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Mom, 81, in LTC. Is on a new anti-biotic for a UTI. The first time, they put her on Marcobid and I did not notice any cognitive improvement after a HUGE decline. So I asked for a retest (at her new LTC facility) which they said was fine. Then a few weeks later they said, hmm, there's a bad pee smell so they retested her again and not surprisingly, another UTI. Treated her with Macrobid again. Since she was still being totally crazy, I asked for a retest and for some general blood work. Retest said - still have a UTI! E-coli. So this time they put her on a different anti-biotic. On day 5 of 7 (or 10?) and she's still crazy. She is seeing her dead relatives and thinks I'm driving her to grandma's house (dead for 30 years) and picking up dad (died in 2016). I play along but it's wearing me down. If this new anti-biotic doesn't help her cognitive situation, I will accept the fact that this is just where she is now.
BUT - how do you deal with it??? I'm thinking that I might have to tell the nurses not to let her call me after dinner any more.

I think that the first way to deal with what MAY BE permanent impairment of this type is that the access to phone is removed, and medication to calm is sought. That means this is both a problem you can handle yourself by speaking to her long term care facility and a problem that you need to be certain is addressed with her doctor.

The fact that this UTI is being treated inadequately is allowing that only the weak bacteria get killed off each time, with the stronger ones remaining, making it more and more difficult to cure. She may need prophylactic antibiotic, a good one such as cipro. MDs no longer like to treat using it as it has complications, but the complications of her UTI, IF that is what this is, are life changing and severe enough to make this a life not worth living for her. If there's incontinence or inadequate cleansing (and even without those problems) this may be an ongoing problem.

Meanwhile, this is a problem for Medical treatment AND a problem that you need the LTC facility to understand must be addressed with removal of the phone past a certain hour. There is also, sadly going to come a time when you may need to turn off your own phone, and turn it on every few hours to collect messages.

There is also Telecalm at 888 701 0411 and telecalmprotects.com. Has certain phones that are scam and spam blocking, and stops multiple outgoing numbers repeated over a short time with family of facility notifications of any 9ll calls. It can also work on corded phone without internet access, so you may want to check this company out. It has been mentioned on AC in the past and I made note of it to pass on. I have no personal history of using it.

Good luck, and I am sorry you're going through this.
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againx100 6 hours ago
Thanks for the helpful response Alva.

She doesn't have her own phone anymore but has to ask the nurses to call me. It would be easy for me to tell them not to have her call me after X hour. I am the one you might have heard about telecalm from. I used it for awhile and really like it but the router kept needing to be reset and there's no way my mother could handle that, never mind remember how to make a phone call. I think I'll give it a day or two more to see if the new anti-biotic helps enough to get the convos more into a tolerable level of confusion. It not, I'll ask them to tell her something like "Oh your daughter said she would be going out to dinner tonight and wouldn't be available to talk tonight" or something like that.

She is currently being given trazadone at 2 (25mg) and bedtime (50mg). The staff thinks this is working pretty well. Me? I'm not so sure. When I ask my mom to give the phone back to the nurse, I usually tell them about the crazy things she is saying and they often say that she's not telling them these kinds of things. Oh boy. So, by a calming med - do you have something other than this one in mind? I know people often mention Ativan. I wonder if that can be paired with the afternoon trazadone which is to try to keep the sundowners at least somewhat under control.

I understand what you're saying about the stronger bacteria surviving. I am going to ask them to retest again after this current course of treatment and lobby for a different and longer course of treatment if the UTI is still active. She is mostly incontinent - tries to make it to the bathroom but pees whenever she stands up at the very least. An aid always helps her as her strength isn't what is could/should be. I really don't want her in the hospital so I'll see what I can push for in LTC.
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My mother was doing the same type of thing shortly before she passed, but w/o having a UTI. She was obsessed with her deceased parents and riding the NYC subway to see them (we live in Colorado). It was awful. Her agitation level was thru the roof, so I asked her PCP for Ativan which did help, thank God. Then I got her evaluated for hospice, and she was approved under the Medicare reason of Senile Degeneration of the Brain. This was in Nov of 2021. She passed in Feb of 2022.


When my father kept getting back to back UTIs, he was at end of life and I got him on hospice too.

I don't know that your mom is approaching end of life herself, but it may be a good idea to get her evaluated for hospice to see what they think. It seems to me when an elder starts talking about seeing their deceased loved ones a lot, they themselves are getting ready to transition.

It's very difficult to get these calls and to stay composed, I know.....its very unsettling. This whole journey is so fraught with worry and uncertainty, it's mind boggling. I pray for inner peace for YOU, my friend, knowing that you're doing everything humanly possible for your mom right now. Be kind to yourself.
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againx100 6 hours ago
Thanks Lea. Your responses always help me. And usually bring a tear to my eye. As many compassionate responses do!

Typically, my mom doesn't seem agitated as much as just talking crazy about dead people. She's usually pretty calm about it and easily distracted like when I told her that I already called grandma to tell her that we wouldn't be able to make it to her house tonight. She bought that quite calmly.

I have been wondering when the appropriate time to ask for a hospice evaluation would be. I guess in the next week or two, if she does not rally at all, then it becomes something more considerable. Her life sucks and I do not believe in artificially extending it. She has level 5 dementia so I don't know if that's enough to qualify. I just want her calm and pain free and comfortable, both mentally and physically.

This dementia journey is certainly unsettling and mind boggling. Seriously, my mind gets blown with the new and strange places her mind goes. It's kind of interesting but mostly just so damn sad.

I know I am doing a lot for her and I feel good about that. If I didn't push this UTI retest, would they do it on their own? Doubtful. Which kind of sucks. I'm trying to be kind to myself but just don't have enough hours to do enough for myself. Hey at least I already got in a nice hot whirlpool tub today!
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I would say she needs to be taken to the hospital and a culture done to find out what bacteria is causing the UTI. Then she needs IV antibiotics. This cannot be done at the facility. Then, she needs to be taking something to keep it from recurring. My Mom was on cranberry tablets and a probiotic. Mom could become septic.

LTC facilities are limited in their care.
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againx100 6 hours ago
Thanks for your response JoAnn. I will not be taking her to the hospital unless I really have to. It's too hard for her. And me. I will have to check to see if my mom is still on the cranberry supplement. And I'll ask for a probiotic. I feel like I am always asking for things but that's OK. LTC are definitely limited in what they provide. Annoying but I guess that's the way it is.
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You can ask the nurses to not allow her to call you, or better yet, just don't answer your phone. I'm sure her facility will contact you if there is a real problem.
There are medications for sundowning, so I would most certainly talk to her doctor about putting her on some of them.
And definitely stay on top of her UTI's as they can turn septic if not treated properly.
And I'll say it again....dementia sucks!
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againx100 6 hours ago
Thanks for responding, funky. Your last words hit home - dementia sucks! I hate it. I NEVER want to be like that. UGH. I would rather be dead.

She is on trazadone which the staff thinks is helping but in light of all these calls about dead people, I'm not really sure. Or maybe it would be worse with a lot of agitation along with the conversations? IDK.
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Tell the nurses not to let her call you every day after dinner. Limit the phone calls to a couple evenings a week.

I did homecare for many, many seniors with dementia over 25 years in the caregiving field. Some of them were completely invalid, bedbound, incontinent clients in diapers 24/7 and they had less problems with UTI's than your mother does. Your mother needs more hygiene care done more often than it's being done now. The best way to treat a UTI is to prevent one.

It's a given that any LTC facility no matter how high-end or expensive is going to cut corners on CNA staff and the patients are going to suffer for it.

Would it be possible to hire a part-time caregiver for your mother? Someone who will go to the facility a couple times a day to make sure she's clean and dry? Even just once a day will help in addition to the CNA toileting/diapering schedule at the facility. It's terrible that families often have to hire private help for a loved one in a fully-staffed LTC facility, but it's reality so much of the time.
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againx100 6 hours ago
Thanks for your response, burnt. If this UTI stuff continues, I will seriously consider an aid to go there and make sure she's really clean, etc. They only shower people once a week which is utterly disgusting, though I have pretty much resigned myself to it!
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It took a number of years but I learned UTI's can be caused as a side effect of some prescription drugs. Is she on Memantine? Or C-Memantine? This can cause the urinary tract issues and cause the user to hold urine and get a UTI. We stopped the C-Memantine and then had zero UTI's after that.
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againx100 6 hours ago
Thanks Brandee. She's not on that med but thanks for the idea.
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Don’t answer! It’s okay not to be available.
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againx100 1 hour ago
Someone from the facility calls me and I can tell her it's not a good time to talk so I can/will start doing that. Thanks.
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