17 research outputs found

    Linking an unlearning context with firm performance through human capital

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    AbstractThe purpose of this paper is to examine the relationship among organisational unlearning, human capital and firm performance. In doing so, this paper comprehensively reviewed the literature on the unlearning concept, and developed and validated a model to measure unlearning in 112 companies listed on the Spanish Stock Exchange. The methodology involved the construction and analysis of a structural model using both subjective and objective criteria in our measurement variables, developed from a relevant literature review. Our findings show that managers need to develop an unlearning context process to create human capital, which is a primordial asset to improve firm performance

    Genomic mutation profile in progressive chronic lymphocytic leukemia patients prior to first-line chemoimmunotherapy with FCR and rituximab maintenance (REM)

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    Chronic Lymphocytic Leukemia (CLL) is the most prevalent leukemia in Western countries and is notable for its variable clinical course. This variability is partly reflected by the mutational status of IGHV genes. Many CLL samples have been studied in recent years by next-generation sequencing. These studies have identified recurrent somatic mutations in NOTCH1, SF3B1, ATM, TP53, BIRC3 and others genes that play roles in cell cycle, DNA repair, RNA metabolism and splicing. In this study, we have taken a deep-targeted massive sequencing approach to analyze the impact of mutations in the most frequently mutated genes in patients with CLL enrolled in the REM (rituximab en mantenimiento) clinical trial. The mutational status of our patients with CLL, except for the TP53 gene, does not seem to affect the good results obtained with maintenance therapy with rituximab after front-line FCR treatment

    Treatment with tocilizumab or corticosteroids for COVID-19 patients with hyperinflammatory state: a multicentre cohort study (SAM-COVID-19)

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    Objectives: The objective of this study was to estimate the association between tocilizumab or corticosteroids and the risk of intubation or death in patients with coronavirus disease 19 (COVID-19) with a hyperinflammatory state according to clinical and laboratory parameters. Methods: A cohort study was performed in 60 Spanish hospitals including 778 patients with COVID-19 and clinical and laboratory data indicative of a hyperinflammatory state. Treatment was mainly with tocilizumab, an intermediate-high dose of corticosteroids (IHDC), a pulse dose of corticosteroids (PDC), combination therapy, or no treatment. Primary outcome was intubation or death; follow-up was 21 days. Propensity score-adjusted estimations using Cox regression (logistic regression if needed) were calculated. Propensity scores were used as confounders, matching variables and for the inverse probability of treatment weights (IPTWs). Results: In all, 88, 117, 78 and 151 patients treated with tocilizumab, IHDC, PDC, and combination therapy, respectively, were compared with 344 untreated patients. The primary endpoint occurred in 10 (11.4%), 27 (23.1%), 12 (15.4%), 40 (25.6%) and 69 (21.1%), respectively. The IPTW-based hazard ratios (odds ratio for combination therapy) for the primary endpoint were 0.32 (95%CI 0.22-0.47; p < 0.001) for tocilizumab, 0.82 (0.71-1.30; p 0.82) for IHDC, 0.61 (0.43-0.86; p 0.006) for PDC, and 1.17 (0.86-1.58; p 0.30) for combination therapy. Other applications of the propensity score provided similar results, but were not significant for PDC. Tocilizumab was also associated with lower hazard of death alone in IPTW analysis (0.07; 0.02-0.17; p < 0.001). Conclusions: Tocilizumab might be useful in COVID-19 patients with a hyperinflammatory state and should be prioritized for randomized trials in this situatio

    Multiparticulate Systems of Meloxicam for Colonic Administration in Cancer or Autoimmune Diseases

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    The aim of this research is the development of new colonic release systems of meloxicam (MLX) a non-steroidal anti-inflammatory drug (NSAIDs) with pH and time-dependent vehicles for cancer or autoimmune diseases. The colon has a higher pH than the rest of the gastrointestinal tract (GIT) and this can be used as a modified release strategy. Eudragit&reg; polymers are the most widely used synthetic products in the design of colonic release formulations because they might offer mucoadhesiveness and pH-dependent release. Colonic delivery systems produced with pH-dependent and permeable polymers (FS-30D) or with pH-independent and low permeability polymers (NM-30D), must dissolve at a pH range of 6.0&ndash;7.0 to delay the release of the drug and prevent degradation in the GIT, before reaching the colon. The conditions prepared to simulate a gastrointestinal transit showed the CNM multiparticulate system, composed of Eudragit&reg; NM and cellulose, as the best release option for MLX with a more sustained release with respect to the other formulations. CNM formulation followed Higuchi and First-order release kinetics, thus MLX release was controlled by a combination of diffusion and polymers swelling/eroding processes

    Long-Term Effects of the Use of Organic Amendments and Crop Rotation on Soil Properties in Southeast Spain

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    The evolution of soil chemical properties over 20 years was monitored to assess the effects of the change in soil management from a rainfed to an irrigated model and the use of organic amendments and crop rotation. Intensive agriculture has been the activity that has caused most degradation and contamination of this soil. Long-term monitoring of the soil profile made it possible to assess its response to the application of sustainable agricultural techniques intended to offset these effects. Three profiles of the same soil were studied&mdash;P1 (1998), P2 (2003), P3 (2017)&mdash;to show the evolution in time and space. An incipient degradation process was detected in the first five years, verified by increases in salinity (2.3 dS m&minus;1), exchangeable Na (0.5 g kg&minus;1), and TN (1.3 g kg&minus;1) in P2 in comparison with P1 (1.0, 0.2, and 1.1, respectively). There was also leaching towards the deep horizons for TN (0.4, 0.9, and 0.7 g kg&minus;1 for P1, P2, and P3, respectively), and for assimilable elements such as P (1.1, 6.4, and 3.8), Fe (2.0, 2.1, and 5.6), Mn (0.3, 6.5, and 1.9), Zn (0.3, 0.5, and 0.9), and Cu (0.5, 0.6, and 1.3) (all mg kg&minus;1, for P1, P2, and P3, respectively). Between 2004 and 2017, organic amendments (sheep manure) were reduced by 50%, crop rotation was intensified, and green fertilization and forage maize cultivation were included. As a result, P3 showed an improvement in comparison with P2, with decreases in EC (1.4 dS m&minus;1), exchangeable Na (0.2 g kg&minus;1), and TN (0.8 g kg&minus;1). The change in soil management enhanced some soil functions (carbon sink and chemical fertility) and attenuated soil degradation

    Multiparticulate Systems of Meloxicam for Colonic Administration in Cancer or Autoimmune Diseases

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    The aim of this research is the development of new colonic release systems of meloxicam (MLX) a non-steroidal anti-inflammatory drug (NSAIDs) with pH and time-dependent vehicles for cancer or autoimmune diseases. The colon has a higher pH than the rest of the gastrointestinal tract (GIT) and this can be used as a modified release strategy. Eudragit® polymers are the most widely used synthetic products in the design of colonic release formulations because they might offer mucoadhesiveness and pH-dependent release. Colonic delivery systems produced with pH-dependent and permeable polymers (FS-30D) or with pH-independent and low permeability polymers (NM-30D), must dissolve at a pH range of 6.0–7.0 to delay the release of the drug and prevent degradation in the GIT, before reaching the colon. The conditions prepared to simulate a gastrointestinal transit showed the CNM multiparticulate system, composed of Eudragit® NM and cellulose, as the best release option for MLX with a more sustained release with respect to the other formulations. CNM formulation followed Higuchi and First-order release kinetics, thus MLX release was controlled by a combination of diffusion and polymers swelling/eroding processes.Ministerio de Ciencia e Innovación, España.Universidad Complutense de MadridDepto. de Farmacia Galénica y Tecnología AlimentariaFac. de FarmaciaTRUEpu

    Proyecto de repositorios de las Bibliotecas Universitarias de Andalucía

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    El Consorcio de Bibliotecas Universitarias de Andalucía (CBUA) ha planificado un repositorio institucional que va a contener los documentos científicos e históricos propios de cada una de las Instituciones en acceso abierto. Se trata de un repositorio distribuido, los documentos se encuentran en diferentes servidores y el acceso a los mismos se realiza a través de los catálogos locales o desde el catálogo colectivo. El modelo se ha concebido también para que la recuperación de la información se pueda realizar desde los buscadores científicos como el Scholar o Scirus, esto implica la construcción de ficheros de metadatos con arquitectura XML y esquema OAI-Dublin Core, estos ficheros se obtienen utilizando un software de conversión a XML a partir de los registros MARC21 existentes en los sistemas locales. Esta concepción de repositorio permite optimizar la tecnología ya existente en las bibliotecas, potenciar el uso de los catálogos locales y del colectivo al no hacer una separación de estos documentos del resto de colecciones, maximizar la visibilidad de la investigación que se produce en las Universidades Andaluzas así como la difusión de los fondos históricos digitalizados a través de los buscadores científicos

    Discovering HIV related information by means of association rules and machine learning

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    Acquired immunodeficiency syndrome (AIDS) is still one of the main health problems worldwide. It is therefore essential to keep making progress in improving the prognosis and quality of life of affected patients. One way to advance along this pathway is to uncover connections between other disorders associated with HIV/AIDS-so that they can be anticipated and possibly mitigated. We propose to achieve this by using Association Rules (ARs). They allow us to represent the dependencies between a number of diseases and other specific diseases. However, classical techniques systematically generate every AR meeting some minimal conditions on data frequency, hence generating a vast amount of uninteresting ARs, which need to be filtered out. The lack of manually annotated ARs has favored unsupervised filtering, even though they produce limited results. In this paper, we propose a semi-supervised system, able to identify relevant ARs among HIV-related diseases with a minimal amount of annotated training data. Our system has been able to extract a good number of relationships between HIV-related diseases that have been previously detected in the literature but are scattered and are often little known. Furthermore, a number of plausible new relationships have shown up which deserve further investigation by qualified medical experts
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