8 research outputs found

    Control de contratistas de Seguridad y Salud en el Trabajo en Instituciones educativas de las localidades de Santa Fe y la Candelaria

    Get PDF
    El control de contratistas en el ámbito de Seguridad y Salud en el Trabajo en las Instituciones Educativas en adelante (IED), es de poco o nulo control a causa a la falta de comprensión por parte de las individuos encargados de las administraciones de los centros educativos, no obstante, es significativo examinar la relevancia de este saber científico a en todos los centros de trabajo o actividades económicas ya que la prevención y control de los peligros propenden a un ambiente laboral saludable y seguro. Por consiguiente, en el presente documento se abordará desde una perspectiva prevencionista la identificación de aspectos claves en las IED sobre la importancia de efectuar y conservar un Sistema de Gestión de Seguridad y Salud en el Trabajo (SG-SST) no solo para los empleados directos sino para todos aquellos empleados de corto tiempo o contratistas

    Canagliflozin and renal outcomes in type 2 diabetes and nephropathy

    Get PDF
    BACKGROUND Type 2 diabetes mellitus is the leading cause of kidney failure worldwide, but few effective long-term treatments are available. In cardiovascular trials of inhibitors of sodium–glucose cotransporter 2 (SGLT2), exploratory results have suggested that such drugs may improve renal outcomes in patients with type 2 diabetes. METHODS In this double-blind, randomized trial, we assigned patients with type 2 diabetes and albuminuric chronic kidney disease to receive canagliflozin, an oral SGLT2 inhibitor, at a dose of 100 mg daily or placebo. All the patients had an estimated glomerular filtration rate (GFR) of 30 to <90 ml per minute per 1.73 m2 of body-surface area and albuminuria (ratio of albumin [mg] to creatinine [g], >300 to 5000) and were treated with renin–angiotensin system blockade. The primary outcome was a composite of end-stage kidney disease (dialysis, transplantation, or a sustained estimated GFR of <15 ml per minute per 1.73 m2), a doubling of the serum creatinine level, or death from renal or cardiovascular causes. Prespecified secondary outcomes were tested hierarchically. RESULTS The trial was stopped early after a planned interim analysis on the recommendation of the data and safety monitoring committee. At that time, 4401 patients had undergone randomization, with a median follow-up of 2.62 years. The relative risk of the primary outcome was 30% lower in the canagliflozin group than in the placebo group, with event rates of 43.2 and 61.2 per 1000 patient-years, respectively (hazard ratio, 0.70; 95% confidence interval [CI], 0.59 to 0.82; P=0.00001). The relative risk of the renal-specific composite of end-stage kidney disease, a doubling of the creatinine level, or death from renal causes was lower by 34% (hazard ratio, 0.66; 95% CI, 0.53 to 0.81; P<0.001), and the relative risk of end-stage kidney disease was lower by 32% (hazard ratio, 0.68; 95% CI, 0.54 to 0.86; P=0.002). The canagliflozin group also had a lower risk of cardiovascular death, myocardial infarction, or stroke (hazard ratio, 0.80; 95% CI, 0.67 to 0.95; P=0.01) and hospitalization for heart failure (hazard ratio, 0.61; 95% CI, 0.47 to 0.80; P<0.001). There were no significant differences in rates of amputation or fracture. CONCLUSIONS In patients with type 2 diabetes and kidney disease, the risk of kidney failure and cardiovascular events was lower in the canagliflozin group than in the placebo group at a median follow-up of 2.62 years

    Design and baseline characteristics of the finerenone in reducing cardiovascular mortality and morbidity in diabetic kidney disease trial

    Get PDF
    Background: Among people with diabetes, those with kidney disease have exceptionally high rates of cardiovascular (CV) morbidity and mortality and progression of their underlying kidney disease. Finerenone is a novel, nonsteroidal, selective mineralocorticoid receptor antagonist that has shown to reduce albuminuria in type 2 diabetes (T2D) patients with chronic kidney disease (CKD) while revealing only a low risk of hyperkalemia. However, the effect of finerenone on CV and renal outcomes has not yet been investigated in long-term trials. Patients and Methods: The Finerenone in Reducing CV Mortality and Morbidity in Diabetic Kidney Disease (FIGARO-DKD) trial aims to assess the efficacy and safety of finerenone compared to placebo at reducing clinically important CV and renal outcomes in T2D patients with CKD. FIGARO-DKD is a randomized, double-blind, placebo-controlled, parallel-group, event-driven trial running in 47 countries with an expected duration of approximately 6 years. FIGARO-DKD randomized 7,437 patients with an estimated glomerular filtration rate >= 25 mL/min/1.73 m(2) and albuminuria (urinary albumin-to-creatinine ratio >= 30 to <= 5,000 mg/g). The study has at least 90% power to detect a 20% reduction in the risk of the primary outcome (overall two-sided significance level alpha = 0.05), the composite of time to first occurrence of CV death, nonfatal myocardial infarction, nonfatal stroke, or hospitalization for heart failure. Conclusions: FIGARO-DKD will determine whether an optimally treated cohort of T2D patients with CKD at high risk of CV and renal events will experience cardiorenal benefits with the addition of finerenone to their treatment regimen. Trial Registration: EudraCT number: 2015-000950-39; ClinicalTrials.gov identifier: NCT02545049

    Carta de Psicología No. 56

    No full text
    Entre los mecanismos de divulgación de la investigación de la Facultad de Psicología se cuenta con la publicación semestral de Carta de Psicología, espacio en el cual se publican artículos cortos resultado de investigaciones desarrolladas en los diferentes escenarios de formación, para visibilizar los productos derivados de los semilleros innovo, de investigación o grupos de estudio; al igual que aquellos derivados de la interacción académica con instituciones de orden nacional e internacional, los derivados de ejercicios de investigación en el aula de clase y de actividades de extensión. Esta publicación parte de un doble reconocimiento: en su comienzo, los artículos científicos fueron epístolas de las comunidades científicas, grupos cercanos de interlocución franca y abierta. En su avance, Carta de Psicología propende por la reflexión y el diálogo a partir del reconocimiento de las experiencias valiosas que construyen universidad y diversidad en la formación, los ejercicios de investigación del aula, los avances de los proyectos de semilleros de investigación, los avances de maestría y doctorado, las voces de los egresados, entre otros, de tal manera que sirva como referencia de lo que hacemos y de lo que somos. Esta filosofía orienta el último desarrollo de la política editorial de Carta de Psicología en cuatro secciones: Investigación formativa, Interacción académica, Investigación de aula y Extensión.Investigación, integración curricular y divulgación como ejes para el cumplimiento de las funciones sustantivas en la Facultad de Psicología. El cambio de la comunicación en las relaciones afectivosexuales debido al uso de las redes sociales. Consumo de sustancias psicoactivas: una problemática juvenil. Flexibilidad cognitiva en el deterioro cognitivo leve. Relación entre clima organizacional y engagement en empleados de Bogotá. Relación entre el estrés y el desempeño laboral: revisión teórica. Percepción del liderazgo transformacional con relación a las variables sociodemográficas de la población colombiana. Programas de Outplacement para trabajadores en relación con su calidad de vida. Violencia sexual y redes sociales. Los juegos en redes y la violencia autoinfligida. El sentido de comunidad y la crisis económica, social y política en Colombia. Consumo de alcohol de estudiantes universitarios antes y durante la pandemia COVID-19. Resultados preliminares. Uso de la tecnología para la aplicación del instrumento para valorar la comprensión de síntesis. Consecuencias de los modelos de pautas de crianza en el desarrollo infantil. La justicia más allá de la equidad: un breve comentario del libro Las fronteras de la justicia, de Martha Nussbaum. Conceptualización y consecuencias del maltrato Infantil Exploración de factores de riesgo y los efectosdel reclutamiento forzado en el desarrollo infantil. Indicadores de aprendizaje para la educación integral de la sexualidad. Instrumento de medición de afectividad y erotismo en trabajadoras sexuales de Bogotá. Toma de decisiones y vida sexual: autocuidado, relaciones afectivas y toma de decisiones en niños/niñas. Convicciones y conductas sobre virginidad. Significado y valor de acuerdo con las diferencias generacionales. Percepción sobre el concepto, situación y vulneración de los derechos humanos en el departamento de Santander, Colombia. Factores que influyen en la vulnerabilidad frente al delito de la trata de personas en estudiantes universitarios de la Universidad Cooperativa de Colombia. Violencia intrafamiliar desde la perspectiva del agresor: un estudio de caso en la cárcel de máxima seguridad de Palogordo de Bucaramanga

    Effect of SGLT2 Inhibitors on Stroke and Atrial Fibrillation in Diabetic Kidney Disease: Results From the CREDENCE Trial and Meta-Analysis

    No full text
    BACKGROUND AND PURPOSE: Chronic kidney disease with reduced estimated glomerular filtration rate or elevated albuminuria increases risk for ischemic and hemorrhagic stroke. This study assessed the effects of sodium glucose cotransporter 2 inhibitors (SGLT2i) on stroke and atrial fibrillation/flutter (AF/AFL) from CREDENCE (Canagliflozin and Renal Events in Diabetes With Established Nephropathy Clinical Evaluation) and a meta-analysis of large cardiovascular outcome trials (CVOTs) of SGLT2i in type 2 diabetes mellitus.METHODS: CREDENCE randomized 4401 participants with type 2 diabetes mellitus and chronic kidney disease to canagliflozin or placebo. Post hoc, we estimated effects on fatal or nonfatal stroke, stroke subtypes, and intermediate markers of stroke risk including AF/AFL. Stroke and AF/AFL data from 3 other completed large CVOTs and CREDENCE were pooled using random-effects meta-analysis.RESULTS: In CREDENCE, 142 participants experienced a stroke during follow-up (10.9/1000 patient-years with canagliflozin, 14.2/1000 patient-years with placebo; hazard ratio [HR], 0.77 [95% CI, 0.55-1.08]). Effects by stroke subtypes were: ischemic (HR, 0.88 [95% CI, 0.61-1.28]; n=111), hemorrhagic (HR, 0.50 [95% CI, 0.19-1.32]; n=18), and undetermined (HR, 0.54 [95% CI, 0.20-1.46]; n=17). There was no clear effect on AF/AFL (HR, 0.76 [95% CI, 0.53-1.10]; n=115). The overall effects in the 4 CVOTs combined were: total stroke (HRpooled, 0.96 [95% CI, 0.82-1.12]), ischemic stroke (HRpooled, 1.01 [95% CI, 0.89-1.14]), hemorrhagic stroke (HRpooled, 0.50 [95% CI, 0.30-0.83]), undetermined stroke (HRpooled, 0.86 [95% CI, 0.49-1.51]), and AF/AFL (HRpooled, 0.81 [95% CI, 0.71-0.93]). There was evidence that SGLT2i effects on total stroke varied by baseline estimated glomerular filtration rate (P=0.01), with protection in the lowest estimated glomerular filtration rate (&lt;45 mL/min/1.73 m2]) subgroup (HRpooled, 0.50 [95% CI, 0.31-0.79]).CONCLUSIONS: Although we found no clear effect of SGLT2i on total stroke in CREDENCE or across trials combined, there was some evidence of benefit in preventing hemorrhagic stroke and AF/AFL, as well as total stroke for those with lowest estimated glomerular filtration rate. Future research should focus on confirming these data and exploring potential mechanisms. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT02065791

    Kidney and Cardiovascular Effects of Canagliflozin According to Age and Sex: A Post Hoc Analysis of the CREDENCE Randomized Clinical Trial

    No full text
    Rationale &amp; Objective: It is unclear whether the effect of canagliflozin on adverse kidney and cardiovascular events in those with diabetic kid-ney disease varies by age and sex. We assessed the effects of canagliflozin among age group categories and between sexes in the Canagli-flozin and Renal Endpoints in Diabetes with Established Nephropathy Clinical Evaluation (CREDENCE) study.Study Design: Secondary analysis of a random-ized controlled trial. Setting &amp; Participants: Participants in the CREDENCE trial. Intervention: Participants were randomly assigned to receive canagliflozin 100 mg/d or placebo.Outcomes: Primary composite outcome of kid-ney failure, doubling of serum creatinine con-centration, or death due to kidney or cardiovascular disease. Prespecified secondary and safety outcomes were also analyzed. Out-comes were evaluated by age at baseline (&lt;60, 60-69, and &gt;_70 years) and sex in the intention-to-treat population using Cox regression models.Results: The mean age of the cohort was 63.0 &amp; PLUSMN; 9.2 years, and 34% were female. Older age and female sex were independently associ-ated with a lower risk of the composite of adverse kidney outcomes. There was no evidence that the effect of canagliflozin on the primary outcome (acomposite of kidney failure, a doubling of serum creatinine concentration, or death from kidney or cardiovascular causes) differed between age groups (HRs, 0.67 [95% CI, 0.52-0.87], 0.63 [0.4 8-0.82], and 0.89 [0.61-1.29] for ages &lt;60, 60-69, and &gt;_70 years, respectively; P = 0.3 for interaction) or sexes (HRs, 0.71 [95% CI, 0.5 4-0.95] and 0.69 [0.56-0.8 4] in women and men, respectively; P = 0.8 for interaction). No differences in safety outcomes by age group or sex were observed.Limitations: This was a post hoc analysis with multiple comparisons.Conclusions: Canagliflozin consistently reduced the relative risk of kidney events in people with diabetic kidney disease in both sexes and across age subgroups. As a result of greater background risk, the absolute reduction in adverse kidney outcomes was greater in younger participants.Funding: This post hoc analysis of the CREDENCE trial was not funded. The CREDENCE study was sponsored by Janssen Research and Development and was conducted collaboratively by the sponsor, an academic-led steering committee, and an academic research organization, George Clinical.Trial Registration: The original CREDENCE trial was registered at ClinicalTrials.gov with study number NCT02065791

    Effects of pre-operative isolation on postoperative pulmonary complications after elective surgery: an international prospective cohort study

    No full text
    corecore