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Comprehensive Geriatric Assessment Domains and Routine Inflammatory Indices in Relation to Clinical Frailty Scale-Defined Frailty: A Cross-Sectional Study in Hospital-Based Older Adults

A study · Healthcare (Basel, Switzerland) · Oct 27, 2026

What this means

BACKGROUND/Frailty in older adults is multidimensional, but the added value of routine blood-based inflammatory indices beyond comprehensive geriatric assessment is uncertain. In a hospital-based sample we examined how Clinical Frailty Scale (CFS)-defined frailty relates to geriatric domains and to inflammatory/prognostic indices, and whether these indices improve the cross-sectional classification of frailty beyond a core geriatric model.

A plain-English summary is on its way. Until then, this is the start of the authors' own summary.

Tested inNot stated
Who it was tested in
Not stated
Kind of research
A study

The science

Original title
Comprehensive Geriatric Assessment Domains and Routine Inflammatory Indices in Relation to Clinical Frailty Scale-Defined Frailty: A Cross-Sectional Study in Hospital-Based Older Adults.
Authors
Yıldız LM, Duman H, Tüfekçi D
Journal
Healthcare (Basel, Switzerland)
Published
Oct 27, 2026
Study type
Study

Abstract

Background

Frailty in older adults is multidimensional, but the added value of routine blood-based inflammatory indices beyond comprehensive geriatric assessment is uncertain. In a hospital-based sample we examined how Clinical Frailty Scale (CFS)-defined frailty relates to geriatric domains and to inflammatory/prognostic indices, and whether these indices improve the cross-sectional classification of frailty beyond a core geriatric model.

What they did

In this single-center, cross-sectional study, 284 of 300 consecutive records of adults aged 65 years or older who underwent comprehensive geriatric assessment at a family medicine-run healthy aging outpatient clinic in a university hospital were analyzed after data-quality checks. Frailty was defined as a CFS score of 5 or higher. Function, nutrition, cognition, mood, and mobility were assessed with Katz Activities of Daily Living (ADL), Lawton Instrumental Activities of Daily Living (IADL), Mini Nutritional Assessment (MNA), Mini-Cog, Geriatric Depression Scale-15, and Timed Up and Go (TUG). Five inflammatory/prognostic indices, including the platelet-to-lymphocyte ratio (PLR), were recalculated from same-day laboratory values. Logistic regression and receiver operating characteristic analyses compared a basic clinical model, a core geriatric model, and index-added models, with bootstrap assessment of calibration and optimism.

What they found

Frailty prevalence was 54.6% (95% confidence interval [CI]: 48.8-60.3). The area under the curve was 0.611 in the basic clinical model and 0.866 (95% CI: 0.821-0.907) in the core geriatric model (optimism-corrected 0.842; calibration slope 0.81). Because several geriatric measures overlap conceptually with CFS grading, reduced models were fitted: omitting Katz ADL, Lawton IADL, and Mini-Cog gave an area under the curve of 0.779 (95% CI: 0.721-0.833), while additionally omitting MNA and TUG gave 0.657 (95% CI: 0.592-0.719), close to the basic clinical model. Inflammatory indices provided no consistent incremental contribution; the small increase with PLR had a bootstrap confidence interval that included zero. In this sample, comprehensive geriatric assessment domains demonstrated a stronger association with same-time CFS-defined frailty classification than routine blood-based inflammatory indices. The findings describe contemporaneous classification in very old, hospital-based patients and do not establish prospective predictive value.

The authors' abstract, grouped under plain headings from its own section labels.

Read it on PubMed ↗

Yıldız LM, Duman H, Tüfekçi D Comprehensive Geriatric Assessment Domains and Routine Inflammatory Indices in Relation to Clinical Frailty Scale-Defined Frailty: A Cross-Sectional Study in Hospital-Based Older Adults. Healthcare (Basel, Switzerland). 2026. doi:10.3390/healthcare14203375. PMID: 42940420. https://pubmed.ncbi.nlm.nih.gov/42940420/

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