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Comparative Effectiveness of Echinocandins vs Triazoles or Amphotericin B Formulations as Initial Directed Therapy for Invasive Candidiasis in Children and Adolescents.
Fisher, Brian T; Zaoutis, Theoklis E; Xiao, Rui; Wattier, Rachel L; Castagnola, Elio; Pana, Zoi Dorothea; Fullenkamp, Allison; Boge, Craig L K; Ross, Rachael K; Yildirim, Inci; Palazzi, Debra L; Danziger-Isakov, Lara; Vora, Surabhi B; Arrieta, Antonio; Yin, Dwight E; Avilés-Robles, Martha; Sharma, Tanvi; Tribble, Alison C; Maron, Gabriela; Berman, David; Green, Michael; Sung, Lillian; Romero, José; Hauger, Sarmistha B; Roilides, Emmanuel; Belani, Kiran; Nolt, Dawn; Soler-Palacin, Pere; López-Medina, Eduardo; Muller, William J; Halasa, Natasha; Dulek, Daniel; Hussain, Ibrahim Zaid Bin; Pong, Alice; Hoffman, Jill; Rajan, Sujatha; Gonzalez, Blanca E; Hanisch, Benjamin; Aftandilian, Catherine; Carlesse, Fabianne; Abzug, Mark J; Huppler, Anna R; Salvatore, Christine M; Ardura, Monica I; Chakrabarti, Arunaloke; Santolaya, Maria E; Localio, A Russell; Steinbach, William J.
Afiliación
  • Fisher BT; Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Zaoutis TE; Department of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia Pennsylvania, USA.
  • Xiao R; Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Wattier RL; Department of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia Pennsylvania, USA.
  • Castagnola E; Department of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia Pennsylvania, USA.
  • Pana ZD; Department of Pediatrics, Division of Infectious Diseases and Global Health, University of California-San Francisco, San Francisco, California, USA.
  • Fullenkamp A; Infectious Diseases Unit, Department of Pediatrics, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
  • Boge CLK; Infectious Disease Unit, 3rd Department of Pediatrics, Aristotle University and Hippokration Hospital, Thessaloniki, Greece.
  • Ross RK; Division of Pediatric Infectious Diseases, Duke University, Durham, North Carolina, USA.
  • Yildirim I; Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Palazzi DL; Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Danziger-Isakov L; Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
  • Vora SB; Division of Infectious Diseases, Department of Pediatrics Emory University, Atlanta, Georgia, USA.
  • Arrieta A; Section of Infectious Diseases, Department of Pediatrics, Baylor College of Medicine and Texas Children's Hospital, Houston, Texas, USA.
  • Yin DE; Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
  • Avilés-Robles M; Department of Pediatrics, University of Washington and Seattle Children's Hospital, Seattle, Washington, USA.
  • Sharma T; Division of Pediatric Infectious Diseases, Children's Hospital - Orange County, Orange, California, US.
  • Tribble AC; Division of Infectious Diseases, Department of Pediatrics, Children's Mercy and University of Missouri-Kansas City School of Medicine, Kansas City, Missouri, USA.
  • Maron G; Infectious Diseases Department, Hospital Infantil de México Federico Gómez, Mexico City, Mexico.
  • Berman D; Division of Infectious Diseases Children's Hospital Boston, Boston, Massachusetts, USA.
  • Green M; Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Sung L; Division of Infectious Diseases, Department of Pediatrics, University of Michigan and CS Mott Children's Hospital, Ann Arbor, Michigan, USA.
  • Romero J; Department of Infectious Diseases St. Jude Children's Hospital, Memphis, Tennessee, USA.
  • Hauger SB; Division of Pediatric Infectious Diseases, Johns Hopkins All Children's Hospital, St. Petersburg, Florida, USA.
  • Roilides E; Division of Infectious Diseases, Department of Pediatrics, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, Pennsylvania, USA.
  • Belani K; Department of Pediatrics, The Hospital for Sick Children, Toronto, Canada.
  • Nolt D; Division of Pediatric Infectious Diseases, Arkansas Children's Hospital Research Institute, Little Rock, Arkansas, USA.
  • Soler-Palacin P; Pediatric Infectious Diseases, Dell Children's Medical Center, Austin, Texas, USA.
  • López-Medina E; Infectious Disease Unit, 3rd Department of Pediatrics, Aristotle University and Hippokration Hospital, Thessaloniki, Greece.
  • Muller WJ; Pediatric Infectious Diseases, Children's Minnesota, Minneapolis, Minnesota, USA.
  • Halasa N; Division of Pediatric Infectious Diseases, Doernbecher Children's Hospital, Oregon Health & Science University, Portland, Oregon, USA.
  • Dulek D; Pediatric Infectious Diseases and Immunodeficiencies Unit, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
  • Hussain IZB; Centro de Estudios en Infectología Pediátrica and Universidad del Valle, Cali Colombia.
  • Pong A; Division of Infectious Diseases, Department of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
  • Hoffman J; Department of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee, US.
  • Rajan S; Department of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee, US.
  • Gonzalez BE; Pediatric Infectious Diseases King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia.
  • Hanisch B; Department of Pediatrics, University of California San Diego, San Diego, California, USA.
  • Aftandilian C; Pediatric Infectious Diseases, University of California Los Angeles, Los Angeles, California, USA.
  • Carlesse F; Division of Pediatric Infectious Diseases, Cohen Children's Medical Center, New Hyde Park, New York, USA.
  • Abzug MJ; Center for Pediatric Infectious Diseases, Cleveland Clinic Foundation, Cleveland, Ohio, USA.
  • Huppler AR; Pediatric Infectious Diseases, Children's National Health System, Washington, DC, USA.
  • Salvatore CM; Pediatric Hematology/Oncology, Stanford University School of Medicine, Palo Alto, California, USA.
  • Ardura MI; Instituto de Oncologia Pediatrica-IOP/GRAACC-UNIFESP, Sao Paulo, Brazil.
  • Chakrabarti A; Division of Pediatric Infectious Diseases, University of Colorado School of Medicine and Children's Hospital Colorado, Aurora, Colorado, USA.
  • Santolaya ME; Department of Pediatrics, Division of Infectious Diseases, Medical College of Wisconsin and Children's Hospital of Wisconsin, Milwaukee, Wisconsin, USA.
  • Localio AR; Department of Pediatrics, Division of Pediatric Infectious Diseases Weill Cornell Medicine, New York, New York, USA.
  • Steinbach WJ; Pediatric Infectious Diseases and Host Defense, Nationwide Children's Hospital, The Ohio State University, Columbus, Ohio, USA.
Article en En | MEDLINE | ID: mdl-34374424
BACKGROUND: Invasive candidiasis is the most common invasive fungal disease in children and adolescents, but there are limited pediatric-specific antifungal effectiveness data. We compared the effectiveness of echinocandins to triazoles or amphotericin B formulations (triazole/amphotericin B) as initial directed therapy for invasive candidiasis. METHODS: This multinational observational cohort study enrolled patients aged >120 days and <18 years with proven invasive candidiasis from January 1, 2014, to November 28, 2017, at 43 International Pediatric Fungal Network sites. Primary exposure was initial directed therapy administered at the time qualifying culture became positive for yeast. Exposure groups were categorized by receipt of an echinocandin vs receipt of triazole/amphotericin B. Primary outcome was global response at 14 days following invasive candidiasis onset, adjudicated by a centralized data review committee. Stratified Mantel-Haenszel analyses estimated risk difference between exposure groups. RESULTS: Seven-hundred and fifty invasive candidiasis episodes were identified. After exclusions, 541 participants (235 in the echinocandin group and 306 in the triazole/amphotericin B group) remained. Crude failure rates at 14 days for echinocandin and triazole/amphotericin B groups were 9.8% (95% confidence intervals [CI]: 6.0% to 13.6%) and 13.1% (95% CI: 9.3% to 16.8%), respectively. The adjusted 14-day risk difference between echinocandin and triazole/amphotericin B groups was -7.1% points (95% CI: -13.1% to -2.4%), favoring echinocandins. The risk difference was -0.4% (95% CI: -7.5% to 6.7%) at 30 days. CONCLUSIONS: In children with invasive candidiasis, initial directed therapy with an echinocandin was associated with reduced failure rate at 14 days but not 30 days. These results may support echinocandins as initial directed therapy for invasive candidiasis in children and adolescents. CLINICAL TRIALS REGISTRATION: NCT01869829.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Observational_studies / Risk_factors_studies Idioma: En Revista: J Pediatric Infect Dis Soc Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Observational_studies / Risk_factors_studies Idioma: En Revista: J Pediatric Infect Dis Soc Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido