The heart of an anencephalic baby can be used as a donor after death. There exists insufficient information in literature, however, for the possible morphological differences in anencephalic hearts. This study compares ventricular myocardial thicknesses of anencephalic fetuses with normal fetuses in the same gestational age group. The comparison was made histologically on the slices taken from three levels of anterior and posterior walls of the left and right ventricles and from two levels of the interventricular septum. When each level was taken into account separately, the middle part of the left ventricular anterior wall was detected thinner in anencephalics (P = 0.010). When the mean value for each wall (anterior and posterior) was taken into account, left ventricular anterior wall was found thinner in anencephalics (P = 0.005). When the mean value for each ventricle was compared, the left ventricular wall was detected thinner in anencephalics (P = 0.025). These results support the idea that absence of the cerebral cortex results in modifications of the fetal heart. Because differences were limited to the left ventricular anterior wall non-homogenously, factors other than the decrease in the heart load (e.g., changes in intrathoracic anatomy) might also affect the myocardial features. When the mean value of right ventricle was compared to the left within the normal and anencephalic groups separately, the left ventricle was thicker than the right in normal fetuses (P = 0.016). In anencephalics the difference between two ventricular walls was insignificant (P = 0.084). This supports the left ventricular dominance in normal fetuses but not in anencephalics for the 27-34 weeks of age group. We suggest that when an anencephalic heart is intended to use as a donor, possible alterations presented in this article should be taken into account.
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http://dx.doi.org/10.1002/ca.20015 | DOI Listing |
Cardiol Rev
January 2025
Departments of Cardiology and Medicine, New York Medical College and Westchester Medical Center, Valhalla, NY.
Right ventricular myocardial infarction (RVMI) is a significant and distinct form of acute myocardial infarction associated with considerable morbidity and mortality. It occurs most commonly due to proximal right coronary artery obstruction, often in conjunction with inferior myocardial infarction. RVMI poses unique diagnostic and therapeutic challenges due to the anatomical and functional differences between the right and left ventricles.
View Article and Find Full Text PDFPLoS One
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Department of Pathology, 906 Hospital of Joint Logistic Support Force of PLA, Ningbo, Zhejiang, China.
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Phys Eng Sci Med
January 2025
School of Electrical Engineering and Electronic Information, Xihua University, Chengdu, China.
Hypertrophic cardiomyopathy (HCM), including obstructive HCM and non-obstructive HCM, can lead to sudden cardiac arrest in adolescents and athletes. Early diagnosis and treatment through auscultation of different types of HCM can prevent the occurrence of malignant events. However, it is challenging to distinguish the pathological information of HCM related to differential left ventricular outflow tract pressure gradients.
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Klinik für Elektrophysiologie/Rhythmologie, Ruhr-Universität Bochum, Bochum, Deutschland.
Atrial fibrillation (AF) ablation is associated with a lower likelihood of death and surgical heart failure (HF) interventions in patients with HF. This effect is mainly driven by reduced all cause and cardiovascular death following ablation. Ablation also results in improved left ventricular (LV) function, decreased AF burden and AF regression.
View Article and Find Full Text PDFMultimed Man Cardiothorac Surg
January 2025
Congenital Heart Center, Division of Cardiovascular Surgery, Department of Surgery, University of Florida, Gainesville, FL, USA.
The Berlin Heart EXCOR is a pulsatile paracorporeal ventricular assist device (VAD) for neonates, infants, children and adults with congenital or acquired severe ventricular dysfunction. Berlin Heart EXCOR VADs are routinely used as either a bridge to a cardiac transplantation, or occasionally as a bridge to ventricular recovery. Our programmatic philosophy is to bridge neonates and infants with functionally univentricular ductal-dependent systemic circulation or functionally univentricular ductal-dependent pulmonary circulation who are at high risk for staged palliation because of important cardiac risk factors with a single-ventricle VAD (sVAD) as a bridge to a cardiac transplant.
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