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Roll Up Your Sleeves: Red Cross Says Blood Need ‘Urgent’

TUESDAY, July 26, 2016 (HealthDay News) — The American Red Cross says it has an urgent need for blood donations, with less than a five-day supply of blood on hand to help those who need it.

“The Red Cross continues to have an emergency need for blood and platelet donors to give now and help save patient lives,” Nick Gehrig, communications director for Red Cross Blood Services, said in a news release.

The organization noted it first alerted Americans to the need for blood and platelet donations back in early July. And while donation levels did rise, “a critical blood shortage remains,” the group said.

“At times, blood and platelets are being distributed to hospitals faster than donations are coming in, which impacts the ability to rebuild the blood supply,” the Red Cross explained.

Right now, the national supply has dipped below the five-day level the Red Cross says it needs to make sure it’s ready for unforeseen emergencies.

“We are grateful for those who have already stepped up this summer to give and want to remind those who are eligible that hospital patients are still counting on them to roll up a sleeve,” Gehrig said.

All blood types are needed, and the Red Cross is even offering donors an incentive in this blood drive. All those who donate by Aug. 31 will receive a $5 Amazon gift card claim code, emailed to them after their donation.

To schedule an appointment to donate, head to redcrossblood.org or call 1-800-RED-CROSS (1-800-733-2767).

Donated blood can save lives. Just ask Ray Poulin, whose liver and kidneys failed after a severe blood infection. Given only a one in 10 chance of survival, he received 77 units of blood — and lived.

“There was a lot that went into saving my life, but if the blood wasn’t available when I needed it, I wouldn’t be here today,” Poulin said in the Red Cross news release.

More information

Find a donation center near you at the American Red Cross.





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Does Dementia Diagnosis Have Silver Lining for Some?

TUESDAY, July 26, 2016 (HealthDay News) — Is it possible that a diagnosis as devastating as dementia could have some positive effects?

Yes, a small study suggests.

Researchers asked 48 people with early dementia or mild cognitive impairment to complete a questionnaire that measured their quality of life and personal outlook after getting their diagnosis.

The “Silver Lining Questionnaire” was designed to measure how much patients believe their illness has a positive impact in areas such as: relationships, appreciation for life, positive influence on others, inner strength and life philosophy.

The questionnaire has been used before with cancer patients. But, this was the first time it was used with dementia/mild cognitive impairment patients, the researchers said.

“The overall assumption is that this diagnosis would have a uniformly negative impact on a patient’s outlook on life, but we were surprised to find that almost half of respondents reported positive scores,” said study author Dr. Gregory Jicha, a professor at the Sanders-Brown Center on Aging at the University of Kentucky.

The patients in the study had high scores on areas such as: appreciation and acceptance of life; less concern about failure; self-reflection, tolerance of others, and courage to face problems in life; stronger relationships and new opportunities to meet people.

“The common stereotype for this type of diagnosis is depression, denial and despair,” Jicha said in a university news release.

“However, this study — while small — suggests that positive changes in attitude are as common as negative ones,” he said.

The study was to be presented Monday at the Alzheimer’s Association International Conference in Toronto. Findings presented at meetings are generally viewed as preliminary until they’ve been published in a peer-reviewed journal.

The next phase in this research is to determine the factors that led some dementia patients to see the positive in their diagnosis. That information can likely be used to help other patients, the researchers said.

More information

The Alzheimer’s Association has more on dementia.





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Flu Shot Tied to Fewer Hospitalizations, Deaths in Type 2 Diabetes Patients

TUESDAY, July 26, 2016 (HealthDay News) — The seasonal flu vaccine may offer people with type 2 diabetes some protection against dying prematurely, a new study suggests.

The flu shot also appeared to protect those with type 2 diabetes from hospitalizations for stroke, as well as heart and breathing problems, the study said.

British researchers looked at a large group — more than 124,500 people — with type 2 diabetes. People with type 2 diabetes normally have a higher risk of cardiovascular problems, the researchers noted.

During the seven-year study, the researchers found that flu vaccination was associated with a 19 percent reduction in flu-season hospital admissions for heart attack in people with type 2 diabetes.

Hospital admissions for stroke were 30 percent lower for those who got a flu vaccination. Admissions were also down 22 percent for heart failure, and 15 percent for pneumonia or influenza in people with type 2 diabetes who got the flu shot.

The death rate among those who received a flu shot was 24 percent lower than in those who weren’t vaccinated, the research said.

The study wasn’t designed to prove a cause-and-effect link between the flu shot and the reduction in death and hospital admissions. However, the study did show a strong connection between those factors.

The results show “that people with type 2 diabetes may derive substantial benefits from current vaccines, including protection against hospital admission for some major cardiovascular outcomes,” wrote study researcher Dr. Eszter Vamos, from Imperial College London, and colleagues.

“These findings underline the importance of influenza vaccination as part of comprehensive secondary prevention in this high-risk population,” the researchers said.

The study was published July 25 in CMAJ.

More information

The U.S. Centers for Disease Control and Prevention has more on type 2 diabetes and the flu.





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‘Heat Dome’ Not Budging Until Week’s End

TUESDAY, July 26, 2016 (HealthDay News) — The massive “heat dome” that has blanketed the eastern United States with oppressive heat and humidity for days will not be budging before the end of the week, weather forecasters said Tuesday.

“With no strong pushes of cool air from Canada on the horizon, people from the mid-Atlantic to the Deep South can expect virtually no relief from the high heat and humidity,” said AccuWeather meteorologist Kyle Elliott.

The Pacific Northwest will not be spared soaring temperatures either, as dangerous heat barrels northward from the Southwest. The core of that heat had covered the southwestern part of the country for much of July, but it will shift toward the states of Washington and Oregon this week, according to AccuWeather.

Later this week, temperatures will be 10 to 15 degrees Fahrenheit above average in cities like Seattle and Portland, and 100 degrees Fahrenheit is a distinct possibility in some areas of the Northwest, the weather service added.

In light of the lingering heat over much of the country, experts offered these tips on how to stay cool, and healthy, in the sweltering weather.

“The heat can be dangerous for your heart. Be careful during this time,” said Dr. Suzanne Steinbaum, director of women’s heart health at Lenox Hill Hospital, in New York City. “Make sure you stay hydrated and drink enough water. Stay in the shade or indoors with air conditioning if possible.”

She added, “Take [the heat wave] seriously. Dehydration can be a critical issue for not only your heart, but can affect your whole body.”

One expert noted that certain groups are more susceptible to heat-related illnesses.

“Some people at especially high risk for heat injury include those under 2 and over 65, as well as those with chronic diseases like diabetes, heart disease and emphysema [COPD],” said Dr. Michael Grosso, medical director at Northwell Health’s Huntington Hospital, in Huntington, N.Y.

In this kind of hot weather, drink water regularly, and before you actually feel thirsty, he stressed. Wearing light, loose-fitting clothing also helps, as well as pacing your activity during the day.

Grosso also suggested people avoid cooking in their homes and that they take cool baths or showers if they get overheated.

Another expert noted that heat-related illnesses are more common than many think.

“Although preventable, many heat-related illnesses, including deaths, occur annually. Older adults, infants and children, and people with chronic medical conditions are particularly susceptible,” said Dr. Barry Rosenthal. He is chair of the department of emergency medicine at Winthrop-University Hospital, in Mineola, N.Y.

“However, even young and healthy individuals can succumb to the heat if one does not take appropriate precautions,” he added.

Rosenthal outlined how to reduce the risk of heat-related illnesses during hot weather. One of the best ways is to be in an air-conditioned building. If your home doesn’t have air conditioning, go to a cooling center or an air-conditioned public place such as a library or shopping mall.

Also, ask your doctor or pharmacist if any medications you’re taking increase your risk of heat-related illness. For example, diuretics (water pills) can pose a risk during hot weather. If you’re taking a medication that raises the risk of heat-related problems, ask your doctor if there are additional steps you need to take to reduce the risk.

If possible, limit strenuous outdoor activity and exercise to early morning or evening, when temperatures are lower. Monitor local news and weather channels or contact your local public health department during extreme heat for health and safety updates.

Check on people who are at increased risk for heat-related illnesses, such as elderly loved ones and neighbors.

“At first signs of heat illness — dizziness, nausea, headaches, muscle cramps — move to a cooler place, rest a few minutes, then slowly drink a cool beverage. Seek medical attention immediately if conditions do not improve,” Rosenthal said.

More information

Visit the U.S. Centers for Disease Control and Prevention for more on the dangers of extreme heat.





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U.S. Panel Says Evidence ‘Insufficient’ to Recommend Skin Cancer Screenings

By Dennis Thompson
HealthDay Reporter

TUESDAY, July 26, 2016 (HealthDay News) — There currently isn’t enough scientific proof to recommend regular full-body exams for skin cancer as a means of preventing deaths from these cancers, a leading panel of U.S. preventive health experts has concluded.

An updated evidence review found scant evidence on either the benefits or harms of a health care professional performing a skin exam as part of a patient’s regular check-up, said Dr. David Grossman. He is vice-chairperson of the U.S. Preventive Services Task Force (USPSTF).

“We don’t know if taking the extra time to examine every inch of someone’s skin actually does yield benefit or causes no harm,” Grossman said.

Despite this, people should regularly check their own bodies for signs of skin cancer, and report anything unusual to their doctor, he added.

“Someone who’s got a mole they’re worried about because it’s growing and changing colors, they’re not a part of this recommendation,” Grossman explained.

More than 5 million basal and squamous cell skin cancers are diagnosed each year in the United States. It’s estimated that around 2,000 people die due to these cancers annually, the American Cancer Society (ACS) says.

Melanoma skin cancer occurs far less often, but is much deadlier. More than 76,000 new melanomas are expected to be diagnosed in 2016. Approximately 10,000 people will die from melanoma in 2016, the ACS says.

The new report doesn’t change the task force’s prior statement on skin cancer screening issued in 2009. That report said the evidence was inconclusive as well.

This latest update is “an explicit call for more evidence,” Grossman said. “We’re pretty clear on what it would take to move this” to a recommendation in favor of regular skin exams.

But, not everyone agrees that the evidence is so meager.

The American Academy of Dermatology (AAD) said its own skin cancer screening program — in place for 30 years — has resulted in detection of more than 255,000 suspected skin cancer lesions and 28,500 melanomas out of more than 2.5 million screenings.

“We know that screenings, which are noninvasive, quick and painless, are the best tool possible to detect skin cancer early when it is most treatable,” AAD President Dr. Abel Torres said in a prepared statement.

Torres added that the AAD “is disappointed with this recommendation, as dermatologists know that skin cancer screenings can save lives.”

In an accompanying editorial, dermatologist Dr. Martin Weinstock argued that “insufficient evidence of benefit” doesn’t mean the same thing as “evidence of no benefit.”

The largest benefit of regular skin exams would be catching a melanoma before it became invasive, Weinstock said. He’s a professor of dermatology and epidemiology with Brown University’s Warren Alpert Medical School in Providence, R.I.

“The worst risk would be unnecessary biopsies that could lead to scarring of a person’s skin and greater health care costs,” he explained.

“Really, the potential harms aren’t great, and the potential benefit is that you could save some lives,” Weinstock said.

Grossman said very little new research has surfaced on either the benefits or the harms of screening for skin cancer during the past seven years.

The largest recent study involved more than 360,000 people in northern Germany who received regular skin screening as well as education on sun protection, Grossman said. That study showed a nearly 50 percent decline in death rates from melanoma in men, and improved melanoma death rates compared with other nearby regions.

But the study design makes it impossible to tell what actually caused the benefits. “It’s unclear whether the drop they saw in mortality is related to the screening or to improved behavioral response, with people using skin protection,” Grossman said.

In addition, the melanoma death rate subsequently jumped back up. “That rate wasn’t sustained over time,” he said.

“If we saw a number of studies like this and they all were consistent and sustained, we would consider such evidence,” Grossman concluded. “But this one had so many limitations and was only a single study, so it wasn’t sufficient.”

The USPSTF is an independent, volunteer panel of national experts who regularly review the scientific evidence and make recommendations regarding health screening procedures and preventive medicine.

The Affordable Care Act has placed tremendous value on the task force’s opinion, as insurance companies are required to provide — free of cost — any screening that the USPSTF recommends, according to the U.S. Department of Health and Human Services.

A recommendation for skin cancer screening would place tremendous pressure on health care providers across the nation to make sure properly trained professionals are available to provide the service, Weinstock said.

“If something is recommended by the task force, it becomes incumbent upon organizations providing health care to keep tabs on whether they are making the services available to their patients,” he said.

“I’m disappointed that we have 10,000 Americans dying every year from melanoma, and that if they were getting screened by appropriately trained people, I think that number would be much less,” Weinstock added.

The task force’s updated evidence review and statement on skin cancer screening appears in the July 26 Journal of the American Medical Association.

More information

For more on melanoma, visit the American Cancer Society.





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Teasing Out Where the Tokers Live

TUESDAY, July 26, 2016 (HealthDay News) — Whether you smoke pot might depend on what part of the United States you live in, a new survey suggests.

Marijuana use by Americans is highest in the West and lowest in the South, according to a federal government report that also examined people’s beliefs about the risk of harms associated with the drug.

Among people 12 and older, rates of marijuana use in the past month were close to 10 percent in the West and slightly over 6 percent in the South, according to the U.S. Substance Abuse and Mental Health Services Administration (SAMHSA).

People in the West were least likely (over 25 percent) to believe that monthly marijuana use poses significant risk, while people in the South were the most likely (over 32 percent) to believe it.

Even among states, there were significant differences in marijuana use and whether people believed regular pot use was risky.

For example, current marijuana use ranged from a low of almost 4 percent in one region in the southernmost part of Texas to a high of 16 percent in San Francisco.

Rates of concern about the risks of regular marijuana use ranged from a high of just over 49 percent in Miami-Dade County and Monroe County in Florida to a low of about 14 percent in Ward 3 of the District of Columbia.

Recreational use of marijuana is legal in Alaska, Colorado, Oregon, Washington state and the District of Columbia, while medical marijuana is legal in 20 other states.

“This report provides a very detailed understanding of marijuana use and perception patterns in communities across the nation,” said Fran Harding, director of SAMHSA’s Center for Substance Abuse Prevention.

“This information can help public health officials and others better gauge the marijuana-related prevention and treatment needs in their communities and fine-tune their programs and services to best address them,” Harding said in an agency news release.

More information

The U.S. National Institute on Drug Abuse has more about marijuana.





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Put Birth Control in Place Right After Childbirth

TUESDAY, July 26, 2016 (HealthDay News) — Obstetrician-gynecologists should counsel pregnant women about use of long-acting reversible contraception, such as implants and IUDs, immediately after they give birth, a leading group of U.S. doctors says.

The goal is to prevent accidental pregnancy or another pregnancy too soon, the American College of Obstetricians and Gynecologists (ACOG) explained in its first clinical opinion on the subject.

“We encourage maternity providers to begin discussions about postpartum contraception prior to delivery to ensure women have the time and information they need to select the best method for them,” statement co-author Dr. Ann Borders said in a news release.

The doctors’ group recommends implementing a long-acting contraceptive in the period between delivery and hospital discharge.

“The period following delivery is a busy, exhausting and often stressful time, and immediate postpartum insertion of [long-acting reversible contraception] may eliminate some of the stressors during that time, like scheduling multiple appointments,” Borders said.

These patient-doctor conversations should cover the benefits and risks of these types of birth control, along with other types of birth control, so that women can make informed decisions, ACOG said.

Contraceptive implants and IUDs are “safe and highly effective birth control options for most females, including adolescents,” according to the statement.

Many women plan to resume or start using birth control at their postpartum follow-up visit. But, up to 40 percent of women don’t attend a follow-up appointment, “and as a result never obtain an IUD, contraceptive implant (or alternate method of contraception),” the group said.

And even if they do attend a postpartum follow-up visit, they may need to schedule an additional appointment for placement or face potential loss of insurance coverage after childbirth, the news release said.

“Although expulsion rates for immediate postpartum placement of IUDs are higher, many women find that the advantages of insertion before leaving the hospital outweigh the disadvantages,” Borders added.

Nearly 50 percent of pregnancies in the United States are unplanned. Poor, younger and minority women are most at risk, according to ACOG.

The American College of Nurse-Midwives and the Society for Maternal-Fetal Medicine endorsed the statement. It’s also supported by the Association of Women’s Health, Obstetric and Neonatal Nurses, and the American Academy of Family Physicians.

The statement is published in the August issue of the journal Obstetrics and Gynecology.

More information

The U.S. Office on Women’s Health has more on birth control.





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Are Stroke Centers Life Savers?

By Steven Reinberg
HealthDay Reporter

TUESDAY, July 26, 2016 (HealthDay News) — The odds of surviving a stroke are slightly better for patients treated at hospitals with a specialized stroke department, known as primary stroke centers, a new study finds.

But that benefit was only seen if stroke patients got to a stroke center in less than 90 minutes, the study authors said.

“Treatment of stroke is very time sensitive. As the saying goes, time is brain,” said lead researcher Dr. Kimon Bekelis.

“So the faster you intervene, the faster the patient recovers,” he said.

Bekelis is an instructor at the Dartmouth Institute for Health Policy and Clinical Practice at Dartmouth-Hitchcock Medical Center in Lebanon, N.H.

Primary stroke centers provide integrated care, including timely administration of medications, such as the clot-busting drug tPA (tissue plasminogen activator, also known as alteplase). They also offer special procedures to reduce the effects of a stroke, Bekelis said.

Many of these treatments are only available at stroke centers or are delivered faster there, which may account for the difference in survival, compared with treatment at a community hospital, he said.

Most Americans live within 90 minutes of a stroke center, but in rural areas the travel time can be longer, Bekelis said. He suggested that to fill this gap, speeding travel time using helicopters might be one way of improving survival.

Dr. Ralph Sacco is chairman of neurology at the University of Miami Miller School of Medicine. He said, “This analysis provides further evidence of the importance of being treated for stroke at a certified primary stroke center, even if it takes up to 90 minutes to get there.”

The study only looked at differences in death rates for stroke centers compared to standard hospitals. But, it’s likely there are other potential benefits — such as reduced disability — for patients treated in certified stroke centers, Sacco suggested.

“Longer delays in getting to a stroke center might lead to decreases in the utilization of acute stroke treatments,” he explained.

“We need to consider other approaches, such as the use of telestroke [which puts doctors who are treating a stroke patient in direct contact with a stroke specialist using technology], and increasing the number of stroke-ready hospitals to increase the access of patients to timely stroke care,” Sacco said.

For the study, the researchers collected data on nearly 866,000 Medicare patients, average age 79. All had a stroke between 2010 and 2013.

Almost 54 percent of these patients were treated at a stroke center. There are 976 stroke centers in the United States, the report noted.

Twenty-four percent of those in the study lived closer to a stroke center than to another hospital, the investigators found.

The study showed that patients who can get to a stroke center within 90 minutes had a nearly 2 percent higher chance of surviving a stroke after seven and 30 days, compared with patients treated at hospitals without such centers.

Bekelis and his colleagues also found that patients treated at a stroke center were twice as likely to receive tPA — 6 percent versus nearly 3 percent — than people treated at a standard hospital.

The report was published online July 25 in JAMA Internal Medicine.

At least one stroke expert expressed concern about sending patients who may not have had a stroke to stroke centers, potentially overwhelming the system.

“It is important to balance the benefit you get by going directly to a stroke center against whether that patient is actually having a stroke, or having a stroke that could be treated as effectively in a community hospital,” said Dr. Lee Schwamm. He’s vice chairman of the department of neurology at Massachusetts General Hospital in Boston.

It can be difficult to diagnose a stroke in the field, said Schwamm, who wrote an accompanying editorial in the journal.

“We need an understanding of how to improve pre-hospital diagnosis so that EMTs [emergency medical technicians] have the guidance they need to make the right choice,” he said. “This might include telephone conferencing with a stroke specialist or a smartphone app.”

More information

To learn more about stroke, visit the American Stroke Association.





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Strawberry chip protein scone recipe

Do you have a soft spot for scones? Try these wheat and sugar free, high-protein scones for your next high tea.

What you'll need

The scones

  • 1 cup oat flour (ground quick oats)
  • ½ cup vanilla protein powder 
  • ¼ cup rolled oats
  • ½ tsp baking soda
  • ¼ tsp sea salt
  • 3 tbsp coconut oil
  • 1 egg white
  • ¼ cup strawberry Greek yogurt
  • 2 tbsp almond milk
  • 3 sachets Stevia
  • 3 tbsp dark chocolate chips

Mixed berry jam

  • 1 cup frozen mixed berries (thawed)
  • 2 sachets of Stevia
  • 2 tsp chia seeds

Natural fat-free whipped 'cream' 

  • ½ cup non-fat dry milk 
  • ½ cup ice water 
  • 1 egg white  
  • 1 tsp lemon juice 
  • ¼ cup powdered sugar, sifted (you can use Stevia, quarter teaspoon or to taste)
  • ½ tsp vanilla extract

What you'll do

The scones

Preheat the oven to 220ºC.

Mix all the dry ingredients together and all the wet ingredients together.

Add the wet to the dry and fold together.

Stir in chocolate chips.

Add heaped tablespoon amounts to a parchment-lined cookie sheet and bake for 12 to 15 minutes. Be careful that the tops reach golden, not brown. Enjoy with tea or cold almond milk.

The jam

Thaw frozen berries and, when thawed, puree. Add the berry puree to a small saucepan and add the Stevia and chia seeds.

Keep stirring the jam over low heat for 5 to 6 minutes – never leaving it unattended or to stick to the saucepan.

Let cool and serve with protein scones or your favourite toast or muffin. 

The cream

Put the ice water, egg white, and non-fat dry milk in the bowl of a stand mixer fitted with the whip attachment. Beat on high for 4  to 5 minutes until it starts to thicken. Stop the machine to scrape down the sides of the bowl to get the milk powder incorporated.

 

Add the lemon juice and continue whipping on the highest speed for another minute or two until thick.

Lower the speed and slowly add sugar or Stevia, then vanilla. Beat until well mixed. 

 

Serve immediately with scones and jam.

 

Cream recipe adapted from Betty Crocker’s Pie and Pastry Cookbook.

Recipe by lifestyle blogger Kris Bitton of I Heart Wellness. 

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‘Managing’ Elderly Patients Without Powerful Antipsychotics

By Randy Dotinga
HealthDay Reporter

MONDAY, July 25, 2016 (HealthDay News) — About 25 percent of dementia patients in U.S. nursing homes are still quieted with risky antipsychotic medications. Now, a small study suggests that managing these difficult patients, instead of medicating them, could obtain better results.

“Drugs have a place, but should not be first-line treatments. They don’t work well, and there are side effects,” said study author Dr. Henry Brodaty, a professor of aging and mental health at the University of New South Wales in Sydney, Australia.

Antipsychotic drugs such as Risperdal (risperidone), Abilify (aripiprazole) and Seroquel (quetiapine) are approved to treat serious psychiatric conditions such as bipolar disorder and schizophrenia. But in seniors, they’re often used to calm aggressive or violent behavior linked to dementia.

“They’re basically a sedative,” said Dean Hartley, director of science initiatives with the U.S.-based Alzheimer’s Association. While he agreed that the drugs are warranted in some situations, he said dementia patients who take the powerful drugs are more susceptible to falls and have a higher risk of death.

The new study touts a program that trains nursing home staff members to focus on resolving specific issues bothering the patients and not to automatically sedate them.

It’s not clear how much this kind of program would cost in the United States or whether nursing homes could adapt to a new way of doing things. But it’s clear that the tranquilizers used on patients with dementia can be dangerous, said Hartley.

U.S. health officials have been trying to reduce the use of antipsychotics in long-term nursing homes. Since 2008, the U.S. Food and Drug Administration has required a boxed warning with all antipsychotic medications noting the increased risk of death in elderly patients with dementia-related psychosis.

The reported percentage of patients using the drugs dipped from 24 percent in late 2011 to 17 percent in 2015, according to background notes with the study.

Still, patients with dementia often need special management. According to Brodaty, 90 percent of people with dementia also experience agitation, depression, aggression, wandering, delusions and/or hallucinations.

His study included 156 patients at 24 nursing homes in Australia. All regularly took antipsychotic medications and were older than 60.

Nurses were trained how to handle difficult-to-manage behaviors without relying on drugs.

Of 135 patients taken off the antipsychotic drugs, 76 percent were still not using them 12 months later, the researchers said.

Hartley, the Alzheimer’s Association scientist, said focusing on the needs of patients requires understanding the issues that burden them. For example, he said, they may suffer pain from urinary tract infections but are unable to tell their caregivers.

Hartley mentioned the case of a patient who kept wanting to leave a facility, saying that it was raining outside. When asked, she explained that her kids — now grown — needed to be picked up at the bus stop. “They said they’d pick them up for her,” Hartley said, and the woman became calmer.

What about cost? This kind of program could actually reduce expenses, Hartley said, because patients would be less disruptive and need fewer emergency room visits due to injuries from falling.

Hartley cautioned that the study was small and needs to be validated. “It’s an important study, but it’s only the beginning,” he said. Still, the approach “may help caregivers or families know that their family members are being treated in a humane way.”

The study was scheduled for presentation Monday at the Alzheimer’s Association International Conference in Toronto. Medical studies released at conferences should be considered preliminary until published in a peer-reviewed journal.

More information

For more about dementia, visit the Alzheimer’s Association.





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