scholarly journals Why a Digitally Enabled Minimum Data Set for Older Adults in Care Homes Might Improve Population Health and Well-Being Outcomes

2019 ◽  
Vol 5 (3) ◽  
Author(s):  
Sally Fowler Davis
2018 ◽  
Vol 31 (2) ◽  
pp. 103-103

Narayan SW, Jamieson HA, Nishtala PS. Evaluation of the National Minimum Data Set for Neurological Conditions in Older Adults. Journal of Geriatric Psychiatry and Neurology. 2017; 30(6):331-336. doi: 10.1177/0891988717732154 In the above-referenced article, the corresponding author’s qualifications were incorrectly listed as BPharm, MPharm, PG DipClinPharm, PhD which is an overlap of another author’s qualifications. The online and print versions have been updated to reflect the correct qualification of the corresponding author as BPharm, MPharmPrac.


Author(s):  
Erin E. Gilbart ◽  
John P. Hirdes

RÉSUMÉAlors qu'il existe une importante documentation sur la relation entre le stress, le soutien social et le bien-etrê chez les aîné(e)s vivant dans la communauté, peu d'études ont examiné la population des institutions. Cette étude a utilisé les données d'enquêtes pilotes du MDS 2.0 de trois hôpitaux ainsi que d'autres enquêtes reliées au bien-être psychologique. On a constaté que les patients les plus engagés socialement avaient tendance à afficher des niveaux plus élevés de bien-être et cette tendance était encore plus frappante chez ceux qui jouissaient d'un meilleur état de santé. La douleur était un prédicteur important de la réduction du bien-être. Étant donné que le MDS 2.0 fournit une approche complète à l'identification des problèmes sociaux, psychologiques et physiques et à leur réponse chez les aîné(e)s vivant en institution, il peut entraîner des effets importants sur le bien-être si on l'utilise à l'appui de la prise de décision et des interventions cliniques.


2017 ◽  
Vol 30 (6) ◽  
pp. 331-336 ◽  
Author(s):  
Sujita W. Narayan ◽  
Hamish A. Jamieson ◽  
Prasad S. Nishtala

2001 ◽  
Vol 7 (3) ◽  
pp. 189-200 ◽  
Author(s):  
Robert J Buchanan ◽  
Suojin Wang ◽  
Chunfeng Huang ◽  
David Graber

This paper profiles nursing home residents with multiple sclerosis (MS) at the time of admission, including sociodemographic characteristics, health status measures, and treatments received. Admission assessments from the Minimum Data Set are used to create these profiles of residents with MS. There are 9013 admission assessments in the MDS for residents with MS between June 22, 1998 and January 17, 2000 analyzed for this study. Residents with MS are distinctly younger at admission than most nursing home residents, averaging 57.98 years of age. Recently admitted residents with MS are more physically dependent than other nursing home residents and tend to have limited range of motion and loss of voluntary movement. About one in three newly admitted residents with MS had some degree of impaired cognitive function. Over one third of residents with MS were depressed at admission, yet only 11.7% of recently admitted residents with MS were evaluated by a licensed mental health specialist. This prompts concern about the psychosocial well-being of MS residents in nursing homes.


2022 ◽  
Vol 22 (1) ◽  
Author(s):  
Massirfufulay Kpehe Musa ◽  
Gizdem Akdur ◽  
Sarah Brand ◽  
Anne Killett ◽  
Karen Spilsbury ◽  
...  

Abstract Background Care homes provide long term care for older people. Countries with standardised approaches to residents’ assessment, care planning and review (known as minimum data sets (MDS)) use the aggregate data to guide resource allocation, monitor quality, and for research. Less is known about how an MDS affects how staff assess, provide and review residents’ everyday care. The review aimed to develop a theory-driven understanding of how care home staff can effectively implement and use MDS to plan and deliver care for residents. Methods The realist review was organised according to RAMESES (Realist And Meta-narrative Evidence Synthesis: and Evolving Standards) guidelines. There were three overlapping stages: 1) defining the scope of the review and theory development on the use of minimum data set 2) testing and refining candidate programme theories through iterative literature searches and stakeholders’ consultations as well as discussion among the research team; and 3) data synthesis from stages 1 and 2. The following databases were used MEDLINE via OVID, Embase, CINAHL (Cumulative Index to Nursing and Allied Health Literature), ASSIA [Applied Social Sciences Citation Index and Abstracts]) and sources of grey literature. Results Fifty-one papers informed the development of three key interlinked theoretical propositions: motivation (mandates and incentives for Minimum Data Set completion); frontline staff monitoring (when Minimum Data Set completion is built into the working practices of the care home); and embedded recording systems (Minimum Data Set recording system is integral to collecting residents’ data). By valuing the contributions of staff and building on existing ways of working, the uptake and use of an MDS could enable all staff to learn with and from each other about what is important for residents’ care Conclusions Minimum Data Sets provides commissioners service providers and researchers with standardised information useful for commissioning planning and analysis. For it to be equally useful for care home staff it requires key activities that address the staff experiences of care, their work with others and the use of digital technology. Registration PROSPERO registration number CRD42020171323.


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