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1.
Marin-Neto, José Antonio; Rassi Jr., Anis; Moraes Oliveira, Gláucia M.; Lemos Correia, Luís Claudio; Novaes Ramos Jr., Alberto; Hasslocher-Moreno, Alejandro Marcel; Luquetti Ostermayer, Alejandro; Sousa, Andréa Silvestre de; Amato Vincenzo de Paola, Angelo; Sobral de Sousa, Antonio Carlos; Pinho Ribeiro, Antonio Luiz; Correia Filho, Dalmo; Moraes de Souza, Dilma do Socorro; Cunha-Neto, Edecio; J. A. Ramires, Felix; Bacal, Fernando; Pereira Nunes, Maria do Carmo; Martinelli Filho, Martino; Ibrahim Scanavacca, Maurício; Magalhães Saraiva, Roberto; Alves de Oliveira Júnior, Wilson; M. Lorga-Filho, Adalberto; de Jesus Benevides de Almeida Guimarães, Adriana; Lopes Latado Braga, Adriana; Sarmento de Oliveira, Adriana; V. L. Sarabanda, Alvaro; Yecê das Neves Pinto, Ana; Assis Lopes do Carmo, André; Schmidt, André; Costa, Andréa Rodrigues da; Ianni, Barbara Maria; Markman Filho, Brivaldo; Eduardo Rochitte, Carlos; Thé Macedo, Carolina; Mady, Charles; Chevillard, Christophe; Bittencourt das Virgens, Cláudio Marcelo; Nery de Castro, Cleudson; De Paoli de Carvalho Britto, Constança Felícia; Pisani, Cristiano; do Carmo Rassi, Daniela; C. Sobral Filho, Dario; Rodrigues Almeida, Dirceu; A. Bocchi, Edimar; T. Mesquita, Evandro; de Souza Nogueira Sardinha Mendes, Fernanda; Pereira, Francisca Tatiana; Sperandio da Silva, Gilberto Marcelo; de Lima Peixoto, Giselle; Glotz de Lima, Gustavo; H. Veloso, Henrique; Turin Moreira, Henrique; Bellotti Lopes, Hugo; Masciarelli Francisco Pinto, Ibraim; Pinto Dias, João Carlos; Bemfica, João Marcos; Silva-Nunes, João Paulo; Soares Barreto-Filho, José Augusto; Kerr Saraiva, José Francisco; Lannes-Vieira, Joseli; Menezes Oliveira, Joselina Luzia; V. Armaganijan, Luciana; Martins, Luiz Cláudio; C. Sangenis, Luiz Henrique; Barbosa, Marco Paulo; Almeida-Santos, Marcos Antônio; Simões, Marcos Vinicius; Shikanai-Yasuda, Maria Aparecida; Vieira Moreira, Maria da Consolação; Higuchi, Maria de Lourdes; Costa Monteiro, Maria Rita de Cássia; Felix Mediano, Mauro Felippe; Maia Lima, Mayara; T. Oliveira, Maykon; Moreira Dias Romano , Minna; Nitz, Nadjar; de Tarso Jorge Medeiros, Paulo; Vieira Alves, Renato; Alkmim Teixeira, Ricardo; Coury Pedrosa, Roberto; Aras, Roque; Morais Torres, Rosália; dos Santos Povoa, Rui Manoel; Rassi, Sérgio Gabriel; Salles Xavier, Sérgio; Marinho Martins Alves , Silvia; B. N. Tavares, Suelene; Lima Palmeira, Swamy; da Silva Junior, Telêmaco Luiz; da Rocha Rodrigues, Thiago; Madrini Junior, Vagner; Maia da Costa , Veruska; Dutra, Walderez.
Preprint in Portuguese | SciELO Preprints | ID: pps-4820

ABSTRACT

This guideline aimed to update the concepts and formulate the standards of conduct and scientific evidence that support them, regarding the diagnosis and treatment of the Cardiomyopathy of Chagas disease, with special emphasis on the rationality base that supported it.  Chagas disease in the 21st century maintains an epidemiological pattern of endemicity in 21 Latin American countries. Researchers and managers from endemic and non-endemic countries point to the need to adopt comprehensive public health policies to effectively control the interhuman transmission of T. cruzi infection, and to obtain an optimized level of care for already infected individuals, focusing on diagnostic and therapeutic opportunistic opportunities.   Pathogenic and pathophysiological mechanisms of the Cardiomyopathy of Chagas disease were revisited after in-depth updating and the notion that necrosis and fibrosis are stimulated by tissue parasitic persistence and adverse immune reaction, as fundamental mechanisms, assisted by autonomic and microvascular disorders, was well established. Some of them have recently formed potential targets of therapies.  The natural history of the acute and chronic phases was reviewed, with enhancement for oral transmission, indeterminate form and chronic syndromes. Recent meta-analyses of observational studies have estimated the risk of evolution from acute and indeterminate forms and mortality after chronic cardiomyopathy. Therapeutic approaches applicable to individuals with Indeterminate form of Chagas disease were specifically addressed. All methods to detect structural and/or functional alterations with various cardiac imaging techniques were also reviewed, with recommendations for use in various clinical scenarios. Mortality risk stratification based on the Rassi score, with recent studies of its application, was complemented by methods that detect myocardial fibrosis.  The current methodology for etiological diagnosis and the consequent implications of trypanonomic treatment deserved a comprehensive and in-depth approach. Also the treatment of patients at risk or with heart failure, arrhythmias and thromboembolic events, based on pharmacological and complementary resources, received special attention. Additional chapters supported the conducts applicable to several special contexts, including t. cruzi/HIV co-infection, risk during surgeries, in pregnant women, in the reactivation of infection after heart transplantation, and others.     Finally, two chapters of great social significance, addressing the structuring of specialized services to care for individuals with the Cardiomyopathy of Chagas disease, and reviewing the concepts of severe heart disease and its medical-labor implications completed this guideline.


Esta diretriz teve como objetivo principal atualizar os conceitos e formular as normas de conduta e evidências científicas que as suportam, quanto ao diagnóstico e tratamento da CDC, com especial ênfase na base de racionalidade que a embasou. A DC no século XXI mantém padrão epidemiológico de endemicidade em 21 países da América Latina. Investigadores e gestores de países endêmicos e não endêmicos indigitam a necessidade de se adotarem políticas abrangentes, de saúde pública, para controle eficaz da transmissão inter-humanos da infecção pelo T. cruzi, e obter-se nível otimizado de atendimento aos indivíduos já infectados, com foco em oportunização diagnóstica e terapêutica. Mecanismos patogênicos e fisiopatológicos da CDC foram revisitados após atualização aprofundada e ficou bem consolidada a noção de que necrose e fibrose sejam estimuladas pela persistência parasitária tissular e reação imune adversa, como mecanismos fundamentais, coadjuvados por distúrbios autonômicos e microvasculares. Alguns deles recentemente constituíram alvos potenciais de terapêuticas. A história natural das fases aguda e crônica foi revista, com realce para a transmissão oral, a forma indeterminada e as síndromes crônicas. Metanálises recentes de estudos observacionais estimaram o risco de evolução a partir das formas aguda e indeterminada e de mortalidade após instalação da cardiomiopatia crônica. Condutas terapêuticas aplicáveis aos indivíduos com a FIDC foram abordadas especificamente. Todos os métodos para detectar alterações estruturais e/ou funcionais com variadas técnicas de imageamento cardíaco também foram revisados, com recomendações de uso nos vários cenários clínicos. Estratificação de risco de mortalidade fundamentada no escore de Rassi, com estudos recentes de sua aplicação, foi complementada por métodos que detectam fibrose miocárdica. A metodologia atual para diagnóstico etiológico e as consequentes implicações do tratamento tripanossomicida mereceram enfoque abrangente e aprofundado. Também o tratamento de pacientes em risco ou com insuficiência cardíaca, arritmias e eventos tromboembólicos, baseado em recursos farmacológicos e complementares, recebeu especial atenção. Capítulos suplementares subsidiaram as condutas aplicáveis a diversos contextos especiais, entre eles o da co-infecção por T. cruzi/HIV, risco durante cirurgias, em grávidas, na reativação da infecção após transplante cardíacos, e outros.    Por fim, dois capítulos de grande significado social, abordando a estruturação de serviços especializados para atendimento aos indivíduos com a CDC, e revisando os conceitos de cardiopatia grave e suas implicações médico-trabalhistas completaram esta diretriz. 

2.
JACC Heart Fail ; 10(3): 184-197, 2022 03.
Article in English | MEDLINE | ID: mdl-35241246

ABSTRACT

OBJECTIVES: This report describes the baseline clinical profiles and management of DELIVER (Dapagliflozin Evaluation to Improve the Lives of Patients With Preserved Ejection Fraction Heart Failure) trial participants and how these compare with those in other contemporary heart failure with preserved ejection fraction trials. BACKGROUND: The DELIVER trial was designed to evaluate the effects of the sodium-glucose cotransporter-2 inhibitor dapagliflozin on cardiovascular death, heart failure (HF) hospitalization, or urgent HF visits in patients with HF with mildly reduced and preserved left ventricular ejection fraction (LVEF). METHODS: Adults with symptomatic HF and LVEF >40%, with or without type 2 diabetes mellitus, elevated N-terminal pro-B-type natriuretic peptide (NT-proBNP) levels, and evidence of structural heart disease were randomized to dapagliflozin 10 mg once daily or matching placebo. RESULTS: A total of 6,263 patients were randomized (mean age: 72 ± 10 years; 44% women; 45% type 2 diabetes mellitus; 45% with body mass index ≥30 kg/m2; and 57% with history of atrial fibrillation or flutter). Most participants had New York Heart Association functional class II symptoms (75%). Baseline mean LVEF was 54.2 ± 8.8% and median NT-proBNP of 1,399 pg/mL (IQR: 962 to 2,210 pg/mL) for patients in atrial fibrillation/flutter compared with 716 pg/mL (IQR: 469 to 1,281 pg/mL) in those who were not. Patients in both hospitalized and ambulatory settings were enrolled, including 10% enrolled in-hospital or within 30 days of a hospitalization for HF. Eighteen percent of participants had HF with improved LVEF. CONCLUSIONS: DELIVER is the largest and broadest clinical trial of this population to date and enrolled high-risk, well-treated patients with HF with mildly reduced and preserved LVEF. (Dapagliflozin Evaluation to Improve the Lives of Patients With Preserved Ejection Fraction Heart Failure [NCT03619213]).


Subject(s)
Atrial Fibrillation , Diabetes Mellitus, Type 2 , Heart Failure , Sodium-Glucose Transporter 2 Inhibitors , Aged , Aged, 80 and over , Diabetes Mellitus, Type 2/complications , Diabetes Mellitus, Type 2/drug therapy , Female , Humans , Male , Middle Aged , Natriuretic Peptide, Brain/therapeutic use , Peptide Fragments , Sodium-Glucose Transporter 2 Inhibitors/pharmacology , Sodium-Glucose Transporter 2 Inhibitors/therapeutic use , Stroke Volume , Ventricular Function, Left
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