Comparing routine inpatient data and death records as a means of identifying children and young people with life-limiting conditions
- PMID: 28849716
- PMCID: PMC5788076
- DOI: 10.1177/0269216317728432
Comparing routine inpatient data and death records as a means of identifying children and young people with life-limiting conditions
Erratum in
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Corrigendum: Comparing routine inpatient data and death records as a means of identifying children and young people with life-limiting conditions.Palliat Med. 2020 Jul;34(7):968. doi: 10.1177/0269216320920164. Epub 2020 May 8. Palliat Med. 2020. PMID: 32383389 Free PMC article. No abstract available.
Abstract
Background: Recent estimates of the number of children and young people with life-limiting conditions derived from routine inpatient data are higher than earlier estimates using death record data.
Aim: To compare routine inpatient data and death records as means of identifying life-limiting conditions in children and young people.
Design: Two national cohorts of children and young people with a life-limiting condition (primary cohort from England with a comparator cohort from Scotland) were identified using linked routinely collected healthcare and administrative data.
Participants: A total of 37,563 children and young people with a life-limiting condition in England who died between 1 April 2001 and 30 March 2015 and 2249 children and young people with a life-limiting condition in Scotland who died between 1 April 2003 and 30 March 2014.
Results: In England, 16,642 (57%) non-neonatal cohort members had a life-limiting condition recorded as the underlying cause of death; 3364 (12%) had a life-limiting condition-related condition recorded as the underlying cause and 3435 (12%) had life-limiting conditions recorded only among contributing causes. In all, 5651 (19%) non-neonates and 3443 (41%) neonates had no indication of a life-limiting condition recorded in their death records. Similar results were seen in Scotland (overall, 16% had no indication of life-limiting conditions). In both cohorts, the recording of life-limiting condition was highest among those with haematology or oncology diagnoses and lowest for genitourinary and gastrointestinal diagnoses.
Conclusion: Using death record data alone to identify children and young people with life-limiting condition - and therefore those who would require palliative care services - would underestimate the numbers. This underestimation varies by age, deprivation, ethnicity and diagnostic group.
Keywords: Palliative medicine; cause of death; child; inpatients.
Conflict of interest statement
References
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- Jarvis S, Parslow RC, Carragher P, et al. How many children and young people with life-limiting conditions are clinically unstable? A national data linkage study. Arch Dis Child 2016, http://adc.bmj.com/content/102/2/131 - PubMed
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- Fraser LK, Miller M, Hain R, et al. Rising national prevalence of life-limiting conditions in children in England. Pediatrics 2012; 129: e923–e929. - PubMed
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- Fraser LK, Jarvis SW, Moran NE, et al. Children in Scotland requiring Palliative Care: identifying numbers and needs (The ChiSP Study). York: University of York, 2015.
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