Norm Norm-Vet 2013

Total Page:16

File Type:pdf, Size:1020Kb

Norm Norm-Vet 2013 2O13 NORM NORM-VET Usage of Antimicrobial Agents and Occurrence of Antimicrobial Resistance in Norway DESIGN, FORSIDE: IDA SKAAR IDA FORSIDE: DESIGN, – SVANEGODKJENT TRYKKSAK – 241 762 241 – TRYKKSAK SVANEGODKJENT – ISSN: 1502-2307 (print) / 1890-9965 (electronic) AS MEDIA LUNDBLAD 2013 NORM NORM-VET Usage of Antimicrobial Agents and Occurrence of Antimicrobial Resistance in Norway ISSN: 1502-2307 (print) / 1890-9965 (electronic) Any use of data from NORM/NORM-VET 2013 should include specific reference to this report. Suggested citation: NORM/NORM-VET 2013. Usage of Antimicrobial Agents and Occurrence of Antimicrobial Resistance in Norway. Tromsø / Oslo 2014. ISSN:1502-2307 (print) / 1890-9965 (electronic). This report is available at www.vetinst.no and www.antibiotikaresistens.no 1 NORM / NORM-VET 2013 CONTRIBUTORS AND PARTICIPANTS Editors: Gunnar Skov Simonsen NORM, Univ. Hosp. of North Norway Anne Margrete Urdahl NORM-VET, Norwegian Veterinary Institute Authors: Cecilie Torp Andersen Candida spp. [email protected] Oslo Univ. Hosp. Trude Margrete Arnesen Tuberculosis [email protected] Norw. Inst. of Pub. Health Hege Salvesen Blix Antibiotic usage in humans [email protected] Norw. Inst. of Pub. Health Dominique Caugant Meningococci [email protected] Norw. Inst. of Pub. Health Petter Elstrøm MRSA [email protected] Norw. Inst. of Pub. Health Kari Grave Antibiotic usage in animals [email protected] Norw. Vet. Inst. Ina Haagensen Enteropathogenic bacteria from humans [email protected] Norw. Inst. of Pub. Health Kjersti Wik Larssen MRSA [email protected] St. Olav Univ. Hosp. Madelaine Norström Bacteria from animals [email protected] Norw. Vet. Inst. Gunnar Skov Simonsen Bacteria from humans [email protected] NORM, Univ. Hosp. of North Norw. Dagfinn Skaare Haemophilus influenzae [email protected] Vestfold Hospital, Tønsberg Jannice Schau Slettemeås Bacteria from animals [email protected] Norw. Vet. Inst. Martin Steinbakk Group A streptococci [email protected] Norw. Inst. of Pub. Health Marianne Sunde Bacteria from animals [email protected] Norw. Vet. Inst. Gaute Syversen Gonococci [email protected] Oslo Univ. Hosp. Ullevål Anne Margrete Urdahl Bacteria from animals [email protected] NORM-VET, Norw. Vet. Inst. Didrik Vestrheim Pneumococci [email protected] Norw. Inst. of Pub. Health Astrid Louise Wester Enteropathogenic baceria from humans [email protected] Norw. Inst. of Pub. Health Frode Width-Gran MRSA [email protected] St. Olav Univ. Hosp. Institutions participating in NORM-VET: Norwegian Food Safety Authority Kjell Hauge Norwegian Veterinary Institute, Dep. of Health Surveillance Anne Margrete Urdahl / Merete Hofshagen / Madelaine Norström / Kari Grave Norwegian Veterinary Institute, Dep. of Diagnostics Marianne Sunde / Jannice Schau Slettemeås / Aina Steihaug Barstad Institutions participating in NORM: Akershus University Hospital, Lørenskog, Department of Microbiology Trond Egil Ranheim / Marit Vattøy Førde Hospital, Department of Microbiology Reidar Hjetland / Astrid Vedde Haugesund Hospital, Department of Microbiology Liv Jorunn Sønsteby / Pirrko-Liisa Kellokumpu Haukeland Univ. Hospital, Bergen, Dep. of Microbiology Haima Mylvaganam / Torunn Sneide Haukeland Innlandet Hospital, Lillehammer, Department of Microbiology Carola Grub / Kari Ødegaard Levanger Hospital, Department of Microbiology Angela Kümmel / Anne-Kristine Lorås Molde Hospital, Department of Microbiology Einar Vik / Lisa Valle Norwegian Insititute of Public Health, Ref. Lab. for Enteropathogenic Bacteria Astrid Louise Wester / Trine-Lise Stavnes Norwegian Insititute of Public Health, Ref. Lab. for H. influenzae Martin Steinbakk / Gunnhild Rødal Norwegian Insititute of Public Health, Ref. Lab. for M. tuberculosis Turid Mannsåker / Kari Nilsen Norwegian Insititute of Public Health, Ref. Lab. for N. meningitidis Dominique Caugant / Inger Marie Saga Norwegian Insititute of Public Health, Ref. Lab. for S. pneumoniae Didrik Vestrheim / Anne Ramstad Alme Norwegian Insititute of Public Health, Ref. Lab. for S. pyogenes Martin Steinbakk / Anne Ramstad Alme Nordland Hospital, Bodø, Department of Microbiology Liisa Mortensen / Hege Elisabeth Larsen Oslo University Hospital, Radiumhospitalet, Laboratory of Microbiology Peter Gaustad / Sunniva Fagerås Røst Oslo University Hospital, Rikshospitalet, Institute of Medical Microbiology Peter Gaustad / Pia Langseth Oslo University Hospital, Rikshospitalet, Ref. Lab. for Mycology Cecilie Torp Andersen / Aina Myhre Oslo University Hospital, Ullevål, Department of Microbiology Gaute Syversen / Thea Bergheim Oslo University Hospital, Ullevål, Ref. Lab. for N. gonorrhoeae Gaute Syversen / Thea Bergheim Stavanger University Hospital, Department of Microbiology Olav Natås / Anita Løvås Brekken St. Olav University Hospital, Trondheim, Department of Microbiology Jan Egil Afset / Toril Nordtømme St. Olav University Hospital, Trondheim, Ref. Lab. for MRSA Lillian Marstein / Hege Snøsen Sørlandet Hospital, Kristiansand, Department of Microbiology Unn Houge / Ann Kristin Øverland-Glastad Unilabs Telelab A/S, Skien Andreas Emmert / Anne Ragnhild Oseid University Hospital of North Norway, Tromsø, Department of Microbiology Gunnar Skov Simonsen / Ellen Haldis Josefsen University Hospital of North Norway, Nat. Adv. Unit on Detection of AMR Ørjan Samuelsen / Bjørg C. Haldorsen Vestfold Hospital, Tønsberg, Department of Microbiology Dagfinn Skaare / Astrid Lia Vestre Viken - Bærum Hospital, Department of Medical Microbiology Annette Onken / Merriam Sundberg Vestre Viken - Drammen Hospital, Department of Medical Microbiology Krisztina Papp / Hanne Fanuelsen Østfold Hospital, Fredrikstad, Department of Microbiology Anita Kanestrøm / Anne Cathrine Hollekim Ålesund Hospital, Department of Microbiology Reidar Hide / Filip Angeles NORM reference group in 2013: Martin Steinbakk Norwegian Institute of Public Health, Oslo Dag Harald Skutlaberg Haukeland University Hospital, Bergen Anita Kanestrøm Østfold Hospital Trust, Fredrikstad Ståle Tofteland Norwegian Society for Medical Microbiology Thea Bergheim Norwegian Society of Engineers and Technologists Dag Berild Norwegian Society for Infectious Diseases Knut Eirik Eliassen Norwegian College of General Practitioners 2 NORM / NORM-VET 2013 CONTENTS CONTENTS I. Introduction ………………………………………………………………………………………............. 5 II. Sammendrag ..........……………………………………………………………………………….............. 6 III. Summary …………………………………………………………………………………………............ 9 IV. Population statistics.…………………………………………………………………………………........ 12 V. Usage of antimicrobial agents Usage in animals……………………………………………………………………………………...14 Usage in humans.…………………………………………………………………………………..... 18 VI. Occurrence of antimicrobial resistance A. Animal clinical isolates Staphylococcus pseudintermedius from dog ………...………………………………………. 28 B. Indicator bacteria from animals and food Escherichia coli from dogs, layers, turkey and turkey meat …............................................... 31 Extended-spectrum beta-lactamase (ESBL) producing Escherichia coli from dogs, layers, turkey and turkey meat ………………………………………………..……... 34 Enterococcus spp. from layers and turkey …………. ……………………..………………. 36 Vancomycin resistant Enterococcus spp. (VRE) from layers and turkey ………………….. 38 C. Zoonotic and non-zoonotic enteropathogenic bacteria Salmonella spp. ……………………….........................………………...................................... 39 Campylobacter spp. …………………………………. .............................................................. 47 Yersinia enterocolitica .. ……….........................……………………....................................... 51 Shigella spp. .………………….............……….........................…….................................. 52 D. Human clinical isolates Distribution of bacterial species in blood cultures .................................................................... 55 Escherichia coli in blood cultures ………………….............................................................. 57 Escherichia coli in urine ……………………………................................................................ 59 Klebsiella spp. in blood cultures .………………….................................................................... 61 Klebsiella spp. in urine ………………………………………………………………………. 63 Haemophilus influenzae in blood cultures and cerebrospinal fluids …………………………. 69 Neisseria meningitidis in blood cultures and cerebrospinal fluids …………………………… 70 Neisseria gonorrhoeae ……………………………………………………………………….. 71 Staphylococcus aureus in blood cultures …………............................................................... 72 Staphylococcus aureus in wound specimens ............................................................................. 73 Methicillin resistant Staphylococcus aureus (MRSA) infections in Norway 2013 …………… 75 Enterococcus spp. in blood cultures ….……………................................................................ 77 Streptococcus pneumoniae in blood cultures and cerebrospinal fluids ...................................... 82 Streptococcus pyogenes in blood cultures …………….. ………………………………......... 84 Streptococcus pyogenes in specimens from the respiratory tract and wounds .......................... 84 Mycobacterium tuberculosis …….……………......................................................................... 86 Candida spp. in blood cultures ............................................................................................
Recommended publications
  • The Role of Nanobiosensors in Therapeutic Drug Monitoring
    Journal of Personalized Medicine Review Personalized Medicine for Antibiotics: The Role of Nanobiosensors in Therapeutic Drug Monitoring Vivian Garzón 1, Rosa-Helena Bustos 2 and Daniel G. Pinacho 2,* 1 PhD Biosciences Program, Universidad de La Sabana, Chía 140013, Colombia; [email protected] 2 Therapeutical Evidence Group, Clinical Pharmacology, Universidad de La Sabana, Chía 140013, Colombia; [email protected] * Correspondence: [email protected]; Tel.: +57-1-8615555 (ext. 23309) Received: 21 August 2020; Accepted: 7 September 2020; Published: 25 September 2020 Abstract: Due to the high bacterial resistance to antibiotics (AB), it has become necessary to adjust the dose aimed at personalized medicine by means of therapeutic drug monitoring (TDM). TDM is a fundamental tool for measuring the concentration of drugs that have a limited or highly toxic dose in different body fluids, such as blood, plasma, serum, and urine, among others. Using different techniques that allow for the pharmacokinetic (PK) and pharmacodynamic (PD) analysis of the drug, TDM can reduce the risks inherent in treatment. Among these techniques, nanotechnology focused on biosensors, which are relevant due to their versatility, sensitivity, specificity, and low cost. They provide results in real time, using an element for biological recognition coupled to a signal transducer. This review describes recent advances in the quantification of AB using biosensors with a focus on TDM as a fundamental aspect of personalized medicine. Keywords: biosensors; therapeutic drug monitoring (TDM), antibiotic; personalized medicine 1. Introduction The discovery of antibiotics (AB) ushered in a new era of progress in controlling bacterial infections in human health, agriculture, and livestock [1] However, the use of AB has been challenged due to the appearance of multi-resistant bacteria (MDR), which have increased significantly in recent years due to AB mismanagement and have become a global public health problem [2].
    [Show full text]
  • National Antibiotic Consumption for Human Use in Sierra Leone (2017–2019): a Cross-Sectional Study
    Tropical Medicine and Infectious Disease Article National Antibiotic Consumption for Human Use in Sierra Leone (2017–2019): A Cross-Sectional Study Joseph Sam Kanu 1,2,* , Mohammed Khogali 3, Katrina Hann 4 , Wenjing Tao 5, Shuwary Barlatt 6,7, James Komeh 6, Joy Johnson 6, Mohamed Sesay 6, Mohamed Alex Vandi 8, Hannock Tweya 9, Collins Timire 10, Onome Thomas Abiri 6,11 , Fawzi Thomas 6, Ahmed Sankoh-Hughes 12, Bailah Molleh 4, Anna Maruta 13 and Anthony D. Harries 10,14 1 National Disease Surveillance Programme, Sierra Leone National Public Health Emergency Operations Centre, Ministry of Health and Sanitation, Cockerill, Wilkinson Road, Freetown, Sierra Leone 2 Department of Community Health, Faculty of Clinical Sciences, College of Medicine and Allied Health Sciences, University of Sierra Leone, Freetown, Sierra Leone 3 Special Programme for Research and Training in Tropical Diseases (TDR), World Health Organization, 1211 Geneva, Switzerland; [email protected] 4 Sustainable Health Systems, Freetown, Sierra Leone; [email protected] (K.H.); [email protected] (B.M.) 5 Unit for Antibiotics and Infection Control, Public Health Agency of Sweden, Folkhalsomyndigheten, SE-171 82 Stockholm, Sweden; [email protected] 6 Pharmacy Board of Sierra Leone, Central Medical Stores, New England Ville, Freetown, Sierra Leone; [email protected] (S.B.); [email protected] (J.K.); [email protected] (J.J.); [email protected] (M.S.); [email protected] (O.T.A.); [email protected] (F.T.) Citation: Kanu, J.S.; Khogali, M.; 7 Department of Pharmaceutics and Clinical Pharmacy & Therapeutics, Faculty of Pharmaceutical Sciences, Hann, K.; Tao, W.; Barlatt, S.; Komeh, College of Medicine and Allied Health Sciences, University of Sierra Leone, Freetown 0000, Sierra Leone 8 J.; Johnson, J.; Sesay, M.; Vandi, M.A.; Directorate of Health Security & Emergencies, Ministry of Health and Sanitation, Sierra Leone National Tweya, H.; et al.
    [Show full text]
  • Infant Antibiotic Exposure Search EMBASE 1. Exp Antibiotic Agent/ 2
    Infant Antibiotic Exposure Search EMBASE 1. exp antibiotic agent/ 2. (Acedapsone or Alamethicin or Amdinocillin or Amdinocillin Pivoxil or Amikacin or Aminosalicylic Acid or Amoxicillin or Amoxicillin-Potassium Clavulanate Combination or Amphotericin B or Ampicillin or Anisomycin or Antimycin A or Arsphenamine or Aurodox or Azithromycin or Azlocillin or Aztreonam or Bacitracin or Bacteriocins or Bambermycins or beta-Lactams or Bongkrekic Acid or Brefeldin A or Butirosin Sulfate or Calcimycin or Candicidin or Capreomycin or Carbenicillin or Carfecillin or Cefaclor or Cefadroxil or Cefamandole or Cefatrizine or Cefazolin or Cefixime or Cefmenoxime or Cefmetazole or Cefonicid or Cefoperazone or Cefotaxime or Cefotetan or Cefotiam or Cefoxitin or Cefsulodin or Ceftazidime or Ceftizoxime or Ceftriaxone or Cefuroxime or Cephacetrile or Cephalexin or Cephaloglycin or Cephaloridine or Cephalosporins or Cephalothin or Cephamycins or Cephapirin or Cephradine or Chloramphenicol or Chlortetracycline or Ciprofloxacin or Citrinin or Clarithromycin or Clavulanic Acid or Clavulanic Acids or clindamycin or Clofazimine or Cloxacillin or Colistin or Cyclacillin or Cycloserine or Dactinomycin or Dapsone or Daptomycin or Demeclocycline or Diarylquinolines or Dibekacin or Dicloxacillin or Dihydrostreptomycin Sulfate or Diketopiperazines or Distamycins or Doxycycline or Echinomycin or Edeine or Enoxacin or Enviomycin or Erythromycin or Erythromycin Estolate or Erythromycin Ethylsuccinate or Ethambutol or Ethionamide or Filipin or Floxacillin or Fluoroquinolones
    [Show full text]
  • AMEG Categorisation of Antibiotics
    12 December 2019 EMA/CVMP/CHMP/682198/2017 Committee for Medicinal Products for Veterinary use (CVMP) Committee for Medicinal Products for Human Use (CHMP) Categorisation of antibiotics in the European Union Answer to the request from the European Commission for updating the scientific advice on the impact on public health and animal health of the use of antibiotics in animals Agreed by the Antimicrobial Advice ad hoc Expert Group (AMEG) 29 October 2018 Adopted by the CVMP for release for consultation 24 January 2019 Adopted by the CHMP for release for consultation 31 January 2019 Start of public consultation 5 February 2019 End of consultation (deadline for comments) 30 April 2019 Agreed by the Antimicrobial Advice ad hoc Expert Group (AMEG) 19 November 2019 Adopted by the CVMP 5 December 2019 Adopted by the CHMP 12 December 2019 Official address Domenico Scarlattilaan 6 ● 1083 HS Amsterdam ● The Netherlands Address for visits and deliveries Refer to www.ema.europa.eu/how-to-find-us Send us a question Go to www.ema.europa.eu/contact Telephone +31 (0)88 781 6000 An agency of the European Union © European Medicines Agency, 2020. Reproduction is authorised provided the source is acknowledged. Categorisation of antibiotics in the European Union Table of Contents 1. Summary assessment and recommendations .......................................... 3 2. Introduction ............................................................................................ 7 2.1. Background ........................................................................................................
    [Show full text]
  • Environmental Risk Assessment of Antibiotics: Investigations Into Cyanobacteria Interspecies Sensitivities and Establishing Appropriate Protection Limits
    Environmental Risk Assessment of Antibiotics: Investigations into Cyanobacteria Interspecies Sensitivities and Establishing Appropriate Protection Limits Submitted by Gareth Curtis Le Page to the University of Exeter as a thesis for the degree of Doctor of Philosophy in Biological Sciences In December 2018 This thesis is available for Library use on the understanding that it is copyright material and that no quotation from the thesis may be published without proper acknowledgement I certify that all material in this thesis which is not my own work has been identified and that no material has previously been submitted and approved for the award of a degree by this or any other University. Signature: …………………………………………………………...(Gareth Le Page) 1 Abstract Antibiotics have been described as a ‘wonder drug’ that have transformed medicine since their discovery at the beginning of the 20th century and are used globally in safeguarding human and animal health. Environmental risk assessment (ERA) aims to ensure their environmental safety by setting protection limits that seek to prevent adverse effects upon populations and ecosystem function. In the case of antibiotics however, there is concern that ERA may not be fully protective of bacterial populations. This thesis examines the ERA of antibiotics and highlights that protection limits may in some cases be under-protective or over-protective for bacteria populations (including cyanobacteria), depending on the antibiotic mode of action and the species on which the protection limit is based. The first section of the thesis contains a systematic review including a meta-analysis of all publically available aquatic ecotoxicity data. The results illustrate that generally bacteria are the most sensitive taxa to antibiotics compared with eukaryotes but that interspecies variability in sensitivity among bacteria can range by up to five orders of magnitude.
    [Show full text]
  • Identification of Macrolide Antibiotic-Binding Human P8 Protein
    J. Antibiot. 61(5): 291–296, 2008 THE JOURNAL OF ORIGINAL ARTICLE ANTIBIOTICS Identification of Macrolide Antibiotic-binding Human_p8 Protein Tetsuro Morimura, Mio Hashiba, Hiroshi Kameda, Mihoko Takami, Hirokazu Takahama, Masahiko Ohshige, Fumio Sugawara Received: December 10, 2007 / Accepted: May 1, 2008 © Japan Antibiotics Research Association Abstract Clarithromycin is a macrolide antibiotic that is widely used in clinical medicine. Macrolide antibiotics Introduction such as clarithromycin specifically bind to the 50S subunit of the bacterial ribosome thereby interfering with protein Launched in 1990 by Abbott Laboratories, clarithromycin biosynthesis. A selected peptide sequence from our former A (CLA: synonym of 6-O-methylerythromycin, 1) [1] is a study, composed of 19 amino acids, which was isolated macrolide antibiotic that is commonly used to treat a from a phage display library because of its ability to bind variety of human bacterial infections. Macrolide clarithromycin, displayed significant similarity to a portion antibiotics, represented by erythromycin A (ERY, 2) and its of the human_p8 protein. The recombinant p8 protein structural homologues, specifically bind to the bacterial binds to biotinylated-clarithromycin immobilized on a 50S ribosomal subunit resulting in the inhibition of streptavidin-coated sensor chip and the dissociation bacterial protein biosynthesis [2]. CLA (1) is also constant was determined. The binding of recombinant p8 commonly used to target gastric Helicobacter pylori, which protein to double-stranded DNA was inhibited by is implicated in both gastric ulcers and cancer [3]. biotinylated-clarithromycin, clarithromycin, erythromycin Numerous studies to develop novel pharmaceutical and azithromycin in gel mobility shift assay. applications for macrolide antibiotics, including CLA (1), Dechlorogriseofulvin, obtained from a natural product ERY (2) and azithromycin (AZM, 3), have been published screening, also inhibited human p8 protein binding to [4].
    [Show full text]
  • Development of a Firefly Luciferase-Based Assay For
    University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Veterinary and Biomedical Sciences, Papers in Veterinary and Biomedical Science Department of February 1999 Development of a Firefly ucifL erase-Based Assay for Determining Antimicrobial Susceptibility of Mycobacterium avium subsp. paratuberculosis Stephanie L. Williams University of Nebraska - Lincoln N. Beth Harris University of Nebraska - Lincoln Raul G. Barletta University of Nebraska - Lincoln, [email protected] Follow this and additional works at: https://digitalcommons.unl.edu/vetscipapers Part of the Veterinary Medicine Commons Williams, Stephanie L.; Harris, N. Beth; and Barletta, Raul G., "Development of a Firefly ucifL erase-Based Assay for Determining Antimicrobial Susceptibility of Mycobacterium avium subsp. paratuberculosis" (1999). Papers in Veterinary and Biomedical Science. 8. https://digitalcommons.unl.edu/vetscipapers/8 This Article is brought to you for free and open access by the Veterinary and Biomedical Sciences, Department of at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Papers in Veterinary and Biomedical Science by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. JOURNAL OF CLINICAL MICROBIOLOGY, Feb. 1999, p. 304–309 Vol. 37, No. 2 0095-1137/99/$04.0010 Copyright © 1999, American Society for Microbiology. All Rights Reserved. Development of a Firefly Luciferase-Based Assay for Determining Antimicrobial Susceptibility of Mycobacterium avium subsp. paratuberculosis 1 1 1,2 STEPHANIE L. WILLIAMS, N. BETH HARRIS, * AND RAU´ L G. BARLETTA * Department of Veterinary and Biomedical Sciences1 and Center for Biotechnology,2 University of Nebraska, Lincoln, Nebraska 68583-0905 Received 29 June 1998/Returned for modification 21 October 1998/Accepted 21 October 1998 Paratuberculosis (Johne’s disease) is a fatal disease of ruminants for which no effective treatment is avail- able.
    [Show full text]
  • Conjunctivitis Or Worse?
    Red Eye in Dogs and CatS: Conjunctivitis or Worse? Tracy Revoir, DVM Senior Manager of Veterinary Support, Dechra Veterinary Products It should come as no surprise that conjunctivitis is Common Causes of Conjunctivitis the most common ophthalmic disorder in dogs and cats. But because the clinical signs of conjunctivitis If you do confirm conjunctivitis, the next step is can mimic those of more serious ophthalmic identifying the cause. If both eyes are affected and diseases (glaucoma and uveitis), it’s important to abnormal clinical signs are apparent in other body confirm your diagnosis. systems, think underlying systemic disease. If only one eye is affected, rule out infection, tear film What are important clues to the severity of the deficiencies, an irritant, anatomical abnormality, condition? With conjunctivitis, the inflammation or deeper ocular disease. should be limited to the conjunctiva. Hyperemic conjunctival vessels are superficial, branching, In dogs, conjunctivitis can result from anatomical and bright red. They are movable over the deeper disorders, irritants, infection (usually bacterial), or episcleral vessels and can be blanched with topical atopy. Most bacterial infections are secondary dilute phenylephrine. With glaucoma and uveitis, the conditions, most often to allergies. In cats, herpes- episcleral vessels are engorged; they are dark red, virus and Chlamydophila felis are the most common deep, straight, and immobile and do not blanch with causes of conjunctivitis. Atopy can also be topical dilute phenylephrine. With conjunctivitis, an issue in cats. the Schirmer tear test and intraocular pressures are normal. And the cornea should be clear and no aqueous flare should be present. The pupil and Addressing the Problem pupillary responses are normal and intraocular structures should be visible.
    [Show full text]
  • Topical Antibiotics for Impetigo: a Review of the Clinical Effectiveness and Guidelines
    CADTH RAPID RESPONSE REPORT: SUMMARY WITH CRITICAL APPRAISAL Topical Antibiotics for Impetigo: A Review of the Clinical Effectiveness and Guidelines Service Line: Rapid Response Service Version: 1.0 Publication Date: February 21, 2017 Report Length: 23 Pages Authors: Rob Edge, Charlene Argáez Cite As: Topical antibiotics for impetigo: a review of the clinical effectiveness and guidelines. Ottawa: CADTH; 2017 Feb. (CADTH rapid response report: summary with critical appraisal). ISSN: 1922-8147 (online) Disclaimer: The information in this document is intended to help Canadian health care decision-makers, health care professionals, health systems leaders, and policy-makers make well-informed decisions and thereby improve the quality of health care services. While patients and others may access this document, the document is made available for informational purposes only and no representations or warranties are made with respect to its fitness for any particular purpose. The information in this document should not be used as a substitute for professional medical advice or as a substitute for the application of clinical judgment in respect of the care of a particular patient or other professional judgment in any decision-making process. The Canadian Agency for Drugs and Technologies in Health (CADTH) does not endorse any information, drugs, therapies, treatments, products, processes, or services. While care has been taken to ensure that the information prepared by CADTH in this document is accurate, complete, and up-to-date as at the applicable date the material was first published by CADTH, CADTH does not make any guarantees to that effect. CADTH does not guarantee and is not responsible for the quality, currency, propriety, accuracy, or reasonableness of any statements, information, or conclusions contained in any third-party materials used in preparing this document.
    [Show full text]
  • Daily Moxifloxacin, Clarithromycin, Minocycline, and Clofazimine In
    ISSN: 2643-461X Neto et al. Int J Trop Dis 2020, 3:035 DOI: 10.23937/2643-461X/1710035 Volume 3 | Issue 2 International Journal of Open Access Tropical Diseases CASE SERIES Daily Moxifloxacin, Clarithromycin, Minocycline, and Clofazimine in Nonresponsiveness Leprosy Cases to Recommended Treatment Regimen Francisco Bezerra de Almeida Neto, MD1,2,3*, Rebeca Daniele Buarque Feitosa, OT3 and Marqueline Soares da Silva, RN3 1Department of Dermatology, Mauricio de Nassau Recife University Center, Brazil Check for 2Department of Tropical Medicine, Federal University of Pernambuco (UFPE), Brazil updates 3Cabo de Santo Agostinho Health Care Hansen's Disease Specialized Center, Cabo de Santo Agostinho, Brazil *Corresponding author: Francisco Bezerra de Almeida Neto, MD, Department of Dermatology, Mauricio de Nassau Recife University Center; Department of Tropical Medicine, Federal University of Pernambuco (UFPE); Cabo de Santo Agostinho Health Care Hansen's Disease Specialized Center, Cabo de Santo Agostinho, R Jonathas de Vasconcelos, 316, Boa Viagem, Recife, PE, CEP 51021140, Brazil, Tel: +5581988484442 Abstract Introduction Background: In hyperendemic countries for leprosy, there Although leprosy is the first infectious disease at- has been a growing increase in clinical multibacillary “non- tributed to a pathogen by Gerard Amauer Hansen, it responsiveness” leprosy cases to the fixed-duration treat- remains a relevant public health problem in countries ment recommended by World Health Organization (MDT- MB). There are no defined protocols to treat these patients. considered hyper-endemic for the disease [1]. Methods: A retrospective, observational case series study The main etiologic agents areMycobacterium leprae was conducted of 4 patients with multibacillary leprosy who and Mycobacterium lepromatosis. The clinical mani- presented to a specialized Leprosy health care.
    [Show full text]
  • Farrukh Javaid Malik
    I Farrukh Javaid Malik THESIS PRESENTED TO OBTAIN THE GRADE OF DOCTOR OF THE UNIVERSITY OF BORDEAUX Doctoral School, SP2: Society, Politic, Public Health Specialization Pharmacoepidemiology and Pharmacovigilance By Farrukh Javaid Malik “Analysis of the medicines panorama in Pakistan – The case of antimicrobials: market offer width and consumption.” Under the direction of Prof. Dr. Albert FIGUERAS Defense Date: 28th November 2019 Members of Jury M. Francesco SALVO, Maître de conférences des universités – praticien hospitalier, President Université de Bordeaux M. Albert FIGUERAS, Professeur des universités – praticien hospitalier, Director Université Autonome de Barcelone Mme Antonia AGUSTI, Professeure, Vall dʹHebron University Hospital Referee Mme Montserrat BOSCH, Praticienne hospitalière, Vall dʹHebron University Hospital Referee II Abstract A country’s medicines market is an indicator of its healthcare system, the epidemiological profile, and the prevalent practices therein. It is not only the first logical step to study the characteristics of medicines authorized for marketing, but also a requisite to set up a pharmacovigilance system, thus promoting rational drug utilization. The three medicines market studies presented in the present document were conducted in Pakistan with the aim of describing the characteristics of the pharmaceutical products available in the country as well as their consumption at a national level, with a special focus on antimicrobials. The most important cause of antimicrobial resistance is the inappropriate consumption of antimicrobials. The results of the researches conducted in Pakistan showed some market deficiencies which could be addressed as part of the national antimicrobial stewardship programmes. III Résumé Le marché du médicament d’un pays est un indicateur de son système de santé, de son profil épidémiologique et des pratiques [de prescription] qui y règnent.
    [Show full text]
  • Neomycin and Polymyxin B Sulfates and Bacitracin Zinc Ophthalmic Ointment, USP)
    NDA 50-417/S-011 Page 3 NEOSPORIN® Ophthalmic Ointment Sterile (neomycin and polymyxin B sulfates and bacitracin zinc ophthalmic ointment, USP) Description: NEOSPORIN Ophthalmic Ointment (neomycin and polymyxin B sulfates and bacitracin zinc ophthalmic ointment) is a sterile antimicrobial ointment for ophthalmic use. Each gram contains: neomycin sulfate equivalent to 3.5 mg neomycin base, polymyxin B sulfate equivalent to 10,000 polymyxin B units, bacitracin zinc equivalent to 400 bacitracin units, and white petrolatum, q.s. Neomycin sulfate is the sulfate salt of neomycin B and C, which are produced by the growth of Streptomyces fradiae Waksman (Fam. Streptomycetaceae). It has a potency equivalent of not less than 600 µg of neomycin standard per mg, calculated on an anhydrous basis. The structural formulae are: [Structure] Polymyxin B sulfate is the sulfate salt of polymyxin B 1 and B 2 , which are produced by the growth of Bacillus polymyxa (Prazmowski) Migula (Fam. Bacillaceae). It has a potency of not less than 6,000 polymyxin B units per mg, calculated on an anhydrous basis. The structural formulae are: [Structure] Bacitracin zinc is the zinc salt of bacitracin, a mixture of related cyclic polypeptides (mainly bacitracin A) produced by the growth of an organism of the licheniformis group of Bacillus subtilis var Tracy. It has a potency of not less than 40 bacitracin units per mg. The structural formula is: [Structure] CLINICAL PHARMACOLOGY: A wide range of antibacterial action is provided by the overlapping spectra of neomycin, polymyxin B sulfate, and bacitracin. Neomycin is bactericidal for many gram-positive and gram-negative organisms.
    [Show full text]