{"title":"Choice of Imaging Methods in Hypertrophic Cardiomyopathy","authors":"M. Antunes, E. Arteaga-Fernández, C. Mady","doi":"10.5935/2318-8219.20190003","DOIUrl":"https://doi.org/10.5935/2318-8219.20190003","url":null,"abstract":"","PeriodicalId":211175,"journal":{"name":"ARQUIVOS BRASILEIROS DE CARDIOLOGIA - IMAGEM CARDIOVASCULAR","volume":"2 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"128528213","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
I. Bispo, Ricardo Volpatto, Fernando Assakawa, Diego Costa, A. Coelho, V. Gimenes
{"title":"Right Atrial Papillary Fibroelastoma","authors":"I. Bispo, Ricardo Volpatto, Fernando Assakawa, Diego Costa, A. Coelho, V. Gimenes","doi":"10.5935/2318-8219.20190054","DOIUrl":"https://doi.org/10.5935/2318-8219.20190054","url":null,"abstract":"","PeriodicalId":211175,"journal":{"name":"ARQUIVOS BRASILEIROS DE CARDIOLOGIA - IMAGEM CARDIOVASCULAR","volume":"4 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"114456837","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Arrhythmogenic Right Ventricular Dysplasia with Right Atrial Thrombus","authors":"Clara Santos, A. Bolonhez, O. Mangili","doi":"10.5935/2318-8219.20190053","DOIUrl":"https://doi.org/10.5935/2318-8219.20190053","url":null,"abstract":"A displasia arritmogênica do ventrículo direito é uma doença genética autossômica dominante caracterizada pela substituição progressiva do miocárdio por tecido fibrogorduroso. Clinicamente, é caracterizada por arritmias, insuficiência cardíaca, síncope e, em alguns casos, morte súbita. Relata-se o caso de um paciente portador de tal patologia em estágio avançado, que evoluiu com flutter atrial e formação de trombo em apêndice atrial direito, cuja opção terapêutica adotada foi a de anticoagulação e posterior cardioversão elétrica.","PeriodicalId":211175,"journal":{"name":"ARQUIVOS BRASILEIROS DE CARDIOLOGIA - IMAGEM CARDIOVASCULAR","volume":"16 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"134568655","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Lisete Lopes, C. Henriques, A. Francisco, D. Rodrigues, A. Pires
{"title":"Postpericardiotomy Syndrome after Nuss Procedure","authors":"Lisete Lopes, C. Henriques, A. Francisco, D. Rodrigues, A. Pires","doi":"10.5935/2318-8219.20200043","DOIUrl":"https://doi.org/10.5935/2318-8219.20200043","url":null,"abstract":"Postpericardiotomy syndrome (PPS) was first described in 1953 in patients with fever and pleuritic chest pain undergoing rheumatic mitral stenosis repair surgery.1, 2 PPS was initially believed to be associated with rheumatic disease reactivation and was subsequently recognized as an autoimmune inflammatory process.1, 2 The proposed diagnostic criteria have changed over time1 but are currently based on the COPPS3 and COPPS-24 studies, which were developed to assess the benefit of colchicine in PPS.2 A PPS diagnosis requires at least two of the following criteria: fever of unknown cause, pain with characteristics of pleuritis or pericarditis, a rubbing sound on auscultation, and evidence of pericardial and/or pleural effusion with increased C-reactive protein level.3,-5 Most patients present a benign and self-limited progression.6 However, the form and severity of clinical presentation can vary widely from asymptomatic patients with mild pleural and/ or pericardial effusion to those with serious complications such as cardiac tamponade.1, 2","PeriodicalId":211175,"journal":{"name":"ARQUIVOS BRASILEIROS DE CARDIOLOGIA - IMAGEM CARDIOVASCULAR","volume":"195 S562","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"132905264","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Carolina Bertoluci, M. Foppa, A. Santos, S. Fuchs, F. Fuchs
{"title":"Echocardiography on Prehypertension and Stage I Hypertension","authors":"Carolina Bertoluci, M. Foppa, A. Santos, S. Fuchs, F. Fuchs","doi":"10.5935/2318-8219.20190020","DOIUrl":"https://doi.org/10.5935/2318-8219.20190020","url":null,"abstract":"Results: Mean systolic and diastolic BP were significantly higher in the stage I hypertension group (141.0/90.4 mmHg) than in the prehypertension group (129.3/81.5 mmHg, P<0,001 for both). Mean age was 55 years old (30 to 70), with an almost equal number of men and women, of which 80% were white and 7% had diabetes. Most parameters of LV mass, LA size and diastolic function were similar between the prehypertension and stage I hypertension groups. Hypertensive individuals had larger LA diameter and posterior wall thickness, and lower lateral e’ velocities, even after adjustment for age, sex and body mass index. Sex-specific analysis showed higher LV mass in stage I hypertension compared to prehypertension only in women (141.1 ± 34.1 g vs. 126.1 ± 29.1 g, P<0.05).","PeriodicalId":211175,"journal":{"name":"ARQUIVOS BRASILEIROS DE CARDIOLOGIA - IMAGEM CARDIOVASCULAR","volume":"54 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"114676637","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Como eu faço o diagnóstico e o tratamento das taquicardias fetais","authors":"Marcia Ferreira Alves Barberato","doi":"10.5935/2318-8219.20200017","DOIUrl":"https://doi.org/10.5935/2318-8219.20200017","url":null,"abstract":"","PeriodicalId":211175,"journal":{"name":"ARQUIVOS BRASILEIROS DE CARDIOLOGIA - IMAGEM CARDIOVASCULAR","volume":"9 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"116279669","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
A. L. Jorge, Deborah Luz Diniz Martins, D. Ávila, Otávio Souza de Martino, M. Ribeiro, D. Neves, W. Martins
{"title":"Heart Failure in Pregnancy – Another Possibility Beyond Peripartum\u0000 Cardiomyopathy","authors":"A. L. Jorge, Deborah Luz Diniz Martins, D. Ávila, Otávio Souza de Martino, M. Ribeiro, D. Neves, W. Martins","doi":"10.5935/2318-8219.20190042","DOIUrl":"https://doi.org/10.5935/2318-8219.20190042","url":null,"abstract":"Resumo O miocárdio não compactado é uma miocardiopatia primária genética rara descrita como anormalidade na morfogênese endomiocárdica na qual se tem a interrupção da compactação das fibras miocárdicas, gerando um tecido frouxo trabecular. Manifesta-se com insuficiência cardíaca, embolias e arritmias ventriculares. Relata-se um caso de miocardiopatia não compactada sistêmica em paciente de 22 anos, puérpera e portadora de diabetes mellitus tipo 1.","PeriodicalId":211175,"journal":{"name":"ARQUIVOS BRASILEIROS DE CARDIOLOGIA - IMAGEM CARDIOVASCULAR","volume":"07 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"127289123","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}