Kubler-Ross Stages of Dying and Subsequent Models of Grief
Introduction
Medical professionals in all disciplines work with dying patients, and doing so effectively can be difficult. In the context of death and dying, patients, their loved ones, and the healthcare team must shift their goals. Where treating acute and chronic illness usually involves finding a tolerable path to eliminating or preventing the progression of a condition, treating terminal illness must involve preparing for death as well as efforts to mitigate symptoms.[1] Understanding the experience of dying and grief allows providers to support the unique needs of patients, their loved ones, and other healthcare team members.[2][3][4]
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Dr. Elizabeth Kubler-Ross introduced the most commonly taught model for understanding the psychological reaction to imminent death in her 1969 book, On Death and Dying. The book explored the experience of dying through interviews with terminally ill patients and outlined the 5 stages of dying: denial, anger, bargaining, depression, and acceptance (DABDA). This work is historically significant as it marked a cultural shift in the approach to conversations regarding death and dying. Before her work, the subject of death was somewhat taboo, often talked around or avoided altogether. Dying patients were not always given a voice or choices in their care plan. Some were not even explicitly told about their terminal diagnosis. Her work was popular in medical and lay cultures and shifted the nature of conversations around death and dying by emphasizing the experience of the dying patient.[4][5] This led to new approaches to working with patients through the final phase of life. She highlighted the importance of listening to and supporting their unique experiences and needs. She spurred new perspectives on ways practitioners can support terminally ill patients and their family members in adjusting to the reality of impending death.[6]
Kubler-Ross and others subsequently applied her model to the loss experience in many contexts, including grief and other significant life changes. Though the stages are frequently interpreted strictly, with an expectation that patients pass through each in sequence, Kubler-Ross noted that this was not her contention and that individual patients could manifest each stage differently, if at all. The model, which resulted from a qualitative and experiential study, was purposely personal and subjective and should not be interpreted as natural law. Rather, the stages provide a heuristic for patterns of thought, emotions, and behavior common in the setting of terminal illness, which may otherwise seem atypical.[7] Facilities with these patterns can help healthcare providers provide empathy and understanding to patients, families, and team members for whom these patterns may cause confusion and frustration.[6]
Kubler-Ross's 5 Stages of Dying
Denial is a common defense mechanism used to protect oneself from the hardship of considering an upsetting reality. Kubler-Ross noted that patients would often reject the reality of the new information after the initial shock of receiving a terminal diagnosis. Patients may directly deny the diagnosis, attribute it to faulty tests or an unqualified physician, or avoid the topic in conversation. While persistent denial may be deleterious, a period of denial is quite normal in the context of terminal illness and could be important for processing difficult information. In some contexts, it can be challenging to distinguish denial from a lack of understanding, and this is one of many reasons that upsetting news should always be delivered clearly and directly. However, unless there is adequate reason to believe the patient truly misunderstands, providers do not need to repeatedly reeducate patients about the truth of their diagnosis, though recognizing the potential confusion can help balance a patient's right to be informed with their freedom to reconcile that information without interference.
Anger is commonly experienced and expressed by patients as they concede the reality of a terminal illness. It may be directed at blaming medical providers for inadequately preventing the illness, family members for contributing to risks or not being sufficiently supportive, or spiritual providers or higher powers for the diagnosis' injustice. The anger may also be generalized and undirected, manifesting as a shorter temper or a loss of patience. Recognizing anger as a natural response can help healthcare providers and loved ones tolerate what might otherwise feel like hurtful accusations. However, they must not disregard criticism that may be warranted by attributing them solely to an emotional stage.[8]
Bargaining typically manifests as patients seeking some measure of control over their illness. The negotiation could be verbalized internally, as well as medical, social, or religious. The patients' proffered bargains could be rational, such as committing to treatment recommendations or accepting help from their caregivers. It could also represent more magical thinking, such as efforts to appease misattributed guilt they may feel is responsible for their diagnosis. While bargaining may mobilize more active participation from patients, healthcare providers, and caregivers should not mislead patients about their power to fulfill the patients' negotiations. Again, caregivers and providers do not need to correct irrational bargaining behavior repeatedly but should recognize that participating too heartily in a patient's bargains may distort their eventual understanding.
Depression is perhaps the most immediately understandable of Kubler-Ross's stages, and patients experience it with unsurprising symptoms such as sadness, fatigue, and anhedonia. Spending time in the first 3 stages is potentially an unconscious effort to protect oneself from this emotional pain. While the patient's actions may potentially be easier to understand, they may be more jarring in juxtaposition to behaviors arising from the first 3 stages. Consequently, caregivers may need to consciously restore compassion that may have waned while caring for patients progressing through the first 3 stages.
Acceptance describes recognizing the reality of a difficult diagnosis while no longer protesting or struggling against it. Patients may focus on enjoying the time they have left and reflecting on their memories. They may begin to prepare for death practically by planning their funeral or helping to provide financially or emotionally for their loved ones. It is often portrayed as the last of Kubler-Ross's stages and a goal of the dying or grieving process. While caregivers and providers may find this stage less emotionally taxing, it is important to remember that it is not inherently more healthy than the other stages. As with denial, anger, bargaining, and depression, understanding the stages has less to do with promoting a fixed progression and more to do with anticipating patients' experiences to allow more empathy and support for whatever they go through.[4][5][6][7]
Issues of Concern
Criticisms of the Kubler-Ross Model
The DABDA model has been increasingly criticized in recent years. The model has historical and cultural significance as 1 of the most well-known models for understanding grief and loss. Many alternative models have been developed based, at least in part, on the original DABDA model. The principal criticisms of Kubler-Ross's stages of death and dying are that the stages were developed without sufficient evidence and are often applied too strictly. Kubler-Ross and her collaborators developed their ideas qualitatively through in-depth interviews with over 200 terminally ill patients.[7]
Critics have focused on the fact that her research and use of "stages" have not been empirically validated. It is also said that "stages" are applied too rigidly and linearly. Instead, she aimed to describe a set of behaviors and emotions that may be experienced by a patient facing the end of life, and by describing them, improve understanding for both the patient and caregivers. Another important criticism of the model arises when it is viewed as prescriptive rather than descriptive, indicating that a patient must move through each stage to reach the final goal of "acceptance." This view holds many assumptions, including that progression through the stages is linear and that some stages are inherently less adaptive than others. Caregivers may view their job as helping a patient move through each stage, such as denial or anger, onto more easily palatable stages, such as bargaining or acceptance. Attempting to push the patient through the stages has the potential to cause harm, as they need to process their grief in their own unique way. Dr. Kubler Ross and others have reminded readers that many patients experience the stages fluidly, often exhibiting more than 1 at a time and moving between them non-linearly. It is also important to note that each stage can serve a protective role, and each patient has a unique experience in their grief process.[4][6]
Other Models of Grief
Four additional models of grief are described below.
Bowlby and Parkes' 4 Phases of Grief
Bowlby and Parkes proposed a reformulated theory of grief based in the 1980s. Their work is based on Kubler-Ross's model and describes 4 phases of grief. It emphasizes that the grieving process is not linear.
Shock and Disbelief
The initial phase replaced the term "denial" due to negative connotations. In this phase, the reality becomes altered as the mind responds to a stressful situation, becoming unresponsive or numb to the new situation. Over time, the mind processes the new reality, and the patient moves to a new phase.
Searching and Yearning
This phase is closely related to the Anger and Bargaining stage of the DABDA model. The patient attempts to undo the new reality and question its reason.
Disorganization and Repair
This phase closely relates to the Depression stage of the DABDA model. The patient experiences full acceptance of the new reality. They show signs of depression and apathy.
Rebuilding and Healing
In this phase, the patient experiences a "renewed sense of identity," which represents overcoming the sense of loss and beginning to feel in control of their destiny. They no longer show signs of depression.
Worden's 4 Basic Tasks In Adapting To Loss
Worden's model of grief does not rely on stages but instead notes that the patient must complete 4 tasks to complete bereavement. These tasks do not occur in any specific order. The grieving person may work on a task intermittently until it is complete. This model applies to the grief of a survivor but may also be applied to a patient facing death.
Accepting Reality of Loss
Initially, the patient may have difficulty accepting the reality of impending death. Typically, acceptance is viewed as being ready to move forward with the process of preparing for death.
Experiencing Pain of Grief
Patients may feel sadness, anger, or confusion. They are experiencing the pain of loss. The task is completed as the patient begins to feel "normal" again.
Adjusting to Environment
An all-consuming focus on impending death causes the patient to ignore other roles in life that are important to them. To complete this task, the patient typically resumes daily activities, such as restarting work or hobbies or becoming engaged as a spouse or parent.
Redirecting Emotional Energy
This task is generally applicable to grieving survivors. Survivors redirect their emotional energy from suffering the loss of a loved one to engaging in new activities that bring pleasure and new experiences. Subsequent theories on grieving have transitioned from stages and tasks of grief to more experiential and narrative methods.
Wolfelt's Companioning Approach to Grieving
Wolfelt's companioning approach views grief as a natural extension of the ability to give and receive love. As such, grief is not something to avoid but should be fully experienced and even embraced on the path to healing. The grieving person must feel their grief and learn to incorporate it into their lives. A person supporting the bereaved serves as a witness and companion alongside the bereaved as they walk through their grief journey. Wolfelt states, "Companioning is about going to the wilderness of the soul with another human being; it is not about thinking you are responsible for finding the way out."[9][10][9]
There are no tasks to complete, and no focus is placed on "fixing" the grief. However, he does describe 6 "needs of grief" or mourning that are more experiential. He acknowledges the need for grief to be both experienced and expressed, confronting the reality of the loss in tolerable doses. The bereaved must lean into or embrace the pain of the loss while focusing on self-compassion and self-care. He includes a narrative component as the bereaved transition their relationship with the departed from one of presence to one of memory and the need to explore their new identity in living without their lost beloved. They find meaning or peace with the loss and possibly confront their spiritual beliefs and framework. After the loss, they also need to explore the positive aspects of their new identity. Finally, he also stresses the need to develop a support system that encourages the bereaved toward self-compassion as grief resurges over the coming months and years.[9]
Neimeyer's Narrative and Constructivist Model
Neimeyer views grieving as a process of meaning-making. He acknowledges that people co-construct their understanding of reality through a narrative of their own life stories, influenced by their beliefs and world views. He describes "6 key realities influenced by death." In these 6 realities, he acknowledges that significant loss can validate or invalidate a person's framework and beliefs in life. It may require developing a new framework to heal and incorporate the loss into their worldview. Grief is simultaneously universal and unique, so the therapy for the bereaved must be tailored to each client's individual needs. The process of griefing is inherently an active rather than passive period, filled with decision-making and reconstruction both practically and existentially.
Emotions during the grieving period are useful and can serve as guides in reconstructing a sense of balance and meaning in life after the disruption caused by significant loss. Reconstructing an identity after a significant loss is an inherently social process, as the new identity is partly defined in relation to their community and social norms. And finally, adapting to loss involves finding a way to incorporate the loss into a new identity and self-narrative, giving the loss a sense of meaning and making sense of the changes. This can enable not only survival after a loss but eventually thriving.[9][11] Therapists using the narrative and constructivist model may have patients re-tell the story of their loss with visual aids, exploring the thoughts and feelings accompanying it. They may also suggest writing goodbye to the deceased or exploring their feelings through metaphors.
Clinical Significance
The transition in care, from attempting to heal the patient to caring for them near death, can be difficult for everyone involved. Healthcare providers sometimes feel as if "their job is done" as they can no longer heal the patient and "drop out" of the patient's care. This can lead patients and their loved ones to feel they are being abandoned as they near death. They often wish for guidance on the complex changes that the patient is going through emotionally and physically. Actions that are a normal part of the dying process, such as anger and refusing visitors, can leave loved ones confused and upset. Understanding the stages of grief allows providers to give support and guidance during the dying process. The explanations provided by medical caregivers hold particular importance for patients and family members as they seek to understand and subsequently make sense of terminal illness. These key moments of communication and connection can be pivotal in making sense of and healing from significant loss.[12][13] Facility with the grieving process is also imperative for the healing and resiliency of medical caregivers as they navigate through grief alongside their patients.[14]
Enhancing Healthcare Team Outcomes
For the healthcare team, caring for patients near death can be uniquely challenging for everyone involved. Healthcare providers sometimes feel as if "their job is done" as they can no longer heal the patient and "drop out" of the patient's care. This can lead to patients and their loved ones feeling abandoned by the healthcare team as they near death.[15] They often wish for guidance emotionally and physically. This is where an end-of-life interdisciplinary team can be very helpful. Physicians can provide clarity on diagnostic and prognostic information. Pharmacists participate by dispensing appropriate comfort medication in a timely fashion and working directly with the nursing staff. Hospice care providers, including social workers and nursing staff, can counsel, administer comfort care, deliver emotional support, and empathize with the patient and the family. The healthcare team should understand the models for grief, which allows providers to give support and guidance during the dying process and provides a coordinated effort to provide the patient and family with much-needed emotional support.
References
Friedrichsdorf SJ, Bruera E. Delivering Pediatric Palliative Care: From Denial, Palliphobia, Pallilalia to Palliactive. Children (Basel, Switzerland). 2018 Aug 31:5(9):. doi: 10.3390/children5090120. Epub 2018 Aug 31 [PubMed PMID: 30200370]
Pravin RR, Enrica TEK, Moy TA. The Portrait of a Dying Child. Indian journal of palliative care. 2019 Jan-Mar:25(1):156-160. doi: 10.4103/IJPC.IJPC_133_18. Epub [PubMed PMID: 30820120]
Thurn T, Borasio GD, Chiò A, Galvin M, McDermott CJ, Mora G, Sermeus W, Winkler AS, Anneser J. Physicians' attitudes toward end-of-life decisions in amyotrophic lateral sclerosis. Amyotrophic lateral sclerosis & frontotemporal degeneration. 2019 Feb:20(1-2):74-81. doi: 10.1080/21678421.2018.1536154. Epub 2019 Feb 21 [PubMed PMID: 30789031]
Corr CA, Should We Incorporate the Work of Elisabeth Kübler-Ross in Our Current Teaching and Practice and, If So, How? Omega. 2021 Sep; [PubMed PMID: 31366311]
Bregman L. Kübler-Ross and the Re-visioning of Death as Loss: Religious Appropriation and Responses. The journal of pastoral care & counseling : JPCC. 2019 Mar:73(1):4-8. doi: 10.1177/1542305019831943. Epub [PubMed PMID: 30895849]
Ross Rothweiler B, Ross K. Fifty Years Later: Reflections on the Work of Elisabeth Kübler-Ross M.D. The American journal of bioethics : AJOB. 2019 Dec:19(12):3-4. doi: 10.1080/15265161.2019.1674551. Epub [PubMed PMID: 31746702]
Corr CA. Elisabeth Kübler-Ross and the "Five Stages" Model in a Sampling of Recent American Textbooks. Omega. 2020 Dec:82(2):294-322. doi: 10.1177/0030222818809766. Epub 2018 Nov 15 [PubMed PMID: 30439302]
Smaldone MC,Uzzo RG, The Kubler-Ross model, physician distress, and performance reporting. Nature reviews. Urology. 2013 Jul; [PubMed PMID: 23609853]
Bruce CA. Helping patients, families, caregivers, and physicians, in the grieving process. The Journal of the American Osteopathic Association. 2007 Dec:107(12 Suppl 7):ES33-40 [PubMed PMID: 18165376]
Schuelke T, Crawford C, Kentor R, Eppelheimer H, Chipriano C, Springmeyer K, Shukraft A, Hill M. Current Grief Support in Pediatric Palliative Care. Children (Basel, Switzerland). 2021 Apr 4:8(4):. doi: 10.3390/children8040278. Epub 2021 Apr 4 [PubMed PMID: 33916583]
Neimeyer RA, Baldwin SA, Gillies J. Continuing bonds and reconstructing meaning: mitigating complications in bereavement. Death studies. 2006 Oct:30(8):715-38 [PubMed PMID: 16972369]
Meert KL,Eggly S,Kavanaugh K,Berg RA,Wessel DL,Newth CJ,Shanley TP,Harrison R,Dalton H,Dean JM,Doctor A,Jenkins T,Park CL, Meaning making during parent-physician bereavement meetings after a child's death. Health psychology : official journal of the Division of Health Psychology, American Psychological Association. 2015 Apr; [PubMed PMID: 25822059]
Berbís-Morelló C, Mora-López G, Berenguer-Poblet M, Raigal-Aran L, Montesó-Curto P, Ferré-Grau C. Exploring family members' experiences during a death process in the emergency department: A grounded theory study. Journal of clinical nursing. 2019 Aug:28(15-16):2790-2800. doi: 10.1111/jocn.14514. Epub 2019 Apr 25 [PubMed PMID: 29752844]
Zhai Y,Du X, Loss and grief amidst COVID-19: A path to adaptation and resilience. Brain, behavior, and immunity. 2020 Jul; [PubMed PMID: 32335197]
Stroebe M, Schut H, Boerner K. Cautioning Health-Care Professionals. Omega. 2017 Mar:74(4):455-473. doi: 10.1177/0030222817691870. Epub [PubMed PMID: 28355991]