Development of an E-learning System for the Endoscopic Diagnosis of Early Gastric Cancer: An International Multicenter Randomized Controlled Trial.

BACKGROUND: In many countries, gastric cancer is not diagnosed until an advanced stage. An Internet-based e-learning system to improve the ability of endoscopists to diagnose gastric cancer at an early stage was developed and was evaluated for its effectiveness. METHODS: The study was designed as a randomized controlled trial. After receiving a pre-test, participants were randomly allocated to either an e-learning or non-e-learning group. Only those in the e-learning group gained access to the e-learning system. Two months after the pre-test, both groups received a post-test. The primary endpoint was the difference between the two groups regarding the rate of improvement of their test results. FINDINGS: 515 endoscopists from 35 countries were assessed for eligibility, and 332 were enrolled in the study, with 166 allocated to each group. Of these, 151 participants in the e-learning group and 144 in the non-e-learning group were included in the analysis. The mean improvement rate (standard deviation) in the e-learning and non-e-learning groups was 1·24 (0·26) and 1·00 (0·16), respectively (P<0·001). INTERPRETATION: This global study clearly demonstrated the efficacy of an e-learning system to expand knowledge and provide invaluable experience regarding the endoscopic detection of early gastric cancer (R000012039).

Unilateral ectopic insertion of the pectoralis minor: Clinical and functional significance.

During routine dissection of a 70-year-old female, we observed a unilateral ectopic insertion of the left pectoralis minor muscle. The tendon was cord-like and passed through a tendon sheath superior to the coracoid process to insert on the greater tubercle of the humerus. Additionally, an aponeurosis extended from the distal aspect of the muscle's tendon and passed medially to insert near the base of the coracoid process. This is the first report of an additional aponeurosis extending from the tendon of the pectoralis minor and attaching to the coracoid process. We also observed that the pectoralis minor tendon caused an unusually smooth deep indentation on the superior aspect of the coracoid process; considering its insertion on the humerus, we hypothesize that the muscle acted as an abductor of the shoulder along with the supraspinatus. The medial extension of an aponeurotic tendon from the pectoralis minor tendon near its insertion, to the base of the coracoid process further suggests that the muscle provided stability to the glenohumeral joint while acting as an abductor. Pectoralis minor variations have been described since 1897; however, few studies have demonstrated functional or clinical significance. The redundancy of the actions of this muscle along with its long tendon suggests a potential source for autograft.

[Relationship between methylenetetrahydrofolate reductase polymorphism and homocysteine levels in women with recurrent pregnancy loss: a nutrigenetic perspective]. / Relación entre los polimorfismos de la metilen-tetrahidrofolato-reductasa y los niveles de homocisteína en mujeres con pérdida gestacional recurrente: perspectiva desde la nutrigenética.

The objective of this study was to evaluate if there is any difference in the proportion of methylenetetrahydrofolate reductase (MTHFR) C677T polymorphisms and the homocysteine levels in a group of women with recurrent pregnancy loss (RPL) and a control group. Ninety-three patients with diagnosis of three or more gestational losses and 206 healthy women with two or more children, were included. After acceptance of informed consent, samples of peripheral blood were taken to determine the genetic polymorphisms of MTHFR C677T and the plasmatic levels of homocysteine. The carriers of the homozygous mutation TT of MTHFR 677T polymorphism were 12.9% (12 of 93) in the group of patients and 14.6% (30 of 206) in the control group; 46.2% (43 of 93) and 40% (83 of 206) in the group of patients and controls respectively, were heterozygous CT for MTHFR gene. The levels of homocysteine were 7.2 micromol/ml in the group of patients and 7.7 mmol/l in controls. There was no relationship between MTHFR gene polymorphisms and the increase of homocysteine levels, nor of these one with RPL. From the nutrigenetics perspective we suggest that studies related to MTHFR polymorphisms and the risk of disease include the levels of folate and B6 and B12 vitamins participating in the tetrahydrofolate cycle for trying to establish a direct relation among the genotype, the level of metabolite and the clinical manifestations. In this regard, we recommend the administration of folic acid in women in search of pregnancy due to the high frequency of heterozygous and homozygous for MTHFR C677T mutation in our population.

Relación entre los polimorfismos de la metilen-tetrahidrofolato-reductasa y los niveles de homocisteína en mujeres con pérdida gestacional recurrente: perspectiva desde la nutrigenética / Relationship between methylenetetrahydrofolate reductase polymorphism and homocysteine levels in women with recurrent pregnancy loss: a nutrigenetic perspective

El objetivo de este estudio fue evaluar si existe diferencia en la proporción de los polimorfismos de la metilen tetrahidrofolato reductasa (MTHFR) C677T y en los niveles de homocisteína, entre una población de mujeres con pérdida gestacional recurrente y un grupo control. Se incluyeron 93 pacientes con diagnóstico de tres o más pérdidas gestacionales y 206 mujeres sanas con dos o más hijos. Previa aceptación del consentimiento informado, a cada mujer se le tomó una muestra de sangre periférica tanto para la genotipificación de los polimorfismos de la MTHFR como para la medición de homocisteína en plasma. Las portadoras de la condición homocigota TT para el polimorfismo de la MTHFR 677T fueron 12,9% (12/93) en el grupo de pacientes y 14,6% (30/206) en el grupo control; un 46,2% (43/93) y 40% (83/206) en el grupo de pacientes y de controles respectivamente, fueron heterocigotos CT para el gen de la MTHFR. Los niveles promedio de homocisteína fueron 7,2 μmol/ml para las pacientes y 7,7 μmol/ml para los controles. No se encontró relación entre los polimorfismos del gen de la MTHFR y el aumento en los niveles de homocisteína, ni de éstos con la PGR. Desde la perspectiva de la nutrigenética, sugerimos que para estudiar la relación entre los polimorfismos de la MTHFR con determinada enfermedad, se tengan en cuenta los niveles de folatos, vitaminas B6 y B12 que intervienen en el ciclo de los tetrahidrofolatos con el fin de intentar establecer una relación más directa entre el genotipo, el nivel del metabolito y las manifestaciones clínicas. En este mismo sentido recomendamos el consumo de ácido fólico en las mujeres que estén buscando embarazo dado la alta frecuencia de heterocigotos y homocigotos para la mutación C677T de la MTHFR en nuestra población (AU)

The objective of this study was to evaluate if there is any difference in the proportion of methylenetetrahydrofolate reductase (MTHFR) C677T polymorphisms and the homocysteine levels in a group of women with recurrent pregnancy loss (RPL) and a control group. Ninety-three patients with diagnosis of three or more gestational losses and 206 healthy women with two or more children, were included. After acceptance of informed consent, samples of peripheral blood were taken to determine the genetic polymorphisms of MTHFR C677T and the plasmatic levels of homocysteine. The carriers of the homozygous mutation TT of MTHFR 677T polymorphism were 12.9% (12 of 93) in the group of patients and 14.6% (30 of 206) in the control group; 46.2% (43 of 93) and 40% (83 of 206) in the group of patients and controls respectively, were heterozygous CT for MTHFR gene. The levels of homocysteine were 7.2 μmol/ml in the group of patients and 7.7 mmol/l in controls. There was no relationship between MTHFR gene polymorphisms and the increase of homocysteine levels, nor of these one with RPL. From the nutrigenetics perspective we suggest that studies related to MTHFR polymorphisms and the risk of disease include the levels of folate and B6 and B12 vitamins participating in the tetrahydrofolate cycle for trying to establish a direct relation among the genotype, the level of metabolite and the clinical manifestations. In this regard, we recommend the administration of folic acid in women in search of pregnancy due to the high frequency of heterozygous and homozygous for MTHFR C677T mutation in our population (AU)

Efecto del consumo de diferentes dosis de café filtrado sobre los niveles plasmáticos de homocisteína y presión arterial en un grupo de voluntarios sanos / Effect of consumption of different doses of filtered coffee on homocysteine plasma levels and blood pressure in a group of healthy volunteers

No está claro si el consumo de café afecta la presión arterial y los niveles de homocisteína. El objetivo fue determinar el cambio en las concentraciones plasmáticas de homocisteína y presión arterial en un grupo de voluntarios sanos. Se realizó un estudio prospectivo, clínico controlado, en el que se conformaron cuatro grupos de 29 sujetos cada uno, quienes, durante un período de seis semanas, se sometieron al consumo diario de café filtrado. El grupo 1 no consumió café, el grupo 2 consumió 200 mL de café, el grupo 3 400 mL y el 4 600 mL. Antes de la intervención se midieron: presión arterial, homocisteína, índice arterial, ácido fólico eritrocitario y vitaminas B12 y B6. Al final de la intervención, se tomó la presión arterial y se midió la concentración de homocisteína. Los resultados mostraron grupos sin diferencias significativas en las condiciones basales. Después de la intervención, el cambio en los valores de homocisteína entre los grupos, no mostró diferencia significativa y permanecieron dentro de los valores de referencia (p = 0,098). El cambio en los niveles de presión arterial sistólica y diastólica, no fue significativo (p=0,510 y 0,430 respectivamente). En conclusión, el consumo de diferentes dosis de café filtrado, no mostró cambios significativos en los niveles séricos de homocisteína como tampoco en los niveles de presión arterial sistólica y diastólica en un grupo de sujetos sanos normotensos; en el grupo que se abstuvo de tomar café, no disminuyeron de manera significativa los niveles de homocisteína y presión arterial.

Balance de energía, composición corporal y actividad física en preescolares eutróficos y obesos / Energy balance, body composition and physical activity in eutrophic and obese preschool children

En Chile, se ha producido un incremento importante de la obesidad como consecuencia de una acelerada transición nutricional, pasando rápidamente de una situación de pre-transición -con predominio de la desnutrición como principal problema de salud pública-a uno de post-transición, con predominio de la obesidad. Esta situación se ha observado principalmente en niños, adultos y embarazadas.

Balance de energia, composición corporal y actividad física en preescolares eutróficos y obesos / Energy balance, body composition and physical activity in eutrophic and obese preschool children

Objetivo: Comparar balance energético, composición corporal y actividad física en párvulos eutróficos y obesos, de 3 a 5 años, asistentes a jardines infantiles JUNJI. Metodología: Se compararon entre eutróficos y obesos: el gasto energético total (GET) con agua doblemente marcada (ADM); la ingesta energética (IE) por pesaje en jardín y registro en el hogar, más la actividad fásica en jardín con sensor de movimiento TRITRAC. Resultados: GET fue mayor en niños obesos (p = 0,006). IE en el jardín fue mayor para obesos de ambos sexos (p = 0,0001), IE en el hogar (semana) fue mayor en niños obesos (p = 0,0001) y en fin de semana IE fue mayor en niñas y niños obesos (p = 0,0001). En actividad física en el jardin, los niños eutróficos tuvieron mayor actividad moderada intensa (p = 0,02). Conclusiones: El hogar condiciona una mayor ingesta energía de los niños obesos. La actividad física tiende a ser sedentaria en el jardín infantil. Un proceso de intervención educativa que busque cambiar esta situación, debe considerar a la familia y educadores

Inherited thrombophilia is associated with deep vein thrombosis in a Colombian population.

The development of venous thromboembolism is influenced by a variety of genetic and environmental risk factors. A few studies have ascertained whether thrombophilic defects are risk factors for venous thromboembolism in Latin American populations with a variable degree of admixture, such as the Colombian population. To address this issue, we conducted a case-control study involving 100 consecutive patients with deep vein thrombosis and 114 healthy controls from the Hospital Universitario San Vicente de Paúl, Medellín, Colombia. Activated protein C resistance (APC resistance) was detected in 25/99 patients vs. 6/114 controls (OR = 6.08, 95% CI = 2.23-17.47). Ten of 100 patients carried the factor V Leiden mutation vs. 1/114 controls (OR = 12.56, 95% CI = 1.61-267). APC resistance was associated with the factor V Leiden mutation in only 10/25 patients. The prothrombin G20210A mutation was found in 4/100 patients, but none of the controls (P < 0.05). There was no significant difference in the proportion of homozygous carriers of methylenetetrahydrofolate reductase C677T variant among patients and controls. In conclusion, in our studied population, factor V Leiden, APC resistance, and prothrombin G20210A were associated with an increased risk of deep vein thrombosis. However, the frequencies of these thrombophilic defects and of APC resistance associated with factor V Leiden was lower than the corresponding frequencies previously reported for Caucasian populations. Further study is required to assess the influence of ethnicity on thrombophilia.

Concentracion sérica de cobre ®libre¼ y ceruloplasmina en niños con desnutricion aguda grave antes de iniciar la terapia nutricional y al momento de recuperar el apetito en turbo, antioquia, colombia / Serum concentrations of free copper and ceruloplasmin in children with severe acute malnutrition before nutritional therapy and after children have recovered the apetite in turbo, antioquia, colombia

Introduction: copper supplementation therapy has been used in children with acute and severe malnutrition. Scientific evidence has shown that malnourished children with edema have free copper in plasma which could produce oxidative stress. Objective: To compared plasma concentrations of free copper between children with acute and severe malnutrition and a control group. Methodology: Cross sectional study where 66 normal and malnourished children were studied. A longitudinal study (before and after type) design was used including 40 children with severe and acute malnutrition; free copper was merasured by high-resolution capillary electrophoresis; ceruloplasmin and PCR by nephelometry. Results: In the cross sectional study children with marasmus had higher free copper serum concentrations than children with oedematous malnutrition, but the difference was not significant. In the control group this metal was not found. Children with oedema showed significant lower ceruloplasmin concentrations than children with marasmus (p=0.00) while the difference in PCR was also no significant for both groups. When the relationship between free copper serum concentrations and the presence of infection was analyzed no significant differences were obtained. However, serum albumin concentration was significantly lower for children with oedematous malnutrition than the marasmic group (p=0.016). After children recovered the appetite in the longitudinal study, serum free copper concentration decreased for both groups and ceruloplasmin concentration increased but no significant differences were observed. Conclusion: Copper supplementation could be considered as nutritional therapy for undernourished children since the beginning of the nutritional treatment, as it is recommended by WHO.

Introducción: La recuperación de los niños con desnutrición aguda grave incluye suplementación con cobre desde el inicio de la terapia; existen evidencias que niños edematosos pueden tener cobre libre en plasma el cual podría generar estrés oxidativo. Objetivo: Comparar concentraciones séricas de cobre libre y ceruloplasmina en un grupo de desnutridos agudos graves y un grupo control Metodología: estudio transversal al ingreso entre niños con y sin desnutrición en una muestra de 66 sujetos y longitudinal de tipo antes y después en 40 niños desnutridos. Se determinó cobre libre por electroforesis capilar de alta resolución; ceruloplasmina y PCR por nefelometría, además de variables clínicas Resultados: En el transversal, los marasmáticos presentaron niveles de cobre libre mayores que los edematosos sin diferencia significativa; en el grupo control este metal no se detectó. En los edematosos la concentración de ceruloplasmina fue significativamente menor con relación a los marasmáticos (p=0.00) y la PCR no presentó diferencia significativa entre ellos. No se encontraron diferencias significativas entre los niveles de cobre libre y presencia o no de infección. La albúmina se encontró más baja en los edematosos con diferencia significativa respecto a los marasmáticos (p=0.016). En el longitudinal, al recuperar el apetito el cobre libre disminuyó y la ceruloplasmina aumentó en los dos grupos sin diferencia significativa Conclusión: el suplemento de cobre como componente de la terapia nutricional puede ser suministrado a los desnutridos desde el inicio como lo propone el protocolo de la OMS.

Atrophic gastritis in young children and adolescents.

BACKGROUND: Helicobacter pylori associated gastric cancer arises via a multistage process, with atrophic gastritis being the precursor lesion. Helicobacter pylori is typically acquired in childhood, yet little is known of the prevalence of atrophic gastritis in childhood. AIM: To study atrophic gastritis among children from countries with high gastric cancer incidence. METHODS: Sections from topographically mapped gastric biopsy specimens from children undergoing clinically indicated endoscopy in Korea and Colombia were evaluated using visual analogue scales. Atrophy was defined as loss of normal glandular components, including replacement with fibrosis, intestinal metaplasia (IM), and/or pseudopyloric metaplasia of the corpus (identified by the presence of pepsinogen I in mucosa that was topographically corpus but phenotypically antrum). RESULTS: One hundred and seventy three children, 58 from Korea (median age, 14 years) and 115 from Colombia (median age, 13 years), were studied. Helicobacter pylori was present in 85% of Colombian children versus 17% of Korean children (p<0.01). Atrophic mucosa near the antrum-corpus border was present in 16% of children, primarily as pseudopyloric metaplasia (31%, IM; 63%, pseudopyloric metaplasia; 6%, both). The median age of children with corpus atrophy was 15 (range, 7-17) years. CONCLUSION: Gastric atrophy occurs in H pylori infected children living in countries with high gastric cancer incidence. Identification and characterisation of the natural history of H pylori gastritis requires targeted biopsies to include the lesser and greater curve of the corpus, starting just proximal to the anatomical antrum-corpus junction, in addition to biopsies targeting the antrum and cardia.

Balance de energía, composición corporal y actividad física en preescolares eutróficos y obesos / Energy balance, body composition and physical activity in eutrophic and obese preschool children

Objetivo: Comparar balance energético, composición corporal y actividad física en párvulos eutróficos y obesos, de 3 a 5 años, asistentes a jardines infantiles JUNJI. Metodología: Se compararon entre eutróficos y obesos: el gasto energético total (GET) con agua doblemente marcada (ADM); la ingesta energética (IE) por pesaje en jardín y registro en el hogar, más la actividad física en jardín con sensor de movimiento TRITRAC. Resultados: GET fue mayor en niños obesos (p = 0,006). IE en el jardín fue mayor para obesos de ambos sexos (p = 0,0001), IE en el hogar (semana) fue mayor en niños obesos (p = 0,0001) y en fin de semana IE fue mayor en niñas y niños obesos (p = 0,0001). En actividad física en el jardín, los niños eutróficos tuvieron mayor actividad moderada intensa (p = 0,02). Conclusiones: El hogar condiciona una mayor ingesta energía de los niños obesos. La actividad física tiende a ser sedentaria en el jardín infantil. Un proceso de intervención educativa que busque cambiar esta situación, debe considerar a la familia y educadores.

CagA in Barrett's oesophagus in Colombia, a country with a high prevalence of gastric cancer.

BACKGROUND: In the USA, atrophic gastritis and gastric cancer are rare, whereas gastro-oesophageal reflux disease (GERD) is common. Infection with Helicobacter pylori, especially a CagA positive strain, is unusual in patients with GERD/Barrett's oesophagus in the USA. AIM: To examine the relation between Barrett's oesophagus and CagA positive H pylori in Colombia, a country with a high prevalence of CagA positive H pylori associated atrophic gastritis and gastric cancer. METHODS: Helicobacter pylori and CagA status was determined among Colombian patients with long segment Barrett's oesophagus and a control group with simple H pylori gastritis. Helicobacter pylori status was determined using a triple stain and CagA status was determined by immunohistochemistry using a specific rabbit anti-CagA serum. RESULTS: Gastric and oesophageal mucosal biopsies were obtained from 51 patients--39 men (mean age, 57.8 years; SD, 13.1) and 12 women (mean age, 51.8 years; SD, 14.4)--with documented long segment Barrett's oesophagus. The results were compared with 24 Colombian patients with H pylori gastritis without oesophageal disease. Thirty two patients with Barrett's oesophagus had active H pylori infection. CagA status was evaluated in a subset of 23 H pylori infected patients with Barrett's oesophagus, and was positive in eight of these patients compared with 19 of 24 controls (p = 0.01). CONCLUSIONS: Although most Colombian patients with Barrett's oesophagus had H pylori infection, CagA positive infections were unusual. These data illustrate how consistent corpus inflammation reduces acid secretion, which prevents Barrett's oesophagus among those with abnormal gastro-oesophageal reflux barriers.

Colonizacion por estreptococo beta hemolitico del grupo B durante el embarazo y prevencion de enfermedad neonatal / Group B streptococcus colonization during pregnancy and prevention of early onset of disease

El estreptococo beta-hemolítico del grupo B (SGB) es uno de los principales agentes causantes de sepsis neonatal precoz. La mortalidad de los afectados oscila entre el 6 y el 20%, y la tasa de secuela neurológica llega al 30%. En 1996 el Centro de Prevención y Control de Enfermedades de Atlanta, el Colegio Americano de Obstetras y Ginecólogos y la Academia Americana de Pediatría sugirieron en consenso que el personal de atención de salud materna-neonatal debía adoptar una estrategia para la prevención de la sepsis por este germen. Los objetivos del presente trabajo prospectivo fueron determinar el porcentaje de colonización por SGB en las pacientes gestantes asistidas del 1° de julio de 2001 al 31 de diciembre de 2002 e implementar un programa de prevención de sepsis neonatal precoz por SGB a través de profilaxis antibiótica intraparto basado en cultivos. Sobre 1756 pacientes, se realizaron cultivos con hisopado vaginal y anal a 1228 (69.9%). El porcentaje de colonización materna por SGB fue del 1.4% (17 pacientes). Se presentó un caso de sepsis neonatal compatible con SGB (0.6‰) en una madre con cultivo negativo. Sólo una paciente portadora de SGB presentó factores de riesgo. Los resultados nos sugieren continuar con la estrategia de prevención basada en cultivos debido a que la mayoría de las pacientes colonizadas no presentaron factores de riesgo. Son necesarios estudios de relación costo-beneficio en nuestro medio para definir si esta estrategia de prevención es aplicable a la realidad sanitaria argentina.

Colonizacion por estreptococo beta hemolitico del grupo B durante el embarazo y prevencion de enfermedad neonatal / Group B streptococcus colonization during pregnancy and prevention of early onset of disease

El estreptococo beta-hemolítico del grupo B (SGB) es uno de los principales agentes causantes de sepsis neonatal precoz. La mortalidad de los afectados oscila entre el 6 y el 20%, y la tasa de secuela neurológica llega al 30%. En 1996 el Centro de Prevención y Control de Enfermedades de Atlanta, el Colegio Americano de Obstetras y Ginecólogos y la Academia Americana de Pediatría sugirieron en consenso que el personal de atención de salud materna-neonatal debía adoptar una estrategia para la prevención de la sepsis por este germen. Los objetivos del presente trabajo prospectivo fueron determinar el porcentaje de colonización por SGB en las pacientes gestantes asistidas del 1º de julio de 2001 al 31 de diciembre de 2002 e implementar un programa de prevención de sepsis neonatal precoz por SGB a través de profilaxis antibiótica intraparto basado en cultivos. Sobre 1756 pacientes, se realizaron cultivos con hisopado vaginal y an

Airtight in Situ Thin-Layer Reflection-Absorption FT-IR Microspectroelectrochemical Cell for the Study of Nonaqueous Systems.

An airtight thin-layer reflection FT-IR microspectroelectrochemical cell suitable for the study of both aqueous and nonaqueous electrochemical systems is described. Due to its design, the cell can be easily assembled using disk microelectrodes. This variable-thickness cell can be used for the voltammetric study of both aqueous and nonaqueous systems under semi-infinite diffusion and thin-layer conditions. Dichloromethane solutions of ferrocene were used to test the in situ FT-IR microspectroelectrochemical performance of the cell. The cyclic voltammetric behavior of an oxygen- and water-free CH(2)Cl(2) solution of Ru(3)(CO)(12), under semi-infinite diffusion conditions, provides evidence of the airtightness of this cell.

Mucosa gástrica heterotópica en esófago cervical: prevalencia, correlación clínica, endoscópica e histológica

Se estudiaron prospectivamente 1.070 pacientes a quienes se les realizó un examen endoscópico por cualquier causa, se les investigó síntomas de reflujo gastroesofágico (RGE) y la presencia de mucosa gástrica heterotópica (MGH) en esófago cervical. Se diagnosticaron 150 casos de MGH (14 por ciento) de los cuales presentamos resultados de 139 de ellos en quienes existe una confirmación histológica. Esta población fue comparada con un grupo control de características similares. El promedio de edad de los dos grupos fue 48.9 años y predominó el sexo masculino (67 por ciento). La presencia del RGE fue significativamente más frecuente en los pacientes con MGH, tanto en las formas típicas (agrieras y pirosis) como en algunas atípicas (disfagia, dolor torácico). Una historia de más de un año de evolución de disfagia alta o sensación de cuerpo extraño aumentaron el riesgo de presentar MGH en 20 veces. El consumo de cigarrillo aumentó también este riesgo aunque en menor importancia. La mayoría de lesiones fueron únicas (70 por ciento) y menores de 1 cm. No se observaron cambios de esofagitis perilesional. El epitelio predominante fue el de tipo fúndico (76 por ciento), apreciándose dos tipos de epitelios en una tercera parte de los casos. No existieron cambios de metaplasia intestinal ni de displasia. Bacterias con la forma de Helicobacter pylori se encontraron en la MGH en el 67 por ciento. No se halló una correlación significativa entre su número, tamaño, tipo histológico predominante, evidencia de H. pylori y la presencia de síntomas. Se encontró un mayor número de casos de esofagitis endoscópica en el grupo control (35 por ciento) que en MGH. No se documentó diferencia entre el número de casos de esófago de Barrett, de hernia hiatal y de patología gastroduodenal en ambos grupos. El examen histológico del esófago distal reveló exocitosis de neutrofilos en el 33 por ciento de casos indicando esofagitis moderada e infiltrando polimorfonuclear a nivel del corion en el 67 por ciento como índice de actividad. En conclusión de acuerdo a nuestro estudio el riesgo de encontrarse un área de MGH está incrementada en pacientes con el antecedente de síntomas de reflujo gastroesofágico crónico y particularmente la disfagia. Se discuten los posibles mecanismos etiopatogénicos

Impaired left atrial function after heart transplantation: disparate contribution of donor and recipient atrial components studied on-line with quantitative echocardiography.

BACKGROUND: Because of a lack of noninvasive techniques, left atrial function after orthotopic heart transplantation has not been well characterized. METHODS: Global left atrial performance and the relative contributions of donor and recipient atrial components were assessed with transthoracic echocardiography with on-line automated border detection in 20 patients with normal left ventricular systolic function 1 to 6 years (mean 3.5 +/- 0.3 years [standard error]) after heart transplantation. RESULTS: The mean left atrial area at ventricular end-systole was 22.9 +/- 1.5 cm2, the mean left atrial emptying fraction ([left atrial area at ventricular end-systole--left atrial area at ventricular end-diastole]/left atrial area at ventricular end-systole) was 29.7% +/- 2.6%, and the fractional area change caused by active contraction was 27.8% +/- 3.1%. Compared with controls, patients had larger atria, depressed emptying, and reduced fractional active contraction. Although the recipient to donor area ratio was 3:2, the proportion of atrial emptying (change in area from mid-to-late ventricular diastole divided by the total left atrial change during ventricular diastole) contributed by the recipient component was greatly diminished when compared with that of the donor component (1.4% +/- 3.5% versus 31% +/- 2.7%) (p = 0.0001). CONCLUSIONS: Despite being anatomically smaller, the functional contractile contribution of the donor component dominated atrial emptying. Thus, after heart transplantation, global left atrial function is depressed, predominantly because of dysfunction of the recipient atrial component.

Quantification of left ventricular dimensions on line with biplane transesophageal echocardiography and lateral gain compensation.

To determine the feasibility and accuracy of biplane transesophageal echocardiography (TEE) with automatic boundary detection (ABD) for the estimation of left ventricular areas, we examined 19 consecutive patients with the use of this technique. In addition, we evaluated the utility of lateral gain compensation (LGC) to improve the online tracking of the ABD algorithm on the lateral endocardial-blood boundary of the echocardiographic image. The transverse plane short-axis TEE view and the longitudinal plane two chamber TEE view were used for the analysis. A semiquantitative estimate (in degrees) of the endocardial circumference, in which the boundary was correctly identified and tracked on line, improved from a mean of 198 degrees to 360 degrees with LGC (P less than 0.001). Results of comparisons of offline and online biplane TEE cavity areas revealed excellent correlations of values for the 16 patients (84%) in whom adequate transverse plane short-axis images were obtained (r values greater than 0.9 at systole and diastole). The correlation was also excellent (r values greater than 0.9) in the nine patients in whom longitudinal plane two-chamber views adequate for ABD analysis were obtained at systole and diastole. LGC significantly improved the accuracy of endocardial detection and tracking, which otherwise would be limited due to the anisotropic properties of the myocardium. Thus, ABD during biplane TEE may be feasible in a significant number of patients and accurately reflects left ventricular areas when compared with offline methods.

Human pharmacokinetics of a new Vinca alkaloid S 12363 with use of a monoclonal antibody-based radio- or enzyme immunoassay.

S 12363 is a new Vinca alkaloid derivative, characterized by the grafting of an alpha-aminophosphonate, onto the Vinca nucleus, facilitating drug penetration and increasing intracellular drug retention. As a high cytotoxic activity had been demonstrated in in vitro and in vivo models recommended by the National Cancer Institute, a phase I trial was initiated in cancer patients. In order to quantify S 12363 systemic levels in humans, two monoclonal antibody-based immunoassays, RIA (radio-) and EIA (enzyme immunoassay) were developed. The gamma-emitting probe used in the RIA, 125I-(deacetyl-O4-vinblastine)-tyramine, bound very tightly to the monoclonal antibody (dissociation constant, Kd = 2.5 x 10(-11) M), demonstrating a high affinity mainly directed toward the catharantine nucleus (vindesine, vincristine, vinblastine, 100% cross-reactivity; vinorelbine, 0.3% cross-reactivity). In the EIA, a deacetyl O4-vinblastine/ovalbumine conjugate was used as the competing antigen. Its binding to the monoclonal antibody was revealed by an anti-mouse immunoglobulin G conjugated to biotin which interacts with streptavidin labeled with alkaline phosphatase. This method permitted obtaining nearly the same sensitivity and reproducibility with EIA as with RIA, their respective minimum quantitation limits being 0.100 and 0.040 ng/ml (106 and 42 pM) of S 12363 in plasma. These assays allowed the study of S 12363 systemic pharmacokinetics in cancer patients during a phase I trial up to 72 h after dosing. As determined by RIA, the S 12363 plasma profile was triphasic with a terminal half-life; t1/2 gamma = 49 +/- 16 h, a plasma clearance, CL = 0.14 +/- 0.04 liter/h/kg, and a volume of distribution at steady state, Vdss = 5.0 +/- 2.8 liter/kg. The pharmacokinetics of S 12363 is linearly related to dose when increased from 0.08 up to 0.84 mg/m2 in humans. Its plasma profile and pharmacokinetic parameters are close to those of other Vinca alkaloids with clearance and terminal half-life being intermediate between those of vinblastine and vincristine. Therapeutic doses are 4 to 10 times lower and should be a direct consequence of the higher uptake and retention by the cells of this new aminophosphonate Vinca alkaloid derivative.

On-line quantification of ventricular function during dobutamine stress echocardiography.

To develop an approach for on-line quantification of left ventricular size and function during pharmacological stress testing we employed echocardiographic automatic edge detection via integrated backscatter imaging during dobutamine infusion in 27 patients. Ventricular cavity areas, fractional area change and rate of cavity area change were obtained on-line with instantaneous graphic display of the data. When compared to baseline image data, patients with a normal response exhibited modest (15%) reduction in end-diastolic cavity areas at peak dobutamine level, but marked (33%) reduction in systolic areas yielding a 52% increase in fractional area change (n = 13; P < 0.001). The second group of patients (n = 14) had an abnormal response characterized by limited changes in measured parameters of ventricular function and reduced fractional area change (P < 0.05). On-line quantification during pharmacological stress echocardiography is a promising addition to the test for surveillance and objective instantaneous evaluation of global cardiac responses.