The effect of sodium-glucose co-transporter 2 inhibitors on outcomes after cardiac resynchronization therapy.

CRT Cardiac resynchronization therapy Optimal medical therapy Remodelling SGLT2i Sodium‐glucose co‐transporter 2 inhibitors

Journal

ESC heart failure
ISSN: 2055-5822
Titre abrégé: ESC Heart Fail
Pays: England
ID NLM: 101669191

Informations de publication

Date de publication:
22 Apr 2024
Historique:
revised: 14 02 2024
received: 08 12 2023
accepted: 10 03 2024
medline: 23 4 2024
pubmed: 23 4 2024
entrez: 22 4 2024
Statut: aheadofprint

Résumé

The trials upon which recommendations for the use of cardiac resynchronization therapy (CRT) in heart failure used optimal medical therapy (OMT) before sodium-glucose co-transporter 2 inhibitors (SGLT2i). Moreover, the SGLT2i heart failure trials included only a small proportion of participants with CRT, and therefore, it remains uncertain whether SGLT2i should be considered part of OMT prior to CRT. We compared electrocardiogram (ECG) and echocardiographic responses to CRT as well as hospitalization and mortality rates in consecutive patients undergoing implantation at a large tertiary centre between January 2019 to June 2022 with and without SGLT2i treatment. Three hundred seventy-four participants were included aged 74.0 ± 11.5 years (mean ± standard deviation), with a left ventricular ejection fraction (LVEF) of 31.8 ± 9.9% and QRS duration of 161 ± 29 ms. The majority had non-ischaemic cardiomyopathy (58%) and were in NYHA Class II/III (83.6%). These characteristics were similar between patients with (n = 66) and without (n = 308) prior SGLT2i treatment. Both groups demonstrated similar evidence of response to CRT in terms of QRS duration shortening, and improvements in LVEF, left ventricular end-diastolic inner-dimension (LVIDd) and diastolic function (E/A and e/e'). While there was no difference in rates of hospitalization (for heart failure or overall), mortality was significantly lower in patients treated with SGLT2i compared with those who were not (6.5 vs. 16.6%, P = 0.049). We observed an improvement in mortality in patients undergoing CRT prescribed SGLT2i compared with those not prescribed SGLT2i, despite similar degrees of reverse remodelling. The authors recommend starting SGLT2i prior to CRT implantation, where it does not delay implantation.

Identifiants

pubmed: 38649305
doi: 10.1002/ehf2.14784
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : British Heart Foundation Senior Clinical Research Fellowships
ID : FS/SCRF/20/32005
Organisme : British Heart Foundation Senior Clinical Research Fellowships
ID : FS/SCRF/22/32014

Informations de copyright

© 2024 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.

Références

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Auteurs

Jonathan J H Bray (JJH)

Oxford Heart Centre, Oxford University Hospitals, NHS Trust, Oxford, UK.

Marco Coronelli (M)

Oxford Heart Centre, Oxford University Hospitals, NHS Trust, Oxford, UK.

Sam G C Scott (SGC)

Oxford Heart Centre, Oxford University Hospitals, NHS Trust, Oxford, UK.

John A Henry (JA)

Oxford Heart Centre, Oxford University Hospitals, NHS Trust, Oxford, UK.

Liam S Couch (LS)

Oxford Heart Centre, Oxford University Hospitals, NHS Trust, Oxford, UK.

Mahmood Ahmad (M)

UCL Medical School, University College London, London, UK.

Julian Ormerod (J)

Oxford Heart Centre, Oxford University Hospitals, NHS Trust, Oxford, UK.

James Gamble (J)

Oxford Heart Centre, Oxford University Hospitals, NHS Trust, Oxford, UK.

Timothy R Betts (TR)

Oxford Heart Centre, Oxford University Hospitals, NHS Trust, Oxford, UK.
Department of Cardiovascular Medicine, University of Oxford, Oxford, UK.

Andrew Lewis (A)

Oxford Heart Centre, Oxford University Hospitals, NHS Trust, Oxford, UK.
Department of Cardiovascular Medicine, University of Oxford, Oxford, UK.

Oliver J Rider (OJ)

Oxford Heart Centre, Oxford University Hospitals, NHS Trust, Oxford, UK.
Department of Cardiovascular Medicine, University of Oxford, Oxford, UK.

Peregrine G Green (PG)

Oxford Heart Centre, Oxford University Hospitals, NHS Trust, Oxford, UK.

Neil Herring (N)

Oxford Heart Centre, Oxford University Hospitals, NHS Trust, Oxford, UK.
Department of Cardiovascular Medicine, University of Oxford, Oxford, UK.
Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford, UK.

Classifications MeSH