Collaborative data familiarisation and quality assessment: Reflections from use of a national dataset to investigate palliative care for Indigenous Australians
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Title
Collaborative data familiarisation and quality assessment: Reflections from use of a national dataset to investigate palliative care for Indigenous Australians
Authors
Keywords
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Journal
Health Information Management Journal
Volume -, Issue -, Pages 183335832090895
Publisher
SAGE Publications
Online
2020-03-27
DOI
10.1177/1833358320908957
References
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Related references
Note: Only part of the references are listed.- Delay in commencement of palliative care service episodes provided to Indigenous and non-Indigenous patients: cross-sectional analysis of an Australian multi-jurisdictional dataset
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- Phase of Illness in palliative care: Cross-sectional analysis of clinical data from community, hospital and hospice patients
- (2017) Harriet Mather et al. PALLIATIVE MEDICINE
- Data Quality in Electronic Health Records Research: Quality Domains and Assessment Methods
- (2017) Shelli L. Feder WESTERN JOURNAL OF NURSING RESEARCH
- Data quality and 30-day survival for out-of-hospital cardiac arrest in the UK out-of-hospital cardiac arrest registry: a data linkage study
- (2017) Sangeerthana Rajagopal et al. BMJ Open
- Physical Symptoms at the Time of Dying Was Diagnosed: A Consecutive Cohort Study To Describe the Prevalence and Intensity of Problems Experienced by Imminently Dying Palliative Care Patients by Diagnosis and Place of Care
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- Linking Data for Mothers and Babies in De-Identified Electronic Health Data
- (2016) Katie Harron et al. PLoS One
- Palliative Care Problem Severity Score: Reliability and acceptability in a national study
- (2015) Malcolm Masso et al. PALLIATIVE MEDICINE
- The REporting of studies Conducted using Observational Routinely-collected health Data (RECORD) Statement
- (2015) Eric I. Benchimol et al. PLOS MEDICINE
- Gaps in Indigenous disadvantage not closing: a census cohort study of social determinants of health in Australia, Canada, and New Zealand from 1981–2006
- (2014) Francis Mitrou et al. BMC PUBLIC HEALTH
- Palliative Care Phase: Inter-rater reliability and acceptability in a national study
- (2014) Malcolm Masso et al. PALLIATIVE MEDICINE
- Improving national hospice/palliative care service symptom outcomes systematically through point-of-care data collection, structured feedback and benchmarking
- (2014) David C. Currow et al. SUPPORTIVE CARE IN CANCER
- A Review of Data Quality Assessment Methods for Public Health Information Systems
- (2014) Hong Chen et al. International Journal of Environmental Research and Public Health
- Data Quality Assessment for Comparative Effectiveness Research in Distributed Data Networks
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- The quality of Indigenous identification in administrative health data in Australia: insights from studies using data linkage
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- Methods and dimensions of electronic health record data quality assessment: enabling reuse for clinical research
- (2012) N. G. Weiskopf et al. JOURNAL OF THE AMERICAN MEDICAL INFORMATICS ASSOCIATION
- False Alarms and Pseudo-Epidemics
- (2012) David A. Grimes et al. OBSTETRICS AND GYNECOLOGY
- Measuring Symptom Distress in Palliative Care: Psychometric Properties of the Symptom Assessment Scale (SAS)
- (2011) Samar M. Aoun et al. JOURNAL OF PALLIATIVE MEDICINE
- The Australian Palliative Care Outcomes Collaboration (PCOC) – measuring the quality and outcomes of palliative care on a routine basis
- (2010) Kathy Eagar et al. Australian Health Review
- Multiple imputation using chained equations: Issues and guidance for practice
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- Methodologies for data quality assessment and improvement
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- What is the impact of missing Indigenous status on mortality estimates? An assessment using record linkage in Western Australia
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