ArticlePloS one2017
Improved data validity in the Swedish Register of Palliative Care.
Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.
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.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
21 citing papers in PubMed.
- Regional cancer care leads´ and patient representatives´ perspectives on national governance and organisation of palliative cancer care.BMC health services research · 2026Article
- Evaluating quality of palliative care from the perspective of healthcare professionals in different care settings: development of the quality of palliative care questionnaire - staff.BMC palliative care · 2026Article
- Quality of end-of-life care among individuals with and without dementia: a Swedish registry-based study.BMC palliative care · 2026Article
- Pain at the end of life in patients with cancer: a population-based study on prevalence, relief, and the role of pain assessment.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2026Article
- What gets measured in palliative care? A review and synthesis of routine data collection in 16 countries.Health policy OPEN · 2025Review
- End-of-life care in hematological malignancies - a nationwide comparative study on the Swedish Register of Palliative Care.PloS one · 2025Observational
- Symptom assessment in the dying: family members versus healthcare professionals.BMJ supportive & palliative care · 2024Article
- Palliative care consultation in the last week of life and associated factors: a cross-sectional general population study.Palliative care and social practice · 2024Article
- Symptom Management and Support in Dying Patients with Cancer and Coronavirus Disease-19-A Register-Based Study.Journal of palliative care · 2023Article
- Article
- Benefits, for patients with late stage chronic obstructive pulmonary disease, of being cared for in specialized palliative care compared to hospital. A nationwide register study.BMC palliative care · 2021Article
- Symptoms, symptom relief and support in COVID-19 patients dying in hospitals during the first pandemic wave.BMC palliative care · 2021Article
- Dying from COVID-19 in nursing homes-sex differences in symptom occurrence.BMC geriatrics · 2021Article
- Were Clinical Routines for Good End-of-Life Care Maintained in Hospitals and Nursing Homes During the First Three Months of the Outbreak of COVID-19? A National Register Study.Journal of pain and symptom management · 2021Article
- Dying From COVID-19: Loneliness, End-of-Life Discussions, and Support for Patients and Their Families in Nursing Homes and Hospitals. A National Register Study.Journal of pain and symptom management · 2020Article
- Better quality of end-of-life care for persons with advanced dementia in nursing homes compared to hospitals: a Swedish national register study.BMC palliative care · 2020Article
- The economic burden of prostate cancer - a Swedish prevalence-based register study.BMC health services research · 2020Article
- Article
- Trends in Hospital-Based Specialty Palliative Care in the United States From 2013 to 2017.JAMA network open · 2019Article
- Quality of care for the dying across different levels of palliative care development: A population-based cohort study.Palliative medicine · 2018Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
introductionThe Swedish Register of Palliative Care (SRPC) is a national quality register that collects data about end-of-life care from healthcare providers that care for dying patients. Data are used for quality control and research. Data are mainly collected with an end-of-life questionnaire (ELQ), which is completed by healthcare staff after the death of a patient. A previous validity assessment of the ELQ showed insufficient validity in some items including symptom relief. The aim of this study was to examine the validity of the revised ELQ. MATERIALS AND
methodsData from 100 consecutive patients' medical records at two specialised palliative care units were used to complete new ELQs, which were then compared to the ELQ registrations from the SRPC for the same patients. The level of agreement was calculated for each ELQ item. To account for the possibility of the agreement occurring by chance, Cohen's kappa was calculated for suitable items. To examine the extent of registration mistakes when transferring the paper form to the web, the original paper versions of the ELQ filled out at the units were compared to data from the ELQs reported to the SRPC.
resultsLevel of agreement between ELQ registrations from the SRPC and the new ELQs based on the medical records varied between 0.55 and 1.00, where 24 items showed level of agreement above 0.80 and 9 items showed level of agreement below 0.80. Cohen's kappa with 95% confidence intervals was calculated for 24 items. The kappa values showed that two items had poor agreement, four fair agreement, 11 moderate agreement, five good agreement and two very good agreement. The level of agreement varied between 0.93 and 1.00 when comparing the ELQ registrations in the SRPC and the paper forms.
conclusionThe revised ELQ contains more items with high levels of agreement between registrations in the SRPC and notes in the patients' medical records when compared to the previous version. Validating issues around symptom assessment remains a challenge in our model of quality assessment.
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.