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1.
J Mycol Med ; 27(2): 261-265, 2017 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-28188050

RESUMEN

Symptomatic candiduria often occurs in patients with indwelling bladder catheters or immunocompromised host. Isolation of Candida in urine in high-risk patients should primarily be considered as a marker for candidemia. Hematological and genitourinary malignancies are one of the main risk factors associated with Candida urinary tract infections (CUTI). Fluconazole is a choice for initial treatment of CUTI, but it is fluctuate depending on the patient's condition including renal failure, site of urinary infection and Candida species. Poor glomerular filtration is the main disadvantage echinocandins resulting in very low urinary concentrations. Therefore, echinocandins have prohibited their use in CUTI. Up to now, there are only 10 cases reported in the literatures with highly effective echinocandins in CUTI because of high concentrations in the tissue are needed to control invasive fungal disease. Herein, we report a candiduria followed by renal candidiasis caused by Candida albicans in a 6-year-old Iranian male with a history of Wilms tumor in left kidney. Direct examination of urine specimen revealed an infection due to budding yeast cells with numerous pseudohyphae and growths of C. albicans was reconfirmed by sequencing of ITS rDNA region. MICs in increasing order were as follows: caspofungin (0.016µg/ml), voriconazole (0.125µg/ml), amphotericin B (0.25µg/ml), itraconazole (0.5µg/ml) and fluconazole (2µg/ml). It seems that successful treatment with caspofungin owes achieved high renal tissue concentrations that are unrelated to glomerular filtration. In conclusion, predisposing factors for better outcome are more important than treatment of CUTI, therefore, management of UTI is essential for critically patients.


Asunto(s)
Candidiasis/tratamiento farmacológico , Equinocandinas/uso terapéutico , Neoplasias Renales/tratamiento farmacológico , Lipopéptidos/uso terapéutico , Infecciones Urinarias/tratamiento farmacológico , Tumor de Wilms/tratamiento farmacológico , Antifúngicos/uso terapéutico , Candida/aislamiento & purificación , Candidiasis/complicaciones , Candidiasis/orina , Caspofungina , Niño , Humanos , Irán , Neoplasias Renales/complicaciones , Neoplasias Renales/microbiología , Masculino , Resultado del Tratamiento , Infecciones Urinarias/complicaciones , Infecciones Urinarias/microbiología , Tumor de Wilms/complicaciones , Tumor de Wilms/microbiología
2.
Eur Rev Med Pharmacol Sci ; 17(22): 3068-72, 2013 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-24302188

RESUMEN

BACKGROUND: Approximately 0.5-2% of upper respiratory tract infections in adults and 6-13% of viral upper respiratory tract infections in children are complicated by acute sinusitis. This study was aimed to evaluate the coadministration effect of fluticasone nasal spray (FNS) with amoxicillin for AS in children. MATERIALS AND METHODS: One hundred children 2 to 14 years of age with acute sinusitis referred to Shahid Mohammadi Pediatric Hospital in Bandar Abbas were randomly allocated into two equal intervention and control groups to receive amoxicillin with fluticasone nasal spray one puff twice daily for 14 days and amoxicillin 80 to 100 mg/kg/ day for 14 days respectively. RESULTS: Twenty one (42%) of children in intervention group were cured completely and 2 (4%) children in control group had complete recovery (p < 0.001). Symptom severity score was 22.98 ± 2.95 before treatment that reduced to 13.26 ± 3.20 after treatment (p < 0.001). CONCLUSIONS: Use of fluticasone can reduce the severity of symptoms of sinusitis in children.


Asunto(s)
Amoxicilina/administración & dosificación , Androstadienos/administración & dosificación , Antibacterianos/administración & dosificación , Antiinflamatorios/administración & dosificación , Sinusitis/tratamiento farmacológico , Enfermedad Aguda , Administración Intranasal , Adolescente , Niño , Preescolar , Femenino , Fluticasona , Humanos , Masculino , Método Simple Ciego
3.
Indian Pediatr ; 41(12): 1232-7, 2004 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-15623904

RESUMEN

Four hundred and fifty three healthy children immunized with a course of hepatitis B vaccine beginning at birth were tested at 10-11 years of age for persistence of anti-hepatitis B-S antigen antibody (anti-HBs); and responses of children without protective antibody to different doses of hepatitis B vaccine booster were evaluated. Although nearly 42% of them were not seroprotected, but most of boosted subjects (87.3%) retained robust immunologic memory and rapidly retained a protective anti-HBs antibody titer of at least 10 IU/L after booster vaccination.


Asunto(s)
Vacunas contra Hepatitis B/uso terapéutico , Hepatitis B/prevención & control , Memoria Inmunológica , Formación de Anticuerpos , Niño , Femenino , Humanos , Inmunización Secundaria , Masculino , Factores de Tiempo
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