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      Empagliflozin and serum potassium in heart failure: an analysis from EMPEROR-Pooled  

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          Abstract

          Aims

          Hyperkalaemia frequently leads to interruption and discontinuation of neurohormonal antagonists, which may worsen heart failure prognosis. Some studies suggested that sodium-glucose cotransporter 2 inhibitors reduce hyperkalaemia, an effect that may have important clinical implications. This analysis evaluates the effect of empagliflozin on the occurrence of hyper- and hypokalaemia in HF.

          Methods and results

          EMPEROR-Pooled (i.e. EMPEROR-Reduced and EMPEROR-Preserved combined) included 9583 patients with available serum potassium levels at baseline (98.6% of the total EMPEROR-Pooled population, n = 9718). Hyperkalaemia was identified by investigators’ reports of adverse events, and by a laboratory serum potassium value above 5.5 mmol/L and 6.0 mmol/L. The main outcome was a composite of investigator-reported hyperkalaemia or initiation of potassium binders. Patients with high potassium at baseline were more frequently diagnosed with diabetes and ischaemic HF aetiology and had lower left ventricular ejection fraction and estimated glomerular filtration rate but were more frequently treated with sacubitril/valsartan or mineralocorticoid receptor antagonists. Empagliflozin (compared with placebo) reduced the composite of investigator-reported hyperkalaemia or initiation of potassium binders [6.5% vs. 7.7%, hazard ratio (HR) 0.82, 95% confidence interval (CI) 0.71–0.95, P = 0.01]. Empagliflozin reduced hyperkalaemia rates regardless of the definition used (serum potassium >5.5 mmol/l: 8.6% vs. 9.9%, HR 0.85, 95% CI 0.74–0.97, P = 0.017; serum potassium >6.0 mmol/l: 1.9% vs. 2.9%, HR 0.62, 95% CI 0.48–0.81, P < 0.001). The incidence of hypokalaemia (investigator-reported or serum potassium <3.0 mmol/l) was not significantly increased with empagliflozin.

          Conclusions

          Empagliflozin reduced the incidence of hyperkalaemia without significant increase in hypokalaemia.

          Structured Graphical Abstract

          Structured Graphical Abstract

          Empagliflozin reduced the incidence of hyperkalemia without increasing the risk of hypokalemia.

          Abstract

          This pooled analysis from the EMPEROR trials showed that empagliflozin reduced the incidence of hyperkalaemia without significant increase in hypokalaemia in patients with heart failure.

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          Most cited references21

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          Cardiovascular and Renal Outcomes with Empagliflozin in Heart Failure

          Sodium-glucose cotransporter 2 (SGLT2) inhibitors reduce the risk of hospitalization for heart failure in patients regardless of the presence or absence of diabetes. More evidence is needed regarding the effects of these drugs in patients across the broad spectrum of heart failure, including those with a markedly reduced ejection fraction.
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            2016 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure: The Task Force for the diagnosis and treatment of acute and chronic heart failure of the European Society of Cardiology (ESC). Developed with the special contribution of the Heart Failure Association (HFA) of the ESC.

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              Empagliflozin in Heart Failure with a Preserved Ejection Fraction

              Sodium-glucose cotransporter 2 inhibitors reduce the risk of hospitalization for heart failure in patients with heart failure and a reduced ejection fraction, but their effects in patients with heart failure and a preserved ejection fraction are uncertain.
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                Author and article information

                Contributors
                Journal
                Eur Heart J
                Eur Heart J
                eurheartj
                European Heart Journal
                Oxford University Press
                0195-668X
                1522-9645
                14 August 2022
                10 June 2022
                10 June 2022
                : 43
                : 31 , Focus Issue on Heart Failure and Cardiomyopathies
                : 2984-2993
                Affiliations
                Université de Lorraine, Inserm, Centre d'Investigations Cliniques Plurithématique 1433, and Inserm U1116, CHRU, F-CRIN INI-CRCT (Cardiovascular and Renal Clinical Trialists) , Nancy, France
                Cardiovascular Research and Development Center, Department of Surgery and Physiology, Faculty of Medicine of the University of Porto , Porto, Portugal
                Université de Lorraine, Inserm, Centre d'Investigations Cliniques Plurithématique 1433, and Inserm U1116, CHRU, F-CRIN INI-CRCT (Cardiovascular and Renal Clinical Trialists) , Nancy, France
                Baylor Heart and Vascular Institute Dallas , TX, USA
                National and Kapodistrian University of Athens School of Medicine , Athens, Greece
                Boehringer Ingelheim International GmbH , Ingelheim, Germany
                mainanalytics GmbH , Sulzbach, Germany
                Boehringer Ingelheim International GmbH , Ingelheim, Germany
                Department of Internal Medicine I, University Hospital Würzburg , Würzburg, Germany
                Comprehensive Heart Failure Centre, University of Würzburg , Würzburg, Germany
                London School of Hygiene and Tropical Medicine , London, UK
                Department of Cardiology (CVK) Berlin Institute of Health Center for Regenerative Therapies (BCRT) German Centre for Cardiovascular Research (DZHK) partner site Berlin, Charité Universitätsmedizin Berlin , Berlin, Germany
                Baylor Heart and Vascular Institute Dallas , TX, USA
                Imperial College , London, UK
                Author notes
                Corresponding author. Tel: +33 (0) 3 83 15 73 15, Fax: +33 (0) 3 83 15 73 24, Email: j.ferreira@ 123456chru-nancy.fr

                Conflict of interest: J.P.F. reports personal fees from Boehringer Ingelheim, during the conduct of the study; personal fees from Boehringer Ingelheim, outside the submitted work. F.Z. reports personal fees from Boehringer Ingelheim, during the conduct of the study; personal fees from Janssen, Novartis, Boston Scientific, Amgen, CVRx, AstraZeneca, Vifor Fresenius, Cardior, Cereno Pharmaceutical, Applied Therapeutics, Merck, Bayer and, Cellprothera, other from CVCT, and Cardiorenal, outside the submitted work. J.B. reports personal fees from Boehringer Ingelheim, during the conduct of the study; personal fees from Boehringer Ingelheim, Cardior, CVRx, Foundry, G3 Pharma, Imbria, Impulse Dynamics, Innolife, Janssen, LivaNova, Luitpold, Medtronic, Merck, Novartis, NovoNordisk, Relypsa, Roche, Sanofi, Sequana Medical, V-Wave and Vifor, outside the submitted work. G.F. reports personal fees from Boehringer Ingelheim, during the conduct of the study; personal fees from Medtronic, Vifor, Servier, Novartis, Bayer, Amgen and Boehringer Ingelheim, outside the submitted work. I.R. and B.J.K. are employees of Boehringer Ingelheim. ES is employee of mainanalytics GmbH, contracted by Boehringer Ingelheim. SJP reports personal fees from Boehringer Ingelheim, during the conduct of the study; personal fees from Boehringer Ingelheim, outside the submitted work. S.A. reports personal fees from Boehringer Ingelheim, during the conduct of the study; grants and personal fees from Abbott Vascular, Vifor, personal fees from Bayer, Boehringer Ingelheim, Brahms GmbH, Cardiac Dimensions, Cordio, Novartis and Servier, outside the submitted work. M.P. reports personal fees from Boehringer Ingelheim, during the conduct of the study; personal fees from Abbvie, Actavis, Amgen, Amarin, AstraZeneca, Boehringer Ingelheim, Bristol Myers Squibb, CSL Behring, Cytokinetics, Johnson & Johnson, Eli Lily & Company, Moderna, Novartis, ParatusRx, Pfizer, Relypsa, Salamandra, Synthetic Biologics, Theravance, and Casana, outside the submitted work.

                Author information
                https://orcid.org/0000-0002-2304-6138
                https://orcid.org/0000-0001-7456-1570
                https://orcid.org/0000-0001-7683-4720
                https://orcid.org/0000-0003-1940-2440
                https://orcid.org/0000-0003-2212-4007
                https://orcid.org/0000-0003-1828-2387
                Article
                ehac306
                10.1093/eurheartj/ehac306
                9375711
                35687107
                cf07b91e-f080-4acf-b337-99bce0a2b001
                © The Author(s) 2022. Published by Oxford University Press on behalf of European Society of Cardiology.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License ( https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

                History
                : 02 December 2021
                : 09 March 2022
                : 24 May 2022
                Page count
                Pages: 10
                Funding
                Funded by: Boehringer Ingelheim, DOI 10.13039/100001003;
                Funded by: Eli Lilly;
                Award ID: NCT03057977
                Award ID: NCT03057951
                Categories
                Clinical Research
                Heart Failure and Cardiomyopathies
                AcademicSubjects/MED00200

                Cardiovascular Medicine
                potassium,hyperkalaemia,heart failure,empagliflozin
                Cardiovascular Medicine
                potassium, hyperkalaemia, heart failure, empagliflozin

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