Evidence map›Paper›PMID 40424377›Full record

ArticlePloS one2025

Eligibility and GDMT up-titration success in heart failure: A real-world assessment.

Annika Weidenhammer, Suriya Prausmüller, Marc Stadler, Noel Panagiotides, Georg Spinka, Gregor Heitzinger, Henrike Arfsten, Guido Strunk, Anush Barkhudaryan, Clemens Partsch and 5 more

Abstract read
In one paragraph

Article in PloS one, 2025. 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

15 authors.

Annika WeidenhammerDepartment of Internal Medicine II, Clinical Division of Cardiology, Medical University of Vienna, Vienna, Austria.ORCID https://orcid.org/0009-0008-3250-0364
Suriya PrausmüllerDepartment of Internal Medicine II, Clinical Division of Cardiology, Medical University of Vienna, Vienna, Austria.
Marc StadlerDepartment of Internal Medicine II, Clinical Division of Cardiology, Medical University of Vienna, Vienna, Austria.
Noel PanagiotidesDepartment of Internal Medicine II, Clinical Division of Cardiology, Medical University of Vienna, Vienna, Austria.ORCID https://orcid.org/0000-0002-5246-8241
Georg SpinkaDepartment of Internal Medicine II, Clinical Division of Cardiology, Medical University of Vienna, Vienna, Austria.
Gregor HeitzingerDepartment of Internal Medicine II, Clinical Division of Cardiology, Medical University of Vienna, Vienna, Austria.
Henrike ArfstenDepartment of Internal Medicine II, Clinical Division of Cardiology, Medical University of Vienna, Vienna, Austria.
Guido StrunkComplexity Research, Schönbrunner Straße 32, Vienna, Austria.ORCID https://orcid.org/0000-0002-0607-5105
Anush BarkhudaryanDepartment of Internal Medicine II, Clinical Division of Cardiology, Medical University of Vienna, Vienna, Austria.
Clemens PartschDepartment of Internal Medicine II, Clinical Division of Cardiology, Medical University of Vienna, Vienna, Austria.
Philipp BartkoDepartment of Internal Medicine II, Clinical Division of Cardiology, Medical University of Vienna, Vienna, Austria.
Georg GoliaschDepartment of Internal Medicine II, Clinical Division of Cardiology, Medical University of Vienna, Vienna, Austria.
Christian HengstenbergDepartment of Internal Medicine II, Clinical Division of Cardiology, Medical University of Vienna, Vienna, Austria.ORCID https://orcid.org/0000-0002-8284-2994
Martin HülsmannDepartment of Internal Medicine II, Clinical Division of Cardiology, Medical University of Vienna, Vienna, Austria.
Noemi PavoDepartment of Internal Medicine II, Clinical Division of Cardiology, Medical University of Vienna, Vienna, Austria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImplementation of GDMT in HFrEF remains incomplete. Prescription manners may vary based on the development of adverse effects. An HFA position paper proposed patient profiling and individualized prescription manners. This study aims to assess the eligibility for GDMT up-titration and its success in the context of clinical profiles in chronic severe HFrEF outpatients.

methodsClinical characteristics of 900 HFrEF patients at first presentation were assessed, and GDMT up-titration limiting factors were identified by applying thresholds of mutual consent. GDMT prescription was analyzed at 6 months and 1 year.

results75% of patients had no GDMT up-titration limiting factor at baseline. Significant up-titration could be achieved in all four HF drug classes, especially within the first 6 months, irrespective of GDMT up-titration limiting factors (p ≤ 0.035 for administration and dosage, all drug classes). During up-titration, there was a balanced transition between up-titration limiting factors. 35% of patients received triple therapy on target dosages with a 2.6% one-year mortality rate. Regarding the HFA profiles, 62% of patients could not be classified into a specific HFA phenotype, including most severe patients. 98% of classifiable patients belonged to only four phenotypes, while GDMT up-titration could be achieved in all of these HFA profiles (p ≤ 0.007).

conclusionIn this real-world study, 75% of patients with chronic severe HFrEF are eligible for GDMT up-titration towards target dosages. The clinical profile concept of the HFA might be adapted, as most classifiable patients can be up-titrated, and most severe patients are missed by the classification.

Indexed as

Heart FailureAgedFemaleHumansMaleMiddle AgedTreatment Outcome

Identifiers

PMID40424377
PMCPMC12112052

What Socratic 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 Socratic graph.