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. 2020 Nov 3;10(1):18942.
doi: 10.1038/s41598-020-76098-y.

Using CHADS2 and CHA2DS2-VASc scores for mortality prediction in patients with chronic kidney disease

Affiliations

Using CHADS2 and CHA2DS2-VASc scores for mortality prediction in patients with chronic kidney disease

Po-Chao Hsu et al. Sci Rep. .

Abstract

Chronic kidney disease (CKD) is a public health issue and is associated with high morbidity and mortality. How to identify the high-risk CKD patients is very important to improve the long-term outcome. CHADS2 and CHA2DS2-VASc scores are clinically useful scores to evaluate the risk of stroke in patients with atrial fibrillation. However, there was no literature discussing about the usefulness of CHADS2 and CHA2DS2-VASc scores for cardiovascular (CV) and all-cause mortality prediction in CKD patients. This longitudinal study enrolled 437 patients with CKD. CHADS2 and CHA2DS2-VASc scores were calculated for each patient. CV and all-cause mortality data were collected for long-term outcome prediction. The median follow-up to mortality was 91 (25th-75th percentile: 59-101) months. There were 66 CV mortality and 165 all-cause mortality. In addition to age and heart rate, CHADS2 and CHA2DS2-VASc scores (both P value < 0.001) were significant predictors of CV and all-cause mortality in the multivariate analysis. Besides, in direct comparison of multivariate model, basic model + CHA2DS2-VASc score had a better additive predictive value for all-cause mortality than basic model + CHADS2 score (P = 0.031). In conclusion, our study showed both of CHADS2 and CHA2DS2-VASc scores were significant predictors for long-term CV and all-cause mortality in CKD patients and CHA2DS2-VASc score had a better predictive value than CHADS2 score for all-cause mortality in direct comparison of multivariate model. Therefore, using CHADS2 and CHA2DS2-VASc scores to screen CKD patients may be helpful in identifying the high-risk group with increased mortality.

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Conflict of interest statement

The authors declare no competing interests.

Figures

Figure 1
Figure 1
Flow chart of patient enrollment. CKD, chronic kidney disease; eGFR, estimated Glomerular filtration rate.
Figure 2
Figure 2
Nested Cox model for cardiovascular mortality (A) and all-cause mortality (B). Basic model in (A) included age, heart rate, and body mass index. Basic model in (B) included age, heart rate, body mass index, and diuretic use.
Figure 3
Figure 3
The Kaplan–Meier curves of different chronic kidney disease (CKD) stages for all-cause mortality-free survival.

References

    1. Vlachopoulos C, et al. Association of estimated pulse wave velocity with survival: a secondary analysis of SPRINT. JAMA Netw. Open. 2019;2:e1912831. doi: 10.1001/jamanetworkopen.2019.12831. - DOI - PMC - PubMed
    1. Go AS, Chertow GM, Fan D, McCulloch CE, Hsu CY. Chronic kidney disease and the risks of death, cardiovascular events, and hospitalization. N. Engl. J. Med. 2004;351:1296–1305. doi: 10.1056/NEJMoa041031. - DOI - PubMed
    1. Hwang SJ, Tsai JC, Chen HC. Epidemiology, impact and preventive care of chronic kidney disease in Taiwan. Nephrology (Carlton) 2010;15(Suppl 2):3–9. doi: 10.1111/j.1440-1797.2010.01304.x. - DOI - PubMed
    1. Tonelli M, et al. Chronic kidney disease and mortality risk: a systematic review. J. Am. Soc. Nephrol. 2006;17:2034–2047. doi: 10.1681/ASN.2005101085. - DOI - PubMed
    1. Whittaker CF, Miklich MA, Patel RS, Fink JC. Medication safety principles and practice in CKD. Clin. J. Am. Soc. Nephrol. 2018;13:1738–1746. doi: 10.2215/CJN.00580118. - DOI - PMC - PubMed

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