32 research outputs found

    COVID-19 symptoms at hospital admission vary with age and sex: results from the ISARIC prospective multinational observational study

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    Background: The ISARIC prospective multinational observational study is the largest cohort of hospitalized patients with COVID-19. We present relationships of age, sex, and nationality to presenting symptoms. Methods: International, prospective observational study of 60 109 hospitalized symptomatic patients with laboratory-confirmed COVID-19 recruited from 43 countries between 30 January and 3 August 2020. Logistic regression was performed to evaluate relationships of age and sex to published COVID-19 case definitions and the most commonly reported symptoms. Results: ‘Typical’ symptoms of fever (69%), cough (68%) and shortness of breath (66%) were the most commonly reported. 92% of patients experienced at least one of these. Prevalence of typical symptoms was greatest in 30- to 60-year-olds (respectively 80, 79, 69%; at least one 95%). They were reported less frequently in children (≀ 18 years: 69, 48, 23; 85%), older adults (≄ 70 years: 61, 62, 65; 90%), and women (66, 66, 64; 90%; vs. men 71, 70, 67; 93%, each P < 0.001). The most common atypical presentations under 60 years of age were nausea and vomiting and abdominal pain, and over 60 years was confusion. Regression models showed significant differences in symptoms with sex, age and country. Interpretation: This international collaboration has allowed us to report reliable symptom data from the largest cohort of patients admitted to hospital with COVID-19. Adults over 60 and children admitted to hospital with COVID-19 are less likely to present with typical symptoms. Nausea and vomiting are common atypical presentations under 30 years. Confusion is a frequent atypical presentation of COVID-19 in adults over 60 years. Women are less likely to experience typical symptoms than men

    Barriers to and Enablers of Implementation of High-Value Interventions by Renal Pharmacists: A Qualitative Study Informed by the Theoretical Domains Framework

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    ABSTRACTBackground: Previous studies have shown that patients with chronic kidney disease who are followed by a renal clinical pharmacist have improved clinical outcomes. In 2016, a consensus list of quality indicator drug therapy problems (QI-DTPs) was developed by renal clinical pharmacists to help prioritize which renal patients should receive interventions. Before QI-DTP interventions can be implemented in clinical practice, barriers to and enablers of their use need to be identified, to allow development of strategies to overcome the barriers and apply the enablers.Objective: To identify modifiable barriers to and enablers of implementation of renal QI-DTP interventions by renal clinical pharmacists.Methods: In this exploratory qualitative descriptive study, one-on-one, semistructured, audio-recorded telephone interviews were conducted with renal clinical pharmacists to identify the barriers to and enablers of implementation of renal QI-DTP interventions. The interviews consisted of questions developed according to the Theoretical Domains Framework.Results: Interviews were conducted with 13 renal pharmacists from across Canada. The main barriers to implementation of renal QI-DTP interventions that participants identified were knowledge gaps, prioritization, and nephrologist acceptance. The main enablers identified were training, colleague support, and better patient care.Conclusion: Three barriers to and three enablers of implementation of renal QI-DTP interventions were identified. These barriers and enablers can be used to help with pharmacist education and to optimize the care that pharmacists provide to renal patients.RÉSUMÉContexte : Des Ă©tudes prĂ©cĂ©dentes dĂ©montrent une amĂ©lioration des rĂ©sultats cliniques de patients souffrant d’une maladie rĂ©nale chronique, qui sont suivis par un pharmacien clinicien en nĂ©phrologie. En 2016, des pharmaciens cliniciens en nĂ©phrologie ont mis au point une liste consensuelle des indicateurs de qualitĂ© des problĂšmes de pharmacothĂ©rapie (QI-DTP) pour les aider Ă  prioriser les patients souffrant d’une insuffisance rĂ©nale, qui doivent subir une intervention. Avant de mettre en place ces QI-DTP en pratique clinique, on doit dĂ©terminer les Ă©lĂ©ments qui entravent et facilitent leur utilisation pour pouvoir Ă©laborer des stratĂ©gies visant Ă  surmonter les obstacles et Ă  appliquer les Ă©lĂ©ments facilitateurs.Objectif :DĂ©terminer les Ă©lĂ©ments modifiables qui entravent et facilitent la mise en place des QI-DTP par les pharmaciens cliniciens en nĂ©phrologie lors d’interventions rĂ©nales.MĂ©thodes : Dans cette Ă©tude exploratoire, descriptive et qualitative, des entretiens tĂ©lĂ©phoniques individuels, semi structurĂ©s et enregistrĂ©s ont Ă©tĂ© menĂ©s auprĂšs de pharmaciens cliniciens en nĂ©phrologie pour determiner les Ă©lĂ©ments qui entravent et facilitent la mise en place de QI-DTP lors d’interventions rĂ©nales. Les entretiens consistaient en des questions prĂ©parĂ©es selon le Theoretical Domains Framework.RĂ©sultats : Les entretiens ont Ă©tĂ© menĂ©s auprĂšs de 13 pharmaciens en nĂ©phrologie de partout au Canada. Les principaux Ă©lĂ©ments entravant la mise en place de QI-DTP lors d’interventions rĂ©nales dĂ©terminĂ©es par les participants Ă©taient : le manque de connaissances, la priorisation et l’acception des nĂ©phrologues. Les principaux Ă©lĂ©ments facilitant la tĂąche Ă©taient : la formation, le soutien des collĂšgues et de meilleurs soins offerts aux patients.Conclusion : Trois Ă©lĂ©ments entravant et trois Ă©lĂ©ments facilitant la mise en place de QI-DTP lors d’interventions rĂ©nales ont Ă©tĂ© dĂ©terminĂ©s. Ils peuvent ĂȘtre utilisĂ©s pour contribuer Ă  la formation du pharmacien et pour optimiser les soins offerts aux patients qui souffrent d’insuffisance rĂ©nale

    Fragment-based discovery of a new family of non-peptidic small-molecule cyclophilin inhibitors with potent antiviral activities

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    International audienceCyclophilins are peptidyl-prolyl cis/trans isomerases (PPIase) that catalyse the interconversion of the peptide bond at proline residues. Several cyclophilins play a pivotal role in the life cycle of a number of viruses. The existing cyclophilin inhibitors, all derived from cyclosporine A or sanglifehrin A, have disadvantages, including their size, potential for side effects unrelated to cyclophilin inhibition and drug–drug interactions, unclear antiviral spectrum and manufacturing issues. Here we use a fragment-based drug discovery approach using nucleic magnetic resonance, X-ray crystallography and structure-based compound optimization to generate a new family of non-peptidic, small-molecule cyclophilin inhibitors with potent in vitro PPIase inhibitory activity and antiviral activity against hepatitis C virus, human immunodeficiency virus and coronaviruses. This family of compounds has the potential for broad-spectrum, high-barrier-to-resistance treatment of viral infections

    Trachelospermum asiaticum Nakai

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    ćŽŸè‘—ć’Œć: ăƒ†ă‚€ă‚«ă‚«ăƒ…ăƒ©ç§‘ć: キョォチクトォ科 = ApocynaceaeæŽĄé›†ćœ°: ćƒè‘‰çœŒ ć››èĄ—é“ćž‚ 物äș• (䞋総 ć››èĄ—é“ćž‚ 物äș•)æŽĄé›†æ—„: 1996/6/16æŽĄé›†è€…: 萩ćș­äžˆćŁœæ•Žç†ç•Șć·: JH033730ć›œç«‹ç§‘ć­Šćšç‰©é€šæ•Žç†ç•Șć·: TNS-VS-98373

    Histone variant H2A.J accumulates in senescent cells and promotes inflammatory gene expression

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    International audienceThe senescence of mammalian cells is characterized by a proliferative arrest in response to stress and the expression of an inflammatory phenotype. Here we show that histone H2A.J, a poorly studied H2A variant found only in mammals, accumulates in human fibroblasts in senescence with persistent DNA damage. H2A.J also accumulates in mice with aging in a tissue-specific manner and in human skin. Knock-down of H2A.J inhibits the expression of inflammatory genes that contribute to the senescent-associated secretory phenotype (SASP), and over expression of H2A.J increases the expression of some of these genes in proliferating cells. H2A.J accumulation may thus promote the signalling of senescent cells to the immune system, and it may contribute to chronic inflammation and the development of aging-associated diseases

    High-risk exposure without personal protective equipment and infection with SARS-CoV-2 in-hospital workers - The CoV-CONTACT cohort.

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