metricas
covid
Buscar en
Enfermedades Infecciosas y Microbiología Clínica
Toda la web
Inicio Enfermedades Infecciosas y Microbiología Clínica Fungal infection in solid organ recipients
Información de la revista
Vol. 30. Núm. S2.
Infections in solid organ transplantation
Páginas 49-56 (marzo 2012)
Compartir
Compartir
Descargar PDF
Más opciones de artículo
Vol. 30. Núm. S2.
Infections in solid organ transplantation
Páginas 49-56 (marzo 2012)
Acceso a texto completo
Fungal infection in solid organ recipients
Infección fúngica en los receptores de órgano sólido
Visitas
2945
Jesús Fortúna,
Autor para correspondencia
fortunabete@gmail.com

Corresponding author.
, Isabel Ruizb, Pilar Martín-Dávilaa, Manuel Cuenca-Estrellac
a Department of Infectious Diseases, Hospital Ramón y Cajal, Madrid, Spain
b Department of Infectious Diseases, Hospital Val d’Hebron, Barcelona, Spain
c Mycology Department, Centro Nacional de Microbiología, Instituto de Salud Carlos III, Madrid, Spain
Este artículo ha recibido
Información del artículo
Resumen
Bibliografía
Descargar PDF
Estadísticas
Abstract

In solid organ recipients, as with other immunosuppressed patients, infections by Candida spp. and Aspergillus spp. are the most frequent invasive mycoses. Infections by Cryptococcus spp. and fungi of the Mucorales order are less common. Infections by Fusarium spp. and Scedosporium spp. are very uncommon, except in patients undergoing hematopoietic stem cell transplant and patients with prolonged neutropenia. The risk factors for fungal infection are immunosuppression, surgery, viral co-infection, and environmental exposure. Diagnosis is challenging: blood culture is of little use, except in candidiasis and cryptococcosis, and the poor accuracy of antigen-based techniques, except in cryptococcosis, favors widespread use of empirical therapy. A delay in the initiation of therapy increases the already high mortality of these infections. The agents used to treat fungal infection are azoles, echinocandins, and lipid amphotericin. Administration depends on antifungal activity, drug-drug interactions with calcineurin inhibitors, and safety profiles (effects on grafts and other side effects).

Keywords:
Fungal infection
Solid organ recipients
Transplant
Resumen

En los receptores de órgano sólido, y en otros pacientes inmunodeprimidos, las infecciones por Candida spp. y Aspergillus spp. son las micosis invasivas más frecuentes. Las infecciones por Cryptococcus spp. y por hongos del orden Mucorales son menos frecuentes. Las infecciones por Fusarium spp. y Scedosporium spp. son muy infrecuentes, excepto en pacientes sometidos a trasplante de células madre hematopoyéticas y pacientes con neutropenia prolongada. Los factores de riesgo para infección fúngica son la inmunosupresión, cirugía, coinfección viral y exposición al entorno. El diagnóstico constituye un reto: la poca utilidad del hemocultivo, excepto en la candidiasis y la criptococcosis, y la poca precisión de las técnicas basadas en antígeno, excepto en la criptococcosis, favorecen el uso extendido del tratamiento empírico. El retraso en el inicio del tratamiento aumenta la ya alta mortalidad de estos procesos. Los fármacos utilizados para tratar las infecciones fúngicas son azoles, equinocandinas y amfotericina asociada a lípido. La administración depende de la actividad antifúngica, las interacciones farmacológicas con los inhibidores de la calcineurina y el perfil de seguridad (efecto sobre el injerto y otros efectos secundarios).

Palabras clave:
Infección fúngica
Receptores de órgano sólido
Trasplante
El Texto completo está disponible en PDF
References
[1.]
S. Gabardi, D.W. Kubiak, A.K. Chandraker, S.G. Tullius.
Invasive fungal infections and antifungal therapies in solid organ transplant recipients.
Transpl Int, 20 (2007), pp. 993-1015
[2.]
R.S. Garrido, J.M. Aguado, C. Díaz-Pedroche, O. Len, M. Montejo, A. Moreno, et al.
A review of critical periods for opportunistic infection in the new transplantation era.
Transplantation, 82 (2006), pp. 1457-1462
[3.]
P.G. Pappas, B.D. Alexander, D.R. Andes, S. Hadley, C.A. Kauffman, A. Freifeld, et al.
Invasive fungal infections among organ transplant recipients: results of the Transplant-Associated Infection Surveillance Network (TRANSNET).
Clin Infect Dis, 50 (2010), pp. 1101-1111
[4.]
A.P. Limaye, P.A. Connolly, M. Sagar, T.R. Fritsche, B.T. Cookson, L.J. Wheat, et al.
Transmission of Histoplasma capsulatum by organ transplantation.
N Engl J Med, 343 (2000), pp. 1163-1166
[5.]
J. Gavaldà, O. Len, R. San Juan, J.M. Aguado, J. Fortún, C. Lumbreras, et al.
Risk factors for invasive aspergillosis in solid-organ transplant recipients: a case-control study.
Clin Infect Dis, 41 (2005), pp. 52-59
[6.]
J. Fortún, P. Martín-Dávila, S. Moreno, E. De Vicente, J. Nuño, A. Candelas, et al.
Risk factors for invasive aspergillosis in liver transplant recipients.
Liver Transpl, 8 (2002), pp. 1065-1070
[7.]
N. Singh, A.P. Limaye, G. Forrest, N. Safdar, P. Muñoz, K. Pursell, et al.
Late-onset invasive aspergillosis in organ transplant recipients in the current era.
Med Mycol, 44 (2006), pp. 445-449
[8.]
F.P. Silveira, E.J. Kwak, D.L. Paterson, J.M. Pilewski, K.R. McCurry, S. Husain.
Posttransplant colonization with non-Aspergillus molds and risk of development of invasive fungal disease in lung transplant recipients.
J Heart Lung Transplant, 27 (2008), pp. 850-855
[9.]
Anonymous.
Fungal infections.
Am J Transp, 4 (2004), pp. 110-134
[10.]
N. Singh, O. Lortholary, B.D. Alexander, K.L. Gupta, G.T. John, K.J. Pursell, et al.
Antifungal management practices and evolution of infection in organ transplant recipients with cryptococcus neoformans infection.
Transplantation, 80 (2005), pp. 1033
[11.]
N. Singh, B.D. Alexander, O. Lortholary, F. Dromer, K.L. Gupta, G.T. John, Cryptococcal Collaborative Transplant Study Group.
Cryptococcus neoformans in organ transplant recipients: impact of calcineurin-inhibitor agents on mortality.
J Infect Dis, 195 (2007), pp. 756-764
[12.]
D.P. Kontoyiannis, R.E. Lewis, B.D. Alexander, O. Lortholary, F. Dromer, K.L. Gupta, et al.
Calcineurin inhibitor agents interact synergistically with antifungal agents in vitro against Cryptococcus neoformans isolates: correlation with outcome in solid organ transplant recipients with cryptococcosis.
Antimicrob Agents Chemother, 52 (2008), pp. 735-738
[13.]
N. Singh, B.D. Alexander, O. Lortholary, F. Dromer, K.L. Gupta, G.T. John, et al.
Pulmonary cryptococcosis in solid organ transplant recipients: clinical relevance of serum cryptococcal antigen.
Clin Infect Dis, 46 (2008), pp. e12-e18
[14.]
M. Cuenca-Estrella, L. Bernal-Martínez, G. Isla, A. Gómez-López, L. Alcázar-Fuoli, M.J. Buitrago.
Incidence of zygomycosis in transplant recipients.
Clin Microbiol Infect, 5 (2009), pp. 37-40
[15.]
D. Neofytos, J.A. Fishman, D. Horn, E. Anaissie, C.H. Chang, A. Olyaei, et al.
Epidemiology and outcome of invasive fungal infections in solid organ transplant recipients.
Transpl Infect Dis, 12 (2010), pp. 220-229
[16.]
N. Singh, J.M. Aguado, H. Bonatti, G. Forrest, K.L. Gupta, N. Safdar, et al.
Zygomycosis in solid organ transplant recipients: a prospective, matched case-control study to assess risks for disease and outcome.
J Infect Dis, 200 (2009), pp. 1002-1011
[17.]
N.G. Almyroudis, D.A. Sutton, P. Linden, M.G. Rinaldi, J. Fung, S. Kusne.
Zygomycosis in solid organ transplant recipients in a tertiary transplant center and review of the literature.
Am J Transplant, 6 (2006), pp. 2365-2374
[18.]
H.Y. Sun, G. Forrest, K.L. Gupta, J.M. Aguado, O. Lortholary, M.B. Julia, et al.
Rhinoorbital-cerebral zygomycosis in solid organ transplant recipients.
Transplantation, 90 (2010), pp. 85-92
[19.]
A. Solé, M. Salavert.
Fungal infections after lung transplantation.
Curr Opin Pulm Med, 15 (2009), pp. 243-253
[20.]
B. Sendid, D. Caillot, B. Baccouch-Humbert, L. Klingspor, M. Grandjean, A. Bonnin, et al.
Contribution of the Platelia Candida-specific antibody and antigen tests to early diagnosis of systemic Candida tropicalis infection in neutropenic adults.
J Clin Microbiol, 41 (2003), pp. 4551-4558
[21.]
M. Mikulski, T. Calandra, M. Sanguinetti, D. Poulain, C. Viscoli, Third European Conference on Infections in Leukemia Group.
The use of mannan antigen and antimannan antibodies in the diagnosis of invasive candidiasis: recommendations from the Third European Conference on Infections in Leukemia.
Crit Care, 14 (2010), pp. R222
[22.]
L. Ostrosky-Zeichner, B.D. Alexander, D.H. Kett, J. Vazquez, P.G. Pappas, F. Saeki, et al.
Multicenter clinical evaluation of the (1-->3) beta-D-glucan assay as an aid to diagnosis of fungal infections in humans.
Clin Infect Dis, 41 (2005), pp. 654-659
[23.]
M.A. Mennink-Kersten, D. Ruegebrink, P.E. Verweij.
Pseudomonas aeruginosa as a cause of 1,3-beta-d-glucan assay reactivity.
Clin Infect Dis, 46 (2008), pp. 1930-1931
[24.]
S. Koo, J.M. Bryar, J.H. Page, L.R. Baden, F.M. Marty.
Diagnostic performance of the (1-->3)-beta-D-glucan assay for invasive fungal disease.
Clin Infect Dis, 49 (2009), pp. 1650-1659
[25.]
T. Avni, L. Leibovici, M. Paul.
PCR diagnosis of invasive candidiasis: systematic review and meta-analysis.
J Clin Microbiol, 49 (2011), pp. 665-670
[26.]
S. Ascioglu, J.H. Rex, B. De Pauw, J.E. Bennett, J. Bille, F. Crokaert, et al.
Defining opportunistic invasive fungal infections in immunocompromised patients with cancer and hematopoietic stem cell transplants: an international consensus.
Clin Infect Dis, 34 (2002), pp. 7-14
[27.]
B. De Pauw, T.J. Walsh, J.P. Donnelly, D.A. Stevens, J.E. Edwards, T. Calandra, et al.
Revised definitions of invasive fungal disease from the European Organization for Research and Treatment of Cancer/Invasive Fungal Infections Cooperative Group and the National Institute of Allergy and Infectious Diseases Mycoses Study Group (EORTC/MSG) Consensus Group.
Clin Infect Dis, 46 (2008), pp. 1813-1821
[28.]
C.D. Pfeiffer, J.P. Fine, N. Safdar.
Diagnosis of invasive aspergillosis using a galactomannan assay: a meta-analysis.
Clin Infect Dis, 42 (2006), pp. 1417-1427
[29.]
J. Fortún, P. Martín-Dávila, M.E. Álvarez, A. Sánchez-Sousa, C. Quereda, E. Navas, Ramon y Cajal Hospital's Liver Transplant Group, et al.
Aspergillus antigenemia sandwich-enzyme immunoassay test as a serodiagnostic method for invasive aspergillosis in liver transplant recipients.
Transplantation, 71 (2001), pp. 145-149
[30.]
A. Aubry, R. Porcher, J. Bottero, S. Touratier, T. Leblanc, B. Brethon, et al.
Occurrence and kinetics of false-positive Aspergillus galactomannan test results following treatment with beta-lactam antibiotics in patients with hematological disorders.
J Clin Microbiol, 44 (2006), pp. 389-394
[31.]
J. Fortún, P. Martín-Dávila, M.E. Álvarez, F. Norman, A. Sánchez-Sousa, L. Gajate, et al.
False-positive results of Aspergillus galactomannan antigenemia in liver transplant recipients.
Transplantation, 87 (2009), pp. 256-260
[32.]
S. Husain, D.L. Paterson, S.M. Studer, M. Crespo, J. Pilewski, M. Durkin, et al.
Aspergillus galactomannan antigen in the bronchoalveolar lavage fluid for the diagnosis of invasive aspergillosis in lung transplant recipients.
Transplantation, 83 (2007), pp. 1330-1336
[33.]
C.J. Clancy, R.A. Jaber, H.L. Leather, J.R. Wingard, B. Staley, L.J. Wheat, et al.
Bronchoalveolar lavage galactomannan in diagnosis of invasive pulmonary aspergillosis among solid-organ transplant recipients.
J Clin Microbiol, 45 (2007), pp. 1759-1765
[34.]
M. Cuenca-Estrella, Y. Meije, C. Díaz-Pedroche, A. Gómez-López, M.J. Buitrago, L. Bernal-Martínez, et al.
Value of serial determinations of fungal DNA by a real-time PCRbased technique for early detection of invasive aspergillosis in patients with febrile neutropenia.
J Clin Microbiol, 47 (2009), pp. 379-384
[35.]
F. Botterel, C. Farrugia, P. Ichai, J.M. Costa, F. Saliba, S. Bretagne.
Real-time PCR on the first galactomannan-positive serum sample for diagnosing invasive aspergillosis in liver transplant recipients.
Liver Transpl, 14 (2008), pp. 1678-1679
[36.]
P.G. Pappas, C.A. Kauffman, D. Andes, D.K. Benjamin, T. Calandra, J.E. Edwards, et al.
Clinical practice guidelines for the management of candidiasis: 2009 update by the Infectious Diseases Society of America.
Clin Infect Dis, 48 (2009), pp. 503-535
[37.]
J.M. Aguado, I. Ruiz-Camps, P. Muñoz, J. Mensa, B. Almirante, L. Vázquez, Grupo de Estudio de Micología Médica de la SEIMC (GEMICOMED), et al.
Guidelines for the treatment of Invasive Candidiasis and other yeasts. Spanish Society of Infectious Diseases and Clinical Microbiology (SEIMC). 2010 Update.
Enferm Infecc Microbiol Clin, 29 (2011), pp. 345-361
[38.]
C.Y. Liu, L.J. Huang, W.S. Wang, T.L. Chen, C.C. Yen, M.H. Yang, et al.
Candidemia in cancer patients: impact of early removal of non-tunneled central venous catheters on outcome.
J Infect, 58 (2009), pp. 154-160
[39.]
N. De Wet, A. Llanos-Cuentas, J. Suleiman, E. Baraldi, E.F. Krantz, M. Della Negra, et al.
A randomized, double-blind, parallel-group, dose-response study of micafungin compared with fluconazole for the treatment of esophageal candidiasis in HIVpositive patients.
Clin Infect Dis, 39 (2004), pp. 842-849
[40.]
D.S. Krause, A.E. Simjee, C. Van Rensburg, J. Viljoen, T.J. Walsh, B.P. Goldstein, et al.
A randomized, double-blind trial of anidulafungin versus fluconazole for the treatment of esophageal candidiasis.
Clin Infect Dis, 39 (2004), pp. 770-775
[41.]
A. Villanueva, E.G. Arathoon, E. Gotuzzo, R.S. Berman, M.J. DiNubile, C.A. Sable.
A randomized double-blind study of caspofungin versus amphotericin for the treatment of candidal esophagitis.
Clin Infect Dis, 33 (2001), pp. 1529-1535
[42.]
J.R. Perfect, W.E. Dismukes, F. Dromer, D.L. Goldman, J.R. Graybill, R.J. Hamill, et al.
Clinical practice guidelines for the management of cryptococcal disease: 2010 update by the infectious diseases society of america.
Clin Infect Dis, 50 (2010), pp. 291-322
[43.]
N. Singh, O. Lortholary, B.D. Alexander, K.L. Gupta, G.T. John, K. Pursell, et al.
An immune reconstitution syndrome-like illness associated with Cryptococcus neoformans infection in organ transplant recipients.
Clin Infect Dis, 40 (2005), pp. 1756-1761
[44.]
D.W. Denning, P. Ribaud, N. Milpied, D. Caillot, R. Herbrecht, E. Thiel, et al.
Efficacy and safety of voriconazole in the treatment of acute invasive aspergillosis.
Clin Infect Dis, 34 (2002), pp. 563-571
[45.]
R. Herbrecht, D.W. Denning, T.F. Patterson, J.E. Bennett, R.E. Greene, J.W. Oestmann, et al.
Voriconazole versus amphotericin B for primary therapy of invasive aspergillosis.
N Engl J Med, 347 (2002), pp. 408-415
[46.]
J. Fortún, P. Martín-Dávila, M.A. Sánchez, V. Pintado, M.E. Álvarez, A. Sánchez-Sousa, et al.
Voriconazole in the treatment of invasive mold infections in transplant recipients.
Eur J Clin Microbiol Infect Dis, 22 (2003), pp. 408-413
[47.]
M. Kleinberg.
Aspergillosis in the CLEAR outcomes trial: working toward a realworld clinical perspective.
Med Mycol, 43 (2005), pp. S289-S294
[48.]
J. Groetzner, I. Kaczmarek, T. Wittwer, J. Strauch, B. Meiser, T. Wahlers, et al.
Caspofungin as first-line therapy for the treatment of invasive aspergillosis after thoracic organ transplantation.
J Heart Lung Transplant, 27 (2008), pp. 1-6
[49.]
J. Maertens, G. Egerer, W.S. Shin, D. Reichert, M. Stek, S. Chandwani, et al.
Caspofungin use in daily clinical practice for treatment of invasive aspergillosis: results of a prospective observational registry.
BMC Infect Dis, 10 (2010), pp. 182
[50.]
M. Winkler, J. Pratschke, U. Schulz, S. Zheng, M. Zhang, W. Li, et al.
Caspofungin for post solid organ transplant invasive fungal disease: results of a retrospective observational study.
Transpl Infect Dis, 12 (2010), pp. 230-237
[51.]
N. Singh, A.P. Limaye, G. Forrest, N. Safdar, P. Muñoz, K. Pursell, et al.
Combination of voriconazole and caspofungin as primary therapy for invasive aspergillosis in solid organ transplant recipients: a prospective, multicenter, observational study.
Transplantation, 81 (2006), pp. 320-326
[52.]
D.W. Denning, K.A. Marr, W.M. Lau, D.P. Facklam, V. Ratanatharathorn, C. Becker, et al.
Micafungin (FK463), alone or in combination with other systemic antifungal agents, for the treatment of acute invasive aspergillosis.
J Infect, 53 (2006), pp. 337-349
[53.]
B.D. Alexander, J.R. Perfect, J.S. Daly, A. Restrepo, A.M. Tobón, H. Patino, et al.
Posaconazole as salvage therapy in patients with invasive fungal infections after solid organ transplant.
Transplantation, 86 (2008), pp. 791-796
[54.]
H. Leather, R.M. Boyette, L. Tian, J.R. Wingard.
Pharmacokinetic evaluation of the drug interaction between intravenous itraconazole and intravenous tacrolimus or intravenous cyclosporin A in allogeneic hematopoietic stem cell transplant recipients.
Biol Blood Marrow Transplant, 12 (2006), pp. 325-334
[55.]
A.H. Saad, D.D. DePestel, P.L. Carver.
Factors influencing the magnitude and clinical significance of drug interactions between azole antifungals and select immunosuppressants.
Pharmacotherapy, 26 (2006), pp. 1730-1744
[56.]
R.N. Greenberg, K. Mullane, J.A. Van Burik, I. Raad, M.J. Abzuq, G. Anstead, et al.
Posaconazole as salvage therapy for zygomycosis.
Antimicrob Agents Chemother, 50 (2006), pp. 126-133
[57.]
C. Reed, A. Ibrahim, J.E. Edwards Jr., I. Walot, B. Spellberg.
Deferasirox, an ironchelating agent, as salvage therapy for rhinocerebral mucormycosis.
Antimicrob Agents Chemother, 50 (2006), pp. 3968-3969
[58.]
C. Reed, R. Bryant, A.S. Ibrahim, J. Edwards Jr., S.G. Filler, R. Goldberg, et al.
Combination polyene-caspofungin treatment of rhino-orbital-cerebral mucormycosis.
Clin Infect Dis, 47 (2008), pp. 364-371
[59.]
F. Barchiesi, E. Spreghini, A. Santinelli, A.W. Fothergill, E. Pisa, D. Giannini, et al.
Posaconazole prophylaxis in experimental systemic zygomycosis.
Antimicrob Agents Chemother, 51 (2007), pp. 73-77
[60.]
P. Troke, K. Aguirrebengoa, C. Arteaga, D. Ellis, C.H. Heath, I. Lutsar, et al.
Treatment of scedosporiosis with voriconazole: clinical experience with 107 patients.
Antimicrob Agents Chemother, 52 (2008), pp. 1743-1750
[61.]
J.L. Rodríguez-Tudela, J. Berenguer, J. Guarro, A.S. Kantarcioglu, R. Horre, G.S. de Hoog, et al.
Epidemiology and outcome of Scedosporium prolificans infection, a review of 162 cases.
Med Mycol, 47 (2009), pp. 359-370
[62.]
B.P. Howden, M.A. Slavin, A.P. Schwarer, A.M. Mijch.
Successful control of disseminated Scedosporium prolificans infection with a combination of voriconazole and terbinafine.
Eur J Clin Microbiol Infect Dis, 22 (2003), pp. 111-113
Copyright © 2012. Elsevier España S.L.. All rights reserved
Descargar PDF
Opciones de artículo
es en pt

¿Es usted profesional sanitario apto para prescribir o dispensar medicamentos?

Are you a health professional able to prescribe or dispense drugs?

Você é um profissional de saúde habilitado a prescrever ou dispensar medicamentos