Evidence map›Paper›PMID 38649305›Full record

ArticleESC heart failure2024

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

Jonathan J H Bray, Marco Coronelli, Sam G C Scott, John A Henry, Liam S Couch, Mahmood Ahmad, Julian Ormerod, James Gamble, Timothy R Betts, Andrew Lewis and 3 more

Open access · goldAbstract read
In one paragraph

Article in ESC heart failure, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.6field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 1 country.

Jonathan J H BrayOxford Heart Centre, Oxford University Hospitals, NHS Trust, Oxford, UK.
Marco CoronelliOxford Heart Centre, Oxford University Hospitals, NHS Trust, Oxford, UK.
Sam G C ScottOxford Heart Centre, Oxford University Hospitals, NHS Trust, Oxford, UK.
John A HenryOxford Heart Centre, Oxford University Hospitals, NHS Trust, Oxford, UK.
Liam S CouchOxford Heart Centre, Oxford University Hospitals, NHS Trust, Oxford, UK.
Mahmood AhmadUCL Medical School, University College London, London, UK.
Julian OrmerodOxford Heart Centre, Oxford University Hospitals, NHS Trust, Oxford, UK.
James GambleOxford Heart Centre, Oxford University Hospitals, NHS Trust, Oxford, UK.
Timothy R BettsOxford Heart Centre, Oxford University Hospitals, NHS Trust, Oxford, UK.
Andrew LewisOxford Heart Centre, Oxford University Hospitals, NHS Trust, Oxford, UK.
Oliver J RiderOxford Heart Centre, Oxford University Hospitals, NHS Trust, Oxford, UK.
Peregrine G GreenOxford Heart Centre, Oxford University Hospitals, NHS Trust, Oxford, UK.
Neil HerringOxford Heart Centre, Oxford University Hospitals, NHS Trust, Oxford, UK.
Oxford University Hospitals NHS Trust · GBScience Oxford · GBUniversity College London · GB

Funding

British Heart Foundation FS/SCRF/20/32005British Heart Foundation Senior Clinical Research Fellowships FS/SCRF/20/32005British Heart Foundation Senior Clinical Research Fellowships FS/SCRF/22/32014
6 · The paper itself

Abstract

aimsThe 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. METHODS AND

resultsWe 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).

conclusionsWe 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.

Indexed as

Cardiac Resynchronization TherapyHeart FailureSodium-Glucose Transporter 2 InhibitorsAgedEchocardiographyElectrocardiographyFemaleFollow-Up StudiesHumansMaleRetrospective StudiesStroke VolumeSurvival RateTreatment OutcomeVentricular Function, LeftSodium-Glucose Transporter 2 InhibitorsCardiac resynchronization therapyCRTOptimal medical therapyRemodellingSGLT2iSodium‐glucose co‐transporter 2 inhibitors

Identifiers

PMID38649305
PMCPMC11287366
OpenAlexW4395047436

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.