Key result
Initiation of a high-dialyzability β-blocker compared with a low-dialyzability β-blocker was associated with a higher risk of death at 180 days (RR 1.4; 95% CI 1.1-1.8; P<0.01).
Why the study?
Does initiation of high-dialyzability beta-blockers compared with low-dialyzability beta-blockers increase mortality in older patients receiving long-term hemodialysis?
Cohort (n=6,588)
Does initiation of high-dialyzability beta-blockers compared with low-dialyzability beta-blockers increase mortality in older patients receiving long-term hemodialysis?
Relative Risk: 1.4 (95% CI 1.1–1.8)
p-value: p=<0.01
In older patients on long-term hemodialysis, initiating high-dialyzability beta-blockers is associated with a significantly higher 180-day mortality risk compared to low-dialyzability beta-blockers.
May warrant preferring low-dialyzability β-blockers in hemodialysis; leaves open causality pending randomized trials.
Some β-blockers are efficiently removed from the circulation by hemodialysis ("high dialyzability") whereas others are not ("low dialyzability"). This characteristic may influence the effectiveness of the β-blockers among patients receiving long-term hemodialysis. To determine whether new use of a high-dialyzability β-blocker compared with a low-dialyzability β-blocker associates with a higher rate of mortality in patients older than age 66 years receiving long-term hemodialysis, we conducted a propensity-matched population-based retrospective cohort study using the linked healthcare databases of Ontario, Canada. The high-dialyzability group (n=3294) included patients initiating atenolol, acebutolol, or metoprolol. The low-dialyzability group (n=3294) included patients initiating bisoprolol or propranolol. Initiation of a high- versus low-dialyzability β-blocker was associated with a higher risk of death in the following 180 days (relative risk, 1.4; 95% confidence interval, 1.1 to 1.8; P<0.01). Supporting this finding, we repeated the primary analysis in a cohort of patients not receiving hemodialysis and found no significant association between dialyzability and the risk of death (relative risk, 1.0; 95% confidence interval, 0.9 to 1.3; P=0.71). β-Blocker exposure was not randomly allocated in this study, so a causal relationship between dialyzability and mortality cannot be determined. However, our findings should raise awareness of this potentially important drug characteristic and prompt further study.
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Weir et al. (2014) conducted a cohort in Long-term hemodialysis (n=6,588). High-dialyzability β-blocker vs. Low-dialyzability β-blocker was evaluated on Death in the following 180 days (RR 1.4, 95% CI 1.1-1.8, p=<0.01). Initiation of a high-dialyzability β-blocker compared with a low-dialyzability β-blocker was associated with a higher risk of death at 180 days (RR 1.4; 95% CI 1.1-1.8; P<0.01).
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