scholarly journals Anatomy and function of the heart and intrathoracic vessels in congenital heart disease: Evaluation with the dynamic spatial reconstructor

1985 ◽  
Vol 5 (1) ◽  
pp. 70S-76S ◽  
Author(s):  
Lawrence J. Sinak ◽  
Yun-He Liu ◽  
Michael Block ◽  
Douglas D. Mair ◽  
Paul R. Julsrud ◽  
...  
2020 ◽  
Vol 22 (12) ◽  
Author(s):  
Benjamin Kelly ◽  
Sheyanth Mohanakumar ◽  
Vibeke Elisabeth Hjortdal

Abstract Purpose of Review Lymphatic disorders have received an increasing amount of attention over the last decade. Sparked primarily by improved imaging modalities and the dawn of lymphatic interventions, understanding, diagnostics, and treatment of lymphatic complications have undergone considerable improvements. Thus, the current review aims to summarize understanding, diagnostics, and treatment of lymphatic complications in individuals with congenital heart disease. Recent Findings The altered hemodynamics of individuals with congenital heart disease has been found to profoundly affect morphology and function of the lymphatic system, rendering this population especially prone to the development of lymphatic complications such as chylous and serous effusions, protein-losing enteropathy and plastic bronchitis. Summary Although improved, a full understanding of the pathophysiology and targeted treatment for lymphatic complications is still wanting. Future research into pharmacological improvement of lymphatic function and continued implementation of lymphatic imaging and interventions may improve knowledge, treatment options, and outcome for affected individuals.


2020 ◽  
Vol 21 (Supplement_1) ◽  
Author(s):  
I Sanz Ortega ◽  
S Velasco Del Castillo ◽  
J J Onaindia Gandarias ◽  
I Rodriguez Sanchez ◽  
J Florido Perena ◽  
...  

Abstract Introduction Due to the complexity of congenital heart disease and limitations of transthorathic echocardiogram (TTE), especially in adult patients, it is not unusual to need other image techniques to assess cardiac anatomy and function. The most common primary anomaly of tricuspid valve (TV) is Ebstein anomaly, but there are other much rarer primary anomalies of this valve consisting in prolapse, cord retraction.... without downward displacement of the leaflet, generally causing tricuspid regurgitation (TR) that can be severe and sometimes intervention is needed, preferably reparation. Due to anatomical issues, it is difficult to assess anatomy of TV in TTE, so sometimes 3D-TTE must be performed to clarify the mechanism and to measure orifice, but when transthoracic view is not enough, 3D transoesophageal echocardiogram (TOE) can be useful for this purpose. Case We report the case of a 15-year-old boy that was referred to our clinic because of shortness of breath and a systolic tricuspid murmur. TTE was performed and an image compatible with tricuspid valve prolapse with no apical displacement of any leaflets (Figure, A) causing severe TR (Figure, B) was noticed, as well as severely dilated right chambers, with good ejection fraction of both ventricles. It was not clear the mechanism so 2D TOE was done, showing a prolapse of a leaflet (Figure, C) causing severe TR (Figure, D). The mechanism was finally clarified by 3D TOE (figure E). This was a prolapse of lateral portion of posterior leaflet (asterisk) with restrictive movement of anterior (triangle) and septal (arrow) ones, causing a huge coaptation defect in systole leading to a very severe tricuspid insufficiency with signs of volume overload of right ventricle. There was no atrial septal defect and pulmonary drainage anomalies were ruled out by cardiac magnetic resonance. Patient was referred to surgery due to symptoms and great dilatation of right chambers. Conclusión: Due to anatomical complexity and limitations of echography, cross and multimodality cardiac imaging is usually needed in assessing congenital heart disease. Apart from Ebstein anomaly, other congenital entities of tricuspid valve such as prolapse and/or retraction can lead to severe tricuspid regurgitation. Due to limitations of 2D TTE in assessing tricuspid valve anatomy, 3D TTE has to be performed, but if it is not enough, 3D TOE can be an option to evaluate mechanism and directly see the orifice of regurgitation in congenital disease of tricuspid valve. Abstract P879 Figure


2016 ◽  
Vol 18 (suppl E) ◽  
pp. E15-E18 ◽  
Author(s):  
Alessandro Giamberti ◽  
Alessandro Varrica ◽  
Giuseppe Pomè ◽  
Angelo Micheletti ◽  
Diana Negura ◽  
...  

2019 ◽  
Vol 6 (3) ◽  
pp. 1130
Author(s):  
Kalpana M. S. ◽  
Vijayanthi Mala J.

Background: Congenital heart disease (CHD) is a defect in the cardiovascular structure and function and represents a heterogeneous group of defects with little known cause. Most of them are diagnosed in newborn period, yet some may be missed only to be diagnosed later. CHDs present with little or no symptoms and hence are under diagnosed in centres with inadequate facilities. So, this study was conducted to find the prevalence of CHDs in neonates delivered in our centre.Methods: The study was conducted in an urban community centre from May 2018 to January 2019. Babies delivered here were subjected to clinical examination, pulse oximetry at our centre and detailed ECHO examination was done at a nearby PHC where a trained cardiologist was available.Results: There were 783 babies delivered during the study period, of which 436 babies underwent echo and formed the study group. Totally 35 (8%) babies had some abnormality on echo. Clinically murmurs were present in 10 newborns. Critical congenital heart disease was seen in 3(0.6%) babies. These babies were diagnosed with severe PS, Bicuspid aortic valve with severe AS and pulmonary atresia. VSD was the commonest malformation followed by ASD and PDA.Conclusions: Screening of CHD helps to detect defects which otherwise would have been missed. Critical CHD could be diagnosed which enabled us to refer the babies for early surgery.


ESC CardioMed ◽  
2018 ◽  
pp. 697-699
Author(s):  
Eloisa Arbustini ◽  
Alessandro Di Toro ◽  
Lorenzo Giuliani ◽  
Nupoor Narula ◽  
Valentina Favalli

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 paradigmatic examples are infantile tafazzinopathies. The prevalence of LVNC in healthy athletes, its possible reversibility, and increasing diagnosis in healthy subjects suggest cautious use of the term LVNC cardiomyopathy, which describes the morphology, but not the functional profile of the cardiomyopathy or the associated congenital disease. Therefore, when associated with left ventricular dilation and dysfunction, hypertrophy, or congenital heart disease, the leading diagnosis is cardiomyopathy or congenital heart disease followed by the addition of the descriptor LVNC.


2011 ◽  
Vol 41 (8) ◽  
pp. 1000-1007 ◽  
Author(s):  
Rowan Walsh ◽  
Yishay Salem ◽  
Amee Shah ◽  
Wyman W. Lai ◽  
James C. Nielsen

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