Reativação do citomegalovírus em pacientes graves aumenta a mortalidade

Detalhes bibliográficos
Ano de defesa: 2024
Autor(a) principal: Sousa, Estefânia Conceição Carmo
Orientador(a): Não Informado pela instituição
Banca de defesa: Não Informado pela instituição
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de Mato Grosso
Brasil
Faculdade de Medicina (FM)
UFMT CUC - Cuiabá
Programa de Pós-Graduação em Ciências da Saúde
Programa de Pós-Graduação: Não Informado pela instituição
Departamento: Não Informado pela instituição
País: Não Informado pela instituição
Palavras-chave em Português:
HIV
Link de acesso: http://ri.ufmt.br/handle/1/6752
Resumo: INTRODUCTION: In critically ill patients, cytomegalovirus (CMV) frequently reactivates. This reactivation is linked to extended hospital and ICU stays, increased need for mechanical ventilation, and higher incidences of sepsis, healthcare-associated infections (HAIs), morbidity and mortality. OBJECTIVES: This study to describe CMV reactivation and outcomes in patients treated at or admitted to a university hospital. METHODS: We conducted a retrospective cohort study of patients with suspected CMV reactivation treated at a university hospital in Central Brazil from November 2021 to July 2023. Data were abstracted from medical charts and entered a form prepared in EpiData Entry software version 3.1(//www.epidata.dk/) for statistical analysis. RESULTS: Among one hundred patients with clinical suspicion of CMV reactivation by the attending medical team, thirty-one cases (31.0%) had detectable viral load in blood samples. In patients with CMV reactivation, mortality reached 19.35%, compared to 5.8% in patients with undetectable viral load (p= 0.045). Mortality and CMV reactivation were significantly (p<0.050) higher in patients infected with the human immunodeficiency virus (HIV), those with shock or healthcare-associated infections (HAIs), and those requiring mechanical ventilation (MV). Patients with suspected CMV reactivation who were treated with ganciclovir had a significantly higher mortality (25.0%) than those who did not use ganciclovir (6.25%) (p=0.025). CONCLUSIONS: CMV reactivation, HIV infection, shock, MV, and HAIs were associated with increase patient mortality. However, further studies on the use of antivirals for treatment or prophylaxis of CMV reactivation in non-transplant critically ill patients are necessary, as ganciclovir may be toxic.