Key result
Discharge RASi after hyperkalemia linked to ~38% lower mortality but higher chronic dialysis risk.
Why the study?
RASi are frequently discontinued during hospitalization for hyperkalemia, but guidance regarding discharge prescribing is limited.
Does prescription of RASi at discharge reduce mortality or impact dialysis initiation in adults hospitalized with hyperkalemia?
Cohort (n=4,388)
No
Does prescription of RASi at discharge reduce mortality or impact dialysis initiation in adults hospitalized with hyperkalemia?
Hazard Ratio: 0.62 (95% CI 0.55–0.71)
Absolute Event Rate: 18.3% vs 29.3%
p-value: p=<0.001
Continuing RASi therapy at discharge after a hospitalization for hyperkalemia is associated with improved survival but an increased risk of initiating chronic dialysis.
May support individualized RASi decisions post-hyperkalemia; leaves open net benefit versus dialysis risk pending RCTs.
Background: Medication changes at hospital discharge may influence post-discharge outcomes. Renin-angiotensin system inhibitors (RASi) are frequently discontinued during hospitalization for hyperkalemia; however, guidance regarding discharge prescribing is limited. We evaluated the association between RASi prescription at discharge and post-discharge outcomes in patients hospitalized with hyperkalemia. Methods: In this single-center retrospective cohort study at a large tertiary hospital, adults admitted between 2005 and 2020 with a potassium level > 5.5 mEq/L while receiving chronic RASi therapy were included and followed through 2022. Exposure was defined as prescription versus non-prescription of RASi at discharge. Propensity score matching was used among survivors of the first hospitalization to balance baseline characteristics. Kaplan-Meier and multivariable Cox models were used to assess all-cause mortality and chronic dialysis. Results: Among 12,326 patients with confirmed hyperkalemia, 9,051 survived the index hospitalization; 4,388 were included after matching (2,194 per group). Prescription of RASi at discharge was associated with lower mortality (401 (18.3%) vs 642 (29.3%); hazard ratio (HR), 0.62; 95% confidence interval (CI), 0.55-0.71) but a higher risk of chronic dialysis initiation (167 (8.2%) vs. 111 (5.7%); HR, 1.57; 95% CI, 1.23-1.99). Conclusions: In patients hospitalized with hyperkalemia, discharge prescription of RASi was associated with lower mortality but a higher incidence of chronic dialysis initiation. Dialysis initiation may reflect both progression of renal disease and longer survival among patients discharged on RASi therapy. Given the observational study design, these findings should be interpreted as associations rather than causal effects and underscore the complex risk-benefit considerations surrounding discharge medication decisions.
No takes yet. Share an insight, caveat, or question.
Weiss et al. (2026) conducted a cohort in Hyperkalemia (n=4,388). Prescription of Renin-Angiotensin System Inhibitors (RASi) at discharge vs. Non-prescription of RASi at discharge was evaluated on All-cause mortality (HR 0.62, 95% CI 0.55-0.71, p=<0.001). Discharge prescription of renin-angiotensin system inhibitors after hyperkalemia was associated with lower mortality (HR 0.62) but higher chronic dialysis initiation compared to non-prescription.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: