144 research outputs found

    Félix Arnaudin : Chants populaires de la Grande-Lande

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    Ces deux recueils forment les volumes III et IV de l’ensemble des huit volumes des Ɠuvres complĂštes de FĂ©lix Arnaudin, dont le Parc RĂ©gional des Landes de Gascogne a entrepris l’édition. Au magnifique album de photos (quelque trois mille plaques de verre), aux Contes (I), aux Proverbes, Dictons, Devinettes, Formulettes, PriĂšres (II), viennent donc s’ajouter ces deux recueils de chants. Doivent suivre le Dictionnaire de la Grande-Lande, Ă©galement en deux volumes, dont la parution a Ă©tĂ© retardĂ©..

    Strategies of initiation and streamlining of antibiotic therapy in 41 French intensive care units

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    CIAR (Club d'infectiologie en AnesthĂ©sie-RĂ©animation) Study Group: Pr B Allaouchiche (HCL, CHU Lyon), Pr C Arich (CHU Nimes), Pr C Auboyer (CHU St-Etienne), Dr JP Caramella (CHG Nevers), Dr JF Cochard (CHU Bordeaux), Dr A Combes (CHG Meaux), Dr P Courant (CHG Avignon), Dr J Durand-Gasselin (CHG Toulon), Pr J Duranteau (APHP, CHU Bicetre), Dr H Floch (CHU Nantes), Dr F Fraisse (CHG St Denis), Pr M Freysz (CHU Dijon), Dr B Garrigues (CHG Aix-en-Provence), Dr B Georges (CHU Toulouse), Pr F Gouin (APHM, CHU Marseille), Pr L Jacob (APHP, CHU St Louis), Pr P Juvin (APHP, CHU Beaujon), Dr J Keinlen (CHU Montpellier), Dr AM Korinek (APHP, CHU Pitie Salpetriere), Dr C Lamer (Institut Mutualiste Montsouris, Paris), Pr JY Lefrant (CHU Nimes), Dr O Lesieur (CHG La Rochelle), Dr Yazine Mahjoub (CHU Amiens), Pr Y Malledant (CHU Rennes), Pr C Martin (APHM, CHU Marseille), Pr O Mimoz (CHU Poitiers), Pr C Paugam-Burtz (APHP, CHU Beaujon, Clichy), Dr PF Perrigault (CHU Montpellier), Pr T Pottecher (CHU Strasbourg), Pr JL Pourriat (APHP, CHU Hotel Dieu), Dr JF Poussel (CHG Metz), Dr A Rabbat (APHP, CHU Hotel Dieu), Dr J Reignier (CHG La Roche sur Yon), Dr P Sichel (CHG Cherbourg), Dr JP Sollet (CHG Argenteuil), Dr D Thevenin (CHG Lens), Dr G Viquesnel (CHU Caen).International audienceINTRODUCTION: Few studies have addressed the decision-making process of antibiotic therapy (AT) in intensive care unit (ICU) patients. METHODS: In a prospective observational study, all consecutive patients admitted over a one-month period (2004) to 41 French surgical (n = 22) or medical/medico-surgical ICUs (n = 19) in 29 teaching university and 12 non-teaching hospitals were screened daily for AT until ICU discharge. We assessed the modalities of initiating AT, reasons for changes and factors associated with in ICU mortality including a specific analysis of a new AT administered on suspicion of a new infection. RESULTS: A total of 1,043 patients (61% of the cohort) received antibiotics during their ICU stay. Thirty percent (509) of them received new AT mostly for suspected diagnosis of pneumonia (47%), bacteremia (24%), or intra-abdominal (21%) infections. New AT was prescribed on day shifts (45%) and out-of-hours (55%), mainly by a single senior physician (78%) or by a team decision (17%). This new AT was mainly started at the time of suspicion of infection (71%) and on the results of Gram-stained direct examination (21%). Susceptibility testing was performed in 261 (51%) patients with a new AT. This new AT was judged inappropriate in 58 of these 261 (22%) patients. In ICUs with written protocols for empiric AT (n = 25), new AT prescribed before the availability of culture results (P = 0.003) and out-of-hours (P = 0.04) was more frequently observed than in ICUs without protocols but the appropriateness of AT was not different. In multivariate analysis, the predictive factors of mortality for patients with new AT were absence of protocols for empiric AT (adjusted odds ratio (OR) = 1.64, 95% confidence interval (95%CI): 1.01 to 2.69), age ≄60 (OR = 1.97, 95% CI: 1.19 to 3.26), SAPS II score >38 (OR = 2.78, 95% CI: 1.60 to 4.84), rapidly fatal underlying diseases (OR = 2.91, 95% CI: 1.52 to 5.56), SOFA score ≄6 (OR = 4.48, 95% CI: 2.46 to 8.18). CONCLUSIONS: More than 60% of patients received AT during their ICU stay. Half of them received new AT, frequently initiated out-of-hours. In ICUs with written protocols, empiric AT was initiated more rapidly at the time of suspicion of infection and out-of-hours. These results encourage the establishment of local recommendations for empiric AT

    A prospective, observational study of fidaxomicin use for Clostridioides difficile infection in France.

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    To describe the characteristics, management and outcomes of hospitalised patients with Clostridioides difficile infection (CDI) treated with and without fidaxomicin. This prospective, multicentre, observational study (DAFNE) enrolled hospitalised patients with CDI, including 294 patients treated with fidaxomicin (outcomes recorded over a 3-month period) and 150 patients treated with other CDI therapies during three 1-month periods. The primary endpoint was baseline and CDI characteristics of fidaxomicin-treated patients. At baseline, the fidaxomicin-treated population included immunocompromised patients (39.1%) and patients with severe (59.2%) and recurrent (36.4%) CDI. Fidaxomicin was associated with a high rate of clinical cure (92.2%) and low CDI recurrence (16.3% within 3 months). Clinical cure rates were ≄90% in patients aged ≄65 years, those receiving concomitant antibiotics and those with prior or severe CDI. There were 121/296 (40.9%) patients with adverse events (AEs), 5.4% with fidaxomicin-related AEs and 1.0% with serious fidaxomicin-related AEs. No fidaxomicin-related deaths were reported. Fidaxomicin is an effective and well-tolerated CDI treatment in a real-world setting in France, which included patients at high risk of adverse outcomes.Trial registration: Description of the use of fidaxomicin in hospitalised patients with documented Clostridium difficile infection and the management of these patients (DAFNE), NCT02214771, www.ClinicalTrials.gov

    Higher third-generation cephalosporin prescription proportion is associated with lower probability of reducing carbapenem use: a nationwide retrospective study

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    The ongoing extended spectrum ÎČ-lactamase-producing Enterobacteriaceae (ESBL-PE) pandemic has led to an increasing carbapenem use, requiring release of guidelines for carbapenem usage in France in late 2010. We sought to determine factors associated with changes in carbapenem use in intensive care units (ICUs), medical and surgical wards between 2009 and 2013

    Antibiotiques chez le patient insuffisant rénal : actualisation des adaptations posologiques à la pratique clinique en infectiologie

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    Antibiotic prescription in chronic kidney disease patients poses a twofold problem. The appropriate use of antibacterial agents is essential to ensure efficacy and to prevent the emergence of resistance, and dosages should be adapted to the renal function to prevent adverse effects. SiteGPR is a French website for health professionals to help with prescriptions to chronic kidney disease patients. A working group of infectious disease specialists and nephrology pharmacists reviewed the indications, dosing regimens, administration modalities, and dose adjustments of antibiotics marketed in France for patients with renal failure. Data available on the SiteGPR website and detailed in the present article aims to provide an evidence-based update of infectious disease recommendations to health professionals managing patients with chronic kidney disease

    Chitosan and cyclodextrin polymer based sponge for the treatment of diabetic foot infections

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    Les infections du pied diabĂ©tique sont la complication la plus frĂ©quente nĂ©cessitant l’hospitalisation des patients atteints de diabĂšte. Ces infections sont la consĂ©quence de plusieurs complications liĂ©es Ă  l’hyperglycĂ©mie chronique. C’est aussi l’évĂšnement le plus commun amenant Ă  une amputation des extrĂ©mitĂ©s. Elles sont associĂ©es Ă  une morbi-mortalitĂ© trĂšs Ă©levĂ©e,particuliĂšrement quand l’os est infectĂ©. Leur prise en charge est lourde, longue avec un risque de rechute important. Leur traitement repose sur des actes chirurgicaux, des soins infirmiers et une antibiothĂ©rapie par voie systĂ©mique. Les artĂ©riopathies dont souffrent les patients diabĂ©tiques et les tissus nĂ©crosĂ©s mal vascularisĂ©s entourant les plaies engendrent une mauvaise pĂ©nĂ©trance des antibiotiques au site infectĂ©, avec de possible sĂ©lections de rĂ©sistances bactĂ©riennes. Ces infections sont donc particuliĂšrement difficiles Ă  soigner. Dans ce contexte, l’objectif de ce travail est de dĂ©velopper un dispositif mĂ©dical pour la libĂ©ration locale d’antibiotiques. Ce dispositif consiste en une Ă©ponge conçue Ă  base de deux polyĂ©lectrolytes, obtenue par lyophilisation. Le chitosan est un polymĂšre cationique en condition acide et le polymĂšre de cyclodextrines est anionique et rĂ©sulte d’une rĂ©action de rĂ©ticulation entre les cyclodextrines et l’acide citrique. Les cyclodextrines sont des molĂ©cules cages capables de former des complexes d’inclusion avec des principes actifs. Ces complexes permettent de libĂ©rer les mĂ©dicaments de façon prolongĂ©e. Les Ă©ponges sont imprĂ©gnĂ©es dans des solutions d’antibiotiques et sont destinĂ©es Ă  ĂȘtre implantĂ©es dans la lĂ©sion infectĂ©e. La libĂ©ration locale permet d’augmenter les concentrations au niveau de la plaie sans risque de toxicitĂ© pour l’organisme et Ă©vite l’émergence de bactĂ©ries rĂ©sistantes.Diabetic foot infections are the most common complication requiring hospitalization ofpatients with diabetes. These infections are the result of many complications related to chronichyperglycemia. They often result in extremities amputation and are associated with a high morbimortality,especially when bone is infected. Their treatment is based on surgical procedures, nursingcare and systemic antibiotic therapy for several weeks, with a significant risk of relapse. Because of abasic low blood flow and diabetic foot infections damages, blood supply is decreased causing a lowantibiotic diffusion in the infected site and possible bacterial resistance selections. Therefore, they are particularly difficult to treat. In this context, the objective of this work is to develop a medical devicefor a local antibiotics release. We designed a sponge based on two polyelectrolytes (chitosan andcylodextrin polymer) and obtained by freeze-drying. Chitosan is a cationic polymer under acid condition and the cyclodextrin polymer is anionic and results from the crosslinking reaction between cyclodextrins and citric acid. Cyclodextrins are molecular cages able to form inclusion complexes with drugs, leading to an extended release. Sponges are impregnated in antibiotics solutions and are intended to be implanted in the infected lesion. Local release increases concentrations in the wound without risks of toxicity to the body and prevents the emergence of resistant bacteria
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