| Q45330320 | "A room full of chairs around his bed": being present at the death of a loved one in Veterans Affairs Medical Centers |
| Q34988154 | "Choice" in end-of-life decision making: researching fact or fiction? |
| Q38198147 | "Don't get weak in your compassion": bereaved next of kin's suggestions for improving end-of-life care in Veterans Affairs Medical Centers |
| Q34125239 | "I'm sitting here by myself ...": experiences of patients with serious illness at an Urban Public Hospital |
| Q36286182 | "They wouldn't pay attention": death without dignity |
| Q50875602 | "What bothers you the most?" Initial responses from patients receiving palliative care consultation. |
| Q43232378 | "You can't always get what you want"--or can you? |
| Q50628575 | 'Doubly deprived': a post-death qualitative study of primary carers of people who died in Western Australia. |
| Q47573135 | 'You only have one chance to get it right': A qualitative study of relatives' experiences of caring at home for a family member with terminal cancer. |
| Q33918030 | A "good death": perspectives of Muslim patients and health care providers. |
| Q38498621 | A Case Study of Hispanics and Hospice Care |
| Q92662954 | A brief, patient- and proxy-reported outcome measure in advanced illness: Validity, reliability and responsiveness of the Integrated Palliative care Outcome Scale (IPOS) |
| Q48360452 | A community-based model of rapid autopsy in end-stage cancer patients |
| Q37138870 | A dimensional analysis of the concept: good death of a child with cancer |
| Q48231058 | A good death from the perspective of palliative cancer patients. |
| Q53409264 | A good death: a qualitative study of patients with advanced AIDS. |
| Q40639068 | A measure of the quality of dying and death. Initial validation using after-death interviews with family members |
| Q74787277 | A model to guide patient and family care: based on nationally accepted principles and norms of practice |
| Q33650382 | A practical approach to the family that expects a miracle |
| Q47762075 | A question prompt list for patients with advanced cancer in the final year of life: development and cross-cultural evaluation |
| Q53037687 | A survey of the views of palliative care healthcare professionals towards referring cancer patients to participate in randomized controlled trials in palliative care. |
| Q86630760 | Acting with dedication and expertise: Relatives' experience of nurses' provision of care in a palliative unit |
| Q93331907 | Advance Care Planning: Contemporary Issues and Future Directions |
| Q34282548 | Advance directives and establishing the goals of care |
| Q47752851 | Advanced cancer patients' reported wishes at the end of life: a randomized controlled trial |
| Q44813030 | Advocating and educating for spiritual screening assessment and referrals to chaplains |
| Q99724505 | After providing end of life care to relatives, what care options do family caregivers prefer for themselves? |
| Q81622710 | Aggressiveness of care in a prospective cohort of patients with advanced NSCLC |
| Q92666114 | An EAPC white paper on multi-disciplinary education for spiritual care in palliative care |
| Q36193365 | Appropriate and inappropriate care in the last phase of life: an explorative study among patients and relatives |
| Q44252353 | As death approaches: a retrospective survey of the care of adults dying in Alice Springs Hospital |
| Q37951881 | Assessing quality of care for the dying: the development and initial validation of a postal self-completion questionnaire for bereaved relatives |
| Q36315803 | Association between physicians' beliefs and the option of comfort care for critically ill patients |
| Q34758350 | Association between the Medicare hospice benefit and health care utilization and costs for patients with poor-prognosis cancer |
| Q40633704 | Associations Between End-of-Life Cancer Care Patterns and Medicare Expenditures |
| Q47609738 | Becky's legacy: personal and professional reflections on loss and hope |
| Q89278303 | Beyond the bucket list: Unfinished and business among advanced cancer patients |
| Q44494868 | Breaking bad news about transitions to dying: a qualitative exploration of the role of the District Nurse. |
| Q61797232 | Breaking silence: a survey of barriers to goals of care discussions from the perspective of oncology practitioners |
| Q40336767 | Breathlessness in cancer and chronic obstructive pulmonary disease: using a qualitative approach to describe the experience of patients and carers. |
| Q51546138 | Burden of Transitions After Invasive Mechanical Ventilation for U.S. Individuals with Severe Chronic Obstructive Pulmonary Disease: Opportunity to Prepare for Preference-Congruent End-of-Life Care? |
| Q48009848 | Cancer patient autonomy and quality of dying-a prospective nationwide survey in Taiwan |
| Q35256731 | Care of the human spirit and the role of dignity therapy: a systematic review of dignity therapy research |
| Q48703765 | Care planning for pressure ulcers in hospice: the team effect |
| Q34770442 | Caregiver evaluation of the quality of end-of-life care (CEQUEL) scale: the caregiver's perception of patient care near death |
| Q53250744 | Caregiving near the end of life: unmet needs and potential solutions. |
| Q48291103 | Centenarians preparing for the end of life? |
| Q33915884 | Challenges Facing Families at the End of Life in Three Settings |
| Q50602056 | Challenges in home-based palliative care in Norway: a qualitative study of spouses' experiences. |
| Q55662402 | Challenges in supporting lay carers of patients at the end of life: results from focus group discussions with primary healthcare providers. |
| Q30202757 | Clergy Views on a Good Versus a Poor Death: Ministry to the Terminally Ill |
| Q37122222 | Clergy-laity support and patients' mood during serious illness: a cross-sectional epidemiologic study |
| Q36902558 | Clinical review: the role of the intensivist and the rapid response team in nosocomial end-of-life care |
| Q91645762 | Closing the Gap in Hospice Utilization for the Minority Medicare Population |
| Q50134121 | Comfort in the last 2 weeks of life: relationship to accessing palliative care services |
| Q35068296 | Communication about cancer near the end of life |
| Q57212970 | Comparison of attitudes towards five end-of-life care interventions (active pain control, withdrawal of futile life-sustaining treatment, passive euthanasia, active euthanasia and physician-assisted suicide): a multicentred cross-sectional survey of |
| Q53070535 | Comparison of patient and family assessments of quality of life of terminally ill cancer patients in Japan. |
| Q41168049 | Comparison of preferences for end-of-life care among patients with advanced cancer and their caregivers: A discrete choice experiment. |
| Q36506576 | Concept analysis of good death in the Japanese community |
| Q92910873 | Conceptualization of a good end-of-life experience with dementia in Japan: a qualitative study |
| Q39375996 | Concerns of family members of patients receiving palliative sedation therapy |
| Q59103454 | Concordance between Experiences of Bereaved Relatives, Physicians, and Nurses with Hospital End-of-Life Care: Everyone Has Their “Own Truth” |
| Q47598809 | Confirmation of the "disability paradox" among hospice patients: preservation of quality of life despite physical ailments and psychosocial concerns |
| Q38534557 | Confronting Therapeutic Failure: A Conversation Guide |
| Q42640930 | Confronting death: perceptions of a good death in adults with lung cancer |
| Q39850432 | Connectedness in Community-Dwelling Older Adults |
| Q47317208 | Coping and Prognostic Awareness in Patients With Advanced Cancer |
| Q33834837 | Correlates of a good death and the impact of hospice involvement: findings from the national survey of households affected by cancer |
| Q92441355 | Costs and outcomes of advance care planning and end-of-life care for older adults with end-stage kidney disease: A person-centred decision analysis |
| Q46301933 | Couples therapy at end of life |
| Q85184253 | Critical Care Nurses' Perceptions of Obstacles, Supports, and Knowledge Needed in Providing Quality End-of-Life Care |
| Q34742763 | Cross-cultural similarities and differences in attitudes about advance care planning |
| Q37407477 | Cultural beliefs about a patient's right time to die: an exploratory study |
| Q101224595 | Current measures of distress may not account for what's most important in existential care interventions: Results of the outlook trial |
| Q35804316 | Death and dying from old people's point of view. A literature review |
| Q50576614 | Death at the Door of the Operating Room. |
| Q48030457 | Death with dignity from the perspective of the surviving family: a survey study among family caregivers of deceased older adults |
| Q35851036 | Decision support: helping patients and families to find a balance at the end of life |
| Q47147188 | Decision-making on therapeutic futility in Mexican adolescents with cancer: a qualitative study |
| Q36788419 | Defining a Good Death (Successful Dying): Literature Review and a Call for Research and Public Dialogue |
| Q34752682 | Defining and determining quality in end-of-life care |
| Q55168340 | Definition of Terms Used in Limitation of Treatment and Providing Palliative Care at the End of Life: The Indian Council of Medical Research Commission Report. |
| Q37396831 | Demographic profile and utilization statistics of a Canadian inpatient palliative care unit within a tertiary care setting. |
| Q74363341 | Desire for physician-assisted suicide: requests for a better death? |
| Q38230308 | Development and validation of a scale for the end of life caregiving appraisal |
| Q57494410 | Development of a Carer Support Needs Assessment Tool (CSNAT) for end-of-life care practice at home: A qualitative study |
| Q35786076 | Development of a prognostic model for six-month mortality in older adults with declining health |
| Q46423930 | Development of a supportive care measure for economic evaluation of end-of-life care using qualitative methods |
| Q93095708 | Development of the PC-7, a Quantifiable Assessment of Spiritual Concerns of Patients Receiving Palliative Care Near the End of Life |
| Q36163513 | Development of the Serious Illness Care Program: a randomised controlled trial of a palliative care communication intervention |
| Q44633473 | Differing management of people with advanced cancer and delirium by four sub-specialties |
| Q53260866 | Dignified dying: phenomenon and actions among nurses in India. |
| Q64105928 | Dignity Therapy Led by Nurses or Chaplains for Elderly Cancer Palliative Care Outpatients: Protocol for a Randomized Controlled Trial |
| Q40455170 | Discussing end-of-life issues with terminally ill cancer patients and their carers: a qualitative study. |
| Q57524673 | Dying Safely |
| Q39833898 | Dying means suffocating: perceptions of people living with severe COPD facing the end of life |
| Q42759428 | Dying on the streets. |
| Q35691469 | Dying on the streets: homeless persons' concerns and desires about end of life care |
| Q47565010 | Dying patients' need for emotional support and personalized care from physicians: perspectives of patients with terminal illness, families, and health care providers |
| Q27308027 | Dying well with reduced agency: a scoping review and thematic synthesis of the decision-making process in dementia, traumatic brain injury and frailty |
| Q30233285 | Dying with dignity: the good patient versus the good death |
| Q38121761 | Early integration of palliative care services with standard oncology care for patients with advanced cancer |
| Q38892901 | Early supportive medication use and end-of-life care among Medicare beneficiaries with advanced breast cancer |
| Q47613916 | Educating Aging Service Agency Staff About Discussing End-of-Life Wishes |
| Q92358910 | Effect of the Serious Illness Care Program in Outpatient Oncology: A Cluster Randomized Clinical Trial |
| Q91226595 | Effectiveness of spiritual care using spiritual pain assessment sheet for advanced cancer patients: A pilot non-randomized controlled trial |
| Q36854902 | Effects of a palliative care intervention on clinical outcomes in patients with advanced cancer: the Project ENABLE II randomized controlled trial. |
| Q36859399 | End of life care in chronic obstructive pulmonary disease: in search of a good death |
| Q34131336 | End of life care policy for the dying: consensus position statement of Indian association of palliative care |
| Q47424820 | End of life is a public health issue |
| Q33363026 | End-of-Life Care Intensity and Hospice Use: A Regional-level Analysis |
| Q39185434 | End-of-Life Care Matters: Palliative Cancer Care Results in Better Care and Lower Costs |
| Q59487291 | End-of-life care for ethnic minority groups |
| Q45331068 | End-of-life care for older cancer patients in the Veterans Health Administration versus the private sector |
| Q37857548 | End-of-life care in ICU: a practical guide |
| Q47401992 | End-of-life care in the critically ill geriatric population |
| Q50193585 | End-of-life care in the neonatal intensive care unit: applying comfort theory |
| Q53172828 | End-of-life care in two Norwegian nursing homes: family perceptions. |
| Q30409127 | End-of-life care pathways as tools to promote and support a good death: a critical commentary |
| Q46045353 | End-of-life care perspectives of patients and health professionals in an Indian health-care setting |
| Q34201626 | End-of-life care policy: An integrated care plan for the dying: A Joint Position Statement of the Indian Society of Critical Care Medicine (ISCCM) and the Indian Association of Palliative Care (IAPC). |
| Q33684137 | End-of-life care preferences and needs: perceptions of patients with chronic kidney disease |
| Q99563790 | End-of-life decision making in the context of chronic life-limiting disease: a concept analysis and conceptual model |
| Q37591329 | End-of-life experiences in adolescents dying with cancer |
| Q45249985 | End-of-life preferences: a theory-driven inventory |
| Q64970645 | End-of-life priorities of older adults with terminal illness and caregivers: A qualitative consultation. |
| Q37671486 | Engaging Patients With Advance Directives Using an Information Visualization Approach |
| Q36308334 | Engaging in patient decision-making in multidisciplinary care for amyotrophic lateral sclerosis: the views of health professionals |
| Q35075593 | Ethics and decision making in end stage lung disease |
| Q40542111 | Existential concerns of terminally ill cancer patients receiving specialized palliative care in Japan |
| Q35853872 | Exploring end of life priorities in Saudi males: usefulness of Q-methodology |
| Q39563012 | Factors Associated with Family Reports of Pain, Dyspnea, and Depression in the Last Year of Life |
| Q34626801 | Factors associated with discussion of care plans and code status at the time of hospital admission: results from the Multicenter Hospitalist Study |
| Q36997325 | Factors contributing to evaluation of a good death from the bereaved family member's perspective |
| Q37250293 | Factors important to patients' quality of life at the end of life |
| Q48463806 | Families' acceptance of near death: a qualitative study of the process for introducing end-of-life care |
| Q73749384 | Family caregiver knowledge of treatment intent in a longitudinal study of patients with advanced cancer |
| Q36440216 | Family decision making at end of life |
| Q34569195 | Family factors in end-of-life decision-making: family conflict and proxy relationship |
| Q50959526 | Family perceptions of prognosis, silence, and the "suddenness" of death. |
| Q36753967 | Feeling like a burden to others: a systematic review focusing on the end of life |
| Q34557395 | Finding common ground to achieve a "good death": family physicians working with substitute decision-makers of dying patients. A qualitative grounded theory study |
| Q39029677 | Finding peace in clinical settings: A narrative review of concept and practice |
| Q35159745 | Focus group interviews: a guide for palliative care researchers and clinicians |
| Q40435685 | Fostering coping and nurturing hope when discussing the future with terminally ill cancer patients and their caregivers. |
| Q46011750 | Functional impairment, race, and family expectations of death. |
| Q41516346 | Good death for children with cancer: a qualitative study |
| Q50784629 | Good death study of elderly patients with terminal cancer in Taiwan. |
| Q53412312 | Good deaths, bad deaths, and preferences for the end of life: a qualitative study of geriatric outpatients. |
| Q47721823 | Handling Challenges Inherent in the Hospice Chaplain Role |
| Q49967384 | Handling Stereotypes of Religious Professionals: Strategies Hospice Chaplains Use When Interacting with Patients and Families |
| Q45333569 | Health care providers' perceptions of spirituality while caring for veterans |
| Q53410511 | Homelessness and clinical ethics. |
| Q48057986 | How do Australian palliative care nurses address existential and spiritual concerns? Facilitators, barriers and strategies |
| Q31074083 | How should nations measure the quality of end-of-life care for older adults? Recommendations for an international minimum data set. |
| Q41126777 | How to implement quality indicators successfully in palliative care services: perceptions of team members about facilitators of and barriers to implementation |
| Q47572369 | Imagining the alternatives to life prolonging treatments: elders' beliefs about the dying experience |
| Q35216419 | Impaired communication capacity and agitated delirium in the final week of terminally ill cancer patients: prevalence and identification of research focus |
| Q30484407 | In their own words: patients and families define high-quality palliative care in the intensive care unit |
| Q48148335 | Informational needs of patients with metastatic breast cancer: what questions do they ask, and are physicians answering them? |
| Q28756636 | Integration of palliative care practices into the ongoing care of children with cancer: individualized care planning and coordination |
| Q35878602 | Internal medicine trainee self-assessments of end-of-life communication skills do not predict assessments of patients, families, or clinician-evaluators |
| Q35031370 | Interventions to encourage discussion of end-of-life preferences between members of the general population and the people closest to them - a systematic literature review |
| Q48017102 | Investigating communication in cancer consultations: what can be learned from doctor and patient accounts of their experience? |
| Q41406445 | Is it acceptable to video-record palliative care consultations for research and training purposes? A qualitative interview study exploring the views of hospice patients, carers and clinical staff |
| Q36440133 | Issues in psychotherapy with terminally ill patients |
| Q39957520 | La Belle Mort En Milieu Rural: A report of An Ethnographic study of the Good Death for Quebec Rural Francophones |
| Q89418771 | Late Transitions and Bereaved Family Member Perceptions of Quality of End-of-Life Care |
| Q40083635 | Learning About Dying and Living: An Applied Approach to End-of-Life Communication. |
| Q39243797 | Living with pleasure in daily life at the end of life: recommended care strategy for cancer patients from the perspective of physicians and nurses |
| Q38494326 | Making explicit the contention in hospice care |
| Q43015091 | Managing chronic diseases: end of life is more than death |
| Q33740569 | Materials to prepare hospice families for dying in the home |
| Q34988135 | Measurement of quality of care and quality of life at the end of life |
| Q35907175 | Measuring quality of dying in end-stage renal disease |
| Q53250849 | Measuring quality of life at the end of life: validation of the QUAL-E. |
| Q57728608 | Metaphors for ‘good’ and ‘bad’ deaths: A health professional view |
| Q36632720 | Moving toward peace: an analysis of the concept of a good death |
| Q46749589 | Myths and Systems: A Response to "'He Needs to Talk!': A Chaplain's Case Study of Nonreligious Spiritual Care". |
| Q54417869 | Nutrition and hydration in dying patients: the perceptions of acute care nurses. |
| Q48621137 | Older persons' ethical problems involving their health |
| Q47377615 | One size does not fit all for a good death. |
| Q96033754 | Optimal goal of management of delirium in end-of-life cancer care |
| Q42151898 | Outcome indicators in palliative care--how to assess quality and success. Focus group and nominal group technique in Germany |
| Q35641129 | Palliative care at the end of life: comparing quality in diverse settings |
| Q30400727 | Palliative care decision making among the elderly and family: a theoretical model |
| Q35646588 | Palliative critical care in the intensive care unit: A 2011 perspective |
| Q36654478 | Patient Home Visits: Measuring Outcomes of a Community Model for Palliative Care Education |
| Q53144187 | Patient awareness of prognosis, patient-family caregiver congruence on the preferred place of death, and caregiving burden of families contribute to the quality of life for terminally ill cancer patients in Taiwan. |
| Q46714856 | Patient-caregiver concordance in symptom assessment and improvement in outcomes for patients undergoing cancer chemotherapy |
| Q34353394 | Patient-focused, family-centered end-of-life medical care: views of the guidelines and bereaved family members |
| Q53308081 | Patients with advanced cancer and family caregivers' knowledge of health and community services: a longitudinal study. |
| Q45187280 | Patients' views on decision making in advanced cancer |
| Q73927602 | Perception of discomfort by relatives and nurses in unresponsive terminally ill patients with cancer: a prospective study |
| Q44701756 | Perceptions of nurses with regard to doctor-patient communication |
| Q60302119 | Period from Loss of the Ability to Access Toilets Independently to Death in End-Stage Cancer Patients |
| Q47782959 | Perspectives on death, dying and advance care planning from patients receiving haemodialysis |
| Q36668030 | Perspectives on spirituality at the end of life: a meta-summary |
| Q90030566 | Physician and Patient Characteristics Associated With More Intensive End-of-Life Care |
| Q47409289 | Physicians in Postgraduate Training Characteristics and Support of Palliative Sedation for Existential Distress |
| Q39006020 | Physicians' perceptions of suffering in people with dementia at the end of life |
| Q34088293 | Planning for the end of life |
| Q33732178 | Preferences for active and aggressive intervention among patients with advanced cancer |
| Q45329746 | Preferences for death and dying among veterans with chronic obstructive pulmonary disease |
| Q53221479 | Preferences of the Dutch general public for a good death and associations with attitudes towards end-of-life decision-making. |
| Q61624780 | Preparing for the End of Life |
| Q40592266 | Pressure Ulcer Prevention and Treatment in Hospices: A Qualitative Analysis |
| Q57071396 | Priorities of a "good death" according to cancer patients, their family caregivers, physicians, and the general population: a nationwide survey |
| Q35105897 | Qualitative methods in end-of-life research: recommendations to enhance the protection of human subjects |
| Q35539687 | Quality indicators for end-of-life care in the intensive care unit* |
| Q38391704 | Quality of death among hospice decedents: Proxy observations from a survey of community-dwelling adults in the contiguous United States |
| Q38825391 | Quality of death, rumination, and posttraumatic growth among bereaved family members of cancer patients in home palliative care. |
| Q92317812 | Quality of dying and death desired by residents of Kagawa Prefecture, Japan: a qualitative study |
| Q53288267 | Quality of dying in head and neck cancer patients: a retrospective analysis of potential indicators of care. |
| Q45821998 | Quality of dying in head and neck cancer patients: the role of surgical palliation |
| Q46461563 | Racial differences in perceptions held by caregivers of long-term ventilator patients at end of life |
| Q33828929 | Raising the bar for the care of seriously ill patients: results of a national survey to define essential palliative care competencies for medical students and residents |
| Q38790605 | Reconsidering long-term care in the end-of-life context in Japan |
| Q89305181 | Regional Practice Patterns and Racial/Ethnic Differences in Intensity of End-of-Life Care |
| Q36566616 | Relatives in end-of-life care--part 1: a systematic review of the literature the five last years, January 1999-February 2004. |
| Q51553813 | Reliability testing of the FAMCARE-2 scale: measuring family carer satisfaction with palliative care. |
| Q34988141 | Research design in end-of-life research: state of science |
| Q37150730 | Research participation by older adults at end of life: barriers and solutions |
| Q34210584 | Researching "good death" in a Hong Kong palliative care program: a clinical data-mining study. |
| Q42678606 | Respiratory practitioners’ experience of end-of-life discussions in COPD |
| Q46563170 | Responding to Requests Regarding Prayer and Religious Ceremonies by Patients Near the End of Life and Their Families |
| Q37638800 | Seriously ill patients' discussions of preparation and life completion: an intervention to assist with transition at the end of life |
| Q38571380 | Setting up a support group for children and their well carers who have a significant adult with a life-threatening illness |
| Q44315914 | Seymour et al. Palliative sedation: Improvement of guidelines necessary, but not sufficient: A reply |
| Q37506016 | Shared decision making and its role in end of life care |
| Q37353172 | Shared priorities for the end-of-life period |
| Q73261010 | Similarity and difference among standard medical care, palliative sedation therapy, and euthanasia: a multidimensional scaling analysis on physicians' and the general population's opinions |
| Q92141864 | Soothing the heart with music: A feasibility study of a bedside music therapy intervention for critically ill patients in an urban hospital setting |
| Q84623915 | Specialist palliative care home care support teams in Spain |
| Q46432414 | Spouses' effectiveness as end-of-life health care surrogates: accuracy, uncertainty, and errors of overtreatment or undertreatment. |
| Q48417829 | Staff opinions about the components of a good death in long-term care |
| Q36154887 | Statement on home care for patients with respiratory disorders |
| Q33836527 | Still Searching: A Meta-Synthesis of a Good Death from the Bereaved Family Member Perspective |
| Q79119188 | Strategies for recruiting patients into randomized trials of palliative care |
| Q59210645 | Strategies for the economic evaluation of end-of-life care: making a case for the capability approach |
| Q37006143 | Sustaining hope when communicating with terminally ill patients and their families: a systematic review |
| Q38945834 | Symptom burden in heart failure: assessment, impact on outcomes, and management. |
| Q35136945 | Symptom trends in the last year of life from 1998 to 2010: a cohort study. |
| Q38687350 | The "good death": An integrative literature review |
| Q39095276 | The Experience of Hospital Death |
| Q34788433 | The Japan HOspice and Palliative Care Evaluation study (J-HOPE study): study design and characteristics of participating institutions |
| Q37796563 | The Oncologist's Role in Care of the Dying Cancer Patient |
| Q33624876 | The Quality of Dying and Death Questionnaire (QODD): empirical domains and theoretical perspectives |
| Q52679961 | The State of the Science on Integrating Palliative Care in Heart Failure. |
| Q50285998 | The VOICE Study: Valuing Opinions, Individual Communication and Experience: building the evidence base for undertaking Patient-Centred Family Meetings in palliative care - a mixed methods study |
| Q88089821 | The Voice Is As Mighty As the Pen: Integrating Conversations into Advance Care Planning |
| Q39178095 | The doctor's role in helping dying patients with cancer achieve peace: a qualitative study |
| Q28274263 | The effect of the Liverpool Care Pathway for the dying: a multi-centre study |
| Q82937380 | The experience of being next of kin to an older person in the last phase of life |
| Q33854975 | The experience of palliative patients and their families of a family meeting utilised as an instrument for spiritual and psychosocial care: A qualitative study |
| Q46734879 | The factors affecting end-of-life decision-making by physicians of patients with intellectual disabilities in the Netherlands: a qualitative study |
| Q38619143 | The feasibility and acceptability of a chaplain-led intervention for caregivers of seriously ill patients: A Caregiver Outlook pilot study |
| Q35089336 | The final phase in acute myeloid leukaemia (AML). A study on bleeding, infection and pain |
| Q51023955 | The health impact of health care on families: a matched cohort study of hospice use by decedents and mortality outcomes in surviving, widowed spouses. |
| Q24614583 | The impact of advance care planning on end of life care in elderly patients: randomised controlled trial |
| Q42761513 | The importance and challenge of measuring family experience with end-of-life care in the ICU. |
| Q47592040 | The importance of good death components among cancer patients, the general population, oncologists, and oncology nurses in Japan: patients prefer "fighting against cancer". |
| Q38720176 | The importance of measuring customer satisfaction in palliative care |
| Q36091826 | The influence of spiritual beliefs and practices on the treatment preferences of African Americans: a review of the literature |
| Q47813726 | The meaning and experience of bereavement support: A qualitative interview study of bereaved family caregivers. |
| Q30343613 | The meaning that young Israeli adults ascribe to the least undesirable death. |
| Q35888217 | The need for safeguards in advance care planning |
| Q35805736 | The quality of medical care at the end-of-life in the USA: existing barriers and examples of process and outcome measures |
| Q45100807 | The quality of supportive care among inpatients dying with advanced cancer |
| Q43782201 | The reluctance to burden others as a value in end-of-life decision making: a source of inaccuracy in substituted judgment |
| Q43575995 | The social stratification of older adults' preparations for end-of-life health care |
| Q36632752 | The state of advance care planning: one decade after SUPPORT. |
| Q88500526 | Themes Addressed by Couples With Advanced Cancer During a Communication Skills Training Intervention |
| Q51937008 | Thoughts of patients with advanced heart failure on dying. |
| Q33840839 | To die, to sleep: US physicians' religious and other objections to physician-assisted suicide, terminal sedation, and withdrawal of life support |
| Q34581281 | Towards a standardized method of developing quality indicators for palliative care: protocol of the Quality indicators for Palliative Care (Q-PAC) study |
| Q37299559 | Treatment at the end of life |
| Q47249570 | Treatment preferences and advance care planning at end of life: the role of ethnicity and spiritual coping in cancer patients |
| Q40091026 | Trends in end-of-life cancer care in the Medicare program. |
| Q24646327 | Two Decades of Research on Euthanasia from the Netherlands. What Have We Learnt and What Questions Remain? |
| Q36924508 | Typology of end-of-life priorities in Saudi females: averaging analysis and Q-methodology |
| Q50588481 | Understanding the concept of a "good death" among bereaved family caregivers of cancer patients in Singapore. |
| Q46600336 | Understanding the continuum of palliative care for patients and their caregivers |
| Q39418585 | Urologist attitudes toward end-of-life care |
| Q54101836 | Using Bedside Rounds to Teach Communication Skills in the Internal Medicine Clerkship. |
| Q57962714 | Using Nominal Group Technique to investigate the views of people with intellectual disabilities on end-of-life care provision |
| Q50796083 | Using the LCP: bereaved relatives' assessments of communication and bereavement. |
| Q36870380 | Using the experiences of bereaved caregivers to inform patient- and caregiver-centered advance care planning |
| Q37326593 | Using the medical record to evaluate the quality of end-of-life care in the intensive care unit |
| Q51017419 | Validation of a New Measure of Concept of a Good Death |
| Q44902176 | Validation of a new measure of the concept of good death among Taiwanese children |
| Q39685552 | Views and preferences of low-literate Hispanics regarding diabetes education: results of formative research |
| Q57404625 | Voices of the terminally ill: uncovering the meaning of desire for euthanasia |
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