Evidence map›Paper›PMID 42814187›Full record

ReviewHeart failure reviews2026

Complication management in hypertrophic cardiomyopathy.

Viktoria Höller, Peter-Paul Zwetsloot, Viktoria Santner, Nora Schwegel, Sophie Luise Pötsch, Nicolas Verheyen, Michelle Michels

Abstract readReview
In one paragraph

Review in Heart failure reviews, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Viktoria Höller *Department of Cardiology, University Heart Center, Medical University of Graz, Graz, Austria.
Peter-Paul Zwetsloot *Department of Cardiology, Thoraxcenter, Cardiovascular Institute, Erasmus MC, Dr. Molewaterplein 40, Rotterdam, 3015GD, The Netherlands.
Viktoria SantnerDepartment of Cardiology, University Heart Center, Medical University of Graz, Graz, Austria.
Nora SchwegelDepartment of Cardiology, University Heart Center, Medical University of Graz, Graz, Austria.
Sophie Luise PötschDepartment of Cardiology, University Heart Center, Medical University of Graz, Graz, Austria.
Nicolas Verheyen *Department of Cardiology, University Heart Center, Medical University of Graz, Graz, Austria.
Michelle Michels *Department of Cardiology, Thoraxcenter, Cardiovascular Institute, Erasmus MC, Dr. Molewaterplein 40, Rotterdam, 3015GD, The Netherlands. m.michels@erasmusmc.nl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiac disorder, yet remains substantially underdiagnosed in clinical practice. Although current guidelines define HCM primarily based on left ventricular wall thickness, this approach alone does not capture the full spectrum of disease expression. Comprehensive phenotyping using multimodality imaging, combined with genetic testing and systematic family screening, allows for more accurate diagnosis and earlier detection, although its integration into routine clinical algorithms remains incomplete. Clinical outcomes and therapeutic strategies in HCM are largely driven by disease-related complications. These include heart failure, atrial fibrillation, ventricular arrhythmias, and sudden cardiac death, where risk stratification and prevention are central. While left ventricular outflow tract obstruction represents a major therapeutic target with rapidly evolving treatment options, alternative obstruction phenotypes and non-obstructive disease have received comparatively less attention. In these patients, symptoms are often determined by microvascular dysfunction, diastolic impairment, and myocardial fibrosis, contributing to myocardial ischemia and heart failure. Recent advances in targeted therapies, particularly cardiac myosin inhibitors, highlight the increasing importance of precise phenotypic characterization for treatment selection. However, their long-term impact on disease progression and clinical outcomes remains to be established. Overall, HCM should be considered a dynamic and heterogeneous disease continuum requiring individualized, phenotype-driven diagnostic and therapeutic strategies.

Indexed as

Arrhythmias, CardiacAtrial FibrillationCardiomyopathy, HypertrophicDeath, Sudden, CardiacDisease ManagementHeart FailureHumansPhenotypeVentricular Outflow Obstruction, LeftArrhythmiaComplication managementHeart failureHypertrophic cardiomyopathyIschemiaObstruction

Identifiers

PMID42814187
PMCPMC13627219

What OpenQuestion holds

Textmetadata
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.