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1.
Tunis Med ; 98(11): 783-788, 2020 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-33479976

RESUMEN

BACKGROUND: The electrocardiogram (ECG) remains one of the most important and commonly used diagnostic tools in medicine. At the faculty of Medicine of Tunis (FMT), teaching ECG interpretation to undergraduate medical students is an important part of the curriculum. AIMS: To assess the effectiveness of pedagogical workshops in ECG learning among students of First-year of the primary cycle of medical studies (PCMS 1). In addition, we aimed to assess the students' perceptions of the tutorials. METHODS: It was an exhaustive cross-sectional study that was carried out at the FMT during the academic year 2017-2018 and that included students from PCMS 1. All participants completed a pre-test, a workshop session and a post-test. Each of the tests consists of five Multiple Choice Questions (MCQs) covering the same topics. An evaluation of students' satisfaction with the tutorial was made at the end of the session. RESULTS: Ten workshops were held at the FMT, including 160 students. The overall score increased from 4 out of 10 points in the pre-test to 6.8 out of 10 points in the post-test (p <0.001). A statistically significant improvement was noted in all tests questions (p<0.001). Sixty-one learners (39.3%) were "Not satisfied" with the number of students per group. On the whole, 83.8% (n=130) of students found the session beneficial. CONCLUSIONS: Students indicated a positive attitude toward the workshop and its utility. More research among similar populations is needed to support these conclusions and to assess the effectiveness of medium- and long-term educational workshops on medical students.


Asunto(s)
Educación de Pregrado en Medicina , Estudiantes de Medicina , Estudios Transversales , Evaluación Educacional , Electrocardiografía , Humanos
2.
Biomed Pharmacother ; 83: 577-583, 2016 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-27459113

RESUMEN

AIM: to investigate the anti-inflammatory effect of the Pistacia lentiscus oil in experimental colitis model. MATERIALS AND METHODS: Colitis was induced in male rats by instillation of 2,4,6-trinitrobenzenesulfonic acid (TNBS) in all groups. The experimental groups consisted of: 5 rats received Lentisc oil 2months before colitis induction (preventive group), 5 rats received the oil on the day of colitis induction (curative group) and 5 control rats. Lentisc oil was extracted from the ripe fruit of the plant by the cold press method and was analyzed by spectro-chromatography. Lentisc oil has been inserted with a standard diet at the dose of 30mg oil/100g of food/rat. RESULTS: The lentisc oil sample is composed mainly by Oleic acid (47.96%), Palmitic acid (27.94%) and Linoleic acid (20.22%).There was a significant difference between control rats and treated rats with lentisc oil concerned body mass (p=0.009), bleeding index (p=0.005 and p=0.018) and diarrhea (p=0.012). Histological examination revealed a clear difference between the control and preventive groups with disappearance of erosion, decreased of cryptitis, irregular crypts and crypt loss in the preventive group. Curative group showed a significant decrease of ulceration, hyperplasia, cryptitis, irregular crypts and crypt loss compared to the control group. There was an attenuation of inflammation in the preventive group compared to the curative group without statistically significant. CONCLUSION: Lentisc oil administration could provide a protective effect on intestinal inflammation in colitis rats induced by TNBS mainly when it is administered at a young age in preventive mode. This beneficial effect would involve a modification of arachidonic acid metabolism.


Asunto(s)
Colitis/tratamiento farmacológico , Colitis/prevención & control , Pistacia/química , Aceites de Plantas/uso terapéutico , Animales , Peso Corporal/efectos de los fármacos , Colitis/inducido químicamente , Colitis/patología , Colon/efectos de los fármacos , Colon/patología , Diarrea/tratamiento farmacológico , Hemorragia/tratamiento farmacológico , Masculino , Aceites de Plantas/farmacología , Ratas Wistar , Recto/efectos de los fármacos , Recto/patología
3.
Med Sci (Paris) ; 29(12): 1145-50, 2013 Dec.
Artículo en Francés | MEDLINE | ID: mdl-24356146

RESUMEN

Crohn's disease (CD) and ulcerative colitis (UC) are the principal inflammatory bowel diseases (IBD) which physiopathology is currently poorly elucidated. During these diseases, the participation of the epithelial cell in the installation and the perpetuation of the intestinal inflammation is now clearly implicated. In fact, the intestinal epithelium located at the interface between the internal environment and the intestinal luminal, is key to the homeostatic regulation of the intestinal barrier. This barrier can schematically be regarded as being three barriers in one: a physical, chemical and immune barrier. The barrier function of epithelial cell can be altered by various mechanisms as occurs in IBD. The goal of this article is to review the literature on the role of the epithelial cell in intestinal homeostasis and its implication in the IBD.


Asunto(s)
Células Epiteliales/fisiología , Enfermedades Inflamatorias del Intestino/fisiopatología , Mucosa Intestinal/fisiopatología , Intestinos/fisiopatología , Animales , Colitis Ulcerosa , Enfermedad de Crohn , Células Epiteliales/inmunología , Homeostasis , Humanos , Inflamación , Enfermedades Inflamatorias del Intestino/inmunología , Mucosa Intestinal/inmunología
4.
BMC Gastroenterol ; 9: 62, 2009 Aug 07.
Artículo en Inglés | MEDLINE | ID: mdl-19664207

RESUMEN

BACKGROUND: The immune responses to bacterial products through the pattern recognition receptor (PRR) play a pivotal role in pathogenesis of Crohn's disease. A recent study described an association between CD and some gene coding for bacterial receptor like NOD2/CARD15 gene and TLR4. In this study, we sought to determine whether TLR4 gene was associated with Crohn's disease (CD) among the Tunisian population and its correlation with clinical manifestation of the disease. METHODS: 90 patients with CD and 80 healthy individuals are genotyped for the Asp299Gly and Thr399Ile polymorphisms by restriction fragment length polymorphism analysis. RESULTS: The allele and genotype frequency of the TLR4 polymorphisms did not differ between patients and controls. The genotype-phenotype correlation permitted to show that the Thr399Ile polymorphism was associated with early onset disease. CONCLUSION: this study reported the absence of association between CD and TLR4 gene in the Tunisian population, but this gene could play a role in clinical expression of the disease.


Asunto(s)
Enfermedad de Crohn/etnología , Enfermedad de Crohn/genética , Fenotipo , Polimorfismo de Nucleótido Simple/genética , Receptor Toll-Like 4/genética , Adulto , Estudios de Casos y Controles , Femenino , Frecuencia de los Genes/genética , Predisposición Genética a la Enfermedad/genética , Genotipo , Humanos , Masculino , Túnez
5.
Eur J Gastroenterol Hepatol ; 19(3): 225-8, 2007 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-17301649

RESUMEN

BACKGROUND AND AIMS: Crohn's disease is a multifactorial disorder with a pivotal role of the genetic component. HSP70-2 gene, located in IBD3 region, has a PstI polymorphic site associated recently with Crohn's disease especially with a perforating form. In this study, we sought to determine whether this polymorphism was associated with Crohn's disease in the Tunisian population and its correlation with clinical manifestation of the disease. METHODS: In all, 148 patients with Crohn's disease and 81 healthy individuals were genotyped for the HSP70-2 PstI polymorphism by restriction fragment length polymorphism analysis. RESULTS: The allele and genotype frequency of the PstI polymorphism did not differ between patients and controls. Furthermore, this polymorphism was not associated with specific disease behavior. CONCLUSION: This study reported the absence of association between Crohn's disease and HSP70-2 gene in the Tunisian population. The allele A of PstI polymorphism was not associated with phenotype of the disease.


Asunto(s)
Enfermedad de Crohn/genética , Proteínas HSP70 de Choque Térmico/genética , Polimorfismo Genético , Adolescente , Adulto , Estudios de Casos y Controles , Enfermedad de Crohn/cirugía , Femenino , Frecuencia de los Genes , Predisposición Genética a la Enfermedad , Genotipo , Humanos , Masculino , Fenotipo , Reacción en Cadena de la Polimerasa/métodos , Factores de Tiempo
6.
Tunis Med ; 84(5): 269-74, 2006 May.
Artículo en Francés | MEDLINE | ID: mdl-16915774

RESUMEN

The irritable bowel syndrome (IBS) is a frequent gastrointestinal disorder (10 -15% of the population). It is characterized by chronic abdominal pain with modification in the bowel habits. The diagnosis is based of ROME II criteria. The pathophysiology of the SII remains unknown . It result from visceral hypersensitivity with anomalies of the digestive motility. These anomalies are secondary of dysfunction of the brain - gut axis modulated by environmental and the psychosocial factors. The understanding of the pathophysiological mechanisms of the SII and in particular the function of the brain-gut axis will permit a better handling of the patients. Indeed, the present knowledge of the neurotransmitter implied in the communication between the central nervous system and the digestive tract are currently the basis of the new therapies aimed to modulate the mechanisms implicated in the causation of the several symptoms of IBS. These novel pharmacotherapy should reduce the indirect societal and costs of IBS.


Asunto(s)
Síndrome del Colon Irritable/fisiopatología , Encéfalo/fisiopatología , Motilidad Gastrointestinal/fisiología , Tracto Gastrointestinal/inervación , Tracto Gastrointestinal/fisiopatología , Humanos , Vías Nerviosas/fisiopatología , Neurotransmisores/fisiología
7.
Dig Dis Sci ; 50(1): 130-5, 2005 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-15712650

RESUMEN

Crohn's disease (CD) is a heterogeneous disorder. A genetic linkage to chromosome 16 (IBD1) has been previously observed and replicated in unrelated populations. Recently, in this region, NOD2/CARD15 has been identified as a susceptibility gene. The aim of this report is to determine whether this gene is implicated in CD in a Tunisian population. One hundred thirty patients with CD and 90 healthy individuals were genotyped for the three common NOD2 variants (C2104T in exon 4, G2722C in exon 8, and 3020insC in exon 11). Furthermore, the 11 exons of the NOD2 gene were sequenced in 20 patients with CD. Results showed that the frequency of the CARD15 variants in the Tunisian population is significantly lower than that observed in the European and American population. Direct sequencing of CARD15 did not permit us to identify a characteristic mutation in our population. No association was confirmed between CD and the NOD2 gene in our Tunisian population. Furthermore, the NOD2/CARD15 gene has a variable association with CD in different populations. These results indicate the genetic variation of CD in different ethnic groups.


Asunto(s)
Enfermedad de Crohn/genética , Variación Genética , Péptidos y Proteínas de Señalización Intracelular/genética , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Arginina , Estudios de Casos y Controles , Exones , Femenino , Frecuencia de los Genes , Genotipo , Glicina , Humanos , Masculino , Persona de Mediana Edad , Proteína Adaptadora de Señalización NOD2 , Triptófano , Túnez
8.
Tunis Med ; 82(7): 635-41, 2004 Jul.
Artículo en Francés | MEDLINE | ID: mdl-15552020

RESUMEN

The Inflammatory Bowel Disease (IBD) are multifactorial diseases involving the interaction of genetic and environmental factors. In genetic terms, the IBD are polygenic and multigenic disorders with incomplete penetrance. In the late decade, investigators have applied the complementary techniques of genome-wide scanning and candidate gene analysis to search susceptibility genes. The IBD susceptibility regions, widely replicated, are in chromosomes 16 (IBD1), 12 (IBD2) and 6 (IBD3). Recently, a significant association have been reported with Crohn's disease and NOD2/ CARD15 gene. This gene is an appropriate candidate gene because its localization and function. More studies is necessary to confirm this association, search an other variants of this gene and other candidate gene. This studies provide best comprehension of the disease pathogenesis and deliver clinical application.


Asunto(s)
Enfermedades Inflamatorias del Intestino , Predisposición Genética a la Enfermedad , Humanos , Enfermedades Inflamatorias del Intestino/epidemiología , Enfermedades Inflamatorias del Intestino/genética
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