Thank You for Nothing

This article details actions of PICU nurses when we care for children who have hopeless prognoses. It explores our emotions as we realize that we have done all we can for a patient and it's time to let them go. Nurses Announcements Archive Article

As nurses, it's our job to make patients better, to improve their lives in some way. For acute care nurses, the goal is to help patients recover from an illness, surgery, or accident. Rehab nurses help patients reach their highest level of functioning. Community health nurses promote wellness and primary prevention. Hospice nurses help a patient die with the most comfort and dignity possible.

As PICU nurses, our job is to fix children. Pediatrics is arguably the most diverse field of nursing, and we see a huge variety or illnesses, injuries and ailments. I'm very pleased to say that the great majority of children go home well. Kids are extremely resilient. A two year old who aspirated his scrambled eggs can be on ECMO one day and smiling and playing only three days later. I've seen kids overcome insurmountable odds on the road to recovery. I've seen the smiles from ecstatic parents, felt their grateful hugs, read their heartfelt thank-you notes. These memories make it especially hard when there is a child so sick we know they won't be going home.

It doesn't help that our unit has recently had several children with chronic conditions and hopeless prognoses: A few progressive genetic disorders, a fatal surgical complication, a routine procedure that ended in brain death. As PICU nurses, these are our least favorite patients. The ones that we cannot fix. The ones we cannot send home better, or cannot send home at all. These cases are hopeless from the beginning, but we run tests and do research and try new treatments until the question of their care changes from 'What can we do?' to 'What should we do?'

Such is the case with the child who weighs heavily on my mind. A little boy just over a year old, the victim of a serious genetic defect who has already outlived his prognosis by several months. He is cherished by his parents. Though his face and body are severely malformed, his mother looks at him like there has never been a more perfect child. She wants desperately to keep her son with her, but he is nearing the end. A string of recent hospitalizations have left his body exhausted and unable to recover from this most recent respiratory infection. He won't leave the hospital. It takes nearly a week and several family meetings to convince the parents it's time to let him go. In that time, the child has nearly died more than once. A 'Full Code' order required that we compress, push medications, even insert an IO, and left the nurses frustrated and questioning the ethics of our work. It's heart-wrenching for us to process. This child has spent months with us over the past year and we have grown to love him. While we hate to let him go, we hate the thought of hurting him even more. We have reached the 'Can' versus 'Should' moment.

After several family meetings, a DNR is signed. The child is placed in the mother's arms. Family is called in to say goodbye. This time, when the child's heart rate and saturations begins to drop, the scene is different. The nurse doesn't press the code button and sound the alarm. She doesn't place the child on a back board, initiate compressions, push epinephrine or begin bagging. Instead, she holds the hand of the crying mother, she silences the alarms, disconnects the child from the monitor and steps out of the room to give the family privacy. In the eyes of an ICU nurse, she is does nothing.

It's the hardest nothing she will ever do.

The parent's see the difference now. Instead of facing their child's death with fear and anxiety, they sense the peace in his body. He is exactly where he should be- being cuddled by his mother and kissed by his father. His last moments are free from pain and full of security and love.

The family spends as much time as they want holding the child, saying goodbye. When they are ready, the nurse places the child in the crib, removes his lines and tubes, washes his tiny body, makes handprints and footprints in ink and cuts a lock of hair as a keepsake. One by one, the family files out of the room. The mother is the last to leave. She turns back for one last look at her son before waddling out the door. She waddles because this mom is also 36 weeks pregnant.

In a couple of weeks she will return to this hospital, to the Labor and Delivery unit, and she will deliver another baby boy. The nurses in the newborn nursery will assess her new son and deliver the news that the baby is perfectly healthy. There will be no five month stay in the NICU. No barrage of tests and procedures. No hopeless prognosis. This baby will not come home with a trach and a shunt and a feeding tube. His mother and father will take him home after two days and he will thrive. A perfectly healthy baby boy who, by the grace of God, his parents will never have to bury.

Staff line up at the door to see the family out. There are tears in the eyes of the family, the nurses, even our attending physician. We offer condolences and encouragement: "Take care of yourself." "Get some rest." One nurse hugs the mother and softly whispers, "You did the right thing" and the hug gets a little tighter.

The mother saves her final hug for her son's nurse. "Thank you," she says, "for everything."

But we know what she really means is, thank you for nothing.

As a student and NOT a nurse yet, you may be better served if you would shut the front door and LISTEN to what nurses are talking about, before you judge what sort of "mindset" they should have.

Just saying........

Just as I expected, a few replies with nothing more than personal attacks with nothing further to add that has any intellectual basis or value....sad

Yep - 1st post!:yeah:

Speaking as a family member who went through what you've described - there's quite a bit more to that "nothing" than you may realize. No - you can't always save a patient, and we family members recognize that, even though we may be remiss in saying so. But, one of the things I found (and ultimately caused me to decide to join the ranks of the nursing profession) was that there comes a time when you have to switch over from seeing the person in the bed (or crib) as the patient, to seeing the person next to the bed (or crib) as the patient. They're the ones you can help, and just the simple act of a pat on the shoulder can mean so very much to those stalwart, exhausted, and ultimately loving folks who take on the challenge of standing by their loved one when it's their time to go.

So - on behalf of all the families who've been there, are there now or who are going there - a heartfelt "thank you" for helping us in our ultimate time of need.

Blessings,

IEDave

Specializes in LTC, assisted living, med-surg, psych.
Just as I expected, a few replies with nothing more than personal attacks with nothing further to add that has any intellectual basis or value....sad

Really? This from the person who admittedly stopped reading [the article] after the first sentence...........

Sorry for the brief hijack. Please carry on. :)

Specializes in CICU.

Lovely article.

I find it difficult to see the futile care that is sometimes inflicted on patients (often elderly in my case). While I do know how difficult these situations are for families, it is also difficult for us. I love that this post shows me that I am not alone in struggling with these feelings.

I hate the nights when I have to pray that a particular "full code" patient does not code on my watch - simply because it would break my heart and my spirit to have to do it.

Specializes in ICU, Telemetry.

I'm sitting here with tears on my face. I know what that situation's like with adults who are in our ICU for months, repeatedly coded when there's nothing good we can do except to stop "doing," and I can't imagine how heartbreaking it must be with a child. And, like Do-over, I've had nights at the bedside where I am silently pleading with the patient and God that they not code until the family finally understands that all a code is going to do is hurt, not help. Many a night I've watched monitors and falling vital signs, praying, "Please, don't make me do this..." It's bad enough to witness this at the end of life, and I can't imagine what it must be like to see this at the beginning....great article about things that needed to be said.

And as for the other stuff....well, the ignore button works wonders. *sigh*

Specializes in CICU.
Yep - 1st post!:yeah:

Speaking as a family member who went through what you've described - there's quite a bit more to that "nothing" than you may realize. No - you can't always save a patient, and we family members recognize that, even though we may be remiss in saying so. But, one of the things I found (and ultimately caused me to decide to join the ranks of the nursing profession) was that there comes a time when you have to switch over from seeing the person in the bed (or crib) as the patient, to seeing the person next to the bed (or crib) as the patient. They're the ones you can help, and just the simple act of a pat on the shoulder can mean so very much to those stalwart, exhausted, and ultimately loving folks who take on the challenge of standing by their loved one when it's their time to go.

So - on behalf of all the families who've been there, are there now or who are going there - a heartfelt "thank you" for helping us in our ultimate time of need.

Blessings,

IEDave

Great first post! Thanks, its nice to hear.

Great article :) I passed our local board exam, now waiting for my license and I want to be a pedia nurse in a pedia ward or a PICU nurse. The child is not the only one needing care here in the scenario of the article, but also the family. We nurses should be strong, brave and be prepared for such cases which are emotionally draining. I am thinking to myself... what if something like this will happen and how can I be therapeutic to these family members? A Patient who is under "CODE" and then has a negative outcome can be really saddening for the family members but when the nurse becomes a partner to the acceptance for the loss or in a way, be a comfort person, I think it can be helpful to lessen their pain.

Yep - 1st post!:yeah:

Speaking as a family member who went through what you've described - there's quite a bit more to that "nothing" than you may realize. No - you can't always save a patient, and we family members recognize that, even though we may be remiss in saying so. But, one of the things I found (and ultimately caused me to decide to join the ranks of the nursing profession) was that there comes a time when you have to switch over from seeing the person in the bed (or crib) as the patient, to seeing the person next to the bed (or crib) as the patient. They're the ones you can help, and just the simple act of a pat on the shoulder can mean so very much to those stalwart, exhausted, and ultimately loving folks who take on the challenge of standing by their loved one when it's their time to go.

So - on behalf of all the families who've been there, are there now or who are going there - a heartfelt "thank you" for helping us in our ultimate time of need.

Blessings,

IEDave

Caregiver role strain is often mislooked or forgotten, whether it be with the parents of a child with developmental difficulties, a child of a parent with dementia and multiple comorbidities, a spouse of a pt with multiple chronic health issues.

A family is a tightly meshed unit, and one that is strained beyond the breaking point is one in which functional grieving cannot occur. Illness, infections, hospitalizations are stressful upon the entire family unit. Sometimes I don't think we have enough nursing diagnoses for the families of pts, nor anywhere near enough resources.

When I have a family sitting in patient hospice that grows close to me, it is the most exhausting nursing I can do. I can say I will always do everything in my power to make it as good a death as it can be. Death doesn't have to be an ugly event. If I can guide the family through the stages of grief to where it is accepted, and to where it is not a traumatic event. Where it is a sigh, a whisper, with holding of hands, a kiss...then I have done the pt a favor, and eased the role strain.

For those family that choose to do everything, I will say to them. "We did everything we could" I will let them have the comfort of knowing that they fought to the end. Just please don't let it happen on my shift. I so regret some of the codes I have had to do.

My dd#2 and sil have a blended family that includes two boys in wheelchairs--a 19 yo (his) with cerebral palsy and a 15 yo (hers) with spina bifida. DD has saved the life of the younger boy a number of times by insisting on speaking to a hospitalist or an attending when the ED resident doesn't "get" that this boy doesn't show a lot of typical s/s when he's in trouble. So far, so good, but he's come closer to the brink than he should have. (The senior residents--neurology, neurosurgery, pulmonolary, ortho, GI and renal usually give her their cell numbers and allow her to email pictures of surgical incisions or other things because they trust her judgment. She has never been wrong about the need for a shunt revision--and he's had a bunch--or an infected site.)

My daughter and her husband are fierce advocates for their boys, and yet they both know that there may come a time when they have to let go. We cry even talking about it, but we understand that someday (far down the road, God willing) it could come to that point.

I'm so thankful for nurses (and docs) who can see that help takes many forms and sometimes the help to let go is the best we have to offer.

Thank you, Ashley, for a heartfelt article with so much wisdom.

Specializes in PCU.

That was a truly beautiful article...thank you so much for sharing.

Specializes in Trauma Surgery, Nursing Management.

Very well written Ashley! Thank you for describing such a beautiful story.

At the risk of sounding like e.e. cummings, sometimes nothing is everything.

Human touch is very much "something"...it may not cure, but it shows the parent/patient that we care...