2020
DOI: 10.1002/ejhf.1793
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Unravelling the interplay between hyperkalaemia, renin–angiotensin–aldosterone inhibitor use and clinical outcomes. Data from 9222 chronic heart failure patients of the ESC‐HFA‐EORP Heart Failure Long‐Term Registry

Abstract: We assessed the interplay between hyperkalaemia (HK) and renin-angiotensin-aldosterone system inhibitor (RAASi) use, dose and discontinuation, and their association with all-cause or cardiovascular death in patients with chronic heart failure (HF). We hypothesized that HK-associated increased death may be related to RAASi withdrawal.

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Cited by 101 publications
(93 citation statements)
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“…61,62 Despite a lack of randomized controlled trial data to document improved clinical outcomes with correction of hyperkalemia and reinitiation of RAASi therapy in patients with an increased hyperkalemia risk, there is an increasing body of real-world evidence of increased morbidity and mortality among patients with CKD, HF, or diabetes who receive suboptimal or no RAASi therapy because of hyperkalemia. [63][64][65] For example, in a cohort study of patients who experienced a decline in eGFR to less than 30 mL/min per 1.73 m 2 while receiving RAASi therapy, discontinuation of RAASi therapy was associated with a higher risk of mortality or major adverse cardiovascular events than continuation of RAA-Sis. 63 In addition, a recent consensus report 9 and a position paper 66 suggest that treatment with the newer K þ binders (discussed subsequently) may allow for optimization of RAASi therapy in patients with HF.…”
Section: Risk Factorsmentioning
confidence: 99%
“…61,62 Despite a lack of randomized controlled trial data to document improved clinical outcomes with correction of hyperkalemia and reinitiation of RAASi therapy in patients with an increased hyperkalemia risk, there is an increasing body of real-world evidence of increased morbidity and mortality among patients with CKD, HF, or diabetes who receive suboptimal or no RAASi therapy because of hyperkalemia. [63][64][65] For example, in a cohort study of patients who experienced a decline in eGFR to less than 30 mL/min per 1.73 m 2 while receiving RAASi therapy, discontinuation of RAASi therapy was associated with a higher risk of mortality or major adverse cardiovascular events than continuation of RAA-Sis. 63 In addition, a recent consensus report 9 and a position paper 66 suggest that treatment with the newer K þ binders (discussed subsequently) may allow for optimization of RAASi therapy in patients with HF.…”
Section: Risk Factorsmentioning
confidence: 99%
“…After adjusting for a wide range of clinical predictors, and NT‐proBNP, the elevation in risk for death associated with higher potassium was modest and less pronounced than in hypokalaemia. Although prior studies have suggested that the elevated risk for death associated with hyperkalaemia may reflect underdosing or even the withholding of RAAS blockers, 22,23 this is not likely to represent the explanation in the present trial given that patients started on the maximum dose of the study drug and every effort was made to maintain the optimal dose during follow‐up. Moreover, the associations between higher potassium and fatal outcomes were similar for all subtypes of death examined, including non‐CV death, which suggests a lack of any specific mechanistic direct effect of hyperkalaemia.…”
Section: Discussionmentioning
confidence: 82%
“…L'étude d'un large registre de 9 222 patients de 31 pays différents [17], montre une prévalence de l'hyperkaliémie de 16,6 %. L'hyperkaliémie et l'hypokaliémie étaient un risque de mortalité.…”
Section: Discussionunclassified