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Intradialytic BP variability is associated with cardiovascular mortality and hospitalization in HD patients
Xuelei Zhang1, Ling Xu2, Peiyi Zhou1
1Department of Nephrology, Daxing Teaching Hospital, Capital Medical University, Beijing, China.
Insights
Intradialytic blood pressure variability (BPV) is a significant predictor of cardiovascular disease (CVD) mortality and hospitalization in hemodialysis (HD) patients. Higher intradialytic BPV is linked to increased CVD risk, highlighting its importance in managing HD patient outcomes.
Area of Science:
- Nephrology
- Cardiology
- Clinical Research
Background:
- Pre-dialysis blood pressure variability (BPV) is a known cardiovascular disease (CVD) risk factor in hemodialysis (HD) patients.
- Limited data exists on the impact of intradialytic BPV on patient prognosis.
Purpose of the Study:
- To investigate the association between intradialytic BPV and CVD outcomes in HD patients.
- To identify predictors of intradialytic BPV.
Main Methods:
- Retrospective cohort study of 202 HD patients.
- Intradialytic blood pressure measurements from November 2017 were analyzed.
- Patients were stratified into four groups based on variability independent of the mean (VIM) interquartiles.
Main Results:
- Higher VIM was associated with increased CVD mortality (p=0.05) and CVD-related hospitalization (OR=1.085, p=0.030).
- VIM and age were independent predictors of CVD death (HR=1.091 and HR=1.059, respectively).
- Predictors of VIM included patient age, dialysis vintage, serum albumin, and intradialytic weight gain.
Conclusions:
- Intradialytic BPV is a significant predictor of CVD mortality and hospitalization in HD patients.
- Higher intradialytic BPV is associated with older age, longer dialysis vintage, lower albumin, and greater ultrafiltration.
- Managing intradialytic BPV may improve CVD outcomes in the HD population.
Introduction:
Studies showed that pre-dialysis BP variability (BPV) was an independent risk factor of cardiovascular disease (CVD) among HD patients, but which is limited on how intradialytic BPV affects prognosis.
Methods:
In this study, we designed a retrospective cohort study to examine the association between intradialytic BPV and CVD outcomes in HD patients. A total of 202 patients who underwent HD in our center were included, and all intradialytic BP measurements of November 2017 were obtained from the database. Patients were divided into four groups according to variability independent of the mean (VIM) interquartile.
Results:
The mean age was 62.1 ± 14.3 years, 60.9% were male, and median VIM was 14.75 (12.60-18.59). Multiple-regression analyses showed patients age, dialysis vintage, serum albumin, and the percentage of intradialytic weight gain as significant predictors of VIM (all p values were <0.05). Kaplan-Meier survival curves showed that CVD mortality was greater in patients with higher VIM (p = 0.05), whereas all-cause mortality had no significant difference between the four groups overall (p = 0.149). Furthermore, multivariate regression analyses demonstrated that VIM (HR = 1.091, p < 0.004) and age (HR = 1.059, p = 0.003) were significant independent predictors for CVD death. Logistic-regression models revealed that higher VIM groups were more likely to have CVD-related hospitalization (OR = 1.085, p = 0.030), whereas the association between VIM and all-cause hospitalization was not statistically significant (OR = 1.015, p = 0.669).
Conclusions:
This retrospective study suggested that higher intradialytic BPV was associated with increasing age, longer dialysis vintage, lower albumin, and greater ultrafiltration; intradialytic BPV could be an effective predictor for CVD mortality and hospitalization in the HD population.
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