19 research outputs found

    Burnout : intervención aplicada a un entrenador durante la competición

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    Burnout surge como respuesta inadecuada al estrés generado por variables de índole familiar/social, deportivo y personal. Debido a su influencia en el ámbito deportivo, se ha investigado mucho sobre burnout, pero son escasos los trabajos que realicen un proceso de intervención con entrenadores. Asumiendo el paradigma de los sistemas dinámicos (el comportamiento final de un sistema, es resultado de la relación de interdependencia establecida entre los distintos elementos presentes), presentamos una intervención realizada con un entrenador de balonmano que presentaba síntomas de burnout. La intervención se realizó en el transcurso de la temporada (mientras se disputaba la competición) y tuvo como objetivo reducir la intensidad del burnout en el entrenador. Se aplicó durante 9 semanas y abordó los elementos del contexto deportivo que previamente, por medio de una entrevista semi-estructurada, se identificaron como estresores para el entrenador (estilo negativo de dirección y de interacción, altas demandas competitivas, excesivas demandas de energía y tiempo, monotonía del entrenamiento, sentimientos del deportista de estar apartado, no adaptación de las expectativas originales con los logros finales obtenidos). Utilizando la versión española del Athlete Burnout Questionnaire, se mide la intensidad del burnout en las tres dimensiones: agotamiento físico/emocional (AFE), reducida sensación de logro (RSL) y devaluación de la práctica deportiva (DPD), antes y después de la intervención.Burnout arises as an inadequate response to the stress generated by familiar / social, sports and personal variables. Due to its influence in sports, much research has been done on burnout, but there is no much work done on the benefits of coach intervention. Assuming the paradigm of dynamic systems (the final system's behavior is the result of interdependence established between elements), we present the results of an intervention performed with a handball coach who presented symptoms of burnout. The intervention was performed during the sport season and aimed to reduce the coach's intensity of burnout. It was applied during 9 weeks and addressed those element that previously and through a semi-structured interview, were identified as trainer stressors (negative style of management and interaction, high competitive demands, excessive energy and time demands, monotonous training, feelings of the athlete being separated, original expectations not matching the final achievements). Using the Spanish version of the Athlete Burnout Questionnaire, burnout intensity is measured by three dimensions: physical / emotional exhaustion (AFE), reduced sense of accomplishment (RSL) and depreciation of sports practice (DPD), before and after intervention. -Pretest: 3.4 in AFE, 4.0 in RSL and 4.0 in DPD. -Postest: 1.8 in AFE, 2.8 in RSL and 2.4 in DPD. The scores show a decrease in the intensity of burnout suffered by the coach

    Comprehensive description of clinical characteristics of a large systemic Lupus Erythematosus Cohort from the Spanish Rheumatology Society Lupus Registry (RELESSER) with emphasis on complete versus incomplete lupus differences

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    Systemic lupus erythematosus (SLE) is an autoimmune disease characterized by multiple organ involvement and pronounced racial and ethnic heterogeneity. The aims of the present work were (1) to describe the cumulative clinical characteristics of those patients included in the Spanish Rheumatology Society SLE Registry (RELESSER), focusing on the differences between patients who fulfilled the 1997 ACR-SLE criteria versus those with less than 4 criteria (hereafter designated as incomplete SLE (iSLE)) and (2) to compare SLE patient characteristics with those documented in other multicentric SLE registries. RELESSER is a multicenter hospital-based registry, with a collection of data from a large, representative sample of adult patients with SLE (1997 ACR criteria) seen at Spanish rheumatology departments. The registry includes demographic data, comprehensive descriptions of clinical manifestations, as well as information about disease activity and severity, cumulative damage, comorbidities, treatments and mortality, using variables with highly standardized definitions. A total of 4.024 SLE patients (91% with ≥4 ACR criteria) were included. Ninety percent were women with a mean age at diagnosis of 35.4 years and a median duration of disease of 11.0 years. As expected, most SLE manifestations were more frequent in SLE patients than in iSLE ones and every one of the ACR criteria was also associated with SLE condition; this was particularly true of malar rash, oral ulcers and renal disorder. The analysis-adjusted by gender, age at diagnosis, and disease duration-revealed that higher disease activity, damage and SLE severity index are associated with SLE [OR: 1.14; 95% CI: 1.08-1.20 (P < 0.001); 1.29; 95% CI: 1.15-1.44 (P < 0.001); and 2.10; 95% CI: 1.83-2.42 (P < 0.001), respectively]. These results support the hypothesis that iSLE behaves as a relative stable and mild disease. SLE patients from the RELESSER register do not appear to differ substantially from other Caucasian populations and although activity [median SELENA-SLEDA: 2 (IQ: 0-4)], damage [median SLICC/ACR/DI: 1 (IQ: 0-2)], and severity [median KATZ index: 2 (IQ: 1-3)] scores were low, 1 of every 4 deaths was due to SLE activity. RELESSER represents the largest European SLE registry established to date, providing comprehensive, reliable and updated information on SLE in the southern European population

    Tocilizumab in refractory Caucasian Takayasu's arteritis: a multicenter study of 54 patients and literature review

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    Objective: To assess the efficacy and safety of tocilizumab (TCZ) in Caucasian patients with refractory Takayasu's arteritis (TAK) in clinical practice. Methods: A multicenter study of Caucasian patients with refractory TAK who received TCZ. The outcome variables were remission, glucocorticoid-sparing effect, improvement in imaging techniques, and adverse events. A comparative study between patients who received TCZ as monotherapy (TCZMONO) and combined with conventional disease modifying anti-rheumatic drugs (cDMARDs) (TCZCOMBO) was performed. Results: The study comprised 54 patients (46 women/8 men) with a median [interquartile range (IQR)] age of 42.0 (32.5-50.5) years. TCZ was started after a median (IQR) of 12.0 (3.0-31.5) months since TAK diagnosis. Remission was achieved in 12/54 (22.2%), 19/49 (38.8%), 23/44 (52.3%), and 27/36 (75%) patients at 1, 3, 6, and 12 months, respectively. The prednisone dose was reduced from 30.0 mg/day (12.5-50.0) to 5.0 (0.0-5.6) mg/day at 12 months. An improvement in imaging findings was reported in 28 (73.7%) patients after a median (IQR) of 9.0 (6.0-14.0) months. Twenty-three (42.6%) patients were on TCZMONO and 31 (57.4%) on TCZCOMBO: MTX (n = 28), cyclosporine A (n = 2), azathioprine (n = 1). Patients on TCZCOMBO were younger [38.0 (27.0-46.0) versus 45.0 (38.0-57.0)] years; difference (diff) [95% confidence interval (CI) = -7.0 (-17.9, -0.56] with a trend to longer TAK duration [21.0 (6.0-38.0) versus 6.0 (1.0-23.0)] months; diff 95% CI = 15 (-8.9, 35.5), and higher c-reactive protein [2.4 (0.7-5.6) versus 1.3 (0.3-3.3)] mg/dl; diff 95% CI = 1.1 (-0.26, 2.99). Despite these differences, similar outcomes were observed in both groups (log rank p = 0.862). Relevant adverse events were reported in six (11.1%) patients, but only three developed severe events that required TCZ withdrawal. Conclusion: TCZ in monotherapy, or combined with cDMARDs, is effective and safe in patients with refractory TAK of Caucasian origin.Funding: This work was partially supported by RETICS Programs, RD08/0075 (RIER), RD12/0009/0013 and RD16/0012 from “Instituto de Salud Carlos III” (ISCIII) (Spain)

    A deletion at Adamts9-magi1 Locus is associated with psoriatic arthritis risk

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    Objective: Copy number variants (CNVs) have been associated with the risk to develop multiple autoimmune diseases. Our objective was to identify CNVs associated with the risk to develop psoriatic arthritis (PsA) using a genome-wide analysis approach. Methods: A total of 835 patients with PsA and 1498 healthy controls were genotyped for CNVs using the Illumina HumanHap610 BeadChip genotyping platform. Genomic CNVs were characterised using CNstream analysis software and analysed for association using the χ2 test. The most significant genomic CNV associations with PsA risk were independently tested in a validation sample of 1133 patients with PsA and 1831 healthy controls. In order to test for the specificity of the variants with PsA aetiology, we also analysed the association to a cohort of 822 patients with purely cutaneous psoriasis (PsC). Results: A total of 165 common CNVs were identified in the genome-wide analysis. We found a highly significant association of an intergenic deletion between ADAMTS9 and MAGI1 genes on chromosome 3p14.1 (p=0.00014). Using the independent patient and control cohort, we validated the association between ADAMTS9-MAGI1 deletion and PsA risk (p=0.032). Using next-generation sequencing, we characterised the 26 kb associated deletion. Finally, analysing the PsC cohort we found a lower frequency of the deletion compared with the PsA cohort (p=0.0088) and a similar frequency to that of healthy controls (p>0.3). Conclusions: The present genome-wide scan for CNVs associated with PsA risk has identified a new deletion associated with disease risk and which is also differential from PsC risk

    Golimumab in refractory uveitis related to spondyloarthritis. Multicenter study of 15 patients

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    Objective: To assess the efficacy of golimumab (GLM) in refractory uveitis associated to spondyloarthritis (SpA). Methods: Multicenter study of SpA-related uveitis refractory to at least one immunosuppressive drug. The main outcome variables were degree of anterior and posterior chamber inflammation, visual acuity, and macular thickness. Results: Fifteen patients (13 men/2 women; 18 affected eyes; mean age 39±6 years) were evaluated. The underlying SpA subtypes were ankylosing spondylitis (n=8), psoriatic arthritis (n=6) and non-radiographic axial SpA (n=1). The ocular involvement patterns were recurrent anterior uveitis in 8 patients and chronic anterior uveitis in 7. Before GLM they have received methotrexate (n=13), sulfasalazine (n=6), pulses of methylprednisolone (n=4), azathioprine (n=3), leflunomide (n=2) and cyclosporine (n=1). Ten of them had also been treated with TNF-? blockers; etanercept (n=7), adalimumab (n=7), infliximab (n=6), and certolizumab (n=1). GLM was given at the standard dose (50 mg/sc/monthly) as monotherapy (n=7) or in combination with conventional immunosuppressive drugs (n=8), mainly methotrexate. Most patients had rapid and progressive improvement of intraocular inflammation parameters. The median number of cells in the anterior chamber at 2 years (0 [0-0]) was significantly reduced compared to baseline findings (1 [0-3]); p=0.04). The mean best corrected visual acuity value also improved (0.84±0.3 at 2 years versus 0.62±0.3 at baseline; p=0.03). Only minor side effects were observed after a mean follow-up of 23±7 months. Conclusions: Our results indicate that GLM may be a useful therapeutic option in refractory SpA-related uveitis

    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

    Burnout : intervención aplicada a un entrenador durante la competición

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    Burnout surge como respuesta inadecuada al estrés generado por variables de índole familiar/social, deportivo y personal. Debido a su influencia en el ámbito deportivo, se ha investigado mucho sobre burnout, pero son escasos los trabajos que realicen un proceso de intervención con entrenadores. Asumiendo el paradigma de los sistemas dinámicos (el comportamiento final de un sistema, es resultado de la relación de interdependencia establecida entre los distintos elementos presentes), presentamos una intervención realizada con un entrenador de balonmano que presentaba síntomas de burnout. La intervención se realizó en el transcurso de la temporada (mientras se disputaba la competición) y tuvo como objetivo reducir la intensidad del burnout en el entrenador. Se aplicó durante 9 semanas y abordó los elementos del contexto deportivo que previamente, por medio de una entrevista semi-estructurada, se identificaron como estresores para el entrenador (estilo negativo de dirección y de interacción, altas demandas competitivas, excesivas demandas de energía y tiempo, monotonía del entrenamiento, sentimientos del deportista de estar apartado, no adaptación de las expectativas originales con los logros finales obtenidos). Utilizando la versión española del Athlete Burnout Questionnaire, se mide la intensidad del burnout en las tres dimensiones: agotamiento físico/emocional (AFE), reducida sensación de logro (RSL) y devaluación de la práctica deportiva (DPD), antes y después de la intervención.Burnout arises as an inadequate response to the stress generated by familiar / social, sports and personal variables. Due to its influence in sports, much research has been done on burnout, but there is no much work done on the benefits of coach intervention. Assuming the paradigm of dynamic systems (the final system's behavior is the result of interdependence established between elements), we present the results of an intervention performed with a handball coach who presented symptoms of burnout. The intervention was performed during the sport season and aimed to reduce the coach's intensity of burnout. It was applied during 9 weeks and addressed those element that previously and through a semi-structured interview, were identified as trainer stressors (negative style of management and interaction, high competitive demands, excessive energy and time demands, monotonous training, feelings of the athlete being separated, original expectations not matching the final achievements). Using the Spanish version of the Athlete Burnout Questionnaire, burnout intensity is measured by three dimensions: physical / emotional exhaustion (AFE), reduced sense of accomplishment (RSL) and depreciation of sports practice (DPD), before and after intervention. -Pretest: 3.4 in AFE, 4.0 in RSL and 4.0 in DPD. -Postest: 1.8 in AFE, 2.8 in RSL and 2.4 in DPD. The scores show a decrease in the intensity of burnout suffered by the coach

    Successful Optimization of Adalimumab Therapy in Refractory Uveitis Due to Behçet's Disease.

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    To assess efficacy, safety, and cost-effectiveness of adalimumab (ADA) therapy optimization in a large series of patients with uveitis due to Behçet disease (BD) who achieved remission after the use of this biologic agent. Open-label multicenter study of ADA-treated patients with BD uveitis refractory to conventional immunosuppressants. Sixty-five of 74 patients with uveitis due to BD, who achieved remission after a median ADA duration of 6 (range, 3-12) months. ADA was optimized in 23 (35.4%) of them. This biologic agent was maintained at a dose of 40 mg/subcutaneously/2 weeks in the remaining 42 patients. After remission, based on a shared decision between the patient and the treating physician, ADA was optimized. When agreement between patient and physician was reached, optimization was performed by prolonging the ADA dosing interval progressively. Comparison between optimized and nonoptimized patients was performed. Efficacy, safety, and cost-effectiveness in optimized and nonoptimized groups. To determine efficacy, intraocular inflammation (anterior chamber cells, vitritis, and retinal vasculitis), macular thickness, visual acuity, and the sparing effect of glucocorticoids were assessed. No demographic or ocular differences were found at the time of ADA onset between the optimized and the nonoptimized groups. Most ocular outcomes were similar after a mean ± standard deviation follow-up of 34.7±13.3 and 26±21.3 months in the optimized and nonoptimized groups, respectively. However, relevant adverse effects were only seen in the nonoptimized group (lymphoma, pneumonia, severe local reaction at the injection site, and bacteremia by Escherichia coli, 1 each). Moreover, the mean ADA treatment costs were lower in the optimized group than in the nonoptimized group (6101.25 euros/patient/year vs. 12 339.48; P ADA optimization in BD uveitis refractory to conventional therapy is effective, safe, and cost-effective
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