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Glicocálix endotelial: relevancia clínica y enfoque traslacional 内皮糖皮质激素:临床意义和翻译方法
Pub Date : 2019-12-06 DOI: 10.24265/horizmed.2019.v19n4.12
Jorge Luis Vélez, Mario Montalvo, Santiago Aguayo, P. Vélez, G. Velarde, F. E. Jara González, Joshuan Barboza-Meca
espanolEl glicocalix endotelial es una estructura sin forma definida que recubre la capa luminal del endotelio vascular y que esta constituido, principalmente, por tres elementos: proteoglicanos, glucosaminoglicanos y glicoproteinas. Cumple distintas funciones, como regular la permeabilidad vascular a las moleculas y liquidos, la transduccion de las fuerzas mecanicas de tension y las cascadas de fibrinolisis y coagulacion vascular; ademas, protege de la adhesion leucocitaria, plaquetaria y de patogenos. Los determinantes de lesion del glicocalix pueden ser de varios tipos, por ejemplo, incremento las fuerzas de tension, especies reactivas de oxigeno (O ), aumento, a nivel plasmatico, de sustancias como el sodio (hipernatremia), glucosa (hiperglicemia) y colesterol (hipercolesterolemia), y las moleculas proinflamatorias. Cualquiera de las noxas citadas, individualmente o combinadas, lesionan el glicocalix y la disfuncion resultante se expresara clinicamente como disfuncion endotelial, aumento de la permeabilidad vascular, paso de lipoproteinas al subendotelio, activacion de la coagulacion o aumento de la adhesion de plaquetas y leucocitos al endotelio. EnglishEndothelial glycocalyx is an undefined structure covering the luminal layer of the vascular endothelium and consisting mainly of three elements: proteoglycans, glycosaminoglycans and glycoproteins. It has different functions, such as the regulation of vascular permeability to liquids and molecules; transduction of the mechanical forces of vascular tension; regulation of coagulation and fibrinolysis cascades; and protection of leukocyte, platelet and pathogen adhesion. The determinants of a glycocalyx lesion can be of several types―e.g., increased tensile forces; reactive oxygen (O ) species; increased plasma level of substances such as sodium (hypernatremia), glucose (hyperglycemia) and cholesterol (hypercholesterolemia); and pro-inflammatory molecules. Any of the above-mentioned noxas, alone or combined, injure the glycocalyx. Its dysfunction will be clinically expressed as endothelial dysfunction, increased vascular permeability, filtration of lipoproteins to the subendothelium, activation of coagulation, or increased adhesion of leukocytes and platelets to the endothelium.
内皮糖蛋白是一种未定义的结构,覆盖着血管内皮的管腔层,主要由三种元素组成:蛋白多糖、氨基葡萄糖和糖蛋白。它具有调节血管对分子和液体的通透性、传递机械应力以及纤维蛋白溶解和血管凝固级联等不同功能;此外,它还可以防止白细胞、血小板和病原体的粘附。GlycoCALIX损伤的决定因素可以有几种类型,例如,压力增加、活性氧物种(O)、血浆中钠(高钠血症)、葡萄糖(高血糖)和胆固醇(高胆固醇血症)等物质的增加以及促炎症分子。上述任何一种NOxas单独或组合都会损害GlycoCALIX,由此产生的功能障碍在临床上表现为内皮功能障碍、血管通透性增加、脂蛋白向内皮下转移、凝血激活或血小板和白细胞与内皮的粘附增加。EnglishEndothelial Glycocalyx是一种未定义的结构,覆盖血管内皮的管腔层,主要由三种元素组成:蛋白多糖、糖胺聚糖和糖蛋白。它具有不同的功能,如调节血管对液体和分子的通透性;血管张力机械力的转导;凝血和纤溶级联的调节;以及对白细胞、血小板和病原体粘附的保护。Glycocalyx损伤的决定因素可以有几种类型,例如,增加的张力;活性氧(O)物种;钠(高钠血症)、葡萄糖(高血糖)和胆固醇(高胆固醇血症)等物质的血浆水平升高;和促炎症分子。上述任何noxas,单独或联合,都会注射Glycocalyx。其功能障碍将在临床上表现为内皮功能障碍、血管通透性增加、脂蛋白向内皮下过滤、凝血激活或白细胞和血小板对内皮的粘附增加。
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引用次数: 2
Clasificación actual del carcinoma de pulmón. Consideraciones histológicas, inmunofenotípicas, moleculares y clínicas 肺癌的当前分类。组织学、免疫表型、分子和临床考虑
Pub Date : 2019-12-05 DOI: 10.24265/horizmed.2019.v19n4.11
Carlos Barrionuevo Cornejo, Daniela Dueñas Hancco
In recent years, the rapid technological development and the better knowledge of genetic and molecular aspects in medicine have allowed a better approach to understand, diagnose and treat various oncological diseases. Regarding lung carcinoma, there has been a remarkable evolution from the first classifications, which were purely morphological, to the last one issued in 2015. This last classification includes histological, immunophenotypic, molecular genetics, clinical and radiological information, which allows a better evaluation and therapeutic management of these patients. In the present article, the first classifications of lung carcinoma to the last one are reviewed, and the most relevant changes and the importance of the molecular genetics findings are examined for a better clinical and therapeutic approach.
近年来,快速的技术发展以及对医学遗传和分子方面的更好了解,为理解、诊断和治疗各种肿瘤学疾病提供了更好的方法。关于肺癌,从最初的纯形态学分类到2015年发布的最后一个分类,已经发生了显著的演变。最后一种分类包括组织学、免疫表型、分子遗传学、临床和放射学信息,可以更好地评估和治疗这些患者。在本文中,对肺癌的第一个分类到最后一个分类进行了综述,并检查了最相关的变化和分子遗传学发现的重要性,以获得更好的临床和治疗方法。
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引用次数: 0
Síndrome de burnout y la satisfacción laboral en profesionales de la salud 职业倦怠综合症与卫生专业人员的工作满意度
Pub Date : 2019-12-05 DOI: 10.24265/horizmed.2019.v19n4.06
Rosario Margarita Yslado Méndez, R. Figueroa, T. Poma, Eva Zarzosa Marquez, L. Castro, Irene Pinto Flores, Angelita Rojas Gamboa
Objetivo: El objetivo del estudio es estimar las relaciones funcionales entre el burnout y la satisfaccion laboral de los profesionales de la salud de dos hospitales del Peru. Se aplico el “Inventario de burnout de Maslach” MBI y la “Escala de satisfaccion laboral (SL-SPC)” Materiales y metodos: Es un estudio cuantitativo, descriptivo correlacional y transversal. Se encuestaron 177 profesionales de la salud (medicos, odontologos, quimicos farmaceuticos, psicologos, enfermeros, obstetras, tecnologos medicos, nutricionistas y trabajadores sociales) Resultados: Mediante el analisis de ecuaciones estructurales se encontro que existe relacion significativa (AGFI = 0,946) y negativa (coeficiente estructural = -0,62) entre el burnout y la satisfaccion laboral en los profesionales de la salud; el burnout es predictor de la satisfaccion laboral. La dimension predominante del burnout fue la despersonalizacion (37%=0,72/ (0,56+0,72+0,65)); y el factor predominante de la satisfaccion laboral fueron los beneficios economicos (35%=0,99/ (0,67+0,99+0,48+0,66)). Conclusiones: Se propone realizar investigaciones futuras sobre las variables moderadoras, que explican la relacion entre el burnout y la satisfaccion laboral e implementar programas de intervencion ocupacional y organizacional.
目的:本研究的目的是评估秘鲁两家医院卫生专业人员的职业倦怠与工作满意度之间的功能关系。采用MBI的“Maslach倦怠量表”和“工作满意度量表”材料和方法:这是一项定量、相关和横向的描述性研究。对177名卫生专业人员(医生、牙医、药剂师、心理学家、护士、产科医生、医学技术人员、营养师和社会工作者)进行了调查。结果:通过对结构方程的分析,发现卫生专业人员的职业倦怠与工作满意度之间存在显著关系(AGFI=0.946)和负相关关系(结构系数=-0.62);工作倦怠是工作满意度的预测因素。倦怠的主要维度是去个性化(37%=0.72/(0.56+0.72+0.65));工作满意度的主要因素是经济效益(35%=0.99/(0.67+0.99+0.48+0.66))。结论:建议未来研究调节变量,解释职业倦怠与工作满意度之间的关系,并实施职业和组织干预计划。
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引用次数: 6
Brote de escabiosis en el Hospital Víctor Lazarte Echegaray, Trujillo, 2017 2017年特鲁希略维克多·拉扎特·埃切加雷医院爆发疫情
Pub Date : 2019-12-05 DOI: 10.24265/horizmed.2019.v19n4.08
Marco Antonio Alfaro Angulo, Ana Maria Ruth Canevaro Alva
Objective: To describe the characteristics of a scabies outbreak and assess the effect of the control measures. Materials and methods: A descriptive and prospective epidemiological study was conducted at a reference hospital with220 inpatient beds. Data was collected by visiting the Medicine Service on a daily basis, interviewing the healthcare personnel and examining the medical records. The description of the outbreak includes epidemiological variables such as subject, place and time. Descriptive statistics was used to determine the absolute and relative frequencies, as well as the attack rate. Patients and healthcare personnel were requested to sign an informed consent and received information about the benefits of the research. The intervention consisted of isolation measures and contact transmission-based precautions. The use of non-sterile gloves was emphasized. Results: The outbreak took place between the epidemiological weeks 29 and 37 in the year 2017. The index case was a 93-year-old male patient who had Norwegian scabies and was admitted to the hospital due to Alzheimer’s disease. The scabies occurred in nine female nurses, seven residents, six nurse technicians, one intern y five inpatients. Conclusions: This propagated-source outbreak lasted nine epidemiological weeks; and affected nurses, residents, interns and inpatients. The attack rate was 40 %. The prevention and control measures were isolation of the index case and patients, hand hygiene before and after patient care, use of non-sterile gloves, use of scrubs, use of individual medical supplies for each patient, handling of clothing from scabies-infected patients in sealed bags and using gloves, surface cleaning, withdrawal of scabies-infected health workers from their duties until 24 hours of treatment onset, and epidemiological surveillance. Medical treatment was 5 % permethrin lotion for three days. Use of biosafety standards is recommended for patient care, especially when patients are admitted to the hospital with skin lesions. The implemented measures must be considered to prevent and control this type of outbreak.
目的:描述一起疥疮暴发的特点,评价控制措施的效果。材料和方法:在一家有220张住院床位的参考医院进行描述性和前瞻性流行病学研究。数据是通过每天访问医疗服务中心、采访医护人员和检查医疗记录来收集的。疫情的描述包括受试者、地点和时间等流行病学变量。描述性统计用于确定绝对频率和相对频率,以及发病率。患者和医护人员被要求签署知情同意书,并收到有关研究益处的信息。干预措施包括隔离措施和基于接触传播的预防措施。强调使用非无菌手套。结果:疫情发生在2017年流行病学第29周至第37周之间。指标病例是一名93岁的男性患者,患有挪威疥疮,因阿尔茨海默病入院。疥疮发生在9名女护士、7名住院医生、6名护理技术人员、1名实习生和5名住院患者身上。结论:本次传播源疫情持续了9个流行病学周;以及受影响的护士、住院医生、实习生和住院病人。发病率为40%。预防和控制措施包括隔离指标病例和患者、患者护理前后的手部卫生、使用非无菌手套、使用磨砂膏、为每位患者使用个人医疗用品、用密封袋处理疥疮感染患者的衣物并使用手套、表面清洁、,感染疥疮的卫生工作者在治疗开始24小时前停止工作,并进行流行病学监测。药物治疗为5%氯氰菊酯洗剂,为期三天。建议使用生物安全标准进行患者护理,尤其是当患者因皮肤损伤入院时。必须考虑采取的措施来预防和控制这种类型的疫情。
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引用次数: 1
Escala de actitud religiosa en estudiantes de Medicina Humana 医学生宗教态度量表
Pub Date : 2019-12-05 DOI: 10.24265/horizmed.2019.v19n4.05
M. T. Rivera-Encinas, J. Huarcaya-Victoria
espanolObjetivo: Establecer la validez y fiabilidad de la Escala de actitud religiosa (EAR) en una muestra de estudiantes de medicina de una universidad privada del Peru. Materiales y metodos: Estudio observacional y transversal. Se aplico la EAR a una muestra de 687 estudiantes de medicina para valorar las propiedades psicometricas. Resultados: El puntaje medio de la EAR fue de 62,97 ± 15,74. Destaca la diferencia en variables genero (p=0,011), ano de estudio (p=0,035), y religion (p=0,000). Se encontraron 3 factores con autovalores de 9,34, 1,53 y 1,02 respectivamente. Cada uno aporta el 35,22 %, 17,68 % y 17,09 % de la varianza total explicada en la rotacion, que es, en conjunto, el 70 % de la varianza total. La EAR tiene una consistencia interna aceptable (alfa de Cronbach=0,94), pero en su version de 14 items aumenta a 0,951. Conclusiones: Se puede inferir que la EAR, en su version de 14 items, cuenta con propiedades psicometricas adecuadas para poder evaluar la actitud de la poblacion de estudiantes peruanos de Medicina Humana hacia la religion. EnglishObjective: To establish the validity and reliability of the Religious Attitude Scale (RAS) in a sample of medical students from a Peruvian private university. Materials and methods: An observational and cross-sectional study was conducted. The RAS was administered to a sample of 687 medical students to assess the psychometric properties. Results: The mean score of the RAS was 62.97 ± 15.74. Differences in gender (p = 0.011), academic year (p = 0.035) and religion (p = 0.000) stand out. Three factors with eigenvalues of 9.34, 1.53 and 1.02 were found, each contributing 35.22 %, 17.68 % and 17.09 % of the total variance explained in t he rotation, which accounts for 70 % of the total variance. The RAS has an acceptable internal consistency (Cronbach's alpha = 0.94); however, in its 14-item version it increases to 0.951. Conclusions: It can be concluded that the RAS, in its 14-item version, has adequate psychometric properties to evaluate the attitude of the population of Peruvian students of human medicine toward religion.
西班牙目标:在秘鲁一所私立大学的医学生样本中建立宗教态度量表的有效性和可靠性。材料和方法:观察和横向研究。EAR应用于687名医科学生的样本,以评估心理测量特性。结果:耳部平均得分为62.97±15.74。性别(p=0.011)、学习年份(p=0.035)和宗教(p=0.000)变量的差异尤为突出。发现3个因子的特征值分别为9.34、1.53和1.02。每个人贡献了旋转中解释的总方差的35.22%、17.68%和17.09%,这总共占总方差的70%。EAR具有可接受的内部一致性(Cronbach的阿尔法=0.94),但在其14项版本中增加到0.951。结论:可以推断,14项版本的EAR具有足够的心理测量特性,可以评估秘鲁人文医学学生对宗教的态度。英语目标:在秘鲁一所私立大学的医学生样本中建立宗教态度量表的有效性和可靠性。材料和方法:进行了观察和跨部门研究。对687名医学生的样本进行了RAS,以评估心理特性。结果:RAS平均得分为62.97±15.74。性别(p=0.011)、学年(p=0.035)和宗教(p=0.000)的差异脱颖而出。发现三个特征值分别为9.34、1.53和1.02的因子,分别贡献了T he轮换解释的总方差的35.22%、17.68%和17.09%,占总方差的70%。RAS具有可接受的内部一致性(克朗巴赫的阿尔法=0.94);然而,在其14项版本中,它增加到0951项。结论:可以得出的结论是,RAS在其14项版本中具有足够的心理特征,可以评估秘鲁人文医学学生对宗教的态度。
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引用次数: 1
Análisis de asociación entre polimorfismos (rs941798 y rs914458) del gen PTPN1 y diabetes tipo 2 en familias de Lima-Perú 秘鲁利马家庭PTPN1基因多态性(RS941798和RS914458)与2型糖尿病的相关性分析
Pub Date : 2019-12-05 DOI: 10.24265/horizmed.2019.v19n4.03
Enrique Eduardo Sanchez-Castro, Renato LaTorre-Ramírez, Carlos Patricio Padilla Rojas, Frank Lizaraso-Soto, J. Calderón Ticona, José Enrique Solís Villanueva, Wilser Andrés García-Quispes, Mónica Yolanda Paredes Anaya
espanolObjetivo: Analizar la asociacion de los polimorfismos de un solo nucleotido (SNP) rs941798 y rs914458 del gen PTPN1 con la diabetes tipo 2 en familias peruanas de Lima. Materiales y metodos: Veintitres trios familiares fueron captados en el Hospital Nacional Arzobispo Loayza. Se extrajeron muestras de sangre periferica para obtener el ADN y luego las frecuencias alelicas y genotipicas de los SNP. La genotipificacion de los SNP se realizo mediante secuenciacion. El analisis de asociacion basado en familias entre los SNP y la diabetes tipo 2 se realizo con el programa FBAT. Resultados: Se observaron los 3 genotipos posibles para cada SNP, rs941798 (A>G) y rs914458 (G>C). Las pruebas de asociacion basada en familias a nivel alelico mostraron al alelo A del SNP rs941798 asociado a la diabetes tipo 2 (p = 0.023) bajo uno de los modelos evaluados; no obstante, tras la correccion de Bonferroni para comparaciones multiples, esta asociacion se perdio. No se evidencio asociacion entre los SNP y la enfermedad en ningun nivel (alelico, genotipico o haplotipico). Conclusiones: No se encontraron evidencias de asociacion significativa entre los SNP rs941798 y rs914458 del gen PTPN1 con la DT2 en familias peruanas de Lima, en ninguno de los niveles estudiados (alelico, genotipico y haplotipico). EnglishObjective: To analyze the association that PTPN1 gene single nucleotide polymorphisms (SNPs) rs941798 and rs914458 have with type 2 diabetes in Peruvian families from Lima. Materials and methods: Twenty-three (23) families consisting of three members each were recruited at the Hospital Nacional Arzobispo Loayza. Peripheral blood samples were collected to obtain the DNA, and then the allele and genotype frequencies of the SNPs. SNP genotyping was performed using the sequencing method. The family-based analysis of the association between SNPs and type 2 diabetes was conducted using the family-based association test (FBAT) program. Results: Three (3) possible genotypes were observed for each SNP, i.e. rs941798 (A>G) and rs914458 (G>C). In one of the assessed models, the family-based association tests showed at the allele level that allele A of SNP rs941798 is associated with type 2 diabetes (p = 0.023). However, after using the Bonferroni correction for multiple comparisons, this association was lost. No association was demonstrated between the SNPs and the disease at any level (allele, genotype or haplotype). Conclusions: No evidence of significant association was found between PTPN1 gene SNPs rs941798 and rs914458 and type 2 diabetes at the studied levels (allele, genotype or haplotype) in Peruvian families from Lima.
西班牙lobjetivo:分析秘鲁利马家庭PTPN1基因rs941798和rs914458单核苷酸多态性与2型糖尿病的关系。本研究的目的是确定在墨西哥洛伊扎大主教国立医院(Loayza大主教国立医院)的23名家庭成员。采集周围血液样本进行dna分析,然后测定等位基因和SNP基因型频率。通过测序对SNP进行基因分型。使用FBAT程序对SNP和2型糖尿病进行基于家庭的关联分析。结果:每个SNP有3种可能的基因型,rs941798 (A>G)和rs914458 (G>C)。基于等位基因水平的家族关联试验显示SNP rs941798的a等位基因与2型糖尿病相关(p = 0.023);然而,在Bonferroni对多次比较进行修正后,这种关联消失了。在任何水平上(等位基因、基因型或单倍型)均未发现SNP与疾病之间的关联。结论:在秘鲁利马家庭中,PTPN1基因的SNP rs941798和rs914458与tt2基因的任何水平(等位基因、基因型和单倍型)均无显著相关性。目的:分析来自利马的秘鲁家庭的PTPN1基因单核苷酸多态性(SNPs) rs941798和rs914458与2型糖尿病的关系。材料和方法:在洛伊扎大主教国立医院招募了23个家庭,每个家庭有3名成员。Peripheral血液samples民工指导to obtain the DNA,然后allele和genotype frequencies of the SNPs。= =地理= =根据美国人口普查,这个县的总面积为,其中土地和(0.964平方公里)水。使用以家庭为基础的关联试验(FBAT)方案对SNPs与2型糖尿病之间的关联进行了基于家庭的分析。结果:在每个SNP中观察到3个可能的基因型,即rs941798 (A>G)和rs914458 (G>C)。在一种评估模型中,基于家庭的关联试验显示,SNP rs941798的水平与2型糖尿病有关(p = 0.023)。然而,在使用Bonferroni修正进行多次比较后,这种关联就消失了。在任何水平(allele、基因型或单倍型),SNPs与疾病之间没有关联。结论:在来自利马的秘鲁家庭中,没有证据表明PTPN1基因SNPs rs941798和rs914458与研究水平(allele、基因型或单倍型)的2型糖尿病之间存在显著关联。
{"title":"Análisis de asociación entre polimorfismos (rs941798 y rs914458) del gen PTPN1 y diabetes tipo 2 en familias de Lima-Perú","authors":"Enrique Eduardo Sanchez-Castro, Renato LaTorre-Ramírez, Carlos Patricio Padilla Rojas, Frank Lizaraso-Soto, J. Calderón Ticona, José Enrique Solís Villanueva, Wilser Andrés García-Quispes, Mónica Yolanda Paredes Anaya","doi":"10.24265/horizmed.2019.v19n4.03","DOIUrl":"https://doi.org/10.24265/horizmed.2019.v19n4.03","url":null,"abstract":"espanolObjetivo: Analizar la asociacion de los polimorfismos de un solo nucleotido (SNP) rs941798 y rs914458 del gen PTPN1 con la diabetes tipo 2 en familias peruanas de Lima. Materiales y metodos: Veintitres trios familiares fueron captados en el Hospital Nacional Arzobispo Loayza. Se extrajeron muestras de sangre periferica para obtener el ADN y luego las frecuencias alelicas y genotipicas de los SNP. La genotipificacion de los SNP se realizo mediante secuenciacion. El analisis de asociacion basado en familias entre los SNP y la diabetes tipo 2 se realizo con el programa FBAT. Resultados: Se observaron los 3 genotipos posibles para cada SNP, rs941798 (A>G) y rs914458 (G>C). Las pruebas de asociacion basada en familias a nivel alelico mostraron al alelo A del SNP rs941798 asociado a la diabetes tipo 2 (p = 0.023) bajo uno de los modelos evaluados; no obstante, tras la correccion de Bonferroni para comparaciones multiples, esta asociacion se perdio. No se evidencio asociacion entre los SNP y la enfermedad en ningun nivel (alelico, genotipico o haplotipico). Conclusiones: No se encontraron evidencias de asociacion significativa entre los SNP rs941798 y rs914458 del gen PTPN1 con la DT2 en familias peruanas de Lima, en ninguno de los niveles estudiados (alelico, genotipico y haplotipico). EnglishObjective: To analyze the association that PTPN1 gene single nucleotide polymorphisms (SNPs) rs941798 and rs914458 have with type 2 diabetes in Peruvian families from Lima. Materials and methods: Twenty-three (23) families consisting of three members each were recruited at the Hospital Nacional Arzobispo Loayza. Peripheral blood samples were collected to obtain the DNA, and then the allele and genotype frequencies of the SNPs. SNP genotyping was performed using the sequencing method. The family-based analysis of the association between SNPs and type 2 diabetes was conducted using the family-based association test (FBAT) program. Results: Three (3) possible genotypes were observed for each SNP, i.e. rs941798 (A>G) and rs914458 (G>C). In one of the assessed models, the family-based association tests showed at the allele level that allele A of SNP rs941798 is associated with type 2 diabetes (p = 0.023). However, after using the Bonferroni correction for multiple comparisons, this association was lost. No association was demonstrated between the SNPs and the disease at any level (allele, genotype or haplotype). Conclusions: No evidence of significant association was found between PTPN1 gene SNPs rs941798 and rs914458 and type 2 diabetes at the studied levels (allele, genotype or haplotype) in Peruvian families from Lima.","PeriodicalId":30557,"journal":{"name":"Horizonte Medico","volume":"19 1","pages":"14-19"},"PeriodicalIF":0.0,"publicationDate":"2019-12-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48583380","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Nivel de conocimiento y práctica de medidas de bioseguridad: Hospital San José, 2016 生物安全措施的知识水平和实践:San jose医院,2016
Pub Date : 2018-12-31 DOI: 10.24265/horizmed.2018.v18n4.06
Frank Dennys Tamariz Chavarria
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引用次数: 4
Resangrado de la úlcera péptica en pacientes con y sin enfermedad renal crónica 有或无慢性肾脏疾病患者消化性溃疡再出血
Pub Date : 2018-12-31 DOI: 10.24265/horizmed.2018.v18n4.03
Gerly Edson Guzmán Calderón
{"title":"Resangrado de la úlcera péptica en pacientes con y sin enfermedad renal crónica","authors":"Gerly Edson Guzmán Calderón","doi":"10.24265/horizmed.2018.v18n4.03","DOIUrl":"https://doi.org/10.24265/horizmed.2018.v18n4.03","url":null,"abstract":"","PeriodicalId":30557,"journal":{"name":"Horizonte Medico","volume":"43 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2018-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.24265/horizmed.2018.v18n4.03","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"68832618","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Cáncer de cérvix y autorresponsabilidad: perfilando el riesgo de abstención al Papanicolaou entre las mujeres chilenas mediante Árboles de Decisión 宫颈癌与自我责任:通过决策树分析智利妇女不做巴氏试验的风险
Pub Date : 2018-12-31 DOI: 10.24265/horizmed.2018.v18n1.03
Carlos René Rodríguez Garcés, Geraldo Bladimir Padilla Fuentes
Objetivo: modelar estadisticamente los niveles de riesgo al absentismo preventivo de Papanicolaou que presentan las mujeres chilenas segun variables sociodemograficas. Materiales y metodos: Encuesta de Caracterizacion Socioeconomica Nacional. Muestra de 73 324 casos segun alcances CASEN. Modelamiento segun Arboles de Decision para establecer perfiles de la mujer que se abstiene y analizar luego los motivos que esgrimen para tal decision. Resultados: el riesgo de abstencion al examen varia considerablemente en razon de tomar otros examenes de prevencion de cancer (no tomar mamografia), encontrarse en determinada etapa de la adultez (tardia) y tener algun tipo de vinculo conyugal; al tradicional deficit de informacion y acceso le sustituyen los motivos personales como excusa frecuente para no considerar el Papanicolaou como accion recurrente. Asi, la percepcion de poca utilidad y la falta de tiempo configuran el comportamiento de abstencion como una decision en lugar de una imposibilidad. Conclusiones: Tales resultados problematizan las caracteristicas de la mujer contemporanea y sus comportamientos, ademas de plantear la necesidad de considerar la intervencion socioeducativa como requisito para generar actitudes favorables hacia la prevencion; factores que debiera considerar la politica social de prevencion del cancer en general y de cervix en particular.
{"title":"Cáncer de cérvix y autorresponsabilidad: perfilando el riesgo de abstención al Papanicolaou entre las mujeres chilenas mediante Árboles de Decisión","authors":"Carlos René Rodríguez Garcés, Geraldo Bladimir Padilla Fuentes","doi":"10.24265/horizmed.2018.v18n1.03","DOIUrl":"https://doi.org/10.24265/horizmed.2018.v18n1.03","url":null,"abstract":"Objetivo: modelar estadisticamente los niveles de riesgo al absentismo preventivo de Papanicolaou que presentan las mujeres chilenas segun variables sociodemograficas. Materiales y metodos: Encuesta de Caracterizacion Socioeconomica Nacional. Muestra de 73 324 casos segun alcances CASEN. Modelamiento segun Arboles de Decision para establecer perfiles de la mujer que se abstiene y analizar luego los motivos que esgrimen para tal decision. Resultados: el riesgo de abstencion al examen varia considerablemente en razon de tomar otros examenes de prevencion de cancer (no tomar mamografia), encontrarse en determinada etapa de la adultez (tardia) y tener algun tipo de vinculo conyugal; al tradicional deficit de informacion y acceso le sustituyen los motivos personales como excusa frecuente para no considerar el Papanicolaou como accion recurrente. Asi, la percepcion de poca utilidad y la falta de tiempo configuran el comportamiento de abstencion como una decision en lugar de una imposibilidad. Conclusiones: Tales resultados problematizan las caracteristicas de la mujer contemporanea y sus comportamientos, ademas de plantear la necesidad de considerar la intervencion socioeducativa como requisito para generar actitudes favorables hacia la prevencion; factores que debiera considerar la politica social de prevencion del cancer en general y de cervix en particular.","PeriodicalId":30557,"journal":{"name":"Horizonte Medico","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2018-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.24265/horizmed.2018.v18n1.03","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"68832636","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Síndrome de Jeune en un paciente pediátrico: Reporte de caso clínico 小儿患者杨氏综合征:临床病例报告
Pub Date : 2018-12-31 DOI: 10.24265/horizmed.2018.v18n3.12
Elert Zapata Aguilar, Víctor Hugo Calderón Arenas, Lizeth Y. Cabanillas Burgos
El sindrome de Jeune es una displasia esqueletica de baja frecuencia, de transmision autosomica recesiva y potencialmente mortal. Clinicamente tiene una amplia variedad de manifestaciones; En forma clasica se presenta con un torax estrecho, hipoplasia pulmonar secundaria, braquimelia, anormalidades pelvicas, cardiacas y renales. El compromiso pulmonar es variable y puede ser letal. El diagnostico puede sospecharse prenatalmente con el estudio ultrasonografico al medir la circunferencia toracica y de la jaula costal, estudiar su relacion entre si y con la circunferencia abdominal. En este articulo se describe el caso clinico de una paciente de 3 meses de edad, con forma de presentacion leve y diagnostico posnatal.
{"title":"Síndrome de Jeune en un paciente pediátrico: Reporte de caso clínico","authors":"Elert Zapata Aguilar, Víctor Hugo Calderón Arenas, Lizeth Y. Cabanillas Burgos","doi":"10.24265/horizmed.2018.v18n3.12","DOIUrl":"https://doi.org/10.24265/horizmed.2018.v18n3.12","url":null,"abstract":"El sindrome de Jeune es una displasia esqueletica de baja frecuencia, de transmision autosomica recesiva y potencialmente mortal. Clinicamente tiene una amplia variedad de manifestaciones; En forma clasica se presenta con un torax estrecho, hipoplasia pulmonar secundaria, braquimelia, anormalidades pelvicas, cardiacas y renales. El compromiso pulmonar es variable y puede ser letal. El diagnostico puede sospecharse prenatalmente con el estudio ultrasonografico al medir la circunferencia toracica y de la jaula costal, estudiar su relacion entre si y con la circunferencia abdominal. En este articulo se describe el caso clinico de una paciente de 3 meses de edad, con forma de presentacion leve y diagnostico posnatal.","PeriodicalId":30557,"journal":{"name":"Horizonte Medico","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2018-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"68832603","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Horizonte Medico
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