Serum Potassium in the PARADIGM-HF trial - Université de Lorraine
Journal Articles European Journal of Heart Failure Year : 2020

Serum Potassium in the PARADIGM-HF trial

Abstract

Background: We studied the association between potassium and outcomes, the effect of sacubitril/valsartan on potassium, and whether potassium level modified the effect of sacubitril/valsartan in patients with heart failure and a reduced ejection fraction in PARADIGM-HF.Aims: We examined several outcomes including cardiovascular death, sudden-death, pump-failure death, non-cardiovascular death and heart failure hospitalization.Methods: 8399 patients were randomized to either enalapril or sacubitril/valsartan. Potassium at randomization and follow-up was examined as a continuous and categorical variable (≤3.5, 3.6-4.0, 4.1-4.9, 5.0-5.4, and ≥5.5mmol/L) in various statistical models. Hyperkalemia was defined as K+ ≥5.5mmol/L and hypokalemia as K+ ≤3.5mmol/L.Results: Compared to potassium 4.1-4.9mmol/L, both hypokalemia (HR 2.40, 95%CI 1.84-3.14) and hyperkalemia (HR 1.42, 1.10-1.83) were associated with a higher risk of cardiovascular death. However, potassium abnormalities were similarly associated with sudden death and pump failure death, as well as non-cardiovascular death and heart failure hospitalization. Sacubitril/valsartan had no effect on potassium overall. The benefit of sacubitril/valsartan over enalapril was consistent across the range of baseline potassium.Conclusions: Although both higher and lower potassium were independent predictors of cardiovascular death, potassium abnormalities may mainly be markers rather than mediators of risk of death.
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Dates and versions

hal-02918319 , version 1 (20-08-2020)

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Joao Pedro Ferreira, Ulrik M Mogensen, Pardeep Jhund, Akshay Desai, Jean-Lucien Rouleau, et al.. Serum Potassium in the PARADIGM-HF trial. European Journal of Heart Failure, 2020, 22 (11), pp.2056-2064. ⟨10.1002/ejhf.1987⟩. ⟨hal-02918319⟩
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