Abstract
Context
With the aging of our population, almost one in five adults, or 19% of the population, will be over the age of 65 years by 2030. Many persons have expressed concern about the inadequate preparation of hospitals to provide high value end-of-life care for the current and anticipated population of older adults.
Objectives
The purpose of this study was to explore the perceptions of nurse executives about the provision of end-of-life care in the hospital setting.
Methods
We conducted a pilot, descriptive, naturalistic, qualitative study using in-person interviews to capture nurse executives’ understandings, beliefs and perceptions of end-of-life care in their facilities.
Results
Data were collected from 10 nurse executives. We identified five major factors, three barriers and two facilitators, in their descriptions of provision of end-of-life care provided in the hospital: 1) communication inadequacies, 2) education inadequacies, 3) hospital system constraints, 4) hospice services availability, and 5) nurse executive advocacy.
Conclusion
These findings highlight the need for interventions that focus on improving communication at the bedside and in transitions of care, enhancing educational interventions, and developing patient-centered care systems, which translate into a higher quality end-of-life experience for patients and their family members. Nurse executives are currently an underutilized resource in end-of-life care but are poised to be able to champion innovative models and a culture of change that integrates high-value care for patients with serious and chronic illnesses.
Keywords: End of life, hospital, nurse, executive, perceptions, communication, constraints, hospice, education
Introduction
Concern has been raised over the preparation of hospitals to provide high value end-of-life care for the current and anticipated population of older adults (1–6). Government statistics estimate that by the year 2030, almost one in five adults will be over the age of 65 years (7). As people age, they typically develop one or more chronic illnesses. These chronically ill patients often have uncertain prognoses and poorly predictable disease trajectories (8–10). Our current health care system is acute and episodic based, and frequently fails to address the needs of patients with serious chronic illnesses (5,11). Many patients require care beyond that provided by physician office visits and home health services, resulting in frequent hospitalizations and long-term care (12).
A report by the Institute of Medicine indicated that approximately 90% of patients wish to end their lives comfortably at home, surrounded by family and friends (13–16). However, the reality is that approximately 56% of adults die in acute care hospitals (17) and 19% die in long-term care facilities, with many receiving aggressive medical treatments by default up to the point of death (17–21). Thus, many do not achieve their wish to end their lives in the manner and place of their choice. There are major barriers to providing effective end-of-life care, including 1) lack of communication among health care providers, patients and families, 2) a focus on cure and technology, and 3) unrealistic patient and family expectations (22–24). However, very little is known about a key stakeholder group, nurse executives, who assist in setting policies that affect the provision of end-of-life care in the acute care settings. A recent series of studies concluded that “A proactive presence of senior management is integral in implementing systematic change in hospital-based end-of-life care,” and improved end of life care will require strategic planning, community education, and evaluation of policies and procedures (25,26). Nurse executives are key to this issue because of their considerable “administrative knowledge, clinical experience, and authority to effect change” (27) in the hospital setting. However, despite the extensive medical and nursing literature on end-of-life care, little is known about nurse executives’ perceptions of the provision of end-of-life care in hospitals. This study, therefore, explored the views of nurse executives about the provision of end-of-life care in the hospital setting.
Methods
Research Design
We conducted a descriptive, naturalistic (28), qualitative study using in-person interviews to capture nurse executives’ understandings, beliefs and perceptions of end-of-life care in the hospital setting. Qualitative methods allowed us to explore nurse executives’ opinions and experiences more fully than might be obtained by other approaches.
Overview and Setting
We recruited experienced nurse executives within Arkansas. Both University of Arkansas and Veterans Administration institutional review board approvals were obtained prior to initiation of the study. We also obtained written consent from participants and addressed privacy protection with the participants prior to conducting the interviews.
Participant Recruitment
In consultation with qualitative research experts from the fields of health services and nursing, we conducted purposive sampling using chain referral sampling to identify high-level nurse executives who were knowledgeable about care provided in the hospital setting. To be included, participants had to be English-speaking and a high-level nurse executive.
Data Collection
An interview guide was developed based on review of the literature and consultation with qualitative research experts (J.C.M. and J.E.K.). We pre-tested the guide with two nurse executives and determined that the questions were understandable and answerable. The interviews were conducted by the first author (K.K.G.) face-to-face in participants’ facilities. Interviews began with a global question about the nurse executives’ perceptions of the provision of end-of-life care currently, followed by probes about ideas, experiences, and knowledge of end-of-life care (28). Interviews lasted 1.0–2.5 hours and were audio-recorded, transcribed verbatim, and verified for accuracy. Each nurse executive received a $25 gift card for participation.
Data Analysis
We entered each transcript into Atlas-ti (version 5.2, Scientific Software Development, Berlin, Germany), a text-based data management program that allows data labeling and sorting by identified variables. The data were coded using content analysis (28) with constant comparison technique (29). After the first author (K.K.G.) coded the initial three interviews, developed definitions for each code, and prepared a preliminary codebook, the fourth author (J.E.K.) reviewed the transcripts and codebook. Emerging codes and coding differences were discussed until consensus was reached. The first and fourth authors then coded the remaining interviews by aggregating similar narratives, forming categories from the aggregates, and developing overarching themes that represented the beliefs and understandings of the nurse executives. After ten interviews, we identified considerable repetition of data, signifying data saturation (30).
Several techniques were used to maximize the validity and reliability of the data, following guidelines for trustworthiness for qualitative studies (31). We enhanced dependability through use of one interviewer and one interview guide for all interviews. Additionally, we used verbatim transcriptions followed by thorough review of the transcripts against the recorded interviews. The first author enhanced credibility and confirmability by keeping a detailed audit trail of coding and theoretical decisions and reaching consensus with the fourth author. Unedited examples of narrative were used to validate the findings. Results of the coding exercise yielded strong agreement (84%).
Results
Sample
Our final sample comprised 10 high-level nurse executives in Arkansas. Nurse executives in this study had a median and average age of 52 and 51.2 years, respectively, with nine of the 10 having a master’s degree (with one nurse executive pursuing a PhD) and one unspecified. They had executive roles in a hospital setting that ranged from vice-president of patient care services to chief nursing officer to nurse executive officer. These nurse executives were in charge of nursing operations in hospitals with a median bed number of 301 but ranged from approximately 20 to over 500 beds. Hospitals were located in communities with a median population size of 55,334. Because of concerns about inadvertent disclosure of the nurse executives’ identity, no further detailed information about hospitals and locations could be provided.
Factors Identified as Barriers to End-of-Life Care in the Hospital Setting
All nurse executive interviewees discussed inadequacies in communication among physicians, patients, their families, and bedside nurses. The following case described by a nurse executive illustrates what she faced in her role as patient, family and bedside nurse advocate.
[W]e had one sister that was here with [her] mom. [This sister] thought we needed to resuscitate [her] and “do everything.” But the “living will said no” and the doctor hadn’t written an order. Another sister on the phone, who was a nurse practitioner, was saying no, “she’s got a living will; we don’t want to do all this.” So you’ve got one sister saying don’t do everything, one sister saying do everything, a piece of paper saying don’t do everything and no order. We ended up having to call a code to intubate her. We did not have an order. The nurses on the floor get in trouble from the doctor. He’s saying “why would you do that, she’s terminal, she’s got cancer, you’ve got a living will.” Well, where were you at? Write an order! You know if you’d just looked at the living will and talked to that daughter and written us an order we wouldn’t be where we’re at, but anyhow. [….] I say that’s a common thread. (Interview 7)
Communication Inadequacies in the Provision of End-of-Life Care
Nurse executives noted that a lack of communication among multiple treating physicians for complex medical conditions predominated. This resulted in a lack of coordination and communication with the patient and his or her family resulting in a failure to discuss the patient’s overall health status and prognosis.
Almost never are they (physicians) talking together, that just does not happen…there’s usually not one physician that’s giving them the whole picture….and that causes more confusion and resource utilization… (Interview 5)
Although hospitals are required to provide patients with information and the option to complete an advance directive, they characterized most advance directives as too vague and not specific enough to direct medical care decisions.
I think somehow knowing people’s wishes more…before they get in a compromised state…because you can sign a piece of paper and we know that they signed that piece of paper…but if we had more knowledge about really what the patient’s wishes were…I think that we would go to bat for them more. (Interview 4)
The nurse executives repeatedly stated effective communication would consist of raising patients’ awareness about the seriousness of their medical conditions, discussing options for treatment, assisting them in making difficult treatment decisions, and promoting use of appropriate health services. They also stated that they felt that most health care providers did not receive sufficient training in initiating and discussing challenging and difficult topics such as end-of-life planning. The participants in our study perceived that the common occurrence of delaying, or deferring to other health care providers, discussions about end-of-life goals of care and treatment decisions influenced the transitions in end-of-life care by making that transition abrupt, laden with conflict or likely not to occur at all.
Education Inadequacies for Provision of End-of-Life Care
All of the participants in this study indicated a need for more effective education for all disciplines and at all levels to address the unique needs patients have at the ends of their lives. Specifically, they spoke more of the educational needs of bedside nurses and nurse executives, given their experience. One nurse executive noted a need for new treatment models based on patient-centered care for providing end-of-life care in the hospital setting, that bedside nurses and nurse executives, as well as other health care providers, needed to be prepared to provide care that is patient centered.
To recognize what their instincts are telling them and to feel comfortable in going outside the norm or expected, to bend rules, if you will, to be less rigid around policy…And you think of things like visiting hours, you think of things like pets, you think of those things that can bring comfort to a patient or family and to take those risks and say why not. Why can’t we do those things? (Interview 8)
Some nurse executives stated that having a mentoring system for bedside nurses (and other health professionals) could be helpful, but noted that end-of-life care is difficult to teach because there are few universal interventions.
I think that’s why it’s so difficult to teach because there’s no one right way to do it or to act….it is about being open to the situation, open to the suggestions of both the patient, if able, and the family and being open to all possibilities, even those that are somewhat unusual. (Interview 6)
The nurse executives identified training to empower bedside nurses, and other health care providers, to actively listen to patients, encouraging questions, and to being receptive when patients are ready to talk about the end of life. They also indicated that all health care providers, but especially bedside nurses, need to know how to establish goals with a patient. They felt that end-of-life training should be offered as an essential component of curriculum for all upcoming health care workers and provided to the current health care workforce through continuing education. A few of the participants in our study suggested a mentoring program that demonstrates communication techniques, which might be an effective method of establishing these skills among both new and experienced health care providers.
Hospital System Constraints for the Provision of End-of-Life Care
All nurse executives acknowledged that acute care hospitals have and continue to play a significant role for patients at the end of life. However, current resource and financial constraints were characterized as major barriers to providing end-of-life care.
You know, the hospital is not the place anymore…It’s not the place for having time to make those kinds of decisions or, you know, to provide palliative care. It just doesn’t, you know we’re all under such pressure for so many reasons to get people in and get them out. And then the next level of care, you know unless it’s been discussed previously… a lot of patients and families are not ready for that. And, you know, you feel like you’re pushing them out the door while they’re dragging their feet and not wanting to go. It’s just not very satisfactory. (Interview 5)
Staffing is another issue that participants felt impacted end-of-life care planning and support. They indicated that shorter hospital stays mean that nurses, as well as other health care providers, have much less time to interact with patients and less time to develop a relationship that supports discussion of goals and communication about sensitive topics such as end-of-life issues.
I don’t have enough staff at any level currently with financial constraints to be able to say, you know, go in there and spend two hours with that patient and their family and do what we were taught to do in nursing school. (Interview 1)
Individualized care planning in light of end-of-life decisions seemed to also concern the nurse executives interviewed:
The plan of care is meant to be interdisciplinary obviously and we’re lucky if we can get nursing, nutrition services, RT, PT maybe to all at least look at it, initial it, have some awareness. But physicians, have no, they have no, at least in a community hospital, no involvement whatsoever. And the plan is pretty cursory and it’s really supposed to be individualized, but it’s really not, very little and just doesn’t work well. And nurses hate it, everybody hates doing them. You know, I thought for a long, long time that we need to find a way to make that more meaningful against that global, I want the global picture. Where is the patient going? How long do we think it’s going to take? What do we have to do to get there? (Interview 6)
Despite attempts at end-of-life care planning in the hospital with hospice or other resources, nurse executives perceived a terminally ill person’s discharge to home as potentially difficult or virtually impossible if symptoms were difficult to manage (e.g., pain). Caregiver stress or burnout and cultural barriers to dying in the home added to the difficulties. Interestingly, nurse executives identified similar barriers when discussing discharge to nursing homes:
I think that we have come a long ways…but I don’t think that we are there yet… You know our nursing homes too, they need a lot of education…I don’t think they feel comfortable with end-of-life care either. So many times they move that end-of-life care from their residential facility into the hospital, when it doesn’t have to be moved into the hospital. (Interview 4)
However, one participant in this study, from a smaller, rural hospital indicated that providing end-of-life care was an important service that her hospital provided in their community and significantly differed when compared to larger, more urban hospitals. For example, she indicated that a substantial portion of their revenue included care for patients at the end of life.
We don’t have internists. We don’t have a lot of specialists…Our inpatient basis is post-operative stuff from surgery and then whatever our family practice admits. We’re happy to take end-of-life care patients because it’s something that… if we can get them on hospice at least we’ll get some payment. (Interview 9)
She indicated that end-of-life care options for patients in rural areas are usually limited to care in the home or a long-term care facility. She stated that long-term care facilities may not able to provide areas for constant attendance by family members. She also stated that if a patient has difficult-to-control or distressing symptoms, the care providers in long-term care or the home may find it difficult to make rapid and frequent adjustments of medications as can occur in the hospital setting.
Factors Identified as Facilitators for End-of-Life Care
Some interviewees discussed aspects that facilitated end-of-life care such as improved access to hospice services and hospice training of health care providers. Additionally, they perceived that, in their role as a nurse executive, they should advocate for individualized patient-centered end-of-life care.
Hospice Services for Provision of End-of-Life Care
Greater accessibility to hospice services was identified by four of the participants as a positive factor for improving end-of-life care in the hospital setting. One nurse executive stated:
We are better at getting hospice involved than again we were. We’ve had several educational things with hospice about when it’s appropriate to come to that level of care. There often is a sense of relief. That the family is getting, I think, really more support when we do that. And there’s a sense of relief from the nurses that we’re doing what’s right for the patient and family.
However, nurse executives indicated that despite this increased availability, many health care providers avoided or delayed discussions about goals of care and end-of-life care planning. They perceived this as related to the inadequate training that most health care providers obtain at both the trainee level and continuing education level. They perceived that many of these health care providers delegated the responsibility for end-of-life care planning to other health care providers or settings. This resulted in hospice assistance or care not being requested until late in the course of treatment
Nurse Executives as Advocates for Provision of End-of-Life Care
The importance of the role of nurse executives as advocates was discussed by seven of the interviewees. Nurse executives explained that they problem solve and advocate for the patients by working with physicians, other administrators and staff to develop policies and procedures to facilitate care. Nurse executives felt that they played an important role in establishing and implementing these policies in the hospital setting especially in the area of end-of-life care, as many current hospital policies are often system oriented and not patient centered.
Well, I’m into breaking all those rules. I’ve done that before, broken a fair amount of rules to help people get whatever they need to give them some comfort…so. I guess that’s why I’m a nurse exec because you have to be able to be the one that’s in charge that can break the rules. (Interview 8)
Nurse executives also function as advocates for patients, their families and bedside nurses regarding communication about prognosis, treatment goals, and end-of-life care. They felt that communication inadequacies lead to more uncertainty, increased resource utilization, longer hospital stays and decreased satisfaction with the care provided.
Oh, the nurses feel definitely fragmented and periodically [nurse executives] have to run interference and get them all together to say who’s the main spokesperson and who’s having the talk with the family because each one of you is sending a different message and the family’s not getting it. (Interview 8)
Another nurse executive felt that administration was not involved soon enough with difficult end-of-life situations. She said:
I sometimes wish people would involve me sooner…because there is no doubt that one patient and family experience can turn an entire unit upside down… (Interview 3)
Nurse executives in this study saw themselves as advocates for patients, families, bedside nurses, other health care workers and the facilities they represent. Many of the nurse executives described their early nursing experience as a bedside nurse, or for some as a nursing assistant, and working their way up to their current executive position. They reported that they used these practical, in-the-trenches experiences to advocate for policies and procedures that address the unique needs of patients at the end of life and their families. They identified the nurse executive as a key individual in hospital administration who can advocate for high-value, patient-centered, end-of-life care in the hospital setting.
Discussion
This study explored nurse executives’ perceptions of the provision of end-of-life care in the hospital setting. Nurse executive participants, in this study, recognized several continuing unmet needs for patients at the end of life, such as communication deficits, educational needs and hospital system constraints that hamper the delivery of optimal end-of-life care in the hospital setting (18,32–34). The nurse executives perceived that the growing awareness and availability of hospice services may facilitate improving the care provided at the end of life. However, they, as others have found, identified that it also requires effective communication about end-of-life wishes and a referral which frequently occurs late in the care or did not occur at all (35–37). They also identified the nurse executive as an underutilized resource and advocate in the hospital setting for improving the provision of end-of-life care.
Without effective communication, patients and their families may not have enough time to accomplish life completion goals or accommodate to the impending loss. They also may suffer more anxiety, more depression or have more difficulty with bereavement (38). Inadequate communication may also impede health care providers’ abilities to address the full range of patients’ and their families’ needs at the end of life (9,39). They reported, as have others, that our health care system is designed to address acute, episodic illness and does not adequately address the needs of patients with serious, chronic illnesses with long-term care needs, including end-of-life planning (26). The nurse executives reported concerns that inadequate communication in the context of multiple health care providers across multiple transitions and levels of care, which also has been identified in recent literature (9), contributes to increased resource utilization and confusion for patients and their families.
Unfortunately, comprehensive and interdisciplinary training in end-of-life care and effective communication is rarely, or inadequately, provided in current curricula (40). Nurse executives indicated, as found in other studies (41–44), that this training should be offered as an essential component of curriculum for all upcoming health care workers and provided to the current health care workforce through mentoring and continuing education (45). The nurse executives acknowledged that it was generally difficult for bedside nurses, and other health care providers, to comprehend and manage these complex conditions and needs with less and less time spent with patients because of shortened hospital stays and increasing workloads. This lack of time reported in this study is consistent with other studies indicating that these pressures play a role in the provision of end-of-life care in the hospital setting (46). They also indicated that nurses have traditionally been patient advocates but because of uncertainty about what the patient may want, this advocacy from bedside nurses is less likely to occur.
This study has several limitations. Qualitative studies are inherently not designed to assess the prevalence of the identified themes but to describe how nurse executives perceived the current provision of end-of-life care in the hospital settings in which they work. This study was not designed to explore solutions to the perceptions that the nurse executives identified and further research is needed to investigate solutions to the barriers and facilitators they identified. In addition, future quantitative research is needed to address whether the perceptions described above are characteristic of more generalizable samples of nurse executives. The sample included high-level nurse executives and did not include other nursing administration that may play a bigger role in end-of-life care provision.
These findings highlight that nurse executives are currently an underutilized resource in end-of-life care but are poised to be able to champion innovative models and a culture of change that integrates high-value care for patients with serious and chronic illnesses (46). Our findings may be used to inform future interventions that engage nurse executives in their administrative role to accomplish the systemic change that is needed to improve the care provided to patients at the end of life in the hospital setting. These include a focus on improving communication at the bedside and in transitions of care, enhancing educational interventions and developing patient-centered care systems that translate into a higher quality end-of-life experience for patients and their family members.
Acknowledgments
This work was supported by the National Institute of Nursing: P20 NR009006 “Research Center for Individualized Nursing Interventions,” J. McSweeney, Principal Investigator. All authors listed have contributed sufficiently to the project to be included as authors, and all those who are qualified to be authors are listed in the author byline.
Footnotes
Publisher's Disclaimer: This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final citable form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.
Disclosures
To the best of our knowledge, no conflicts of interest, financial or other, exist.
References
- 1.Whelan CT, Jin L, Meltzer D. Pain and satisfaction with pain control in hospitalized medical patients: no such thing as low risk. Arch Intern Med. 2004;164(2):175–180. doi: 10.1001/archinte.164.2.175. [DOI] [PubMed] [Google Scholar]
- 2.Morrison RS, Ahronheim JC, Morrison GR, et al. Pain and discomfort associated with common hospital procedures and experiences. J Pain Symptom Manage. 1998;15(2):91–101. [PubMed] [Google Scholar]
- 3.Desbiens NA, Mueller-Rizner N, Connors AF, Jr., Wenger NS, Lynn J. The symptom burden of seriously ill hospitalized patients. SUPPORT Investigators. Study to Understand Prognoses and Preferences for Outcome and Risks of Treatment. J Pain Symptom Manage. 1999;17(4):248–255. doi: 10.1016/s0885-3924(98)00149-3. [DOI] [PubMed] [Google Scholar]
- 4.Knaus WA, Harrell FE, Jr., Lynn J, et al. The SUPPORT prognostic model. Objective estimates of survival for seriously ill hospitalized adults. Study to understand prognoses and preferences for outcomes and risks of treatments. Ann Intern Med. 1995;122(3):191–203. doi: 10.7326/0003-4819-122-3-199502010-00007. [DOI] [PubMed] [Google Scholar]
- 5.Nelson JE, Meier DE, Litke A, et al. The symptom burden of chronic critical illness. Crit Care Med. 2004;32(7):1527–1534. doi: 10.1097/01.ccm.0000129485.08835.5a. [DOI] [PubMed] [Google Scholar]
- 6.Eues SK. End-of-life care: improving quality of life at the end of life. Prof Case Manag. 2007;12(6):339–344. doi: 10.1097/01.PCAMA.0000300408.00325.1c. [DOI] [PubMed] [Google Scholar]
- 7.Department of Health and Human Services, Administration on Aging. [Accessed November 20, 2010];Aging statistics. 2010 Jun 30; Available from http://www.aoa.gov/aoaroot/aging_statistics/index.aspx.
- 8.Lynn J, Teno JM, Phillips RS, et al. Perceptions by family members of the dying experience of older and seriously ill patients. SUPPORT Investigators. Study to Understand Prognoses and Preferences for Outcomes and Risks of Treatments. Ann Intern Med. 1997;126(2):97–106. doi: 10.7326/0003-4819-126-2-199701150-00001. [DOI] [PubMed] [Google Scholar]
- 9.Reinke LF, Shannon SE, Engelberg R, et al. Nurses' identification of important yet under-utilized end-of-life care skills for patients with life-limiting or terminal illnesses. J Palliat Med. 2010;13(6):753–759. doi: 10.1089/jpm.2009.0423. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Gill TM, Gahbauer EA, Han L, Allore HG. Trajectories of disability in the last year of life. N Engl J Med. 2010;362(13):1173–1180. doi: 10.1056/NEJMoa0909087. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Nierman DM. A structure of care for the chronically critically ill. Crit Care Clin. 2002;18(3):477–491. doi: 10.1016/s0749-0704(02)00010-6. [DOI] [PubMed] [Google Scholar]
- 12.Hamel MB, Davis RB, Teno JM, et al. Older age, aggressiveness of care, and survival for seriously ill, hospitalized adults. SUPPORT Investigators. Study to Understand Prognoses and Preferences for Outcomes and Risks of Treatments. Ann Intern Med. 1999;131(10):721–728. doi: 10.7326/0003-4819-131-10-199911160-00002. [DOI] [PubMed] [Google Scholar]
- 13.Townsend J, Frank AO, Fermont D, et al. Terminal cancer care and patients' preference for place of death: a prospective study. BMJ. 1990;301(6749):415–417. doi: 10.1136/bmj.301.6749.415. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.McCormick WC, Inui TS, Deyo RA, Wood RW. Long-term care preferences of hospitalized persons with AIDS. J Gen Intern Med. 1991;6(6):524–528. doi: 10.1007/BF02598221. [DOI] [PubMed] [Google Scholar]
- 15.Higginson IJ, Sen-Gupta GJ. Place of care in advanced cancer: a qualitative systematic literature review of patient preferences. J Palliat Med. 2000;3(3):287–300. doi: 10.1089/jpm.2000.3.287. [DOI] [PubMed] [Google Scholar]
- 16.The George H. Gallup International Institute. Spiritual beliefs and the dying process. Princeton, NJ: The Nathan Cummings Foundation and Fetzer Institute; 1997. [Google Scholar]
- 17.Center for Disease Control, National Center for Health Statistics. [Accessed on July 27, 2010];New study of patterns of death in the United States. 1998 Available from http://www.cdc.gov/nchs/pressroom/98facts/98facts.htm.
- 18.Braun UK, McCullough LB. Preventing life-sustaining treatment by default. Ann Fam Med. 2011;9(3):250–256. doi: 10.1370/afm.1227. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Emanuel LL. Advance directives. Annu Rev Med. 2008;59:187–198. doi: 10.1146/annurev.med.58.072905.062804. [DOI] [PubMed] [Google Scholar]
- 20.Institute of Medicine. Approaching death: Improving care at the end of life. Washington, DC: National Academy Press; 1997. [Google Scholar]
- 21.Pritchard RS, Fisher ES, Teno JM, et al. Influence of patient preferences and local health system characteristics on the place of death. SUPPORT Investigators. Study to Understand Prognoses and Preferences for Risks and Outcomes of Treatment. J Am Geriatr Soc. 1998;46(10):1242–1250. doi: 10.1111/j.1532-5415.1998.tb04540.x. [DOI] [PubMed] [Google Scholar]
- 22.Oberst MT. Methodology in behavioral and psychosocial cancer research. Patients' perceptions of care. Measurement of quality and satisfaction. Cancer. 1984;53(10 Suppl):2366–2375. [PubMed] [Google Scholar]
- 23.Burton MV, Parker RW. Satisfaction in breast cancer patients with their medical and psychological care. J Psychosoc Oncol. 1994;12(2):41–61. [Google Scholar]
- 24.Rogers AE, Addington-Hall JM, Abery AJ, et al. Knowledge and communication difficulties for patients with chronic heart failure: qualitative study. BMJ. 2000;321(7261):605–607. doi: 10.1136/bmj.321.7261.605. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Cooney JP, Jr., Landers GM, Williams JM. Hospital executive leadership: a critical component for improving care at the end of life. Hosp Top. 2002;80(3):25–29. doi: 10.1080/00185860209598000. [DOI] [PubMed] [Google Scholar]
- 26.Morrison RS. Health care system factors affecting end-of-life care. J Palliat Med. 2005;8(Suppl 1):S79–S87. doi: 10.1089/jpm.2005.8.s-79. [DOI] [PubMed] [Google Scholar]
- 27.Nelson JE, Angus DC, Weissfeld LA, et al. End-of-life care for the critically ill: a national intensive care unit survey. Crit Care Med. 2006;34(10):2547–2553. doi: 10.1097/01.CCM.0000239233.63425.1D. [DOI] [PubMed] [Google Scholar]
- 28.Morse JM, Field PA. Qualitative research methods for health professionals. 2nd ed. London: Sage; 1995. [Google Scholar]
- 29.Glaser BG, Strauss AL. The discovery of grounded theory. 1st ed. Chicago: Aldine; 1967. [Google Scholar]
- 30.Speziale H, Carpenter D. Qualitative research in nursing. 3rd ed. Philadelphia: Lippincott; 2003. [Google Scholar]
- 31.Lincoln YS, Guba EG. Naturalistic inquiry. Beverly Hills, CA: Sage; 1985. [Google Scholar]
- 32.Singer PA, Martin DK, Kelner M. Quality end-of-life care: patients' perspectives. JAMA. 1999;281(2):163–168. doi: 10.1001/jama.281.2.163. [DOI] [PubMed] [Google Scholar]
- 33.Hawkins NA, Ditto PH, Danks JH, Smucker WD. Micromanaging death: process preferences, values, and goals in end-of-life medical decision making. Gerontologist. 2005;45(1):107–117. doi: 10.1093/geront/45.1.107. [DOI] [PubMed] [Google Scholar]
- 34.Hickman SE, Hammes BJ, Moss AH, Tolle SW. Hope for the future: achieving the original intent of advance directives. Hastings Cent Rep. 2005 Nov-Dec;:S26–S30. doi: 10.1353/hcr.2005.0093. (Spec No.) [DOI] [PubMed] [Google Scholar]
- 35.Herth K. Fostering hope in terminally-ill people. J Adv Nurs. 1990;15(11):1250–1259. doi: 10.1111/j.1365-2648.1990.tb01740.x. [DOI] [PubMed] [Google Scholar]
- 36.Koopmeiners L, Post-White J, Gutknecht S, et al. How healthcare professionals contribute to hope in patients with cancer. Oncol Nurs Forum. 1997;24(9):1507–1513. [PubMed] [Google Scholar]
- 37.Delvecchio MJ, Good MJ, Breen CM, Abernathy AP, Tulsky JA. American oncology and the discourse on hope. Cult Med Psychiatry. 1990;14:59–79. doi: 10.1007/BF00046704. [DOI] [PubMed] [Google Scholar]
- 38.Higginson I, Priest P. Predictors of family anxiety in the weeks before bereavement. Soc Sci Med. 1996;43(11):1621–1625. doi: 10.1016/s0277-9536(96)00062-7. [DOI] [PubMed] [Google Scholar]
- 39.Fried TR, Bradley EH, O'Leary JR, Byers AL. Unmet desire for caregiver-patient communication and increased caregiver burden. J Am Geriatr Soc. 2005;53(1):59–65. doi: 10.1111/j.1532-5415.2005.53011.x. [DOI] [PubMed] [Google Scholar]
- 40.Gauthier DM. Challenges and opportunities: communication near the end of life. Medsurg Nurs. 2008;17(5):291–296. [PubMed] [Google Scholar]
- 41.Reinke LF, Shannon SE, Engelberg RA, Young JP, Curtis JR. Supporting hope and prognostic information: nurses' perspectives on their role when patients have life-limiting prognoses. J Pain Symptom Manage. 2010;39(6):982–992. doi: 10.1016/j.jpainsymman.2009.11.315. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Jackson LD, Duffy BK. Health communication research. Westport, CT: Greenwood; 1998. [Google Scholar]
- 43.Science Panel on Interactive Communication and Health. Wired for health and wellbeing: The emergence of interactive health communication. Washington, DC: U.S. Department of Health and Human Services, U.S. Government Printing Office; 1999. [Google Scholar]
- 44.Krimshtein NS, Luhrs CA, Puntillo KA, et al. Training nurses for interdisciplinary communication with families in the intensive care unit: an intervention. J Palliat Med. 2011;14(12):1325–1332. doi: 10.1089/jpm.2011.0225. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 45.Back AL, Arnold RM, Tulsky JA, Baile WF, Edwards K. "Could I add something?": teaching communication by intervening in real time during a clinical encounter. Acad Med. 2010;85(6):1048–1051. doi: 10.1097/ACM.0b013e3181dbac6f. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 46.Siu AL, Spragens LH, Inouye SK, Morrison RS, Leff B. The ironic business case for chronic care in the acute care setting. Health Aff (Millwood) 2009;28(1):113–125. doi: 10.1377/hlthaff.28.1.113. [DOI] [PubMed] [Google Scholar]
