Moral Distress In Nursing

Have you ever felt a sense of constraint in the healthcare setting as a result of being unable to pursue what you believe is the most ethical course of action? The purpose of this article is to discuss moral distress and offer some suggestions on how to effectively address the issue. Nurses Announcements Archive Article

Moral distress occurs when an individual judges that they know the right action in a particular situation, but internal or external constraints prohibit taking action (Volpe, 2011). Nurses are routinely placed in the difficult situation of being expected to stand behind the care decisions made by physicians and family members, even if we know that their choices may result in prolonged suffering.

Nurses are expected to help patients and address their physical pain, but at the same time, we might participate in very painful interventions that seem to offer little in the way of help. This leads to a moral conflict that can mentally rip apart the strongest members of our ranks.

Moral distress can be discouraging, especially when the interventions are carried out at the whim of unrealistic family members. For instance, a 96-year-old female with end-stage dementia ends up on the acute rehabilitation unit at a specialty hospital where she must endure three hours per day of physical, occupational, and speech therapy after undergoing a bilateral total knee replacement. Her eldest son, the medical power of attorney, insisted that the patient have this major surgery despite the risks and the fact that she has not walked in nearly two years. When she stopped eating approximately one year ago, her son refused a consult for hospice, and instead, ensured that she had a feeding tube inserted.

After one month of various therapies at the rehab hospital that proved to be unsuccessful, the patient was discharged back to the skilled nursing facility where she had been residing prior to the surgery. She never regained the ability to walk, frequently wails in pain, never gets out of bed, stares at the wall inside her room all day, and pulls her feeding tube out at least once per month.

The attending physician at the facility recently informed her son that the patient would now need hemodialysis. The son said, "Do whatever it takes. I want everything done for my mother." The staff at the nursing home cringed because they must continue to provide heroic measures for a patient with a terminal disease process.

Nurses have used unhealthy methods to deal with moral distress such as resentment, anger, job-hopping, casting blame on themselves and others, reducing hours to part-time, leaving the bedside for a position that involves no direct patient care, or leaving the profession altogether. However, more adaptive techniques exist. First of all, the most important thing we can do is speak up and identify the distressing situation, although this might be discouraged in certain settings. Since moral distress is not solely a nursing issue, the other disciplines need to be involved, especially social work and medicine. Management needs to support floor nurses by openly allowing dialogue regarding moral distress and conducting support groups. If possible, get the ethics committee involved. Also, a supportive network outside of the workplace is of great value to nurses who grapple with moral distress.

Most importantly, education is the key. We must educate patients and families about the inevitable end of life. By insisting that 'everything be done' for someone with a terminal prognosis, well-meaning family members are unwittingly reducing the patients' quality of life while prolonging the inevitable outcome. The circle of life naturally ends with death, and this is an outcome that no one will ever escape.

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I don't think this should be our moral distress. We have to treat the patient. This is not our decision to make, not our life to lead, it is our occupation. And when it comes to our own moral compass, it needs to be left at the door. We are not privvy to pre-hospital family dynamics, What plans were spoken about, promised...

If said patient said to family some years back as they were talking about end of life issues and wills and things "I want EVERYTHING done", then it is up to said family member who is authorized to make those decisions to do so. Even if they personally don't think it right. That we don't think it is right gets into us passing judgement on patient's and their choices.

Would I personally put my family member through any such thing? No way. But being health care proxy to my parents--if they say "do everything" (and thankfully they did not) then you need to abide by that choice. Patients need to be mindful of who they choose to be their HCP. If it is spelled out in a living will that someone doesn't want life substaining interventions, the HCP can boycott that. But one would hope that whomever they choose would abide by the patient's wishes, and we are not in a position to judge that choice.

Specializes in Case mgmt., rehab, (CRRN), LTC & psych.
If it is spelled out in a living will that someone doesn't want life substaining interventions, the HCP can boycott that.

And too many HCPs and POAs go against the written wishes of the patients.

About four years ago, one of my patients was a demented lady in her 80s who was declining. The daughter said, "I want everything possible done."

After a feeding tube had been inserted and several surgical procedures had been performed (to no avail), the daughter produces a packet of papers and says, "Oh. I just found these in my closet this morning."

The patient had expressed in writing that she wanted to be a DNR. She also indicated that she wanted no life-sustaining measures such as being vented. She also declared that she did not want a G-tube. The daughter, who had signed these papers in the presence of a notary public back in the 1990s, knew of their existence but hid them because she "wanted everything done," even if it was against mother's wishes.

I think that there always comes a time when the thinking of "I want everything done" needs to change to the perspective of "Would my ... be happy being in the situation that they are in now. Sometimes, it is difficult for the family members or proxies to see past the way things were or the way things should have been and really see how things are now. As I was told today, sometimes you need to remind people "Where is the patient/resident in all of this."

Specializes in Peds Medical Floor.
I think that there always comes a time when the thinking of "I want everything done" needs to change to the perspective of "Would my ... be happy being in the situation that they are in now. Sometimes, it is difficult for the family members or proxies to see past the way things were or the way things should have been and really see how things are now. As I was told today, sometimes you need to remind people "Where is the patient/resident in all of this."

I also think it's hard for the public to realize what "I want everything done" really REALLY looks like. Nothing on TV or what you read would show what it really is like to be a vegetable hooked to tubes and machines for years.

Specializes in PCCN.

ahhh, this explains why I was so upset at a situation my last shift. I just did not know that was why. But the decisions of others that I had to abide by not willingly ( or right) put me in to a deep hole that I am slowly coming out of. But I just didnt realize it would affect me so much. Or the poor pt, who had a developmental disability and didnt understand what was going on. :-(.

I think the Medical profession as a whole also has to say "No. This will not be done. " The ortho sugeon should refused to operate. The Gastro doc should refused to insert the g-tube. As long as we continue to bow to the wishes of the family, they will push for more.

As easy as it sounds on paper, it's very hard to do that in practice, especially in the current day where the threat of a lawsuit drives so many things in medical practice. I'd like to think that, once I'm an attending, I'd be the kind of doc who'd be able to refuse wishes of the family if I feel they're not in the best interest of the patient. However, as a resident, I'm absolutely not faced with the same pressures and responsibility that attendings face, so I could easily change my view over the next coming years.

but we do not want to be in the position where someone, ANYONE, has the right to determine who lives or dies. The above scenario probably would not exist in real life since the patient would not meet rehab goals. I do agree that education for the family, and maybe counseling, should be resources since family may feel guilty about making the wrong decision. This is not an easy call.

I never really understood this argument. If someone doesn't want anyone "determining" whether someone lives or dies, don't ever go to see a health care professional. The moment you see someone and start taking medication or whatever, you're already putting your life in someone else's hands.

It's really weird. When lives are extended, no one complains that the practitioner is "playing God." But, when it comes to death, all of a sudden medical practice is severely restricted to ensure that no one "plays God." It's cool to extend someone's life beyond what nature "dictates" but it's not cool once decisions regarding death come into play? :confused:

Specializes in SICU/CVICU.

I think that this agressiveness with which patients are frequently treated is often related to the conversations the physician has with the family. When my aunt was admitted to a nursing home one of the first questions she was asked was whether or not she wanted her heart "restarted" if it stopped. She of course said yes. I had her power of attorney for health care (which was already activated secondary to end stage dementia) and told them in no uncertian terms that she was to be a DNR. These were her wishes before she became demented. I had to be very "firm" to ensure this was done.

When the end was near and I wanted only comfort measures and did not want her admitted to a hospital and have here GI bleed worked up, the nursing home staff started calling my mother (the secondary on the power of attorney for health care) to try to get another response. My mom went along with me, but it caused her a lot of distress and second guessing the decisions that were made.

It exists! This is my job! Sometimes I feel that my patients feel like they are in Hell.

68, end-stage Alzheimers, metastatic cancer, decub the size of a dinner plate, trach/vent, PEG, Full Code.

84, end-stage Alzheimers, ETT/vent (trach later this week) PEG, retraints, fearful eyes, Full Code.

82 years-old, dementia, trach, PEG, Full Code.

68, metatistic cancer, decub the size of dinner plate, frankly bleeding foley AND suprapubic, 2 units of blood every 48 hours, PEG but not tolerating feeds so TPN, HD M-W-F,94, complete dementia, pressure sores on legs, trach, PEG, severe contractures, Full Code.

Not one able to get out of bed, not one able to communicate, not one able to do the smallest thing for themselves. All with the most minimal pain releif (TYLENOL q 6,1 Vicodin q 8, Dilaudid 0.5 q 4) so that the pulmonoligists can "wean" them. Every day, always like this. Always.

It really is so sad. especially the look in the pt's eyes. Dilaudid IV 0.5 mg, tylenol? some of our drs order dilaudid/morphine like it is candy along with a narcan order. Others it is a big deal for them to even order 1 oxy ir5mg q 8 hours. Is this a hospital?do you have palliative medicine there? Whether that consult gets placed often depends on the dr and the family but sometimes it does help A LOT especially with the medications that get ordered prn.

I don't think this should be our moral distress. We have to treat the patient. This is not our decision to make, not our life to lead, it is our occupation. And when it comes to our own moral compass, it needs to be left at the door. We are not privvy to pre-hospital family dynamics, What plans were spoken about, promised...

If said patient said to family some years back as they were talking about end of life issues and wills and things "I want EVERYTHING done", then it is up to said family member who is authorized to make those decisions to do so. Even if they personally don't think it right. That we don't think it is right gets into us passing judgement on patient's and their choices.

Would I personally put my family member through any such thing? No way. But being health care proxy to my parents--if they say "do everything" (and thankfully they did not) then you need to abide by that choice. Patients need to be mindful of who they choose to be their HCP. If it is spelled out in a living will that someone doesn't want life substaining interventions, the HCP can boycott that. But one would hope that whomever they choose would abide by the patient's wishes, and we are not in a position to judge that choice.

Many/most shifts I leave my feelings and thoughts at the door. Check out. that means not only do I not become distressed by the 98 year old peg, going for a trach, 10 stage 4 decubs, etc. I also do not get distressed for the walkie talkies or others who then whine about a robot nurse, comfort cares and their crying families etc. . In order to close off one I have to close off EVERYTHING. I want everything done, just like on television......................

Specializes in Trauma, ER, ICU, CCU, PACU, GI, Cardiology, OR.
thanks all for your condolences :hug:

i'm sorry for your lost, i shall keep you and your relatives in my prayers :hug:...aloha~

Specializes in Acute Care Psych, DNP Student.

Moral distress weighs on you like nothing else in nursing. It hits up against the usual feeling that we are doing something good and makes us question if the opposite is occurring.

I remember when my facility hired an agency MD who seemed odd. One day I was assisting him as he was doing an I & D on a GSW. That MD was digging around forever. Ok, maybe an hour. It's like he was lost in the tissue. I had assisted with similar procedures and never seen anything like this.

Moral distress for me was that sinking feeling of working with a questionable practitioner and fearing the patient could be harmed. I voiced my concerns to an administrator, but nothing was done.

There are so many issues in nursing that can cause us moral distress. It's tough to know what to press and what to let go.

Specializes in ICU.
but we do not want to be in the position where someone, ANYONE, has the right to determine who lives or dies. The above scenario probably would not exist in real life since the patient would not meet rehab goals. I do agree that education for the family, and maybe counseling, should be resources since family may feel guilty about making the wrong decision. This is not an easy call.

The above situation happens ALL THE TIME. Its disgusting. The medical profession needs to change. Sorry but we can't save everyone, yet we let these people waste away in bed unable to move, staring at the wall. Man I hope I die an awesome death, because how many of these people end up dying is tragic.