Rheumatic heart disease (RHD) remains to be a very important health issue worldwide, mainly in underdeveloped countries. It continues to be a leading cause of morbidity and mortality throughout developing countries. RHD is a delayed... more
Rheumatic heart disease (RHD) remains to be a very important health issue worldwide, mainly in underdeveloped countries. It continues to be a leading cause of morbidity and mortality throughout developing countries. RHD is a delayed non-suppurative immunologically mediated inflammatory response to the throat infection caused by a hemolytic streptococcus from the A group (Streptococcus pyogenes). RHD keeps position 1 as the most common cardiovascular disease in young people aged <25 years considering all the continents. The disease can lead to valvular cardiac lesions as well as to carditis. Rheumatic fever valvular injuries lead most commonly to the fusion and thickening of the edges of the cusps and to the fusion, thickening, and shortening of the chordae and ultimately to calcification of the valves. Valvular commissures can also be deeply compromised, leading to severe stenosis. Atrial and ventricular remodeling is also common following rheumatic infection. Mixed valvular lesi...
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Left ventricular noncompaction (LVNC) is a condition characterized by prominent ventricular trabeculae and deep intertrabecular recesses and has been described as a possible substrate for arrhythmias, thromboembolism, and heart failure.... more
Left ventricular noncompaction (LVNC) is a condition characterized by prominent ventricular trabeculae and deep intertrabecular recesses and has been described as a possible substrate for arrhythmias, thromboembolism, and heart failure. Herein, we explored the prevalence of LVNC morphology among hearts with congenital heart defects (CHD). We examined 259 postnatal hearts with one of the following CHD: isolated ventricular septal defect (VSD); isolated atrial septal defect (ASD); atrioventricular septal defect (AVSD); transposition of the great arteries (TGA); isomerism of the atrial appendages (ISOM); Ebstein’s malformation (EB); Tetralogy of Fallot (TF). Eleven hearts from children who died of non-cardiovascular causes were used as controls. The thickness of the compacted and non-compacted left ventricular myocardial wall was determined and the specimens classified as presenting or not LVNC morphology according to three criteria, as proposed by Chin, Jenni, and Petersen. Normal hea...
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Research Interests: Cardiology, Medicine, Electrocardiography, Humans, Internal Medicine, and 12 moreFemale, Aged, Coronary Angiography, Myocardial Infarction, Chest Pain, Infarction, Cardiogenic shock, Inferior Wall myocardial Infarction, QRS complex, Cardiovascular medicine and haematology, Coronary Vessels, and Fatal outcome
Background— Puncture of the atrial appendage may provide access to the pericardial space. The aim of this study was to evaluate the feasibility of epicardial mapping and ablation through an endocardial transatrial access in a swine model.... more
Background— Puncture of the atrial appendage may provide access to the pericardial space. The aim of this study was to evaluate the feasibility of epicardial mapping and ablation through an endocardial transatrial access in a swine model. Methods and Results— An 8-F Mullins sheath was used to perforate the right (n=16) or left (n=1) atrial appendage in 17 pigs (median weight, 27.5 kg; first and third quartiles [Q1, Q3], 25.2, 30.0 kg). A 7-F ablation catheter was introduced into the pericardial space to perform epicardial mapping and deliver radiofrequency pulses on the atria. The pericardial space was entered in all 17 animals. In 15 (88%) animals, there was no hemodynamic instability (mean blood pressure monitoring, initial median, 80 mm Hg; Q1, Q3, 70, 86 mm Hg; final median, 88 mm Hg; Q1, Q3, 80, 96 mm Hg; P =0.426). In these 15, a mild hemorrhagic pericardial effusion was identified and aspirated (median, 20 mL; Q1, Q3, 15, 30 mL) during the procedure, and postmortem gross anal...
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Research Interests: Pathology, Cardiology, Electron Microscopy, Evolution, Medicine, and 15 moreCatheterization, Cell morphology, Internal Medicine, Animals, Cell, Optical microscopy, Exploration, Morphological Analysis, Clinical Sciences, Gout, Right Ventricle, Catheter, Balloon Catheter, Pulmonary Artery, and Cardiovascular medicine and haematology
Research Interests: Cardiology, Immunohistochemistry, Medicine, Echocardiography, Internal Medicine, and 15 moreANOVA, Animals, PT, Heart, Mechanism, Hyperplasia, Hypertrophy, Clinical Sciences, Goats, Analysis of Variance, Cell Proliferation, Heart Ventricles, Pulmonary Artery, Sirius Red, and Cardiovascular medicine and haematology
Research Interests: Cardiology, Immunohistochemistry, Medicine, Extracellular Matrix, Humans, and 15 moreInternal Medicine, Capillaries, Left Ventricular Assist Device, Female, Male, Infant, Fibrosis, Clinical Sciences, Left ventricular hypertrophy, Age Factors, Thoracic and cardiovascular surgery, Atresia, Left Ventricular, Cardiovascular medicine and haematology, and ventricle
Background— Fetal atrioventricular (AV) block is an uncommon lesion with significant mortality. Because of the rarity of this disorder, the natural course, extensive evaluation of untreated fetuses, and late follow-up remain unclear.... more
Background— Fetal atrioventricular (AV) block is an uncommon lesion with significant mortality. Because of the rarity of this disorder, the natural course, extensive evaluation of untreated fetuses, and late follow-up remain unclear. Methods and Results— Of the 116 consecutive cases of fetal AV block studied from 1988 to 2006, only 1 was terminated, and 75% were live births. Fifty-nine cases of AV block were associated with major structural heart disease, mainly left atrial isomerism (n=40), with only 26% of neonatal survivors. Of the 57 fetuses with normal cardiac anatomy, 41 (72%) were positive for maternal antinuclear antibodies, and 32 of these seropositive mothers did not receive any treatment. This untreated group had live-birth and 1-year infant survival rates of 93% and 90%, respectively. Five fetuses from seronegative mothers showed regression to sinus rhythm during pregnancy. The presence of major structural heart disease, hydrops, an atrial rate ≤120 bpm, and a ventricula...
Research Interests: Treatment Outcome, Medicine, Pregnancy, Humans, Internal Medicine, and 13 moreFemale, Infant, Follow-up studies, Heart Disease, Clinical Sciences, Public health systems and services research, Retrospective Studies, Circulation, Fetus, Perinatal Outcome, University Hospitals, Perinatal Care, and Cardiovascular medicine and haematology
Surgical banding of the pulmonary artery in patients with transposition of the great arteries leads to a rapid increase of the left ventricular mass. The purpose of this animal experiment was to induce ventricular systolic hypertension in... more
Surgical banding of the pulmonary artery in patients with transposition of the great arteries leads to a rapid increase of the left ventricular mass. The purpose of this animal experiment was to induce ventricular systolic hypertension in the “subpulmonary ventriclerdquo; by intravascular obstruction to pulmonary flow. The first experiment was performed in an anesthetized animal with an open thorax. A balloon-tipped catheter was introduced into the femoral vein and advanced to the pulmonary artery. The balloon was positioned in the pulmonary trunk and was progressively inflated until a systemic pressure was achieved in the “pulmonary ventricle”. This was accomplished within 40 minutes without a significant reduction in cardiac output, which was continuously monitored by an electromagnetic flowprobe. In the second experiment an analogous procedure was performed in a closed chest, awake, spontaneously breathing animal. The catheter was maintained in proper place for 24 hours. Subseque...
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Aim of our study was to investigate the feasibility of use and possible additional value of real-time 3D transesophageal echocardiography (RT-3D-TEE) compared to conventional 2D-TEE in patients undergoing elective mitral valve repair.... more
Aim of our study was to investigate the feasibility of use and possible additional value of real-time 3D transesophageal echocardiography (RT-3D-TEE) compared to conventional 2D-TEE in patients undergoing elective mitral valve repair. After ethical committee approval, patients were included in this prospective study. After induction of anesthesia, a comprehensive 2D-TEE examination was performed, followed with RT-3D-TEE. The intraoperative surgical finding was used as the gold standard for segmental analysis. Only such segments which were surgically corrected either by resection or insertion of artificial chords were judged pathologic. A total of 50 patients were included in this study; usable data were available from 42 of these patients . Based on the Carpentier classification, the pathology found was type I in 2 (5%) patients, type II in 39 (93%) patients and type IIIb in 1 (2%) patient. We found that 3D imaging of complex mitral disease involving multiple segments, when compared to 2D-TEE did not show any statistically significant difference.RT-3D-TEE did not show any major advantage when compared to conventional 2D-TEE for assessing mitral valve pathology, although further study in a larger population is required to establish the validity of this study.
Research Interests: Cardiology, Medicine, Echocardiography, Prospective studies, Humans, and 11 moreInternal Medicine, Computer Systems, Female, Male, Mitral Valve Repair, Clinical Sciences, Mitral valve prolapse, Heart Valve Prosthesis Implantation, Cardiovascular medicine and haematology, minimally invasive surgical procedures, and Mitral valve
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To study the pathogenesis, evolution and prognosis of the complete heart block of the fetus. Bidimensional echocardiography associated to M-mode and doppler was performed in 600 patients. All cases of congenital heart block were referred... more
To study the pathogenesis, evolution and prognosis of the complete heart block of the fetus. Bidimensional echocardiography associated to M-mode and doppler was performed in 600 patients. All cases of congenital heart block were referred because the fetuses presented hydrops, bradycardia and/or cardiac malformation suspected by routine ultrasound. Isolated heart block was found in 6 fetuses (5 cases of complete type and 1 case of 2nd degree type 2:1). Heart block associated with complex cardiac disease and left atrial isomerism was found in 6 fetuses with no survivors (5 cases of complete type and 1 case of 2nd degree type 2:1). Heart block associated with atrioventricular discordante was found in 1 case. The findings of this study agree the literature about the relation between maternal anti-RO antibodies and isolated complete heart block. We also found a poor prognosis in the group with heart block and complex cardiac malformations.
Research Interests: Cardiology, Brazil, Medicine, Electrocardiography, Echocardiography, and 14 morePregnancy, Humans, Internal Medicine, Female, Incidence, Heart Disease, Newborn Infant, Prognosis, Fetus, Bradycardia, Arquivos brasileiros, Heart Block, Cardiovascular medicine and haematology, and Connective Tissue Diseases
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Neste trabalho, quantificamos fatores de crescimento em fragmentos de miocárdio de 19 cardiopatas chagásicos crônicos com insuficiência cardíaca congestiva, através da técnica da imunoperoxidase. Pesquisamos: antígenos de T. cruzi ,... more
Neste trabalho, quantificamos fatores de crescimento em fragmentos de miocárdio de 19 cardiopatas chagásicos crônicos com insuficiência cardíaca congestiva, através da técnica da imunoperoxidase. Pesquisamos: antígenos de T. cruzi , fatores de crescimento (GM-CSF, TGF-beta1, PDGF-A e PDGF-B) e células inflamatórias (CD4+, CD8+, CD20+ e CD68+). A razão média CD4+/CD8+ foi 0,6 ± 0,3. O número médio de macrófagos (CD68+) foi 5,9±3,1; de células intersticiais PDGF-A+ foi 7,5 ± 4,3; PDGF-B+ 2,9 ± 2,7, TGF-beta1+ 2,2 ± 1,9 e GM-CSF+ 2,3 ± 1,9. A marcação para PDGF-A foi geralmente intensa, ocorrendo também em endotélio, células musculares lisas e sarcolema; não houve correlação dessa positividade com a quantidade de células intersticiais positivas para os mesmos fatores. TGF-beta1 ocorreu em baixa expressão em 100% dos casos. Em conclusão, PDGF-A e B são, provavelmente, os fatores de crescimento mais relacionados às lesões proliferativas na cardiopatia chagásica crônica e, conseqüentement...
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A newborn with transposition of the great arteries presented with rupture of the ductus arteriosus after balloon catheter atrioseptostomy. The necropsy study demonstrated persistent ductus patency, and a 0.5‐cm‐long horizontal fissure... more
A newborn with transposition of the great arteries presented with rupture of the ductus arteriosus after balloon catheter atrioseptostomy. The necropsy study demonstrated persistent ductus patency, and a 0.5‐cm‐long horizontal fissure could be observed. On microscopy, there was laceration of the intimal layer, with wall dissection and focal hemorrhage extending to the adventitia. Ductus rupture was attributed to the wall weakess, as a consequence of prostaglandin E1 administration.
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Research Interests: Cardiology, Microscopy, Medicine, Instrumentation, Internal Medicine, and 15 moreHemodynamics, Blood Pressure, Animals, Clinical Sciences, Goats, Dimensional, Left ventricular hypertrophy, Right Ventricle, Equipment Design, Heart Ventricles, Pressure Gradient, Control Group, Experimental Model, Pressure Overload, and Cardiovascular medicine and haematology
The membrane attack complex (MAC) of complement participates in several inflammatory and proliferative processes by releasing pro‐inflammatory cytokines and growth factors from target cells. Chronic Chagasic cardiomyopathy (CCH) is a... more
The membrane attack complex (MAC) of complement participates in several inflammatory and proliferative processes by releasing pro‐inflammatory cytokines and growth factors from target cells. Chronic Chagasic cardiomyopathy (CCH) is a parasitic dilated cardiopathy, characterized by severe fibrosis and inflammation, which differs from idiopathic dilated cardiomyopathy (DCM). Trypanosoma cruzi, the pathogenic organism of CCH, is a strong complement activator and can also induce alternative pathway activation by mammalian cells. This study explored whether the myocardium in CCH patients has increased MAC deposition, an expression of complement activation, compared to DCM patients. MAC was semi‐quantified in endomyocardial human samples (29 CCH subjects, 18 DCM subjects, and four controls) by immunohistochemistry. MAC was present in the sarcolemma of 38% of CCH, 5.5% of DCM (p<0.02), and 0% of controls, and in interstitial inflammatory cells of CCH. No difference was observed in the e...
Research Interests: Complement activation, Inflammation, Immunohistochemistry, Medicine, Complement System, and 15 moreHumans, Chronic Disease, Fibrosis, CD, Dilated cardiomyopathy, Chagas disease, Clinical Sciences, Middle Aged, Adult, Myocardium, Cardiomyopathy, Complement, Chagas Cardiomyopathy, Membrane attack complex, and Coronary Vessels
Fetal echocardiography has recently caused an impact on the treatment of congenital heart disease and in the field of therapeutic, cardiological intervention. The present study reports on a case of critical aortic stenosis, diagnosed in... more
Fetal echocardiography has recently caused an impact on the treatment of congenital heart disease and in the field of therapeutic, cardiological intervention. The present study reports on a case of critical aortic stenosis, diagnosed in utero at 27 weeks’ gestation, and in which balloon dilatation was attempted to improve the poor prognosis associated with this condition. Since the endocardium at
Research Interests: Cardiology, High Pressure, Medicine, Internal Medicine, Aortic stenosis, and 12 moreCongenital Heart Disease, Fetal Echocardiography, Aortic Valve, Left Ventricle, Hypoplastic Left Heart Syndrome, Endocardial Fibroelastosis, Aortic valve stenosis, stenosis, Paediatrics and reproductive medicine, endocardium, ventricle, and In Utero
To investigate the mechanism of expression of atrial natriuretic polypeptide (ANP) in human ventricles, we conducted an immunohistochemical study of ANP in biventricular endomyocardial biopsy specimens obtained from a total of 49 patients... more
To investigate the mechanism of expression of atrial natriuretic polypeptide (ANP) in human ventricles, we conducted an immunohistochemical study of ANP in biventricular endomyocardial biopsy specimens obtained from a total of 49 patients with cardiac dilatation due to dilated cardiomyopathy (21 patients), postmyocarditis (18 patients), or volume overload (five patients) and subjects with no dilatation as controls (five patients). Four-micron thick sections were stained by an indirect immunoperoxidase method using monoclonal antibody to alpha-human ANP as the primary antibody. The frequency of ANP-present myocytes was calculated in each specimen and compared with clinical, echocardiographic, hemodynamic, angiographic, and histologic parameters. ANP-present myocytes were noted in all of the 21 patients with dilated cardiomyopathy, in 11 of the 18 patients with postmyocarditis, in four of the five patients with volume overload, and in zero of the five controls. The mean percentage of ...
Research Interests: Cardiology, Medicine, Biopsy, Humans, Internal Medicine, and 15 moreHemodynamics, Female, Male, Myocarditis, Dilated cardiomyopathy, Clinical Sciences, Adult, Cardiomyopathy, Circulation, Ejection Fraction, Heart Ventricles, Atrial Natriuretic Factor, Cardiomegaly, Diastole, and Cardiovascular medicine and haematology
In the primary form of pulmonary hypertension (PH), the involvement of inflammation in the physiopathology of the vascular lesions is well established. Its role in secondary PH is yet to be investigated. We quantified the inflammatory... more
In the primary form of pulmonary hypertension (PH), the involvement of inflammation in the physiopathology of the vascular lesions is well established. Its role in secondary PH is yet to be investigated. We quantified the inflammatory cells on the walls of peripheral pulmonary arteries from patients with congenital heart shunts. Twenty-six lung biopsies from patients with increased pulmonary flow and 10 lung fragments from control participants were examined. B-lymphocytes (CD20), T-lymphocytes (CD3), recently recruited macrophages (MAC387) and granulocytes (CD15) were quantified by area of the adventitia in arteries &amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;gt;50 microm. An index of inflammatory cells infiltrating the medial and intimal layers was also determined. There was no difference in the sum of densities of adventitial inflammatory cells between the groups. A prevalence of MAC387-labeled cells was detected in the PH group and of CD3-labeled cells in the controls. There was a lower density of T-lymphocytes in the PH group (P&amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;lt;.004). Patients with intimal proliferative lesions showed prevalence of MAC387-labeled cells (P=.004). PH participants showed a higher index of MAC387-labeled cells infiltrating the arterial medial and intimal layers (P&amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;amp;lt;.001). The predominance of recently recruited macrophages in the PH group is compatible with ongoing inflammatory reaction in the arterial walls. This could be related to the pathogenesis of the vascular lesions, as a consequence of cytokines produced by the inflammatory cells. The smaller number of adventitial T-lymphocytes in patients with congenital shunts can reflect an impairment of their immune response.
Research Interests: Pathology, Macrophages, Medicine, Pathophysiology, Congenital Heart Defects, and 15 moreHumans, Child, Female, Male, Infant, Lung, CD, Immune system, Biological markers, Cardiovascular Pathology, Peripheral, Pulmonary Artery, Child preschool, Cause of death, and Cardiovascular medicine and haematology
We describe two infants having an atrioventricular septal defect in the setting of a double inlet atrioventricular connection, but with patency of the left-sided valvar orifice and an imperforate right-sided valvar component, and a... more
We describe two infants having an atrioventricular septal defect in the setting of a double inlet atrioventricular connection, but with patency of the left-sided valvar orifice and an imperforate right-sided valvar component, and a further case with atrioventricular septal defect and an imperforate Ebstein's malformation, all producing the haemodynamic effect of tricuspid atresia. We make comparisons with the arrangement in trisomy 16 mice, in whom deficient atrioventricular septation is seen at times with the common atrioventricular junction exclusively connected to the left ventricle, a situation similar to that seen in two of our infants. We also review previous reports emphasising the important theoretical implication of the findings despite their rarity.