My mom has kindly refused formal testing in the past. Yesterday she cooperated and participated in the Mini Mental State Examination test with her doctor. I knew we were probably heading towards severe dementia but was not expecting her to score a 2! I'm struggling with how - and what - to tell her siblings and friends. I've been keeping them updated on her current status, but the doctors wouldn't provide me any guidance on what to expect - and possibly when. I understand each patient is different...but a score of 2! I just need some kind of guidance.
Questions;
5 points
“What is the year? Season? Date? Day? Month?”
5 points
“Where are we now? State? County? Town/city? Hospital? Floor?”
3 points
The examiner names three unrelated objects clearly and slowly, then the instructor asks the patient to name all three of them. The patient’s response is used for scoring. The examiner repeats them until patient learns all of them, if possible.
5 points
“I would like you to count backward from 100 by sevens.” (93, 86, 79, 72, 65, ...)
Alternative: “Spell WORLD backwards.” (D-L-R-O-W)
3 points
“Earlier I told you the names of three things. Can you tell me what those were?”
2 points
Show the patient two simple objects, such as a wristwatch and a pencil, and ask the patient to name them.
1 point
“Repeat the phrase: ‘No ifs, ands, or buts.’”
3 points
“Take the paper in your right hand, fold it in half, and put it on the floor.” (The examiner gives the patient a piece of blank paper.)
1 point
“Please read this and do what it says.” (Written instruction is “Close your eyes.”)
1 point
“Make up and write a sentence about anything.” (This sentence must contain a noun and a verb.)
1point
“Please copy this picture.” (The examiner gives the patient a blank piece of paper and asks him/her to draw the symbol below. All 10 angles must be present and two must intersect.)
30 TOTAL
Score
25-30-Questionably significant
If clinical signs of cognitive impairment are present, formal assessment of cognition may be valuable.
May have clinically significant but mild deficits. Likely to affect only most demanding activities of daily living.
20-25-Mild
Formal assessment may be helpful to better determine pattern and extent of deficits.
Significant effect. May require some supervision, support and assistance.
10-20-Moderate
Formal assessment may be helpful if there are specific clinical indications.
Clear impairment. May require 24-hour supervision.
0-10-Severe
Patient not likely to be testable.
Marked impairment. Likely to require 24-hour supervision and assistance with ADL.
Source:
• Folstein MF, Folstein SE, McHugh PR: “Mini-mental state: A practical method for grading the cognitive state of patients for the clinician.” J Psychiatr Res 1975;12:189-198.
The 0-10 "Severe" does not seem to "fit" your mother's abilities. I'm not too sure if you should place a lot of faith in just this test.
Shute, I can't count backwards by 7's (without fingers ha ha) and would need to write the word out to be able to spell it backwards. My brain just doesn't run in "backwards" mode, I guess.)
Funny thing, I can write backwards in cursive. example: .llew stset ekat t'nod I
(I don't take tests well.) Go figure? YOU are the best prediction of what her abilities are. She can be better tested by a geriatric neurologist.
I knew she had problems but she did so poorly that there is another test they do especially for people with higher education & they said that even as she was a university graduate, she wouldn't be tested further as she did so poorly
She was diagnosed as severe dementia where before test I thought it was mild - I often have been glad that I sat outside & heard her answers as well as saw her 'written' work also because I know how gentle the tester was, how she answered & how she couldn't really answer simple questions -
This made my future actions done with much more surety & confidence - mom had hidden her inability from all but my dad who was in major denial but those tests showed how little she was able to understand - FYI this was about time I invoked her P.O.A. to be able to assist her in the choices she could no longer make herself
Moecam--I enjoyed your story about the person who had it sufficiently together to explain WHY she didn't know the date. When giving these tests, I wonder if the scoring distinguish between those who have no idea and those who answer "I'm not quite sure whether today is January 20 or 21 (2018)", the latter being something that could happen to anyone, especially one who doesn't have any appointments or events scheduled.
That said the instrument is designed as a screening tool, and her low score suggests further evaluation is warranted. As other posters,have pointed out, too, the human mind is tough to quantify in any meaningful way, cognition is changeable, and the subjects attitude and interest in the testing process make a difference. More evaluation sounds like a good idea.
After reviewing the test, I’m not surprised as I know she wouldn’t be able to answer / complete with answers
Instead, it's probably better for you to familiarize yourself (if you haven't done so already) with the way dementia usually progresses, and how most people die of the condition. (Sorry, this is sad to learn about, but it's still worth doing so you'll better understand what to expect.)
People vary and your mother might have a more unusual course (she's already on the young side).
But generally: in the early stage, people have difficulties with things that require more complicated brain processes, like driving, finances, judgment, organizing meals or trips, learning something new, making complicated decisions. They also often have difficulty with short-term memory. They may have difficulty saying certain things, or with visual-spatial processing. They usually are able walk and talk, although what they say doesn't always make sense.
In the middle stages, people start to lose their abilities to manage basic skills like continence, getting dressed, and they have more difficulties with walking. Also the type of mental processing activities they can do becomes more and more limited.
As they go from middle stage to late, they lose the ability to walk and make sentences and manage continence. They recognize even familiar people less and less, and eventually they forget how to put the fork or spoon in their mouth, so they have to be hand-fed. Eventually they lose the ability to sit up without support. As a geriatrician this is what I consider "severe/late-stage," but I have noticed that many people -- including many doctors -- will label someone severe just because their thinking and memory are very scrambled, even if they still are able to manage walking and talking.
If you google for the FAST stages of Alzheimer's, you will probably find this laid out. How long it takes for people to go through the stages is quite variable.
People will score very low on the mini-mental well before they reach late-stage, because to do those cognitive tests, you need to be able to understand the instructions, remember things, speak, and draw/write.
If your mom can call you on her iPhone and manage other tasks, she doesn't sound that severe to me. In terms of what to tell your friends and family, maybe focus on what she's able to do now and what she has trouble with.
Medical complications related to dementia are possible at any stage, but become most common when people are bedbound and have lost most of their mental abilities. In very advanced dementia people have basically lost all their mental abilities, but their bodies are well enough to keep living. Again, how long people last in this stage varies; some people live this way for a few years.
But that only lasts so long, and eventually people will start showing signs of illness related to end-stage dementia. These include repeated pneumonias (which may be related to swallowing difficulties), other recurrent infections, pressure sores that don't heal, weight loss, or fevers. A study found that when people with advanced dementia develop those signs, they had a 40-50% chance of dying within 6 months.
nejm.org/doi/full/10.1056/NEJMoa0902234#t=article
So...I hope some of this information helps. Good luck w your mom and take care.
My husband's MMSE score bounced all over the place. He was in a study, so he took it at least once a year. I don't think it was ever 2, but it went from the teens to 28. He had Lewy Body Dementia. It is characteristic of that disease to have fluctuating cognition. The varying scores were just evidence they had the diagnosis right! A score much lower than last year did not mean he was much worse than last year -- discussion of symptoms was more useful as a measure -- it just meant he tested at a low point in his up-and-down cognition.
It sounds like your mom is doing reasonably well in her interactions with visitors. If she isn't drastically worse than she has been recently, I'd not be overly worried about the test score.
(My mother could pass all kinds of tests, well into her dementia. The tests just give clues, not a diagnosis.)
Hopefully your Mom will agree to a more thorough exam to determine her status more clearly.
As others have suggested there is no actual way of making a prognosis for any dementia. However getting a definite diagnosis will make getting any treatment possible.
I think the idea of doing the test yourself under calm conditions would also be a good idea. At least it would give you a better idea of what is going on.
I used to administer this to people for applications for Long Term care Insurance. Most people scored well enough on the tests and when there was a failure it was very bad. I remember two, one was an elderly lady who without the testing clearly was not competent although her son was furious when her application was refused. The other was a man who when asked to read something totally lost his temper and ordered me out of the house. I think he was illiterate. Another was a man who admitted that he could not read or write. That was fine because I was allowed to read the questions to him.
Enjoy the time you have left with your Mom and let the "what ifs" take care of themselves.
Oo.
Theatre? Cinema?
But it was eight hours ago that I read the list! How long before it's okay to forget what the words were? :/
Ask the doctor for a detailed breakdown of what she couldn't do.
We definitely need to remember what other posters have pointed out, the MMSE and others like it are only the first step, not a diagnosis.
And in this case - do we ever! 2? Impressive! But sadly not in a good way.
It's just flitting across my mind that Mohammed Ali, may his memory be for a blessing, scored virtually undetectably on IQ tests (decades before his later difficulties set in). Nothing wrong with his IQ. It was about his absolute lack of interest in, and his opposition to the basis of, the tests.
My mother declined to answer "trivial" questions. I think she might have found some of them an effort, and indeed been unable to answer some. But instead she preferred to reject them altogether.
So how much is won't, how much is can't, how much is just not able or willing to pay attention in the first place, and join any necessary thought processes into a coherent chain?
Given that MW's mother is still socialising so well, and functioning in many ways, although undoubtedly there is something going on it doesn't seem to fit the obvious things that would produce *this* low a score.
I think I'd do two things.
1. Ask what further investigations might be useful.
2. Celebrate how much of life she is clearly continuing to enjoy. You can't have too many friends or too much music :)
Three things.
3. Take deep breaths. This needn't be the end of the world.
If you knew there was dementia, but didn't think it was severe, I would be concerned about a score that low. To me it would indicate some other underlying issue such as a urinary tract infection, dehydration or severe anxiety/depression. I would not take the doctor's "do nothing" approach at face value. I would ask them to look for an underlying cause, do blood work, a urinalysis and have her see psychiatrist.
You can also print out the test an administer it yourself to see what the issue might be. She might be way more relaxed with you asking her the questions than with a doctor. Just be sure not to help with the answers. This way you get a better idea of what specifically she is having the most trouble with. I have been to the tests with my mom and she always has issues remembering the three words a few minutes later and cannot do the subtraction from 100. She also has trouble with the town and county, but since she doesn't know where the doctor is located and isn't driving, I don't really get bothered by her not getting points for that. She also is never sure what floor we are on, but at the doctor's office we go to, we take an elevator to the 2nd floor, but the elevator is the parking lot, so when you push the button it says 1. If she says either first or second floor, they give it to her.
There is a documentary I'd like to share that you may find helpful on TVO (an Ontario public television station) called Much Too Young
tvo.org/video/documentaries/much-too-young-feature-version
Even though you are living it you may find comfort and inspiration in knowing that others are sharing your journey.
Not dementia but one of the aphasias.
There is a risk of misdiagnosing aphasia as dementia with Folstein. “Is Folstein mini an aphasia test?”, Article, Author: Vigliecca. ncbi.nlm.nih.gov.