Improvement in the outcome of invasive fusariosis in the last decade

Detalhes bibliográficos
Autor(a) principal: Nucci, M.
Data de Publicação: 2014
Outros Autores: Marr, K. A., Vehreschild, M. J. G. T., Souza, C. A. de, Velasco, E., Cappellano, P. [UNIFESP], Carlesse, F. [UNIFESP], Queiroz-Telles, F., Sheppard, D. C., Kindo, A., Cesaro, S., Hamerschlak, N., Solza, C., Heinz, W. J., Schaller, M., Atalla, A., Arikan-Akdagli, S., Bertz, H., Castro, C. Galvao, Herbrecht, R., Hoenigl, M., Haerter, G., Hermansen, N. E. U., Josting, A., Pagano, L., Salles, M. J. C., Mossad, S. B., Ogunc, D., Pasqualotto, A. C., Araujo, V., Troke, P. F., Lortholary, O., Cornely, O. A., Anaissie, E.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1111/1469-0691.12409
http://repositorio.unifesp.br/handle/11600/37794
Resumo: Invasive fusariosis (IF) has been associated with a poor prognosis. Although recent series have reported improved outcomes, the definition of optimal treatments remains controversial. the objective of this study was to evaluate changes in the outcome of IF. Weretrospectively analysed 233 cases of IF from 11 countries, comparing demographics, clinical findings, treatment and outcome in two periods: 1985-2000 (period 1) and 2001-2011 (period 2). Most patients (92%) had haematological disease. Primary treatment with deoxycholate amphotericin B was more frequent in period 1 (63% vs. 30%, p <0.001), whereas voriconazole (32% vs. 2%, p <0.001) and combination therapies (18% vs. 1%, p <0.001) were more frequent in period 2. the 90-day probabilities of survival in periods 1 and 2 were 22% and 43%, respectively (p <0.001). in period 2, the 90-day probabilities of survival were 60% with voriconazole, 53% with a lipid formulation of amphotericin B, and 28% with deoxycholate amphotericin B (p 0.04). Variables associated with poor prognosis (death 90 days after the diagnosis of fusariosis) by multivariable analysis were: receipt of corticosteroids (hazard ratio (HR) 2.11, 95% CI 1.18-3.76, p 0.01), neutropenia at end of treatment (HR 2.70, 95% CI 1.57-4.65, p <0.001), and receipt of deoxycholate amphotericin B (HR 1.83, 95% CI 1.06-3.16, p 0.03). Treatment practices have changed over the last decade, with an increased use of voriconazole and combination therapies. There has been a 21% increase in survival rate in the last decade.
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spelling Improvement in the outcome of invasive fusariosis in the last decadeEpidemiologyfusariosisoutcometreatmentvoriconazoleInvasive fusariosis (IF) has been associated with a poor prognosis. Although recent series have reported improved outcomes, the definition of optimal treatments remains controversial. the objective of this study was to evaluate changes in the outcome of IF. Weretrospectively analysed 233 cases of IF from 11 countries, comparing demographics, clinical findings, treatment and outcome in two periods: 1985-2000 (period 1) and 2001-2011 (period 2). Most patients (92%) had haematological disease. Primary treatment with deoxycholate amphotericin B was more frequent in period 1 (63% vs. 30%, p <0.001), whereas voriconazole (32% vs. 2%, p <0.001) and combination therapies (18% vs. 1%, p <0.001) were more frequent in period 2. the 90-day probabilities of survival in periods 1 and 2 were 22% and 43%, respectively (p <0.001). in period 2, the 90-day probabilities of survival were 60% with voriconazole, 53% with a lipid formulation of amphotericin B, and 28% with deoxycholate amphotericin B (p 0.04). Variables associated with poor prognosis (death 90 days after the diagnosis of fusariosis) by multivariable analysis were: receipt of corticosteroids (hazard ratio (HR) 2.11, 95% CI 1.18-3.76, p 0.01), neutropenia at end of treatment (HR 2.70, 95% CI 1.57-4.65, p <0.001), and receipt of deoxycholate amphotericin B (HR 1.83, 95% CI 1.06-3.16, p 0.03). Treatment practices have changed over the last decade, with an increased use of voriconazole and combination therapies. There has been a 21% increase in survival rate in the last decade.Univ Fed Rio de Janeiro, Univ Hosp, BR-2251030 Rio de Janeiro, BrazilJohns Hopkins Univ, Sch Med, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD USAUniv Hosp Cologne, First Dept Internal Med, Cologne, GermanyUniv Estadual Campinas, UNICAMP, Haematol & Chemotherapy Ctr, Campinas, SP, BrazilNatl Canc Inst, Rio de Janeiro, BrazilUniversidade Federal de São Paulo, Univ Hosp, São Paulo, BrazilUniversidade Federal de São Paulo, Inst Paediat Oncol, GRAACC, São Paulo, BrazilUniv Fed Parana, Univ Hosp, BR-80060000 Curitiba, Parana, BrazilMcGill Univ, Dept Med, Montreal, PQ, CanadaMcGill Univ, Dept Microbiol & Immunol, Montreal, PQ, CanadaSri Ramachandra Med Coll, Res Inst 1, Dept Microbiol, Madras, Tamil Nadu, IndiaPoliclin G B Rossi, Oncoematol Pediat, Verona, ItalyHosp Albert Einstein, São Paulo, BrazilUniv Estado Rio de Janeiro, Rio de Janeiro, BrazilUniv Klinikum Wurzburg, Wurzburg, GermanyUniv Hautklin Tubingen, Uniklin Tubingen, Tubingen, GermanyUniv Fed Juiz Fora, Juiz de Fora, BrazilHacettepe Univ, Sch Med, Dept Med, Infect Dis Sect, TR-06100 Ankara, TurkeyUniv Freiburg Klinikum, Freiberg, GermanyHop Hautepierre, Strasbourg, FranceMed Univ Graz, Dept Med, Graz, AustriaComprehens Infect Dis Ctr CIDC, Ulm, GermanyUniv Copenhagen Hosp, Dept Haematol, Rigshosp, DK-2100 Copenhagen, DenmarkOnkoBer, Hamatoonkol Gastroenterol & Palliativmed, Berlin, GermanyUniv Cattolica Sacro Cuore, Dipartimento Ematol, Rome, ItalySanta Casa São Paulo Sch Med, São Paulo, BrazilCase Western Reserve Univ, Lerner Coll Med, Cleveland Clin, Sect Transplant Infect Dis,Dept Infect Dis,Med In, Cleveland, OH 44106 USACase Western Reserve Univ, Lerner Coll Med, Cleveland Clin, Transplant Ctr, Cleveland, OH 44106 USAAkdeniz Univ, Fac Med, Dept Clin Microbiol, TR-07058 Antalya, TurkeyUFCSPA, Porto Alegre, RS, BrazilHosp Governador Celso Ramos, Florianopolis, SC, BrazilOld Court, Broadstairs, Kent, EnglandCtr Natl Reference Mycol & Antifong, Inst Pasteur, Unite Mycol Mol, Paris, FranceUniv Cologne, Clin Trials Ctr Cologne, ZKS Koln, BMBF 01KN1106, D-50931 Cologne, GermanyUniv Cincinnati, Div Hematol & Oncol, Cincinnati, OH USAUniversidade Federal de São Paulo, Univ Hosp, São Paulo, BrazilUniversidade Federal de São Paulo, Inst Paediat Oncol, GRAACC, São Paulo, BrazilWeb of ScienceAstellas PharmaGilead SciencesMSD/MerckPfizer Pharma GmbHWiley-BlackwellUniversidade Federal do Rio de Janeiro (UFRJ)Johns Hopkins UnivUniv Hosp CologneUniversidade Estadual de Campinas (UNICAMP)Natl Canc InstUniversidade Federal de São Paulo (UNIFESP)Univ Fed ParanaMcGill UnivSri Ramachandra Med CollPoliclin G B RossiHosp Albert EinsteinUniversidade do Estado do Rio de Janeiro (UERJ)Univ Klinikum WurzburgUniv Hautklin TubingenUniv Fed Juiz ForaHacettepe UnivUniv Freiburg KlinikumHop HautepierreMed Univ GrazComprehens Infect Dis Ctr CIDCUniv Copenhagen HospOnkoBerUniv Cattolica Sacro CuoreSanta Casa São Paulo Sch MedCase Western Reserve UnivAkdeniz UnivUFCSPAHosp Governador Celso RamosOld CourtCtr Natl Reference Mycol & AntifongUniv CologneUniv CincinnatiNucci, M.Marr, K. A.Vehreschild, M. J. G. T.Souza, C. A. deVelasco, E.Cappellano, P. [UNIFESP]Carlesse, F. [UNIFESP]Queiroz-Telles, F.Sheppard, D. C.Kindo, A.Cesaro, S.Hamerschlak, N.Solza, C.Heinz, W. J.Schaller, M.Atalla, A.Arikan-Akdagli, S.Bertz, H.Castro, C. GalvaoHerbrecht, R.Hoenigl, M.Haerter, G.Hermansen, N. E. U.Josting, A.Pagano, L.Salles, M. J. C.Mossad, S. B.Ogunc, D.Pasqualotto, A. C.Araujo, V.Troke, P. F.Lortholary, O.Cornely, O. A.Anaissie, E.2016-01-24T14:37:19Z2016-01-24T14:37:19Z2014-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion580-585application/pdfhttp://dx.doi.org/10.1111/1469-0691.12409Clinical Microbiology and Infection. Hoboken: Wiley-Blackwell, v. 20, n. 6, p. 580-585, 2014.10.1111/1469-0691.12409WOS000340197000023.pdf1198-743Xhttp://repositorio.unifesp.br/handle/11600/37794WOS:000340197000023engClinical Microbiology and Infectioninfo:eu-repo/semantics/openAccesshttp://olabout.wiley.com/WileyCDA/Section/id-406071.htmlreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-08T09:36:52Zoai:repositorio.unifesp.br/:11600/37794Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-08T09:36:52Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Improvement in the outcome of invasive fusariosis in the last decade
title Improvement in the outcome of invasive fusariosis in the last decade
spellingShingle Improvement in the outcome of invasive fusariosis in the last decade
Nucci, M.
Epidemiology
fusariosis
outcome
treatment
voriconazole
title_short Improvement in the outcome of invasive fusariosis in the last decade
title_full Improvement in the outcome of invasive fusariosis in the last decade
title_fullStr Improvement in the outcome of invasive fusariosis in the last decade
title_full_unstemmed Improvement in the outcome of invasive fusariosis in the last decade
title_sort Improvement in the outcome of invasive fusariosis in the last decade
author Nucci, M.
author_facet Nucci, M.
Marr, K. A.
Vehreschild, M. J. G. T.
Souza, C. A. de
Velasco, E.
Cappellano, P. [UNIFESP]
Carlesse, F. [UNIFESP]
Queiroz-Telles, F.
Sheppard, D. C.
Kindo, A.
Cesaro, S.
Hamerschlak, N.
Solza, C.
Heinz, W. J.
Schaller, M.
Atalla, A.
Arikan-Akdagli, S.
Bertz, H.
Castro, C. Galvao
Herbrecht, R.
Hoenigl, M.
Haerter, G.
Hermansen, N. E. U.
Josting, A.
Pagano, L.
Salles, M. J. C.
Mossad, S. B.
Ogunc, D.
Pasqualotto, A. C.
Araujo, V.
Troke, P. F.
Lortholary, O.
Cornely, O. A.
Anaissie, E.
author_role author
author2 Marr, K. A.
Vehreschild, M. J. G. T.
Souza, C. A. de
Velasco, E.
Cappellano, P. [UNIFESP]
Carlesse, F. [UNIFESP]
Queiroz-Telles, F.
Sheppard, D. C.
Kindo, A.
Cesaro, S.
Hamerschlak, N.
Solza, C.
Heinz, W. J.
Schaller, M.
Atalla, A.
Arikan-Akdagli, S.
Bertz, H.
Castro, C. Galvao
Herbrecht, R.
Hoenigl, M.
Haerter, G.
Hermansen, N. E. U.
Josting, A.
Pagano, L.
Salles, M. J. C.
Mossad, S. B.
Ogunc, D.
Pasqualotto, A. C.
Araujo, V.
Troke, P. F.
Lortholary, O.
Cornely, O. A.
Anaissie, E.
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal do Rio de Janeiro (UFRJ)
Johns Hopkins Univ
Univ Hosp Cologne
Universidade Estadual de Campinas (UNICAMP)
Natl Canc Inst
Universidade Federal de São Paulo (UNIFESP)
Univ Fed Parana
McGill Univ
Sri Ramachandra Med Coll
Policlin G B Rossi
Hosp Albert Einstein
Universidade do Estado do Rio de Janeiro (UERJ)
Univ Klinikum Wurzburg
Univ Hautklin Tubingen
Univ Fed Juiz Fora
Hacettepe Univ
Univ Freiburg Klinikum
Hop Hautepierre
Med Univ Graz
Comprehens Infect Dis Ctr CIDC
Univ Copenhagen Hosp
OnkoBer
Univ Cattolica Sacro Cuore
Santa Casa São Paulo Sch Med
Case Western Reserve Univ
Akdeniz Univ
UFCSPA
Hosp Governador Celso Ramos
Old Court
Ctr Natl Reference Mycol & Antifong
Univ Cologne
Univ Cincinnati
dc.contributor.author.fl_str_mv Nucci, M.
Marr, K. A.
Vehreschild, M. J. G. T.
Souza, C. A. de
Velasco, E.
Cappellano, P. [UNIFESP]
Carlesse, F. [UNIFESP]
Queiroz-Telles, F.
Sheppard, D. C.
Kindo, A.
Cesaro, S.
Hamerschlak, N.
Solza, C.
Heinz, W. J.
Schaller, M.
Atalla, A.
Arikan-Akdagli, S.
Bertz, H.
Castro, C. Galvao
Herbrecht, R.
Hoenigl, M.
Haerter, G.
Hermansen, N. E. U.
Josting, A.
Pagano, L.
Salles, M. J. C.
Mossad, S. B.
Ogunc, D.
Pasqualotto, A. C.
Araujo, V.
Troke, P. F.
Lortholary, O.
Cornely, O. A.
Anaissie, E.
dc.subject.por.fl_str_mv Epidemiology
fusariosis
outcome
treatment
voriconazole
topic Epidemiology
fusariosis
outcome
treatment
voriconazole
description Invasive fusariosis (IF) has been associated with a poor prognosis. Although recent series have reported improved outcomes, the definition of optimal treatments remains controversial. the objective of this study was to evaluate changes in the outcome of IF. Weretrospectively analysed 233 cases of IF from 11 countries, comparing demographics, clinical findings, treatment and outcome in two periods: 1985-2000 (period 1) and 2001-2011 (period 2). Most patients (92%) had haematological disease. Primary treatment with deoxycholate amphotericin B was more frequent in period 1 (63% vs. 30%, p <0.001), whereas voriconazole (32% vs. 2%, p <0.001) and combination therapies (18% vs. 1%, p <0.001) were more frequent in period 2. the 90-day probabilities of survival in periods 1 and 2 were 22% and 43%, respectively (p <0.001). in period 2, the 90-day probabilities of survival were 60% with voriconazole, 53% with a lipid formulation of amphotericin B, and 28% with deoxycholate amphotericin B (p 0.04). Variables associated with poor prognosis (death 90 days after the diagnosis of fusariosis) by multivariable analysis were: receipt of corticosteroids (hazard ratio (HR) 2.11, 95% CI 1.18-3.76, p 0.01), neutropenia at end of treatment (HR 2.70, 95% CI 1.57-4.65, p <0.001), and receipt of deoxycholate amphotericin B (HR 1.83, 95% CI 1.06-3.16, p 0.03). Treatment practices have changed over the last decade, with an increased use of voriconazole and combination therapies. There has been a 21% increase in survival rate in the last decade.
publishDate 2014
dc.date.none.fl_str_mv 2014-06-01
2016-01-24T14:37:19Z
2016-01-24T14:37:19Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1111/1469-0691.12409
Clinical Microbiology and Infection. Hoboken: Wiley-Blackwell, v. 20, n. 6, p. 580-585, 2014.
10.1111/1469-0691.12409
WOS000340197000023.pdf
1198-743X
http://repositorio.unifesp.br/handle/11600/37794
WOS:000340197000023
url http://dx.doi.org/10.1111/1469-0691.12409
http://repositorio.unifesp.br/handle/11600/37794
identifier_str_mv Clinical Microbiology and Infection. Hoboken: Wiley-Blackwell, v. 20, n. 6, p. 580-585, 2014.
10.1111/1469-0691.12409
WOS000340197000023.pdf
1198-743X
WOS:000340197000023
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Clinical Microbiology and Infection
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
http://olabout.wiley.com/WileyCDA/Section/id-406071.html
eu_rights_str_mv openAccess
rights_invalid_str_mv http://olabout.wiley.com/WileyCDA/Section/id-406071.html
dc.format.none.fl_str_mv 580-585
application/pdf
dc.publisher.none.fl_str_mv Wiley-Blackwell
publisher.none.fl_str_mv Wiley-Blackwell
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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