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1.
J Vet Intern Med ; 36(2): 694-701, 2022 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-35170074

RESUMEN

BACKGROUND: Seizures in the early postoperative period after intracranial surgery may affect outcome in dogs. OBJECTIVES: To determine the incidence of early postoperative seizures (EPS) in dogs with brain tumors, identify specific risk factors for EPS, and determine if EPS affects outcome. ANIMALS: Eighty-eight dogs that underwent 125 intracranial surgeries for diagnosis and treatment of rostrotentorial brain tumors. METHODS: Retrospective cohort study. All patients with a diagnosis of rostrotentorial brain tumor from 2006 to 2020 were included. Early postoperative seizures were diagnosed by observation of seizure activity within 14 days of neurosurgery. Previously diagnosed structural epilepsy, perioperative anticonvulsant drug (ACD) use, magnetic resonance imaging (MRI), and tumor characteristics were evaluated. Outcome measures included neurologic and nonneurologic complications, duration of hospitalization, and survival to discharge. RESULTS: Dogs with rostrotentorial brain tumors had EPS after 16/125 (12.8%) neurosurgical procedures (95% confidence interval [CI], 7%-19%). Presence of previous structural epilepsy was not associated with EPS risk (P = 1). Perioperative ACD use also was not associated with EPS (P = .06). Dogs with EPS had longer hospitalization (P < .001), were more likely to have neurologic complications postsurgery (P = .01), and were less likely to survive to discharge (P = .01). CONCLUSIONS AND CLINICAL IMPORTANCE: It is difficult to predict which dogs are at risk of EPS because the presence of previous structural epilepsy and the use of perioperative ACDs was not associated with EPS. However, seizures in the early postoperative period are clinically important because affected dogs had prolonged hospitalization, more neurologic complications, and decreased short-term survival.


Asunto(s)
Neoplasias Encefálicas , Enfermedades de los Perros , Animales , Neoplasias Encefálicas/complicaciones , Neoplasias Encefálicas/cirugía , Neoplasias Encefálicas/veterinaria , Enfermedades de los Perros/epidemiología , Enfermedades de los Perros/patología , Enfermedades de los Perros/cirugía , Perros , Humanos , Incidencia , Complicaciones Posoperatorias/veterinaria , Periodo Posoperatorio , Estudios Retrospectivos , Factores de Riesgo , Convulsiones/epidemiología , Convulsiones/etiología , Convulsiones/veterinaria
2.
Breast Cancer Res Treat ; 189(1): 15-23, 2021 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-34218359

RESUMEN

PURPOSE: Endocrine therapy (ET) is an effective strategy to treat hormone receptor-positive, human epidermal growth factor receptor 2-negative (HR+/HER2-) advanced breast cancer (ABC) but nearly all patients eventually progress. Our goal was to develop and validate a web-based clinical calculator for predicting disease outcomes in women with HR+ABC who are candidates for receiving first-line single-agent ET. METHODS: The meta-database comprises 891 patient-level data from the control arms of five contemporary clinical trials where patients received first-line single-agent ET (either aromatase inhibitor or fulvestrant) for ABC. Risk models were constructed for predicting 24-months progression-free survival (PFS-24) and 24-months overall survival (OS-24). Final models were internally validated for calibration and discrimination using ten-fold cross-validation. RESULTS: Higher number of sites of metastases, measurable disease, younger age, lower body mass index, negative PR status, and prior endocrine therapy were associated with worse PFS. Final PFS and OS models were well-calibrated and associated with cross-validated time-dependent area under the curve (AUC) of 0.61 and 0.62, respectively. CONCLUSIONS: The proposed ABC calculator is internally valid and can accurately predict disease outcomes. It may be used to predict patient prognosis, aid planning of first-line treatment strategies, and facilitate risk stratification for future clinical trials in patients with HR+ABC. Future validation of the proposed models in independent patient cohorts is warranted.


Asunto(s)
Neoplasias de la Mama , Protocolos de Quimioterapia Combinada Antineoplásica , Neoplasias de la Mama/tratamiento farmacológico , Femenino , Fulvestrant/uso terapéutico , Humanos , Receptor ErbB-2 , Receptores de Estrógenos
3.
PLoS One ; 10(7): e0132024, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-26214312

RESUMEN

Several aspects of the human nervous system and associated motor and cognitive processes have been reported to be modulated by extremely low-frequency (ELF, < 300 Hz) time-varying Magnetic Fields (MF). Due do their worldwide prevalence; power-line frequencies (60 Hz in North America) are of particular interest. Despite intense research efforts over the last few decades, the potential effects of 60 Hz MF still need to be elucidated, and the underlying mechanisms to be understood. In this study, we have used functional Magnetic Resonance Imaging (fMRI) to characterize potential changes in functional brain activation following human exposure to a 60 Hz MF through motor and cognitive tasks. First, pilot results acquired in a first set of subjects (N=9) were used to demonstrate the technical feasibility of using fMRI to detect subtle changes in functional brain activation with 60 Hz MF exposure at 1800 µT. Second, a full study involving a larger cohort of subjects tested brain activation during 1) a finger tapping task (N=20), and 2) a mental rotation task (N=21); before and after a one-hour, 60 Hz, 3000 µT MF exposure. The results indicate significant changes in task-induced functional brain activation as a consequence of MF exposure. However, no impact on task performance was found. These results illustrate the potential of using fMRI to identify MF-induced changes in functional brain activation, suggesting that a one-hour 60 Hz, 3000 µT MF exposure can modulate activity in specific brain regions after the end of the exposure period (i.e., residual effects). We discuss the possibility that MF exposure at 60 Hz, 3000 µT may be capable of modulating cortical excitability via a modulation of synaptic plasticity processes.


Asunto(s)
Encéfalo/fisiología , Campos Magnéticos , Imagen por Resonancia Magnética , Adulto , Mapeo Encefálico , Cognición , Femenino , Humanos , Masculino , Actividad Motora , Desempeño Psicomotor , Factores de Tiempo , Adulto Joven
4.
J Vet Sci ; 14(4): 433-40, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-23820168

RESUMEN

This study describes the neuropathologic features of normal canine brain ablated with non-thermal irreversible electroporation (N-TIRE). The parietal cerebral cortices of four dogs were treated with N-TIRE using a dose-escalation protocol with an additional dog receiving sham treatment. Animals were allowed to recover following N-TIRE ablation and the effects of treatment were monitored with clinical and magnetic resonance imaging examinations. Brains were subjected to histopathologic and ultrastructural assessment along with Bcl-2, caspase-3, and caspase-9 immunohistochemical staining following sacrifice 72 h post-treatment. Adverse clinical effects of N-TIRE were only observed in the dog treated at the upper energy tier. MRI and neuropathologic examinations indicated that N-TIRE ablation resulted in focal regions of severe cytoarchitectural and blood-brain-barrier disruption. Lesion size correlated to the intensity of the applied electrical field. N-TIRE-induced lesions were characterized by parenchymal necrosis and hemorrhage; however, large blood vessels were preserved. A transition zone containing parenchymal edema, perivascular inflammatory cuffs, and reactive gliosis was interspersed between the necrotic focus and normal neuropil. Apoptotic labeling indices were not different between the N-TIRE-treated and control brains. This study identified N-TIRE pulse parameters that can be used to safely create circumscribed foci of brain necrosis while selectively preserving major vascular structures.


Asunto(s)
Encéfalo/patología , Procedimientos Neuroquirúrgicos/efectos adversos , Animales , Encéfalo/metabolismo , Encéfalo/cirugía , Encéfalo/ultraestructura , Caspasa 3/metabolismo , Caspasa 9/metabolismo , Perros , Electroporación/veterinaria , Imagen por Resonancia Magnética/métodos , Microscopía Electrónica de Transmisión , Necrosis/metabolismo , Necrosis/patología
5.
J Wildl Dis ; 44(4): 922-9, 2008 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-18957648

RESUMEN

Aural abscesses are a common health problem in free-ranging eastern box turtles (Terrapene carolina carolina), and they have been associated with high body burdens of organochlorine (OC) compounds, which are known disruptors of vitamin A. The objective of this study was to determine if the presence of pathologic lesions in box turtles were correlated with increased and decreased levels of hepatic OC compounds and vitamin A, respectively. A graded scale for the pathologic changes observed in tissue samples collected from abscessed and nonabscessed box turtles over a 2-yr period (2003-04) was developed, and the levels of OC compounds and vitamin A in livers collected from the same turtles were determined through chemical analysis. Sixty-eight turtles (40 with aural abscesses and 28 without) were included in the study. Relationships between variables were analyzed using Spearman's Rank Correlation Test, where P

Asunto(s)
Absceso/veterinaria , Contaminantes Ambientales/efectos adversos , Hidrocarburos Clorados/efectos adversos , Insecticidas/efectos adversos , Tortugas , Deficiencia de Vitamina A/veterinaria , Absceso/etiología , Absceso/patología , Animales , Animales Salvajes , Relación Dosis-Respuesta a Droga , Oído Medio/patología , Exposición a Riesgos Ambientales , Contaminantes Ambientales/administración & dosificación , Contaminantes Ambientales/análisis , Femenino , Hidrocarburos Clorados/administración & dosificación , Hidrocarburos Clorados/análisis , Insecticidas/administración & dosificación , Insecticidas/análisis , Hígado/química , Hígado/patología , Masculino , Estadísticas no Paramétricas , Vitamina A/metabolismo , Deficiencia de Vitamina A/inducido químicamente , Deficiencia de Vitamina A/patología
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