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Death came to visit

Nurses Article   (5,430 Views 9 Comments 1,008 Words)
by madwife2002 madwife2002 (Member)

madwife2002 has 26 years experience and works as a Director of Nursing Services.

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Did you know that in 2016 death is still a taboo subject where many people don't make living wills. A sad fact is that two thirds of Americans still don't have a living will. It has been suggested that many people are not ready to make important life changing decisions.

Death came to visit

Death came to visit Friday, it was not kind, and it was not peaceful for my friend's mom-it was hard, she struggled so much, her mind was ready, but her body fought her to the bitter end; causing trauma to her loved ones who stayed by her side so she did not die alone. The family had discussed end of life choices, and treatment was stopped on Tuesday, with the only intervention being pain medication.

Death is still a taboo subject that many of us prefer not to discuss. Why is this? Unless you work as a healthcare professional, the clergy and funeral directors, many people are not able to talk about it freely.

As a nurse who has been with many patients as the end of their life, I know you cannot prepare their loved ones for the final end. You cannot say that it will be peaceful, you cannot give a timeline and you cannot promise how it will be because you really don't know. There are relatives who have no clue about what their loved one wanted. There is often no discussion about end of live choices.

I have been fortunate to be with my sister and my mom when they breathed their last breath and it was peaceful, calm and a relief that their struggle was over. I have been with patients who have passed away peacefully without pain, without struggle and without suffering. I have also been with patients who have fought to the bitter end, every last breath being a struggle for them. It was like something from a horror movie only it was real life.

My question is why? Why do some people have horrible deaths and some people go quietly. It certainly doesn't pertain to how they lived their life; I can vouch for that with my own eyes, experience and knowledge. My mother was a feisty firecracker of a woman who fought for everything in life, never gave in to anybody and would never hold her tongue. Yet her death was one of the most calm, peaceful I have ever experienced.

When somebody passes what determines if it is peaceful? What would determine if death is going to be horrible? Is planning important, should patients and relatives make known what they want near the end of life? You still cannot guarantee that death will be peaceful, however everybody involved knows what their loved ones want.

Is it the environment they pass in? Can we choose where to die?

Hospice is a wonderful environment, where the nurses, aides and doctors are amazing. I have never seen such caring individuals. When my mom passed many years ago they were amazing, I will never ever forget the kindness my mom received and how supportive they were to my husband and myself. The atmosphere was incredible in a hospice where everything is available for support. Nothing was too much trouble; nobody seemed rushed or didn't have the time to spend with her.

Hospital can be a frightening place for many people, yet many will die in the hospital this year. Some expected deaths and some unexpected deaths. Relatives can add peace or trauma when their loved one is dying. The circumstances of impending death play a huge role for end of life decisions.

Is the hospital environment a good one for a peaceful death? Yes it can be. It can also be a very traumatic experience. How many things can contribute to peaceful versus traumatic-who or what determines the definition?

Hands up! How many of us nurses have witnessed needless interventions, pain and suffering? How many of us have experienced relatives prolonging life as long as they possibly can? Does this add to the trauma of their dying?

End of life discussions can be very difficult; but it shouldn't be; as it is something we are all going to experience as our only guarantee in life. Many people do not have a living will. Many people do not even understand the terminology 'Living Will'. It makes no sense to them, although we as healthcare professionals are much better at promoting living wills.

Even with a living will there can be struggles to make sure your wishes are followed, but without one relatives can fight and disagree with each other about what they want. Clear precise instructions can at least highlight your choices helping relatives to make better decisions on your behalf.

In 2007 only 41% of the population in the United States had a living will.

In 2009 President Obama made it more popular by publically talking about his living will, saying it is a sensible choice.

In 2013 only 1 in 3 people had a living will, 32%, Findlaw.com

In March 2016 "American College of Emergency Physicians' stated that two thirds of Americans don't have a living will!

Quote
The sad fact is that even with an advance directive, your designated decision-maker may still face a fight in trying to follow your instructions. It's not uncommon for doctors to disagree with a family about what should be done; it's not uncommon for family members to disagree - sharply and painfully - with one another. But, as Mr. Kottkamp said, "It's an uglier fight if you don't have the documents."

Question of the day-Do you have a living will? Or are you part of the 2/3rd's that don't have one?

Less Than One in Three Americans Have a Living Will, Says New FindLaw.com Survey

http://newsroom.acep.org/2016-03-21-Nearly-Two-Thirds-of-Americans-Dont-Have-Living-Wills-Do-

The living will needs resuscitation

For young and old, it's wise to have a living will to state health-care wishes - The Washington Post

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RN with 26 years of experience many of those years spent in dialysis. I have worked in acute care, home, ICHD as a CN, FA, and currently a director.

1 Follower; 74 Articles; 120,069 Visitors; 4,777 Posts

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I think you make a great point when you point out that advanced directives are an important matter to ensure that there is somewhat control over one's care.

I also agree that we need to establish a culture within our society that permits the discussion of end-of-life wishes or general thoughts on what constitutes quality of life.

However, a living will is not the most important document and there seems to be some ongoing confusion around advanced care planning.

I would like to add some information:

- the one single document that any competent adult over the age of 18 years should have is the Health Care Power of Attorney, also called Health Care Proxy (HCP). In this form, that differs from state to state, any competent adult over the age of 18 can name a person (or several) who will make healthcare decisions in case that person is unable to do so (as determined by a physician). Anybody above the age of 18 should have one. If something happens to somebody and they are now unable to convey wishes or are not competent due to an illness/accident, and there is no decision maker named, it can place a huge burden on the next of kin. In some cases and states the next of kin has to go to court to ask for guardianship, which takes time but also restricts the guardian in a different way. A person who does not have a health care proxy form filled out, usually also does not get accepted to rehab. In any way - if there is one form that anybody should do - it is that form. Usually no expensive lawyer is needed, the form needs to be witnessed by adults.

- Living Will - this is a document where a person conveys what they would like to be done or not done or how in case of certain circumstances.While it is great to have a document that provides guidance, it is also a document that is not statutorily recognized in all states. For example, the state of Massachusetts does not recognize a "living will" as binding. If somebody presents a living will, the health care proxy can still use it for their own guidance in decision making. So - since not all states recognize the living will it is really the most important thing to do the health care proxy form and to talk to that person about the wishes. Otherwise they may struggle with decision making or not make the decision that the person would want.

And - a living will depends still on the interpretation by the medical professional and how the HCP understands the circumstances. When people write in their will "if there is no meaningful recovery" - what does that really mean???

And - a living will cost money that a lot of people do not have or want to spend, especially if it is a state that does not recognize the document as binding.

And - when there is a situation where the living will says one thing but the HCP says something different - the physicians will usually do what the HCP wants. Nobody wants to get sued. I have seen patients who never wanted to be intubated, who even had a provider order not to intubate. When the HCP panicked or thought that they are not ready to accept death and ask the MD "to do everything" that patient will still get intubated.

POLST/MOLST: Provider order for life sustaining treatments - this is a medical order (!) for people with serious illness or high age that is filled out with the MD/NP/PA and details if the patient should get intubated/chest compressions/ dialysis/ artificial nutrition and so on and forth. It is a portable order and goes with the patient.

It is always good to have conversations about one's wishes. I could get into a terrible car accident tomorrow and end up in the ICU on a vent - hopefully my spouse knows my wishes and would enforce them. We have talked about those situations so we know what the other one would want. My spouse would want extreme measures unless his head is "cut off" or he "can't think anymore". I asked my oldest child before he left for college and we had discussions, I gave him a health care proxy form to fill out.

There is a huge amount of confusion out there about advanced directives ....

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My mother passed away last January.

Mom had talked with us extensively about what she would and would not want. Whenever a difficult case was in the news, mom talked about what she would want if that were her.

Mom had a lawyer complete a living will.

She gave Medical Power of Attorney to her children and her husband.

We still had a difficult time with the medical staff particularly a palliative care NP.

If mom hadn't raised a hoard of strong, assertive children, we might have been badgered into doing what the medical staff wanted instead of what mom wanted.

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Davey Do has 35 years experience and works as a Behavioral Health RN.

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Great article, madwife.

Belinda, my wife who is a medical nurse, and I regularly talk about death. If we're watching some movie where a major health crisis is invovled, I'll pause the movie to bring it back home. "What would you do if that victim was me?" "What would you wish to have done?" Etc.

I have had a living will, designated Power of Attorney for Healthcare and Finances backup in case something happens to Belinda, along with pre-paid funeral arrangements for several years now.

Doing so has given me some piece of mind.

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My mother passed away last January.

Mom had talked with us extensively about what she would and would not want. Whenever a difficult case was in the news, mom talked about what she would want if that were her.

Mom had a lawyer complete a living will.

She gave Medical Power of Attorney to her children and her husband.

We still had a difficult time with the medical staff particularly a palliative care NP.

If mom hadn't raised a hoard of strong, assertive children, we might have been badgered into doing what the medical staff wanted instead of what mom wanted.

I am sorry to hear that you had a difficult time despite knowing what your mom wanted.

You bring up an important issue in end-of-life care.

The cornerstone of ethics in the United States is autonomy / independence - patients are encouraged and asked to participate in decision-making regarding their wishes. Thus, we have to respect patient's liberty to make decisions that may be not congruent with our own ideas or clinician's recommendations.

But - and like everything in healthcare - this has become much more complicated. To enforce autonomy and liberty, patient-centered care with shared decision-making was introduced more into the medical community. Patients and their families are often lay people when it comes to medical decision-making but need to make decisions that will have impact on their life, quality of life, or even end their life. The idea is that the patient trusts the provider who also provides a recommendations - which should include considerations about what is in the patient's best interest.

Nowadays, with our growing arsenal of technology and "advances", we can easily border on futility. When the "highest" goal is to maximize the life-span, aggressive interventions and treatments are often chosen even though the outcome may be negative and leads to "suffering". A patient has the right to "suffer" if that is what they decide to accept and to go through in order to gain more time. They are allowed to sacrifice comfort for the sake of more time but it is important that they understand this implication.

Physicians can not be forced to provide futile treatments. After all, many interventions are medical orders and a physician has the right to "not offer" this treatment if the patient is not a candidate because the risk is too high or the outcome negative. Examples are surgeries or heart catheter interventions but could also include dialysis. Patients accept more easily when the surgeon or cardiologist says that the risk is too high and that is not an option because it would most likely result in death. That option is not available and thus patient autonomy does not include to choose a futile options. The same with dialysis - only that patients and families have a hard time with that decision. Nowadays patients who are 90 year old undergo dialysis to extend their life but if a person has other comorbidities, the nephrologist may not offer this treatment and refer to medical management.

There is also technology like high flow oxygen, which was thought to be a bridge until a person gets better or dies. But I think nobody really thought about the consequences of this device. When offered to end-stage COPD or similar patients who are so sick that they cannot come off but also do not wish to be trached and live on a ventilator - there is no place for them to go. They "live" in the hospital, which is not the same as home. Lately, I heard more often "if I had known that this is not like regular oxygen and I cannot go home with this - I would have not wanted it".

There are a lot of dilemmas all around.

As a palliative care nurse, I have no "agenda" - my goal is to provide information and care to help patients to live best with a serious illness. There is a huge grey zone where patients do not want to have pain for example or shortness of breath - but also want to be a full code - and though are limited in what can be realized. But it is not my place to pressure somebody into a decision or coerce them - that would take away the liberty in decision-making.

Nurses feel different about suffering than physicians, which is researched. Nurses care and have a hard time when patients suffer "needlessly". Patients and families on the other hand often have their own agenda and are not up front. We see a lot of problems related to not being able to cope with death and not being able to face "loosing somebody" - which ultimately can lead to requests for futile care.

As a palliative care nurse I also have a responsibility to realize when the patient asks for palliative care in the sense of "hospice" but this decision is driven by not understanding ones choices. There are cases where nurses or physicians request a palliative care consult because "the patient does not want any treatment and is ready to die" indicating they respect autonomy but the patient is not competent to make this decision due to mental illness or otherwise incapacitated. Or the patient clearly does not understand that for example life with dialysis is possible or that people can live at home with tube feeds.

There is a lot of room for conflict and friction at the end of life that can make everything more stressful for everybody.

Here is a good article:

What's the Role of Autonomy in Patient- and Family-Centered Care When Patients and Family Members Don't Agree?, Jan 16 - AMA Journal of Ethics (formerly Virtual Mentor)

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madwife2002 has 26 years experience and works as a Director of Nursing Services.

1 Follower; 74 Articles; 120,069 Visitors; 4,777 Posts

Nutella a great insight-In 2000 my mother was diagnosed with a stage 4 uterine ca. The specialist said nothing they could do-too far gone and was not operable. My mother and I had talked for years about end of life care.

I lived 5 hours away and would visit at the weekend. I missed a weekend and while I was gone my mother was offered radiotherapy, when I arrived at the hospital she was screaming in agony, was red raw between her legs and was in a horrible condition. The hospital had stopped pain meds because they said her mind was befuddled.

I talked with my mother, we agreed enough was enough and it was time for hospice-to control pain and move her down to where I lived. The RN on duty informed me that I was a cruel wicked daughter for asking for treatment to be stopped, that my mother had lots of life in her.

We moved her to hospice and my mother died peacefully 3 days later!!!!!!

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madwife2002 has 26 years experience and works as a Director of Nursing Services.

1 Follower; 74 Articles; 120,069 Visitors; 4,777 Posts

We have to be so strong when advocating for our loved ones! Sorry for your loss

My mother passed away last January.

Mom had talked with us extensively about what she would and would not want. Whenever a difficult case was in the news, mom talked about what she would want if that were her.

Mom had a lawyer complete a living will.

She gave Medical Power of Attorney to her children and her husband.

We still had a difficult time with the medical staff particularly a palliative care NP.

If mom hadn't raised a hoard of strong, assertive children, we might have been badgered into doing what the medical staff wanted instead of what mom wanted.

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Not_A_Hat_Person has 10 years experience as a RN.

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When my mother got her cancer diagnosis, even with 2 lawyers in the family, we were all very surprised to discover that Massachusetts does not recognize living wills. You can write your wishes down, but it's not legally binding. When she was actively dying a few years later, we had to fight hard for me to be named her health care proxy because of her mental state.

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A cautionary tale: Children are not always the best medical POA. Appoint someone who is able to listen to medical advice and understand it.

My mother-in-law appointed her daughter as her medical POA. She spent her last 3 months of life in and out of hospitals and nursing homes. The daughter made terrible decisions that were against the advice of the doctors and nursing staff at both facilities. This caused my mother-in-law to spend her last few months in a tremendous amount of pain. She could have had a peaceful transition with the help of hospice. But the daughter refused to listen to anyone except herself.

Make sure that your medical POA can listen to medical advice, is able to understand or ask people who do understand to explain what is being said AND asks you what you want. This person can have a lot of input into how you end your life.

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