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Métodos Terapéuticos y Terapias MTCI
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1.
Rhinology ; 61(6): 561-567, 2023 Dec 01.
Artículo en Inglés | MEDLINE | ID: mdl-37566791

RESUMEN

PURPOSE: To provide real-life data on azole treatment outcomes and the role of surgery in the current management of invasive fungal rhinosinusitis complicated by orbitocranial fungal infection (OCFI). METHODS: Data was collected retrospectively from a chart review from four participating centers and a systematic literature review. The study group included patients with OCFI treated with azole antifungals. The control cases were treated with other antifungal agents. The cranial and orbital involvement degree was staged based on the imaging. The extent of the surgical resection was also classified to allow for inter-group comparison. RESULTS: There were 125 patients in the azole-treated group and 153 in the control group. Among the patients with OCFI cranial extension, 23% were operated on in the azole-treated group and 18% in the control group. However, meninges and brain resection were performed only in the controls (11% of patients) and never in the azole antifungals group. Orbital involvement required surgery in 26% of azole-treated cases and 39% of controls. Despite a more aggressive cranial involvement, azole-treated patients' mortality was significantly lower than in controls, with an OCFI-specific mortality rate of 21% vs. 52%. A similar, though not statistically significant, trend was found for the extent of the orbital disease and surgery. CONCLUSION: Despite less aggressive surgical intervention for cranial involvement, OCFI patients treated with azoles had a higher survival rate. This finding suggests we may improve morbidity with a more conservative surgical approach in conjunction with azole treatment. The same trend is emerging for orbital involvement.


Asunto(s)
Antifúngicos , Micosis , Humanos , Antifúngicos/uso terapéutico , Azoles/uso terapéutico , Pruebas de Sensibilidad Microbiana , Micosis/tratamiento farmacológico , Micosis/cirugía , Estudios Retrospectivos , Resultado del Tratamiento , Revisiones Sistemáticas como Asunto
2.
J Trop Pediatr ; 48(4): 227-33, 2002 08.
Artículo en Inglés | MEDLINE | ID: mdl-12200985

RESUMEN

The purpose of this study was to evaluate the effectiveness of early treatment with erythropoietin (EPO) in two different treatment regimes (high vs. low dose) in comparison to the conventional treatment of packed red blood cell (PRBC) transfusions in the management of anaemia of prematurity in a country with limited resources. An open controlled trial was conducted on 93 preterm infants (7 days postnatal age, 900-1500 g birthweight). Patients were randomly assigned either to a low dose (250 IU/kg), a high dose (400 IU/kg), or a control group. EPO was administered subcutaneously three times a week and all infants received 6 mg/kg iron orally from study entry to endpoint of therapy. Haematological parameters were measured and compared. The success was defined as an absence of transfusions and a haematocrit that did not fall below 30 per cent during the time period that the infants were in the study. The three groups were statistically comparable at study entry with respect to gestational age, birthweight, Apgar scores, and haematological values. Over the period that the infants were in the study, 75 per cent of the low dose group and 71 per cent of the high dose group met the criteria for success compared with 40 per cent in the control group (p < 0.001). However, there was no significant difference in the number of transfusions when the low and high EPO dose groups (9.5 per cent) were combined and compared with the control group (26.7 per cent) p = 0.0587. It was concluded that in stable infants, 900-1500 g, where phlebotomy losses are minimized and stringent transfusion guidelines are adhered to, EPO does not significantly decrease the number of transfusions. A conservative approach in the management of anaemia of prematurity, is a viable alternative in areas with limited resources.


Asunto(s)
Anemia Neonatal/tratamiento farmacológico , Transfusión de Eritrocitos/métodos , Eritropoyetina/administración & dosificación , Recien Nacido Prematuro , Anemia Neonatal/etiología , Distribución de Chi-Cuadrado , Países en Desarrollo , Relación Dosis-Respuesta a Droga , Femenino , Estudios de Seguimiento , Humanos , Recién Nacido , Inyecciones Subcutáneas , Masculino , Probabilidad , Proteínas Recombinantes , Valores de Referencia , Sudáfrica , Resultado del Tratamiento
3.
Cereb Cortex ; 10(10): 1005-13, 2000 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-11007551

RESUMEN

Approximately 50% of New Zealand Black mice (NZB/BINJ) and 80% of NXSM-D/EiJ mice prenatally develop neocortical layer I ectopias, mostly in somatosensory cortices. These cortical anomalies are similar to those seen in the brains of individuals with dyslexia. Neurofilament staining revealed a radial column of tightly packed fiber bundles in the layers underlying ectopias. This suggested that the connectivity of the ectopic neurons was aberrant. The present study used the tracers 1,1'-dioctadecyl- 3,3,3',3'-tetramethylindo- carbocyanine perchlorate (DiI) and biotinylated dextran amine (BDA) to more thoroughly explore the cortical and thalamic connectivity of the ectopias. DiI placement into ectopias again revealed a distinct bundle of fibers extending from the ectopic neurons to the deep cortical layers. This bundle split in the white matter with some fibers traveling to the corpus callosum and others to the internal capsule. Thalamic connections were concentrated in the ventrobasal com- plex (VB) and posterior thalamic nucleus group (Po). Injections of BDA into VB revealed reciprocal connections between VB and the ectopic cortical neurons. Ipsilateral corticocortical projections were seen between ectopias in primary somatosensory and motor and secondary somatosensory cortices, but no contralateral connections of the ectopic neurons were seen. These findings confirm the notion that layer I ectopias are anomalously connected by comparison to neurons in homologous cortex, which may underlie widespread dysfunction of brains containing ectopias.


Asunto(s)
Autoinmunidad , Biotina/análogos & derivados , Encefalopatías/fisiopatología , Coristoma/fisiopatología , Neuronas/fisiología , Corteza Somatosensorial/fisiopatología , Animales , Encefalopatías/genética , Encefalopatías/inmunología , Carbocianinas , Coristoma/genética , Coristoma/inmunología , Dextranos , Femenino , Colorantes Fluorescentes , Masculino , Ratones , Ratones Endogámicos/genética , Corteza Motora/fisiopatología , Vías Nerviosas/fisiopatología , Núcleos Talámicos/fisiopatología
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