Evidence map›Paper›PMID 39187605›Full record

ReviewHeart failure reviews2024

Embracing an era of targeted combination therapy for heart failure with preserved ejection fraction.

Satoshi Shoji, Stephen J Greene, Robert J Mentz

Abstract readReview
PubMed Publisher
In one paragraph

Review in Heart failure reviews, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

3 authors.

Satoshi ShojiDuke Clinical Research Institute, 300 W Morgan St, Durham, NC, 27701, USA. satoshi.shoji@duke.edu.ORCID 0000-0002-2223-7215
Stephen J GreeneDuke Clinical Research Institute, 300 W Morgan St, Durham, NC, 27701, USA.
Robert J MentzDuke Clinical Research Institute, 300 W Morgan St, Durham, NC, 27701, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The concept of quadruple therapy as a "one-size-fit-all" approach is effective among all eligible patients with heart failure with reduced ejection fraction, with consistent and significant clinical benefits including reduced mortality across various subgroups. However, with exception of sodium-glucose cotransporter 2 inhibitors, the consistency of benefit with therapies does not extend to patients with heart failure with preserved ejection fraction. The clinical benefits of other promising medical therapies, such as angiotensin receptor-neprilysin inhibitors, mineralocorticoid receptor antagonists, and glucagon-like peptide-1 receptor agonists, have been demonstrated only in certain phenotypes of the highly heterogenous heart failure with preserved ejection fraction population. This variability can confuse frontline practicing cardiologists, potentially leading to the under-implementation of these medications. Therefore, we propose a simple approach: "targeted" combination therapy. This strategy aims to optimize evidence-based medications in heart failure with preserved ejection fraction by tailoring treatments to specific subgroups within the heart failure with preserved ejection fraction population where significant benefits are most evident.

Indexed as

Drug Therapy, CombinationHeart FailureMineralocorticoid Receptor AntagonistsStroke VolumeAngiotensin-Converting Enzyme InhibitorsAngiotensin Receptor AntagonistsHumansSodium-Glucose Transporter 2 InhibitorsAngiotensin-Converting Enzyme InhibitorsAngiotensin Receptor AntagonistsMineralocorticoid Receptor AntagonistsSodium-Glucose Transporter 2 InhibitorsAngiotensin receptor–neprilysin inhibitorGlucagon-like peptide-1 receptor agonistHeart failure with preserved ejection fractionMineralocorticoid receptor antagonistsSodium-glucose cotransporter 2 inhibitorWorsening heart failure

Identifiers

What OpenQuestion holds

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Registered trials

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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.