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Lack of evidence for a reciprocal interaction between bacterial and cytomegalovirus infection in the allogeneic stem cell transplantation setting.
Vinuesa, Víctor; Solano, Carlos; Giménez, Estela; Piñana, José L; Boluda, Juan Carlos Hernández; Amat, Paula; Navarro, David.
Afiliação
  • Vinuesa V; Microbiology Service, Fundación INCLIVA, Hospital Clínico Universitario, Valencia, Spain.
  • Solano C; Hematology Service, Fundación INCLIVA, Hospital Clínico Universitario, Valencia, Spain.
  • Giménez E; Department of Medicine, School of Medicine, University of Valencia, Valencia, Spain.
  • Piñana JL; Microbiology Service, Fundación INCLIVA, Hospital Clínico Universitario, Valencia, Spain.
  • Boluda JC; Hematology Service, Fundación INCLIVA, Hospital Clínico Universitario, Valencia, Spain.
  • Amat P; Hematology Service, Fundación INCLIVA, Hospital Clínico Universitario, Valencia, Spain.
  • Navarro D; Hematology Service, Fundación INCLIVA, Hospital Clínico Universitario, Valencia, Spain.
Transpl Int ; 29(11): 1196-1204, 2016 Nov.
Article em En | MEDLINE | ID: mdl-27529151
ABSTRACT
Pathogenic interactions between bacteria and cytomegalovirus (CMV) may potentially occur early after allogeneic stem cell transplantation (allo-SCT). This possibility nevertheless has not been investigated in depth. This was a retrospective study that included 170 consecutive patients who underwent 173 allo-SCTs. Both bacterial infection (most of which were bacteremic) and CMV DNAemia were detected in 78 allo-SCTs (62.9%). In total, 51 and 32 episodes of bacterial infection preceded or occurred after CMV DNAemia detection, respectively. Both events were diagnosed concurrently in four allo-SCTs. The cumulative incidence of bacterial infection (of any type) over the study period was comparable in patients with or without a preceding episode of CMV DNAemia (P = 0.321). Cox proportional hazards regression analysis failed to identify CMV DNAemia as a significant risk factor for bacterial infection. Likewise, the cumulative incidence of CMV DNAemia within the study period was not significantly different in patients with or without a preceding episode of bacterial infection (P = 0.189). Furthermore, the occurrence of bacterial infection within episodes of active CMV infection had no apparent impact on the kinetics of CMV DNAemia. Our data, thus, do not support the existence of a bidirectional synergistic effect between bacterial infection and active CMV infection in the allo-SCT setting.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2016 Tipo de documento: Article