiologists who work at Harlem Hospital Center, acknowledged the problem in a joint statement on Tuesday, after being asked about it by The New York Times. “While the process the doctors followed may have alerted cardiologists to those echocardiograms that were most likely to be abnormal, the failure to read the echocardiograms in a timely manner is inexcusable and may have placed patients at risk,” Alan D. Aviles, hospitals corporation president, said in the statement. It was unclear who developed the screening system, hospital officials said. Aviles said he had fired the clinical director of Harlem Hospital’s department of medicine, Dr. Alfred Ashford, and demoted the medical director, Dr. Glendon Henry, to attending physician at another hospital. The two doctors were also reported to the state Office of Professional Medical Misconduct for further investigation, the statement said. Hospital officials said the backlog was discovered during a routine review of records by Columbia University’s affiliation staff, and reported to the city hospitals corporation on Thursday. A team of 15 to 20 doctors from other city hospitals was assembled to begin reviewing the records on Friday. By Tuesday, they had reviewed 1,500 and found no patients who needed treatment, officials said. All patients will be notified of the problem and told if they need follow-up treatment, officials said. Harlem Hospital conducts about 2,500 echocardiograms a year, officials said, which means more than half the tests conducted in the past three years were never reviewed by cardiologists.
Corporation officials said the system of having technicians screen test
results and prioritize them for doctors to review was unique to Harlem
Hospital. To prevent anything similar in the future, the city and
Columbia
have revised their policy to require that all echocardiograms are reported
to physicians within two working days, the hospital corporation said. The
hospital’s medical director will make monthly reviews of the number of
unread tests and report those numbers to the corporation’s board every three
months.
Visit the New York Times for the article.
Study of healthcare law rebuts state protests on Medicaid costs The federal government will bear virtually the entire cost of expanding Medicaid under the new healthcare law, according to a comprehensive new study by the Kaiser Family Foundation that directly rebuts the loud protests of governors warning about its impact on their strapped state budgets. About half of the increase in health insurance coverage under the new law is expected to come from expanding Medicaid in 2014 to a new nationwide eligibility threshold of 133 percent of the poverty level -- $14,400 for a single adult or $29,300 for a family of four. A disproportionate share of the 16 million people expected to enroll in the expanded Medicaid live in states in the South and West that until now have had very stringent eligibility rules for low-income adults. Governors of many of those states have predicted fiscal calamity for their budgets, and some have cited the Medicaid expansion in the suits they have filed against the new law, saying it violates their states' rights. But the Kaiser study released Wednesday predicts that the increase in state spending will be relatively small when weighed against the broad expansion of health coverage for their residents and the huge influx of federal dollars to cover most of the cost. Even the small increase in Medicaid costs may be canceled out by the savings states will enjoy from no longer having to subsidize the uncompensated care of uninsured people who will be on Medicaid, study co-author John Holahan said. The federal government splits the cost of Medicaid with the states, ranging from a 50-50 split in wealthy states to more than 75 percent in poor states, for a nationwide average of 57 percent, although it has been paying higher rates under the economic stimulus package. Under the new law, the federal government will pick up 100 percent of the cost for all newly eligible people through 2016, a rate that will drop gradually to a 90 percent match in 2020 and beyond. The federal government will continue to pay its existing match rates for people who would have already been eligible under their states' current rules. But the study's authors predict that there will be relatively few of these people among the new enrollees. As a result, the overall federal share of the expansion cost will be somewhere between 92 and 95 percent from 2014 through 2019. Although Medicaid enrollment nationally is estimated to increase by 27 percent by 2019, state spending will increase only 1.4 percent, on average, and federal spending will increase by 22 percent, the report finds. The
study used the same assumptions as the Congressional Budget Office for what
the participation levels will be in the expanded Medicaid but also produced
a second set of estimates assuming a higher participation, with Medicaid
expanding by 22.8 million people, if outreach efforts and the goad of the
individual insurance mandate succeed beyond expectations. Even under this
higher enrollment, the increase in state Medicaid costs would be relatively
small -- 3.4 percent in
California
and 5.1 percent in Texas.
Visit the Washington Post for the article.
Hundreds of EMTs, paramedics said to be working with fake credentials More than 200 emergency medical technicians and paramedics in Massachusetts and New Hampshire have been practicing without legitimate certification, having paid certificate mills for fake credentials without taking any medical training, an investigation by Massachusetts public health officials has found. Initial reports suggested that in some cases, medics used the fake credentials to allow them to begin treating patients for the first time, but state officials now say that technicians bought the credentials to renew their state certification. The outfits peddling certificates provided them during the past two years to emergency medical technicians, paramedics, police officers, and firefighters in at least a dozen communities, including Boston, according to two public officials briefed on the investigation. Some 18 Boston firefighters are among those responding to medical emergencies without legitimate accreditation. The state Department of Public Health discovered the ruse last year, when some properly certified EMTs complained to state officials that a number of colleagues had not been trained but received certification. The investigation expanded in recent weeks when an ambulance company reported some of its employees had falsified documentation. The
investigation is ongoing and is expected to grow to include more
communities, said the officials who spoke on condition of anonymity because
they did not have permission to speak publicly. In the meantime, the state
is forcing the unaccredited technicians and paramedics to undergo training
to ensure safe medical care for the public, they said.
Visit the Boston Globe for the article.
Proton Pump Inhibitors (PPI): Class labeling change due to fracture risk FDA notified healthcare professionals and patients of revisions to the prescription and over-the-counter [OTC] labels for proton pump inhibitors - including Nexium, Dexilant, Prilosec, Zegerid, Prevacid, Protonix, Aciphex, Vimovo, Prilosec OTC, Zegerid OTC, and Prevacid 24HR - which work by reducing the amount of acid in the stomach, to include new safety information about a possible increased risk of fractures of the hip, wrist, and spine with the use of these medications. The new safety information is based on FDA's review of several epidemiological studies that found those at greatest risk for these fractures received high doses of proton pump inhibitors or used them for one year or more. The majority of the studies evaluated individuals 50 years of age or older and the increased risk of fracture primarily was observed in this age group. While the greatest increased risk for fractures in these studies involved people who had been taking prescription proton pump inhibitors for at least one year or who had been taking high doses of the prescription medications (not available over-the-counter), as a precaution, the "Drug Facts" label on the OTC proton pump inhibitors (indicated for 14 days of continuous use) also is being revised to include information about this risk. FDA recommends healthcare professionals, when prescribing proton pump inhibitors, should consider whether a lower dose or shorter duration of therapy would adequately treat the patient's condition.
Read the complete MedWatch safety summary.
Sisters of Charity of Leavenworth Health System renews agreement with Broadlane Sisters of Charity of Leavenworth Health System (SCLHS) has renewed its supply chain management agreement with Broadlane. Since 2005, Broadlane has delivered recurring, sustainable cost savings to Kansas-based SCLHS, more than doubling the company’s expectations. SCLHS comprises 11 hospitals and four stand-alone clinics in California, Colorado, Kansas and Montana. The system has 2,500 staffed beds, 16,000 employees and admits approximately 200,000 patients annually.
SCLHS chose Broadlane as its cost-management partner because the health
system shared Broadlane’s vision for finding innovative ways to reduce costs
while enhancing clinical excellence. At SCLHS, Broadlane implemented its
full range of Supply Chain Solutions and Strategic Sourcing Solutions. These
services include a fully centralized supply chain management program
comprised of sourcing, procurement, materials management and system-wide
value analysis. At the heart of SCLHS’ cost-savings was its decision to
centralize purchasing operations from its individual facilities to
Broadlane’s National Procurement Center in Dallas. To learn more visit
www.sclhealthsystem.org.
Kentucky healthcare system expands Premier healthcare alliance relationship to further increase patient safety The Premier healthcare alliance announced that three more hospitals from Edgewood, KY-based St. Elizabeth Healthcare selected Premier’s SafetyConnect patient safety program to further increase patient safety. All six St. Elizabeth hospitals now use SafetyConnect to protect patients more effectively while safely reducing hospital costs. As part of SafetyConnect, St. Elizabeth Florence, St. Elizabeth Ft. Thomas and St. Elizabeth Falmouth will use SafetySurveillor, Premier’s automated solution to help prevent healthcare-associated infections (HAIs) and optimize antibiotic use. The St. Elizabeth facilities (Covington, Grant and Edgewood) that have used the solution since 2002 have, among their many improvements, decreased surgical surveillance by Infection Control Professionals (ICPs) by an average of three hours per day. More than 270 hospitals rely on SafetyConnect for data analytics and software, performance improvement support services and collaborative knowledge sharing to improve overall patient safety and eliminate hospital waste. The Infection Control and Pharmacy modules in SafetySurveillor allow pharmacists and infection preventionists to obtain precise alerts and reports on hospital-defined parameters to help improve outcomes, reducing patient length of stay and associated costs.
Additionally, SafetySurveillor helps hospitals meet state-mandated public
reporting of certain HAIs, including Clostridium difficile and screening for
methicillin-resistant Staphylococcus aureus (MRSA), some of the most common
and harmful infections found in hospitals today. With the automated
SafetySurveillor system, hospitals can detect HAIs, alert staff and
facilitate timely intervention to reduce and prevent infections. Visit
www.premierinc.com.
Rising maternal mortality rate causes alarm, calls for action The
U.S. rate nearly doubled in a decade and is higher than in 40 other
industrialized countries. Experts cite numerous possible reasons and steps
that could be taken. Each day in the U.S., two women die of problems related
to pregnancy or childbirth. The numbers have been rising, for reasons that
are not entirely clear. After plunging in the 1900s, maternal mortality
rates in California tripled between 1996 and 2006, from 5.6 deaths per
100,000 births to 16.9. Nationally, the rate, defined as deaths from
obstetrical causes within one year of giving birth, rose from 7.6 per
100,000 to 13.3 per 100,000. Weight-loss drugs and risk of liver failure There is a potential, rare occurrence of liver failure in people who take the weight-loss medications Xenical or Alli, according to the Food and Drug Administration (FDA). The active ingredient in both of these drugs is orlistat. Xenical (orlistat 120 mg) is a prescription product. Alli (orlistat 60 mg) is sold over-the-counter without a prescription. Contact a healthcare professional immediately if you experience itching, yellow eyes or skin, dark urine, loss of appetite, or light-colored stools. These may be signs of liver injury. FDA has identified and reviewed 12 cases of severe liver injury reported in people taking Xenical and one case reported with the use of Alli. In some of these cases, other factors or drugs may have contributed to the development of severe liver injury. A
cause-and-effect relationship of severe liver injury with orlistat use has
not been established; however, because of the seriousness of this possible
side effect, FDA has revised the drug labels for Xenical and Alli to include
new safety information about the rare occurrence of severe liver injury.
Visit the FDA for more information.
Green Guide for Health Care launches newly redesigned website MedAssets to provide spend management solutions to RehabCare FDA and NIH launch electronic safety reporting portal Report finds control of high blood pressure improving Britain bans doctor who linked autism to vaccine Green Guide for Health Care launches newly redesigned website The Green Guide for Health Care announces the launch of its newly redesigned, restructured, and user-friendly website www.gghc.org! Join the Green Guide community today, with ready access to the Green Guide for Health Care core documents– the Design & Construction and revised Operations sections—and much more. Link to our updated library of Resources, and participate in Green Guide Events and activities! Register a Project. Become a Supporter. Take a tour of the new Green Guide for Health Care website and rediscover your role in accelerating healthcare’s transformation towards high performance healing environments.
The
original Green Guide for Health Care website served over 20,000 registrants
since 2004, providing free access to open access documents for audiences in
over 110 countries. In 2009, the Green Guide leadership team embarked on a
complete restructuring of our website presence. Key features include a new
Forum on Green Healthcare Construction, case study upload/ access
capabilities, and alternative ways for you to support the work of the Green
Guide. As a website registrant, you will have access to a multitude of
online user benefits. As a member of a registered project team, you can
track your project’s greening activities. Everyone enriches our ever-growing
learning community of green healthcare facilities and the people who design,
construct and operate them. Visit the website at
www.gghc.org.
MedAssets to provide spend management solutions to RehabCare
MedAssets
announced that it will provide its spend management solutions to RehabCare,
a national provider of long-term acute care and rehabilitation services, in
order to drive cost savings and standardization in RehabCare's supply
procurement process. MedAssets is working with RehabCare to develop a spend
management strategy designed to meet the specific commodity and operations
needs of long-term and post-acute care providers in order to lower
acquisition costs while maintaining its commitment to patient care.
MedAssets will serve as RehabCare's primary group purchasing organization
(GPO), using the company’s flexible contracting model to enhance efficiency
and reduce costs across its entire supply chain. RehabCare will also be able
to better analyze and control its pharmacy spend at all of its facilities
using MedAssets' supply chain analytics solutions. Visit
www.medassets.com.
The
Healthcare Laundry Accreditation Council is pleased to announce it has
accredited its 100th healthcare laundry in May. “We’re proud to have reached
this milestone in HLAC’s history,” says HLAC Chairperson Patti Costello.
“Laundries voluntarily seeking accreditation demonstrate they understand the
importance of continuous benchmarking, process improvement, patient safety,
and providing hygienically clean textiles to customers,” Costello says.
“Since it began accrediting laundry organizations in 2006, the Healthcare
Laundry Accreditation Council has seen a growing commitment to voluntary
industry excellence and a much greater awareness of the unique role
healthcare textile processing plays in national patient safety goals. As the
demand for healthcare grows, so too will the need for qualified healthcare
laundry providers who are well prepared to handle the increasing needs of
its healthcare customers.” To learn more about the Standards, and the
inspection and accreditation program, visit
www.hlacnet.org.
Genzyme Corp. signs consent decree to correct violations at manufacturing plant and give up $175 million in profits Genzyme Corp. has signed a consent decree agreeing to correct manufacturing quality violations at its Allston, MA, manufacturing facility and will turn over to the federal government $175 million in unlawful profits from the sale of products that were made at the plant, the U.S. Food and Drug Administration announced today. Under the consent decree of permanent injunction, the Cambridge, MA-based company agreed to adhere to a strict timetable to bring the plant in line with the regulatory requirements of the FDA. The payment is known as a disgorgement in which a company must give up profits obtained by improper or illegal acts. Genzyme is a sole supplier of several enzyme replacement drugs for injection that are used to treat rare genetic disorders. During an inspection of the Allston plant from Oct. 8, 2009, until Nov.13, 2009, FDA inspectors found that the company's systems for ensuring manufacturing quality were inadequate resulting in production delays, critical shortages of medically necessary products to consumers and drugs contaminated with metal, fiber, rubber and glass particles. These manufacturing problems violated the FDA’s regulations for manufacturing practice. Genzyme also temporarily suspended manufacturing of some products due to a viral contamination in a bioreactor that makes bulk amounts of its drugs. This resulted in additional drug shortages. Cerezyme, Fabrazyme, Myozyme, and Thyrogen are drug products that undergo all or some stages of manufacture at the Allston plant. Cerezyme treats Gaucher’s disease, which causes fatty substances to accumulate in the liver, spleen and other organs. Fabrazyme treats Fabry disease, which prevents the body from breaking down oils and fats that build up in the eyes and the kidneys. Myozyme treats Pompe disease, a muscular disorder, and Thyrogen is used to diagnose thyroid cancer.
Genzyme has
agreed to a work plan for making facility improvements. It begins with
selecting, within 10 days of entry of the decree by the court, an
independent expert who will inspect the plant and issue recommendations.
Genzyme will use the expert’s recommendations to create a work plan, subject
to FDA approval, that requires specific steps for bringing its Allston plant
into compliance within given dates. If Genzyme fails to complete any step
specified in the work plan, the company will have to pay a substantial fine.
In addition, the consent decree provides a deadline for Genzyme to transfer
its operations for filling drug vials from its Allston facility to other
manufacturing sites or else it will have to disgorge further profits from
the sales of drugs filled at Allston after that specific date.
Visit the FDA for the story.
FDA and NIH launch electronic safety reporting portal The Food and Drug Administration and the National Institutes of Health launched a new Web site that, when fully developed, will provide a mechanism for the reporting of pre- and post-market safety data to the federal government. Currently the Web site can be used to report safety problems related to foods, including animal feed, and animal drugs, as well as adverse events occurring on human gene transfer trials. The new site, called the Safety Reporting Portal (SRP), provides greater and easier access to online reporting. The new Web portal includes different features for different types of reporting: Reportable Food Registry: Industry will have a more user-friendly electronic portal for submitting reportable food reports that are required by law. This electronic portal collects reports from the food industry and public health officials regarding problems with articles of food, including animal feed, that present a reasonable probability of causing serious adverse health consequences or death to humans or animals. Pets: Pet owners and veterinarians will be able to use the portal to report product problems with pet foods and pet treats. Animal drugs: Animal drug manufacturers can report adverse drug events associated with animal drugs. Clinical Trials: Biomedical researchers involved in human gene transfer clinical trials can report an adverse event, indicating whether it might be an unanticipated consequence of the product being tested. Trial sponsors can use the portal to prepare a report, print it and send it to the agency to satisfy reporting requirements for investigational new drugs.
In the
future, the system will encompass other types of clinical trials and,
eventually, safety problems arising from products regulated by a broad array
of federal agencies. This is a first step toward a common electronic
reporting system that will offer one-stop shopping, allowing an individual
to file a single report to multiple agencies that may have an interest in
the event. See
the FDA Release for more information.
Report finds control of high blood pressure improving While the number of Americans with high blood pressure has not declined in recent years, researchers report that the good news is that more people with the condition have it under control. High blood pressure, also known as hypertension, is a major risk factor for heart attack, stroke and other cardiovascular problems; it was considered such an important health issue that achieving a 50 percent control rate was made an official Healthy People 2010 goal. That goal has been achieved, said Dr. Brent M. Egan, a professor of medicine and pharmacology at the Medical University of South Carolina and lead author of the report in the May 26 issue of the Journal of the American Medical Association. That report used data from a series of national health surveys running from 1988 to 2008. "The good news is that blood pressure control has improved very substantially over the years," Egan said. "It went from 27 percent of all hypertensives to 50 percent, with most of the progress since 2000. Awareness of high blood pressure improved from 69 to 81 percent, and the number of hypertensives on treatment improved from 54 percent to 72 percent." The bad news is that the number of Americans with high blood pressure has not gone down. "We're doing a lousy job of trying to prevent it," Egan said. An estimated 65 million Americans, about 29 percent of the population, now have high blood pressure, a far cry from the national goal of 16 percent. The study defined high blood pressure as a reading of 140/90 or higher, self-reported use of blood pressure medications, or both. Control was defined as getting the reading below 140/90.
The survey
found a slightly lower rate of hypertension control among blacks than the
general population, but the difference is small enough so that it might be a
matter of chance, Egan said. A recent study found an overall reduction of
stroke incidence in the United States, but not in blacks.
Visit Healthday for the article.
By taking scans of sleeping children, researchers are discovering what occurs in the brains with autism Using functional magnetic resonance imaging, or fMRI, to peer at images of the children's brains, researchers from the University of California, San Diego, found that autistic children as young as 14 months use different brain regions than youngsters with more typical development when hearing bedtime stories. The findings suggest that even very early on, the brains of those with autism work differently than typical babies. They also help explain why failure of language comprehension is a "red flag" for babies with autism, according to the study's author, Eric Courchesne, director of the UCSD Autism Center of Excellence. The small study of 43 subjects, believed to be the first to examine the brains of young children with autism and related disorders, was presented at the International Meeting for Autism Research in Philadelphia last week. This type of work "is going to tell us an awful lot about how the brain goes wrong in the first place and then gives us insight into how we'll be able to help at an earlier age," says Dr. Courchesne. Learning when and where brain changes occur can also help rule out some suspected causes of autism. For instance, if brain differences are already present at birth, then environmental toxins or vaccine exposure in childhood can't be responsible, according to Dr. Courchesne. Regular MRIs examine the structure of the brain, but by asking subjects to perform a task in the scanner, an fMRI can examine brain function through blood flow and response in response to neural activity. Unlike X-rays, they don't use radiation. But scientists have had trouble figuring out how to get young children to lie still in the noisy, claustrophobic brain scanners. The UCSD group came up with a solution: Put babies and children in the scanner in the wee hours of the night when they are naturally asleep. While the children were in the scanner, researchers played a repeating tape of a female voice reading a bedtime story and the scanner recorded the children's brain activity. (Dr. Courchesne's lab has shown in a separate, published study of older children that even when children sleep, they hear and react to language.) This study showed that in the typically developing babies, both the right and left temporal regions of the brain—parts that help us understand different aspects of language—were activated. In older children, there was evidence that the left side became even more active compared with the right side. But in the babies and children with autism-spectrum disorders the use of the right brain was far stronger. The left temporal region of the brain usually deals with understanding the meaning of words, in a "dictionary" manner, he says. The right side helps us understand social language based on context, like how people sound when they are angry rather than happy, even if they're speaking the same words.
One theory
is that in autism, the right side is needed to learn the basic definitions
of words, crowding out the ability to develop skills to process more social,
nuanced aspects of language, Dr. Courchesne says. The research could one day
help clinicians diagnose children more reliably and younger than 2 or 3
years old, the age when they currently are consistently diagnosed, according
to David Mandell, a psychiatry and pediatrics professor at University of
Pennsylvania and scientific chair of the autism meeting, who wasn't involved
with the study.
Visit the Wall Street Journal for the article.
Britain bans doctor who linked autism to vaccine The doctor whose research linking autism and the vaccine for measles, mumps and rubella influenced millions of parents to refuse the shot for their children was banned Monday from practicing medicine in his native Britain. Dr. Andrew Wakefield's 1998 study was discredited — but vaccination rates have never fully recovered and he continues to enjoy a vocal following, helped in the U.S. by endorsements from celebrities like Jim Carrey and Jenny McCarthy Wakefield was the first researcher to publish a peer-reviewed study suggesting a connection between autism and the vaccine for measles, mumps and rubella. Legions of parents abandoned the vaccine, leading to a resurgence of measles in Western countries where it had been mostly stamped out. There are outbreaks across Europe every year and sporadic outbreaks in the U.S. Wakefield's discredited theories had a tremendous impact in the U.S. In Britain, Wakefield's research led to a huge decline in the number of children receiving the MMR vaccine: from 95 percent in 1995 — enough to prevent measles outbreaks — to 50 percent in parts of London in the early 2000s. Rates have begun to recover, though not enough to prevent outbreaks. In 2006, a 13-year-old boy became the first person to die from measles in Britain in 14 years. "The false suggestion of a link between autism and the MMR vaccine has done untold damage to the UK vaccination program," said Terence Stephenson, president of the Royal College of Paediatrics and Child Health. "Overwhelming scientific evidence shows that it is safe." On Monday, Britain's General Medical Council, which licenses and oversees doctors, found Wakefield guilty of serious professional misconduct and stripped him of the right to practice medicine in the U.K. Wakefield said he plans to appeal the ruling, which takes effect within 28 days. The council was acting on a finding in January that Wakefield and two other doctors showed a "callous disregard" for the children in their study, published in 1998 in the medical journal Lancet. The medical body said Wakefield took blood samples from children at his son's birthday party, paying them 5 pounds (about $7.20) each and later joked about the incident. The study has since been widely rejected. From 1998-2004, studies in journals including the Lancet, the New England Journal of Medicine, Pediatrics and BMJ published papers showing no link between autism and the measles vaccine. Wakefield told The Associated Press Monday's decision was a sad day for British medicine. "None of this alters the fact that vaccines can cause autism," he said. Wakefield claimed the U.S. government has been settling cases of vaccine-induced autism since 1991. However, two rulings by a special branch of the U.S. Court of Federal Claims in March and last year found no link between vaccines and autism. More than 5,500 claims have been filed by families seeking compensation for children they claim were hurt by the vaccine. In Monday's ruling, the medical council said Wakefield abused his position as a doctor and "brought the medical profession into disrepute." At the time of his study, Wakefield was working as a gastroenterologist at London's Royal Free Hospital and did not have approval for the research. The study suggested autistic children had a bowel disease and raised the possibility of a link between autism and vaccines. He had also been paid to advise lawyers representing parents who believed their children had been hurt by the MMR vaccine.
Ten of the
study's authors later renounced its conclusions and it was retracted by the
Lancet in February. At least a dozen British medical associations,
including the Royal College of Physicians, the Medical Research Council and
the Wellcome Trust have issued statements verifying the safety of the
measles, mumps and rubella vaccine.
Visit MSNBC for the article.
New way bacterium spreads in hospital Toxic spider bite causes woman to lose breast US aims to reduce drug addiction deaths New threats to U.S. blood supply As longevity grows, the world might become a better place Pregnancy doubles HIV risk in men; first trial of a microbicide in pregnant women Medtronic profit rises on growth in rhythm devices New way bacterium spreads in hospital Healthcare workers and patients have yet another source of hospital-acquired infection to worry about, British researchers are reporting. Clostridium difficile, a germ that causes deadly intestinal infections in hospital patients, has long been thought to be spread only by contact with contaminated surfaces. But a new study finds that it can also travel through the air. The researchers emphasized that there is no evidence that C. difficile can be contracted by inhaling the germs. Rather, they float on the air, landing in places where more people can touch them. The bug is commonly spread by contact with infected feces, and the British scientists said the new study made it even more urgent to isolate hospital patients with diarrhea as soon as possible — even before tests confirm a C. difficile infection. Healthcare workers who touch contaminated feces can spread the disease by direct contact with other people or just by touching objects. The spores are resistant to disinfectants and can survive in open areas for months. The British researchers began with a six-month investigation of 50 patients, symptomatic and not, with confirmed infection. The air near 12 percent of them was found to be contaminated with C. difficile. The more active their diarrheal symptoms, the more likely they were to have spores in the air around them. Then the scientists repeatedly tested 10 patients with symptomatic illness over a 10-hour period, and the air near 7 was positive for C. difficile, usually during visiting hours or when there was activity in patient rooms like food delivery, ward rounds or bedding changes. Surfaces around 9 of the 10 patients were also contaminated. The scientists believe that the movement of people and the opening and closing of doors stir up spores on contaminated surfaces, helping them disperse and increasing the possibility of them spreading. The finding is unlikely to change current preventive practice, said Dr. L. Clifford McDonald, an epidemiologist at the Centers for Disease Control and Prevention. He said that the study supported putting patients in a single room, “which is the norm here in the U.S.”
The amounts
of C. difficile found in the air were generally modest. There were no clouds
of germs circulating in patients’ rooms. This may suggest a genuinely low
level of airborne contamination, the researchers write, or it may be a
result of methodological problems in collecting air samples: the initial
location of the sampling devices, their design, or their movement to
accommodate patient care or the arrival of visitors.
Visit the New York Times for the article.
Toxic spider bite causes woman to lose breast By the time Victoria Franklin called her twin sister to take her to the hospital in Atlanta on April 9, her breast had turned black and had blown up to the size of a loaf of bread. "Her breast was three times the size, black as tar and had a horrible smell," said Valerie Dapaa, 51, who took her nearly unconscious sister to the hospital, where they removed her breast after finding it ravaged by gangrene. Doctors told Franklin that she had been bitten by a brown recluse spider, a virulent little arachnid that is seen mainly in the south central part of the United States. The brown recluse occurs in 15 states, one of them the northern part of Georgia where Franklin lives, according to the Burke Museum of Natural History and Culture in Seattle. Inside the home, these spiders can be found in dark spots in the bath, garages, closets and cellars. They can nest in boxes of stored clothes and books. Franklin's doctors were not available to talk to ABCNews.com, but some experts say these spiders are often erroneously blamed for skin infections turned septic -- and without finding the spider, no one will ever know for sure. Franklin's condition is known as necrotic arachnidism. Patients report "an abrupt stinging or itching sensation," followed in hours by a painful pimple that within 24 to 48 hours becomes black and necrotic. "It's a nasty little spider that can cause skin destruction and make an ulcer and let infection in, and in some reported cases it can be very dramatic," said Dr. Marcel Casavant, chief of pharmacology and toxicology at Nationwide Children's Hospital in Columbus, Ohio. About 60 percent of all brown recluse spider bites are false reports, according to the Burke Museum. "Any small infection in a diabetic can turn into that she had," said toxicologist Casavant. "I wouldn't assume it was a spider." Experts say the brown recluse spider is often cited in medical and pharmaceutical school training, and doctors are often fooled. These types of infections can arise when patients have metabolic, endocrine or autoimmune conditions, but more often they are caused by the superbug MRSA (methicillin-resistant staphylococcus aureus). "In pharmacy school, everybody has a story: That the brown recluse spider likes to hide in the pockets of long coats in dark places and you reach into the pocket of the coast you haven't worn and get bit," said Paul Doering, professor at the College of Pharmacy at the University of Florida. "But it should be MRSA-phobia and not arachnophobia," he said.
Doering,
who did research on the spider as part of a lawsuit against a pharmacist,
said that any infection that becomes systemic is cause for concern. "With
skin infections today, especially in the world of resistant organisms, you
shouldn't take a chance," he said. "The first sign of something, when you
feel poorly and there is a red lesion, go to the ER or the doc-in-box."
Visit ABC News for the article.
US aims to reduce drug addiction deaths For the first time, the federal government has set a goal of reducing diseases and deaths caused by drug addiction, as well as the number of American teens and adults who use illegal substances. The surgeon general will produce a report to try to focus attention on the escalating abuse of legal but dangerous prescription drugs. And federal officials are urging family doctors and public clinics to help detect addictions early by paying closer attention to whether their patients use illicit drugs. Such emphases, part of the maiden National Drug Control Strategy to emerge from the Obama administration, set a different tone from its predecessors under the Bush administration, which focused more on slowing the flow of illegal drugs. But in the two weeks since the White House issued the 117-page strategy, a growing chorus of drug-policy specialists has begun to complain that President Obama and his aides are not putting enough money behind their efforts to reconfigure the nation’s drug-fighting approach. Overall, the White House seeks to increase spending next year by 3.5 percent on the broad spectrum of drug-control activities — from curbing drugged driving and expanding drug courts to subsidizing opium and coca farmers in other countries to switch to legal crops.
That
increase is less than the 4.1 percent increase that President George W. Bush
sought to combat drug abuse in 2002. Visit
the Boston Globe for the article.
New threats to U.S. blood supply Public health officials are battling a host of new infectious threats to the nation's blood supply. Blood centers, which have long tested for risks like hepatitis C and AIDS, have added a number of new tests on donated blood in recent years, including checks for West Nile virus and Chagas, a tropical parasitic disease. But new screening tests are hard to develop and can take years to win government approval. Currently, for instance, there's no way to screen for newer threats like babesiosis, a parasitic infection that has been linked to 10 U.S. deaths through blood transfusions since 2006. And a dangerous virus known as Chikungunya has spread to the U.S. and Europe from Africa in the last several years. Blood supply officials are urging the U.S. government to adopt so-called pathogen-reduction technology that can kill a wide range of contaminants in blood after it has been donated. One method already in use in about a dozen countries in Europe, Asia and elsewhere destroys most pathogens with a combination of chemicals and ultraviolet light. The Food and Drug Administration declined to approve the technology several years ago, citing possible side effects. But the agency is continuing to evaluate it. More pathogens have shown up as people travel more and bugs get ever more resistant to antibiotics. Researchers last year identified 68 emerging infectious agents with a potential to threaten the blood supply. Though some of the infections may cause mild illness in healthy people, they can be fatal in the patients with weakened immune systems who most need donated blood. Without tests for many risks, blood centers have steadily added new prohibitions for people wanting to give blood as a way to keep out potentially harmful supplies. Donors must answer nearly 50 questions, most of which are required by the FDA and by the American Association of Blood Banks, the lead accrediting body, to determine disease exposures from travel, risky sexual behaviors, medical conditions, and medication and drug use. That's up from about 20 questions in the 1970s. The heightened scrutiny has sharply reduced the pool of eligible donors. In 2006, 12.4 million people showed up to donate blood but nearly 2.6 million were turned away during screening, the most recent government data show. Donors are rejected if they have traveled to regions where malaria is present or lived in Europe since 1980, which may put them at risk of carrying variant Creutzfeldt-Jakob disease, which causes the human form of so-called Mad Cow disease. Also rejected are would-be donors who have ever taken the psoriasis drug Tegison, which was removed from the market because of the risk it can cause birth defects. Blood found to carry disease after testing is discarded. In 2006, 1.2% of donor blood was thrown out. Since 2004 most platelets have been tested for bacterial contamination, a danger because they must be stored at room temperature, an environment that encourages bacteria to grow. Red blood cells, by contrast, can be refrigerated. Other new risks from blood transfusion have emerged in recent years, including lung injury and deadly reactions caused by white blood cells and antibodies in donor blood. The Center for Disease Control and Prevention this year began a "hemovigilance" program to encourage hospitals to track such events more closely. Louis Katz, executive vice president of medical affairs for the Mississippi Valley Regional Blood Center, says that in his blood center, testing accounts for $50 to $60 of the $195 cost of a unit of red blood cells. Still, he says, current testing and questionnaires meant to weed out potentially infected donors are not enough to guarantee safety, especially if there is a potential threat on the scale of HIV, the virus that causes AIDS and was spread in transmitted blood before tests were developed to screen for it. The CDC last week, for instance, reported the first outbreak of dengue fever in the U.S. outside the Texas-Mexico border region since 1945. Dengue, a debilitating mosquito-borne disease, kills 25,000 people a year world-wide and has been increasingly found in travelers returning from the Caribbean, South America and Asia. The Red Cross currently is using an investigational test to screen blood for dengue in Puerto Rico where it is highly prevalent, but the test is not yet approved for wide use. The difficulty of developing new screening tests, and the absence in the U.S. of pathogen-reduction technologies, means "the U.S. blood system is becoming more vulnerable to new pathogens," says Richard Benjamin, chief medical officer at the American Red Cross. "We need to take a more proactive approach to emerging infections." Dr. Katz says pathogen-reduction technology could be the "Holy Grail" for blood safety because it has been shown to kill or inactivate most viruses and bacteria along with potentially harmful white blood cells that naturally occur in donated blood. The white cells, called leukocytes, can carry hidden viruses and can react badly with the recipient's immune system. The most widely used system, called Intercept, is sold in 11 countries by Concord, CA-based Cerus Corp., and kills most contaminants in platelets and plasma using a combination of chemicals and UV light. Intercept also inactivates white blood cells. Over the last decade, many blood centers and the Red Cross have started using filtering systems to reduce the number of white blood cells, but some of them still remain in blood. Cerus says Intercept costs about $50 per unit of platelets. The company says the technology saves blood banks about $25 per unit of platelets by allowing them to eliminate various tests and roughly another $25 per unit by lengthening the shelf life of platelets. Cerus says it is developing a version of the technology to use for red blood cells. Other companies operating overseas offer different technologies to kill pathogens in donated blood. These include adding a mix of vitamin B and various chemicals to the blood or using solvents and dyes to kill pathogens in different blood components.
The FDA
declined to approve Intercept in the U.S. after a 2003 clinical trial showed
a slight risk of a respiratory injury from blood treated with the system.
Cerus Chief Medical Officer Laurence Corash says that in more than 75,000
transfusions in Europe there hasn't been any increased incidence of lung
injuries with Intercept-treated platelets. The FDA doesn't accept European
data. But Dr. Corash says the company is discussing "requirements for the
size of a new clinical trial with the FDA, as well as preparing an
alternative clinical study approach."
Visit the Wall Street Journal for the article.
As longevity grows, the world might become a better place The Land of the Rising Sun has become the land of the setting sun with staggering speed. As recently as 1984, Japan had the youngest population in the developed world, but by 2005 it had become the world's most elderly country. Soon it will become the first country where most people are older than 50. This is partly because Japanese people live so long: Men can expect to reach 79 and women 86. It is also partly because the Japanese have almost given up having babies: The fertility rate is just 1.2 children per woman, far lower than the 2.1 needed to maintain a steady population. The rest of the world is following Japan's example. In 19 countries, from Singapore to Iceland, people have a life expectancy of about 80 years. Of all the people in human history who have reached the age of 65, half are alive now. Meanwhile, women around the world have half as many children as their mothers. And if Japan is the model, their daughters may have half as many as they do. Homo sapiens are aging fast, and the implications of this may overwhelm all other factors shaping the species over the coming decades -- with more wrinkles than pimples, more walkers than training wheels, and more gray power than student power. The longevity revolution affects every country, every community and almost every household. It promises to restructure the economy, reshape the family, redefine politics and even rearrange the geopolitical order over the coming century. The revolution has two aspects. First, we are not producing babies at the rate we used to. In just a generation, world fertility has halved, to just 2.6 babies per woman. In most of Europe and much of east Asia, fertility is closer to one child per woman than two, way below long-term replacement levels. The notion that the populations of places such as Brazil and India will go on expanding looks misplaced; in fact, they could soon be contracting. Meanwhile, except in a handful of AIDS-ravaged countries in Africa, people are living longer everywhere. Some worry that an older workforce will be less innovative and adaptable, but there is evidence that companies with a decent proportion of older workers are more productive than those addicted to youth. This is sometimes called the Horndal effect, after a Swedish steel mill where productivity rose by 15 percent as the workforce got older. Age brings experience and wisdom. Think what it could mean when the Edisons and Einsteins of the future, the doctors and technicians, the artists and engineers, have 20 or 30 more years to give us.
If the 20th
century was the teenage century, the 21st will be the age of the old: It
will be pioneered by the baby boomers who a generation ago took the cult of
youth to new heights. Without the soaring population and so many young
overachievers, the tribal elders will return. More boring maybe, but
hopefully wiser.
Visit the Washington Post for the article.
Pregnancy doubles HIV risk in men; first trial of a microbicide in pregnant women Young women of reproductive-age are among those at greatest risk of acquiring HIV, and several studies have suggested that during pregnancy women are even more susceptible to infection. Now, a new study finds that pregnancy is a time when men also are at greater risk. In fact, their risk doubles if their partner is both HIV-infected and pregnant. Between 70 and 90 percent of all HIV infections in women are acquired through heterosexual intercourse, and women are twice as likely as their male partners to acquire HIV during sex, due in part to biological factors that make them more susceptible. Many women remain sexually active during pregnancy. Although correct and consistent use of male condoms has been shown to prevent HIV infection, women often cannot or do not wish to negotiate condom use with their male partners. And for many women, especially those who wish to become pregnant, abstinence is not an option they can consider. Microbicides -- substances designed to be applied topically on the inside of the rectum or vagina – are under active investigation as a method for women to use to protect against HIV. While a number of studies have shown that during pregnancy women are at increased risk of acquiring HIV from an infected partner, a new study has found pregnancy is a time when men also are at greater risk – double the risk, in fact. The study, which involved 3,321 couples in which one partner was HIV-infected and the other not, is the first to show that a man in a relationship with an HIV-positive woman has a greater chance of becoming infected while she is pregnant than when she is not. Even after accounting for behavioral and other factors that usually contribute to HIV risk, the increased risk associated with pregnancy remained. Biological changes that occur during pregnancy may make women more infectious than they would be otherwise, explains Nelly Mugo, M.D., M.P.H., of the University of Nairobi & Kenyatta National Hospital in Nairobi and the University of Washington in Seattle, who presented results of the study on behalf of the Partners in Prevention HSV/HIV Transmission Study team. The study was conducted in Botswana, Kenya, Rwanda, South Africa, Tanzania, Uganda and Zambia. Results of the first study of a vaginal microbicide tested in pregnant women found only small amounts of drug are absorbed into the bloodstream, amniotic fluid and umbilical cord blood. The study, which involved applying a single dose of tenofovir gel hours before women gave birth by cesarean delivery, was conducted as a first step toward determining if use of a vaginal microbicide during pregnancy is safe for women and their babies. The findings support continuing with further studies of tenofovir gel in pregnant women, said Richard Beigi, M.D, MSc., of the University of Pittsburgh and Magee-Womens Hospital of UPMC, who led the study for the Microbicide Trials Network.
The active
ingredient in tenofovir gel is an antiretroviral that is approved as an oral
drug and used as part of the standard HIV treatment regimen. Both research
and clinical experience with the oral drug have indicated its use is safe in
HIV-infected women during pregnancy. In previous studies looking at the use
of oral tenofovir for the prevention of mother-to-child transmission of HIV,
researchers found that low amounts of drug pass to the baby. In the current
trial, which involved healthy, uninfected pregnant women, the amount of drug
found in umbilical cord blood was 40-times lower than cord blood levels
noted in these other studies after oral dosing, and the amount that got
absorbed into the maternal blood was at levels 50- to 100-times lower. Based
on these results, researchers now plan to conduct a larger study of
tenofovir gel in both pregnant and breastfeeding women.
Visit here for the article.
Medtronic profit rises on growth in rhythm devices Medtronic Inc., the biggest maker of heart-rhythm devices, said fourth-quarter profit surged eightfold on higher sales of defibrillators after rival Boston Scientific Corp. had to pull their devices from the market. Net income rose to $954 million, or 86 cents a share, in the three months ended April 30 from $103 million, or 9 cents, a year earlier, the Minneapolis-based company said in a statement. Earnings excluding some items were 89 cents a share beating by one cent the average estimate of 24 analysts surveyed by Bloomberg.
Chief
Executive Officer William Hawkins revamped the company’s line of products
used in back surgery to revive growth in its second-biggest business unit.
The company also benefited from the recall of Boston Scientific’s
heart-rhythm devices, which were pulled from the market for a month starting
Match 15, said Jan Wald, a Boston-based analyst at Noble Financial Group.
Visit Bloomberg for the article.
High-tech alternatives to high-cost care Insurers may slash rates to hospitals People with AIDS more likely to develop cancers, research says Blood test for early ovarian cancer may be recommended for all Global death rate for children lower than thought Alcohol consumption may protect against risk of AD, particularly in female nonsmokers Contaminants in groundwater used for public supply High-tech alternatives to high-cost care Mention healthcare reform and the image that instantly comes to mind is a big government program. But there is another broad transformation in healthcare under way, a powerful force for decentralized innovation. It is fueled in good part by technology — low-cost computing devices, digital sensors and the Web. The trend promises to shift a lot of the diagnosis, monitoring and treatment of disease from hospitals and specialized clinics, where treatment is expensive, to primary care physicians and patients themselves — at far less cost. The new models emphasize early detection of health problems, prevention and management of chronic disease. The approaches have adopted a range of labels including “wellness,” “consumer-directed healthcare” and the “medical home.” The potential transformation faces formidable obstacles, to be sure. Some of those hurdles include getting patients to embrace healthier lifestyles and persuading the government and insurers to reimburse at-home testing and monitoring devices. Yet the promise, according to Dr. David M. Lawrence, the former chief executive of Kaiser Permanente, the nation’s largest private healthcare provider, is “an array of technology-enabled, consumer-based services that constitute a new form of primary healthcare.” To glimpse the business opportunity — and the challenge — at the forefront of this emerging, decentralized healthcare market, let’s look at a start-up in the field of sleep medicine. The start-up, Watermark Medical, offers an at-home device and a Web-based service for diagnosing sleep apnea. Characterized by snoring and pauses in breathing, sleep apnea is a serious health problem that often goes undiagnosed. Typically caused by tissue in the back of the throat obstructing the airway to the lungs, it contributes to the severity of chronic conditions including diabetes, heart disease, obesity, hypertension and depression, adding an estimated $3.4 billion to the nation’s health costs. Today, sleep apnea diagnoses are mainly done in specialized sleep clinics, where the patient sleeps under observation for a night or two, at a cost of up $4,000 — with the expense usually shared by insurers and patients. Given the cost and inconvenience, physicians say, patients often do not go to a clinic and seek treatment until their sleep troubles are severe. Watermark Medical traces its technical origins to the work of Dr. Philip Westbrook, a Stanford-educated sleep expert who led the sleep disorder centers at the Mayo Clinic in Rochester, Minn., and at Cedars-Sinai Medical Center in Los Angeles. But during a brief period in private practice in California, seeing the expense and trouble sleep-testing was for patients, Dr. Westbrook decided there had to be a simpler, more efficient way. He teamed up with a pair of medical-device technologists and won an innovation grant from the National Institutes of Health to finance a prototype. They came up with a headband that holds a blue plastic device — smaller than a deck of cards and resting on the forehead — equipped with a microprocessor and sensors, and a tube that fits into a patient’s nose. If the tube falls out, the patient hears a voice prompt. But there also wasn’t a real market, until the Centers for Medicare and Medicaid Services approved reimbursement for home sleep-testing in 2008. That was when two young entrepreneurs, Sean Heyniger and Charles Alvarez, who had recently sold PDSHeart, a remote heart-monitoring company, to a larger corporation, were looking for another opportunity. They researched the sleep market and found Dr. Westbrook, who is now Watermark’s chief medical officer. They founded Watermark in March 2008, tweaked Dr. Westbrook’s device, produced a business model and conducted pilot projects. Watermark began introducing its testing device last September. Its sensor-equipped headband, powered by Intel’s Atom microprocessor, measures 10 things, including blood-oxygen saturation, air flow, pulse rate and snoring levels. The patient wears the device for a night or two, then returns the device to the doctor’s office. The data is downloaded to a personal computer, then sent on the Web to a network of sleep professionals, one of whom delivers a report to the physician within 48 hours, with a diagnosis and suggested treatment. The physicians typically charge from $250 to $450 a test, and a doctor collects $100 to $150 of that. Watermark also charges the physicians $4,000 for each digital headband.
So far,
35,000 patients have been tested using the Watermark device, with more than
1,000 doctors prescribing about 4,000 tests a month. If successful with
sleep, Watermark plans to branch out to other kinds of Web-based personal
devices to monitor chronic conditions like heart disease and diabetes.
Visit the New York Times for the article.
Insurers may slash rates to hospitals Massachusetts health insurers say they want to freeze or slash payments to some hospitals and large physician groups this year, setting up the toughest contract negotiations in memory and creating the potential for disruptions in where patients get their care. Other providers would get small increases, at most. Unlike in past years, insurers believe they have widespread backing from politicians, regulators, and employers to aggressively push back against large price increases, even if it means some unhappy providers drop out of insurers’ networks, forcing patients to find new doctors and hospitals. Blue Cross Blue Shield of Massachusetts, the state’s largest insurer, this month sent letters to hospitals and large physicians groups “putting them on alert that the world has changed,’’ said chief executive William Van Faasen. Blue Cross recently began negotiations with 25 hospitals whose contracts expire in October, about one-third of its network. Two other large insurers, Harvard Pilgrim Health Care and Tufts Health Plan, also have sent letters in recent weeks, requesting rate rollbacks from some hospitals and doctors groups. Many providers are in no mood to back down, however, after recently released data showed that some hospitals and doctors groups are paid vastly more than others for providing similar services, because of their market power. The lower-paid providers are demanding more equitable rates. Hospital executives acknowledged that their industry must help control costs by becoming more efficient, but they said many hospitals are struggling and cannot withstand rate freezes or reductions, particularly since the state has cut Medicaid payments and they expect the federal government to reduce Medicare rates under the new national health insurance law. “The cumulative impact is unprecedented,’’ said Lynn Nicholas, president of the Massachusetts Hospital Association. She said “payers feel a mandate to do something and do something quickly’’ and are not being “sensitive to unique situations. Hospitals in the red are being asked to make payment reductions,’’ which could lead to layoffs, mergers, and closures. Contract negotiations between health insurers and hospitals always have been tense and long, and often disappointing for those providers with little market clout. But hospitals and doctors groups with top name brands, large numbers of patients, or geographical dominance have been able to substantially raise their prices, sometimes with the backing of employers. Investigations this year by Attorney General Martha Coakley’s staff and the administration of Governor Deval Patrick blamed the rise in medical spending partly on price increases demanded by powerful providers. Last month, the Division of Insurance blocked insurers from substantially raising premiums for small businesses and individuals who buy their own coverage, and the state Senate last week passed Senate President Therese Murray’s measure to expand regulators’ authority over insurance premiums. Blue Cross executives said their negotiating strategy will depend on a hospital’s situation; some providers that are highly paid or are earning a healthy profit on the insurer’s members will be asked to take rate cuts; those that are struggling may be offered small increases. Harvard Pilgrim sent letters to 25 of its biggest hospitals and physician groups, asking them to reopen contracts and roll back previously agreed-upon increases this year. For those providers, and those with contracts expiring in January, the insurer will offer payment freezes or small increases of up to 3 percent, depending on the situation, said Rick Weisblatt, senior vice president for health services. “It is not our intention to beat up on the smallest providers,’’ he said.
The
hospital association projects that hospitals, nursing homes, and home
healthcare agencies in Massachusetts face about $5.3 billion in cuts in the
next decade, as the federal government redirects funding for health
insurance. A portion of those cuts will be made up by increases in other
types of Medicare funding, but hospitals don’t believe the federal
government will offset all of the cuts.
Visit the Boston Globe for the article.
People with AIDS more likely to develop cancers, research says When science turned AIDS several years ago from a fatal disease to a chronic illness that often can be managed with drugs, patients and doctors breathed a sigh of relief. Now they have a new worry. As people live longer with the virus, they are becoming far more likely than the rest of the population to develop cancers that were not previously associated with AIDS, research has found. "We're seeing high rates of head and neck cancer, lung cancer, kidney cancer, liver cancer and anal cancer," said John F. Deeken, the director of head and neck oncology at Georgetown University Medical Center. Researchers have detected the trend for years in separate studies around the world, but their findings were not widely publicized or known. On Thursday, the American Society of Clinical Oncology released an abstract by Deeken outlining a clinical trial by the AIDS Malignancy Consortium to study the effects and safety of a chemotherapy drug to treat non-AIDS-related cancers in HIV-positive patients. Robert Yarchoan, chief of the HIV and AIDS Malignancy Branch of the National Cancer Institute, said that medical advances have saved lives but noted that people with HIV "have to take pills the rest of their lives. The pills have side effects," he said. "There's premature aging and heart attacks. And now there are these cancers."
HIV-positive patients were excluded from clinical trials for
non-AIDS-related cancers until recently because of their fragile immune
systems. Yarchoan said the National Cancer Institute led the effort to
include them in trials as improved drug therapies strengthen their immune
systems.
Visit the Washington Post for the article.
Blood test for early ovarian cancer may be recommended for all For the majority of ovarian cancer patients, tumors go undiagnosed until the disease progresses to its fatal stages. Researchers were able to detect early development of three aggressive cancer cases and two borderline tumors when doctors monitored fluctuations of a protein known as CA-125, according to the study of 3,252 women released by the MD Anderson Cancer Center in Houston. About 21,550 patients were diagnosed with ovarian cancer in the U.S. last year, and 14,600 died from the disease, according to the National Cancer Institute. The cancer can be permanently removed if caught before it spreads. The new CA-125 testing method is now being evaluated in 200,000 women in the U.K., and results are expected by 2015. The ovarian cancer study was highlighted among 4,500 research project summaries released yesterday ahead of the annual meeting of the American Society of Clinical Oncology, which begins June 4 in Chicago. More than 30,000 cancer doctors and researchers are expected to attend, according to conference organizers. The CA-125 protein was identified as a tumor marker in the 1980s and has long been used by doctors to watch for relapse in patients who have been treated for ovarian cancer. However, until now the test was considered a failure at detecting new cases, because it missed some tumors and falsely identified too many healthy women as having cancer. Researchers in the MD Anderson study used an algorithm that took into consideration age and subtle changes in the CA-125 score. When a score rose too much, the patient was asked to come in for another test three months later. If the tests were still high, they were given an ultrasound and moved into surgery if necessary. The testing regimen was a success. Abbott Laboratories in Abbott Park, Illinois, and Roche Holding AG in Basel, Switzerland, make versions of the CA-125 blood test and other measures to help differentiate between benign and aggressive tumors. Quest Diagnostics Inc., a laboratory that evaluates the tests, is paid $29.81 for each test by Medicare, the government health program for people ages 65 and older, Quest spokesman Patrick George said in an e-mail. Patients without health coverage are charged $148. The algorithm in the ovarian cancer study isn’t publicly available yet, and healthy women shouldn’t rush out and be tested until the U.K. study results are released. Without the testing method, the CA-125 test leads to too many unnecessary surgeries and would miss cases where levels remain low.
Using the
algorithm, three women had benign tumors that were unnecessarily removed.
That’s considered an acceptably low rate of false positives, making the test
viable for broad use. Two cases of borderline tumors were missed by the
method and later detected.
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Global death rate for children lower than thought The global death rate for children under the age of 5 appears to be significantly lower -- by as much as 800,000 fewer deaths -- than the latest mortality estimates released by UNICEF in 2008. The fresh numbers gleaned from number-crunching conducted by researchers at the Institute for Health Metrics and Evaluation (IHME) at the University of Washington in Seattle also indicate that many poorer nations are demonstrating faster progress at stemming the tide of under-5 deaths. The current figures raise some hope for achieving the objectives established by the "Millennium Development Goal 4 (MDG 4)," which is aiming for a two-thirds drop in deaths among children under 5 from 1990 to 2015. Prior statistical analyses suggested that fewer than a quarter of the world's nations were on track to meet this target. Yet despite some encouraging signs, the current review doesn't paint a much better picture overall, revealing that only 31 developing nations and a total of 54 countries out of 187 worldwide appear to be heading towards the MDG 4 finish line. That observation comes from the IHME team's look at levels and trends for child deaths in 187 countries for the period 1970 through 2010. The authors relied on the participating country's censuses, surveys, birth records and registration systems for their data. The researchers found that while 11.9 million children under 5 died across the world in 1990, that figure had dropped to an estimated 7.7 million in 2010. One-third of such deaths occur in south Asia, they found, while one-half take place in sub-Saharan Africa. In the three decades since 1970, there has been a 60 percent overall drop in worldwide child mortality rates, the team noted. In the same timeframe, infant deaths in the first 27 days after birth (neonatal period) and in the first 28 days to 12 months of age (postnatal period) dropped by 57 and 62 percent, respectively. In another positive trend, 1970 saw 40 nations with a death rate above 200 per 1000 live births, but only 12 nations hit that mark by 1990, and none crossed that threshold by 2010. Overall, the fastest rates of decline in childhood mortality appear to be occurring in Latin America and North Africa. On a less optimistic note, however, the authors found that not all high-income countries -- where child death rates are typically much lower than in poorer nations -- are on equal footing with one another, the IHME analysis finds. For example, although the UK has experienced a drop in child deaths of 75 percent since 1970, the nation still has the unfortunate distinction of having the highest child mortality rates in all of Western Europe.
And rates
of child death have declined by just two to three percent per year in both
the U.S. and Canada since 1990 -- a significantly poorer improvement than
the three to five percent decline rates experienced in most other
high-income countries. The finding is reported in the May 23 online issue of
The Lancet.
Visit Healthday for the article.
Alcohol consumption may protect against risk of AD, particularly in female nonsmokers Knowledge regarding environmental factors influencing the risk of Alzheimer's disease is surprisingly scarce, despite substantial research in this area. In particular, the roles of smoking and alcohol consumption still remain controversial. A new study published this month in the Journal of Alzheimer's Disease suggests a protective effect of alcohol consumption on the risk of Alzheimer's disease, particularly in women who do not smoke. Researchers at the University of Valencia, the Generalitat Valenciana, and the Institut Municipal d'Investigació Mèdica, Barcelona, in Spain, carried out a study comparing personal and clinical antecedents of subjects affected with Alzheimer's disease with healthy people, both groups with the same age and gender distribution. Women included in the study were mainly light or moderate alcohol consumers. The risk of Alzheimer's disease was unaffected by any measure of tobacco consumption, but a protective effect of moderate alcohol consumption was observed, this effect being more evident in nonsmoker women.
"Our
results suggest a protective effect of alcohol consumption, mostly in
nonsmokers, and the need to consider interactions between tobacco and
alcohol consumption, as well as interactions with gender, when assessing the
effects of smoking and/or drinking on the risk of AD," according to lead
investigator Ana M. Garcia, PhD, MPH, Department of Preventive Medicine and
Public Health, University of Valencia. "Interactive effects of smoking and
drinking are supported by the fact that both alcohol and tobacco affect
brain neuronal receptors."
Visit eScience News for the story.
Contaminants in groundwater used for public supply More than 20 percent of untreated water samples from 932 public wells across the nation contained at least one contaminant at levels of potential health concern, according to a new study by the U.S. Geological Survey. About 105 million people — or more than one-third of the nation’s population — receive their drinking water from one of the 140,000 public water systems across the United States that rely on groundwater pumped from public wells. The USGS study focused primarily on source (untreated) water collected from public wells before treatment or blending rather than the finished (treated) drinking water that water utilities deliver to their customers. Findings showed that naturally occurring contaminants, such as radon and arsenic, accounted for about three-quarters of contaminant concentrations greater than human-health benchmarks in untreated source water. Naturally occurring contaminants are mostly derived from the natural geologic materials that make up the aquifers from which well water is withdrawn. Man-made contaminants were also found in untreated water sampled from the public wells, including herbicides, insecticides, solvents, disinfection by-products, nitrate, and gasoline chemicals. Man-made contaminants accounted for about one-quarter of contaminant concentrations greater than human-health benchmarks, but were detected in 64 percent of the samples, predominantly in samples from unconfined aquifers. Most (279) of the contaminants analyzed in this study are not federally regulated in finished drinking water under the Safe Drinking Water Act. The USGS also sampled paired source and finished (treated) water from a smaller subset of 94 public wells. Findings showed that many man-made organic contaminants detected in source water generally were detected in finished water at similar concentrations. Organic contaminants detected in both treated and source water typically were detected at concentrations well below human-health benchmarks, however. Additionally, the study shows that contaminants found in public wells usually co-occurred with other contaminants as mixtures. Mixtures can be a concern because the total combined toxicity of contaminants in water may be greater than that of any single contaminant. Mixtures of contaminants with concentrations approaching benchmarks were found in 84 percent of wells, but mixtures of contaminants above health benchmarks were found less frequently, in 4 percent of wells. This USGS study identifies which contaminant mixtures may be of most concern in groundwater used for public-water supply and can help human-health researchers to target and prioritize toxicity assessments of contaminant mixtures. The USGS report identifies the need for continued research because relatively little is known about the potential health effects of most mixtures of contaminants.
Treated
drinking water from public wells is regulated under the Safe Drinking Water
Act. Water utilities, however, are not required to treat water for
unregulated contaminants. The EPA uses USGS information on the occurrence of
unregulated contaminants to identify contaminants that may require
drinking-water regulation in the future.
Visit USGS for the story.
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