6 research outputs found

    Cambios en la presión intraocular en pacientes con neuralgia trigeminal sometidos a radiofrecuencia del ganglio de Gasser

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    ABSTRACT Introduction: Trigeminal neuralgia is characterized by paroxysmal attacks of intense pain, lancinating as electric shocks, accompanied by burning sensation and periodic appearance in the distribution of one or more trigeminal branches. The anatomical relationship between the Gasser ganglion and the cavernous sinus could produce an increase in the intraocular tension after the application of the radiofrequency of the trigeminal ganglion when modifying the venous drainage of the eye, a situation that until now has not been studied. The objective was to determine if the application of conventional radiofrequency in the Gasser ganglion produces changes in the intraocular tension in patients with primary trigeminal neuralgia of second and / or third branch. Material and methods: Longitudinal study that included patients diagnosed with trigeminal neuralgia of second and / or third branch; In the operating room and under general anesthesia, radiofrequency procedure was performed in Gasser ganglion, with generator Neurotherm R 500, needles of 100 mm in length and 22 G, with active tip of 5 mm, sensory stimulation at 50 Hertz with 0.3 - 0.5 V applying 80º C for 60 seconds in 2 or 3 phases. Intraocular pressure was measured 24 hours before the procedure, 24 hours after the procedure and seven days after the procedure. The analysis of the intraocular pressure, as well as the EVA scale of pain was determined by an ANOVA analysis of repeated measures. Results: Thirty patients were included of which 26 were women, the average age was 59.6 ± (SD 11.16). Intraocular tension 24 h before, one day after and one week after performing radiofrequency of the Gasser ganglion, did not show significant changes with ANOVA for repeated samples (p 0.916). Conclusions: Intraocular tension was not modified in the short term after radiofrequency of the Gasser ganglion.RESUMEN Introducción: La neuralgia del trigémino es un cuadro caracterizado por ataques paroxísticos de dolor intenso, lancinante como descargas eléctricas, acompañado de sensación urente y de aparición periódica en la distribución de una o más ramas trigeminales. La relación anatómica entre el ganglio de Gasser y el seno cavernoso pudiera producir un incremento en la tensión intraocular después de la aplicación de la radiofrecuencia del ganglio trigeminal al modificar el drenaje venoso del ojo, situación que hasta el momento no se ha estudiado. El objetivo fue determinar si la aplicación de radiofrecuencia convencional en el ganglio de Gasser produce modificaciones en la tensión intraocular en pacientes con neuralgia trigeminal primaria de segunda y/o tercera rama. Material y métodos: Estudio longitudinal que incluyó a pacientes con diagnóstico de neuralgia del trigémino de segunda y/o tercera rama; en quirófano y bajo anestesia general, se les realizó procedimiento de radiofrecuencia en Ganglio de Gasser, con generador Neurotherm R 500, agujas de 100 mm de longitud y 22 G, con punta activa de 5 mm, estimulación sensitiva a 50 Hertz con 0,3-0,5 V aplicando 80 °C por 60 segundos en dos o tres fases. La presión intraocular se midió 24 horas previas al procedimiento, 24 horas posteriores al procedimiento y siete días después del mismo. El análisis de la presión intraocular, así como la escala EVA de dolor, se determinó mediante un análisis de ANOVA de medidas repetidas. Resultados: Se incluyeron 30 pacientes de los cuales 26 fueron mujeres, la edad promedio fue de 59,6 ± (DE 11,16). La tensión intraocular 24 h antes, un día después y una semana después de la realización de la radiofrecuencia del ganglio de Gasser no mostró modificaciones significativas con ANOVA para muestras repetidas (p = 0,916). Conclusiones: La tensión intraocular no se modificó a corto plazo después de realizar radiofrecuencia del ganglio de Gasser

    An Uncommon Case of Bilateral Breast Enlargement Diagnosed as Tumoral Pseudoangiomatous Stromal Hyperplasia: Imaging and Pathological Findings

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    The incidence of reported pseudoangiomatous stromal hyperplasia (PASH), as well as the variability and severity of clinical presentations, is increasing in the literature. In parallel, several authors posit the need for an improved classification of PASH to avoid possible variables associated with this diagnosis. Here, we present a 25-year-old woman with PASH accompanied by severe bilateral and symmetrical breasts enlargement, highlighting an uncommon clinical presentation of PASH as much as the careful interdisciplinary review and correlation of histology and all available imaging studies to confirm the definitive diagnosis

    Risk of COVID-19 after natural infection or vaccinationResearch in context

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    Summary: Background: While vaccines have established utility against COVID-19, phase 3 efficacy studies have generally not comprehensively evaluated protection provided by previous infection or hybrid immunity (previous infection plus vaccination). Individual patient data from US government-supported harmonized vaccine trials provide an unprecedented sample population to address this issue. We characterized the protective efficacy of previous SARS-CoV-2 infection and hybrid immunity against COVID-19 early in the pandemic over three-to six-month follow-up and compared with vaccine-associated protection. Methods: In this post-hoc cross-protocol analysis of the Moderna, AstraZeneca, Janssen, and Novavax COVID-19 vaccine clinical trials, we allocated participants into four groups based on previous-infection status at enrolment and treatment: no previous infection/placebo; previous infection/placebo; no previous infection/vaccine; and previous infection/vaccine. The main outcome was RT-PCR-confirmed COVID-19 >7–15 days (per original protocols) after final study injection. We calculated crude and adjusted efficacy measures. Findings: Previous infection/placebo participants had a 92% decreased risk of future COVID-19 compared to no previous infection/placebo participants (overall hazard ratio [HR] ratio: 0.08; 95% CI: 0.05–0.13). Among single-dose Janssen participants, hybrid immunity conferred greater protection than vaccine alone (HR: 0.03; 95% CI: 0.01–0.10). Too few infections were observed to draw statistical inferences comparing hybrid immunity to vaccine alone for other trials. Vaccination, previous infection, and hybrid immunity all provided near-complete protection against severe disease. Interpretation: Previous infection, any hybrid immunity, and two-dose vaccination all provided substantial protection against symptomatic and severe COVID-19 through the early Delta period. Thus, as a surrogate for natural infection, vaccination remains the safest approach to protection. Funding: National Institutes of Health
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