Evidence map›Paper›PMID 41574038›Full record

ArticleEuropean heart journal. Digital health2026

Development of a smartphone-based app to support the differential diagnosis in patients with primary left ventricular hypertrophy.

Niccolò Maurizi, Emanuele Monda, Maurizio Pieroni, Elena Biagini, Ella Field, Silvia Passantino, Gabriella Dallaglio, Carlo Fumagalli, Panagiotis Antiochos, Ioannis Skalidis and 10 more

Abstract read
In one paragraph

Article in European heart journal. Digital health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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.

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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

20 authors.

Niccolò MauriziCardiomyopathy Unit, Careggi University Hospital, Largo Brambilla 3, Florence 50121, Italy.ORCID https://orcid.org/0000-0001-5819-204X
Emanuele MondaInherited and Rare Cardiovascular Diseases Unit, Department of Translational Medical Sciences, University of Campania 'Luigi Vanvitelli', Monaldi Hospital, Naples, Italy.
Maurizio PieroniCardiomyopathy Unit, Careggi University Hospital, Largo Brambilla 3, Florence 50121, Italy.ORCID https://orcid.org/0000-0002-6830-4292
Elena BiaginiCardiology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.ORCID https://orcid.org/0000-0003-0295-0440
Ella FieldCentre for Paediatric Inherited and Rare Cardiovascular Disease, Institute of Cardiovascular Science, University College London, London, UK.
Silvia PassantinoService of Cardiology, Meyer Children's Hospital IRCCS, Florence, Italy.
Gabriella DallaglioCardiomyopathy Unit, Careggi University Hospital, Largo Brambilla 3, Florence 50121, Italy.
Carlo FumagalliCardiomyopathy Unit, Careggi University Hospital, Largo Brambilla 3, Florence 50121, Italy.
Panagiotis AntiochosService of Cardiology, University Hospital of Lausanne (CHUV), Lausanne, Switzerland.
Ioannis SkalidisInstitut Cardiovasculaire Paris Sud, Mancy, Paris, France.ORCID https://orcid.org/0000-0002-4374-0389
Henri LuService of Cardiology, University Hospital of Lausanne (CHUV), Lausanne, Switzerland.ORCID https://orcid.org/0000-0002-9074-6505
Ioannis KachrimanidisService of Cardiology, Ippokrateio General Hospital, Athens, Greece.
Alessia ArgiròCardiomyopathy Unit, Careggi University Hospital, Largo Brambilla 3, Florence 50121, Italy.ORCID https://orcid.org/0000-0002-6394-9948
Francesca GirolamiService of Cardiology, Meyer Children's Hospital IRCCS, Florence, Italy.ORCID https://orcid.org/0000-0001-9143-3597
Franco CecchiCardiomyopathy Unit, Careggi University Hospital, Largo Brambilla 3, Florence 50121, Italy.
Francesco CappelliCardiomyopathy Unit, Careggi University Hospital, Largo Brambilla 3, Florence 50121, Italy.
Perry M ElliottCentre for Heart Muscle Disease, Institute of Cardiological Sciences, University College London and St. Bartholomew's Hospital, London, UK.
Juan Pablo KaskiCentre for Paediatric Inherited and Rare Cardiovascular Disease, Institute of Cardiovascular Science, University College London, London, UK.
Giuseppe LimongelliInherited and Rare Cardiovascular Diseases Unit, Department of Translational Medical Sciences, University of Campania 'Luigi Vanvitelli', Monaldi Hospital, Naples, Italy.
Iacopo OlivottoCardiomyopathy Unit, Careggi University Hospital, Largo Brambilla 3, Florence 50121, Italy.ORCID https://orcid.org/0000-0003-1751-9266

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aims: Patients with primary left ventricular hypertrophy (LVH) often experience a diagnostic delay of several years, largely related to fragmented knowledge among different specialties and the rarity of the conditions. We developed and validated a digital support tool to guide the physician in the differential diagnostic process of patients presenting with primary LVH. Methods and results: A total of 818 patients with definitive diagnosis of sarcomeric hypertrophic cardiomyopathy (HCM) or one of its phenocopies [479 (62%) males, 48 ± 24 years] were included. Pre-specified disease-specific red flags (RFs) were categorized into five domains: family history, signs/symptoms, electrocardiography, echocardiographic, and laboratory. Each patient's characteristics were inserted by two independent and blind investigators into the app. The diagnostic outcome, based on the presence/absence of RF, was categorized as follows: (i) most likely diagnosis, (ii) possible diagnosis, and (iii) less likely diagnosis. A total of 2979 RFs were identified and non-sarcomeric phenocopies exhibited a higher RF burden than sarcomeric HCM (3.9 vs. 2.7 RFs per patient, Conclusion: The Thick-Heart App correctly classified 93% of cases into the most-likely diagnosis category (sensitivity 88-100%, specificity 97%). Our study underscores the potential clinical value of digital decision support tools to enable timelier identification of specific cardiomyopathies, by promoting awareness in non-reference settings.

Indexed as

AppHypertrophic cardiomyopathyPhenocopiesRed flags

Identifiers

PMID41574038
PMCPMC12821060

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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.