| Literature DB >> 32618086 |
Petar M Seferović1,2, Gabriele Fragasso3, Mark Petrie4, Wilfried Mullens5,6, Roberto Ferrari7, Thomas Thum8, Johann Bauersachs9, Stefan D Anker10,11, Robin Ray12, Yuksel Çavuşoğlu13, Marija Polovina1,14, Marco Metra15, Giuseppe Ambrosio16, Krishna Prasad17, Jelena Seferović1,18, Pardeep S Jhund19, Giuseppe Dattilo20, Jelena Čelutkiene21, Massimo Piepoli22, Brenda Moura23, Ovidiu Chioncel24,25, Tuvia Ben Gal26, Stefan Heymans27, Rudolf A de Boer28, Tiny Jaarsma29, Loreena Hill30, Yuri Lopatin31, Alexander R Lyon32, Piotr Ponikowski33, Mitja Lainščak34,35, Ewa Jankowska33, Christian Mueller36, Francesco Cosentino37, Lars Lund38, Gerasimos S Filippatos39, Frank Ruschitzka40, Andrew J S Coats41, Giuseppe M C Rosano42.
Abstract
Heart failure (HF) is common and associated with a poor prognosis, despite advances in treatment. Over the last decade cardiovascular outcome trials with sodium-glucose co-transporter 2 (SGLT2) inhibitors in patients with type 2 diabetes mellitus have demonstrated beneficial effects for three SGLT2 inhibitors (empagliflozin, canagliflozin and dapagliflozin) in reducing hospitalisations for HF. More recently, dapagliflozin reduced the risk of worsening HF or death from cardiovascular causes in patients with chronic HF with reduced left ventricular ejection fraction, with or without type 2 diabetes mellitus. A number of additional trials in HF patients with reduced and/or preserved left ventricular ejection fraction are ongoing and/or about to be reported. The present position paper summarises recent clinical trial evidence and discusses the role of SGLT2 inhibitors in the treatment of HF, pending the results of ongoing trials in different populations of patients with HF.Entities:
Keywords: Cardiovascular outcomes; Heart failure; Quality of life; Sodium-glucose co-transporter 2 inhibitors; Type 2 diabetes mellitus
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Year: 2020 PMID: 32618086 DOI: 10.1002/ejhf.1954
Source DB: PubMed Journal: Eur J Heart Fail ISSN: 1388-9842 Impact factor: 15.534