ArticleBMC palliative care2014
Bereaved family member perceptions of patient-focused family-centred care during the last 30 days of life using a mortality follow-back survey: does location matter?
Article in BMC palliative care, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03566732 (International Care Of the Dying Evaluation), which is not on this map. Cited by 22 papers, 1 of them a synthesis that pooled it.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
International Care Of the Dying Evaluation (CODE): Quality of Care for Cancer Patients as Perceived by Bereaved Relatives
Who cites it
22 citing papers in PubMed, 1 synthesis or guideline pooled it, 52 citations in OpenAlex.
- Dying in the hospital setting: A systematic review of quantitative studies identifying the elements of end-of-life care that patients and their families rank as being most important.Palliative medicine · 2015Pooled it
- Measuring End-of-Life Care: Development of a National Questionnaire for Bereaved Family Members.Healthcare (Basel, Switzerland) · 2026Article
- Patients' and relatives' perspectives on the quality of end-of-Life care in advanced cancer: From the final months to bereavement.PloS one · 2026Article
- Factors related to the quality of death and family satisfaction among cancer patients at home: an analysis using death certificate data and a national bereaved family survey.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2025Article
- Translation and cultural adaptation of the Chinese version of the International 'Care Of the Dying Evaluation' (CODE™) tool for assessing the quality of care for dying patients from the perspective of bereaved family members.BMC palliative care · 2025Article
- "Walk me through the final day": A thematic analysis study on the family caregiver experience of the Medical Assistance in Dying procedure day.Palliative medicine · 2024Article
- Navigation programs to support community-dwelling individuals with life-limiting illness: determinants of implementation.BMC health services research · 2024Article
- Cultural Adaption and Validation of the Arabic Version of the CANHELP Lite Bereavement Questionnaire.Journal of patient experience · 2024Article
- How do navigation programs address the needs of those living in the community with advanced, life-limiting Illness? A realist evaluation of programs in Canada.BMC palliative care · 2023Article
- Putting the Patient First: A Scoping Review of Patient Desires in Canada.Healthcare policy = Politiques de sante · 2021Article
- Cultural Adaptation and Validation of the Portuguese Version of the CANHELP Lite Bereavement Questionnaire.Healthcare (Basel, Switzerland) · 2020Article
- Unmet needs of patients with cancer in their last year of life as described by caregivers in a developing world setting: a qualitative study.BMC palliative care · 2020Article
- Dying in acute hospitals: voices of bereaved relatives.BMC palliative care · 2019Article
- Healthcare Received in the Last Months of Life in Portugal: A Systematic Review.Healthcare (Basel, Switzerland) · 2019Review
- Assessing quality of care for the dying from the bereaved relatives' perspective: Using pre-testing survey methods across seven countries to develop an international outcome measure.Palliative medicine · 2019Observational
- Feasibility of hospital-initiated non-facilitator assisted advance care planning documentation for patients with palliative care needs.BMC palliative care · 2018Article
- Achieving Goal-Concordant Care: A Conceptual Model and Approach to Measuring Serious Illness Communication and Its Impact.Journal of palliative medicine · 2018Review
- Organization-level principles and practices to support spiritual care at the end of life: a qualitative study.BMC palliative care · 2017Article
- Patients' perceptions of palliative care quality in hospice inpatient care, hospice day care, palliative units in nursing homes, and home care: a cross-sectional study.BMC palliative care · 2016Article
- Patients' perceptions of palliative care: adaptation of the Quality from the Patient's Perspective instrument for use in palliative care, and description of patients' perceptions of care received.BMC palliative care · 2015Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors at 3 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundImproving end-of-life care is an important international issue. Recently Nova Scotia researchers conducted a mortality follow-back survey to provide a population-based description of care provided to adults during their last 30 days of life as perceived by knowledgeable bereaved family members. Here we describe the relationship between the location where the decedent received the majority of care during their last 30 days and the informant's perception of the extent of unmet need, as defined by multiple domains of patient-focused, family-centred care.
methodDeath certificate identified informants (next-of-kin) of eligible adults who died between June 2009 and May 2011, in Nova Scotia, Canada were invited to participate in a telephone interview based on the After-Death Bereaved Family Member Interview. Whether or not the informant expressed unmet need or concerns for six patient-focused, family-centred care domains were assessed in relation to the location where the majority of care occurred during the decedent's last 30 days.
results1358 informants took part (25% response rate). Results of 1316 eligible interviews indicated home (39%) was the most common location of care, followed by long-term care (29%), hospital (23%) and hospital-based palliative-care units (9%). Unmet need ranged from 5.6% for dyspnea help to 66% for the emotional and spiritual needs of the family. Although the mean score for overall satisfaction was high (mean = 8.7 in 1-10 scale; SD 1.8), 57% were not completely satisfied. Compared to home, adjusted results indicated greater dissatisfaction with overall care and greater communication concerns in the hospital. Greater unmet need occurred at home for dyspnea. Less overall dissatisfaction and unmet need were expressed about care provided in long-term care facilities and hospital-based palliative-care units.
conclusionBereaved informants were generally highly satisfied with the decedent's care during their last 30 days but variations were evident. Overall, no one location stood out as exceptionally different in terms of perceived unmet need within each of the patient-focused, family-centred care domains. Communication in various forms and family emotional and spiritual support were consistently viewed as lacking in all locations and identified as targeted areas for impacting quality care at end of life.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.