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SARS-Cov-2 Prevalence and Seroprevalence Among Healthcare Workers in Belgian Hospitals: Baseline Results of a Prospective Cohort Study
medRxiv preprint doi: https://doi.org/10.1101/2020.10.03.20204545; this version posted October 6, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license . Title: SARS-CoV-2 Prevalence and Seroprevalence among Healthcare Workers in Belgian Hospitals: Baseline Results of a Prospective Cohort Study Authors*: Laure Mortgat1,2, MD Cyril Barbezange3, PhD Natalie Fischer3,4, PhD Leo Heyndrickx5, MSc Veronik Hutse3, PhD Isabelle Thomas3, PhD Bea Vuylsteke6, PhD Kevin Arien5,7,8, PhD Isabelle Desombere3,8, PhD Els Duysburgh1,8, PhD Affiliations: 1. Department of Epidemiology and Public Health, Sciensano, Brussels, Belgium 2. European Programme for Intervention Epidemiology Training (EPIET), European Centre for Disease Prevention and Control (ECDC), Stockholm, Sweden 3. Department of Infectious diseases in humans, Sciensano, Brussels, Belgium 4. European Public Health Microbiology Training (EUPHEM), European Centre for Disease Prevention and Control (ECDC), Stockholm, Sweden 5. Department of Biomedical Sciences, Institute of Tropical Medicine, Antwerp, Belgium 6. Department of Public Health, Institute of Tropical Medicine, Antwerp, Belgium 7. University of Antwerp 8. Equal contributions as last author *alphabetical order for middle authors Corresponding author: Laure Mortgat, Rue Juliette Wytsman 14, 1050 Brussels, BelgiumNOTE: This preprint reports new research that has not been certified by peer review and should not be used to guide clinical practice. [email protected], + 32 2 642 57 42 medRxiv preprint doi: https://doi.org/10.1101/2020.10.03.20204545; this version posted October 6, 2020. -
Moves to Amend HF No. 2711 As Follows
05/05/20 REVISOR KLL/JK A20-0767 1.1 .................... moves to amend H.F. No. 2711 as follows: 1.2 Delete everything after the enacting clause and insert: 1.3 "ARTICLE 1 1.4 APPROPRIATIONS 1.5 Section 1. APPROPRIATIONS. 1.6 The sums shown in the column under "APPROPRIATIONS" are added to or reduce the 1.7 appropriations in Laws 2019, First Special Session chapter 5, to the agencies and for the 1.8 purposes specified in this article. The appropriations are from the general fund, or another 1.9 named fund, and are available for the fiscal year indicated for each purpose. 1.10 APPROPRIATIONS 1.11 Available for the Year 1.12 Ending June 30 1.13 2020 2021 1.14 Sec. 2. CORRECTIONS 1.15 Subdivision 1. Total Appropriation $ 205,000 $ 5,545,000 1.16 The amounts that may be spent for each 1.17 purpose are specified in the following 1.18 subdivisions. 1.19 Subd. 2. Correctional Institutions -0- (2,545,000) 1.20 To account for overall bed impact savings of 1.21 reductions in the penalties for controlled 1.22 substances offenses involving the possession 1.23 of marijuana, investments in community 1.24 supervision, and increased penalties for sex 1.25 trafficking offenses, the fiscal year 2021 Article 1 Sec. 2. 1 05/05/20 REVISOR KLL/JK A20-0767 2.1 appropriation from Laws 2019, First Special 2.2 Session chapter 5, article 1, section 15, 2.3 subdivision 2, is reduced by $2,545,000. 2.4 Subd. -
Covid-19 Surveillance in Residential Institutions
HEALTHCARE-ASSOCIATED INFECTIONS AND ANTIMICROBIAL RESISTANCE COVID-19 SURVEILLANCE IN RESIDENTIAL INSTITUTIONS Version 4.2 – 11/01/2021 _ S. DEQUEKER • K. LATOUR • E. ISLAMAJ • L. INT PANIS • M. CALLIES • L. CATTEAU • B. CATRY • E. VANDAEL W HO WE ARE _ SCIENSANO can count on more than 700 staff members who commit themselves, day after day, to achieving our motto: Healthy all lifelong. As our name suggests, science and health are central to our mission. Sciensano’s strength and uniqueness lie within the holistic and multidisciplinary approach to health. More particularly we focus on the close and indissoluble interconnection between human and animal health and their environment (the “One health” concept). By combining different research perspectives within this framework, Sciensano contributes in a unique way to everybody’s health. For this, Sciensano builds on the more than 100 years of scientific expertise of the former Veterinary and Agrochemical Research Centre (CODA-CERVA) and the ex-Scientific Institute of Public Health (WIV-ISP). 2 Sciensano Epidemiology and public health - Healthcare-associated infections and antimicrobial resistance Long-term care facilities December 2020 • Brussels • Belgium _ S. Dequeker1 • K. Latour1 • E. Islamaj1 • L. Int Panis1 • M. Callies1 • L. Catteau1 • B. Catry1 • E. Vandael1 1 Sciensano, Epidemiology and public health, Healthcare-associated infections and antimicrobial resistance, Brussels Contactperson: S. Dequeker • T+32 2 642 52 34 • [email protected] Please cite as: S. Dequeker, K. Latour, E. Islamaj, L. Int Panis, M. Callies, L. Catteau, B. Catry, E. Vandael. COVID-19 surveillance in residential institutions. Brussels, Belgium : Sciensano ; 2020 24p. TABLE OF CONTENTS TABLE OF CONTENTS ........................................................................................................................................ -
Belgium-Luxembourg-7-Preview.Pdf
©Lonely Planet Publications Pty Ltd Belgium & Luxembourg Bruges, Ghent & Antwerp & Northwest Belgium Northeast Belgium p83 p142 #_ Brussels p34 Wallonia p183 Luxembourg p243 #_ Mark Elliott, Catherine Le Nevez, Helena Smith, Regis St Louis, Benedict Walker PLAN YOUR TRIP ON THE ROAD Welcome to BRUSSELS . 34 ANTWERP Belgium & Luxembourg . 4 Sights . 38 & NORTHEAST Belgium & Luxembourg Tours . .. 60 BELGIUM . 142 Map . 6 Sleeping . 62 Antwerp (Antwerpen) . 144 Belgium & Luxembourg’s Eating . 65 Top 15 . 8 Around Antwerp . 164 Drinking & Nightlife . 71 Westmalle . 164 Need to Know . 16 Entertainment . 76 Turnhout . 165 First Time Shopping . 78 Lier . 167 Belgium & Luxembourg . .. 18 Information . 80 Mechelen . 168 If You Like . 20 Getting There & Away . 81 Leuven . 174 Getting Around . 81 Month by Month . 22 Hageland . 179 Itineraries . 26 Diest . 179 BRUGES, GHENT Hasselt . 179 Travel with Children . 29 & NORTHWEST Haspengouw . 180 Regions at a Glance . .. 31 BELGIUM . 83 Tienen . 180 Bruges . 85 Zoutleeuw . 180 Damme . 103 ALEKSEI VELIZHANIN / SHUTTERSTOCK © SHUTTERSTOCK / VELIZHANIN ALEKSEI Sint-Truiden . 180 Belgian Coast . 103 Tongeren . 181 Knokke-Heist . 103 De Haan . 105 Bredene . 106 WALLONIA . 183 Zeebrugge & Western Wallonia . 186 Lissewege . 106 Tournai . 186 Ostend (Oostende) . 106 Pipaix . 190 Nieuwpoort . 111 Aubechies . 190 Oostduinkerke . 111 Ath . 190 De Panne . 112 Lessines . 191 GALERIES ST-HUBERT, Beer Country . 113 Enghien . 191 BRUSSELS P38 Veurne . 113 Mons . 191 Diksmuide . 114 Binche . 195 MISTERVLAD / HUTTERSTOCK © HUTTERSTOCK / MISTERVLAD Poperinge . 114 Nivelles . 196 Ypres (Ieper) . 116 Waterloo Ypres Salient . 120 Battlefield . 197 Kortrijk . 123 Louvain-la-Neuve . 199 Oudenaarde . 125 Charleroi . 199 Geraardsbergen . 127 Thuin . 201 Ghent . 128 Aulne . 201 BRABO FOUNTAIN, ANTWERP P145 Contents UNDERSTAND Belgium & Luxembourg Today . -
Semaine / Week 11 (09/02/2020 – 15/03/2020)
INFECTIOUS DISEASES IN HUMANS - VIRAL DISEASES – NRC INFLUENZA EPIDEMIOLOGY AND PUBLIC HEALTH - EPIDEMIOLOGY OF INFECTIOUS DISEASES W EKELIJKS I NFLUENZA BULLETIN B ULLETIN HEBDOMADAIRE I NFLUENZA W EEKLY I NFLUENZA BULLETIN Semaine / week 11 (09/02/2020 – 15/03/2020) 1 Sciensano Epidemiology and public health - Epidemiology of infectious diseases Infectious diseases in humans - Viral diseases – NRC Influenza Met de financiële steun van Contact Persons: Epidemiological data: Nathalie Bossuyt • [email protected] Dieter Van Cauteren • [email protected] Natalia Bustos Sierra • [email protected] (Mortality) Virological data: Isabelle Thomas • [email protected] Cyril Barbezange • [email protected] Report number: ISSN 2593-4309 Available on: https://epidemio.wiv-isp.be/ID/diseases/Pages/Influenza.aspx 2 OVERZICHT WEEK 11 R ÉSUMÉ SEMAINE 11 OVERVIEW WEEK 11 In de afgelopen week steeg de to- La semaine passée, l’incidence de Last week, the incidence of visits to tale incidentie van raadplegingen consultations chez le médecin géné- the general practitioner for influ- voor griepaal syndroom tot 448 raliste pour syndrome grippal a aug- enza like illness increased to 448 raadplegingen per 100.000 inwo- menté jusqu’à 448 consultations consultations per 100,000 inhabit- ners (inclusief telefonische raadple- pour 100.000 habitants (consulta- ants (including contact by phone). gingen). De incidentie stijgt in alle tions téléphoniques inclus). L’inci- The incidence increases in all age leeftijdsgroepen in Wallonië en dence augmente dans chaque groups in the Walloon and Brussels Brussel en bij kinderen in Vlaande- tranche d’âge en Wallonie et chez Region and among children in the ren. -
The Expression of Hemagglutinin by a Recombinant Newcastle Disease Virus Causes Structural Changes and Alters Innate Immune Sensing
Article The Expression of Hemagglutinin by a Recombinant Newcastle Disease Virus Causes Structural Changes and Alters Innate Immune Sensing Fiona Ingrao 1,* , Victoria Duchatel 1, Isabel Fernandez Rodil 2, Mieke Steensels 1, Eveline Verleysen 3, Jan Mast 3 and Bénédicte Lambrecht 1 1 Service of Avian Virology and Immunology, Sciensano, 1180 Brussels, Belgium; [email protected] (V.D.); [email protected] (M.S.); [email protected] (B.L.) 2 Institut de Biologie et Médecine Moléculaire, Université Libre de Bruxelles, 6041 Gosselies, Belgium; [email protected] 3 Service of Trace Elements and Nanomaterials, Sciensano, 1180 Brussels, Belgium; [email protected] (E.V.); [email protected] (J.M.) * Correspondence: fi[email protected] Abstract: Recombinant Newcastle disease viruses (rNDV) have been used as bivalent vectors for vaccination against multiple economically important avian pathogens. NDV-vectored vaccines ex- pressing the immunogenic H5 hemagglutinin (rNDV-H5) are considered attractive candidates to protect poultry from both highly pathogenic avian influenza (HPAI) and Newcastle disease (ND). However, the impact of the insertion of a recombinant protein, such as H5, on the biological charac- teristics of the parental NDV strain has been little investigated to date. The present study compared Citation: Ingrao, F.; Duchatel, V.; a rNDV-H5 vaccine and its parental NDV LaSota strain in terms of their structural and functional Rodil, I.F.; Steensels, M.; Verleysen, E.; characteristics, as well as their recognition by the innate immune sensors. Structural analysis of the Mast, J.; Lambrecht, B. The rNDV-H5 demonstrated a decreased number of fusion (F) and a higher number of hemagglutinin- Expression of Hemagglutinin by a Recombinant Newcastle Disease neuraminidase (HN) glycoproteins compared to NDV LaSota. -
Page 1 1 HEALTHCARE-ASSOCIATED
HEALTHCARE-ASSOCIATED INFECTIONS AND ANTIMICROBIAL RESISTANCE S URVEILLANCE OF ANTIMICROBIAL RESISTA NT BACTERIA IN B ELGIAN HOSPITALS Report 2018 – 1 EXECUTIVE SUMMARY W HO WE ARE – SCIENSANO can count on more than 700 staff members who commit themselves, day after day, to achieving our motto: Healthy all life long. As our name suggests, science and health are central to our mission. Sciensano’s strength and uniqueness lie within the holistic and multidisciplinary approach to health. More particularly we focus on the close and indissoluble interconnection between human and animal health and their environment (the “One health” concept). By combining different research perspectives within this framework, Sciensano contributes in a unique way to everybody’s health. For this, Sciensano builds on the more than 100 years of scientific expertise of the former Veterinary and Agrochemical Research Centre (CODA-CERVA) and the ex-Scientific Institute of Public Health (WIV-ISP). 2 Sciensano Epidemiology and public health – Healthcare-associated infections and antimicrobial resistance January 2020 • Brussels • Belgium Internal reference number: D/2020/14.440/8 ISSN: 2593-7073 – Latour K.1 In collaboration with Prof. Dr. Herman Goossens2, Dr. Marie Hallin3, Prof. Dr. Te-Din Huang4 1 Sciensano, Epidemiology and public health, Healthcare-associated infections and antimicrobial resistance, Brussels 2 National reference centre for resistant enterococci, Universiteit Antwerpen, UZ Antwerpen, Antwerpen 3. National reference centre for Staphylococcus aureus, Université Libre de Bruxelles, Hôpital Erasme, Brussels 4. National reference centre for resistant Gram-negative bacilli, Université Catholique de Louvain, CHU UCL Namur (Godinne), Yvoir Katrien Latour • T+32 2 642 57 62 • [email protected] Partners The surveillances of antimicrobial resistant bacteria are organised with the support of the Belgian Antibiotic Policy Coordination Committee (BAPCOC) and are financially supported by the Federal Public Service Public Health, Food Chain Safety and Environment. -
Model Scheduling New/Novel Psychoactive Substances Act (Third Edition)
Model Scheduling New/Novel Psychoactive Substances Act (Third Edition) July 1, 2019. This project was supported by Grant No. G1799ONDCP03A, awarded by the Office of National Drug Control Policy. Points of view or opinions in this document are those of the author and do not necessarily represent the official position or policies of the Office of National Drug Control Policy or the United States Government. © 2019 NATIONAL ALLIANCE FOR MODEL STATE DRUG LAWS. This document may be reproduced for non-commercial purposes with full attribution to the National Alliance for Model State Drug Laws. Please contact NAMSDL at [email protected] or (703) 229-4954 with any questions about the Model Language. This document is intended for educational purposes only and does not constitute legal advice or opinion. Headquarters Office: NATIONAL ALLIANCE FOR MODEL STATE DRUG 1 LAWS, 1335 North Front Street, First Floor, Harrisburg, PA, 17102-2629. Model Scheduling New/Novel Psychoactive Substances Act (Third Edition)1 Table of Contents 3 Policy Statement and Background 5 Highlights 6 Section I – Short Title 6 Section II – Purpose 6 Section III – Synthetic Cannabinoids 13 Section IV – Substituted Cathinones 19 Section V – Substituted Phenethylamines 23 Section VI – N-benzyl Phenethylamine Compounds 25 Section VII – Substituted Tryptamines 28 Section VIII – Substituted Phenylcyclohexylamines 30 Section IX – Fentanyl Derivatives 39 Section X – Unclassified NPS 43 Appendix 1 Second edition published in September 2018; first edition published in 2014. Content in red bold first added in third edition. © 2019 NATIONAL ALLIANCE FOR MODEL STATE DRUG LAWS. This document may be reproduced for non-commercial purposes with full attribution to the National Alliance for Model State Drug Laws. -
Appendix-2Final.Pdf 663.7 KB
North West ‘Through the Gate Substance Misuse Services’ Drug Testing Project Appendix 2 – Analytical methodologies Overview Urine samples were analysed using three methodologies. The first methodology (General Screen) was designed to cover a wide range of analytes (drugs) and was used for all analytes other than the synthetic cannabinoid receptor agonists (SCRAs). The analyte coverage included a broad range of commonly prescribed drugs including over the counter medications, commonly misused drugs and metabolites of many of the compounds too. This approach provided a very powerful drug screening tool to investigate drug use/misuse before and whilst in prison. The second methodology (SCRA Screen) was specifically designed for SCRAs and targets only those compounds. This was a very sensitive methodology with a method capability of sub 100pg/ml for over 600 SCRAs and their metabolites. Both methodologies utilised full scan high resolution accurate mass LCMS technologies that allowed a non-targeted approach to data acquisition and the ability to retrospectively review data. The non-targeted approach to data acquisition effectively means that the analyte coverage of the data acquisition was unlimited. The only limiting factors were related to the chemical nature of the analyte being looked for. The analyte must extract in the sample preparation process; it must chromatograph and it must ionise under the conditions used by the mass spectrometer interface. The final limiting factor was presence in the data processing database. The subsequent study of negative MDT samples across the North West and London and the South East used a GCMS methodology for anabolic steroids in addition to the General and SCRA screens. -
Schifano, F., Napoletano, F., Chiappini, S., Orsolini, L., Guirguis, A., Corkery, J
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by University of Hertfordshire Research Archive Citation for the published version: Schifano, F., Napoletano, F., Chiappini, S., Orsolini, L., Guirguis, A., Corkery, J. M., ... vento, A. (2019). New psychoactive substances (NPS), psychedelic experiences, and dissociation: clinical and clinical pharmacological issues. Current Addiction Reports, 6(2), 140-152. https://doi.org/10.1007/s40429-019-00249-z Document Version: Accepted Version The final publication is available at Springer Nature via https://doi.org/10.1007/s40429-019-00249-z © 2019 Springer Nature Publishing AG General rights Copyright© and Moral Rights for the publications made accessible on this site are retained by the individual authors and/or other copyright owners. Please check the manuscript for details of any other licences that may have been applied and it is a condition of accessing publications that users recognise and abide by the legal requirements associated with these rights. You may not engage in further distribution of the material for any profitmaking activities or any commercial gain. You may freely distribute both the url (http://uhra.herts.ac.uk/) and the content of this paper for research or private study, educational, or not-for-profit purposes without prior permission or charge. Take down policy If you believe that this document breaches copyright please contact us providing details, any such items will be temporarily removed from the repository pending investigation. -
Alcohol and Drug Abuse Subchapter 9
Chapter 8 – Alcohol and Drug Abuse Subchapter 9 Regulated Drug Rule 1.0 Authority This rule is established under the authority of 18 V.S.A. §§ 4201 and 4202 which authorizes the Vermont Board of Health to designate regulated drugs for the protection of public health and safety. 2.0 Purpose This rule designates drugs and other chemical substances that are illegal or judged to be potentially fatal or harmful for human consumption unless prescribed and dispensed by a professional licensed to prescribe or dispense them and used in accordance with the prescription. The rule restricts the possession of certain drugs above a specified quantity. The rule also establishes benchmark unlawful dosages for certain drugs to provide a baseline for use by prosecutors to seek enhanced penalties for possession of higher quantities of the drug in accordance with multipliers found at 18 V.S.A. § 4234. 3.0 Definitions 3.1 “Analog” means one of a group of chemical components similar in structure but different with respect to elemental composition. It can differ in one or more atoms, functional groups or substructures, which are replaced with other atoms, groups or substructures. 3.2 “Benchmark Unlawful Dosage” means the quantity of a drug commonly consumed over a twenty-four-hour period for any therapeutic purpose, as established by the manufacturer of the drug. Benchmark Unlawful dosage is not a medical or pharmacologic concept with any implication for medical practice. Instead, it is a legal concept established only for the purpose of calculating penalties for improper sale, possession, or dispensing of drugs pursuant to 18 V.S.A. -
G.S. 90-89 Page 1 § 90-89. Schedule I Controlled Substances. This
§ 90-89. Schedule I controlled substances. This schedule includes the controlled substances listed or to be listed by whatever official name, common or usual name, chemical name, or trade name designated. In determining that a substance comes within this schedule, the Commission shall find: a high potential for abuse, no currently accepted medical use in the United States, or a lack of accepted safety for use in treatment under medical supervision. The following controlled substances are included in this schedule: (1) Opiates. – Any of the following opiates or opioids, including the isomers, esters, ethers, salts and salts of isomers, esters, and ethers, unless specifically excepted, or listed in another schedule, whenever the existence of such isomers, esters, ethers, and salts is possible within the specific chemical designation: a. Acetyl-alpha-methylfentanyl (N[1-(1-methyl-2-phenethyl)-4-piperidinyl]-N-phenylacet amide). b. Acetylmethadol. c. Repealed by Session Laws 1987, c. 412, s. 2. d. Alpha-methylthiofentanyl (N-[1-methyl-2-(2-thienyl)ethyl/-4-piperidinyl]-N-phenylpro panamide). e. Allylprodine. f. Alphacetylmethadol (except levo-alphacetylmethadol, also known as levomethadyl acetate and LAAM). g. Alphameprodine. h. Alphamethadol. i. Alpha-methylfentanyl (N-(1-(alpha-methyl-beta-phenyl) ethyl-4-piperidyl) propionalilide; 1(1-methyl-2-phenyl-ethyl)-4-(N-propanilido) piperidine). j. Benzethidine. k. Betacetylmethadol. l. Beta-hydroxfentanyl (N-[1-(2-hydroxy-2-phenethyl)-4-piperidinyl]-N-phenylpropanamide ). m. Beta-hydroxy-3-methylfentanyl (N-[1-(2-hydroxy-2-phenethyl)-3-methyl-4-piperidinyl]-N-phenylpro panamide). n. Betameprodine. o. Betamethadol. p. Betaprodine. q. Clonitazene. r. Dextromoramide. s. Diampromide. t. Diethylthiambutene. u.