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      Clinical clustering of eight orthostatic haemodynamic patterns in The Irish Longitudinal Study on Ageing (TILDA)

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          Abstract

          Background

          Orthostatic hypotension (OH) can be assessed with non-invasive continuous beat-to-beat haemodynamic monitoring during active stand (AS) testing; this yields large volumes of data outside the scope of the traditional OH definition. We explored clinical associations of different AS patterns in participants from Wave 1 of the Irish Longitudinal Study on Ageing.

          Methods

          AS patterns were generated based on three sequential binary systolic blood pressure features: drop ≥40 mmHg within 10 sec post-stand (“immediate deficit”), failure to return to within 20 mmHg of supine level at 40 sec after standing (“stabilisation deficit”) and drop ≥20 mmHg between >40 and 120 sec post-stand (“late deficit”). Eight AS groups resulted from combining the presence/absence of these three features. The groups were cross-sectionally characterised, and their ability to independently predict orthostatic intolerance (OI) during AS, and falls or syncope in the past year, was evaluated using multivariate logistic regression models.

          Results

          A total of 4,899 participants were included (mean age 61), of which 3,312 (68%) had no deficits. Older age was associated with stabilisation deficit and late deficits were seen in groups with higher proportions of beta blockers and psychotropic medications. Regression models identified independent associations between OI and three immediate-deficit groups; associations seemed stronger as more deficits were present. There was a significant association between falls history and the three-deficit group (odds ratio 1.54, 95% confidence interval: 1.15–2.07, P = 0.004).

          Conclusions

          More deficits seemed associated with the higher risk of OI and falls history. Observations are not causal but the recognition of these patterns may help clinicians focus on careful prescribing.

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          Most cited references32

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          Frailty in Older Adults: Evidence for a Phenotype

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            Frailty in older adults: evidence for a phenotype.

            Frailty is considered highly prevalent in old age and to confer high risk for falls, disability, hospitalization, and mortality. Frailty has been considered synonymous with disability, comorbidity, and other characteristics, but it is recognized that it may have a biologic basis and be a distinct clinical syndrome. A standardized definition has not yet been established. To develop and operationalize a phenotype of frailty in older adults and assess concurrent and predictive validity, the study used data from the Cardiovascular Health Study. Participants were 5,317 men and women 65 years and older (4,735 from an original cohort recruited in 1989-90 and 582 from an African American cohort recruited in 1992-93). Both cohorts received almost identical baseline evaluations and 7 and 4 years of follow-up, respectively, with annual examinations and surveillance for outcomes including incident disease, hospitalization, falls, disability, and mortality. Frailty was defined as a clinical syndrome in which three or more of the following criteria were present: unintentional weight loss (10 lbs in past year), self-reported exhaustion, weakness (grip strength), slow walking speed, and low physical activity. The overall prevalence of frailty in this community-dwelling population was 6.9%; it increased with age and was greater in women than men. Four-year incidence was 7.2%. Frailty was associated with being African American, having lower education and income, poorer health, and having higher rates of comorbid chronic diseases and disability. There was overlap, but not concordance, in the cooccurrence of frailty, comorbidity, and disability. This frailty phenotype was independently predictive (over 3 years) of incident falls, worsening mobility or ADL disability, hospitalization, and death, with hazard ratios ranging from 1.82 to 4.46, unadjusted, and 1.29-2.24, adjusted for a number of health, disease, and social characteristics predictive of 5-year mortality. Intermediate frailty status, as indicated by the presence of one or two criteria, showed intermediate risk of these outcomes as well as increased risk of becoming frail over 3-4 years of follow-up (odds ratios for incident frailty = 4.51 unadjusted and 2.63 adjusted for covariates, compared to those with no frailty criteria at baseline). This study provides a potential standardized definition for frailty in community-dwelling older adults and offers concurrent and predictive validity for the definition. It also finds that there is an intermediate stage identifying those at high risk of frailty. Finally, it provides evidence that frailty is not synonymous with either comorbidity or disability, but comorbidity is an etiologic risk factor for, and disability is an outcome of, frailty. This provides a potential basis for clinical assessment for those who are frail or at risk, and for future research to develop interventions for frailty based on a standardized ascertainment of frailty.
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              Accumulation of Deficits as a Proxy Measure of Aging

              This paper develops a method for appraising health status in elderly people. A frailty index was defined as the proportion of accumulated deficits (symptoms, signs, functional impairments, and laboratory abnormalities). It serves as an individual state variable, reflecting severity of illness and proximity to death. In a representative database of elderly Canadians we found that deficits accumulated at 3% per year, and show a gamma distribution, typical for systems with redundant components that can be used in case of failure of a given subsystem. Of note, the slope of the index is insensitive to the individual nature of the deficits, and serves as an important prognostic factor for life expectancy. The formula for estimating an individual's life span given the frailty index value is presented. For different patterns of cognitive impairments the average within-group index value increases with the severity of the cognitive impairment, and the relative variability of the index is significantly reduced. Finally, the statistical distribution of the frailty index sharply differs between well groups (gamma distribution) and morbid groups (normal distribution). This pattern reflects an increase in uncompensated deficits in impaired organisms, which would lead to illness of various etiologies, and ultimately to increased mortality. The accumulation of deficits is as an example of a macroscopic variable, i.e., one that reflects general properties of aging at the level of the whole organism rather than any given functional deficiency. In consequence, we propose that it may be used as a proxy measure of aging.
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                Author and article information

                Contributors
                Journal
                Age Ageing
                Age Ageing
                ageing
                Age and Ageing
                Oxford University Press
                0002-0729
                1468-2834
                May 2021
                04 September 2020
                04 September 2020
                : 50
                : 3
                : 854-860
                Affiliations
                The Irish Longitudinal Study on Ageing (TILDA) , Trinity College Dublin, Dublin, Ireland
                Falls and Syncope Unit , Mercer’s Institute for Successful Ageing, St James’s Hospital, Dublin, Ireland
                The Irish Longitudinal Study on Ageing (TILDA) , Trinity College Dublin, Dublin, Ireland
                The Irish Longitudinal Study on Ageing (TILDA) , Trinity College Dublin, Dublin, Ireland
                The Irish Longitudinal Study on Ageing (TILDA) , Trinity College Dublin, Dublin, Ireland
                The Irish Longitudinal Study on Ageing (TILDA) , Trinity College Dublin, Dublin, Ireland
                The Irish Longitudinal Study on Ageing (TILDA) , Trinity College Dublin, Dublin, Ireland
                Falls and Syncope Unit , Mercer’s Institute for Successful Ageing, St James’s Hospital, Dublin, Ireland
                The Irish Longitudinal Study on Ageing (TILDA) , Trinity College Dublin, Dublin, Ireland
                Falls and Syncope Unit , Mercer’s Institute for Successful Ageing, St James’s Hospital, Dublin, Ireland
                Author notes
                Address correspondence to: Dr David Moloney, The Irish Longitudinal Study on Ageing (TILDA), Trinity Central, 152-160 Pearse Street, Dublin D02 R590, Republic of Ireland. Tel: (+353) 1 896 2509; Fax: (+353) 1 896 3407. Email: moloned3@ 123456tcd.ie
                Author information
                http://orcid.org/0000-0001-6969-0175
                http://orcid.org/0000-0001-7090-9293
                Article
                afaa174
                10.1093/ageing/afaa174
                8098799
                32894746
                2382d979-4574-41f9-8e18-1cd697af9cc5
                © The Author(s) 2020. Published by Oxford University Press on behalf of the British Geriatrics Society. All rights reserved. For permissions, please email: journals.permissions@oup.com

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

                History
                : 6 April 2020
                : 4 July 2020
                Page count
                Pages: 7
                Funding
                Funded by: Science Foundation Ireland, DOI 10.13039/501100001602;
                Award ID: 18/FRL/6188
                Categories
                AcademicSubjects/MED00280
                Research Paper

                Geriatric medicine
                physiologic monitoring,active stand,orthostatic hypotension,orthostatic intolerance,falls,older people

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