Observational studyInternational journal for quality in health care : journal of the International Society for Quality in Health Care2021
Patient-reported outcome measurement of symptom distress is feasible in most clinical scenarios in palliative care: an observational study involving routinely collected data.
Observational study in International journal for quality in health care : journal of the International Society for Quality in Health Care, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 2 of them syntheses that pooled it.
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Who cites it
15 citing papers in PubMed, 2 syntheses or guidelines pooled it, 38 citations in OpenAlex.
- EASL position paper on palliative care in advanced chronic liver disease.JHEP reports : innovation in hepatology · 2026Guideline
- Use and Reporting of Patient-Reported Outcomes in Trials of Palliative Radiotherapy: A Systematic Review.JAMA network open · 2022Pooled it
- Frailty and the confidence to plan ahead: Decision-making self-efficacy and advance care planning among older adults receiving home healthcare.Palliative & supportive care · 2026Article
- Monitoring patients' symptom improvement in palliative care units using patient-reported outcomes: a multicenter prospective observational study.BMC palliative care · 2026Observational
- Development and validation of the distress inventory for altered bowel functioning in patients undergoing sphincter-preserving surgery for rectal cancer.Asia-Pacific journal of oncology nursing · 2025Article
- Psychometric properties of palliative care outcome measures: a multi-centre study.Journal of patient-reported outcomes · 2025Article
- Healthcare professionals' perspectives on assessing selected patient-reported outcome measures in specialist palliative care institutions: a multi-country mixed-methods study.BMC palliative care · 2025Article
- Development and validation of clinical implementation methods for patient-reported outcomes in Japanese multi-center palliative care units.Journal of patient-reported outcomes · 2024Article
- Utilising patient-reported outcomes for goal-directed therapy of hip fracture patients: a sequential controlled trial.BMJ open quality · 2023Article
- Considering community care in public health responses: A national study regarding palliative care during a prolonged coronavirus disease 2019 lockdown.Australian and New Zealand journal of public health · 2023Article
- Feasibility, use and benefits of patient-reported outcome measures in palliative care units: a multicentre observational study.BMC palliative care · 2023Observational
- Integrating patient- and caregiver-reported outcome measures into the daily care routines of specialised outpatient palliative care: a qualitative study (ELSAH) on feasibility, acceptability and appropriateness.BMC palliative care · 2022Article
- Observational
- Medical Cannabis: Toward a New Policy and Health Model for an Ancient Medicine.Frontiers in public health · 2022Article
- Home Versus Hospital Rehabilitation of Older Adults Following Hip Fracture Yields Similar Patient-Reported Outcome Measures.Inquiry : a journal of medical care organization, provision and financingObservational
Corrections and comments
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Authors and funding
7 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundImplementation of routinely collected patient-reported outcome measures (PROMs) ensures patients' priorities are at the forefront of care planning and helps to standardize approaches to quality improvement. In palliative care, barriers to PROMs are widely known but what are not understood are the clinical and care settings in which patients are more likely to report and when proxy reporting is needed.
objectiveTo examine the incidence of patient-reported symptom distress compared to the incidence of proxy reporting in palliative care and influencing factors.
methodsA national observational study using routinely collected PROMs data with influencing factors investigated by logistic regression modelling. Participants were patients with an advanced life-limiting illness receiving palliative care in an inpatient or a community healthcare setting in Australia.
resultsSixteen thousand one hundred and fifty-eight reports of symptom distress were collected from 1117 patients seen by 21 palliative care services. The majority of respondents were diagnosed with cancer (76%), were older (≥65 years, 72%) and had nominated English as their first language (88%). The majority of symptom distress reports were completed by patients (61%). The odds of a patient providing a self-report where grater when they were receiving community versus inpatient palliative care (odds ratio (OR): 3.0; 95% confidence interval (CI): 2.25-4.01), for patients diagnosed with malignant versus non-malignant disease (OR 1.7; 95% CI: 1.26-2.31), and for those who required an urgent change in their care plan versus those whose symptoms and problems were adequately managed (OR: 1.38; 95% CI: 1.04-1.83).
conclusionThree factors are associated with an increased likelihood of patient versus proxy reporting in palliative care: healthcare setting, diagnosis, and the acuity and urgency of the patient's clinical needs. PROMs are feasible in most clinical scenarios in palliative care, including when an urgent clinical response is required.
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