Journal
BMC GERIATRICS
Volume 20, Issue 1, Pages -Publisher
BMC
DOI: 10.1186/s12877-020-01739-w
Keywords
Frailty; Frailty phenotype; Older adult; Medicare administrative data
Categories
Funding
- National Institute on Aging (NIA) [R01AG062713]
- Paul B. Beeson Clinical Scientist Development Award in Aging from NIA [K08AG051187]
- American Federation for Aging Research
- John A. Hartford Foundation
- Atlantic Philanthropies
- Harvard Translational Research in Aging Training Program [T32 AG023480]
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BackgroundCapturing frailty within administrative claims data may help to identify high-risk patients and inform population health management strategies. Although it is common to ascertain frailty status utilizing claims-based surrogates (e.g. diagnosis and health service codes) selected according to clinical knowledge, the accuracy of this approach has not yet been examined. We evaluated the accuracy of claims-based surrogates against two clinical definitions of frailty.MethodsThis cross-sectional study was conducted in a Health and Retirement Study subsample of 3097 participants, aged 65years or older and with at least 12-months of continuous fee-for-service Medicare enrollment. We defined 18 previously utilized claims-based surrogates of frailty from Medicare data and evaluated each against clinical reference standards, ascertained from a direct examination: a deficit accumulation frailty index (FI) (range: 0-1) and frailty phenotype. We also compared the accuracy of the total count of 18 claims-based surrogates with that of a validated claims-based FI model, comprised of 93 claims-based variables.Results19% of participants met clinical criteria for the clinical frailty phenotype. The mean clinical FI for our sample was 0.20 (standard deviation 0.13). Hospital Beds and associated supplies was the claims-based surrogate associated with the highest clinical FI (mean FI 0.49). Claims-based surrogates had low sensitivity ranging from 0.01 (cachexia, adult failure to thrive, anorexia) to 0.38 (malaise and fatigue) and high specificity ranging from 0.79 (malaise and fatigue) to 0.99 (cachexia, adult failure to thrive, anorexia) in discriminating the clinical frailty phenotype. Compared with a validated claims-based FI, the total count of claims-based surrogates demonstrated lower Spearman correlation with the clinical FI (0.41 [95% CI 0.38-0.44] versus 0.59 [95% CI, 0.56-0.61]) and poorer discrimination of the frailty phenotype (C-statistics 0.68 [95% CI, 0.66-0.70] versus 0.75 [95% CI, 0.73-0.77]).ConclusionsClaims-based surrogates, selected according to clinical knowledge, do not accurately capture frailty in Medicare claims data. A simple count of claims-based surrogates improves accuracy but remains inferior to a claims-based FI model.
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