Long-term complications according to silicone oil type. A single center cohort study.

PURPOSE: To study the incidence of macular edema (ME), ocular hypertension (OHT), emulsification and migration to the anterior chamber (AC) of silicone oil (SO) in patients after complex retina surgery, stratified by SO type. METHODS: Retrospective, cohort study. Patients who underwent retina surgery with SO injection and extraction in our center were included. We compared the complication rates of ME, OHT, emulsification and migration to the AS according to SO type (1300cSt, 5700cSt and heavy SO). Data on age, sex, emulsification time, duration of the tamponade, previous retina surgeries and diagnosis were also gathered and included in a multivariate analysis. RESULTS: We included 163 patients (mean age of 64.8 years; mean duration of the tamponade: 11 months). Rates of emulsification, ME, OHT and SO migration to the AC were similar in all groups (p = 0.998, 0.668, 0.915 and 0.360). ME was the most frequent complication (33.3-47.8%), which resolved after SO extraction in 77.6% of cases. The majority of cases with OHT persisted (61.7%). Emulsification was related to younger age (OR 0.94) and longer duration of the tamponade (OR 1.04). The odds of SO migration to the AC increased with emulsification (OR 2.78), recurrent retinal detachment (OR 0.99) and aphakia (OR 4.05). CONCLUSIONS: We propose SO extraction as the preferred treatment for ME during SO tamponade. SO extraction should be performed sooner in younger patients to avoid emulsification. In selected patients, we suggest a longer duration of the tamponade up to 11 months with a reasonable safety profile, regardless of the SO type.

The effect of six-month oral vitamin K supplementation on calcification propensity time in individuals with type 2 diabetes mellitus: A post hoc analysis of a randomized, double-blind, placebo-controlled trial.

BACKGROUND AND AIMS: Experimental studies suggested that vitamin K supplementation may retard arterial calcification. Recently, serum calcification propensity time (T50) has been suggested as a functional biomarker for arterial wall calcification propensity. In this post-hoc analysis of a clinical trial, we evaluated the effect of six-month oral vitamin K supplementation on T50 and assessed the correlation between T50 and imaging arterial calcification parameters in people with type 2 diabetes (T2DM). METHODS: This double-blind, randomized, placebo-controlled trial included 68 participants (age = 69 ± 8 years, 76% male) with T2DM. Participants were assigned to menaquinone-7 (360 µg/day; n = 35) or placebo (n = 33). T50 was measured via nephelometry in serum collected at baseline, three and six months. Arterial calcification was measured at baseline and six months via 18F-Na PET-CT and conventional CT using Target-to-Background ratio (TBR) and Agatston score. Longitudinal analysis of covariance adjusted for baseline T50 was used to study the treatment effect. Spearman's correlation was used to assess the correlation between T50 and imaging calcification parameters. RESULTS: Median baseline T50 was similar in the vitamin K (350 [321-394] minutes) and placebo groups (363 [320-398]). There was no significant difference in T50 between treatment arms over time (ẞ = 1.00, 95%C.I. = 0.94-1.07, p = 0.982). The correlation coefficient of T50 with TBR and Agatston score at baseline were -0.185 (p = 0.156) and -0.121 (p = 0.358), respectively. CONCLUSIONS: No effect of vitamin K supplementation on T50 was observed in T2DM. Moreover, T50 did not correlate with TBR and Agatston score. Further research on vitamin K in arterial calcification and on the validity of T50 as arterial calcification marker is warranted.

Cirugía robótica en el tratamiento de la acalasia / Robotic surgery for the treatment of achalasia

Objetivo Describir la experiencia del abordaje robótico en la cirugía de la acalasia en un centro de tercer nivel. Material y métodos Se analizaron los pacientes con acalasia intervenidos mediante cirugía robótica entre mayo de 2010 y abril de 2019. Las variables a estudio se recogieron en una base de datos prospectiva y se realizó un análisis descriptivo. Resultados Se incluyeron 45 pacientes (55,6% varones) con edad media de 44 años. El síntoma principal al diagnóstico fue la disfagia. Diecinueve pacientes (42,2%) habían recibido tratamiento endoscópico previo a la cirugía, mayoritariamente dilatación neumática (84,2%). La técnica quirúrgica empleada fue la miotomía de Heller asociada a funduplicatura tipo Toupet, con un tiempo operatorio medio de 211 minutos. La estancia media fue 5 días. Se produjeron 2 perforaciones postoperatorias (4,4%). La mortalidad peroperatoria fue del 0%. El seguimiento medio fue de 64 meses. A 3 y 5 años se evidenció una importante disminución del Eckardt score y el estudio manométrico mostró una disminución de la presión del esfínter esofágico inferior en reposo media del 58% y del 70%, respectivamente, con persistencia de hipomotilidad del cuerpo esofágico. En dos pacientes (5,4%) se diagnosticó reflujo gastroesofágico patológico y 4 (10,8%) presentaron recurrencia de los síntomas, requiriendo dilataciones neumáticas endoscópicas. En 2 casos las dilataciones no fueron efectivas por lo que se planteó la realización de una miotomía endoscópica. Conclusiones Según nuestra experiencia, la cirugía robótica constituye un procedimiento seguro y efectivo para el tratamiento de la acalasia (AU)

Objective To describe the experience of the robotic approach for achalasia surgery in a tertiary center. Material and methods Patients with achalasia who underwent robotic surgery between May 2010 and April 2019 were analyzed. The study variables were collected in a prospective database and a descriptive analysis was performed. Results 45 patients (55.6% male) with a mean age of 44 years were included. The main symptom at diagnosis was dysphagia. 19 patients (42.2%) received endoscopic treatment prior to surgery, mostly pneumatic dilation (84.2%). Heller's myotomy associated with Toupet fundoplication was the surgical technique of choice, with a mean operative time of 211minutes. The average stay was 5 days. There were 2 postoperative perforations (4.4%). Perioperative mortality was 0%. The mean follow-up was 64 months. At 3 and 5 years, a significant decrease in the Eckardt score was observed and the manometric study showed a decrease in the lower esophageal sphincter pressure at rest of 58% and 70%, respectively, with persistence of hypomotility of the esophageal body. Pathological gastroesophageal reflux was diagnosed in two patients (5.4%) and 4 (10.8%) presented recurrence of symptoms, requiring endoscopic pneumatic dilations. In 2 cases, the dilations were not effective, so an endoscopic myotomy was considered. Conclusions In our experience, robotic surgery is a safe and effective procedure for the treatment of achalasia (AU)

Pectus excavatum, manejo mínimamente invasivo con técnica de Nuss: experiencia Instituto Nacional del Tórax / Pectus excavatum, minimally invasive management with Nuss technique

Resumen Objetivo Comunicar la experiencia en el tratamiento de pectus excavatum en el Instituto Nacional del Tórax. Material y Método: Estudio descriptivo con seguimiento. Se recolectaron datos de las variables de interés, mediante la revisión de fichas clínicas. Se incluyeron pacientes operados entre marzo de 2007 y abril de 2018. Resultados Se incluyeron 86 pacientes operados con técnica mínimamente invasiva en el período descrito. De ellos, 74 pacientes de sexo masculino. El promedio de edad al momento de la cirugía fue de 17,8 años. El principal motivo de consulta fue por desmedro estético que correspondió al 41,8% de los pacientes. Salvo en 1 paciente, en todo el resto se ocupó una sola barra. En nuestra serie hubo 12 pacientes que presentaron alguna complicación operatoria y 1 paciente fallecido. Hasta el cierre del seguimiento se retiraron 61 barras, 2 de ellas previo al período estipulado de tratamiento, por morbilidad. Hay 20 barras in situ y 4 pacientes de los cuales no se tiene registro por abandono de controles. Discusión El pectus excavatum es la más frecuente de las deformidades de la pared torácica, es 4 a 6 veces más frecuente en hombres que en mujeres. En general los pacientes son asintomáticos, aunque algunos pueden presentar síntomas cardiopulmonares. La reparación con cirugía mínimamente invasiva con técnica de Nuss aparece hoy en día como el gold standard de manejo. Conclusión El manejo de los pacientes con pectus excavatum en nuestra Institución se asemeja a lo reportado en la literatura internacional. Nuestros esfuerzos deben apuntar a disminuir la morbimortalidad asociada.

Aim To communicate the experience in the treatment of pectus excavatum in the National Institute of Thorax. Materials and Method: Descriptive study with follow-up. Data of variables of interest were collected through the review of clinical records. Patients operated between March 2007 and April 2018 were included. Results 86 patients operated with the Nuss technique were included in the period described. Of them, 74 male patients. The average age at the time of surgery was 17.8 years. The main reason for consultation was due to cosmetic detriment that corresponded to 41.8% of the patients. Except in 1 patient, in all the rest a single bar was occupied. In our series, there were 12 patients who presented some operative complication and 1 patient died. Up to the end of the follow-up, 61 bars were removed, 2 of them in non-scheduled surgery. There are 20 bars in situ and 4 patients of which there is no registration due to abandonment of controls. Discussion Pectus excavatum is the most frequent of the deformities of the chest wall, it is 4 to 6 times more frequent in men than in women. In general, patients are asymptomatic, although some may have cardiopulmonary symptoms. The repair with minimally invasive surgery with Nuss technique appears today as the goldstandard of management. Conclusion The management of patients with pectus excavatum in our Institution is similar to that reported in the international literature. Our efforts should aim to reduce the associated morbidity and mortality.

Isolated vascular "v" lesions in liver allografts: How to approach this unusual finding.

According to the Banff criteria for kidney allografts, isolated vascular or "v" lesions are defined as intimal inflammation, age-inappropriate fibro-intimal hyperplasia, or both, without the presence of associated interstitial T cell-mediated rejection (TCMR). In general, these lesions portend a worse outcome for kidney allografts, particularly in those where the "v" lesions are identified in patients with coexistent donor specific antibodies (DSA) or later after transplantation. Although affected arteries are rarely sampled in liver allograft biopsies, we identified nine patients at a mean of 1805 days posttransplantation and compared these to matched controls. Almost half (4 of 9) of the study patient biopsies showed inflammatory arteritis associated with focal or diffuse C4d positivity, which was not observed in matched controls. One "v" lesion patient progressed to rejection-related graft failure and two developed moderate/severe TCMR in subsequent biopsies, whereas only one rejection episode occurred in follow-up biopsies, and no rejection-related deaths or graft failures were detected in controls. In conclusion, patients with liver allograft isolated "v" lesions should undergo further evaluation and closer follow-up for impending TCMR and/or underlying co-existent chronic antibody-mediated rejection (AMR).

[Necrobiotic xanthogranuloma. Differential diagnosis, treatment and systemic involvement. Case report]. / Xantogranuloma necrobiótico. Diagnóstico diferencial, tratamiento e implicaciones sistémicas. A propósito de un caso.

CASE REPORT: A 48-year-old male was referred to our hospital for further evaluation of eyelid edema with bilateral yellowish ulcerated nodules. Suspecting a xanthogranulomatosis, imaging tests and biopsy were performed with diagnosis of necrobiotic xanthogranuloma. IgG monoclonal gammapathy was diagnosed in a systemic study. Systemic corticosteroids and cyclosporine were initiated unsuccessfully; therefore intra-lesional injections of triamcinolone were started, which controlled the orbital disease. DISCUSSION: Necrobiotic xanthogranuloma is a rare condition that usually affects the eyelids and anterior orbit. Its diagnosis is important as it is associated with malignant lymphoproliferative processes. Intra-lesional corticosteroids were effective in our patient.

[Orbital alveolar rhabdomyosarcoma masked by ethmoid sinusitis in a 25-year-old]. / Rabdomiosarcoma alveolar orbitario enmascarado por sinusitis etmoidal en un adulto de 25 años.

CASE REPORT: A 25-year-old woman with right subacute sinusitis, complained about discomfort in her right eye. Clinical manifestations and computed tomography were suggestive of sub-periosteal orbital ethmoid wall abscess, for which the patient underwent urgent drainage. A solid tumor was found, with a positive biopsy for alveolar rhabdomyosarcoma. Complete remission and resolution of orbital symptoms were achieved with chemotherapy and radiation therapy. DISCUSSION: Alveolar orbital rhabdomyosarcoma in adults is uncommon. Rhabdomyosarcoma has a high risk of spreading. It can simulate a sinusitis, as in our patient, early diagnosis and early treatment being especially important in these patients.

Duodenosis linfocítica: estudio etiológico y formas de presentación clínica / Lymphocytic duodenosis: etiological study and clinical presentations

INTRODUCCIÓN: La duodenosis linfocítica (DL) es una lesión característica en las fases iniciales de la enfermedad celíaca (EC), pero puede asociarse a otras muchas entidades. El objetivo de este trabajo fue evaluar la prevalencia de las diferentes causas de DL y valorar posibles diferencias en la presentación clínica según la etiología responsable. Métodos Estudio retrospectivo que incluye 194 pacientes diagnosticados de una DL (más de 25 linfocitos intraepiteliales por 100 células epiteliales). Se siguió una estrategia de evaluación etiológica definida que incluyó serología celíaca (anticuerpos antitransglutaminasa), genotipos HLA-DQ2/DQ8, diagnóstico Helicobacter pylori (H. pylori) y sobrecrecimiento bacteriano intestinal (SBID). El diagnóstico de EC se estableció en función de la respuesta clínica e histológica a una DSG en pacientes con serología positiva o un estudio HLA-DQ2 (al menos uno de los alelos) o −DQ8 (ambos alelos) compatibles. Resultados La EC (39%) resultó la causa más frecuente de DL, seguida por SBID (22%), H. pylori (14%), EC y SBID (12%) y otras causas (13%). La mayoría (83%) de los pacientes presentaron un genotipo HLA-DQ2 o −DQ8 compatible. En estos pacientes el diagnóstico más frecuente fue la EC (46%), mientras que en ausencia de HLA-DQ2/DQ8 los diagnósticos más frecuentes fueron el SBID (44%) y H. pylori (22%). En los pacientes enviados por dispepsia, diarrea y anemia, la EC fue el diagnóstico más frecuente, mientras que H. pylori lo fue en los pacientes con dolor abdominal. Conclusiones La EC, seguida del SBID y la infección por H. pylori, constituyen las causas más frecuentes de DL en nuestro medio

INTRODUCTION: Lymphocytic duodenosis (LD) is a characteristic lesion in the initial phases of celiac disease (CD) but can be associated with many other entities. The aim of this study was to evaluate the prevalence of distinct causes of LD and possible differences in clinical presentation according to etiology. METHODS: A retrospective study was performed that included 194 patients diagnosed with LD(more than 25 intraepithelial lymphocytes per 100 epithelial cells). A preestablished strategy to evaluate the cause of the disease was followed that included celiac serology (antitransglutaminase antibodies), HLA-DQ2/DQ8 genotypes, diagnosis of Helicobacter pylori and small intestinal bacterial overgrowth (SIBO). Diagnosis of CD was established on the basis of clinical and histological response to a gluten-free diet in patients with positive serology or compatible findings on HLA-DQ2 (at least one of the alleles) or -DQ8 (both alleles) study. RESULTS: The most frequent cause of LD was CD (39%), followed by SBBO (22%), H.pylori (14%), CD and SIBO (12%), and other causes (13%). Most of the patients (83%) had a compatible HLA-DQ2 or -DQ8 genotype. In these patients, the most frequent diagnosis was CD (46%), while in the absence of HLA-DQ2/DQ8, the most frequent diagnoses were SIBO (44%) and H. pylori (22%). CD was the most frequent diagnosis in patients referred for dyspepsia, diarrhea and anemia, while H. pylori was the most frequent diagnosis in patients with abdominal pain. CONCLUSIONS: The most common causes of LD in our environment are CD, followed by SIBO and H. pylori infection

[Lymphocytic duodenosis: etiological study and clinical presentations]. / Duodenosis linfocítica: estudio etiológico y formas de presentación clínica.

INTRODUCTION: Lymphocytic duodenosis (LD) is a characteristic lesion in the initial phases of celiac disease (CD) but can be associated with many other entities. The aim of this study was to evaluate the prevalence of distinct causes of LD and possible differences in clinical presentation according to etiology. METHODS: A retrospective study was performed that included 194 patients diagnosed with LD (more than 25 intraepithelial lymphocytes per 100 epithelial cells). A preestablished strategy to evaluate the cause of the disease was followed that included celiac serology (antitransglutaminase antibodies), HLA-DQ2/DQ8 genotypes, diagnosis of Helicobacter pylori and small intestinal bacterial overgrowth (SIBO). Diagnosis of CD was established on the basis of clinical and histological response to a gluten-free diet in patients with positive serology or compatible findings on HLA-DQ2 (at least one of the alleles) or -DQ8 (both alleles) study. RESULTS: The most frequent cause of LD was CD (39%), followed by SBBO (22%), H.pylori (14%), CD and SIBO (12%), and other causes (13%). Most of the patients (83%) had a compatible HLA-DQ2 or -DQ8 genotype. In these patients, the most frequent diagnosis was CD (46%), while in the absence of HLA-DQ2/DQ8, the most frequent diagnoses were SIBO (44%) and H. pylori (22%). CD was the most frequent diagnosis in patients referred for dyspepsia, diarrhea and anemia, while H. pylori was the most frequent diagnosis in patients with abdominal pain. CONCLUSIONS: The most common causes of LD in our environment are CD, followed by SIBO and H. pylori infection.

La seguridad del paciente crítico pediátrico relacionada con errores de medicación / Pediatric critical patient safety regarding medication errors

La utilización de fármacos en pacientes pediátricos es un tema controvertido, ya que, las condiciones de su uso no están siempre bien definidas y en ocasiones se utilizan en situaciones no aprobadas en la ficha técnica. Los errores de medicación son una complicación con la que nos encontramos los profesionales de Enfermería en nuestra práctica habitual, dada la implicación en todo el proceso de utilización de los medicamentos. Con el propósito de mejorar la atención de salud del paciente crítico pediátrico y neonatal durante todo el proceso farmacoterapéutico, y ofrecer una práctica asistencial responsable y segura en nuestro entorno laboral, se llevó a cabo una revisión de la bibliografía para determinar el estado del conocimiento actual sobre la seguridad de este tipo de pacientes relacionada con los errores de medicación y la actuación enfermera. En este trabajo se presenta la información sobre qué es y por qué se produce un error de medicación, las características del paciente crítico pediátrico con pluripatología y politerapia, la diferencia entre un niño y un adulto en la administración de medicamentos, las causas que sitúan al paciente críticopediátrico y neonatal en situación de riesgo de error en la utilización de medicamentos, la incidencia de errores de medicación en pediatría, así como la relevancia del papel del profesional de Enfermería en todo el proceso farmacoterapéutico, las recomendaciones para la administración correcta de los medicamentos y las estrategias de prevención de errores de medicación (AU)

Drug use in pediatric patients is a controversial subject, because conditions of use are not always well defined, and sometimes drugs are used in situations not approved in the product specifications. Medication errors are a complication that we nursing professionals face in our daily practice, because of our involvement in the entire process of medication use. With the aim to improve healthcare for pediatric and neonatal patients during the whole drug therapy process, and to offer a responsible and safe healthcare practice in our work setting, a bibliographic review was conducted in order to establish the current knowledge about pediatric and neonatal patient safety regarding medication errors and nursing staff action. Information about what a medication error is and why it happens is presented in this paper, as well as the characteristics of pediatric critical patients with multiple pathology and multiple therapies, the difference between an infant and an adult in terms of drug administration, causes which place pediatric and neonatal critical patients in a risk situation in terms of errors inmedication use, incidence of medication errors in Pediatrics, as well as the relevance of the nursing professional’s role in the entire drug therapy process, recommendations for correct medication administration, and strategies for preventing medication errors (AU)

Spectrum of gluten-sensitive enteropathy in patients with dysmotility-like dyspepsia / Espectro de la enteropatía sensible al gluten en pacientes con dispepsia de tipo dismotilidad

Background Dysmotility-like dyspepsia symptoms are frequent in patients with gluten-sensitive enteropathy (GSE). Current data suggest that patients with mild enteropathy may be present with gluten-sensitive symptoms and complications. Aim To investigate the prevalence of GSE, including mild enteropathy, in patients with dysmotility-like dyspepsia symptoms. Methods We retrospectively studied 142 patients who presented dysmotility-like dyspepsia symptoms and normal upper gastrointestinal endoscopy. Endoscopic duodenal biopsies were taken and processed using hematoxylin–eosin staining and CD3 immunophenotyping. In patients with enteropathy (number of intraepithelial lymphocytes greater than 25 per 100 enterocytes) we also performed coeliac serology (anti-tissue transglutaminase IgA) and HLA-DQ2/DQ8 genotyping. A gluten-free diet was offered if one of these markers was positive. The final GSE diagnosis was established based on clinical and histopathological response to the gluten-free diet after 18 months of follow-up. Results Fifty-one patients (35.9%) had enteropathy; 4 (2.8%) Marsh type 3b, 24 (16.9%) Marsh type 3a, 3 (2.1%) Marsh type 2, and 20 (14.1%) Marsh type 1. A positive serology result was extremely low (6.7%) in mild enteropathy (Marsh type 1–3a) in contrast with Marsh type 3b patients (50%). Most patients with enteropathy had positive HLA DQ2 or -DQ8 genotyping (84.1%). Out of the 37 patients who started a gluten-free diet, 34 (91.9%) improved their symptoms, and 28 of 32 (87.5%) had a histopathological or serological response. A final GSE diagnosis was established in 28 of the 142 patients (19.7%).Conclusion Gluten-sensitive enteropathy can be a frequent and unsuspected cause of dysmotility-like dyspepsia (AU)

Antecedentes La dispepsia de tipo dismotilidad es frecuente en pacientes con enteropatía sensible al gluten (ESG). Los datos actuales sugieren que los pacientes con enteropatía leve pueden presentar síntomas y complicaciones gluten dependientes. Objetivo Investigar la prevalencia de ESG, incluida la enteropatía leve, en pacientes con dispepsia tipo dismotilidad. Métodos Estudio retrospectivo de 142 pacientes que presentaban dispepsia de tipo dismotilidad y normalidad en la endoscopia digestiva alta. Se realizaron biopsias duodenales y se procesaron mediante tinción de hematoxilina-eosina e inmunofenotipo CD3. En los pacientes con enteropatía (número de linfocitos intraepiteliales superior a 25 por cada 100 enterocitos) también se realizó una serología celíaca (anti-transglutaminasa tisular IgA) y genotipado HLA-DQ2/DQ8. Si uno de estos marcadores resultaba positivo, se ofrecía al paciente iniciar una dieta sin gluten. El diagnóstico final de ESG se estableció en función de la respuesta clínica e histopatológica a la dieta sin gluten después de 18 meses de seguimiento. Resultados Cincuenta y un pacientes (35,9%) presentaban enteropatía, 4 (2,8%) de Marsh tipo 3b, 24 (16,9%) Marsh tipo 3a, 3 (2,1%) Marsh tipo 2, y 20 (14,1%) Marsh tipo 1. La positividad serológica fue extremadamente baja (6,7%) en la enteropatía leve (Marsh tipo 1-3a), al contrario que en los pacientes con una lesión Marsh tipo 3b (50%). La mayoría de los pacientes con enteropatía presentaban valores positivos para el genotipado HLA DQ2 o -DQ8 (84,1%). De los 37 pacientes que iniciaron una dieta sin gluten, en 34 (91,9%) mejoraron los síntomas, y 28 de 32 (87,5%) presentaron respuesta histopatológica o serológica. Un diagnóstico final de ESG se estableció en 28 de los 142 pacientes (19,7%).Conclusión La enteropatía sensible al gluten puede ser una causa frecuente e insospechada de dispepsia de tipo dismotilidad (AU)

Spectrum of gluten-sensitive enteropathy in patients with dysmotility-like dyspepsia.

BACKGROUND: Dysmotility-like dyspepsia symptoms are frequent in patients with gluten-sensitive enteropathy (GSE). Current data suggest that patients with mild enteropathy may be present with gluten-sensitive symptoms and complications. AIM: To investigate the prevalence of GSE, including mild enteropathy, in patients with dysmotility-like dyspepsia symptoms. METHODS: We retrospectively studied 142 patients who presented dysmotility-like dyspepsia symptoms and normal upper gastrointestinal endoscopy. Endoscopic duodenal biopsies were taken and processed using hematoxylin-eosin staining and CD3 immunophenotyping. In patients with enteropathy (number of intraepithelial lymphocytes greater than 25 per 100 enterocytes) we also performed coeliac serology (anti-tissue transglutaminase IgA) and HLA-DQ2/DQ8 genotyping. A gluten-free diet was offered if one of these markers was positive. The final GSE diagnosis was established based on clinical and histopathological response to the gluten-free diet after 18 months of follow-up. RESULTS: Fifty-one patients (35.9%) had enteropathy; 4 (2.8%) Marsh type 3b, 24 (16.9%) Marsh type 3a, 3 (2.1%) Marsh type 2, and 20 (14.1%) Marsh type 1. A positive serology result was extremely low (6.7%) in mild enteropathy (Marsh type 1-3a) in contrast with Marsh type 3b patients (50%). Most patients with enteropathy had positive HLA DQ2 or -DQ8 genotyping (84.1%). Out of the 37 patients who started a gluten-free diet, 34 (91.9%) improved their symptoms, and 28 of 32 (87.5%) had a histopathological or serological response. A final GSE diagnosis was established in 28 of the 142 patients (19.7%). CONCLUSION: Gluten-sensitive enteropathy can be a frequent and unsuspected cause of dysmotility-like dyspepsia.

Neoplasias epiteliales del timo: timoma y carcinoma tímico: caracterización, tratamiento y variables asociadas a supervivencia / Thymic epithelial tumors. Retrospective review of 54 patients

Background: Thymic epithelial tumors are uncommon and can be associated with myasthenia gravis. Aim: To describe variables associated with survival and treatment of thymic epithelial tumors. Material and Methods: Retrospective review of surgical databases of a respiratory diseases hospital, identifying patients operated for a thymic epithelial tumor between 2000 and 2010. Follow up lasted from 12 to 156 months and information was obtained from medical records and death certificates of the Chilean national identification service. Results: Data from 54 patients aged 52.5 +/- 16.4 years (33 women) was retrieved. Forty two patients were symptomatic and 47 were subjected to resective surgery. The pathological diagnosis was thymoma in 46 cases and thymic carcinoma in eight. Fourteen patients had postoperative complications and one died. Mean survival time was 101.8 +/- 10.2 months. One, three and five years survival was 90.7 +/- 3.9, 81.4 +/- 5.7 and 71.8 +/- 8.2 percent, respectively. Preoperative performance status of patients, histological type of the tumor and associated myasthenia gravis were predictors of survival. Conclusions: More commonly, thymic epithelial tumors appear in women, their histological type corresponds to thymomas and their resection is feasible.

Objetivos: Describir características, tratamiento y variables asociadas a supervivencia de neoplasias epiteliales del Timo (NET). Material y Método: Revisión retrospectiva de pacientes con NET. Período: enero de 2000 - agosto de 2010. Se describen características, tratamiento, morbilidad, mortalidad y supervivencia global. Se comparó supervivencias según variables seleccionadas. Se utilizó programa SPSS 15.0. Se consideró significativo p < 0,05. Resultados: 54 pacientes, 33 mujeres, edad promedio 52,5 años. Sintomáticos 42 pacientes. Se realizó cirugía resectiva en 47. Histología: 46 Timomas y 8 Carcinomas Tímicos. Complicaciones en 14 y 1 falleció. Rango seguimiento: 12-156 meses. Tiempo promedio supervivencia 101,8 +/- 10,2 meses. Supervivencia global a 1, 3 y 5 años: 90,7 +/- 3,9 por ciento, 81,4 +/- 5,7 por ciento y 71,8 +/- 8,2 por ciento respectivamente. Se encontraron variables asociadas a supervivencia. Conclusiones: Las NET son más frecuentes en mujeres, la mayoría son sintomáticos e histológicamente son timoma. La cirugía es resectiva en la mayoría. Se identifican variables asociadas a supervivencia.

Caracterización y resultados inmediatos en pacientes con tratamiento quirúrgico de bocio intratorácico / Characterization and immediate results in patients with surgical treatment of intrathoracic goiter

Objectives: To describe characteristics and immediate results of surgical treatment of patients with intrathoracic goiter (ITG). Methods: Retrospective review. Period: October 2003 - March 2010. We describe general characteristics, morbidity and mortality. Results: 33 patients, 23 women, mean age 59.1 +/- 14.3 years. Preoperative thyroid function: 32 euthyroid and 1 hyperthyroid. Asymptomatic 10 patients. ITG rate: 31 cervico-mediastinal and 2 mediastinal. Approach: 24 cervicotomy, 7 cervicotomy and sternotomy and 2 sternotomy. Type of resection: 19 total thyroidectomy and 14 subtotal thyroidectomy. Histology: 29 benign and 4 malignant neoplasms. Postoperative stay: median of 4.5 days. Complications in 12 patients: 10 hypo-parathyroidism (9 transient and 1 permanent), 2 dysphonia, 2 cervical hematoma (one redo), 1 wound infection and 1 ventilator associated pneumonia. One patient died (pneumonia). Conclusions: The ITG is more common in women, most are euthyroid and may be asymptomatic. Most can be resected by cervicotomy. The histology is benign in most but may represent malignancies. The surgery is not free of morbidity and mortality.

Objetivos: Describir características y resultados inmediatos del tratamiento quirúrgico de pacientes con Bocio Intratorácico (BIT). Material y Método: Revisión retrospectiva. Período: octubre de 2003 - marzo de 2010. Se describen características generales y morbi-mortalidad. Resultados: 33 pacientes, 23 mujeres, edad promedio 59,1 +/- 14,3 años. Comorbilidades: 12 hipertensos y 1 diabético. Función tiroidea preoperatoria: 32 eutiroideos y 1 hipertiroideo. Asintomáticos 10 pacientes. Tipo BIT: 31 cérvico-mediastínicos y 2 mediastínicos. Abordaje: 24 cervicotomía, 7 cervicotomía más esternotomía y 2 esternotomía. Tipo de resección: 19 tiroidectomía total y 14 tiroidectomía subtotal. Histología: 29 benignos y 4 neoplasias malignas. Estadía postoperatoria: mediana de 4,5 días. Complicaciones en 12 pacientes: 10 hipoparatiroidismos (9 transitorios y 1 permanente), 2 disfonías, 2 hematomas cervicales (uno se reexploró), 1 infección herida operatoria y 1 neumonía asociada a ventilación mecánica. Fallece un paciente (neumonía). Conclusiones: El BIT es más frecuente en mujeres, la mayoría son eutiroideos y pueden ser asintomáticos. La mayoría pueden ser resecados por cervicotomía. La histología es benigna en la mayoría aunque pueden corresponder a neoplasias malignas. La cirugía no está exenta de morbi-mortalidad.

[Influence of pregnancy on refractive parameters after LASIK surgery]. / Influencia del embarazo sobre los parámetros refractivos tras cirugía laser in situ keratomileusis.

OBJECTIVES: Different ocular changes and complications of refractive surgery such as photorefractive keratectomy (PRK) due to pregnancy have been described in the last few years. However there is no information about the possible problems of laser in situ keratomileusis (LASIK) in pregnant women. Our objective was to study how physiological changes secondary to pregnancy could alter the refractive situation in pregnant women who have undergone LASIK surgery. We show the results obtained due to the changes between the first two trimesters of the pregnancy. METHODS: A prospective and observational study was conducted in which one study group, made up of 9 patients who had undergone LASIK surgery before becoming pregnant, was compared with a control group of 9 patients with non-surgically corrected refractive problems. The following measurements were made in both groups in the first and second trimesters of the pregnancy; visual acuity, the best corrected visual acuity, tonometry, ocular anatomical characteristics by biometry, and refractive and corneal study by Pentacam(®). RESULTS: Signicant changes were observed in the cylinder and spherical equivalent between the two trimesters in both groups. Visual acuity and spherical equivalent show a strong trend towards worsening, which was more significant in the study group. The patients of this group who had a larger pre-surgical defect showed lower modifications during the six first months of pregnancy. CONCLUSIONS: The majority of women who require laser refractive surgery are are between 20-30 years old, thus in many cases corneal surgery is followed by at least one pregnancy, with different possible ophthalmological effects. The conclusions that may be derived from this study are that the assessment of the refractive changes in surgically operated corneas may be biomechanically weakened on being subjected to physiological hormone stimulation as happens during gestation.