My dad has very advanced Lewy Body Dementia. He is completely aware of his toileting needs but has a difficult time verbalizing it and of course can’t use a call light. He has also lost his ability to stand alone or ambulate but can assist with a single person transfer. Since he feels the need to relieve his bladder or bowels, he stands to get up. The staff see this as agitation and want to medicate him. After 10 years of living as his caregivers we know his agitation means one of two things. Need for toileting or pain. The staff at night have begun to park my dad at the nurses station in his Geri chair after his first trip to the bathroom for his safety. I realize that he is a huge fall risk and there are rules against restraints him in bed but this feels like a worse restraint and it doesn’t allow for position changes. He is forced to sleep in the hallway on his back all night. I feel like we should be able to override the side rails rule as they are allowed for paralyzed patients. Since dad can’t remember that he can’t stand, he should not be allowed the chance to try. He is a danger to himself.
The place dad is in, is overall giving excellent care and I know they truly care for him and they are only trying to keep him safe at night. Is there any way around these rules for bed restraints so he can sleep in bed at night on his side? It doesn’t help that his room is the furthest from the nurses station with no possibilities for room changes
Otherwise the service was good. The home where my godmother was in was just a rotten home. Nothing about that place was good. Yes, shortage of help, theft, closed door so they could watch soap opera while working. You would not believe the crap I caught them doing in that home. She was constantly bruised. I would bring it up and they said she was violent. So who knows what goes on when visiting hours are over in some places. I cried every time I went to see her.
So, they do still use them. They had him so heavily drugged and I suppose it was for his own protection so he wouldn’t fall. Still, it’s heartbreaking to see because he kept trying to turn and get comfortable and he couldn’t.
I saw restraints used in a nursing home when I went to see my godmother. They still use them. Perhaps they are not supposed to but my godmother became violent and they used them on her. Her ALZ had progressed pretty far by then.
It’s sad.
Unfortunately, with dementia, people's sleep cycles can be thrown completely off with A LOT of restless activity at night (which is demanding for a smaller night staff who are trying to keep people safe). It's not uncommon for someone who causes many repeated visits to the person's room to end up close to the nurse's station at night. They may spend the day sleeping (and that could be in the bed). Just something to think about. Maybe you should set up a meeting with the facility and review the care plan.
Good luck!
Restraint vests are incredibly dangerous--they can slide down and hang themselves.
Have you been there at all hours to see if this is actually happening? If not I would stop in at various times during the night to see where he is. Or if it is legal in your area place a camera in the room so you can see when he tries to get up and if and when they bring him back to bed.
Bed alarms can be used.
Beds can be lowered to the floor.
If they are in fact leaving him in the hall all night I would report this, I would almost consider this abuse. It feels like some punishment. Not to mention there is no way he could get a restful night sleep in a well lit, noisy hallway.
Here’s what I would do: call a Care Meeting with as much of the staff who care for your father as are available. Brainstorm ideas of how to keep him safe but not parked in a chair all night. Be open to all suggestions, but mention the pressure sores. That’s serious business. Infections from those can be deadly. Let us know what happens.