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Targeted potassium levels to decrease arrhythmia burden in high risk patients with cardiovascular diseases (POTCAST): Study protocol for a randomized controlled trial - 02/09/22

Doi : 10.1016/j.ahj.2022.07.003 
Ulrik Winsløw, MD a, , Tharsika Sakthivel, MD a, Chaoqun Zheng, MD c, Helle Bosselmann, MD, PhD c, Ketil Haugan, MD, PhD c, Niels Bruun, MD, DMSc c, d, Charlotte Larroudé, MD, PhD b, Kasper Iversen, MD, DMSc b, d, Hillah Saffi, BSc med a, Emil Frandsen, BSc med a, Niels Risum, MD, PhD a, Henning Bundgaard, MD, DMSc a, d, #, Christian Jøns, MD, PhD a, #
a Department of Cardiology, Copenhagen University Hospital – Rigshospitalet, Denmark 
b Department of Cardiology, Copenhagen University Hospital – Herlev and Gentofte, Denmark 
c Department of Cardiology, Zealand University Hospital – Roskilde, Denmark 
d Faculty of Health and Medical Sciences, University of Copenhagen, Denmark 

Reprint requests: Ulrik Winsløw, MD, Department of Cardiology, Copenhagen University Hospital – Rigshospitalet, Blegdamsvej 9, 2100, Copenhagen, Denmark.Department of CardiologyCopenhagen University Hospital – RigshospitaletBlegdamsvej 9Copenhagen2100Denmark

Riassunto

Background

Low plasma potassium (p-K) is associated with increased risk of malignant arrhythmia and observational studies indicate protective effects of p-K in the upper reference level. However, randomized clinical studies are needed to document whether actively increasing p-K to high-normal levels is possible and safe and improves cardiovascular outcomes.

Objective

To investigate if increased p-K reduces the risk of malignant arrhythmia and all-cause death in high-risk patients with a cardiovascular disease treated with an implantable cardioverter defibrillator (ICD) for primary or secondary preventive causes. Secondly, to investigate whether high-normal p-K levels can be safely reached and maintained using already available medications and potassium-rich dietary guidance.

Methods

This is a prospective, randomized, and open-labelled study enrolling patient at high-risk of malignant arrhythmias. According to sample size calculations, 1,000 patients will be randomized 1:1 to either an investigational regiment that aims to increase and maintain p-K at high-normal levels (4.5-5.0 mmol/L) or to usual standard of care and followed for an expected four years. The trial will run until a total of 291 events have occurred providing an α = 0.05 and 1-β = 0.80. The composite primary endpoint includes ventricular tachycardia >125 bpm lasting >30 seconds, any appropriate ICD-therapy, and all-cause mortality. At present, 739 patients have been randomized.

Conclusions

We present the rationale for the design of the POTCAST trial. The inclusion was initiated 2019 and is expected to be finished 2022. The study will show if easily available treatments to increase p-K may be a new treatment modality to protect against malignant arrythmias.

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Abbreviations : MRA, ICD, HM, ATP, VT, VF, CRT


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 Author Disclosures: The authors report no competing interests. HB receives lecture fees from Amgen and BMS. All authors have read and agree to the manuscript as written. The work described has not been published previously. The individuals listed as authors are solely responsible for the design and conduct of this study, all study analyses as well as drafting and editing of the paper and its final contents.
 This study was supported by Copenhagen University Hospital - Rigshospitalet, The Danish Council for Independent Research, Medical Science (FFS), The Hartmanns Foundation, The Danish Heart Foundation, Snedkermester Sophus Jacobsen og hustru Astrid Jacobsens Fond, Direktør Jacob Madsens og Hustru Olga Madsens Fond, and The Novo Nordisk Foundation.


© 2022  The Authors. Pubblicato da Elsevier Masson SAS. Tutti i diritti riservati.
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P. 59-66 - Novembre 2022 Ritorno al numero
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