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Systemic Hypertension in Pediatric Veno-Venous Extracorporeal Membrane Oxygenation

Abstract Systemic hypertension (HTN) is a recognized complication of veno-venous (VV) extracorporeal membrane oxygenation (ECMO) in children. We sought to determine the prevalence and associated features of HTN in a..

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Microcirculatory Changes in Pediatric Patients During Congenital Heart Defect Corrective Surgery

Abstract A prospective, observational single-center study was carried out. Pediatric patients undergoing congenital heart defect surgery were evaluated before, during, and after surgery. At each time point, sublingual microcirculation and..

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Directing a dispersion cannula tip toward the aortic root during thoracic aortic arch surgery does not adversely affect cardiac function

Abstract Introduction: Neurologic complications of open thoracic aortic surgery are devastating problems in patients with severely diseased aortas. This study aimed to clarify whether directing the aortic cannula tip toward..

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Scavenging right atrial Bretschneider histidine-tryptophan-ketoglutarate cardioplegia: Impact on hyponatremia and seizures in pediatric cardiac surgery patients

Abstract Objective Custodiol-HTK  (Custodiol-HTK Koheler Chemie, GmbH, Bensheim, Germany) causes fluctuations in serum sodium levels, , and is associated with postoperative seizures. We investigated the influence of scavenging right atrial effluent during..

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Initial experience with del Nido cardioplegia solution at a Pediatric and Congenital Cardiac Surgery Program in Brazil

Abstract Objective: The aim of this study was to evaluate outcome measures between our standard multidose cardioplegia protocol and a del Nido cardioplegia protocol in congenital heart surgery patients. Methods:..

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Fluid Status After Cardiac Surgery Assessed by Bioelectrical Impedance Vector Analysis and the Effects of Extracorporeal Circulation

Abstract Objective  after cardiac surgery can be difficult to assess, often requiring invasive measurements. Bioelectrical impedance vector analysis (BIVA) is based on patterns of resistance (R) and reactance (Xc), corrected..

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Influence of cardiopulmonary bypass set-up and management on clinical outcomes after minimally invasive aortic valve surgery

Abstract Introduction: Minimally invasive aortic valve replacement (MIAVR) requires changes in cannulation strategy and cardiopulmonary bypass (CPB) management when compared to the conventional approach (CAVR). We aimed at evaluating if..

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FISIOLOGIA CARDÍACA - Webinar 12

Aula sobre fisiologia cardíaca. A nossa primeira aula de uma série para falar do coração. Prof. Elio Carvalho é Biomédico, Microbiologista e Perfusionista pela Unicamp, CLAP e SBCEC. É perfusionista..

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Right pulmonary artery (RPA) stenosis

Pulmonary artery stenosis is a heart defect that causes a narrowing of the pulmonary artery, the large blood vessel that takes blood from the right ventricle of the heart to..

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Tricuspid valve stenosis

Very little is known about tricuspid valve when compared to other valves, and tricuspid stenosis is rarely described. It most often co-exists with mitral valve pathology especially in patients with..

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Uhl anomaly

Uhl's Anomaly is a rare cardiac condition in which there is total absence of right ventricular myocardium resulting in apposition of the endocardium and epicardium. We report a case of..

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Turner syndrome

Turner syndrome, a condition that affects only females, results when one of the X chromosomes (sex chromosomes) is missing or partially missing. Turner syndrome can cause a variety of medical..

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Single ventricle

A single ventricle is an uncommon occurrence in embryogenesis, which results in the anatomical or functional loss of a ventricular cavity. These malformations are life-threatening and necessitate quick revision to..

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Shone Syndrome

Shone syndrome is a collection of eight left-sided obstructive heart lesions. These affect blood flow to and from the left ventricle, or lower left heart chamber. Shone syndrome was identified..

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Right cervical arch

Cervical aortic arches are a rare  characterized by an elongated, high-lying aortic arch extending at or above the level of the medial ends of the .

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Right aortic arch

Right aortic arch anomalies occur in approximately 0.01 to 0.1 percent of the general population. In general, these anomalies do not directly cause any cardiovascular problems. However, in some patients,..

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Retroesophagial aortic arch

Right aortic arch is an uncommon anatomic anomaly, which occurs in approximately 0.05% to 0.1% of the population. “Mirror-image” right aortic arch is by itself generally asymptomatic, but it is usually..

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Pulmonary atresia with ventricular septal defect (PAVSD) with major pulmonary confluens

The surgical management of pulmonary atresia with ventricular septal defect (VSD), extreme hypoplasia of the pulmonary arteries (PA), major aorto–pulmonary collaterals (MAPCAS) represents a major challenge. Two main basic concepts..

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Pulmonary valve stenosis

Pulmonary valve stenosis is a condition in which a deformity on or near your pulmonary valve narrows the pulmonary valve opening and slows the blood flow. The pulmonary valve is..

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Persistent left superior caval vein draining into the upper left pulmonary vein

Persistent left superior vena cava (PLSVC) is the most common congenital malformation of thoracic venous return and is present in 0.3 to 0.5% of individuals in the general population. This..

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Persistent left superior caval vein

Persistent left superior vena cava (PLSVC) is the most common congenital malformation of thoracic venous return and is present in 0.3 to 0.5% of individuals in the general population. This..

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Patent ductus arteriosus (PDA)

The ductus arteriosus is a normal fetal artery connecting the main body artery (aorta) and the main lung artery (pulmonary artery). The ductus allows blood to detour away from the..

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Partial cor triatriatum sinister

Cor Triatriatum Sinister is a rare congenital abnormality, usually diagnosed in childhood; few cases remain asymptomatic and are diagnosed in adulthood. In this review article we focus on classification and..

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Partial cor triatriatum sinister with partial pulmonary vein connection

Cor Triatriatum Sinister is a rare congenital abnormality, usually diagnosed in childhood; few cases remain asymptomatic and are diagnosed in adulthood. In this review article we focus on classification and..

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