CCS/CHFS Heart Failure Guidelines: Clinical Trial Update on Functional Mitral Regurgitation, SGLT2 Inhibitors, ARNI in HFpEF, and Tafamidis in Amyloidosis.

Journal Article (Journal Article)

In this update, we focus on selected topics of high clinical relevance for health care providers who treat patients with heart failure (HF), on the basis of clinical trials published after 2017. Our objective was to review the evidence, and provide recommendations and practical tips regarding the management of candidates for the following HF therapies: (1) transcatheter mitral valve repair in HF with reduced ejection fraction; (2) a novel treatment for transthyretin amyloidosis or transthyretin cardiac amyloidosis; (3) angiotensin receptor-neprilysin inhibition in patients with HF and preserved ejection fraction (HFpEF); and (4) sodium glucose cotransport inhibitors for the prevention and treatment of HF in patients with and without type 2 diabetes. We emphasize the roles of optimal guideline-directed medical therapy and of multidisciplinary teams when considering transcatheter mitral valve repair, to ensure excellent evaluation and care of those patients. In the presence of suggestive clinical indices, health care providers should consider the possibility of cardiac amyloidosis and proceed with proper investigation. Tafamidis is the first agent shown in a prospective study to alter outcomes in patients with transthyretin cardiac amyloidosis. Patient subgroups with HFpEF might benefit from use of sacubitril/valsartan, however, further data are needed to clarify the effect of this therapy in patients with HFpEF. Sodium glucose cotransport inhibitors reduce the risk of incident HF, HF-related hospitalizations, and cardiovascular death in patients with type 2 diabetes and cardiovascular disease. A large clinical trial recently showed that dapagliflozin provides significant outcome benefits in well treated patients with HF with reduced ejection fraction (left ventricular ejection fraction ≤ 40%), with or without type 2 diabetes.

Full Text

Duke Authors

Cited Authors

  • O'Meara, E; McDonald, M; Chan, M; Ducharme, A; Ezekowitz, JA; Giannetti, N; Grzeslo, A; Heckman, GA; Howlett, JG; Koshman, SL; Lepage, S; Mielniczuk, LM; Moe, GW; Swiggum, E; Toma, M; Virani, SA; Zieroth, S; De, S; Matteau, S; Parent, M-C; Asgar, AW; Cohen, G; Fine, N; Davis, M; Verma, S; Cherney, D; Abrams, H; Al-Hesayen, A; Cohen-Solal, A; D'Astous, M; Delgado, DH; Desplantie, O; Estrella-Holder, E; Green, L; Haddad, H; Harkness, K; Hernandez, AF; Kouz, S; LeBlanc, M-H; Lee, D; Masoudi, FA; McKelvie, RS; Rajda, M; Ross, HJ; Sussex, B

Published Date

  • February 2020

Published In

Volume / Issue

  • 36 / 2

Start / End Page

  • 159 - 169

PubMed ID

  • 32036861

Electronic International Standard Serial Number (EISSN)

  • 1916-7075

Digital Object Identifier (DOI)

  • 10.1016/j.cjca.2019.11.036

Language

  • eng

Conference Location

  • England