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Eleven themes were identified, and each consisted of 2 to 4 subthemes, which are presented in Table 2 . The most frequently appearing theme for a good death across all groups was “preferences for the dying process,” which was reported in 94% of the articles in the sample. These preferences for the dying process included the following subthemes: the death scene (how, who, where, and when), dying during sleep, and preparation for death (e.g., advanced directives, funeral arrangements). “Pain-free status” was the second most frequent core theme of good death in the sample (81%) followed by “emotional well-being” (64%). Examples from patients included the following statements: “Painless. I mean pain is my biggest fear, you know. I don’t want to die in pain,” “a good death would be having the things that you wanted to have taken care of before you die done so you can be at peace with it.” 42 Additionally, some statements included that thinking about death and dying made individuals feel “afraid and depressed.” 50
Core Themes and Subthemes of a Good Death and/or Successful Dying
Core Theme | Subtheme |
---|---|
Preferences for dying process | Death scene (how, who, where, and when) |
Dying during sleep | |
Preparation for death (e.g., advanced directives, funeral arrangements) | |
Pain-free status | Not suffering |
Pain and symptom management | |
Emotional well-being | Emotional support |
Psychological comfort | |
Chance to discuss meaning of death | |
Family | Family support |
Family acceptance of death | |
Family is prepared for death | |
Not be a burden to family | |
Dignity | Respect as an individual |
Independence | |
Life completion | Saying goodbye |
Life well lived | |
Acceptance of death | |
Religiosity/spirituality | Religious/spiritual comfort |
Faith | |
Meet with clergy | |
Treatment preferences | Not prolonging life |
Belief that all available treatments were used | |
Control over treatment | |
Euthanasia/physician-assisted suicide | |
Quality of life | Living as usual |
Maintaining hope, pleasure, gratitude | |
Life is worth living | |
Relationship with HCP | Trust/support/comfort from physician/nurse |
Physician comfortable with death/dying | |
Discuss spiritual beliefs/fears with physician | |
Other | Recognition of culture |
Physical touch | |
Being with pets | |
Healthcare costs |
Four themes—life completion, treatment preferences, dignity, and family—were endorsed by more than 50% of all three stakeholder groups ( Table 3 ). The theme of life completion contained subthemes of saying goodbye, feeling that life was well lived, and acceptance of impending death. Treatment preferences included subthemes related to not prolonging life, a belief that all available treatments were used, a sense of control over treatment choices, and euthanasia/physician-assisted suicide. The theme of dignity consisted of being respected as an individual and maintaining independence, whereas the theme of family included family support, family accepting of death, the family is prepared for the death, and not being a burden to family.
Number of Articles (N = 36) that Included Specific Core Themes
No. of Articles on Patients (N = 20) | No. of Articles on Prebereaved/Bereaved Family (N = 10) | No. of Articles on HCPs (N = 18) | |
---|---|---|---|
Preferences for dying process | 20 (100) | 10 (100) | 17 (94) |
Pain-free status | 17 (85) | 9 (90) | 15 (83) |
Religiosity/spirituality | 13 (65) | 5 (50) | 9 (59) |
Emotional well-being | 12 (60) | 7 (70) | 12 (67) |
Life completion | 11 (55) | 8 (80) | 10 (56) |
Treatment preferences | 11 (55) | 7 (70) | 11 (61) |
Dignity | 11 (55) | 7 (70) | 12 (67) |
Family | 11 (55) | 7 (70) | 11 (61) |
Quality of life | 7 (35) | 7 (70) | 4 (22) |
Relationship with HCP | 4 (20) | 4 (40) | 7 (39) |
Other | 8 (40) | 4 (40) | 5 (28) |
Note: Values in parentheses are percent of the stakeholders endorsing themes.
Prebereaved and bereaved family members rated eight of the core themes at 70% and higher, the most frequent themes being preferences for dying process (100%), pain-free status (90%), and life completion (80%). Relationship with HCPs was found to be the least important specific theme among all three stakeholders.
Among HCPs, preference for dying process (94%) was the most frequently endorsed core theme of a good death, followed by pain-free status (83%), dignity (67%), and emotional well-being (67%). HCPs had the lowest endorsement for three core themes: life completion (56%), relationship with HCPs (39%), and quality of life (22%). Examples from HCPs included statements such as “having a patient pass quietly so not to disturb other patients,” “having the death occur at a time when there was adequate staff,” and “not having used excessive or futile treatments.” 53 , 54 Some statements included regret for administered treatment or a concern that the medical staff was unable to provide appropriate care.
Differences in frequencies of themes among the stakeholder groups were greatest for quality of life, which was rated more frequently in family perspective articles (70%) than in patient and HCP perspective articles (35% and 22%, respectively) ( Table 3 ). Similarly, prebereaved and bereaved family members identified the importance of family and maintaining dignity at a rate (70%) somewhat higher than that in the patient perspective articles (55% each). In contrast, religiosity/spirituality was endorsed somewhat more in patient perspective articles (65%) than in family perspective articles (50%). Supplementary Table S1 lists core themes endorsed by each stakeholder group in individual articles.
In this review we identified a number of themes important to a good death that both converge and diverge across stakeholders. To our knowledge, this review is the first systematic attempt to review the empirical literature on both the definition of a good death or successful dying according to patients, family members, and HCPs and differences across these stakeholder perspectives. Our review identified a general consensus among patients, family members, and HCPs in regard to pain-free status and specific preferences for the dying process; however, there were some notable discrepancies, for example, family members rated quality of life as more important than patient and HCP articles.
This review has several limitations. The first challenge is the variability among the articles reviewed in reporting data such as respondent characteristics. There were no common measures of a “good death” used in different investigations, which limited our capacity to aggregate results for conducting a meta-analysis or meta-regression. There was also an imbalance in sample sizes across qualitative and quantitative studies. We restricted our search to English-language and peer-reviewed articles, which might have limited the scope of our review. Also, some differences in perspectives of different stakeholders discussed below are rather small in magnitude, compounded by the limited amount of published literature in this emerging area of empirical research; consequently, we were underpowered to make statistical comparisons across study groups.
Empirical research on what comprises a good death began only a couple of decades ago, and several aspects of the methodology used in previously published studies were suboptimal. Most articles reviewed did not report information regarding specific demographics of patients, including age, culture/ethnicity, diagnoses, study inclusion/exclusion criteria, and recruitment procedures. Additionally, there was no mention of the length of time between the interview or survey and the patients’ death, which might have an important impact on specific wishes, desires, and needs as one nears the end of life as well as perceptions of what constitutes a good death, which could change over time and as the process is experienced. In regards to the investigations of family members, most studies included postbereavement family members, and therefore perspectives of prebereavement family members were not well represented. Finally, HCPs were often grouped together in the reports, and it is not known what percentage of HCPs were physicians, nurses, social workers, spiritual counselors, and so on. Furthermore, there was little information on how many, if any, of these HCPs had directly cared for dying patients or received training in such care.
Despite these limitations, we were able to identify some consistency among the three stakeholder groups in their perceptions of what constituted a good death. In more than 85% of the articles reviewed, having patient-focused preferences for the dying process and being pain-free were key components of achieving a good death according to patients, prebereaved and bereaved family members, and HCPs. Physicians, nurses, and other HCPs viewed optimal pain control and keeping the patient comfortable as a requirement for a good death. 17 , 29 , 33 , 51 This is also consistent with the overall philosophy of hospice and palliative care, which focuses on decreasing pain and suffering while improving quality of life for both patients and family members. 55
Although family members’ perspectives seemed to be more in tune with the patients’ needs and desires for end-of-life care than HCPs’, there were also some differences between family members and patients in what themes they believed to be important for a good death. For example, quality of life was rated as an important component of a good death twice as often by family members (70%) as by patients (35%). Most family perspective articles were conducted with bereaved family members who were often asked to recall the death of a loved one. Although we cannot make assumptions regarding the inferences of these findings, it could be argued that family members and patients define quality of life differently. The quality of life literature is large and beyond the scope of this review; however, it is worth further investigating how patients, family members, and HCPs define quality of life near the end of life to help understand and define this construct more precisely.
Additionally, “dignity” was reported to be an important component of a good death in 70% of family articles compared with 55% of the articles that included patient perspectives. Although the difference is not large, the finding is counterintuitive to previous research, which has argued that patients greatly value maintaining dignity during the late phase of their life. 56 , 57 However, definitions of dignity vary, and the concept of dignity may have been absorbed into other themes from the stakeholders’ perspectives. Over the last 17 years, The Oregon Death with Dignity Act has consistently publicized that the three most important concerns reported among patients near the end of their lives include a loss of autonomy (91%), a decrease in the ability to participate in activities that made life enjoyable (86%), and a loss of dignity (71%). 58 Furthermore, in a study conducted in 2002 by Chochinov et al., 56 palliative care patients reported that “not being treated with respect or understanding” (87%) and “feeling a burden to others” (87%) significantly impacted their sense of dignity. Therefore, our findings do not necessarily mean that dignity is less important for dying patients but that perhaps patients have a difficult time expressing the need for or concept of dignity to others.
The role of religiosity/spirituality was also somewhat discrepant between patients and other groups. Nearly two-thirds of patients (65%) in the articles reviewed expressed a desire to have religious or spiritual practices fulfilled as a theme of a good death; in contrast, only 50% of family members rated this theme as important. It should be added that hospice care teams are typically supposed to be composed of physicians, nurses, home health aides, social workers, as well as clergy or spiritual counselors. 59 However, in our current sample not all the patients were receiving hospice services, which might have contributed to a lack of recognition of the importance of religiosity/spirituality, because many organizations and hospitals do not have clergy members or spiritual counselors available on site, especially for diverse groups of patients.
Finally, although some literature exists on pain and physical symptoms, there is a dearth of research examining the psychological aspects of a good death, particularly from a patient perspective. 12 Our review indicates that patients view emotional well-being as a critical component of a successful death, as do family members and HCPs. Although it is important that we attend to the patient’s physical symptoms and pain control, it is crucial that the healthcare system expand the care beyond treating these symptoms and more closely address psychological, social, and religiosity/spirituality themes in end-of-life care for both patients and families. Patients view the end of life as encompassing not only the physical components of death but also psychosocial and spiritual concerns. 33 Both the American Psychological Association and the European Association for Palliative Care have identified a need for mental health professionals to address and measure psychological concerns at the end of life. 60 , 61 Further research regarding the psychological components of a good death is needed, especially in developing effective screening measures and appropriate interventions for dying patients. 12
This review suggests an obvious need for more research to examine the concept of a good death from patients’ perspectives to deliver quality care that is individualized to meet each patient’s needs 8 , 62 as well as the needs of their families. The discrepancies among patient, family member, and HCP perspectives on successful dying in this review indicate a critical need for a dialogue about death among all stakeholders involved in the care of each individual patient. It is important that we not only understand but also further investigate how addressing the themes identified in this review, both convergent and discrepant among stakeholders, may influence patient-related outcomes.
Well-designed studies are also necessary to qualitatively and quantitatively examine the concept of successful dying according to patients themselves, because this would have the potential to influence HCP care practices and to help family members meet the needs of their dying loved ones. Qualitative research could lead to the development of measurement tools for successful dying that allow for real-time modifications in care and examine how specific diseases and interventions intersect values and beliefs that are most important to patients nearing the end of their lives. Future studies would also benefit from mixed qualitative–quantitative method designs that compare people at the end of life with others who have chronic but earlier stage diseases (e.g., heart or lung disease). Additionally, it would be important to include different age cohorts (young, middle-aged, and older adults) to determine whether age impacts the themes that constitute a good death. Investigations of large numbers of demographically, medically, and psychosocially well-characterized patients from diverse ethnic and cultural groups, using standardized and validated instruments for successful dying, and seeking perspectives of these patients along with their prebereaved and bereaved family members and HCPs are recommended to inform the best practices in caring for dying patients and their families. Finally, future studies should use a clearly delineated sampling strategy that would then allow generalization to a larger population of patients, family members, and HCPs.
Finally, an important goal of this review is to issue a call for action to the professional and lay community to accelerate its open dialogue regarding death and dying, as the United States has a largely “death-phobic” culture. 63 Although individuals in many states in the country are formally asked and encouraged to consider advanced directives and organ donations, should we, as clinicians, also not ask our older patients to stipulate their preferences for the dying process? If, as a society, we begin to address the question of how people want to die and what they actually need and want at the end of their lives, perhaps we can enable more people to obtain a good death, reaching their full potential, with dignity and whole-person well-being. As stated eloquently by Gawande, 7 “…our most cruel failure in how we treat the sick and the aged is the failure to recognize that they have priorities beyond merely being safe and living longer; that the chance to shape one’s story is essential to sustaining meaning in life; that we have the opportunity to refashion our institutions, our culture, and our conversations in ways that transform the possibilities for the last chapters of everyone’s lives.”
Acknowledgments.
Funding for this research came, in part, from the Sam and Rose Stein Institute for Research on Aging at UC San Diego, American Cancer Society: MRSG-13-233-01 PCSM, and UC San Diego Moores Cancer Center.
Supplementary data to this article can be found online at doi:10.1016/j.jagp.2016.01.135.
Few issues in the United States are more contentious than the use of the death penalty as a punishment for severe crimes. Capital punishment has been recorded almost since the dawn of written history, but in today’s world, many people have come to see it as unnecessary and inhumane. Although some people are opposed to taking the lives of criminals, other people argue that it’s the best way to deal with serious crimes. They feel that these people have committed such terrible atrocities that they can never realistically be rehabilitated and reintroduced into society. The debate has been ongoing for a long time, with both sides expressing strong opinions.
Because the death penalty is so contentious, it’s a great subject for an argumentative essay. This type of essay revolves around the presentation of a particular stance on an issue, which you need to defend with logic, facts, and sound reasoning. You’ll need to do some research to gather relevant facts that support your point of view, then tie them together in a cohesive paper that presents a lucid argument based on the evidence. Because argumentative essays are such a useful tool for developing and evaluating critical thinking skills, you’ll have to write several of them during high school and college.
There are many arguments that you can make for, or against, the death penalty. Here are a few potential topics regarding capital punishment, which you can consider if you’re writing an argumentative essay.
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As physician-assisted dying becomes more available, psychologists are finding opportunities to study people’s motivations and the potential benefits and harms of aid in dying
By Kirsten Weir
December 2017, Vol 48, No. 11
Print version: page 26
13 min read
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It's been two decades since Oregon enacted the nation's first Death with Dignity Act, allowing people with terminal illnesses to hasten their deaths by self-administering medications prescribed by a physician. Since then, California, Colorado, Vermont, Washington state and Washington, D.C., have passed similar statutes.
Yet the topic arouses strong feelings—and raises plenty of questions. Can a person with depression rationally choose to hasten death? Would the option be less appealing if people received better care for physical symptoms and emotional distress? Could aid in dying put marginalized groups at risk?
As physician-assisted dying becomes available in more places, research psychologists are finding opportunities to study people's motivations and the potential benefits and harms of aid in dying. On the clinical side, psychologists' skills are helpful as people sort through their feelings and desires at the end of life, says Elizabeth Goy, PhD, a psychologist at the Portland VA Medical Center and associate professor at Oregon Health and Science University, and chair of the APA Working Group on End-of-Life Issues and Care.
"The very best thing we can do as psychologists is to improve communication and make sure that we are attending to the needs and suffering of patients who are at the end of life," Goy says. "Dying is universal, and it behooves all of us to have some foundational knowledge about end-of-life issues."
Goy and her colleagues on the working group were charged with updating APA's previous resolution on assisted suicide, adopted in 2001. In August, APA's Council of Representatives voted to approve the updated resolution. Like the previous resolution, the 2017 update states that APA neither endorses nor opposes assisted dying at this time.
"It was the consensus of the working group that this is a matter between the psychologist and the person considering aid in dying," says group member and Jonesville, Virginia–based psychologist James L. Werth Jr., PhD. "Psychologists have to be aware of their own biases, and if they can't be a part of the discussion without those biases getting in the way, they should refer the person to someone else. But we determined that APA shouldn't be a limiter of that discussion."
The most notable update to the resolution was linguistic. When the 2001 resolution was passed, the topic was known as "assisted suicide." Today, providers prefer the term "assisted dying" to reflect the distinction between suicide and the process of hastening death to alleviate pain and suffering.
Still, the specter of depression and suicide hangs over public opinion of assisted dying. Since Oregon first raised the possibility of legalized dying in the 1990s, researchers have grappled with the question of whether it can ever be considered a rational choice, Rosenfeld says. "Some people felt that almost everyone who seeks this option is doing so out of a rational appraisal of their situation. Others argued this is just a form of suicide and we should protect them from themselves," he says.
But research in the intervening years has suggested the truth lies in the gray area between, he adds. "Of the people who pursue this option, a sizable portion are rationally appraising their situation. And a sizable proportion are appraising it through a lens of depression."
In a study of terminally ill patients, for instance, Rosenfeld and his colleagues found that desire for death was associated with depression, and that desire decreased in patients who responded to antidepressants ( Psychosomatics , Vol. 51, No. 2, 2010). Other research, however, suggests that depression is not a major driver for most people who request aid in dying. When Oregon's law was passed, Goy teamed up with psychiatrist Linda Ganzini, MD, MPH, at Oregon Health and Science University, to study the moods, values, needs, concerns and symptom burdens of 58 Oregon residents with terminal illnesses who pursued assisted death. They found that most of those people did not have depressive disorders.
However, they also concluded that the Death with Dignity Act, as written, might fail to protect some patients with depression from making the choice to hasten death ( BMJ , Vol. 337, 2008).
Still, some advocates note that depression shouldn't necessarily make a person ineligible for physician-assisted death. "In the normal world of decision-making, we wouldn't say people lose autonomy to make decisions because they're moderately depressed," Rosenfeld says. Indeed, he adds, there's too little research to indicate how a person should feel or act as they approach their final days. "How cheerful should you be when you have a terminal illness?" he asks.
Some proponents of legalized aid in dying suggest that the option may be unfairly singled out because of cultural beliefs about the morality of suicide. "Assisted dying gets a lot of attention because of the values and emotions that get brought into it," says Werth. Yet many more people with serious illness end their lives through some other negotiated means, he says, such as ceasing medications, withholding food or drink, refusing life-sustaining treatment or signing "do not resuscitate" orders. "Most people will die those ways," he says.
After two decades of evidence from Oregon, research is answer-ing many questions about aid in dying. That evidence suggests that the desire to hasten death often comes from wanting to maintain some power over one's own life, Goy says. "In our research, the main reason people voiced for wanting the option was that they really wanted to have control over the circumstances of dying."
The wish for control can be for a variety of reasons, they found, including loss of autonomy and function or worries about future pain ( JAMA Internal Medicine , Vol. 169, No. 5, 2009). But reassuringly, when Goy and her colleagues compared people who expressed a desire for aid in dying with others with terminal illness who did not seek that option, they found no indication that the former group was motivated by financial concerns or being a burden to their loved ones, Goy says.
More research is needed to fully understand why and when some people ultimately make that choice, Shead notes. But it may be that just having the option provides a sense of control over the circumstances of one's death, allowing the person to focus on the quality of life that remains rather than fear of future suffering.
Research also shows that the choice to hasten death doesn't negatively impact surviving family members. Months or years after the death of the patients in their study, Goy and Ganzini interviewed their family caregivers. When they compared family members of those who requested aid in dying with those who did not, the researchers found no differences in depression, grief or use of mental health services. In fact, families of people who chose aid in dying reported that they felt more prepared and accepting of their loved one's death ( Journal of Pain and Symptom Management , Vol. 38, No. 6, 2009).
That could be because family discussions of hastened death often force families to discuss difficult topics they might otherwise not have spoken about, suggests Judith Gordon, PhD, a Seattle-based psychologist and clinical professor of psychology at the University of Washington who has studied end-of-life decision-making since 1996. "In this culture, there's still a lot of resistance to talking about dying, even if someone is diagnosed with a terminal disease," she says. "When people want to use this option, they need the support of their doctors and typically also want the support of their families."
Most people who receive a prescription for lethal medication talk to their families about their decision. "One of the gifts when someone makes this choice is that it brings the discussion to the table. The whole family or support group talks not just about this particular way of dying, but about all the issues related to how they feel about the death and what they will do later. It's an enormous benefit," Gordon says.
Despite those potential benefits, critics express concerns about the possible harms of assisted death.
One worry surrounds access. So far, most of the people who have requested aid in dying are white, middle-class and typically well-educated, notes Carol Gill, PhD, APA working group member and professor of disability and human development at the University of Illinois at Chicago. "This sector of the population generally has access to options and seeks control of their life circumstances up to the end of life," she points out. "In contrast, there are underrepresented communities who have very different views of assisted dying."
The biggest concern to Gill and others is that people from disadvantaged groups might consider hastened death because their health-care needs are not being met. There are well-documented disparities in access to health-care services, with people from lower socioeconomic backgrounds, those with lower health literacy, and members of ethnic or racial minorities being less likely to receive adequate care, including palliative care services.
"There are a number of marginalized populations that are legitimately concerned about whether they are getting all of the best options in care at the end of life," Goy says. "We want to be sure we are attentive to treating pain adequately and addressing emotional experiences such as hopelessness, depression and despair, so that assisted dying does not seem like the only option."
Gill says that many in the disability-rights community have expressed unease with aid in dying because of concerns that people won't receive the resources they need to live meaningful lives despite physical limitations. "There are no assisted-dying laws that guarantee those resources, and that feels discriminatory to a lot of people with disabilities," she says.
Indeed, the very idea of "death with dignity" is an affront to many people who have physical limitations that require daily assistance, Gill says. "Some right-to-die activists have written about assisted dying as an antidote for indignity that occurs at the end of life, such as needing help to dress or use the bathroom. If you're a person with functional limitations, that's a real slap in the face," she says.
For most people, including those with disabilities and those facing functional loss at the end of life, social connection is what makes life worth living, she adds. "Having a meaningful life doesn't necessarily mean that life needs to be pain-free or without physical impairment or functional limitations. What it means is to remain engaged humanly, and get enough support from others or technology to engage in the activities that matter, that make life meaningful."
Even advocates of physician-assisted death say it's crucial that researchers continue to explore the process to ensure it's used responsibly. More work is needed to understand how terminally ill people make treatment decisions, Rosenfeld says, including the decision to end one's life. "The fact that assisted-dying laws aren't used that often has made people more confident that the law isn't being misused. But could that number go down a notch further by having more services available? That's where more research could be really informative," he says.
Gill adds that too little is known about how people make the decision to take lethal medication after they request the prescription. "We don't follow these individuals and hear what they're thinking day to day in the period before they ingest the drugs, and we don't know what happens to people who express interest but don't end up going through with it," she says.
Gill also hopes that researchers will further explore how the availability of aid in dying will affect medical practice. "Will it seem more and more reasonable for people to want their death hastened? Will we remember that life, even when it includes suffering, can still be considered meaningful given adequate support and resources? What will happen to the balance of those resources when assisted dying becomes more common?"
There's an open opportunity for psychology researchers to answer such questions, Rosenfeld says. "I think we are uniquely poised to do the kind of research that would inform these issues."
Psychologists can also fill an important role by evaluating and counseling people who have expressed a wish to pursue aid in dying. Though it's not a topic taught in graduate school, some state psychological associations have prepared guidelines for mental health professionals who do such evaluations, Gordon says. (For example, the Washington State Psychological Association issued the Washington Death with Dignity Act WSPA Guidelines for Mental Health Professionals , and the California Psychological Association recently published its guidelines, California's End of Life Option Act: CPA Guidance for Psychologists .)
Although it's not an easy job to work with people facing their final days, it is often a gratifying one, says Goy. "All of psychology comes to bear when you are working with people at the end of life. It calls for skills in every area that psychologists are trained in," she says. "There are a lot of emotions around this topic and it's ethically sensitive. The best we can do is be open to the concerns, continually be looking for data and challenge our own biases as best we can."
APA End of Life Issues and Care www.apa.org/pi/aging/programs/eol
Physician-Assisted Dying: A Turning Point? Gostin, L.O., & Roberts, A.E., JAMA , 2016
Mental Disorders and the Desire for Death in Patients Receiving Palliative Care for Cancer Wilson, K.G., et al., BMJ Supportive & Palliative Care , 2016
The Relief of Existential Suffering Kissane, D.W., JAMA Internal Medicine , 2012
The Oregon Death with Dignity Act: A Guidebook for Health Care Professionals The Center for Ethics in Health Care, Oregon Health and Science University, 2008
Table of Contents
The death penalty is highly discussed all around the world. The main aspect of the problem is its moral side: is there any crime worth being punished with death?
Writing a death penalty research paper would demand to state your personal position on the question. It is better to define it for yourself before you start.
Still, you’ve got time for that. No need to rush. Think about it while we explain the basic requirements for a research paper on the topic.
First of all, the structure… An essential part of any written work.
It consists of:
While researching the topic, find out about the death penalty procedure, legislation, countries, that practice it, what kinds of crimes are condemned with the death penalty, what are the terms and conditions, etc.
WWhile there’s a need to know much on the topic, it’s obvious that you have to do a lot of college research paper work. That is why you have to choose the best sources. So here are some ideas where you can take useful, reliable and up to date information:
Capital punishment research paper writing may cover a vast variety of issues related to capital punishment. The main task here is to choose a narrow, specialized topic so that it would be interesting and won’t make you get lost in the number of facts.
If you face troubles composing a topic for your work , try this:
Didn’t help? Well, we’ve got some ideas for you. Check ‘em out below.
As the issue is very multifaceted, it might get quite difficult to decide where to start.
Whichever topic you choose, it’s better to know general information on the case. Here are the most helpful stats!
More statistics, visualized for your convenience:
Since there is a lot to examine within the issue of capital punishment, you would need to come up with a specific topic for your research paper.
Below are some prewritten death penalty research paper topics which may be of great help:
To sum up, we’d say that a capital punishment research paper is indeed a tough but still thought-provoking assignment.
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A valid and provocative thesis statement on Arthur Miller’s Pulitzer-prize-winning play “Death of a Salesman” should focus on one of the major themes of the play. These themes revolve around the ideas of denial, abandonment and the disorder of madness.
Because everyone in the Loman family in “Death of a Salesman” is either living in denial or enabling another family member’s denial, this theme is a strong choice for a thesis. In particular, Willy Loman cannot face the truth about his own mediocrity and must cling to his denial of failure to preserve any emotional stability. Willy also feels abandoned by various members of his family and finally abandons them completely when he commits suicide. Willy’s madness and disorder also provide a strong starting place for a thesis statement, as Willy’s denial of the truth ultimately leads him to living in an alternate reality.
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Americans spend a lot of time thinking about what it means to live a good life. But what about a good death? In 2022 researchers at the Duke University Global Health Institute ranked countries by the quality of their end-of-life care, and the United States ranked only 43, just below Colombia, Romania, Nigeria and Guatemala.
So what does this country need to do? Recent Middlebury College graduate Samara Gordon Wexler is thinking about that question. The 22-year-old winner of a prestigious Watson Fellowship is about to embark on a five-continent journey. She'll visit, work and train with end-of-life practitioners from Ghanaian coffin artists to Indian trekkers to find out what it means to die a good death and how to make it happen here.
Here & Now host Deepa Fernandes talks to Gordon Wexler about the project and why it matters.
This segment aired on July 5, 2024.
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To explore the perception of good death of patients with end-stage cancer by nurses in the oncology department.
In the study we used a phenomenological approach and semi-structured interviews. A total of 11 nurses from the oncology department of a Grade A hospital in Taizhou were interviewed on the cognition of good death from July 1 to September 30, 2022. Colaizzi’s analysis method was used to analyse the interview data. This study followed the consolidated criteria for reporting qualitative research (COREQ).
Four themes were identified: a strong sense of responsibility and mission; To sustain hope and faith; The important role of family members; Improve patients’ quality of life.
The nurses in the department of oncology have a low level of knowledge about the “good death”, and the correct understanding and view of the “good death” is the premise of the realization of " good death”. The ability of nursing staff to improve the “good death”, attention, and meet the needs and wishes of individuals and families, is the guarantee of the realization of “good death”.
Peer Review reports
The 2020 Global Cancer Statistics, published by the American Cancer Society shows that there were 10 million cancer deaths worldwide in 2020, and the global cancer burden is projected to reach 28.4 million by 2040, a 47% increase over 2020 [ 1 ]. Our country leads the world in cancer incidence and mortality [ 1 ], and the health damage caused by cancer is almost twice the world average [ 2 , 3 ].
Patients with end-stage cancer are defined as those who have no hope of a cure in modern medicine and are expected to survive for 3–6 months [ 4 , 5 ]. The terminal cancer patient’s condition can not be reversed, and has not yet effectively alleviated the pain, and the use of life support measures such as breathing machines to some extent prolonged the pain, resulting in patients can not die in comfort and dignity [ 6 ]. Death represents a significant and inevitable stage in the cycle of life, marking its final chapter for all living beings. It is a profound and crucial period that holds tremendous significance in the grand scheme of existence [ 7 ]. Hospice care is a holistic approach aimed at addressing the physical, psychosocial, and spiritual needs of individuals with a terminal illness and their family members. It provides comprehensive support and services to ensure comfort, dignity, and quality of life during this challenging time [ 8 ]. There is substantial evidence demonstrating the positive impacts of hospice care. It has been shown to enhance the quality of end-of-life (EoL) care, reduce medical costs, align with individuals’ preferences for comfort-focused care, and minimize the use of burdensome therapies. These findings support the value and effectiveness of hospice care in providing appropriate and compassionate support to patients and their families during the terminal stages of illness [ 9 , 10 ].
Hospice care in China is still in its early stages compared to certain Western countries. Efforts are being made to expand access to hospice services, raise awareness about the benefits of palliative care, and improve the quality of care provided to individuals with life-limiting illnesses in China [ 11 ]. As the concept of “eugenics” and “optimal parenting” gains popularity, the idea of a “good death” is gradually being brought to the forefront. It not only reflects the respect for life but also signifies the progress of society and civilization. The hospice concept was introduced in China in the 1980s. The concept and characteristics of a “good death” originated from early end-of-life care, with the ultimate goal of advocating for people’s support in the field of end-of-life care and drawing attention to the well-being of terminally ill patients. In 1998, Emanuel et al. proposed the framework for a good death, providing a comprehensive explanation of the multidimensional personal experience encompassed by death. Researchers divided the process of death into four key components: the inherent characteristics of the patient, the variable factors within the patient’s experience, the interventions by the healthcare system, and the outcomes. A “good death” can be described as one that occurs without the knowledge of the exact time of death, enables the individual to bid farewell to loved ones, avoids unnecessary interventions, allows the person to have some control over the place of death, minimizes distress and suffering, respects the patient’s and their family’s wishes, and aligns reasonably with clinical, cultural, and ethical standards. This comprehensive definition encompasses multiple aspects that contribute to a positive and meaningful end-of-life experience for both the individual and their loved ones [ 12 , 13 ].
Across different cultures, certain attributes of a good death are often emphasized. These include maintaining a pain-free status through effective pain management, providing emotional comfort and support to the person and their loved ones, and ensuring that individuals are prepared for the inevitability of death through open communication and appropriate end-of-life planning. These attributes are recognized as important factors in promoting a more peaceful and dignified transition at the end of life, regardless of cultural backgrounds [ 14 , 15 ]. Nurses who have a good understanding of the concept of a “good death” are better equipped to provide more effective end-of-life care to patients [ 16 ]. When providing care to individuals who are dying, nurses may experience a range of emotions, including anger, despair, distress, and guilt [ 17 , 18 ]. Understanding the concept of a good death and accepting the inevitability of death can aid nurses in coping with these complex emotions. However, it is worth noting that the acceptance of hospice care in Chinese society has been relatively slow, despite its introduction to mainland China as early as 1988 [ 19 ]. With the aging population, there is an increasing demand for end-of-life care. To measure this demand, an index system can be used, taking into account factors such as the burden caused by diseases, the dependency ratio of the elderly population, and the speed of aging [ 20 ]. In China, the objective demand for end-of-life care is indeed increasing. However, traditional cultural influences often make discussions about death taboo, and the concept of a “good death” is not widely accepted by most people [ 19 ].
Good Death (GD) is one of the core objectives of hospice care [ 21 , 22 ]. This study conducted in-depth interviews with nurses in the department of oncology to understand the current implementation of good death technology, the cognitive status of medical staff on good death, and the clinical coping strategies for patients with end-stage cancer, to determine the cognitive deficiencies of medical staff in good death and the aspects of continuous learning. The study mentioned focused on oncology inpatient unit nurses because they are frequently involved in providing end-of-life care. As patients with cancer often face end-of-life issues, it is important to understand the experiences and perspectives of nurses working in this specific setting.
We used phenomenological qualitative research and face-to-face semi-structured interviews to explore the perception of good death of patients with end-stage cancer by nurses in the oncology department in Taizhou Hospital of Zhejiang Province from July 1 to September 30, 2022. In qualitative research, phenomenological methods focus on describing common experiences shared by the entirepopulation, which also helps researchers to engage with participants from an in-depth perspective and to understand their experiences. Our research team has extensive experience in qualitative research.
Purposive sampling was employed to select the participants who were eligible and could provide rich information about the research question.
Inclusion criteria: (1) Nurses with a license to practice nursing; (2) Oncology nurses with a minimum of 6 months of clinical nursing experience; (3) Providing care services to terminally ill cancer patients, and have work experience in hospice; (4) Ability to clearly articulate their views; (5) Providing informed consent and voluntary participation in this study. Exclusion criteria: (1) Nurses who withdrew from the interview process; (2) Nurses who were on leave or engaged in training, resulting in an absence from their position for more than 3 months; (3) Nurses who were unwilling to discuss their experiences in caring for terminally ill cancer patients.
In this study, the report will replace each participant with a code, and the interviewee’s identity, contact information will not be disclosed to others. Sound content is also used only in this study. The study was reviewed and approved by the Ethics Committee of Taizhou Hospital, Zhejiang Province, China (approval number: K20220789).
The qualitative data collection method employed for this study involved semi-structured, face-to-face interviews. Prior to the start of each interview, all nurses were provided with written informed consent to participate in the research. All interviews were digitally recorded, assigned pseudonyms, and transcribed verbatim. We took measures to ensure that the participants understood the purpose and process of the study, and we emphasized the privacy of the interview environment and the confidentiality of the data. The interviews will take place within the confines of the hospital’s designated conversational chambers, ensuring utmost privacy for the participants. Saturation was considered to be reached when no new themes emerged from the inductive content analysis. In total, we conducted interviews with 11 members of the oncology nursing team (See Table 1 ).
During the interview, subjects were also given the opportunity to read the consent form, confirm understanding, and ask questions. Verbal consent was obtained to preserve the anonymity of the subjects. During the interviews, participants were offered explanations for any inquiries they had. Additionally, participants had the option to refuse further interviews and withdraw from the study for any reason. In addition, two oncology nurses were selected for a pre-interview prior to data collection to ensure the clarity of the questions and to identify any potential problems. The data from preliminary interviews was not included in this study but was utilized to modify the interview structure based on the preliminary findings. The preinterviews were treated as tests and were excluded from the analysis. The final interview used in this study included the items are listed in Table 2 . Interviews were conducted in a quiet consultation room at the hospital between July 1 and September 30, 2022. Each person was interviewed one time, and each interview lasted approximately 30–50 min. All the interviews were conducted by a nurse with master who was trained in qualitative research. A research assistant played an auxiliary role which included recording the interviews.
The investigator audio recorded with permission, and participants’ responses, including nonverbal cues and body language during the interviews, were noted. The results will be returned to each participant within 24 h of each interview, to verify the interview details, thus ensuring the accuracy and credibility of the analysis. Before this interview, investigators were trained in interview and communication skills, including effective listening and giving positive feedback, establishing good relationships with interviewees, maintaining eye contact, not interrupting interviewees, not judging their views, etc.
Audio recordings were transcribed verbatim and checked for accuracy by repeated listening within 24 h of the interviews. After the interview, the data were analysed separately and immediately by two researchers with skilled analysis experience. Interview data was analysed using Nvivo12.0, a computer-assisted qualitative data management software. Colaizzi’s phenomenological seven-stepmethod was used for data analysis to complete theextraction of themes and sub-themes regarding the perception of good death of patients with end-stage cancer among oncology nurses (see Table 3 ). Any disagreement between researchers was resolved by making decisions through discussion until a consensus was reached. The final transcribed data, as well as the extracted themesand sub-themes, were sent to the participants simultaneously, and all participants agreed to be contacted again. This study met the criteria of Consolidated Criteria for Reporting Qualitative Studies (COREQ).
To ensure the study’s dependability, the methods and analyses used were described in detail. The study interviewer was a master’s degree student in nursing. The interviewer received systematic qualitative training to master qualitative research methods, was experienced in oncology practices, and established a good relationship with the participants before the interviews commenced. This facilitated the acquisition of real information. The researcher maintained a neutral attitude during the interview, did not lead or hint, did not interrupt the interviewee at will, and only asked timely follow-up questions, rhetorical questions, and clarifications until no new information emerged. Therefore, credibility was ensured. The collection, analysis, and interpretation of data were continually reviewed and detailed to ensure its dependability. The data extracted from the survey results were described in detail to achieve confirmability. Regarding transferability, this study described in detail the inclusion criteria, exclusion criteria, and demographic characteristics involved. Simultaneously, the Consolidated Criteria for Reporting Qualitative Research (COREQ) checklist was used to report the findings (See Appendix I for details).
Characteristics of the 11 participants are shown in Table 1 . All eleven participants were female. The shortest term of employment as a Registered Nurse was one and a half years, and the longest was 17 years (Fig. 1 ). Four distinct themes emerged from analysis of the interview data: (1) A strong sense of responsibility and mission; (2) Sustaining hope and faith; (3) The important role of family members; and (4) Improving patients’ quality of life. Each theme included three–four subthemes (see Table 4 ).
A visual analysis of the working years of the 11 participants included
Most respondents said that when they realized that a patient was dying, their presence was more important than ever, triggering a strong sense of responsibility and mission. “End-stage patients will leave at any time, when in the dying patient evaluation period, I will often ward, observe the patient’s vital signs, keep the comfort of family members, at this time of the patients and family members are in great need of medical personnel to accompany and support, especially families, at this point the heart is very fragile, especially need a psychological support.” (A5, female, 28 y.o) “For the families of the patients whose death is imminent, I will tell them to tell the patients as soon as possible if there is anything they need to tell them. If there is anything that needs the help of our doctors and nurses, they can tell us at any time. We will do our best to help.” (A7, female, 39 y.o).
Patient confidentiality.
Under the influence of traditional Chinese culture, when patients enter the terminal stage of cancer, considering the patients’ physical and psychological conditions and psychological acceptance of the disease, medical staff needs to inform the patients’ families and seek treatment advice, whether to conceal the true condition of patients [ 23 ], whether to continue treatment or give up treatment and so on so that the whole family is faced with a major choice. In this interview, the interviewees discussed their views on the confidentiality of the patient’s condition from the point of view of good death, and the nurses had better cognition of the confidentiality of the patient’s condition. “We have a lot of family members who are concerned about the patient’s ability to cope. They tell us in advance not to discuss the patient’s condition in front of the patient, and they ask us to keep it confidential when the patient asks. We usually comply with their request at this time. “(A9, female, 32 y.o).
“A lot of family members ask for the patient’s condition to be kept confidential. Our doctors and nurses usually communicate on how to settle accounts with patients in a unified way. “(A3, female, 42 y.o).
Patients and family members experience a complex range of emotions after being informed of a cancer diagnosis, and how to make patients and family members accept the reality that cancer is incurable is a challenge for healthcare professionals [ 24 , 25 , 26 , 27 ]. In the interview, the interviewees mentioned the importance of spiritual support for cancer families. “Many patients have no faith. I have seen many patients who have been in a period of anger after learning that they have cancer. They think why they are so unlucky. They have this disease and have no interest in doing anything. They think that the world is unfair and cruel to them. If we can help them to seek their faith, such as religion, it may have some spiritual comfort for them. " (A8, female, 37 y.o) “I met a retired civil servant in my work who, after learning that he had cancer, organized his years of Work Records and compiled a memoir by year. I think he would review his experiences and values when he read these memoirs, and his heart would be at peace for a while. I got an idea from him that I could use a similar approach to help other patients and their families find value in their lives and live more peacefully in the final stages of their lives. " (A6, female, 29 y.o).
The accompanying role of family members.
Influenced by our traditional culture, most terminal cancer patients want their closest family members to be with them at the end of their lives. Most of the interviewees indicated that the accompany of family members is a comfort to the patients, which makes them feel that they are loved and meets their psychological needs [ 28 ]. “Patients at this stage are more psychologically vulnerable than those with other diseases. At the end of their lives, the company of their family members is a great psychological comfort to them. Although I can’t have a lot of company during an epidemic, I usually ask one of the family members to stay here to accompany the patient. “(A2, female, 36 y.o) “At this time, the family member will stay by the patient’s side. Even if they don’t do anything or say anything, the patient will feel that they are cared for by someone and feel that they are still loved. “(A10, female, 30 y.o).
Under the influence of the Chinese traditional concept of life and death, there are still some difficulties in implementing and promoting euthanasia, especially for cancer patients, whose families often choose to hide the true situation from them, medical staff can only discuss it with their families [ 29 , 30 ]. The nurses mentioned that most of the family members lack the methods of psychological care and the experience of taking care of terminal cancer patients, do not know the psychological needs of the terminal cancer patients, and can not do the psychological work of the patients in time and effectively. “During the work process, some patients’ psychological needs are very high, but the family members accompanying them don’t understand the patients’ psychological needs. The two of them can’t chat together and have nothing to say for a whole day. “(A4, female, 26 y.o).
Family members accompany patients for a long time, know the daily living habits of patients best, can provide wholehearted care, and can timely detect and feedback on the symptoms of patients and changes in their condition, the care of family members for patients is an important component of the medical staff to evaluate the patient’s good death. “Many patients at this stage due to pain and other effects, the ability to move limited, and many daily activities need family care.” (A11, female, 25 y.o) “Terminally ill patients, ECG monitoring everyday detection of vital signs, we usually also one hour patrol, family members beside can pay attention to the patient’s vital signs changes. " (A1, female, 33 y.o).
Symptom control.
Most interviewees believed that end-stage patients should focus on symptom control and pain relief. “In the end, the most uncomfortable thing for many patients is the cancer pain, which makes them unable to move when they turn over. Taking painkillers and injecting painkillers can no longer control the pain. If it can reduce their pain, it is very meaningful for good death.” (A8, female, 37 y.o) “When patients enter the terminal stage, some other treatments are meaningless and try not to disturb them, so that patients can quietly go through the final stage of life.” (A7, female, 39 y.o).
During the interview, most interviewees expressed that they should try their best to meet the reasonable requirements of patients, reduce invasive operations on patients, listen to the voice of patients and their families more, improve the comfort level of patients, and give more tolerance and understanding to patients and their families. “During the epidemic, patients and their families are required to reduce going out and order meals in the department. However, patients with advanced stage do have a poor appetite. Some of their families will prepare meals and send them to the first floor of the hospital building. (A9, female, 32 y.o) “When I perform a blood gas analysis or an infusion on this type of patient, if I feel that I cannot successfully puncture the vein on the first try, I will seek assistance from other colleagues to avoid subjecting the patient to the pain of a second puncture.” (A1, female, 33 y.o).
The aim of this study was to explore the perceptions of oncology nurses regarding end-of-life care for patients with advanced-stage cancer in China. The interviews conducted in this study revealed that oncology nurses have generated numerous ideas and understandings about end-of-life care for patients. This demonstrates their strong concern for end-of-life care issues and their utmost efforts to help patients achieve a good death. The cognition of healthcare professionals regarding a good death is influenced by traditional cultural factors, and their ability to assist patients in achieving a good death is also limited by their level of knowledge and skills.
In contemporary times, the majority of individuals pass away within the confines of a hospital setting, necessitating the presence of nurses during their final days. As patients approach the end of their lives, nurses provide companionship and support throughout this significant transition [ 31 ]. The attitudes exhibited by nurses play a pivotal role in shaping the quality of end-of-life care. A positive attitude towards death can signify that nurses possess a more effective adaptation to the practices related to end-of-life care. This also implies that they are better equipped to provide compassionate and supportive care to patients during this sensitive stage [ 32 , 33 ]. By fostering positive attitudes towards the dying, nurses can overcome their own fears of death. This allows them to create a safe and supportive environment where patients can experience a peaceful and dignified process of dying. Such an atmosphere fosters a sense of respect and enables patients to feel valued as individuals during this vulnerable time [ 34 ]. The research conducted by Ceyhan et al. revealed a positive correlation between the perception of a good death and the attitudes of intensive care nurses towards providing care for patients in their final moments. These nurses exhibited favorable attitudes towards end-of-life care and possessed a strong belief in the concept of a good death. The study suggests that nurses in the intensive care setting are more inclined to embrace and prioritize the well-being and comfort of dying patients [ 35 ].
This is similar to the findings of Hilal Türkben Polat and others [ 34 ]. The concept of death often evokes negative emotions in patients, patient relatives, and nurses. Consequently, it is typically avoided and sometimes even considered a taboo in certain regions. Patients in Eastern countries encounter unique challenges when it comes to preparing for death. This is primarily due to lower frequencies of receiving bad news, such as diagnoses and prognoses, as well as cultural practices that discourage discussions about death. Moreover, stronger taboos surrounding death discussions exist in Eastern countries compared to Western countries [ 36 ]. In western countries, the disclosure of diagnoses is regarded as a fundamental patient right and an essential practice. Within the western ethical tradition, there is significant emphasis on providing patients with truthful information. Medical practitioners have a responsibility to respond to patients’ questions regarding their diagnosis in an honest and forthright manner [ 37 ].
Under the influence of Eastern philosophy, the challenges related to diagnosis disclosure are further magnified in Eastern countries. Traditional Eastern philosophical beliefs, such as the emphasis on harmony, collective well-being, and the idea of protecting patients from distress, can create barriers to open and direct communication about diagnoses. Balancing the values of truthfulness and preserving emotional well-being becomes a particular challenge within the Eastern cultural context [ 38 ]. In China, it is common for family members to withhold cancer diagnoses from the patient, as they believe it may help protect the patient from potential emotional distress and depression. This practice stems from a desire to shield loved ones from the potentially negative impact of such news. However, it is important to note that this approach may differ from the Western emphasis on patient autonomy and the right to access complete information about one’s own health condition [ 26 ]. As highlighted by Jiang Yu et al., the decision to withhold cancer diagnoses in China is often a collective consensus among family members. This collective decision-making process is influenced by cultural norms, where the family plays a central role in matters of health and well-being. In such cases, the family members believe that keeping the diagnosis concealed is in the best interest of the patient, aiming to maintain emotional well-being and alleviate potential distress. It is important to recognize and respect these cultural differences and the role of familial decision-making in the context of healthcare practices [ 39 ].
The concept of “Avoid death” in our traditional culture will affect the expression of the needs of terminal cancer patients. Compared with patients, their families have more difficulty accepting the concept of good death, which they believe means giving up treatment, waiting for death, and being difficult to accept psychologically [ 40 ]. The medical personnel should strengthen the family members’ correct understanding of good death and make them realize the importance of respecting the patient’s right to know and independent decision-making to realize good death, it is suggested that family decision-making should be gradually changed into a way of discussion between patients and their families, to lighten the psychological burden of both sides and let patients realize their wishes. Fully pay attention to the needs of end-stage patients and their families, and take targeted measures to help patients to achieve good death [ 41 ].
The attitude of professional nurses to death greatly influences the treatment decision of terminal cancer patients and affects the quality of patients’ death. The more skilled the nursing skills, the better the communication skills, and the terminal attitude of terminal cancer patients, the better the quality of life of the patients.
Based on the interview results, it is evident that nurses have insufficient competency in implementing end-of-life care. They make efforts to help patients manage clinical symptoms and enhance the caregiving abilities of family members through their own capabilities, aiming to assist patients in a better end-of-life experience. However, the nurses’ level of competence directly affects the patient’s experience of end-of-life care. They have limited opportunities for formal end-of-life care training and education, resulting in a relative lack of knowledge in this area. The end-of-life experience is unique and personal for each individual, with most people desiring to avoid pain during this period, while others may prioritize prolonging life at any cost. End-of-life care may be provided by doctors, physicians, nurses, emergency personnel, or volunteers. However, nurses play a significant role and bear primary responsibilities in this regard [ 14 ]. A study indicated that nurses, as moral agents, possess a profound commitment to upholding the moral integrity of end-of-life care, particularly when it involves assisted death. This suggests that nurses play a crucial role in ensuring that ethical principles and values are upheld throughout the process. Their dedication to promoting the well-being and dignity of patients in these complex situations highlights their ethical and moral responsibility in providing compassionate and supportive end-of-life care [ 15 ]. In addition, another research study highlighted the indispensable role of nurses in providing compassionate care to patients in their final stages of life [ 16 ]. Nurses are entrusted with the responsibility to deliver exceptional care to terminally ill patients and their families. Insufficient knowledge has been identified as a major obstacle in providing optimal care for individuals nearing the end of their lives [ 18 ]. A lack of education and training in end-of-life care has been recognized as a significant contributing factor to insufficient recognition and management of symptoms, as well as challenges in effective communication with patients and their families [ 17 ].
At present, the level of knowledge and skills of our palliative care is not high, and they lack the skills of psychological, social, and spiritual support and are difficult to implement skillfully [ 42 ]. The limited awareness of hospice care in Mainland China can be attributed to various factors, such as the absence of systematic policy support, limited public educational campaigns, and the lack of comprehensive academic and practical curricula and training programs on hospice care. These factors have collectively contributed to the insufficient understanding and recognition of hospice care among the general public and healthcare professionals in Mainland China [ 43 ].
Healthcare professionals need professional knowledge and skills should use a variety of ways to educate professionals, and guide them not only care about patient survival rate, and quality of life, at the same time, we should also pay attention to the physical and psychological needs of incurable patients [ 44 ], educate patients with end-stage cancer and their families, provide a suitable environment and the necessary help, improve the quality of patient’s death, and meeting the needs of patients who are nearing the end of life. By enhancing the medical curriculum to include comprehensive education on hospice care and establishing hospice care programs within hospitals, opportunities can be increased for physicians, nurses, patients, and their family members to enhance their awareness and utilization of hospice care services. This would ultimately contribute to improving end-of-life care and ensuring that individuals receive the support and comfort they need during this crucial time [ 45 ]. In addition, the whole society should widely carry out life education and Death Education, guide people to look at life and death correctly, a planned, leisurely life with, a good start, and a good finish.
In the Chinese cultural context, there is a strong emphasis on the centrality of the family and social relationships [ 12 ]. Family dynamics are considered crucial for a good death, and Asian populations, influenced by Confucian teachings, place great importance on the cohesion of the family and the significance of familial relationships [ 46 ]. Nurses take care of terminal cancer patients for a long time, and they are familiar with the patients and their families. Clinical nurses should play an active role as a good communication bridge, which can help them communicate their needs or promote communication among themselves, at the same time, teach family members to play a better role in family support to meet the needs of patients with end-stage cancer to receive family warmth and care [ 47 , 48 , 49 ].
This study still has some limitations. Primarily, the participants were confined exclusively to a solitary tertiary hospital, thereby potentially limiting the generalizability of the findings. To augment representativeness, future investigations could contemplate sampling participants from nontertiary hospitals. Furthermore, the inclusion of solely female nurses in the analysis neglects male nurses, thus introducing a predisposed bias into the results. Within the targeted population of this inquiry, the dearth of male nurses serving escalates the complexity of ameliorating this bias. Secondly, the study lacked the amalgamation of quantitative research, impeding the determination of specific domains and the magnitude of improvement required in nurses’ competencies. To rectify this, future research endeavors should endeavor to broaden the sample size and scope, employing quantitative research methods to scrutinize the precise cognitive facets and knowledge modules necessitating enhancement in nurses. Additionally, there exists a demand for further exploration of culturally tailored competency models in the Chinese context. This would assist in confronting and resolving the challenges impeding the current competency development process. Furthermore, interviews were conducted in Chinese and subsequently analyzed and translated into English. Despite efforts by professional English editors to guarantee accurate translation, there remains a small risk that the translation process may have influenced the study outcomes. Lastly, further exploration is still required to ascertain the appropriate cultural backdrop of our model, and to refine and address the prevailing complications encountered in the euthanasia procedure.
This study explored the general cognition of nurses in the oncology department about good death from the perspective of Chinese nurses. The results showed that nurses in the oncology department had a low level of knowledge about good death, and had a correct understanding and view of “good death”. Indeed, strengthening hospice education is crucial to improve public awareness and acceptance of hospice care, leading to better quality end-of-life care. To enhance public education on hospice care, it is essential to develop and implement culturally appropriate educational programs systematically. By tailoring these programs to the specific cultural context, we can effectively address the barriers and taboos surrounding discussions about death and promote understanding and acceptance of hospice care [ 50 ]. It is the premise of realizing “good death”, and the ability of nurses should be improved. It is the guarantee of realizing “good death” to pay attention to and satisfy the needs and wishes of individuals and families.
The datasets generated during the current study are available from the corresponding author on reasonable request.
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This work was supported in part by Medical Science and Technology Project of Zhejiang Province (2024KY1788), Major Research Program of Taizhou Enze Medical Center Grant (19EZZDA2), Program of Taizhou Enze Medical Center Grant (22EZD06), Open Project Program of Key Laboratory of Minimally Invasive Techniques & Rapid Rehabilitation of Digestive System Tumor of Zhejiang Province (21SZDSYS01), Program of Taizhou Science and Technology Grant (23ywa33).
Wei-dan Wu, Yi Wang and Xin-yu Fu contributed equally to this work.
Department of Gastroenterology, Taizhou Hospital of Zhejiang Province affiliated to Wenzhou Medical University, Linhai, Zhejiang Province, China
Wei-dan Wu, Yi Wang, Jin-hua Zhang, Xin-Li Mao & Shao-wei Li
Key Laboratory of Minimally Invasive Techniques & Rapid Rehabilitation of Digestive System Tumor of Zhejiang Province, Taizhou Hospital of Zhejiang Province affiliated to Wenzhou Medical University, Linhai, Zhejiang Province, China
Wei-dan Wu, Yi Wang, Xin-Li Mao & Shao-wei Li
Institute of Digestive Disease, Taizhou Hospital of Zhejiang Province Affiliated to Wenzhou Medical University, Linhai, Zhejiang Province, China
Taizhou Hospital of Zhejiang Province affiliated to Wenzhou Medical University, Linhai, Zhejiang Province, China
Xin-yu Fu & Chen-yang Zhang
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W-D W, W Y, X-L M and S-W L identified the research topic and designed the research process; W-D W, W Y, X-Y F were involved in writing the article; W-D W, J-H Z, X-Y F, W Y and C-Y Z were involved in interviewing and summarizing; W-D W, X-Y F, X-L M and S-W L were involved in correcting and revising the article.
Correspondence to Xin-Li Mao or Shao-wei Li .
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All methods were carried out in accordance with the Declaration of Helsinki. The study was reviewed and approved by the Ethics Committee of Taizhou Hospital of Zhejiang Province affiliated to Wenzhou Medical University Institutional Review Board (approval No. K20220789). Researchers contacted and explained the research procedures and recruitment criteria to the participants and emphasised that participants’ responses would remain anonymous and confidential. Informed consent was obtained from all study participants.
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Wu, Wd., Wang, Y., Fu, Xy. et al. Qualitative study on the perception of good death in patients with end-stage cancer in oncology nurses. BMC Nurs 23 , 431 (2024). https://doi.org/10.1186/s12912-024-02081-x
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Carol Bongiovi died on Tuesday, July 9, at 83.
Jon Bon Jovi is mourning the loss of his mother Carol Bongiovi who died on Tuesday, July 9, at 83, according to an obituary provided by the rock star's representative.
"Our mother was a force to be reckoned with, her spirit and can-do attitude shaped this family. She will be greatly missed," wrote Jon Bon Jovi in a statement on behalf of his family.
Born Carol Sharkey, Carol Bongiovi was born in Erie, Pennsylvania, and joined the U.S. Marine Corps in 1959, where she met her husband, John Biongiovi, Sr. The couple moved to New Jersey, where their sons John Bongiovi Jr. -- later known as Jon Bon Jovi -- Anthony and Matthew were born.
Described as an entrepreneur who operated several businesses, Carol Bongiovi also worked as a Playboy Bunny and founded the Bon Jovi fan club.
According to the obituary, she's survived by her husband, John Bongiovi Sr., her three sons and daughters-in-law and eight grandchildren.
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Death of a Salesman is Arthur Miller’s multiple award-winning stage play that explores such ideas as American Dream and family. Our writers have prepared a list of topics and tips on writing the Death of a Salesman thesis statement, essay, or literary analysis.
Breaking news, gov. gretchen whitmer says it ‘wouldn’t hurt’ for biden to take cognitive assessment as prez denies need.
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Michigan Gov. Gretchen Whitmer said Wednesday that it “wouldn’t hurt” for President Biden to take a cognitive test.
Whitmer acknowledged that the assessment would be a good idea in an interview Wednesday, despite the octogenarian president denying that there’s a need for him to undergo such testing.
“I don’t think that it’d hurt, to be honest,” Whitmer told CNN in response to a question about Biden taking a mental acuity test.
The White House has been plagued with questions about Biden’s mental abilities since the June 27 debate, when he appeared to be confused and stumbled over his responses at times.
Polls show a majority of Americans are concerned about his mental fitness — and an increasing number of congressional Democrats and close allies are calling for him to drop out of the 2024 race.
The president tried to alleviate concerns about his age by sitting down for an interview with ABC’s George Stephanopoulos, but his performance there spurred even more allies to call on him to drop out.
Whitmer, a Democrat who has been a fierce supporter of Biden and is rumored to be a potential replacement if the president were to choose to suspend his campaign, also admitted that “the first presidential debate was not a success for President Biden.”
But, Whitmer said, Democrats need to continue to rally behind Biden while he’s in the race if they want to defeat former President Donald Trump.
“We can’t lose sight of how high these stakes are. We have a field. And unless one person, Joe Biden, makes an alternative decision, this is the field, and we’ve gotta go.”
Whitmer’s remarks echo a similar comment made by former House Speaker Nancy Pelosi (D-Calif.), who said Biden needs to “make that decision” on whether he’s going to stay in the race.
The president has been firm that he’s going to continue his bid. He wrote a letter to congressional Democrats on Monday stressing that he’s not dropping out, and later went on “Morning Joe” to say he is the Democratic nominee.
Biden has also laid out several excuses for his bad performance against Trump in the first debate. In his interview with Stephanopoulos , Biden argued that he was “exhausted” and “sick” with a “bad cold,” before pivoting to saying Trump’s points “distract me.”
He has never publicly released the results of a mental acuity test and has argued over the years that his time in the Oval Office is proof that he doesn’t need one.
“Look, I have a cognitive test every single day,” Biden told Stephanopolous. “Every day, I’ve had tests. Everything I do. You know, not only am I campaigning, I’m running the world. And that’s not — it sounds like hyperbole, but we are the central nation of the world.”
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Dorothy Parker was Lopatto's cat, a stray adopted from a local vet. And Dorothy Parker, known mostly as Dottie, died peacefullywhen she passed away earlier this month. Lopatto's essay is, in part ...
Writing an essay about death can be a profound and thought-provoking experience, allowing individuals to reflect on their own mortality and explore existential questions. To inspire your writing, here are 115 death essay topic ideas and examples. The concept of death in different cultures. The role of death in religious beliefs.
If so, reading essays about death, grief, and even near-death experiences can potentially help you begin addressing your own death anxiety. This list of essays and articles is a good place to start. The essays here cover losing a loved one, dealing with grief, near-death experiences, and even what someone goes through when they know they're ...
1. Life After Death. Your imagination is the limit when you pick this prompt for your essay. Because no one can confirm what happens to people after death, you can create an essay describing what kind of world exists after death. For instance, you can imagine yourself as a ghost that lingers on the Earth for a bit.
Death is defined as the permanent cessation of all biological functions that sustain a living organism. This can occur as a result of illness, injury, or simply old age. Death is a natural process that occurs to all living things, but it is also a process that is often accompanied by fear and uncertainty.
All Are Equal in Death. Death refers to the lasting termination of all life's tasks in a human being. Death chances on its prey in the middle of their actions and strikes equally to all. Socrates: His Life, Philosophy, & Death. The Philosopher, Socrates was a Greek and he was born in the proximities of 470 B.
She died before her 60th birthday - her terminal illness was discovered very late, and she passed away less than a year after receiving the diagnosis. Such a rapid change in my life left a mark on my memory and reshaped my view of life and death. Get a custom essay on Death, Dying, and Bereavement: Reflection. 187 writers online.
Death, loss, and grief are universal experiences that have been explored and portrayed in literature for centuries. These themes often serve as a reflection of the human condition, providing insights into the emotional, psychological, and cultural dimensions of these experiences. This essay will delve into the interpretations of death, loss ...
This article considers several questions concerning the philosophy of death. First, it discusses what it is to be alive. This topic arises because to die is roughly to lose one's life. The second topic is the nature of death, and how it bears on the persistence of organisms and persons. The third topic is the harm thesis, the claim that death ...
Step 2: Write your initial answer. After some initial research, you can formulate a tentative answer to this question. At this stage it can be simple, and it should guide the research process and writing process. The internet has had more of a positive than a negative effect on education.
Any thesis statement should be determined by what the author really believes. This question about the death penalty is one that really tries to force the author to take a position for or against.
Defining death helps refine the central question of the essay. There are good reasons to believe that dying can harm the person who dies. For example, dying can harm someone because it is frightening or painful. This essay, however, is an attempt to determine whether death, as opposed to dying, can harm the person who dies.
82 essay samples found. The death penalty, also known as capital punishment, remains a contentious issue in many societies. Essays on this topic could explore the moral, legal, and social arguments surrounding the practice, including discussions on retribution, deterrence, and justice. They might delve into historical trends in the application ...
Capital punishment has been a debatable issue for decades. Some people believe that the death penalty plays a crucial role in the criminal justice system, while others think that this procedure is highly unethical. We will write. a custom essay specifically for you by our professional experts. 192 writers online.
This thesis statement is not debatable. First, the word pollution implies that something is bad or negative in some way. Furthermore, all studies agree that pollution is a problem; they simply disagree on the impact it will have or the scope of the problem. No one could reasonably argue that pollution is unambiguously good.
Of the quantitative and mixed-methods studies (N = 9), 3 articles used standardized measures of a good death, including the Preferences about Death and Dying questionnaire, 26 The Concept of a Good Death scale, 27 and The Good Death Inventory. 28 The other six studies had developed their own quantitative measures (e.g., attitudinal measures of ...
Share Cite. Possible thesis statements: While Hamlet suffers a tragedy in death, he died as a hero, finally avenging his father's death. Hamlet is a tragic hero because he dies while avenging his ...
3. Methods. This review synthesised concept analyses on a good death to create a shared understanding of a good death within nursing. One researcher found the concept analyses by searching PubMed, CINAHL Complete, and Medline (Ebsco). The search terms used were "concept analysis" and "good death "or "peaceful death."
Here are a few potential topics regarding capital punishment, which you can consider if you're writing an argumentative essay. The death penalty is a deterrent that prevents potential criminals from committing serious crimes like murder. The death penalty is not effective at preventing crime. Capital punishment is more cost-effective than ...
That evidence suggests that the desire to hasten death often comes from wanting to maintain some power over one's own life, Goy says. "In our research, the main reason people voiced for wanting the option was that they really wanted to have control over the circumstances of dying."
Set an alarm clock for 5-10 minutes and concentrate on noting ideas for your topic. Find the aspect of your most genuine interest. Make sure that the issue you chose is well covered with decent materials. Note keywords of your topic to be. Experiment on phrasing. Determine your topic as the main research question.
A valid and provocative thesis statement on Arthur Miller's Pulitzer-prize-winning play "Death of a Salesman" should focus on one of the major themes of the play. These themes revolve around the ideas of denial, abandonment and the disorder of madness. Because everyone in the Loman family in "Death of a Salesman" is either living in ...
In 2022 researchers at the Duke University Global Health Institute ranked countries by the quality of their end-of-life care, and the United States ranked only 43.
Death is the only allowable reason for a candidate to drop out according to Wisconsin law, impeding potential replacement of Biden on the 2024 ballot. Getty Images
Letexier's average of 3.33 yellow cards per game is also among the lowest at Euro 2024, which could be good news for a Spain side who have been among the most prolific foulers in Germany.
News. Calls for justice grow in death of Black man outside Milwaukee hotel as GOP convention approaches. D'Vontaye Mitchell's death on June 30 has become the most recent flashpoint in how the ...
Objective To explore the perception of good death of patients with end-stage cancer by nurses in the oncology department. Method In the study we used a phenomenological approach and semi-structured interviews. A total of 11 nurses from the oncology department of a Grade A hospital in Taizhou were interviewed on the cognition of good death from July 1 to September 30, 2022. Colaizzi's ...
Carol Bongiovi died on Tuesday, July 9, at 83. Jon Bon Jovi is mourning the loss of his mother Carol Bongiovi who died on Tuesday, July 9, at 83, according to an obituary provided by the rock star ...
12 min. Death of a Salesman is Arthur Miller's multiple award-winning stage play that explores such ideas as American Dream and family. Our writers have prepared a list of topics and tips on writing the Death of a Salesman thesis statement, essay, or literary analysis. Table of Contents.
Michigan Gov. Gretchen Whitmer said Wednesday that it "wouldn't hurt" for President Biden to take a cognitive test. Whitmer acknowledged that the assessment would be a good idea in an ...