Open Operatory Dental Setting Infection Control Practices and Risk Of
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Antiseptics and Disinfectants for the Treatment Of
Verstraelen et al. BMC Infectious Diseases 2012, 12:148 http://www.biomedcentral.com/1471-2334/12/148 RESEARCH ARTICLE Open Access Antiseptics and disinfectants for the treatment of bacterial vaginosis: A systematic review Hans Verstraelen1*, Rita Verhelst2, Kristien Roelens1 and Marleen Temmerman1,2 Abstract Background: The study objective was to assess the available data on efficacy and tolerability of antiseptics and disinfectants in treating bacterial vaginosis (BV). Methods: A systematic search was conducted by consulting PubMed (1966-2010), CINAHL (1982-2010), IPA (1970- 2010), and the Cochrane CENTRAL databases. Clinical trials were searched for by the generic names of all antiseptics and disinfectants listed in the Anatomical Therapeutic Chemical (ATC) Classification System under the code D08A. Clinical trials were considered eligible if the efficacy of antiseptics and disinfectants in the treatment of BV was assessed in comparison to placebo or standard antibiotic treatment with metronidazole or clindamycin and if diagnosis of BV relied on standard criteria such as Amsel’s and Nugent’s criteria. Results: A total of 262 articles were found, of which 15 reports on clinical trials were assessed. Of these, four randomised controlled trials (RCTs) were withheld from analysis. Reasons for exclusion were primarily the lack of standard criteria to diagnose BV or to assess cure, and control treatment not involving placebo or standard antibiotic treatment. Risk of bias for the included studies was assessed with the Cochrane Collaboration’s tool for assessing risk of bias. Three studies showed non-inferiority of chlorhexidine and polyhexamethylene biguanide compared to metronidazole or clindamycin. One RCT found that a single vaginal douche with hydrogen peroxide was slightly, though significantly less effective than a single oral dose of metronidazole. -
Mitigation of Aerosol Generating Procedures in Dentistry a Rapid Review Version 1.2
Mitigation of Aerosol Generating Procedures in Dentistry A Rapid Review Version 1.2 19 April 2021 The content of this review might change as new information becomes available. Please ensure that you are using the most recent version of this document by referring to www.sdcep.org.uk. SDCEP Mitigation of Aerosol Generating Procedures in Dentistry Version history Version Date Summary of changes V1.0 25/09/2020 First publication V1.1 25/01/2021 Agreed positions and conclusions of the review unchanged. New members added to Working Group in Appendix 1. Post-publication update added in Appendix 4. V1.2 19/04/2021 Agreed positions and conclusions of the review unchanged. Changes to Working Group membership noted in Appendix 1. Post-publication update in Appendix 4 amended to reflect the outcome of the literature searches conducted up to 2 March 2021. i SDCEP Mitigation of Aerosol Generating Procedures in Dentistry Contents Summary iii 1 Introduction 1 2 The COVID-19 Pandemic – Risk and Impact on Dental Care 2 2.1 Risk 2 2.2 Underlying SARS-CoV-2 risk 3 2.2.1 Prevalence of COVID-19 and transmission rate 3 2.2.2 Level of virus present in saliva 5 2.2.3 SARS-CoV-2 and aerosols 5 2.3 Impact on dental services and patient care 5 2.3.1 Dental services and personnel 6 2.3.2 Patient care 6 3 Aerosol Generating Procedures 9 3.1 Definitions of aerosol and aerosol generating procedures 9 3.2 Categorisation of dental procedures 9 3.2.1 Dental drill speeds 11 3.2.2 3-in-1 syringe 11 4 Procedural Mitigation 12 4.1 High volume suction 12 4.2 Rubber dam 14 4.3 -
Dental Aerosol As a Hazard Risk for Dental Workers
materials Article Dental Aerosol as a Hazard Risk for Dental Workers Jacek Matys 1 and Kinga Grzech-Le´sniak 1,2,* 1 Laser Laboratory, Oral Surgery Department, Wroclaw Medical University, 50-367 Wroclaw, Poland; [email protected] 2 Department of Periodontics School of Dentistry, Virginia Commonwealth University, VCU, Richmond, VA 23298, USA * Correspondence: [email protected] Received: 23 October 2020; Accepted: 9 November 2020; Published: 12 November 2020 Abstract: Standard dental procedures, when using a water coolant and rotary instruments, generate aerosols with a significantly higher number of various dangerous pathogens (viruses, bacteria, and fungi). Reducing the amount of aerosols to a minimum is mandatory, especially during the new coronavirus disease, COVID-19. The study aimed to evaluate the amount of aerosol generated during standard dental procedures such as caries removal (using dental bur on a high and low-speed handpiece and Er:YAG laser), ultrasonic scaling, and tooth polishing (using silicon rubber on low-speed handpiece) combined with various suction systems. The airborne aerosols containing particles in a range of 0.3–10.0 µm were measured using the PC200 laser particle counter (Trotec GmbH, Schwerin, Germany) at three following sites, manikin, operator, and assistant mouth, respectively. The following suction systems were used to remove aerosols: saliva ejector, high volume evacuator, saliva ejector with extraoral vacuum, high volume evacuator with extraoral vacuum, Zirc® evacuator (Mr.Thirsty One-Step®), and two customized high volume evacuators (white and black). The study results showed that caries removal with a high-speed handpiece and saliva ejector generates the highest amount of spray particles at each measured site. -
1 Brief Report: the Virucidal Efficacy of Oral Rinse Components Against SARS-Cov-2 in Vitro Evelina Statkute1†, Anzelika Rubin
bioRxiv preprint doi: https://doi.org/10.1101/2020.11.13.381079; this version posted November 13, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-ND 4.0 International license. Brief Report: The Virucidal Efficacy of Oral Rinse Components Against SARS-CoV-2 In Vitro Evelina Statkute1†, Anzelika Rubina1†, Valerie B O’Donnell1, David W. Thomas2† Richard J. Stanton1† 1Systems Immunity University Research Institute, Division of Infection & Immunity, School of Medicine, Heath Park, Cardiff, CF14 4XN 2Advanced Therapies Group, School of Dentistry, Cardiff University, Heath Park, Cardiff CF14 4XY, UK †These authors contributed equally * Correspondence: [email protected], [email protected] Running title: Virucidal Activity of Mouthwashes Keywords: SARS-CoV2, mouthwash, lipid, envelope Disclosure: Venture Life Group plc provided information on mouthwash formulations employed in the study, but had no role in funding, planning, execution, analysis or writing of this study. A separate study funded to Cardiff University by Venture Life Group is assessing in vivo efficacy of CPC in patients with COVID19. The investigators declare no direct conflicts exist. 1 bioRxiv preprint doi: https://doi.org/10.1101/2020.11.13.381079; this version posted November 13, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-ND 4.0 International license. -
Tonsillopharyngitis - Acute (1 of 10)
Tonsillopharyngitis - Acute (1 of 10) 1 Patient presents w/ sore throat 2 EVALUATION Yes EXPERT Are there signs of REFERRAL complication? No 3 4 EVALUATION Is Group A Beta-hemolytic Yes DIAGNOSIS Streptococcus (GABHS) • Rapid antigen detection test infection suspected? (RADT) • roat culture No TREATMENT EVALUATION No A Supportive management Is GABHS confi rmed? B Pharmacological therapy (Non-GABHS) Yes 5 TREATMENT A EVALUATE RESPONSEMIMS Supportive management TO THERAPY C Pharmacological therapy • Antibiotics Poor/No Good D Surgery, if recurrent or complicated response response REASSESS PATIENT COMPLETE THERAPY & REVIEW THE DIAGNOSIS© Not all products are available or approved for above use in all countries. Specifi c prescribing information may be found in the latest MIMS. B269 © MIMS Pediatrics 2020 Tonsillopharyngitis - Acute (2 of 10) 1 ACUTE TONSILLOPHARYNGITIS • Infl ammation of the tonsils & pharynx • Etiologies include bacterial (group A β-hemolytic streptococcus, Haemophilus infl uenzae, Fusobacterium sp, etc) & viral (infl uenza, adenovirus, coronavirus, rhinovirus, etc) pathogens • Sore throat is the most common presenting symptom in older children TONSILLOPHARYNGITIS 2 EVALUATION FOR COMPLICATIONS • Patients w/ sore throat may have deep neck infections including epiglottitis, peritonsillar or retropharyngeal abscess • Examine for signs of upper airway obstruction Signs & Symptoms of Sore roat w/ Complications • Trismus • Inability to swallow liquids • Increased salivation or drooling • Peritonsillar edema • Deviation of uvula -
Dental Aerosol Management Interim Guidance from CDA’S COVID-19 Clinical Care Workgroup
BACK TO PRACTICE California Dental Association 1201 K Street, Sacramento, CA 95814 PATIENT CARE 800.232.7645 | cda.org ® Dental Aerosol Management Interim Guidance from CDA’s COVID-19 Clinical Care Workgroup Updated May 26, New: Resources for Upper-Room UV and portable HEPA room filtration, per CDC Guidance for Dental Settings, May 19 Introduction As part of its overall charge to assist dental professionals during the COVID-19 pandemic, the California Dental Association COVID-19 Clinical Care Workgroup initiated an in-depth investigation into aerosol management in dentistry. This document reflects that work. It is important to note that the environment is rapidly evolving and we are constantly learning more about the virus, its transmission and how to reduce risk during the provision of dental care. In particular, new products for dental aerosol management are being introduced almost daily and the evidence on the efficacy of these in the dental setting is just beginning to develop. We anticipate evidence on this will continue to emerge well after this resource is published. Therefore, this document should be considered a living document that will be updated over time as information becomes available. What’s more, the California Dental Association is not a regulatory agency, therefore the guidance offered here is not intended to be construed as the “standard of care,” and should be considered along with guidance from local, state, and federal government agencies, local/regional hospital systems and/or other authorities. Background The delivery of dental services routinely involves exposure of dental health personnel and patients to the contents of saliva and blood through droplets, spatter and aerosols produced during patient care. -
NINDS Custom Collection II
ACACETIN ACEBUTOLOL HYDROCHLORIDE ACECLIDINE HYDROCHLORIDE ACEMETACIN ACETAMINOPHEN ACETAMINOSALOL ACETANILIDE ACETARSOL ACETAZOLAMIDE ACETOHYDROXAMIC ACID ACETRIAZOIC ACID ACETYL TYROSINE ETHYL ESTER ACETYLCARNITINE ACETYLCHOLINE ACETYLCYSTEINE ACETYLGLUCOSAMINE ACETYLGLUTAMIC ACID ACETYL-L-LEUCINE ACETYLPHENYLALANINE ACETYLSEROTONIN ACETYLTRYPTOPHAN ACEXAMIC ACID ACIVICIN ACLACINOMYCIN A1 ACONITINE ACRIFLAVINIUM HYDROCHLORIDE ACRISORCIN ACTINONIN ACYCLOVIR ADENOSINE PHOSPHATE ADENOSINE ADRENALINE BITARTRATE AESCULIN AJMALINE AKLAVINE HYDROCHLORIDE ALANYL-dl-LEUCINE ALANYL-dl-PHENYLALANINE ALAPROCLATE ALBENDAZOLE ALBUTEROL ALEXIDINE HYDROCHLORIDE ALLANTOIN ALLOPURINOL ALMOTRIPTAN ALOIN ALPRENOLOL ALTRETAMINE ALVERINE CITRATE AMANTADINE HYDROCHLORIDE AMBROXOL HYDROCHLORIDE AMCINONIDE AMIKACIN SULFATE AMILORIDE HYDROCHLORIDE 3-AMINOBENZAMIDE gamma-AMINOBUTYRIC ACID AMINOCAPROIC ACID N- (2-AMINOETHYL)-4-CHLOROBENZAMIDE (RO-16-6491) AMINOGLUTETHIMIDE AMINOHIPPURIC ACID AMINOHYDROXYBUTYRIC ACID AMINOLEVULINIC ACID HYDROCHLORIDE AMINOPHENAZONE 3-AMINOPROPANESULPHONIC ACID AMINOPYRIDINE 9-AMINO-1,2,3,4-TETRAHYDROACRIDINE HYDROCHLORIDE AMINOTHIAZOLE AMIODARONE HYDROCHLORIDE AMIPRILOSE AMITRIPTYLINE HYDROCHLORIDE AMLODIPINE BESYLATE AMODIAQUINE DIHYDROCHLORIDE AMOXEPINE AMOXICILLIN AMPICILLIN SODIUM AMPROLIUM AMRINONE AMYGDALIN ANABASAMINE HYDROCHLORIDE ANABASINE HYDROCHLORIDE ANCITABINE HYDROCHLORIDE ANDROSTERONE SODIUM SULFATE ANIRACETAM ANISINDIONE ANISODAMINE ANISOMYCIN ANTAZOLINE PHOSPHATE ANTHRALIN ANTIMYCIN A (A1 shown) ANTIPYRINE APHYLLIC -
Inactivation of SARS-Cov-2 Through Treatment with the Mouth Rinsing Solutions Viruprox® and Bacterx® Pro
microorganisms Communication Inactivation of SARS-CoV-2 through Treatment with the Mouth Rinsing Solutions ViruProX® and BacterX® Pro Julia Koch-Heier 1,†, Helen Hoffmann 1,†, Michael Schindler 2 , Adrian Lussi 3,4 and Oliver Planz 1,* 1 Interfaculty Institute for Cell Biology, Department of Immunology, Eberhard Karls University of Tuebingen, 72076 Tuebingen, Germany; [email protected] (J.K.-H.); [email protected] (H.H.) 2 Institute for Medical Virology and Epidemiology of Viral Disease, Department of Molecular Virology, 72076 Tuebingen, Germany; [email protected] 3 Department of Operative Dentistry and Periodontology, University Medical Centre, 79106 Freiburg, Germany; [email protected] 4 School of Dental Medicine, University of Bern, 3010 Bern, Switzerland * Correspondence: [email protected] † These authors contributed equally to this work. Abstract: The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic effects daily dental work. Therefore, infection control measures are necessary to prevent infection of dental personnel during dental treatments. The use of a preprocedural mouth rinse with chlorhexidine (CHX), cetylpyridinium chloride (CPC), or hydrogen peroxide (H2O2) solution for 30–60 s may reduce the viral load and may protect the personnel in a dental practice. In the present study the ® virucidal effect of the mouth rinsing solutions ViruProX with 0.05% CPC and 1.5% H2O2 and Citation: Koch-Heier, J.; Hoffmann, BacterX® pro containing 0.1% CHX, 0.05% CPC, and 0.005% sodium fluoride (F-) was investigated H.; Schindler, M.; Lussi, A.; Planz, O. in vitro. The mouth rinsing solutions successfully inactivated infectious SARS-CoV-2 particles, the Inactivation of SARS-CoV-2 through causative agent of coronavirus disease 2019 (COVID-19), within 30 s. -
Chemical Modulators of Fibrinogen Production and Their Impact on Venous Thrombosis
Published online: 2020-12-10 Coagulation and Fibrinolysis 433 Chemical Modulators of Fibrinogen Production and Their Impact on Venous Thrombosis Rui Vilar1 Samuel W. Lukowski1,2 Marco Garieri1 Corinne Di Sanza1 Marguerite Neerman-Arbez1,3 Richard J. Fish1 1 Department of Genetic Medicine and Development, University of Address for correspondence Richard J. Fish, Department of Genetic Geneva Faculty of Medicine, Geneva, Switzerland Medicine and Development, Faculty of Medicine, University of 2 Institute for Molecular Bioscience, The University of Queensland, Geneva, 1, rue Michel-Servet, Geneva 1206, Switzerland Saint Lucia, Queensland, Australia (e-mail: [email protected]). 3 iGE3, Institute of Genetics and Genomics in Geneva, Geneva, Switzerland Thromb Haemost 2021;121:433–448. Abstract Thrombosis is a leading cause of morbidity and mortality. Fibrinogen, the soluble substrate for fibrin-based clotting, has a central role in haemostasis and thrombosis and its plasma concentration correlates with cardiovascular disease event risk and a prothrombotic state in experimental models. We aimed to identify chemical entities capable of changing fibrinogen production and test their impact on experimental thrombosis. A total of 1,280 bioactive compounds were screened for their ability to alter fibrinogen production by hepatocyte-derived cancer cells and a selected panel was tested in zebrafish larvae. Anthralin and all-trans retinoic acid (RA) were identified as fibrinogen-lowering and fibrinogen-increasing moieties, respectively. In zebrafish larvae, anthralin prolonged laser-induced venous occlusion times and reduced thrombocyte accumulation at injury sites. RA had opposite effects. Treatment with RA, a nuclear receptor ligand, increased fibrinogen mRNA levels. Using an antisense morpholino oligonucleotide to deplete zebra- fish fibrinogen, we correlated a shortening of laser-induced venous thrombosis times with RA treatment and fibrinogen protein levels. -
Pharmaceutical Appendix to the Tariff Schedule 2
Harmonized Tariff Schedule of the United States (2006) – Supplement 1 (Rev. 1) Annotated for Statistical Reporting Purposes PHARMACEUTICAL APPENDIX TO THE HARMONIZED TARIFF SCHEDULE Harmonized Tariff Schedule of the United States (2006) – Supplement 1 (Rev. 1) Annotated for Statistical Reporting Purposes PHARMACEUTICAL APPENDIX TO THE TARIFF SCHEDULE 2 Table 1. This table enumerates products described by International Non-proprietary Names (INN) which shall be entered free of duty under general note 13 to the tariff schedule. The Chemical Abstracts Service (CAS) registry numbers also set forth in this table are included to assist in the identification of the products concerned. For purposes of the tariff schedule, any references to a product enumerated in this table includes such product by whatever name known. Product CAS No. Product CAS No. ABACAVIR 136470-78-5 ACEXAMIC ACID 57-08-9 ABAFUNGIN 129639-79-8 ACICLOVIR 59277-89-3 ABAMECTIN 65195-55-3 ACIFRAN 72420-38-3 ABANOQUIL 90402-40-7 ACIPIMOX 51037-30-0 ABARELIX 183552-38-7 ACITAZANOLAST 114607-46-4 ABCIXIMAB 143653-53-6 ACITEMATE 101197-99-3 ABECARNIL 111841-85-1 ACITRETIN 55079-83-9 ABIRATERONE 154229-19-3 ACIVICIN 42228-92-2 ABITESARTAN 137882-98-5 ACLANTATE 39633-62-0 ABLUKAST 96566-25-5 ACLARUBICIN 57576-44-0 ABUNIDAZOLE 91017-58-2 ACLATONIUM NAPADISILATE 55077-30-0 ACADESINE 2627-69-2 ACODAZOLE 79152-85-5 ACAMPROSATE 77337-76-9 ACONIAZIDE 13410-86-1 ACAPRAZINE 55485-20-6 ACOXATRINE 748-44-7 ACARBOSE 56180-94-0 ACREOZAST 123548-56-1 ACEBROCHOL 514-50-1 ACRIDOREX 47487-22-9 ACEBURIC -
Unduh File PDF
Majalah Farmasetika, 3 (5) 2018, 98-101 https://doi.org/10.24198/farmasetika.v3i5.21633 e-ISSN : 2686-2506 Perkembangan Obat Sariawan dan Terapi Alternatifnya Prilly Mutiara Sandy*, Fira Burhanisa Irawan Program Studi Sarjana Farmasi, Fakultas Farmasi, Universitas Padjadjaran, Sumedang 45363 email: [email protected] Abstrak : Sariawan merupakan penyakit mulut yang sudah tidak asing lagi. Berbagai kalangan mulai dari balita, remaja, orang tua, maupun lanjut usia tentu pernah mengalami penyakit tersebut. Efek dari sariawan itu sendiri ialah bisa menyebabkan para penderitanya tidak nafsu makan dan mulut terasa perih. Pengobatan yang dapat dilakukan adalah dengan mengonsumsi zat pemati rasa dan antiseptika.Pemakaiannya obat bisa dilakukan sebanyak 2-3 kali dalam sehari. Selain dengan zat pemati rasa, sariawan juga dapat diobati dengan antiseptika. Hasil terbaik dari penggunaan antiseptika terbukti oleh obat kumur provid-ion (Betadine) dan klorheksidin dalam bentuk tablet hisap srta larutan peroksida 3%. Selain itu juga bisa menggunakan obat kumur yang mengandung Chlorhexidine gluconate 2%, sodium hyaluronate, PVP , dan glycyrrhetinic. BPOM menganjurkan penggunaan obat-obat yang memiliki kandungan enzydamine HCL, providone iodine 1%, atau kombinasi dequalinium chloride dan vitamin C. Bagi yang ingin menyembuhkan sariawan dengan bahan-bahan alami, yaitu: tanaman gambir, daun sirih, air garam, dan cabai. Keyword : obat, sariawan, terapi alternative Outline • Pendahuluan • Terapi sariawan • Albothyl (policresulen) • Terapi alternatif • Kesimpulan Pendahuluan Sariawan atau aphtous stomatitis adalah luka yang terdapat di dalam mulut yang biasanya berbentuk oval atau bulat berwarna putih dan dapat menimbulkan rasa tidak sakit serta tidak nyaman. Sariawan disebabkan oleh beberapa hal, diantaranya ialah kurangnya vit C, vit B12 dan bisa juga karena adanya infeksi yang disebabkan oleh bakteri, virus, atau jamur. -
Evaluating Dental Aerosol and Splatter in an Open Plan Clinic Environment
Evaluating dental aerosol and splatter in an open plan clinic environment: implications for the COVID-19 pandemic Running title: Open dental clinic aerosol R Holliday1,2 *#, JR Allison1,2 #, CC Currie1,2, DC Edwards1,2, C Bowes 1,2, K Pickering 2, S Reay2, J Durham1,2, J Lumb2, N Rostami1, J Coulter1,2, C.Nile1, N Jakubovics1 *Corresponding Author #Joint First Authors Affiliations: 1. School of Dental Sciences, Newcastle University, United Kingdom 2. Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle Upon Tyne, United Kingdom Corresponding Author: Dr Richard Holliday School of Dental Sciences Newcastle University Framlington Place Newcastle Upon Tyne NE2 4BW Telephone: 07876 580022 Email: [email protected] Keywords: Aerosols, Dental Equipment; Dental Fallow Time; Dental High-Speed Equipment; Dental Infection Control; SARS-CoV-2; Suction Abstract Aim: To identify splatter and aerosol distribution resulting from dental aerosol generating procedures (AGPs) in the open plan clinic environment. A secondary aim is to explore the detailed time course of aerosol settling after an AGP. Methodology: Dental procedures were undertaken on a dental mannequin. Fluorescein dye was placed into the irrigation system of the high-speed air turbine handpiece for the first experimental design, and in the second, fluorescein dye was entered into the mannequin's mouth via artificial salivary ducts. Filter papers were placed at set distances around the open plan clinic environment to collect aerosol and splatter under various mitigating conditions, including ventilation and aspiration flow rate. An 8-metre diameter rig was set up to investigate the effect of fallow time. Filter papers were analysed using imaging software and spectrofluorometric analysis.