End Of Life Issues---The Good, The Bad, and the Ugly

If I ever become a hospice nurse (which is what I've decided I want to be when I grow up), the varied experiences I'm collecting in long-term care should stand me in good stead. Nurses Announcements Archive Article

Right now I have three different residents in three different stages in the process of casting off the human shell that has housed their souls for over eight decades. One of them, Allie*, had been in fairly good shape until the night she had a massive GI bleed and was going into shock while I wrangled with the 911 dispatcher ("She's HOW old? What's her advanced directive say?"). After the EMTs saw for themselves that I wasn't exaggerating---why do they assume we LTC nurses know nothing?---they scooped and ran, and after a few days in the hospital she was returned to us with a DNR order and an inoperable, fast-growing mass in her lower colon that could rebleed at any time. Her family, however, was unwilling to give up, and it wasn't until this past week, when she had a stroke that destroyed her ability to speak and paralyzed half her body, that they finally began to understand that whatever quality of life she had was gone.

While they have declined our suggestion to bring in hospice, they agreed to comfort measures such as liquid morphine and stopping unnecessary medications, and they've been coming in every few hours to do mouth care and lotioning. Allie is still with us, and though it's clear to all that she won't be much longer, at least she's surrounded by acceptance and can die in peace.

Not so, I'm sorry to say, with another of our ladies, whom I've known since the night she arrived at my assisted living facility four years ago, utterly exhausted from a day of flying across the country with her cat and two suitcases filled to bursting with expensive clothing, hats, and jewelry. Maryann* later followed me to the nursing home, where she has declined slowly but steadily over the past year; now her kidneys are just about gone and her once-sharp sense of humor right along with them. She's been in and out of the hospital now for several months, and each time she returns it's with a diagnosis of "dehydration" and we are once again urged to push fluids, push fluids, push fluids.

Well, guess what? Maryann doesn't LIKE to drink fluids. They make her go to the bathroom too often. She also doesn't like to take her meds---too many pills, she says. She's tired of taking pills. She's tired of living. She wants to stop taking all those pills so that she can be with her husband and her cat again. I don't blame her.

But Maryann's son, who brought her out here from Philadelphia after his father's death, is having none of it. There is a grandson's wedding coming up in June, he tells us, and "if Mom were in her right mind" she'd want to be around for the event. So we are to encourage/force her to drink at least 2 liters of fluids per day, take all of the 20+ medications she's on PLUS the new ones that were prescribed after her most recent hospital stay. "If she wants to 'go' after the wedding, she can," says the son, "but she really WOULD want to stick around for this. We can't let her die yet, so whatever it takes to keep her going, just do it." All this despite an advanced directive that says no resuscitation, no feeding tubes, not even antibiotics except for "comfort".

I want to tell him that this is the most inhumane thing I've ever heard of, that his ideas are so wrong on so many levels that I can't even wrap my mind around it, but I can't. Why? Because this ISN'T the worst thing I've ever seen happen to a resident with a controlling family. That distinction is reserved for the 95-year-old gentleman down the hall whose fate is in the hands of a late-middle-aged couple, neither of whom is related to him by blood. This unfortunate fellow has outlived all but one of his children, who is estranged for unknown reasons; and if he were in his right mind, I think he would be madder than a wet cat at having to live like this. "Grampa" is as demented as they come; his speech is unintelligible, he is combative at times and incontinent ALL the time, he's missing half his right foot due to infection and doesn't know he can't stand up without falling. He has ischemic colitis, CHF, chronic renal failure with a GFR of about 8, degenerative joint disease, osteoporosis.........yet this couple just can't seem to let nature take its course.

We've sent Grampa to the ER no fewer than five times this year, despite the belief of facility staff that we are flogging his failing body for absolutely NO useful purpose. I've sent him out for diarrhea that wouldn't stop. I've sent him out for pneumonia. I've sent him out for low BPs, twice. And yesterday I had to send him yet again, this time because he was obtunded AND his BP was in the toilet AND the diarrhea was back. Why? His POA demanded it, despite the fact that he has a DNR order and the paramedics give us hell every time we call about this man. Yes, we all know that "do not resuscitate" doesn't mean "do not treat", but every time he's sent out he winds up being admitted to the hospital for several days on the insistence of the POA. While he's there, he's tied down and force-fed medicines and IV fluids to rehydrate his body; when he returns to us he goes back to swatting at the hands holding a cup or a spoon to his lips. Doesn't anyone understand what he's trying to tell us?

I won't even go into the reasons why this is a waste of limited healthcare resources or how selfish it seems to me for families not to let their loved ones go when they fall into hopeless circumstances and life becomes a burden. No, what keeps me awake at night sometimes is the conflict between my job and my ethics, which holds that forcing people to stay alive is as morally wrong as killing them outright via euthanasia.

It's not that I would ever impose my personal beliefs on a resident or family, but as a nurse I've seen some of the worst sorts of suffering there is......and not all of it is physical in origin. Some of it is the loss of who the individual was; another large part of it is the loss of independence and dignity. But when those things are combined with medical problems that cause one to feel miserable every day of his or her life, well......would YOU want to live like that? I know I wouldn't. But even though I have an advanced directive (and have threatened my family that I would haunt them forever if they don't let me die when it's my time!), I'm less than confident that my future caregivers will know when to say "we've done enough".

They used to call pneumonia the "old man's friend" back in the days before antibiotics. While I wouldn't trade today's technology for yesterday's more realistic approach to end-of-life issues, I wonder sometimes if we as a society have become so arrogant that we keep people alive long past their natural lifespans merely because we can.

Just a few thoughts on an evening when I have more quiet time than usual to contemplate. If you've read this far, thanks for hanging in there this long. What are your thoughts?

*Names have been changed to protect privacy.

That's just plain selfish of the families to keep these people from moving on to the next life. I'm currently a first semester student working in LTC now and I have had so many people tell me they just wish to die. We need to educate the families that sometimes the best miracle is "to let go and let GOD". It breaks my heart the way some of these people are kept alive for no one's good except the family that isn't willing to let go yet. And bless you hospice and LTC nurses for doing this day in and day out!!!!

Specializes in cardiac, ortho, med surg, oncology.
Maybe so many of us are afraid to let go because that means we're next; maybe we cling to our forbears so fiercely simply because they are our last connection with the younger selves that we will never be again.

Anyway, that's a lot of generalization, but it sort of makes my point. :coollook:

I agree, when our parents die there is no longer a generation between us and the grave. I do think being nurses helps us to get there more gracefully though

I work in the ICU at a fairly large hospital. I totally understand about the inability for people to have a 'good death' because of family members that are clueless. Too bad everyone is afraid of trial lawyers or we could practice medicine in an ethical, sensible and financially responsible fashion. Until things change however I guess we are stuck letting lay persons run the show. What we see is appauling to say the least!! I totally hear ya!

Specializes in Community, OB, Nursery.

This goes on at the other end of the spectrum too - with tiny preemies. But the core issue is still the same. Just because we can, should we? In whose best interest is it to keep people alive that are trying to tell us (verbally or otherwise) that they are dying? I think too many times we fight to keep bodies around when souls want to go gracefully.

Great post.

Would it make you feel better if I told you there is one person who will not allow it to happen to their family member. My mom will be 86 shortly and her dementia is getting worse. She made it perfectly clear to me when she started to feel herself slip that she did not want what you are describing to happen to her. She always disliked medical treatment, the more invasive it was the more she disliked it. It would be obscene to subject her to treatments she would refuse if she were in her correct mind. I do worry how far we can go with this. Take for instance the fact that she has mild heart failure and her feet swell on some days. I know she would refuse treatment for the heart failure and accept whatever the consequences of that would be, but could it be misconstrued as neglect on my part if I follow that path? I worry about that. I do have her medical and durable power of attorney.

I think as nurses we have to be reminded every day that dying with dignity is important to everyone. I, too, don't understand why some family members don't understand this. But as patient advocates we must offer our understanding to both patients and family.

It's not just the families that don't understand that death happens. So many in our profession and so many physicians see death as 'giving up' and 'losing' the battle. And so many are woefully ignorant about what hospice does and why we use the drugs we use. The medical profession needs WAY more education about hospice as well.

Specializes in hospice, corrections.

Thank You! Thank You! Thank You! :bow: to all of the nurses who do LTC. I can't for all the reasons that are listed above. I LOVE working at Hospice. Occasionally we get the family members that do not want the patient medicated because they want them to be "alert". I have become very good at pain control education. If the patient comes to us and can still verbalize pain, we medicate per patient. If they cannot, I teach the family the non-verbal signs and symptoms I look for and explain what I am doing and why. Usually, the family will get on board and look for those symptoms with me. :yeah:

I too am one that has made it very clear to my family what I want when I cannot advocate for myself. I want standing orders for a glass of wine after dinner (or two!) I expect to have chocolate readily available. If I can't eat or drink, then I'm done. NO FEEDING TUBES. I've threatened to have that tattooed on my stomach so that if my family decides I need one, the doctor will see how I really feel.

Again, Thank you! LTC nurses do a job I know I couldn't do. You are truly angels.:saint::hug:

Specializes in burn, geriatric, rehab, wound care, ER.
It's not just the families that don't understand that death happens. So many in our profession and so many physicians see death as 'giving up' and 'losing' the battle. And so many are woefully ignorant about what hospice does and why we use the drugs we use. The medical profession needs WAY more education about hospice as well.

I wonder if some of these docs don't want to lose the gravy train i.e. a dead patient doesn't earn them any money. I have suspicions about one particular doc who works at my facility who seems to dissuade pts/family members from DNR's and always wants aggressive treatment for his frail elderly pts with poor quality of life.

When a patient goes on hospice, does their PMD lose a patient-does the hospice MD effectively become their PMD ? I would appreciate clarification from any hospice nurses out there.

Specializes in lots of different areas.

Well put. Too bad we can't post this in the hall for all the "POA's" to read!

Specializes in Hospice.

Don't look now, Viva, but you're already a hospice nurse ... and a pretty good one judging from the original post.

It would be a great thing to learn more about what LTC/AL/Rehab nurses need or want from those of us working for the more formal hospice industry.

One of the medical directors for my hospice ... 2 owners ago ... was trying to get a consultation service started. If our respective owners can figure out how to make money out of it ... what a great thing to have as a resource for the work you're doing for these elders.

Specializes in LTC, assisted living, med-surg, psych.

That's a great idea, heron!

Speaking for my peers in LTC, I'd have to say that our primary need is EDUCATION---about what hospice is, what it does for the patient, family, AND facility staff, and especially its philosophy regarding medications and comfort. So many LTC nurses are so afraid to give meds in the amounts recommended---afraid they'll be accused of killing the patient, or hastening his/her death---that they don't medicate properly, thereby causing unnecessary suffering and perhaps even prolonging the dying process.

In fact, I'm one of the few LTC nurses I know who's comfortable with giving meds in the amounts needed to relieve pain, air hunger, terminal agitation etc. I've had to do a lot of encouragement with my fellow nurses to get them on board with comfort care procedures........usually when I've spent most of my shift working to get on top of a hospice patient's pain and distress because the previous shift gave only 5 mg of morphine all day.:(