Evidence map›Paper›PMID 36136796›Full record

ArticleGeriatrics (Basel, Switzerland)2022

The Prognostic and Discriminatory Utility of the Clinical Frailty Scale and Modified Frailty Index Compared to Age.

Ben Carter, Victoria L Keevil, Atul Anand, Christopher N Osuafor, Robert J B Goudie, Jacobus Preller, Matthew Lowry, Sarah Clunie, Susan D Shenkin, Kathryn McCarthy and 2 more

Abstract read
In one paragraph

Article in Geriatrics (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Observational
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Ben CarterDepartment of Biostatistics and Health Informatics, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London SE5 8AF, UK.ORCID 0000-0003-0318-8865
Victoria L KeevilDepartment of Medicine for the Elderly, Addenbrooke's Hospital, Cambridge University Hospitals NHS Foundation Trust, Hills Road, Cambridge CB2 0QQ, UK.ORCID 0000-0001-6148-0640
Atul AnandCentre for Cardiovascular Science, Queens Medical Research Institute, University of Edinburgh, Edinburgh EH16 4TJ, UK.ORCID 0000-0002-6428-4554
Christopher N OsuaforDepartment of Medicine for the Elderly, Addenbrooke's Hospital, Cambridge University Hospitals NHS Foundation Trust, Hills Road, Cambridge CB2 0QQ, UK.ORCID 0000-0002-3537-6521
Robert J B GoudieMedical Research Council Biostatistics Unit, University of Cambridge, Cambridge CB2 0SR, UK.ORCID 0000-0001-9554-1499
Jacobus PrellerDepartment of Acute Internal Medicine and Intensive Care, Cambridge University Hospitals NHS Foundation Trust, Cambridge CB2 0QQ, UK.
Matthew LowryGeriatric Medicine, Usher Institute, University of Edinburgh; Edinburgh EH16 4UX, UK.ORCID 0000-0001-8972-5136
Sarah ClunieGeriatric Medicine, Usher Institute, University of Edinburgh; Edinburgh EH16 4UX, UK.
Susan D ShenkinGeriatric Medicine, Usher Institute, University of Edinburgh; Edinburgh EH16 4UX, UK.ORCID 0000-0001-7375-4776
Kathryn McCarthyDepartment of Surgery and Care of the Elderly, Southmead Hospital, North Bristol NHS Trust, Bristol BS10 5NB, UK.
Jonathan HewittDivision of Population Medicine, Cardiff University, Cardiff CF10 3AT, UK.ORCID 0000-0002-7924-1792
Terence J QuinnInstitute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow G12 8TA, UK.ORCID 0000-0003-1401-0181

Funding

Medical Research Council MC_UU_00002/2Medical Research Council MR/T023902/1Medical Research Council MR/W000598/1
6 · The paper itself

Abstract

Background: There is no consensus on the optimal method for the assessment of frailty. We compared the prognostic utility of two approaches (modified Frailty Index [mFI], Clinical Frailty Scale [CFS]) in older adults (≥65 years) hospitalised with COVID-19 versus age. Methods: We used a test and validation cohort that enrolled participants hospitalised with COVID-19 between 27 February and 30 June 2020. Multivariable mixed-effects logistic modelling was undertaken, with 28-day mortality as the primary outcome. Nested models were compared between a base model, age and frailty assessments using likelihood ratio testing (LRT) and an area under the receiver operating curves (AUROC). Results: The primary cohort enrolled 998 participants from 13 centres. The median age was 80 (range:65−101), 453 (45%) were female, and 377 (37.8%) died within 28 days. The sample was replicated in a validation cohort of two additional centres (n = 672) with similar characteristics. In the primary cohort, both mFI and CFS were associated with mortality in the base models. There was improved precision when fitting CFS to the base model +mFI (LRT = 25.87, p < 0.001); however, there was no improvement when fitting mFI to the base model +CFS (LRT = 1.99, p = 0.16). AUROC suggested increased discrimination when fitting CFS compared to age (p = 0.02) and age +mFI (p = 0.03). In contrast, the mFI offered no improved discrimination in any comparison (p > 0.05). Similar findings were seen in the validation cohort. Conclusions: These observations suggest the CFS has superior prognostic value to mFI in predicting mortality following COVID-19. Our data do not support the use of the mFI as a tool to aid clinical decision-making and prognosis.

Indexed as

clinical frailty scaleCOVID-19frailtymodified frailty indexolder peopleprognosis

Identifiers

PMID36136796
PMCPMC9498791

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.