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Praying your efforts on behalf of dad are successful.
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Ok, now I do know of a case where someone was going to be discharged early to rehab. He had a fever, and could not be discharged to rehab.
After 18 months in the hospital following spinal surgery error, leg amputation, etc. this patient would have died of infection going to rehab early.
THE FEVER, pneumonia may be key. These medical incompetents are not aware of people @97 wanting to live!
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GardenArtist, what has worked for me in the past is notifying via fax the hospital social worker assigned to his case, the nurse unit manager and the physician that this man lives alone and that they are discharging him to live alone. They bear the responsibility for whatever happens to him. You are going to be out of town. Ask for an occupational therapist to do a home safety evaluation and report prior to discharge. Do not offer to pick him up, do not be available by phone. Insist on all communications in writing. Appear as though you are getting ready to sue their sorry a$$es and they will perk up and behave. (hopefully).
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GA, on the discharge planner piece I was trying to say that I too had been told that dad could get rehab services after going home first. When I called to follow-up I was told he couldn't get it and that I needed to call his PCP. I never got a call back from the person who told me this and made a note to myself to always get it in writing in the future, lesson learned. Since his PCP stunk we found a new doctor that did order it and got him help. Sorry for the confusion.
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GA, just catching up with this and happy that things have resolved. Can't wait to hear what magic you worked!
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JB, thanks for sharing your experience. This is one of the kinds of issues that I found objectionable in PCPs - perhaps by nature of their scope of care being so broad that it can miss facts more discernible by specialists. We'd always relied on specialists and still do. There were only a few PCPs that were thorough, but only at the beginning. And they were all medicine first as a solution. Even things that could have been solved by food changes or additions were treated as conditions that medicines should address. After a while I began to wonder if they were groups targeted by pharmaceutical reps.

I'm not sure what you mean to "check behind the discharge planner." This is not a group with which I'm particularly impressed, so I approach them as I might as porcupine ready to extend its quills. I even try to thank them when they provide me with basic information I already have. "Stroking" plays a big part of deaing with discharge planners.


Update on my situation: things have resolved well and are moving forward; I've been on the phone literally since about 8:30 and just ate while sitting by the phone.

More details later, for anyone else who has to face this. Now it's time for a nice nap.
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GA, really sorry. Like others I can sense your pain and frustration but I'm sure it pales in comparison to being there with you. In reading some of your posts it seemed your dad was still doing fairly well given all that's happened and I know things can change on a dime.

When my dad was sick years ago and looked like he was going to die we took him to the ER but he was released said to make appt with PCP which we did. PCP said let him rest and bring him back in three weeks. I lost it and said look at this man who has been your patient too long for you to have that answer. I know he's a pain in the butt but you can clearly see he is not well. I said never mind I'll take him to another ER and see what they say. And when they ask I'll let them know by name you were the one who refused to have him tested and admitted. He quickly changed his mind and found out he had a blocked prostate issue where he couldn't urinate. The urologist said three more days he would have died. You now have a plan in place, but I was going to suggest you take him to another hospital if it seemed like a viable option at this point.

Check behind the discharge planner. I was told a similar thing back in April when my dad was in the hospital again for a different issue and ran into an issue with it. As long as his PCP approves and you have it in writing before you leave you will be fine. But please make sure you get it then.
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Houseplant,

I have thought of refusing to take him home, but honestly don’t have the will or nerve to do it. It would hurt my father so much; he’d feel as if he was being abandoned. I would probably cry all day and end up going to the hospital to get him.

The issue of a rehab facility was raised, and the Discharge Planner was amenable to considering it. But my father refuses to go. Even a week would make a big difference. We’ve already decided to use the home care agency we had earlier this year; they were very good and contact has already been made. They’ll be on board the day after his discharge, but that still leaves the evening of the discharge day.

The Discharge Planner did tell me that even if he does go home, he can go into a rehab facility within 30 days, which surprised me. I thought that had to be a direct hospital to rehab facility transfer. The DPs have made mistakes before though, so I’d call Medicare to verify that.

My father is adamant that he is going to die in his own home. We’ve discussed this for years, and he will not reconsider. So I’ve accepted it. And I think he would be happier to die near his beloved wood shop than in a facility.
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Refuse to take him home. Request that he be transferred to a skilled nursing facility. Ask Medicare about the 100 benefit days per year for hospitalization/rehab/snf stays. This may apply because he cannot care for himself. If he gets transferred, this gives him more recovery time and gives you a chance to plan for some in-home care. His age and overall health may not permit him to stay home much longer anyway. This may be a good time for you to start touring local nursing homes to see what's out there and start determining what assets he may have to apply toward his care.
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FYI: here's the site; I do already have the IM; it was given to me Friday night when Dad was admitted.

https://www.medicare.gov/claims-and-appeals/right-to-fast-appeal/hospital/fast-appeals-in-hospitals.html
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Yoga Girl,

Answering your question, the doctor who wants to shoo Dad out the door is the PCP we've seen a few times. He's not a doctor we go to on a regular basis. And we've had disagreements in the past when he wanted Dad to take Fosamax, which Dad had taken some years before and found the side effects too unpleasant. The doctor said "he HAS to be on something!" Yet never did he even mention the benefits of weight-bearing exercise for osteoporosis prevention.

That attitude is one of the reasons we never went back.

That's a great idea to involve the Pulmonary physician; Dad's treated with her for years; perhaps she'll even take over the case. And she's really a great doctor.

I think I've answered all your suggestions, and noted them in my phone log for the next phase.

I was even thinking of renting a motel room for the night, but we don't have enough portable oxygen and there's no way I can even haul the larger concentrator out the door.

Guess I'm going to have to bribe my father to go to the rehab facility, if even just for a week.
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CWillie,

Dad's plan was to return home and start walking immediately, as he did up until the day he deteriorated and we ended up in ER. My plan was to go to the place he rehabbed after his 2 femur fractures. He liked it, they liked him, the PT and OT were great, as was the food.

But he's refusing to go. I think this is going to have to change as I'm going to have to refuse to participate if he won't agree to the best option available.

If I refused to take him home, one of his church friends would. I thought about refusing, and it's also something I would really hate to do - it's like abandoning him and would really crush his spirit if he though I was in fact abandoning him.

I will refuse to sign the Discharge Orders and will advise Dad to do so as well.


SendMe,

One of the things I've learned is that this PCP business can be a burden when it comes to hospital admissions. Before, I would state we had no PCP (because I honestly don't think much of the field), but decided to "play the game" and stated that this particular one, who we saw a few times, was the PCP.

What I've learned is that if I say there is no PCP, the hospitalist team will be involved. And they're really, really terrific. They're a young group of go-getter, highly knowledgeable and teamwork oriented doctors.

That's what I'm doing tomorrow - calling the hospital to find out how to release the PCP and get the hospitalists on board.

I was in fact somewhat annoyed that the PCP hadn't even consulted the cardiologist about the elevated heart rate.

No, hospice isn't even on the horizon. Even at almost 97, Dad still walks with his rollator about 300 - 400 ft to the lake when the weather is nice.

Re your second post: I'm thinking maybe the PCP doesn't even want to be involved and is just pushing Dad out b/c Dad hasn't been to see him in 1.5 years, and he might not even want an oldster for a patient.

I caregive from a distance, about 27 miles.

And I'm adding the DON on my list of people to talk to. Never thought of the DON - good suggestion.
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FF,

We had a similar situation once when Dad was rehabbing after his first femur fracture. The Alpha Male director of rehab wanted to discharge Dad right about the 30th day of his stay. Dad was a bit uncomfortable being on his own and wanted to stay another week, but Mr. Alpha Male wouldn't back down.

There was an interesting tete-a-tete in which my father opined on "educated idiots", which I agreed without saying it that the rehab director was one. He definitely was a paper pusher and not a hands on person. I figure he was the relative of someone in high places and that's how he got his job.

Still, he refused to change his discharge Dx and Dad came home early, with much anxiety.


GSA,

I will Google the right to fast appeal info as soon as I post here. Fortunately, Medicare does make it easy with the notice that's provided on admission. So I do have all the data and contact numbers.

But I also know that Medicare doesn't honor its appellate practices. So I don't know how realistically they handle urgent appeals.

I've appealed a hospital price gouging med list for an "observational" stay, and discovered that Medicare doesn't even bother after a preliminary appeal decision.

There is a second level; Medicare just wrote and asked if we wanted to continue the appeal; I wrote and responded yes (replied by cert. mail) but Medicare never did anything else. Never heard from them on the issue again.

Also, the "care in place" will be visiting home care, but that's only 2 - 3x weekly, and only for an hour or so more. It's not 24/7 care. I was surprised the discharge planner didn't raise that issue; instead she wanted to give me one of those advertising booklets listing dozens of AL, IL and other facilities.

When in doubt, hand out free literature!

You hit on a good point though - it was a Eureka! moment when I read it. In the past nurses have told me that Dad tells them what good care I provide for him. (I think he just likes to brag!) I'll bet he did that again and they assumed that we live together and I provide in-home care for him, notwithstanding the fact that the ER doctor, the admitting intern and one of the nurses were all told that he lives alone.

I'm wondering what I can do to convince them that Dad would be in an "unsafe" environment if home alone. This happened the last time this PCP was handling Dad's case and one of the nurses told me I had better plan to stay with him overnight. I asked "where"? There's no room at his house. I can't bring him to mind and lug an oxygen concentrator in the care and we were never given enough tanks from the then supplier.
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guestshopadmin, that's a good point about one's parent saying they have someone at home who can help. I remember one time my Mom [97] saying she has a husband who can take care of her at home. Oh really? My 94 year old Dad is a major fall risk, who can't make a sandwich for himself much less for Mom.
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Talk to the DON, director of nursing immediately. The doctor is having a bad day and it's about to get worse because he/she did not read the patient's chart. Then, there might be a patient's rights advocate or Ombudsman, the nursing office or administration can give you contact info.
OR, you can call the doctor, inform him/her of the missing details.
Call the hospital administrator next.
GA, you are there or caregiving from a distance?
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Sorry GA. Wasn't sure if you had gotten copy of IM for Medicare.gov yet. Have a friend whose stepdad has MRSE infection and already had to appeal once. She said they push out but if you don't have care in place they cannot discharge to unsafe. The advantage plans are bad about this especially if failure to improve. "no my father lives alone and has no care at home." Lather rinse repeat. Is your father telling the doc you can cover?
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GardenArtist, Sorry you have this worry. Is the Dr who wrote the order to discharge his private primary care physician or the Hospitalist employed at the hospital who manages his case? Sometimes I got different answers depending on which of dad's Dr's I asked. Also the pulmonary Dr could hopefully pull some strings. Good luck.
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No experience whatsoever!
Wouldn't a second opinion from a specialist be faster?
Also, you are correct to disagree, because if a patient has pneumonia, they have a fever, isn't hospital protocol that a patient should not be discharged with fever, or was that back in the olden-days of proper medical care?
Is hospice involved?
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GA, I have no answers for you but I sympathize with your frustration. Was the plan that he return home eventually or are you hoping to find a placement for him? What would happen if you refused to pick him up until you have a plan in place?
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Hey garden. Google right to fast appeal. Should take you to Medicare.gov which explains your rights if you think discharge too early!
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GardenArtist, no experience with a hospital wanting to do an early discharge, but am dealing with the rehab/long term care that is talking about discharging my Mom. It's like are we talking about the same person??? No way on earth is that woman ready to come home, she needs long term care, some place, some where. Not in a 3 story home when she is now in a wheelchair, and probably doesn't even know her name anymore :(

I know what you mean about getting caregivers out to the house. The agency I use need 24 hour notice and they charge 1.5x for the first day because everything is so last minute. So I had to stay over with my Dad at my parents house one night and got maybe one hour of sleep because I don't have the strength to help Dad upstairs.

I tell ya, I really hate what my parents are putting me through. It wasn't a life well planned on their part. They should have been in independent living or assisted living years ago.
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Forgot to add that he has pneumonia which isn't yet resolved and has a pleural effusion as well.

Thanks for any suggestions.
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