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Piloting a minimum data set for older people living in care homes in England: a developmental study

Gordon, Adam L. and Rand, Stacey and Crellin, Elizabeth and Allan, Stephen and Tracey, Freya and De Corte, Kaat and Lloyd, Therese and Brine, Richard and Carroll, Rachael E and Towers, Ann-Marie and Burton, Jennifer Kirsty and Akdur, Gizdem and Hanratty, Barbara and Webster, Lucy and Palmer, Sinead and Jones, Liz and Meyer, Julienne and Spilsbury, Karen and Killett, Anne and Wolters, Arne T and Peryer, Guy and Goodman, Claire (2024) Piloting a minimum data set for older people living in care homes in England: a developmental study. [Preprint] (doi:10.1101/2024.06.07.24308589) (The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided) (KAR id:108061)

The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided.
Official URL:
https://doi.org/10.1101/2024.06.07.24308589

Abstract

Background: We developed a prototype minimum data set (MDS) for English care homes, assessing feasibility of extracting data directly from digital care records (DCRs) with linkage to health and social care data.

Methods: Through stakeholder development workshops, literature reviews, surveys and public consultation we developed an aspirational MDS. We identified ways to extract this from existing sources including DCRs and routine health and social care datasets. To address gaps we added validated measures of delirium, cognitive impairment, functional independence and Quality of Life to DCR software. Following routine health and social care data linkage to DCRs, we compared variables recorded across multiple data sources, using a hierarchical approach to reduce missingness where appropriate. We reported proportions of missingness, mean and standard deviation (SD) or frequencies (%) for all variables.

Results: We recruited 996 residents from 45 care homes in three English Integrated Care Systems. 727 residents had data included in the MDS. Additional data were well completed (<35% missingness at wave 1). Competition for staff time, staff attrition, and software-related implementation issues contributed to missing DCR data. Following data linkage and combining variables where appropriate, missingness was reduced (<=4% where applicable).

Discussion: Integration of health and social care is predicated on access to data and interoperability. Despite governance challenges we safely linked care home DCRs to statutory health and social care datasets to create a viable prototype MDS for English care homes. We identified issues around data quality, governance, data plurality and data completion essential to MDS implementation going forward.

Item Type: Preprint
DOI/Identification number: 10.1101/2024.06.07.24308589
Refereed: No
Name of pre-print platform: medRxiv
Uncontrolled keywords: care homes; minimum dataset; data linkage; quality of life; digital care record
Subjects: H Social Sciences > HV Social pathology. Social and public welfare > HV59 Institutional care/home care
Divisions: Divisions > Division for the Study of Law, Society and Social Justice > School of Social Policy, Sociology and Social Research > Personal Social Services Research Unit
Divisions > Division for the Study of Law, Society and Social Justice > School of Social Policy, Sociology and Social Research > Centre for Health Services Studies
Depositing User: Stacey Rand
Date Deposited: 05 Dec 2024 09:43 UTC
Last Modified: 06 Dec 2024 11:09 UTC
Resource URI: https://kar.kent.ac.uk/id/eprint/108061 (The current URI for this page, for reference purposes)

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