13 research outputs found

    Politiche, azioni e strumenti: la sperimentazione del servizio "Garanzia di originalità" dell'Università di Bologna

    Get PDF
    Nel 2010 l’Università di Bologna ha avviato una sperimentazione per testare l’utilizzo di strumenti automatici a supporto della rilevazione del plagio negli elaborati finali dei suoi studenti. Nell’intervento verranno illustrate le finalità del progetto, le modalità di realizzazione e i risultati della sperimentazione che ha coinvolto i docenti e gli studenti di 27 Corsi di Studio e 3 dottorati di ricerca. Verranno sottolineati, inoltre, gli aspetti giuridici relativi alla corretta gestione dei profili del diritto d’autore, affrontati preliminarmente all’avvio della sperimentazione

    Prevalence, associated factors and outcomes of pressure injuries in adult intensive care unit patients: the DecubICUs study

    Get PDF
    Funder: European Society of Intensive Care Medicine; doi: http://dx.doi.org/10.13039/501100013347Funder: Flemish Society for Critical Care NursesAbstract: Purpose: Intensive care unit (ICU) patients are particularly susceptible to developing pressure injuries. Epidemiologic data is however unavailable. We aimed to provide an international picture of the extent of pressure injuries and factors associated with ICU-acquired pressure injuries in adult ICU patients. Methods: International 1-day point-prevalence study; follow-up for outcome assessment until hospital discharge (maximum 12 weeks). Factors associated with ICU-acquired pressure injury and hospital mortality were assessed by generalised linear mixed-effects regression analysis. Results: Data from 13,254 patients in 1117 ICUs (90 countries) revealed 6747 pressure injuries; 3997 (59.2%) were ICU-acquired. Overall prevalence was 26.6% (95% confidence interval [CI] 25.9–27.3). ICU-acquired prevalence was 16.2% (95% CI 15.6–16.8). Sacrum (37%) and heels (19.5%) were most affected. Factors independently associated with ICU-acquired pressure injuries were older age, male sex, being underweight, emergency surgery, higher Simplified Acute Physiology Score II, Braden score 3 days, comorbidities (chronic obstructive pulmonary disease, immunodeficiency), organ support (renal replacement, mechanical ventilation on ICU admission), and being in a low or lower-middle income-economy. Gradually increasing associations with mortality were identified for increasing severity of pressure injury: stage I (odds ratio [OR] 1.5; 95% CI 1.2–1.8), stage II (OR 1.6; 95% CI 1.4–1.9), and stage III or worse (OR 2.8; 95% CI 2.3–3.3). Conclusion: Pressure injuries are common in adult ICU patients. ICU-acquired pressure injuries are associated with mainly intrinsic factors and mortality. Optimal care standards, increased awareness, appropriate resource allocation, and further research into optimal prevention are pivotal to tackle this important patient safety threat

    Performance assessment of ultra-high durability concrete produced from recycled ultra-high durability concrete

    Get PDF
    The purpose of the work reported in this paper is to assess the performance of recycled ultra-high durability concrete (R-UHDC), produced using different fractions of recycled aggregate obtained from crushed ultra-high durability concrete (UHDC), as a substitute for the natural aggregate. Four different recycled ultra-high durability concrete (R-UHDC) mixes were designed and manufactured with a reference mix based on the natural aggregate and three mixes with the natural aggregate replaced using recycled UHDC according to two percentage replacement values (50 and 100%). The effect of environmental degradation of the recycled parent concrete was also addressed, using recycled aggregates subjected to accelerated carbonation (replacement percentage equal to 50%). The work has been conducted in the framework of the activities of the Horizon 2020 ReSHEALience Project in ultra-high durability concrete. One key objective of the project was to formulate the concept and experimentally validate the performance of ultra-high durability concrete for structures and infrastructures exposed to extremely aggressive scenarios. The ReSHEALience consortium has defined UHDC as a “strain-hardening (fiber-reinforced) cementitious material with functionalizing micro- and nano-scale constituents especially added to deliver high durability in the cracked state under extremely aggressive exposure conditions.” In this context, the research was conducted to investigate the potential of recycling the UHDC mixes, developed and validated in previous research and employing them as a partial or even total replacement of the natural fine aggregate in the production of new UHDC. This supports the cradle-to-cradle approach in life cycle engineering applications. The research confirmed the effective regeneration of new UHDC based on the recycled aggregate obtained from crushed UHDC, attaining the required rheological characteristics, mechanical properties (compressive strength, flexural strength, and toughness), and durability performance (chloride penetration resistance, chloride migration, water capillary suction, and resistivity). This work is intended as the first step toward the sustainability assessment of the end of life of UHDC materials and structures and the potential of recycled UHDC for new structures and retrofit structural applications.peer-reviewe

    High dose esomeprazole as an anti-inflammatory agent in sepsis: Protocol for a randomized controlled trial

    No full text
    Background: Sepsis is caused by dysregulated immune responses due to infection and still presents high mortality rate and limited efficacious therapies, apart from antibiotics. Recent evidence suggests that very high dose proton pump inhibitors might regulate major sepsis mediators' secretion by monocytes, which might attenuate excessive host reactions and improve clinical outcomes. This effect is obtained with doses which are approximately 50 times higher than prophylactic esomeprazole single daily administration and 17 times higher than the cumulative dose of a three day prophylaxis. We aim to perform a randomized trial to investigate if high dose esomeprazole reduces organ dysfunction in patients with sepsis or septic shock. Methods: This study, called PPI-SEPSIS, is a multicenter, randomized, double blind, placebo-controlled clinical trial on critically ill septic patients admitted to the emergency department or intensive care unit. A total of 300 patients will be randomized to receive high dose esomeprazole (80 mg bolus followed by 12 mg/h for 72 h and a second 80 mg bolus 12 h after the first one) or equivolume placebo (sodium chloride 0.9%), with 1:1 allocation. The primary endpoint of the study will be mean daily Sequential Organ Failure Assessment (SOFA) score over 10 days. Secondary outcomes will include antibiotic-free days, single organ failure severity, intensive care unit-free days at day 28, and mortality. Discussion: This trial aims to test the efficacy of high dose esomeprazole to reduce acute organ dysfunction in patients with septic shock. Trial registration: This trial was registered on ClinicalTrials.gov with the trial identification NCT03452865 in March 2018
    corecore