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1.
Diagn. tratamento ; 26(4): 137-9, out-dez. 2021. Este editorial foi publicado em inglês na revista São Paulo Medical Journal, volume 139, edição número 6, de novembro e dezembro de 2021 (https://doi.org/10.1590/1516-3180.2021.139628062021)
Artigo em Português | LILACS | ID: biblio-1348606
2.
Clinics ; 71(11): 635-638, Nov. 2016. tab
Artigo em Inglês | LILACS | ID: biblio-828550

RESUMO

OBJECTIVES: Recent studies have revealed a relationship between beta-blocker use and worse prognosis in acute coronary syndrome, mainly due to a higher incidence of cardiogenic shock. However, the relevance of this relationship in the reperfusion era is unknown. The aim of this study was to analyze the outcomes of patients with acute coronary syndrome that started oral beta-blockers within the first 24 hours of hospital admission (group I) compared to patients who did not use oral beta-blockers in this timeframe (group II). METHODS: This was an observational, retrospective and multicentric study with 2,553 patients (2,212 in group I and 341 in group II). Data regarding demographic characteristics, coronary treatment and medication use in the hospital were obtained. The primary endpoint was in-hospital all-cause mortality. The groups were compared by ANOVA and the chi-square test. Multivariate analysis was conducted by logistic regression and results were considered significant when p<0.05. RESULTS: Significant differences were observed between the groups in the use of angiotensin-converting enzyme inhibitors, enoxaparin, and statins; creatinine levels; ejection fraction; tabagism; age; and previous coronary artery bypass graft. Significant differences were also observed between the groups in mortality (2.67% vs 9.09%, OR=0.35, p=0.02) and major adverse cardiovascular events (11% vs 29.5%, OR=4.55, p=0.02). CONCLUSIONS: Patients with acute coronary syndrome who underwent early intervention with oral beta-blockers during the first 24 hours of hospital admission had a lower in-hospital death rate and experienced fewer major adverse cardiovascular events with no increase in cardiogenic shock or sustained ventricular arrhythmias compared to patients who did not receive oral beta-blockers within this timeframe.


Assuntos
Humanos , Masculino , Feminino , Pessoa de Meia-Idade , Idoso , Síndrome Coronariana Aguda/tratamento farmacológico , Síndrome Coronariana Aguda/mortalidade , Antagonistas Adrenérgicos beta/administração & dosagem , Infarto do Miocárdio/tratamento farmacológico , Brasil/epidemiologia , Mortalidade Hospitalar , Modelos Logísticos , Análise Multivariada , Infarto do Miocárdio/mortalidade , Estudos Retrospectivos , Choque Cardiogênico/mortalidade , Resultado do Tratamento
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