Relevant bibliographies by topics / Non-compacted cardiomyopathy

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Academic literature on the topic 'Non-compacted cardiomyopathy'

Author: Grafiati
Published: 3 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "Non-compacted cardiomyopathy"

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Di Toro, Alessandro, Lorenzo Giuliani, Alexandra Smirnova, et al. "Myths to debunk: the non-compacted myocardium." European Heart Journal Supplements 22, Supplement_L (2020): L6—L10. http://dx.doi.org/10.1093/eurheartj/suaa124.

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Abstract Left ventricular non-compaction (LVNC) is defined by the triad: prominent trabecular anatomy, thin compacted layer, and deep inter-trabecular recesses. No person, sick or healthy, demonstrates identical anatomy of the trabeculae; their configuration represents a sort of individual dynamic ‘cardiac fingerprinting’. LVNC can be observed in healthy subjects with normal left ventricular (LV) size and function, in athletes, in pregnant women, as well as in patients with haematological disorders, neuromuscular diseases, and chronic renal failure; it can be acquired and potentially reversibl
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Rodriguez-Fanjul, Javier, Sheila Tubio-Gómez, Juan Manuel Carretero Bellón, Carles Bautista-Rodríguez, and Joan Sanchez-de-Toledo. "Neonatal Non-compacted Cardiomyopathy: Predictors of Poor Outcome." Pediatric Cardiology 41, no. 1 (2019): 175–80. http://dx.doi.org/10.1007/s00246-019-02241-w.

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Nikolayeva, N. V., and O. V. Zotova. "NON-COMPACTED MYOCARDIUM OF THE LEFT VENTRICULAR." Health and Ecology Issues, no. 3 (September 28, 2015): 93–97. http://dx.doi.org/10.51523/2708-6011.2015-12-3-21.

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Non-compacted myocardium of the left ventricular refers to poorly studied diseases of the heart muscle. According to the WHO classification, it belongs to the category of unclassified cardiomyopathy. It develops in congenital heart disease, neuromuscular pathology, defects of the facial skull and has no specific clinical manifestations. The main signs are heart failure, ventricular and supraventricular arrhythmias, systemic and pulmonary embolism.
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Casanova, José David, Josefa González Carrillo, Jesús Martín Jiménez, et al. "Trabeculated Myocardium in Hypertrophic Cardiomyopathy: Clinical Consequences." Journal of Clinical Medicine 9, no. 10 (2020): 3171. http://dx.doi.org/10.3390/jcm9103171.

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Aims: Hypertrophic cardiomyopathy (HCM) is often accompanied by increased trabeculated myocardium (TM)—which clinical relevance is unknown. We aim to measure the left ventricular (LV) mass and proportion of trabeculation in an HCM population and to analyze its clinical implication. Methods and Results: We evaluated 211 patients with HCM (mean age 47.8 ± 16.3 years, 73.0% males) with cardiac magnetic resonance (CMR) studies. LV trabecular and compacted mass were measured using dedicated software for automatic delineation of borders. Mean compacted myocardium (CM) was 160.0 ± 62.0 g and trabecul
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Loo-Valverde, María, Vivian Tuesta-García, Michael Zárate-Quispe, Consuelo Luna-Muñoz, Lucy Correa-Lopez, and Willer Chanduví-Puicón. "Echocardiographic Monitoring of Anatomical Changes in the Myocardium of Pediatric Patients with a Diagnosis of Non-Compaction Cardiomyopathy. 2017 – 2021." Revista de la Facultad de Medicina Humana 24, no. 4 (2024): 138–44. http://dx.doi.org/10.25176/rfmh.v24i4.6688.

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Background: Non-compaction cardiomyopathy (NCM) is known as the lack of maturation of the myocardium that is evidenced by prominent trabeculations and the presence of recesses in newborns and infants that can manifest clinically as heart failure. The purpose of the research is to evaluate the anatomical development of pediatric patients diagnosed with NCM at an early age. Clinical Case: Retrospective case series study of patients diagnosed with non-compaction cardiomyopathy during the first year of life, confirmed according to Jenni criteria, with echocardiographic follow-up every 6 months, fr
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Shlopak, L. B. "A case of lef t ventricular non-compaction (differential diagnosis with hypertrophic cardiomyopathy)." Spravočnik vrača obŝej praktiki (Journal of Family Medicine), no. 7 (July 8, 2023): 46–51. http://dx.doi.org/10.33920/med-10-2307-06.

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Non-compacted myocardium is a condition characterized by changes in the myocardium in the form of a slight thickening of the epicardial layer with pronounced trabecularity and deep spaces that communicate with the left ventricle cavity, but not with the coronary arteries. The non-compacted myocardium is characterized by the presence of areas of a two-layer myocardium structure with a pronounced spongy layer and a large number of trabeculae and intertrabecular spaces freely communicating with the heart cavity according to imaging study methods.
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Jagminas, Rokas, Rokas Šerpytis, Pranas Šerpytis, and Sigita Glaveckaitė. "Left Ventricular Hypertrabeculation (LVHT) in Athletes: A Negligible Finding?" Medicina 61, no. 1 (2024): 32. https://doi.org/10.3390/medicina61010032.

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Left ventricular hypertrabeculation (LVHT) used to be a rare phenotypic trait. With advances in diagnostic imaging techniques, LVHT is being recognised in an increasing number of people. The scientific data show the possibility of the overdiagnosis of this cardiomyopathy in a population of people who have very high levels of physical activity. We describe the case of a young athlete with no medical history, who presented with syncope during a marathon running race. Initial evaluation showed elevated troponin I; transthoracic echocardiography showed a trabeculated ventricle and subsequent cardi
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Fatima, Safa, Lintu Ramachandran, and Mohammad Khan. "COMPACTED CARDIA: LEFT VENTRICULAR NON-COMPACTION CARDIOMYOPATHY IN A YOUNG MALE." Journal of the American College of Cardiology 79, no. 9 (2022): 2605. http://dx.doi.org/10.1016/s0735-1097(22)03596-3.

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Rovira, I., G. Fita, P. Matute, C. Roux, J. Fontanals, and C. Gomar. "Non-compacted cardiomyopathy associated with acute mitral chordae rupture: case report." European Journal of Anaesthesiology 22, Supplement 35 (2005): 42. http://dx.doi.org/10.1097/00003643-200506001-00108.

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MJ, Tino-Martinez, Lerma-Espinosa R, Llaguno-López R, Trejo-Bahena NI, Ocaña-Sánchez MA, and Cortés-Benítez A. "Efecto de la rehabilitación cardiaca fase II en pacientes con insuficiencia cardiaca diagnosticados con miocardio no compacto." Revista de Sanidad Militar 72, no. 2 (2018): 84–89. http://dx.doi.org/10.56443/rsm.v72i2.157.

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Background: Non-compacted myocardium is a recently described cardiomyopathy. It can present itself at any age as different clinical entities, such as heart failure syndrome, arrhythmias, systemic embolism, or sudden death. Scientifi c evidence demonstrates a decrease in mortality in patients with heart failure who are admitted to cardiac rehabilitation programs. Objective: To evaluate the effect of phase II cardiac rehabilitation programs in patients diagnosed with heart failure secondary to non-compacted myocardium. Material and methods: An observational and retrospective study was performed,
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Books on the topic "Non-compacted cardiomyopathy"

1

Weidemann, Frank, Gilbert Habib, and Clara Vazquez. Isolated ventricular non-compaction. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780198726012.003.0045.

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Isolated ventricular non-compaction (IVNC) in adults is a rare congenital cardiomyopathy characterized by the presence of prominent myocardial trabeculations in the apical segments of the left ventricle with deep inter-trabecular recesses in communication with the ventricular cavity. Until now there is no clear genetic or laboratory test for the diagnosis of IVNC and thus the diagnosis is defined by clinical and imaging criteria. During echocardiography a maximal end-systolic ratio between the non-compacted endocardial layer and the compacted layer of greater than 2 is consistent with IVNC. Th
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Book chapters on the topic "Non-compacted cardiomyopathy"

1

Arbustini, Eloisa, Alessandro Di Toro, Lorenzo Giuliani, Nupoor Narula, and Valentina Favalli. "Genetics of cardiomyopathies: left ventricular non-compaction." In ESC CardioMed. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198784906.003.0156.

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Left ventricular non-compaction (LVNC) describes a ventricular wall anatomy characterized by prominent left ventricular trabeculae, a thin compacted layer, and deep intertrabecular recesses. Individual variability is extreme. The trabecular configuration represents a type of individual ‘cardioprinting’. By itself, the diagnosis of LVNC does not coincide with that of a ‘cardiomyopathy’ because it can be observed in healthy subjects with normal left ventricular size and function, and it can be acquired and reversible. Rarely, LVNC is intrinsically part of a cardiomyopathy: the paradigmatic examp
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Arbustini, Eloisa, Alessandro Di Toro, Lorenzo Giuliani, Nupoor Narula, and Valentina Favalli. "Genetics of cardiomyopathies: left ventricular non-compaction." In ESC CardioMed. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198784906.003.0156_update_001.

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Abstract:
Left ventricular non-compaction (LVNC) describes a ventricular wall anatomy, characterized by prominent left ventricular trabeculae, a thin compacted layer, and deep intertrabecular recesses. Individual variability is extreme. The trabecular configuration represents a type of individual dynamic ‘cardioprinting’. On its own, the diagnosis of LVNC does not coincide with that of a ‘cardiomyopathy’ because it can be observed in healthy subjects with normal left ventricular size and function, and it can be acquired and reversible. Rarely, LVNC is intrinsically part of a cardiomyopathy: the paradigm
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