Development and validation of multivariable mortality risk-prediction models in older people undergoing an interRAI home-care assessment (RiskOP).

Mortality Older people Risk prediction

Journal

EClinicalMedicine
ISSN: 2589-5370
Titre abrégé: EClinicalMedicine
Pays: England
ID NLM: 101733727

Informations de publication

Date de publication:
Dec 2020
Historique:
received: 09 06 2020
revised: 08 10 2020
accepted: 13 10 2020
entrez: 13 1 2021
pubmed: 14 1 2021
medline: 14 1 2021
Statut: epublish

Résumé

Currently, one-year survival of older people with complex co-morbidities is unpredictable. Identifying older adults with a reduced life expectancy will lead to more targeted care and better healthcare resource allocation. Development and validation of one-year and three-month mortality risks in people aged ≥65 years who had completed an International Resident Assessment Instrument-Home Care (interRAI-HC) assessment between July 2012 and March 2018. Data was split into development (90%) and validation data sets (10%). A multivariable logistic regression model using data from 108 interRAI questions across multiple domains was developed and validated using discrimination metrics and calibration curves. Variables each explaining at least 1% of the model were then used to develop and validate a parsimonious model. Subgroups by sex, age, ethnicity, and comorbidities were evaluated. There were 104,436 persons (60.2% female; mean age 82.1 years) in the study cohort of whom 20,972 (20.1%) died within one year. The full multivariable model had area under the curves (AUCs) of 0.778 to 0.795 in the 5 validation datasets and was well calibrated. After variable reduction a parsimonious model consisted of 16 variables and was well calibrated and the AUC remained high: 0.773 (0.769 to 0.777). The three-month parsimonious model comprised 22 variables and was well calibrated with an AUC of 0.843 (95%CI: 0.839 to 0.848). These community-based risk prediction models accurately predict mortality in older people with complex co-morbidities. They may contribute to both forecasting for policy making and clinical decision making regarding an individual's needs. The New Zealand Health Research Council.

Sections du résumé

BACKGROUND BACKGROUND
Currently, one-year survival of older people with complex co-morbidities is unpredictable. Identifying older adults with a reduced life expectancy will lead to more targeted care and better healthcare resource allocation.
METHODS METHODS
Development and validation of one-year and three-month mortality risks in people aged ≥65 years who had completed an International Resident Assessment Instrument-Home Care (interRAI-HC) assessment between July 2012 and March 2018. Data was split into development (90%) and validation data sets (10%). A multivariable logistic regression model using data from 108 interRAI questions across multiple domains was developed and validated using discrimination metrics and calibration curves. Variables each explaining at least 1% of the model were then used to develop and validate a parsimonious model. Subgroups by sex, age, ethnicity, and comorbidities were evaluated.
FINDINGS RESULTS
There were 104,436 persons (60.2% female; mean age 82.1 years) in the study cohort of whom 20,972 (20.1%) died within one year. The full multivariable model had area under the curves (AUCs) of 0.778 to 0.795 in the 5 validation datasets and was well calibrated. After variable reduction a parsimonious model consisted of 16 variables and was well calibrated and the AUC remained high: 0.773 (0.769 to 0.777). The three-month parsimonious model comprised 22 variables and was well calibrated with an AUC of 0.843 (95%CI: 0.839 to 0.848).
INTERPRETATION CONCLUSIONS
These community-based risk prediction models accurately predict mortality in older people with complex co-morbidities. They may contribute to both forecasting for policy making and clinical decision making regarding an individual's needs.
FUNDING BACKGROUND
The New Zealand Health Research Council.

Identifiants

pubmed: 33437945
doi: 10.1016/j.eclinm.2020.100614
pii: S2589-5370(20)30358-8
pmc: PMC7788437
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100614

Informations de copyright

© 2020 The Author(s).

Déclaration de conflit d'intérêts

All authors declare no conflicts of interest.

Références

Aust N Z J Public Health. 2016 Aug;40(4):349-55
pubmed: 27197797
JBI Database System Rev Implement Rep. 2017 Apr;15(4):1154-1208
pubmed: 28398987
J Gerontol A Biol Sci Med Sci. 2019 Jan 16;74(2):219-225
pubmed: 29514187
PLoS One. 2014 Jun 10;9(6):e99066
pubmed: 24914546
J Am Geriatr Soc. 2003 Jan;51(1):96-100
pubmed: 12534853
Lancet. 2015 Aug 8;386(9993):533-40
pubmed: 26049253
J Am Geriatr Soc. 2003 Feb;51(2):213-21
pubmed: 12558718
BMJ. 2017 May 23;357:j2099
pubmed: 28536104
J Am Geriatr Soc. 2018 May;66(5):976-981
pubmed: 29500822
J Am Coll Surg. 2018 May;226(5):784-795
pubmed: 29382560
Am J Gastroenterol. 2017 Sep;112(9):1431-1437
pubmed: 28762377
J Clin Epidemiol. 2015 Feb;68(2):134-43
pubmed: 25579640
JAMA. 2012 Jan 11;307(2):182-92
pubmed: 22235089
Eur J Intern Med. 2018 Nov;57:7-18
pubmed: 30017559

Auteurs

John W Pickering (JW)

Department of Medicine, University of Otago, Christchurch, New Zealand.

Rebecca Abey-Nesbit (R)

Department of Medicine, University of Otago, Christchurch, New Zealand.

Heather Allore (H)

Department of Biostatistics, Yale School of Public Health, and Department of Internal Medicine, School of Medicine, New Haven, Connecticut, USA.

Hamish Jamieson (H)

Department of Medicine, University of Otago, Christchurch, New Zealand; Burwood Hospital, Christchurch, New Zealand.

Classifications MeSH