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Campo DCValorIdioma
dc.creatorCastello Branco, Renan Carvalho-
dc.date.accessioned2025-09-09T16:45:59Z-
dc.date.available2027-08-
dc.date.available2025-09-09T16:45:59Z-
dc.date.issued2025-08-08-
dc.identifier.urihttps://repositorio.ufba.br/handle/ri/42876-
dc.description.abstractIntroduction: Chagas disease is an important cause of heart failure (HF) and stroke, affecting over six million people. High intensity transient signals (HITS) are detected on transcranial Doppler (TCD) in patients with Chagas disease, but the effect of antithrombotic treatment on HITS is unknown The aim To evaluate the role of cerebral HITS as a risk marker and as a surrogate outcome in patients with HF of Chagasic etiology Methods: In a prospective, open-label, blinded pilot clinical trial (PROBE), patients underwent TCD recording of the unilateral middle cerebral artery for 60 minutes, seeking HITS. Patients with Chagas disease and HITS were selected 2:1 for use of 300 mg aspirin for seven days and standard HF treatment or standard HF treatment alone (control group). Recruitment took place at the outpatient clinic of Edgar Santos Hospital and Ana Nery Hospital. The primary endpoint was the proportion of HITS after one week, verified using the chi-square test. Results: 373 patients with HF were evaluated, HITS occurred in 22/190 (12%) chagasic patients and in 16/183 (8%) non-chagasic patients (p=0.531). Twelve of the 22 (54%) chagasic patients were randomized to treatment with ASA (n = 8) or without ASA (n = 4). Two patients in the control group (50%) persisted with HITS after 7 days of treatment, compared to none in the ASA group, p=0.028. Median number of HITS decreased from 3.5 to 0 with ASA (p=0.012) and 4.0 to 0.5 in the control group (p=0.095), with no significant between-group difference (p=0.262). No adverse events were reported. Conclusion: In this pilot clinical trial, ASA reduced the proportion of HITS in patients with Chagas disease HF.pt_BR
dc.languageporpt_BR
dc.publisherUniversidade Federal da Bahiapt_BR
dc.rightsAcesso Restrito/Embargadopt_BR
dc.subjectCardiomiopatiapt_BR
dc.subjectDoença de Chagaspt_BR
dc.subjectDoença cerebrovascularpt_BR
dc.subjectMicroemboliaspt_BR
dc.subject.otherCardiomyopathypt_BR
dc.subject.otherChagas diseasept_BR
dc.subject.otherCerebrovascular diseasept_BR
dc.subject.otherMicroembolismspt_BR
dc.titleO papel dos sinais de microembolia cerebral como marcador de risco e como desfecho em pacientes de ensaio clínico piloto na insuficiência cardíaca de etiologia chagásicapt_BR
dc.title.alternativeThe role of signs of cerebral microembolism as a risk marker and as an outcome in patients of a pilot clinical trial in heart failure of chagas etiologypt_BR
dc.typeTesept_BR
dc.publisher.programPós-Graduação em Ciências da Saúde (POS_CIENCIAS_SAUDE) pt_BR
dc.publisher.initialsUFBApt_BR
dc.publisher.countryBrasilpt_BR
dc.subject.cnpqCNPQ::CIENCIAS DA SAUDEpt_BR
dc.contributor.advisor1Oliveira-Filho, Jamary-
dc.contributor.advisor1Latteshttp://lattes.cnpq.br/0078761969684137pt_BR
dc.contributor.referee1Oliveira-Filho, Jamary-
dc.contributor.referee2Jesus, Pedro Antônio Pereira de-
dc.contributor.referee3Fukuda, Thiago Gonçalves-
dc.contributor.referee4Ramos, Eva Carolina Rocha-
dc.contributor.referee5Rocha, Mário de Seixas-
dc.creator.ID0000-0002-6942-9521pt_BR
dc.creator.Latteshttp://lattes.cnpq.br/3490909243647402pt_BR
dc.description.resumoIntrodução: A doença de Chagas é uma causa importante de insuficiência cardíaca (IC) e acidente vascular cerebral, afetando mais de seis milhões de pessoas no mundo. Sinais transitórios de alta intensidade (HITS) são detectados no Doppler transcraniano (DTC) em pacientes com doença de Chagas, mas o efeito do tratamento antitrombótico em HITS é desconhecido Objetivo: Avaliar o papel dos SME cerebral como marcador de risco e como desfecho substitutivo em pacientes com IC de etiologia chagásica Métodos: Ensaio clínico piloto prospectivo, randomizado, aberto e cego (PROBE), os pacientes foram submetidos ao DTC para registro da artéria cerebral média, unilateral, por 60 minutos buscando os SME, onde pacientes com Chagas e SME foram randomizados 2:1 para uso do AAS 300 mg por sete dias e tratamento padrão para IC ou tratamento padrão para IC sozinho (grupo controle). O recrutamento foi feito no ambulatório do Hospital Edgar Santos e Hospital Ana Nery. O desfecho primário foi a proporção de SME após uma semana, analisada usando o teste qui-quadrado. Resultados: 373 pacientes com IC foram avaliados, SME ocorreram em 22/190 (12%) pacientes chagásicos e em 16/183 (8%) pacientes não chagásicos (p=0,531). Doze dos 22 (54%) pacientes chagásicos foram randomizados para tratamento com AAS (n = 8) ou sem AAS (n = 4). Dois pacientes no grupo controle (50%) persistiram com SME após 7 dias de tratamento, em comparação a nenhum, no grupo AAS, p=0,028. A mediana do número de SME diminuiu de 3,5 para 0 com AAS (p=0,012) e 4,0 para 0,5 no grupo controle (p=0,095), sem diferença significativa entre os grupos (p=0,262). Nenhum evento adverso foi relatado. Conclusão: Neste ensaio clínico piloto, o AAS reduziu a proporção de SME em pacientes com IC da doença de Chagas.pt_BR
dc.publisher.departmentFaculdade de Medicina da Bahiapt_BR
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