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Association of short-term blood pressure variability with cardiovascular mortality among incident hemodialysis patients

Objective: To investigate the association of short-term blood pressure variability (BPV) with cardiovascular mortality in hemodialysis (HD) patients, using a reliable index called average real variability (ARV), and to assess the factors associated with ARV in incident HD population. Methods: A tota...

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Detalles Bibliográficos
Autores principales: Feng, Yiduo, Li, Ziqian, Liu, Jing, Sun, Fang, Ma, Lijie, Shen, Yang, Zhou, Yilun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014398/
https://www.ncbi.nlm.nih.gov/pubmed/29619872
http://dx.doi.org/10.1080/0886022X.2018.1456456
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author Feng, Yiduo
Li, Ziqian
Liu, Jing
Sun, Fang
Ma, Lijie
Shen, Yang
Zhou, Yilun
author_facet Feng, Yiduo
Li, Ziqian
Liu, Jing
Sun, Fang
Ma, Lijie
Shen, Yang
Zhou, Yilun
author_sort Feng, Yiduo
collection PubMed
description Objective: To investigate the association of short-term blood pressure variability (BPV) with cardiovascular mortality in hemodialysis (HD) patients, using a reliable index called average real variability (ARV), and to assess the factors associated with ARV in incident HD population. Methods: A total of 103 HD patients were recruited, with 44-h ambulatory blood pressure monitoring performed after the midweek HD session. Systolic BPV was assessed by SD, coefficient of variation (CV), and ARV, respectively. Laboratory data were obtained from blood samples before the midweek HD. All patients were followed up for 24 months. Results: According to the median of BPV indices, the comparisons between patients with the low and high values were conducted. Kaplan–Meier analysis showed the survival curves corresponding to median of SD and CV exhibit similar performance for the low and high groups (p = .647, p = .098, respectively). In contrast, patients with higher ARV had a lower survival rate than those with lower ARV (77.8% vs. 98.0%, p = .002). After adjustment for demographics and clinical factors, ARV (HR: 1.143; 95% CI: 1.022–1.279, p = .019) and high-sensitivity C-reactive protein (HR: 1.394; 95% CI: 1.025–1.363, p = .021) were associated with increased risk of cardiovascular mortality in HD patients. Age and interdialytic weight gain (IDWG) were related factors for ARV (β = 0.065, p = .005; β = 0.825, p = .003, respectively). Conclusions: Greater ARV was independently associated with increased risk of cardiovascular mortality in HD patients. Age and IDWG were independent related factors for ARV.
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spelling pubmed-60143982018-06-28 Association of short-term blood pressure variability with cardiovascular mortality among incident hemodialysis patients Feng, Yiduo Li, Ziqian Liu, Jing Sun, Fang Ma, Lijie Shen, Yang Zhou, Yilun Ren Fail Clinical Study Objective: To investigate the association of short-term blood pressure variability (BPV) with cardiovascular mortality in hemodialysis (HD) patients, using a reliable index called average real variability (ARV), and to assess the factors associated with ARV in incident HD population. Methods: A total of 103 HD patients were recruited, with 44-h ambulatory blood pressure monitoring performed after the midweek HD session. Systolic BPV was assessed by SD, coefficient of variation (CV), and ARV, respectively. Laboratory data were obtained from blood samples before the midweek HD. All patients were followed up for 24 months. Results: According to the median of BPV indices, the comparisons between patients with the low and high values were conducted. Kaplan–Meier analysis showed the survival curves corresponding to median of SD and CV exhibit similar performance for the low and high groups (p = .647, p = .098, respectively). In contrast, patients with higher ARV had a lower survival rate than those with lower ARV (77.8% vs. 98.0%, p = .002). After adjustment for demographics and clinical factors, ARV (HR: 1.143; 95% CI: 1.022–1.279, p = .019) and high-sensitivity C-reactive protein (HR: 1.394; 95% CI: 1.025–1.363, p = .021) were associated with increased risk of cardiovascular mortality in HD patients. Age and interdialytic weight gain (IDWG) were related factors for ARV (β = 0.065, p = .005; β = 0.825, p = .003, respectively). Conclusions: Greater ARV was independently associated with increased risk of cardiovascular mortality in HD patients. Age and IDWG were independent related factors for ARV. Taylor & Francis 2018-04-05 /pmc/articles/PMC6014398/ /pubmed/29619872 http://dx.doi.org/10.1080/0886022X.2018.1456456 Text en © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Feng, Yiduo
Li, Ziqian
Liu, Jing
Sun, Fang
Ma, Lijie
Shen, Yang
Zhou, Yilun
Association of short-term blood pressure variability with cardiovascular mortality among incident hemodialysis patients
title Association of short-term blood pressure variability with cardiovascular mortality among incident hemodialysis patients
title_full Association of short-term blood pressure variability with cardiovascular mortality among incident hemodialysis patients
title_fullStr Association of short-term blood pressure variability with cardiovascular mortality among incident hemodialysis patients
title_full_unstemmed Association of short-term blood pressure variability with cardiovascular mortality among incident hemodialysis patients
title_short Association of short-term blood pressure variability with cardiovascular mortality among incident hemodialysis patients
title_sort association of short-term blood pressure variability with cardiovascular mortality among incident hemodialysis patients
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014398/
https://www.ncbi.nlm.nih.gov/pubmed/29619872
http://dx.doi.org/10.1080/0886022X.2018.1456456
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