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Monday, April 13, 2009

Doctors not Good at Detecting Alzheimer's and Dementia



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Diagnosing mild-to-moderate dementia cases can be difficult. Indeed, more than half of such cases are not recognized by physicians, according to a recent review of the literature at the Medical College of Wisconsin in Milwaukee.
This comes as no surprise to me.

When most people think of dementia and Alzheimer's disease, they think of memory loss. The image in their mind is of someone laying in a bed, unable to recall their loved one's. This is the end stage and sometimes comes a decade or more after the initial diagnosis.

The inability of physicians and family to recognize mild cognitive impairment indicates that we have a long way to go in raising public awareness about dementia. As most caregivers look back, they can tell you about telltale signs of the disease that they missed. Most of us are in this club.

To me, early detection of Alzheimer's and dementia is all about recognizing subtle behavioral changes in older people. Tiny little behavioral changes that gnaw at your stomach. The dragging and scrapping of the feet on the ground. The inability to find the bathroom in a relatives home that they have been visiting all their lives. Trouble paying bills.

The typical reaction to these subtle behavior changes is to think and believe the person is getting old. When you talk to your friends about these little subtle changes you are likely to get reinforced about your conclusion when they say to you--she is getting old.

This is what happened to me. It stayed that way until that little gnawing in my stomach became a stomach ache.

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Best Practices Identified for Early Alzheimer’s Detection

Diagnosing mild-to-moderate dementia cases can be difficult. Indeed, more than half of such cases are not recognized by physicians, according to a recent review of the literature at the Medical College of Wisconsin in Milwaukee. In fact, family members and caregivers, in addition to many physicians, often overlook a decline in cognitive function as well.

To improve prompt diagnosis, Diana Kerwin, MD, assistant professor of medicine and geriatrics, offers the following recommendations published in a recent issue of The Journal of Family Practice:

• Avoid age bias when determining the need for cognitive screening

• Screen the vulnerable elderly, or individuals 65 years of age and older who are at high risk of death or functional decline, at the initial visit and annually after

• Test all patients undergoing cognitive screening for depression as well.

According to Dr. Kerwin, because of the low diagnosis rate by physicians, and the lack of awareness by caregivers, physicians should perform cognitive screening on all high risk patients who are suspected of Alzheimer’s disease, regardless of their age.

Physicians should also perform initial and annual screenings on the vulnerable elderly, and screen suspected Alzheimer’s patients for depression in addition to cognitive function in order to improve early detection of the disease.

As the Baby-Boom generation ages, the number of Alzheimer’s disease cases is expected to surge from the already significant amount of five million cases. Increased awareness and diagnosis will provide optimal care for the aging population.

Early detection of cognitive impairment is also extremely important because the impairment may be related to other medical conditions, such as head trauma, Parkinson’s disease, human immunodeficiency virus (HIV), and thyroid disorder.

Additionally, early detection provides medical, behavioral, and social intervention that may delay cognitive and functional decline.

The US Preventive Services Task Force guidelines recommend that physicians evaluate patients for dementia whenever there is a suggestion of cognitive impairment, based on clinical observation, or based on family or patient concern.

Because psychiatric disorders can impersonate dementia, or can be present simultaneously, suspected dementia patients should also be screened for depression. Depressed patients often complain of memory problems more than those with cognitive dysfunction.

Additionally, depressed patients exhibit impaired function more so than dementia patients. Depression usually interferes with concentration; however, dementia patients appear to concentrate normally, but have greater intellectual strain when answering questions.

The following is a list of optimal screening tests and tools to prevent delayed diagnosis of mild-to-moderate dementia patients:

• The Mini-Mental State Examination (MMSE)

• The Mini-Cog
• The Montreal Cognitive Assessment (MoCA)

• The AD 8 Dementia Screening Interview

• The 7-Minute Neurocognitive Screen

The MMSE is the most widely used cognitive screening tool because it is easy to administer, tracks changes easily, is widely accepted, and is available in more than 50 languages; however, it is not sensitive to mild dementia, and is influenced by age, education, and language skills.

The Mini-Gog is easy to administer, is unaffected by education and language skill, and is highly sensitive to mild dementia.

The MoCA is more time consuming than other tools, but is highly sensitive to mild dementia, available in greater than 20 languages, and diagnoses patients who have memory complaints, but normal MMSE scores.

The AD 8 Dementia screening interview identifies the earliest stages of dementia, but is intended for a family member or caregiver. The 7-Minute Neurocognitive Screen is highly sensitive to early stages of dementia.

Family, friends, and caregivers can also watch for early cognitive decline, thereby helping physicians with early Alzheimer’s detection.

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Bob DeMarco is the editor of the Alzheimer's Reading Room and an Alzheimer's caregiver. The Alzheimer's Reading Room is the number one website on the Internet for news, advice, and insight into Alzheimer's disease. Bob has written more than 800 articles with more than 18,000 links on the Internet. Bob resides in Delray Beach, FL.
Original content Bob DeMarco, Alzheimer's Reading Room

2 comments:

  1. The comment on Doctors detecting early Alzheimer’s and Dementia is so important. If only my mom’s doctor detected the disease 7 years ago, maybe I could of prolonged the later stage she is in now. Instead he treated her for Thyroid and depression, then over the course of the last year telling us to put her in a nursing home for Old Age. But why I asked, so she forgets what she ate for lunch, or what day it is or repeats things, who does at times forget, she knows who I am and my Dad, why put her in a Nursing Facility. Then he gives my Dad a test to take home and work with her, now knowing my dad will not even admit to Alzheimers, only to Dementia, not knowing they are linked, so the test is thrown away and not mentioned. The WWII generation will not admit or understand Alzheimer;s Disease, this is a non-spoken, dirty word to be locked away for crazy people. So how do we, the baby boomers, the age of intense knowledge in the world of space exploration, electronics, internet and Skyp know how to understand and help our loved ones deal with Alzheimer’s Disease if the Doctors will not admit to it. My Dad who is 83 talked with his granddaughter on Skyp the other night and was fascinated. He never thought in his life time to be able to talk and see someone on the computer, the same way his mother was fascinated with TV, she asked “how do they do that”. So why is Alzheimer’s Disease still locked away, where is the research and the Grants for research, instead of all the silly pet projects, what about saving lives??

    Where would we be today if Breast Cancer was still thought of this way, Millions and Millions of women would be dead, my mom being one of them. But because of research and “speaking the unspoken word’ my mom survived Breast Cancer in 1993 and Ovarian Cancer in 1998. Only to fall prey to Alzheimers. Now she does know why she had a breast removed, but years ago was proud to a survivor.

    Why all the medical research and drugs to keep people alive longer only for them to lose all memory of their precious life, a life that made a difference in this world. Why do the doctors deny it or not tell us unless we insist. We all have to do our own research, as I have done night after night on the internet, to find out how to give my mom and dad in their remaining years the quality of life they deserve.

    Let us all SPEAK UP, and be proud to know the word Alzheimers instead of denying it. Make everyone aware of the disease so maybe someday my grandchildren can say “I survived Alzheimers” !! Please email me at aaz1926@gmail.com to make Alzheimers a spoken, proud word.
    ReplyDelete
  2. The comment on Doctors detecting early Alzheimer’s and Dementia is so important. If only my mom’s doctor detected the disease 7 years ago, maybe I could of prolonged the later stage she is in now. Instead he treated her for Thyroid and depression, then over the course of the last year telling us to put her in a nursing home for Old Age. But why I asked, so she forgets what she ate for lunch, or what day it is or repeats things, who does at times forget, she knows who I am and my Dad, why put her in a Nursing Facility. Then he gives my Dad a test to take home and work with her, now knowing my dad will not even admit to Alzheimers, only to Dementia, not knowing they are linked, so the test is thrown away and not mentioned. The WWII generation will not admit or understand Alzheimer;s Disease, this is a non-spoken, dirty word to be locked away for crazy people. So how do we, the baby boomers, the age of intense knowledge in the world of space exploration, electronics, internet and Skyp know how to understand and help our loved ones deal with Alzheimer’s Disease if the Doctors will not admit to it. My Dad who is 83 talked with his granddaughter on Skyp the other night and was fascinated. He never thought in his life time to be able to talk and see someone on the computer, the same way his mother was fascinated with TV, she asked “how do they do that”. So why is Alzheimer’s Disease still locked away, where is the research and the Grants for research, instead of all the silly pet projects, what about saving lives??

    Where would we be today if Breast Cancer was still thought of this way, Millions and Millions of women would be dead, my mom being one of them. But because of research and “speaking the unspoken word’ my mom survived Breast Cancer in 1993 and Ovarian Cancer in 1998. Only to fall prey to Alzheimers. Now she does know why she had a breast removed, but years ago was proud to a survivor.

    Why all the medical research and drugs to keep people alive longer only for them to lose all memory of their precious life, a life that made a difference in this world. Why do the doctors deny it or not tell us unless we insist. We all have to do our own research, as I have done night after night on the internet, to find out how to give my mom and dad in their remaining years the quality of life they deserve.

    Let us all SPEAK UP, and be proud to know the word Alzheimers instead of denying it. Make everyone aware of the disease so maybe someday my grandchildren can say “I survived Alzheimers” !! Please email me at aaz1926@gmail.com to make Alzheimers a spoken, proud word.
    ReplyDelete