Patients' reports of adverse events: a data linkage study of Australian adults aged 45 years and over

2017 ◽  
Vol 26 (9) ◽  
pp. 743-750 ◽  
Author(s):  
Merrilyn Margaret Walton ◽  
Reema Harrison ◽  
Patrick Kelly ◽  
Jennifer Smith-Merry ◽  
Elizabeth Manias ◽  
...  
2021 ◽  
Vol Publish Ahead of Print ◽  
Author(s):  
Jennifer Case ◽  
Merrilyn Walton ◽  
Reema Harrison ◽  
Elizabeth Manias ◽  
Rick Iedema ◽  
...  

2018 ◽  
Author(s):  
Francisco Schneuer ◽  
Elizabeth Milne ◽  
Sarra E. Jamieson ◽  
Gavin Pereira ◽  
Michele Hansen ◽  
...  

Author(s):  
Jia-Li Feng ◽  
Suzanne C. Dixon-Suen ◽  
Susan J. Jordan ◽  
Penelope M. Webb

2021 ◽  
pp. bmjspcare-2020-002708
Author(s):  
Katharina Diernberger ◽  
Xhyljeta Luta ◽  
Joanna Bowden ◽  
Marie Fallon ◽  
Joanne Droney ◽  
...  

BackgroundPeople who are nearing the end of life are high users of healthcare. The cost to providers is high and the value of care is uncertain.ObjectivesTo describe the pattern, trajectory and drivers of secondary care use and cost by people in Scotland in their last year of life.MethodsRetrospective whole-population secondary care administrative data linkage study of Scottish decedents of 60 years and over between 2012 and 2017 (N=274 048).ResultsSecondary care use was high in the last year of life with a sharp rise in inpatient admissions in the last 3 months. The mean cost was £10 000. Cause of death was associated with differing patterns of healthcare use: dying of cancer was preceded by the greatest number of hospital admissions and dementia the least. Greater age was associated with lower admission rates and cost. There was higher resource use in the urban areas. No difference was observed by deprivation.ConclusionsHospitalisation near the end of life was least frequent for older people and those living rurally, although length of stay for both groups, when they were admitted, was longer. Research is required to understand if variation in hospitalisation is due to variation in the quantity or quality of end-of-life care available, varying community support, patient preferences or an inevitable consequence of disease-specific needs.


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