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.

Excellent article! I was a long term care nurse and am now a hospice nurse, and your comments about the desires of families, moves, upcoming weddings that people are being kept alive for are all about the family member, NOT the patient. As a caregiver, I can only recommend education, education, education. I have often told families when doing a hospice admission that we are programmed to live, not to die. As such facing something we don't know provokes anxiety and fear in everyone, especially the caregivers. There is fear about having someone die in their own home, yet it can be a natural, peaceful process. If you can get past some of the issues surrounding keeping the patient alive, you may have more luck with honoring the patient's wishes. Sometimes it takes an outside, objective opinion to make people see that what they are asking for, while they may see it as advocating for the patient, is really a need they have themselves. Moving a family member to be closer to a caregiving relative speaks to a certain guilt that they cannot be in attendance to take care of Mom or Dad. The patient being kept alive for an upcoming wedding....she will have no more knowledge of the fact that there is a celebration if there is pain, discomfort or shortness of breath. Yet, a patient on hospice who cannot be at the wedding may cast a negative light on the festivities, so let's just keep her alive to attend. The topic of dying is very uncomfortable in general, and the reality of someone you love who may be dying is something that has to be eased into. The hospice admissions I do, when the family and patient are both ready and understanding, are usually after a long and, at times, debilitating illness. The family and patient are both understanding there is no more quality of life, and the reasons for keeping them alive diminish. With a sudden change, decline or rapidly progressing terminal illness, I often see families tend to want to look for another avenue besides acceptance of death. It's really not a bad thing, I think more a human thing. As health care professionals, we need to educate about the body's way of shutting down and keeping the topic of death as a pleasant, almost humane thing for the patient. Your article provided a wonderful group of examples about why hospice care is needed in our ever growing population of elderly and terminally ill patients.

I had have a question about end-of-life care that maybe someone can answer. I'm a Jr BSN student, and am currently watching my grandfather as he dies from stage 5 melanoma. The edema is seeping into his lungs, and I can hear the breath sounds change as his death draws nearer. He will soon drown in his own fluid...

My family is asking many questions, but the one I do not know, nor can I find the answer to, is how long after his death can we expect his bowels to evacuate? He has a Foley cath, but is not wearing Depends or anything, and we want to prevent my grandma from witnessing him having a bowel movement if possible.

Thanks guys.

Specializes in OB, critical care, hospice, farm/industr.
Amen!

I work LTC and I, too, cringe at the things we are supposed to do to these poor souls who want nothing more than to be set free.

I am of the thinking, that just because we CAN make people live longer and longer doesn't mean we SHOULD! I see no benefit of living to see 99 if my mind and body are just a shell that houses my being, with no quality of life, I'd rather be in the better place.

I promise you, if my family EVER did to me what I see some families do to those they love, (tube feeds, full codes, treat at all costs, force feed meds/food etc) I will come back from the afterlife with a vengance and haunt them to the very end.

The hospice nurses who come to my facility are always trying to get me to go work hospice for their company, I have the "knack" they say. Hospice has always been an area i'd love to try.

Go for it! We always have room for one more good nurse.

Specializes in Med nurse in med-surg., float, HH, and PDN.

Great blog going on here. I've worked so many hospice cases and I feel so very blessed being able to take this walk with patients and families. I've had family members say "What should we/can I do NOW?", looking for some guidance for medical interventions......I always say "Talk to her/him. Even if you don't think they can't hear or understand. Talk about shared experiences/memories. Tell them things you never felt comfortable about saying, like what he/she has meant to you in your life. Tell them you love them. Tell them you'll miss them, but that you will be okay and that it's OK to let go." At first, they may be dismayed when you say that to a family member; but I can't tell you how many people have told me later they were so thankful for that advice.If they are religious it's okay to remind both patient and family that Jesus is standing beside the still waters and He is holding out His hand, and it's likely that_________(previously deceased loved one) is there with Him. I also will sometimes say that dying is the easiest thing they will ever do, it's just getting there that is difficult. I'll tell the family that our bodies are built to try to survive and that what might be seen from the outside as suffering is the body doing what it is supposed to do, but there is at some point for the patient a kind of mental disconnect from what the body is going through as it is winding down and shutting down. Since I live in the Bible-belt, there isn't alot of resistance to spiritual stuff, and I have a little ritual I do with a patient going through the bodily struggle of fighting to keep living; I say the Lord"s Prayer and the Twenty-third Psalm into the patient's ear, and sing a verse, quietly, of "I Come To The Garden Alone". Believe it or not the patient passes within 5-10 minutes of that! Some of my co-workers say they hope I will be on-duty when "the time comes". I sometimes tell the patient that I will hold their hand on this side until Jesus takes their hand on the other side. I am so blessed by this work and I know some folks would think I'm nuts to say this, but I love that God has given me such inner peace about death and dying, and I love when I can be the one to accompany someone on this part of their lifes journey..................For myself, I'm with mariehas4kids; I want to tatoo DNR on my chest along wiyh a notary-public's seal and my doc's signature!!and the words:" I MEAN IT!"

End of life is a very touchy subject. All families handle it differently. As stated in the blog, some families will hold on despite the consequences to the family member dieing. Other families are realistic and don't want their family member's to suffer. Its hard to say in some situations when enough is enough. The bottom line unfortunately is when a person's life gets to this point it is truly in the hands of the family or caregivers as to how far medical care will go.

I feel this is sad. If a patient has an advanced directive, it is clearly written what that person wanted and in some situations is "sent to the waste side." Therefore, I have learned it is very important to choose carefully who is in charge of you when you are unable to communicate. So your wishes are cared through.

Specializes in Trauma, ER, ICU, CCU, PACU, GI, Cardiology, OR.

enlightening article, once again "viva las viejas" you out shine yourself......aloha~