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      CHA 2DS 2-VASc score stratifies mortality risk in heart failure patients aged 75 years and older with and without atrial fibrillation

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          Abstract

          Background

          During the last decade, the CHA 2DS 2-VASc score has been associated with adverse clinical outcomes in several cardiovascular (CV) and non-cardiovascular diseases beyond atrial fibrillation (AF). Whether the CHA 2DS 2-VASc score stratifies mortality risk in elderly patients with AF and without AF is not well established.

          Methods

          All consecutive patients aged ≥ 75 yrs hospitalized due to heart failure (HF), between January 2020 and November 2020, were retrospectively enrolled. All patients underwent physical examination, blood tests, electrocardiography and conventional transthoracic echocardiography. Primary endpoint was all-cause mortality, while secondary endpoint was the composite of all-cause mortality + rehospitalizations for all causes over mid-term follow-up.

          Results

          The study included 261 HF patients (86.3 ± 6.4 years, 60.5% females). 85 AF and 176 non-AF patients were separately analyzed. Compared to non-AF patients, those with AF had significantly higher CHA 2DS 2-VASc score (5.6 ± 1.4 vs 5.1 ± 1.4, p = 0.007) and lower ejection fraction (47.4 ± 16.5 vs 56.7 ± 15.1%, p < 0.001). Mean follow-up was 1.7 ± 0.5 yrs. During follow-up, 96 patients died (58.3% due to CV causes) and 79 were rehospitalized (58.2% due to CV causes). CHA 2DS 2-VASc score was independently associated with all-cause mortality in whole study population (HR 1.61, 95% CI 1.36–1.92) and in both AF (HR 1.41, 95% CI 1.09–1.82) and non-AF patients (HR 1.84, 95% CI 1.40–2.40). CHA 2DS 2-VASc score also predicted the secondary endpoint in the same study groups. CHA 2DS 2-VASc score ≥ 5 was the best cut-off value for predicting both outcomes.

          Conclusion

          At mid-term follow-up, a CHA 2DS 2-VASc score ≥ 5 predicts increased risk of all-cause mortality and re-hospitalizations for all causes in elderly HF patients, regardless of AF.

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          Most cited references49

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          A new method of classifying prognostic comorbidity in longitudinal studies: Development and validation

          The objective of this study was to develop a prospectively applicable method for classifying comorbid conditions which might alter the risk of mortality for use in longitudinal studies. A weighted index that takes into account the number and the seriousness of comorbid disease was developed in a cohort of 559 medical patients. The 1-yr mortality rates for the different scores were: "0", 12% (181); "1-2", 26% (225); "3-4", 52% (71); and "greater than or equal to 5", 85% (82). The index was tested for its ability to predict risk of death from comorbid disease in the second cohort of 685 patients during a 10-yr follow-up. The percent of patients who died of comorbid disease for the different scores were: "0", 8% (588); "1", 25% (54); "2", 48% (25); "greater than or equal to 3", 59% (18). With each increased level of the comorbidity index, there were stepwise increases in the cumulative mortality attributable to comorbid disease (log rank chi 2 = 165; p less than 0.0001). In this longer follow-up, age was also a predictor of mortality (p less than 0.001). The new index performed similarly to a previous system devised by Kaplan and Feinstein. The method of classifying comorbidity provides a simple, readily applicable and valid method of estimating risk of death from comorbid disease for use in longitudinal studies. Further work in larger populations is still required to refine the approach because the number of patients with any given condition in this study was relatively small.
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            A new equation to estimate glomerular filtration rate.

            Equations to estimate glomerular filtration rate (GFR) are routinely used to assess kidney function. Current equations have limited precision and systematically underestimate measured GFR at higher values. To develop a new estimating equation for GFR: the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation. Cross-sectional analysis with separate pooled data sets for equation development and validation and a representative sample of the U.S. population for prevalence estimates. Research studies and clinical populations ("studies") with measured GFR and NHANES (National Health and Nutrition Examination Survey), 1999 to 2006. 8254 participants in 10 studies (equation development data set) and 3896 participants in 16 studies (validation data set). Prevalence estimates were based on 16,032 participants in NHANES. GFR, measured as the clearance of exogenous filtration markers (iothalamate in the development data set; iothalamate and other markers in the validation data set), and linear regression to estimate the logarithm of measured GFR from standardized creatinine levels, sex, race, and age. In the validation data set, the CKD-EPI equation performed better than the Modification of Diet in Renal Disease Study equation, especially at higher GFR (P < 0.001 for all subsequent comparisons), with less bias (median difference between measured and estimated GFR, 2.5 vs. 5.5 mL/min per 1.73 m(2)), improved precision (interquartile range [IQR] of the differences, 16.6 vs. 18.3 mL/min per 1.73 m(2)), and greater accuracy (percentage of estimated GFR within 30% of measured GFR, 84.1% vs. 80.6%). In NHANES, the median estimated GFR was 94.5 mL/min per 1.73 m(2) (IQR, 79.7 to 108.1) vs. 85.0 (IQR, 72.9 to 98.5) mL/min per 1.73 m(2), and the prevalence of chronic kidney disease was 11.5% (95% CI, 10.6% to 12.4%) versus 13.1% (CI, 12.1% to 14.0%). The sample contained a limited number of elderly people and racial and ethnic minorities with measured GFR. The CKD-EPI creatinine equation is more accurate than the Modification of Diet in Renal Disease Study equation and could replace it for routine clinical use. National Institute of Diabetes and Digestive and Kidney Diseases.
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              2021 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure

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                Author and article information

                Contributors
                sonaglioniandrea@gmail.com
                Journal
                Aging Clin Exp Res
                Aging Clin Exp Res
                Aging Clinical and Experimental Research
                Springer International Publishing (Cham )
                1594-0667
                1720-8319
                16 March 2022
                : 1-14
                Affiliations
                [1 ]GRID grid.416367.1, ISNI 0000 0004 0485 6324, Division of Cardiology, , Ospedale San Giuseppe MultiMedica IRCCS, ; Via San Vittore 12, 20123 Milan, Italy
                [2 ]GRID grid.416367.1, ISNI 0000 0004 0485 6324, Division of Internal Medicine, , Ospedale San Giuseppe MultiMedica IRCCS, ; Milan, Italy
                [3 ]GRID grid.416367.1, ISNI 0000 0004 0485 6324, Division of Hepatology, , Ospedale San Giuseppe MultiMedica IRCCS, ; Milan, Italy
                [4 ]Division of Cardiology, Policlinico San Giorgio, Pordenone, Italy
                [5 ]GRID grid.4708.b, ISNI 0000 0004 1757 2822, Department of Clinical Sciences and Community Health, , Università Di Milano, ; Milan, Italy
                [6 ]GRID grid.511455.1, Geriatric Unit, IRCCS Istituti Clinici Scientifici Maugeri, ; Milan, Italy
                [7 ]GRID grid.415992.2, ISNI 0000 0004 0398 7066, Liverpool Centre for Cardiovascular Science, , University of Liverpool and Liverpool Heart and Chest Hospital, ; Liverpool, UK
                Author information
                http://orcid.org/0000-0001-7641-8831
                Article
                2107
                10.1007/s40520-022-02107-x
                8925288
                35294768
                efc85134-7d09-435f-9b2c-5b1deeaec051
                © The Author(s), under exclusive licence to Springer Nature Switzerland AG 2022

                This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.

                History
                : 16 January 2022
                : 27 February 2022
                Categories
                Original Article

                elderly,cha2ds2-vasc score,atrial fibrillation,heart failure,mortality

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