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Epidemiology, clinical aspects, outcomes and prognostic factors associated with Trichosporon fungaemia: results of an international multicentre study carried out at 23 medical centres.
Nobrega de Almeida, João; Francisco, Elaine Cristina; Holguín Ruiz, Alexis; Cuéllar, Luis E; Rodrigues Aquino, Valério; Verena Mendes, Ana; Queiroz-Telles, Flávio; Santos, Daniel Wagner; Guimarães, Thais; Maranhão Chaves, Guilherme; Grassi de Miranda, Bianca; Araújo Motta, Fabio; Vargas Schwarzbold, Alexandre; Oliveira, Márcio; Riera, Fernando; Sardi Perozin, Jamile; Pereira Neves, Rejane; França E Silva, Ivan Leonardo A; Sztajnbok, Jaques; Fernandes Ramos, Jéssica; Borges Botura, Monica; Carlesse, Fabianne; de Tarso de O E Castro, Paulo; Nyirenda, Themba; Colombo, Arnaldo L.
Afiliação
  • Nobrega de Almeida J; Center for Discovery and Innovation, Hackensack Meridian Health, Nutley, NJ, USA.
  • Francisco EC; Central Laboratory Division-LIM03, Hospital das Clínicas da FMUSP, São Paulo, Brazil.
  • Holguín Ruiz A; Division of Infectious Diseases, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil.
  • Cuéllar LE; Instituto Nacional de Enfermedades Neoplásicas, Lima, Peru.
  • Rodrigues Aquino V; Instituto Nacional de Enfermedades Neoplásicas, Lima, Peru.
  • Verena Mendes A; Hospital de Clínicas, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
  • Queiroz-Telles F; Hospital São Rafael, Salvador, Brazil.
  • Santos DW; Hospital de Clínicas, Infectious Diseases Department, Universidade Federal do Paraná, Curitiba, Brazil.
  • Guimarães T; Division of Infectious Diseases, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil.
  • Maranhão Chaves G; Hospital do Servidor Público Estadual, São Paulo, Brazil.
  • Grassi de Miranda B; Laboratory of Medical and Molecular Mycology, Department of Clinical and Toxicological Analyses, Universidade Federal do Rio Grande do Norte, Natal, Brazil.
  • Araújo Motta F; Hospital Samaritano, São Paulo, Brazil.
  • Vargas Schwarzbold A; Hospital Pequeno Príncipe, Curitiba, Brazil.
  • Oliveira M; Internal Medicine Department, Universidade Federal de Santa Maria, Santa Maria, Brazil.
  • Riera F; Hospital São Rafael, Salvador, Brazil.
  • Sardi Perozin J; Sanatório Allende Córdoba, Córdoba, Argentina.
  • Pereira Neves R; Hospital do Câncer de Londrina, Londrina, Brazil.
  • França E Silva ILA; Universidade Federal de Pernambuco, Recife, Brazil.
  • Sztajnbok J; A.C. Camargo Cancer Center, São Paulo, Brazil.
  • Fernandes Ramos J; Instituto da Criança, Hospital das Clínicas da FMUSP, São Paulo, Brazil.
  • Borges Botura M; Hospital Sírio Libanês, São Paulo, Brazil.
  • Carlesse F; Infectious Diseases Department, Hospital de Clínicas, Hospital das Clínicas da FMUSP, São Paulo, Brazil.
  • de Tarso de O E Castro P; Hospital de Clínicas, Universidade Federal da Bahia, São Paulo, Brazil.
  • Nyirenda T; Departamento de Pediatria, Escola Paulista de Medicina-Universidade Federal de São Paulo, São Paulo, Brazil.
  • Colombo AL; Instituto de Oncologia Pediátrica-IOP-GRAACC-UNIFESP, São Paulo, Brazil.
J Antimicrob Chemother ; 76(7): 1907-1915, 2021 06 18.
Article em En | MEDLINE | ID: mdl-33890055
ABSTRACT

BACKGROUND:

Trichosporon fungaemia (TF) episodes have increased in recent years and mortality rates remain high despite the advances in the management of sepsis. New concepts about its clinical course, treatment and microbiology need to be investigated for the better management of this infection.

OBJECTIVES:

To describe the aetiology, natural history, clinical management and prognostic factors of TF.

METHODS:

TF episodes documented between 2005 and 2018 in 23 South American centres were retrospectively investigated by using a standard clinical form. Molecular identification, antifungal susceptibility testing and biofilm production were also performed.

RESULTS:

Eighty-eight TF episodes were studied. Patients had several underlying conditions, including haematological diseases (47.7%), post-operative status (34%), solid organ transplants (n = 7, 7.9%), among others. Seventy-three (82.9%) patients had a central venous catheter (CVC) at TF diagnosis. The 30 day mortality rate was 51.1%. Voriconazole-based therapy was given to 34 patients (38.6%), with a 30 day mortality rate of 38.2%. Multivariate predictors of 30 day mortality were age (OR 1.036), mechanical ventilation (OR 8.25) and persistent neutropenia (OR 9.299). CVC removal was associated with over 75% decreased risk of 30 day mortality (OR 0.241). Microbiological analyses revealed that 77.7% of the strains were identified as Trichosporon asahii, and voriconazole showed the strongest in vitro activity against Trichosporon spp. Most of the strains (63%) were considered medium or high biofilm producers.

CONCLUSIONS:

Older age, mechanical ventilation and persistent neutropenia were associated with poor prognosis. CVC may play a role in the pathogenicity of TF and its removal was associated with a better prognosis.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Trichosporon / Fungemia Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Trichosporon / Fungemia Idioma: En Ano de publicação: 2021 Tipo de documento: Article