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1.
Transpl Infect Dis ; 19(2)2017 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-28083955

RESUMEN

We report the recent isolation of Cryptococcus laurentii from the feces of a patient with Hodgkin's lymphoma who underwent autologous hematopoietic stem cell transplant (HSCT). The organism was identified using microscopic morphology, cultural characteristics, and biochemical tests including sugar assimilation. Minimum inhibitory concentration of various antifungals was determined by microbroth dilution method. The recovery of pure culture of C. laurentii from stool culture, and the patient's response to treatment with voriconazole support its potential etiological role. To the best of our knowledge, we report the first case of diarrhea caused by C. laurentii in an HSCT recipient.


Asunto(s)
Antifúngicos/uso terapéutico , Criptococosis/microbiología , Cryptococcus/aislamiento & purificación , Diarrea/microbiología , Trasplante de Células Madre Hematopoyéticas/efectos adversos , Enfermedad de Hodgkin/cirugía , Voriconazol/uso terapéutico , Administración Intravenosa , Administración Oral , Adulto , Profilaxis Antibiótica , Antifúngicos/administración & dosificación , Protocolos de Quimioterapia Combinada Antineoplásica/efectos adversos , Protocolos de Quimioterapia Combinada Antineoplásica/uso terapéutico , Proteína C-Reactiva/análisis , Carmustina/efectos adversos , Carmustina/uso terapéutico , Criptococosis/sangre , Criptococosis/tratamiento farmacológico , Citarabina/efectos adversos , Citarabina/uso terapéutico , Diarrea/sangre , Diarrea/tratamiento farmacológico , Etopósido/efectos adversos , Etopósido/uso terapéutico , Heces/microbiología , Fluconazol/uso terapéutico , Humanos , Melfalán/efectos adversos , Melfalán/uso terapéutico , Pruebas de Sensibilidad Microbiana , Acondicionamiento Pretrasplante/efectos adversos , Acondicionamiento Pretrasplante/métodos , Trasplante Autólogo/efectos adversos , Voriconazol/administración & dosificación
2.
Mycoses ; 60(2): 112-117, 2017 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-27696562

RESUMEN

Cryptococcus albidus and Cryptococcus laurentii are uncommon species of this genus that in recent decades have increasingly caused opportunistic infections in humans, mainly in immunocompromised patients; the best therapy for such infection being unknown. Using a murine model of systemic infection by these fungi, we have evaluated the efficacy of amphotericin B (AMB) at 0.8 mg/kg, administered intravenously, fluconazole (FLC) or voriconazole (VRC), both administered orally, at 25 mg/kg and the combination of AMB plus VRC against three C. albidus and two C. laurentii strains. All the treatments significantly reduced the fungal burden in all the organs studied. The combination showed a synergistic effect in the reduction in fungal load, working better than both monotherapies. The histopathological study confirmed the efficacy of the treatments.


Asunto(s)
Antifúngicos/uso terapéutico , Criptococosis/tratamiento farmacológico , Criptococosis/microbiología , Cryptococcus/efectos de los fármacos , Administración Intravenosa , Administración Oral , Anfotericina B/uso terapéutico , Animales , Criptococosis/sangre , Modelos Animales de Enfermedad , Sinergismo Farmacológico , Quimioterapia Combinada , Fluconazol/uso terapéutico , Huésped Inmunocomprometido , Pulmón/microbiología , Ratones , Pruebas de Sensibilidad Microbiana , Bazo/microbiología , Voriconazol/uso terapéutico
3.
J Antimicrob Chemother ; 26(3): 387-97, 1990 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-2172199

RESUMEN

We studied the pharmacokinetics and efficacy of BAY R3783, a new antifungal azole compound, in rabbits and compared it with fluconazole and itraconazole. BAY R3783 has at least two active metabolites, BAY U3624 and BAY U3625. We measured serum concentrations of all three compounds; the peak serum level for the parent compound was approximately two hours post dose. BAY R3783 and its metabolites also crossed the blood-CSF barrier; the mean CSF level of BAY R3783 was 30.5% of simultaneous serum levels. The in-vivo activity of the azoles was compared in a model of cryptococcal meningitis in immunosuppressed rabbits. BAY R3783, fluconazole and itraconazole all reduced yeast counts in the CSF with equal efficacy over ten days of therapy at 100 mg/day. In this model, BAY R3783 was effective in the treatment of cryptococcal meningitis.


Asunto(s)
Criptococosis/metabolismo , Fluconazol/farmacocinética , Cetoconazol/análogos & derivados , Meningitis/metabolismo , Triazoles/farmacocinética , Animales , Criptococosis/sangre , Criptococosis/líquido cefalorraquídeo , Criptococosis/tratamiento farmacológico , Cryptococcus neoformans/patogenicidad , Itraconazol , Cetoconazol/farmacocinética , Meningitis/sangre , Meningitis/líquido cefalorraquídeo , Meningitis/tratamiento farmacológico , Conejos , Triazoles/farmacología , Triazoles/uso terapéutico
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