|:Colo Spgs Gazette;
||:Feb 7, 2012;
TRYING TO GET A GRIP ON DEMENTIA
A NATIONAL PLAN IS BEING SOUGHT TO AID DETECTION
the associated Press —
• Alexis McKenzie’s mother had mild dementia, but things sounded OK when she phoned home: Dad was with her, finishing his wife’s sentences.
Then their phone service was cut off. “I mailed that check,” McKenzie’s father insisted. No, he’d mailed the phone company a bank deposit slip instead. McKenzie visited and discovered spoiling food. Dad the caregiver was in trouble, too.
Dementia can sneak up on families. Its sufferers are pretty adept at covering lapses early on, and spouses are sometimes there to compensate. Doctors too frequently are fooled as well. Now specialists are pushing for the first National Alzheimer’s Plan to help overcome this barrier to early detection, urging what’s called dementia-capable primary care, more screenings for warning signs and regular checks of caregivers’ own physical and mental health.
For a doctor to ask someone with brewing dementia, “How are you?” isn’t enough, said Dr. Laurel Coleman, a geriatric physician at Maine Medical Center who is part of a federal advisory council tackling the issue.
Family input should be mandatory, she told a recent council meeting. It’s the only way to know if the person really is eating and taking her medicines as she claims and not forgetting to turn off the stove.
The question is how to square that input with patient confidentiality, especially if the person never filed the legal forms clearing family members to intervene, as happened with McKenzie.
Plus, regularly seeking that input takes more time than the typical 15-minute visit and is poorly reimbursed, Coleman said. But more primary-care physicians are starting to be trained in dementia’s challenges, she said.
More than 5 million Americans are estimated to have Alzheimer’s or similar forms of dementia, although as many as half may not be formally diagnosed. The toll is projected to reach as much as 16 million by 2050. The Obama administration is drafting a national strategy to try to slow that coming avalanche — with research aiming for some effective treatments by 2025 — plus find ways for struggling families to better cope now.
Step 1 is earlier detection. McKenzie directs an Alzheimer’s assisted-living facility in Washington, so she knows about dementia. Still, it took some sleuthing to determine how much her 82-year-old parents, living in Maryland, were deteriorating. She says her father refused any assistance in caring for her mother, and together the couple put up such a good front that even their regular physician hadn’t realized their shared answers to standard checkup questions weren’t true.
Sure, dementia patients’ stories can be believable.
“It happens in doctors’ offices all the time,” said Beth Kallmyer, vice president of constituent services at the Alzheimer’s Association. That’s why it’s crucial that family members are part of the screening process.
How to get around the hidden-dementia conundrum?
• Medicare’s new annual wellness visit pays for cognitive screening, simple tests that signal who should be referred for more extensive brain exams.
• The government’s Alzheimer’s advisers want doctors to steer families toward advanced-care planning, including designating a health care power of attorney, as soon as dementia is diagnosed.
• A health care proxy won’t be used until the person is quite sick. So Kallmyer advises signing what’s called a “release of information” allowing the doctor to discuss the person’s care with whoever is named right away.
Such steps are important, said Dr. Gary Kennedy, geriatric psychiatry chief at New York’s Montefiore Medical Center Kennedy, because advancing dementia leaves people so unaware of their deficits that they can take family or doctor input “as an affront.” He always asks new patients if he can fill in their loved ones or invite them in from the waiting room, as a way of starting that conversation.
• Doctors can violate patient confidentiality if they believe the person’s decisions or behavior has become a danger, Kennedy said.
McKenzie said her father would never discuss naming a health care proxy and her parents were furious that she’d voiced concerns to their physician. She had to think up nonconfrontational ways to get invited back into their doctor visits: “I’ll drive you, and then why don’t I take notes in case you have any questions later?”
It turned out that McKenzie’s father had a noncancerous brain tumor causing his own gradual dementia symptoms, which started becoming apparent with the phone mix-up, unrefrigerated food and eventually delusions. Finally, she had to go to court to get her parents the care they needed in an assisted living facility near their hometown.
Some people with mild Alzheimer’s might be reclassified as having a less serious brain disease called mild cognitive impairment, according to a new analysis of the evolving terminology. Last year, a work group convened by the National Institute on Aging and the Alzheimer’s Association issued revised criteria for diagnosing mild cognitive impairment. According to this new definition, people with mild cognitive impairment still have “functional independence” and no dementia. But a researcher at Washington University in St. Louis sought to evaluate the impact of the revised criteria. He studied the diagnoses and neurological evaluations of 17,535 people with normal cognition, mild cognitive impairment or Alzheimer’s. The study found that 99.8 percent of the people now diagnosed with very mild Alzheimer’s disease and 92.7 percent of people now diagnosed with mild Alzheimer’s disease would be considered as having mild cognitive impairment under the revised criteria. The confusion seems to stem from what is meant by “functional independence.” The work group allows for a broad view of the term. The study appears online in the journal Archives of Neurology.
los angeles times