Code Status: When Should We Talk About It!

During the past month of my practicum on the neurosciences unit, I have seen and cared for numerous patients. Some have had do not resuscitate (DNR) orders; one had compassionate terminal care (CTC) order, and others a full code status. Nurses Announcements Archive Article

As a student, the anticipation of a code being called is anxiety-laden, to say the least. In talking with the staff it became apparent that no matter how many times they have been in a code situation it is equally as anxiety causing for them. Since starting on the unit I have witnessed two code calls and have been involved with calling the CCA down twice. Although none of these particular codes involved performing CPR, I decided to explore some of the ethical issues and communication barriers involved with code status. One particular patient was incapacitated and showed little hope for any recovery but yet had full code status. Both I and other staff expressed great concern of how a code would progress should this patient suffer respiratory and or cardiac arrest. In order to fully understand the ethical issues I felt surrounded this situation, I will present a relatively detailed history of the case prior to critically reflecting on the question of code status and CPR.

Just over two weeks prior to us caring for our 80-year-old patient, he was admitted to the coronary care unit (CCU) post-MI from a small town hospital. After seeing physicians in our hospital, he was deemed fit for a coronary artery bypass graft, times eight. From what I gathered in the chart, he had a history of hypertension and although recovering from a heart attack he was in sound mind prior to the surgery. On his first postoperative day he went into cardiogenic shock, and eight days later suffered a massive stroke. He required pleural drains, a tracheostomy, a dobhoff feeding tube, and a heparin infusion. Days later he was transferred to the neuro unit with a Glasglow Coma Scale rating of three to six. He was occasionally a six when he would very slightly withdraw his right leg from pain. He was in persistent atrial fibrillation and had plus four oozing edema in all of his limbs. His hemoglobin was dropping and thus we were ordered to administer packed red blood cells. As I cared for him during the night shift I only encountered his family briefly, but while I was in the room I opened the door to any questions that they might have. In spite of my uncertainty with any potential I felt he had for recovery, I was able to explain his medications and need for a blood transfusion. The patient's son expressed hope and excitement at the prospect of his father receiving a blood transfusion, stating "Oh, that's great! That will perk him right up". I was still unsure at this point if he remained a full code because his physician had not yet had an opportunity to discuss it, or if this is what the family wanted. Yet it became clear as the son further went on to talk about the recent death of his mother, and how they weren't ready to let their father go. I felt strong empathy for the family at this point but questioned how forthcoming and honest the physicians involved in the case had been with them regarding not only their fathers minimal or nonexistent chance for recovery, but what code status really means. In addition, I wanted to explore what the nurse's role is in code status decisions with physicians and their families.

It seems there is much confusion regarding the term DNR, particularly but not exclusive to patients and their families. Murphy & Price (2007) assert that although succinct descriptions and procedures are available for health professionals regarding DNR orders, they are insufficient. They further that due to our profound emotional discomfort with death, DNR orders are written not often enough or too late. Part of the problem roots in the confusion over what the term actually means. A DNR order is supposed to mean that in the event that a patient suffers a cardiac or respiratory arrest, CPR will not be initiated. A DNR order does not mean, however, that the patient will not receive maximal therapeutic care and be left to die. I would further that it is this miscommunication that leads to families such as one of our patients, to decide they want full code status. They had stated that they wanted everything done for their father, but one wonders if they knew the violence that can occur during CPR in a code situation and the evidence regarding outcomes if they would still make the same decision.

Brindley, Markland, Mayers & Kutsogiannis (2002) stated that "Resuscitation was never originally recommended for all patients, and its goal should be to reverse premature death not prolong an inevitable death. The current situation is often to attempt CPR unless it is explicitly refused." While Murphy, Murray, Robinson & Campion (1989) conclude that not only is CPR inappropriate for some patients, elderly patients with chronic or acute diseases rarely leave the hospital alive after CPR. With this patient, we all felt that CPR would only prolong the inevitable and furthermore would have caused undue harm on this patient after a sternotomy and the multiple other health problems he suffered from. With a GCS of three, not only did it seem unacceptable to have this patient on a regular nursing ward and not in intensive care, it seemed unacceptable that this family had not had the direness of their fathers' situation explained to them in a manner in which they could understand. This was evident in their hopes of how a blood transfusion would turn things around for him. They were clearly unaware that he had suffered massive brain trauma from his stroke to which he would not recover.

Although it is not a nurse's place to discuss prognosis with the families prior to the physicians doing so, it is my belief that DNR orders have many implications for nursing practice on an ethical level. Firstly nurses have a responsibility to be a patient's advocate and that starts from the moment a patient is in your care (CNA, 2008). Prior to this patient being taken in for this very risky procedure, a nurse could advocate that the physician discuss advanced directives in a family conference, so as the family is not left to make those hard decisions which can often not be agreed upon amongst family members. Robinson, Cupples & Corrigan (2007) assert that is the lack of advanced planning regarding CPR that leads to poor care when people have passed into an advanced stage of illness. Their research suggests that it is most common to postpone discussions about resuscitation until the patient is no longer competent. As it stands it is left to physicians initiate these discussions and research shows that many are uncomfortable doing so, which could be attributed to poor communication skills or a fear that they will undermine patients hope by discussing resuscitation while they are still in the early stage of illness. Robinson et al. (2007) go on to say that it is often nurses who have to take the lead and bring resuscitation issues to the physician's attention. Families deserve to know that their loved ones are unlikely to recover and it is the physicians' responsibility to be honest and openly discuss this. It is proposed that physicians are reluctant to accept that their patients are in fact terminally ill and can no longer recover from what ails them. In contrast to doctors' disease-centered model of care, nurses' holistic patient-centered approach makes them more attuned to getting involved with end of life decisions, as they are likely better informed about a patients total physical condition and preferences (De Gendt, Bilsen, Vander Stiche, Van Den Noortgate, Lambert & Deliens, 2007).

Secondly, both nurses and physicians have an ethical mandate for non-maleficence Performing CPR on an elderly patient who has recently had a sternotomy and has no chance of recovering from a massive stroke would contradict our code of ethics. Advanced CPR has been proven to be a violent intervention that can break thoracic bones, puncture and collapsed lungs, rupture pericardial sacs, cause burns and lead to permanent brain impairment (Davey, 2001). I question how we as nurses can continue this practice when clearly it puts us ethical dilemmas. Lazaruk (2006), a CCU nurse agrees that this harsh, life-sustaining intervention does allow patients a dignified death and that CPR actually leads to significant harm to the patients. She concurs that when possible, code status should be address by medical residents as soon as a patient arrives at the hospital. It could become routine practice to allow patients to be involved in planning their care, and empowering them to make decisions about their own end of life care. Storch (as cited in Lazaruk, 2006) stresses that inappropriate use of CPR is an extremely troubling issue if not the most troubling issue for registered nurses. The CNA Code of Ethics for Registered Nurses (2008) compels us to respect the dignity of our patients and advocate for the use of appropriate interventions. Studies show that in Canada nurses are involved in DNR decision making only half or less of the time (De Gente et al.).

Despite all the evidence this practice continues. Storch suggests that perhaps the fear of death or failing keeps this practice alive, and I would agree. I think our society is very uncomfortable with the dying process. As previously mentioned, I had also cared for a patient who was CTC status. Unfortunately, this was the first time I had ever seen this. This patient received only treatment to keep her comfortable so as she could pass away peacefully, in a dignified manner, with her family at her side. She too had a massive stroke, although had maintained more function than the patient with the full code status. She had ten daughters who took shifts staying with her, holding her hand and providing care and love for her. I found the whole situation very touching, and it was refreshing to see a family so closely embracing the beauty of death as a part of life. As it turned out some of her daughters were nurses. I suspect that they are privy to the pain and suffering that the healthcare system can put patients through, even when they have no hope for recovery.

Obviously, this is a complex issue, but with more education for both nurses and physicians on how to discuss code status and end of life care with patients and their families, we could make it a less distressing part of regular admission. If it was more commonplace and people knew that it was always discussed, then it would cause less fear and decisions could be made in a more timely fashion. I think we need to talk about death as a part of life and start treating all aspects of our patients, not just their bodies. As health care professionals I believe it is our responsibility to be honest with patients and their families so they can make informed decisions and ultimately ease our moral distress and their own. In an age where technology and health care advances can sustain life for so long, perhaps we could ease the fear of death and dying for patients, families, and healthcare providers and allow people to die with dignity.

References

Brindley, P.G., Marland, D.M., Mayers, I., & Kutsogiannis, D.J. (2002). Predictors of survival following in-hospital adult cardiopulmonary resuscitation. CMAJ. 167(4). Retrieved July 26, 2008, from Predictors of survival following in-hospital adult cardiopulmonary resuscitation | CMAJ

Canadian Nurses Association (2008) Code of ethics for registered nurses.

Davey, B. (2001). Do-not-resuscitate decisions: too many, too few, too late? Mortality 6(3), 247-262.

De Gente, C., Bilsen, J., Vander Stichele, R., Van Den Noortgate, N., Lambert, M., & Deliens, L. (2007). Nurses involvement in 'do not resuscitate' decisions on acute elder care wards. Journal of Advanced Nursing 75(4), 404-409.

Lauzaruk, T.(2006). The CPR question. Canadian Nurse, 102, 23-24

Murphy, D.J., Murray, A.M., Robinson, B.E. & Campion, E.W. (1989). Outcomes of cardiopulmonary resuscitation in the elderly. Annals of Internal Medicine, 111, 199-205.

Murphy, P., & Price, D. (2007). How to avoid DNR miscommunications. Nursing Management, 38(3), 17-20.

Robinson, F., Cupples, M. & Corrigan, M. (2007). Implementing a resuscitation policy for patients at the end of life in an acute hospital setting: qualitative study. Palliative Medicine, 21, 305-312.

Specializes in critical care, med/surg.

First off I hope you submitted this to be published and secondly, Bravo! for the in depth research. AS ONE OTHER POST STATED THERE WAS A MASSIVE BREAKDOWN IN COMMUNICATION AND i'M WONDERING...???WAS THIS A TEACHING INSTITUTION? Sorry didn't mean to shout! This sort of thing happens more often in teaching facilities where pts become guinea pigs and if the families are not directly involved things happen that shouldn't. This is a great teaching example that I hope is shared throughout cyberspace! I teach critical care for a local BSN program and have lately began to include an entire clinical day reviewing DNR's, code dynamics, nurse-pt-family interactions about death and dying and this essential need for communication. For all those newbie nurses out there...remember this...you MUST think of what would happen if it were your loved one lying there! So what if you **** off an attending or fellow, the family will remember your compassion and dedication. Peace out!

I wanted to add my Thank You to the first message re DNR status. In my hospital it is part of the nursing admission form. We ask if the pt has a living will/advanced directive, many times we hear "Oh my wife/husband takes care of the will, but I don't think it has anything in it about the hospital." Then we need to explain what a living will/advanced directive is in more detail. I also want to relate a story of a 68 yr old woman with 6 children, the youngest being 22, collapsed at home and was vented in our ICU/CCU. The family had many questions about her care and I made many phone calls to the cardiologist from the room...one question the cardiologist had was "is she still a full code?" when I said yes he wanted to know why?? The family was getting used to the fact that their mother was laying in an ICU bed attached to a ventilator not knowing if she was going to live or not. They made the decision at 3am to make her a DNR and wanted to talk to the doctor about what that would mean. I explained the difference code status' that they could make her: full, partial, DNR. I also explained to them that DNR does not mean don't treat. I also explained to them that this decision was the hardest one that they had to make, and went on to say that their next hardest decision would be how long they wanted mom to be on the vent with all of the pressors and cardiac meds that we were giving her (8 IV pumps all with drips of one form or another). Their response was we know that she doesn't want this (vent prolonging her life) but we aren't ready to let her go. After a long 30 min discussion on this topic I empathized with them, and also told them that what I was hearing is that their head is saying make her comfortable according to her wishes, but their hearts are saying NO and they need to talk amongst themselves and listen to their heads, which is extremely hard to do. I was asked what would I do if it was my parent in this situation, and told them that I would have the same conflict about keeping them with me longer and going with their wishes...but would ultimately go with their wishes. They went home and when they came back the next day, the pt was extubated and made comfort care. She lived for another 36 hrs before peacefully passing with all 6 of her children at her side.

We find that the male doctors that come from foreign countries are the ones that refuse/fight us to make pts DNR when their condition is such that they won't survive if we put them through the torture of CPR and ACLS.

As part of the admission assessment/history, my hospital asks whether the patient has a living will/advanced directive and what it states. I work MICU at a teaching hospital and our unit recently started requiring physicians to address code status on admission. Our attending physicians are also good about discussing code status changes with families when appropriate.

Specializes in Hospice.

With all the respect in the world, I'd like to point out that code status and advance directives are NOT physicians' decisions, except in relatively extreme cases of futile tx at the end of life.

I agree with those policies that make this a discussion that happens at the time of admission. It takes time for pts and families to wrap their heads around a terminal dx, especially if the pt is considered "too young" to die. Sometimes repeated and candid (not cruel) descriptions of exactly what happens during resuscitation are needed to get the info into pt's/POA's/next of kin's awareness so that they can be realistic about their expectations. It is part of the grieving process and cannot be rushed, IMHO.

Specializes in OB, HH, ADMIN, IC, ED, QI.

What does IMHO mean?

Specializes in psych. rehab nursing, float pool.

On admission patients are asked if they have living wills, power of attorneys or medical proxies. This can be a time to discuss the subject further if appropriate.

IMHO= in my humble opinion

In my hospital advanced directives are included in the plan of care upon admission. Determining when to shift from a Full code to a DNR status is the primary responsibilty of the physicians and nurses directly involved with patient care, to inform, educate the pt as well as the family. Ultimately leading to a written order from the physician.

Medicare requires that we discuss advanced directives with our patients upon admission. However, I know that this is poorly done. Most nurses and/or admission clerks just ask if they have one and do they want to execute oen if they don't. The discussion is not really gone into real detail until it is too late and the family is required to make the decision at the last moment.

My sister was 46 years old when we were asked to make a decision about DNR. First of all, the nurses expected me to initiate the conversation with my family since I was a nurse. They forgot that at that point I was a sister and not a nurse. However, I did discuss this with my family and they were able to make an informed decision. Thank God they did not want to see her suffer and agreed to let her go.

I believe that as nurses we have an obligation, not just by law, to find out the wishes of our patients.

Specializes in Education and oncology.

I just wanted to add to the many comments commending the author on the well thought out and well researched article on this very important topic. I'm actually presenting a CEU for nurses in April and will use this article (and it's references-thanks!) in my presentation.

One poster stated advanced directives and code status are not the MD's decisions- no! Of course not- it's the patient and the family. But IT IS the responsibility of the MD to present accurate information re: pt condition and prognosis and choices of treatments. I work in bone marrow transplant and am SICK of the MD "oh, he's got a treatable disease." Smile. AML (form of leukemia) has a 20% five year survival rate. Our patients don't know that.

It's been a miserable Christmas and weekend. Our beloved pt with AML coded and died Christmas- her husband and son just stunned. We had 3 more codes over the weekend and 1 didn't make it. Well well. Isn't that what the author stated? CPR was NOT intended to be used on one who is terminally ill, ie refractory cancer.

Our beloved lady died without her friends- all who are in shock and grieving. "IF only we could have seen her 1 more time, held her hand, told her we love her." Palliative care/hospice care- humane, compassionate and vastly underutilized. I believe it's because we haven't gotten the message out- that you DO have a choice. Tube down throat and broken ribs on the way out. Or morphine, cup of tea and your dog and cat and grandchildren cuddled up next to you. Comfortable and dignified.

We see way too much "ER", "Grey's Anatomy" etc etc. that show coded people waking up and walking out. Come on people! We need a dose of reality and some education to go with it...

sorry for the long post. Can ya tell it's been a tough week and I'm a bit interested in the topic? :yldhdbng:

Doctors are sold the image of themselves as knights in shining armor battling disease. They have lost the image of themselves as people who try to buy their patients the most good time humanly possible, and sometimes that means taking off the suit of armor and doing nothing.

Until medical schools shift their focus, we're going to be stuck in the role of patient advocate, asking doctors just what the hell they're doing offering heroics as the standard of care when common sense would dictate they offer the patients and their families a choice and informing those patients and families directly that a choice exists.

It will continue to put us into a terrible position, but it's part of the job for the foreseeable future.

Specializes in Hospice.
I just wanted to add to the many comments commending the author on the well thought out and well researched article on this very important topic. I'm actually presenting a CEU for nurses in April and will use this article (and it's references-thanks!) in my presentation.

One poster stated advanced directives and code status are not the MD's decisions- no! Of course not- it's the patient and the family. But IT IS the responsibility of the MD to present accurate information re: pt condition and prognosis and choices of treatments. I work in bone marrow transplant and am SICK of the MD "oh, he's got a treatable disease." Smile. AML (form of leukemia) has a 20% five year survival rate. Our patients don't know that.

It's been a miserable Christmas and weekend. Our beloved pt with AML coded and died Christmas- her husband and son just stunned. We had 3 more codes over the weekend and 1 didn't make it. Well well. Isn't that what the author stated? CPR was NOT intended to be used on one who is terminally ill, ie refractory cancer.

Our beloved lady died without her friends- all who are in shock and grieving. "IF only we could have seen her 1 more time, held her hand, told her we love her." Palliative care/hospice care- humane, compassionate and vastly underutilized. I believe it's because we haven't gotten the message out- that you DO have a choice. Tube down throat and broken ribs on the way out. Or morphine, cup of tea and your dog and cat and grandchildren cuddled up next to you. Comfortable and dignified.

We see way too much "ER", "Grey's Anatomy" etc etc. that show coded people waking up and walking out. Come on people! We need a dose of reality and some education to go with it...

sorry for the long post. Can ya tell it's been a tough week and I'm a bit interested in the topic? :yldhdbng:

I wholeheartedly agree that dnr and other advance directive discussions need to happen way sooner than is often the case.

As a hospice nurse, I've seen the chaos that ensues when such decisions are left to the bitter end. Too often, our palliative skills are wasted when a pt comes to us within days, sometimes hours of death. In those cases, about all we can do is hold the families' hands and medicate the pt to a fare-thee-well trying to achieve some semblance of a peaceful death. Sometimes that's unavoidable ... as in cases of fatal trauma or sudden catastrophic illness ... but usually not.

I think my previous post meant to address those situations where we, as professionals, can see a bit further down the road and assume that all it takes is a candid description of the probable course of a disease and voila!, the family makes the leap. Many of us tend to become a bit outraged when a pt or family insists on a full code status even in the face of declining condition and an increasingly bleak outlook. We throw around such words as "selfish"

or "unrealistic" without recognizing the fact that these decisions are part of a grieving process...and that it takes the time that it takes.

Repeated discussions over time are usually necessary to help the pt/family wrap their minds around what's going on. MDs need to take the lead, for sure ... and many of them are as unable to grapple with this as the families and the pts ... often because they don't want to take away all hope prematurely.

In hospice, we are not allowed to require that pts be dnr in order to receive services. I've participated in my share of deathbed code discussions ... a painful and unnecessary added strain in what is already an unbearably sad time.

Specializes in Geriatrics.

WOW, absolutely wonderfully written and well researched, thank you for sharing it.

This was my family just over a year ago with my oldest brother, I thought he had a DNR already, however he ended up in ER, coded and was down for an unknown amount of time(not being monitored-but thats another story). Full code was obviously performed he ended up vented and in ICU. Along with my dad, sister, brother and neice we drove down(we live in Michigan, he lived in Tennessee). He was basically unresponsive, his wife was in denial. I remember the nurse and the physician(ICU) talking to his wife and I in the hall but she didnt get it. I remember the nurse saying "sometimes our interventions and technology interfere with what life has planned". I knew what she meant. There were many times during the 10 days trecking to the ICU 4x day for visiting hours that I felt very alone, I remember having a conversation with my brother just about 6 weeks before this incident when he told me he was sick of being sick, he said it sucked for his kids but he was done with the whole business. I tried to talk to my sister in law but she was convinced he was going to recover, go to rehab and be ok, although she said he might not be 100% ever again she thought he was going to be functional on some level. Even his surgeon came in with what I am calling false hope and they put in a GI tube, I was furious. He was still on the vent and going down hill fast, he didnt tolerate the NG tube so they had discontinued that and when they began using the GI tube no surprise to me (and only a nursing student) that wasnt tolerated either.!!*&^*@! Finally maybe about day 8 my sister in law, neice and I were talking and she asked me what I thought so I said I know he doesnt want to live like this and THIS is what we have-- no change since he has been there, his body is giving up and they are doing dialysis (which he made very clear he never wanted) He was weaned off the vent in here somewhere and to their suprirse he continued breathing on his own. She agreed to the DNR and he passed away 2 days later. ( I think he was waiting for my youngest brother to get there)

Now I do want to say that perhaps some of what happened was for the benefit of my family as we would not have had the chance to say goodbye like we did had he died in the ER. I would however wish we would have been able to initiate palliative care instead.