Cardio-selective versus non-selective β-blockers for cardiovascular events and mortality in long-term dialysis patients: A systematic review and meta-analysis
Abstract:Background
Trials in patients receiving dialysis have demonstrated that β-blockers reduce all-cause mortality and cardiovascular events. However, differences still exist within-class comparative effectiveness studies of the therapeutic benefits of β-blockers in dialysis patients.
Objective
The purpose of this systematic review is to examine whether cardiovascular events and all-cause mortality differed between dialysis patients receiving cardio-selective and non-selective agents.
Methods
A comprehensive se… Show more
“…Some studies showed better clinical outcomes with dialyzable and/or cardioselective β-blockers than with non-dialyzable and/or non-cardioselective ones, despite overall inconsistent results between the types of β-blockers and the clinical outcomes [7][8][9][10][11][12][13][14][15][16][17][18]. However, our study did not show superiority in patient survival based on the type of β-blockers.…”
Section: Discussioncontrasting
confidence: 81%
“…However, they have different characteristics based on dialyzability and/or cardioselectivity, which may result in different effects on the survival of patients with HD. Previous studies have evaluated the association between types of β-blockers and outcomes in patients with HD [7][8][9][10][11][12][13][14][15][16][17][18]. However, results regarding this association were inconsistent.…”
Previous results regarding the association between types of β-blockers and outcomes in patients on hemodialysis (HD) were inconsistent. Our study aimed to evaluate patient survival according to the type of β-blockers administered using a large sample of patients with maintenance HD. Our study included patients on maintenance HD patients from a national HD quality assessment program (n = 54,132). We divided included patients into four groups based on their use and type; Group 1 included patients without a prescription of β-blockers, Group 2 included patients with a prescription of dialyzable and cardioselective β-blockers, Group 3 included patients with a prescription of non-dialyzable and non-cardioselective β-blockers, and Group 4 included patients with prescription of non-dialyzable and cardioselective β-blockers. The number of patients in Groups 1, 2, 3, and 4 were 34,514, 2789, 15,808, and 1021, respectively. The 5-year survival rates in Groups 1, 2, 3, and 4 were 69.3%, 66.0%, 68.8%, and 69.2%, respectively. Univariate Cox regression analyses showed the hazard ratios to be 1.10 (95% CI, 1.04–1.17) in Group 2 and 1.05 (95% CI, 1.02–1.09) in Group 3 compared to Group 1. However, multivariate Cox regression analyses did not show statistical significance among the four groups. Our study showed that there was no significant difference in patient survival based on the use or types of β-blockers.
“…Some studies showed better clinical outcomes with dialyzable and/or cardioselective β-blockers than with non-dialyzable and/or non-cardioselective ones, despite overall inconsistent results between the types of β-blockers and the clinical outcomes [7][8][9][10][11][12][13][14][15][16][17][18]. However, our study did not show superiority in patient survival based on the type of β-blockers.…”
Section: Discussioncontrasting
confidence: 81%
“…However, they have different characteristics based on dialyzability and/or cardioselectivity, which may result in different effects on the survival of patients with HD. Previous studies have evaluated the association between types of β-blockers and outcomes in patients with HD [7][8][9][10][11][12][13][14][15][16][17][18]. However, results regarding this association were inconsistent.…”
Previous results regarding the association between types of β-blockers and outcomes in patients on hemodialysis (HD) were inconsistent. Our study aimed to evaluate patient survival according to the type of β-blockers administered using a large sample of patients with maintenance HD. Our study included patients on maintenance HD patients from a national HD quality assessment program (n = 54,132). We divided included patients into four groups based on their use and type; Group 1 included patients without a prescription of β-blockers, Group 2 included patients with a prescription of dialyzable and cardioselective β-blockers, Group 3 included patients with a prescription of non-dialyzable and non-cardioselective β-blockers, and Group 4 included patients with prescription of non-dialyzable and cardioselective β-blockers. The number of patients in Groups 1, 2, 3, and 4 were 34,514, 2789, 15,808, and 1021, respectively. The 5-year survival rates in Groups 1, 2, 3, and 4 were 69.3%, 66.0%, 68.8%, and 69.2%, respectively. Univariate Cox regression analyses showed the hazard ratios to be 1.10 (95% CI, 1.04–1.17) in Group 2 and 1.05 (95% CI, 1.02–1.09) in Group 3 compared to Group 1. However, multivariate Cox regression analyses did not show statistical significance among the four groups. Our study showed that there was no significant difference in patient survival based on the use or types of β-blockers.
“…A propensity-matched retrospective cohort study comparing dialysis clearance and morbidity and mortality in dialysis patients on different medications showed that in HD patients, the use of DBBs is associated with an increased risk of death in the subsequent 6 months compared with NDBBs [ 148 ]. It has been suggested [ 149 ] that the use of cardio-selective BB may be associated with fewer CV events and lower all-cause mortality compared with dialysis patients on non-selective BB. A propensity-matched retrospective cohort study [ 150 ] of 3400 HD patients with HF showed lower all-cause mortality in patients treated with BB and even lower mortality in patients treated concomitantly with BB and ACEIs or ARBs.…”
Section: Drug Treatment For Dialysis Patientsmentioning
Chronic heart failure (CHF) is a common complication and cause of death in
dialysis patients. Although several clinical guidelines and expert consensus on
heart failure (HF) in the general population have been issued in China and
abroad, due to abnormal renal function or even no residual renal function (RRF)
in dialysis patients, the high number of chronic complications, as well as the
specificity, variability, and limitations of hemodialysis (HD) and peritoneal
dialysis (PD) treatments, there are significant differences between dialysis
patients and the general population in terms of the treatment and management of
HF. The current studies are not relevant to all dialysis-combined HF populations,
and there is an urgent need for high-quality studies on managing HF in dialysis
patients to guide and standardize treatment. After reviewing the existing
guidelines and literature, we focused on the staging and diagnosis of HF,
management of risk factors, pharmacotherapy, and dialysis treatment in patients
on dialysis. Based on evidence-based medicine and clinical trial data, this
report reflects new perspectives and future trends in the diagnosis and treatment
of HF in dialysis patients, which will further enhance the clinicians’
understanding of HF in dialysis patients.
“…A reduction of heart rate might result in increased diastolic filling and improved stroke volume, which is energetically convenient. The use of β-blockers has been shown to improve outcome in ESKD [ 105 , 106 ]. Improvement of diastolic function can be achieved by managing structural, haemodynamic and biological conditions impairing mechanisms of active relaxation and passive filling.…”
Chronic kidney disease (CKD) is characterized by clustered age-independent concentric LV geometry, geometry-independent systolic dysfunction, and age and heart rate-independent diastolic dysfunction. Concentric LV geometry is always associated with echocardiographic markers of abnormal LV relaxation and increased myocardial stiffness, two hallmarks of diastolic dysfunction. Non hemodynamic mechanisms such as metabolic and electrolyte abnormalities, activation of biological pathways, and chronic exposure to cytokine cascade and myocardial macrophage system also impact myocardial structure and impair the architecture of myocardial scaffold, producing and increasing reactive fibrosis, and altering myocardial distensibility. This review addresses pathophysiology of diastole in CKD, and relations with cardiac mechanics, hemodynamic loading, structural conditions, non-hemodynamic factors, and metabolic characteristics. The three mechanisms of diastole will be examined: elastic recoil, active relaxation, and passive distensibility and filling. Based on current evidence, we briefly give indications on methods for quantification of diastolic function and discuss on whether diastolic dysfunction represents a distinct characteristic in CKD or rather a proxy of the severity of cardiovascular condition, with the potential to be predicted by the general cardiovascular phenotype. Finally, the review discusses the opportunity of assessment of diastolic function in the context of CKD, with special emphasis on end-stage kidney disease, to indicate whether and when in-depth measurements might be helpful for clinical decision making in this context.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.