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Please use this identifier to cite or link to this item: http://hdl.handle.net/1843/57820
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dc.creatorCatherine Pastorius Benzigerpt_BR
dc.creatorGabriel Assis Lopes do Carmopt_BR
dc.creatorAntonio Luiz Pinho Ribeiropt_BR
dc.date.accessioned2023-08-14T22:04:14Z-
dc.date.available2023-08-14T22:04:14Z-
dc.date.issued2017-
dc.citation.volume35pt_BR
dc.citation.issue1pt_BR
dc.citation.spage31pt_BR
dc.citation.epage47pt_BR
dc.identifier.doihttps://doi.org/10.1016/j.ccl.2016.08.013pt_BR
dc.identifier.issn0733-8651pt_BR
dc.identifier.urihttp://hdl.handle.net/1843/57820-
dc.description.resumoThe diagnosis and treatment of Chagas disease require specific knowledge about the acute and chronic forms of the disease. The initial Chagas infection is typically asymptomatic but after a decade or longer, approximately 30% of people will progress to a chronic cardiac form of Chagas cardiomyopathy with symptoms including heart failure, arrhythmias, and thromboembolism.Death is often premature and sudden due to arrhythmias or progressive heart failure.Prevention of infection through vector control programs, along with strengthened surveillance sys tems and rapid information sharing, are key to addressing the continued challenges of Chagas disease control globallypt_BR
dc.format.mimetypepdfpt_BR
dc.languageengpt_BR
dc.publisherUniversidade Federal de Minas Geraispt_BR
dc.publisher.countryBrasilpt_BR
dc.publisher.departmentMED - DEPARTAMENTO DE CLÍNICA MÉDICApt_BR
dc.publisher.initialsUFMGpt_BR
dc.relation.ispartofCardiology Clinics-
dc.rightsAcesso Restritopt_BR
dc.subjectCardiomyopathiespt_BR
dc.subjectChagas Diseasept_BR
dc.subject.otherCardiomiopatiaspt_BR
dc.subject.otherDoença de Chagaspt_BR
dc.titleChagas Cardiomyopathy: Clinical Presentation and Management in the Americaspt_BR
dc.typeArtigo de Periódicopt_BR
dc.url.externahttps://www.sciencedirect.com/science/article/abs/pii/S0733865116300741?via%3Dihubpt_BR
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