012000 Ingestion of Toxic Substances by Children

Total Page:16

File Type:pdf, Size:1020Kb

012000 Ingestion of Toxic Substances by Children The New England Journal of Medicine Primary Care of such agents in the home rather than their inher- ent toxicity. On the basis of hazard-factor analysis (in which the number of episodes of major toxic effects INGESTION OF TOXIC SUBSTANCES or death is divided by the total number of reported cases of exposure to the substance, normalized to the BY CHILDREN rate of major toxic effects or death for all substances in the age group in question), the substances asso- MICHAEL SHANNON, M.D., M.P.H. ciated with the greatest risk of death to children in- clude cocaine, anticonvulsant drugs, antidepressant drugs, and iron supplements.6 NGESTION of a harmful substance is among the TREATMENT most common causes of injury to children less The ability to reduce morbidity and mortality Ithan six years of age. Fortunately, in most cases, among children who have ingested a toxic substance the ingested agent has minimal or no clinically im- depends on prompt, appropriate intervention. A tele- portant toxic effect. Occasionally, however, such in- phone call by the parent to a physician or poison cen- gestion can be life-threatening or can even result in ter is often the first step in obtaining treatment. In death. Although preventive measures have been re- most circumstances, after the substance and its toxic- markably successful in reducing the frequency and ity have been identified and the amount ingested severity of poisoning in children, poisoning continues has been determined, treatment can be carried out at to occur and requires strategies for treatment and pre- home without the need for referral to an emergency vention that are safe and effective. In this review, I dis- department. cuss the management of poisoning in children, with In children brought or referred to a health care fa- an emphasis on current guidelines for treatment. cility, assessment and stabilization of vital signs are the initial steps of treatment. Rarely, emergency manage- EPIDEMIOLOGY ment involves the administration of an antidote (e.g., According to the Toxic Exposure Surveillance Sys- naloxone after an overdose of an opioid drug) or tem of the American Association of Poison Control measures to enhance the elimination of toxins that Centers, 1.08 million instances of ingestion of a tox- have already been absorbed (e.g., multiple doses of ac- ic substance by a child less than six years of age were tivated charcoal after an overdose of carbamazepine). reported to poison centers in 1998.1 However, the Laboratory analysis of serum or urine should be guid- proportion of incidents reported to poison centers is ed by the substance ingested, its anticipated degree estimated to be as low as 26 percent,2 suggesting a of toxicity, and the value of measuring these concen- true incidence of more than 4 million poisonings an- trations; there is rarely a need for toxicologic screen- nually. According to the Consumer Product Safety ing tests in children, since the ingested substance is Commission, approximately 85,000 young children usually known.7 were treated for poisoning in emergency departments The term “gastrointestinal decontamination” in- in the same year (Schroeder T: personal communica- cludes interventions that are used to prevent the ab- tion), for a projected incidence of 450 per 100,000 sorption of an ingested toxin. Gastrointestinal de- population. The toxic substances most commonly in- contamination has three distinct components: gastric gested by children are listed in Table 1. Substances emptying, administration of an adsorbent agent, and that are most accessible to children, such as cosmetics catharsis. and personal care products, cleaning products, anal- gesics, and cough and cold preparations, account for Gastric Emptying 58 percent of the products listed.1,3-5 In principle, if the contents of the stomach can be Table 2 lists the primary agents involved in deaths rapidly and completely evacuated after the ingestion from poisoning among children from 1995 through of a toxin, the toxin will not have the opportunity 1998. Medications, both prescription drugs and over- to enter the small intestine, the main site of absorp- the-counter drugs, were responsible for 52 percent tion. Consequently, the clinical effects of the poison- of the deaths from poisoning. The distribution of re- ing can be mitigated. Gastric evacuation can be ac- sponsible agents also reflects the common presence complished either by chemically induced emesis or by mechanical removal with a lavage tube. Emesis is mediated in the central nervous system, From the Division of Emergency Medicine and the Program in Clinical either by direct stimulation of the chemoreceptor trig- Toxicology, Children’s Hospital and Harvard Medical School; and the Mas- ger zone in the area postrema or by gastric irritation sachusetts Poison Control System — all in Boston. Address reprint requests mediated by vagal afferent fibers, with resulting stim- to Dr. Shannon at Children’s Hospital, 300 Longwood Ave., Boston, MA 8,9 02115, or at [email protected]. ulation of the vomiting center in the medulla. ©2000, Massachusetts Medical Society. Agents that have been used in children in the past for 186 · January 20, 2000 Downloaded from www.nejm.org at ST MATTHEWS UNIV SCH MED on May 29, 2004. Copyright © 2000 Massachusetts Medical Society. All rights reserved. PRIMARY CARE this purpose include parenteral apomorphine, copper TABLE 1. AGENTS MOST COMMONLY INGESTED sulfate, fluid extract of ipecac, hydrogen peroxide, and BY CHILDREN LESS THAN SIX YEARS OF AGE, ipecac syrup. Among these, ipecac syrup has proved 1995 TO 1998.* to be the safest, most reliable emetic agent; the others are contraindicated for the treatment of poisoning. NO. OF Ipecac syrup contains two active alkaloids, cephaline AGENT INGESTED CHILDREN and emetine. Both stimulate gastric sensory receptors Cosmetics and personal care products 568,856 linked to the vomiting center in the brain. In addi- Cleaning products 500,791 tion, cephaline acts at the chemoreceptor trigger zone. Analgesics 354,722 The primary advantage of ipecac syrup is its ease of Plants 322,991 administration by parents or caretakers. Cough and cold preparations 278,460 Foreign bodies 256,263 Emesis usually begins about 20 minutes after ipe- 10 Topical agents 234,997 cac syrup is given. Eighty-two percent of children Pesticides 164,277 will vomit after a single 15-ml dose, and 99 percent Vitamins 151,871 will vomit after two doses.11 The duration of vomit- Hydrocarbons 106,269 ing is typically one to two hours. Guidelines for doses are presented in Table 3. Administration can be re- 1,3-5 *Data are from Litovitz et al. peated if vomiting does not begin within 20 to 30 minutes. The administration of additional fluid after ipecac syrup does not appear to improve the efficacy of the agent.12 The use of ipecac syrup should be con- sidered in cases in which children have ingested a po- tentially toxic substance in the preceding hour. How- ever, the efficacy of ipecac syrup, even under these TABLE 2. PRIMARY AGENTS INVOLVED IN FATAL POISONINGS circumstances, has not been proved.10 Because un- AMONG CHILDREN LESS THAN SIX YEARS OF AGE, 1995 TO 1998.* controlled vomiting will occur for at least one to two hours, ipecac syrup should not be administered after CATEGORY the ingestion of certain substances or under certain (NO. OF DEATHS REPORTED)SPECIFIC AGENTS clinical conditions (Table 4). Analgesic drugs (11) Acetaminophen, ibuprofen, metha- Increasingly, both the safety and the efficacy of ip- done, oxycodone, salicylates, 10 morphine ecac syrup have been questioned. Although the drug Cleaning products (6) Corrosives, fluoride-based solutions has an impressive safety profile, there have been re- Electrolytes and minerals (6) Elemental iron ports of adverse effects, including prolonged vomit- Hydrocarbons (6) Gasoline, paint thinner, lamp oil ing, sedation, Mallory–Weiss syndrome, gastric rup- Antidepressant drugs (4) Amitriptyline, imipramine, desipra- ture, and fatal aspiration.13,14 The efficacy of ipecac mine syrup, measured in terms of the elimination of ingest- Insecticides and pesticides (4) Propoxur, organophosphates ed toxins or improvement in outcomes, also appears Cosmetics and personal care Ethanol, baby oil products (2) to be limited. In studies in animals, ipecac syrup re- Anticonvulsant drugs (2) Carbamazepine, valproate sodium moves 10 to 60 percent of an ingested substance; in Stimulants and illicit drugs (2) “Crack” cocaine, heroin clinical studies, within one hour after ingestion, a Plants (2) Cayenne pepper, pennyroyal tea mean of 30 percent of a toxin can be recovered.10 Foreign bodies (2) Activated charcoal† When administered 90 minutes or more after a toxic Sedatives and hypnotic drugs (2) Promethazine, chloral hydrate substance has been ingested, ipecac syrup has no iden- Cardiovascular agents (1) Nifedipine tifiable benefit.15 Saincher et al. have suggested that Tobacco (1) Cigarette butts ipecac syrup is no longer beneficial between 5 and 30 Cough and cold preparations (1) Phenylpropanolamine 16 Hormones and hormone antago- Glipizide minutes after the ingestion of a toxic substance. nists (1) Gastric lavage is an alternative method of remov- Chemicals (1) Diethylene glycol ing the contents of the stomach. For lavage to be Alcohols (1) Ethanol performed properly, competence of the gag reflex Gastrointestinal preparations (1) Bismuth subsalicylate should first be confirmed. Once properly restrained, *Data are from Litovitz et al.1,3-5 the child should be placed in a left lateral decubitus †Deaths were attributed to the administration of activated charcoal. Trendelenburg’s position in order to limit the move- ment of the gastric contents into the duodenum and minimize the risk of aspiration.17,18 A large-bore (24- to-32-French), single-lumen tube should be placed by an orogastric route. The proper placement of the tube is confirmed by the spontaneous or aspirated return of gastric contents or by auscultation of in- Volume 342 Number 3 · 187 Downloaded from www.nejm.org at ST MATTHEWS UNIV SCH MED on May 29, 2004.
Recommended publications
  • EH&S COVID-19 Chemical Disinfectant Safety Information
    COVID-19 CHEMICAL DISINFECTANT SAFETY INFORMATION Updated June 24, 2020 The COVID-19 pandemic has caused an increase in the number of disinfection products used throughout UW departments. This document provides general information about EPA-registered disinfectants, such as potential health hazards and personal protective equipment recommendations, for the commonly used disinfectants at the UW. Chemical Disinfectant Base / Category Products Potential Hazards Controls ● Ethyl alcohol Highly flammable and could form explosive Disposable nitrile gloves Alcohols ● ● vapor/air mixtures. ● Use in well-ventilated areas away from o Clorox 4 in One Disinfecting Spray Ready-to-Use ● May react violently with strong oxidants. ignition sources ● Alcohols may de-fat the skin and cause ● Wear long sleeve shirt and pants ● Isopropyl alcohol dermatitis. ● Closed toe shoes o Isopropyl Alcohol Antiseptic ● Inhalation of concentrated alcohol vapor 75% Topical Solution, MM may cause irritation of the respiratory tract (Ready to Use) and effects on the central nervous system. o Opti-Cide Surface Wipes o Powell PII Disinfectant Wipes o Super Sani Cloth Germicidal Wipe 201 Hall Health Center, Box 354400, Seattle, WA 98195-4400 206.543.7262 ᅵ fax 206.543.3351ᅵ www.ehs.washington.edu ● Formaldehyde Formaldehyde in gas form is extremely Disposable nitrile gloves for Aldehydes ● ● flammable. It forms explosive mixtures with concentrations 10% or less ● Paraformaldehyde air. ● Medium or heavyweight nitrile, neoprene, ● Glutaraldehyde ● It should only be used in well-ventilated natural rubber, or PVC gloves for ● Ortho-phthalaldehyde (OPA) areas. concentrated solutions ● The chemicals are irritating, toxic to humans ● Protective clothing to minimize skin upon contact or inhalation of high contact concentrations.
    [Show full text]
  • Expert Consensus Guidelines for Stocking of Antidotes in Hospitals That Provide Emergency Care
    TOXICOLOGY/CONCEPTS Expert Consensus Guidelines for Stocking of Antidotes in Hospitals That Provide Emergency Care Richard C. Dart, MD, PhD From the Rocky Mountain Poison & Drug Center - Denver Health, Denver, CO (Dart, Heard, Schaeffer, Stephen W. Borron, MD, MS Bogdan, Alhelail, Buchanan, Hoppe, Lavonas, Mlynarchek, Phua, Rhyee, Varney, Zosel); Department of E. Martin Caravati, MD, MPH Surgery, University of Texas Health Sciences Center, San Antonio, TX (Borron); Division of Emergency Daniel J. Cobaugh, PharmD Medicine, Utah Poison Control Center, University of Utah Health Sciences Center, Salt Lake City, UT Steven C. Curry, MD (Caravati); ASHP Research and Education Foundation, Bethesda, MD (Cobaugh); Department of Jay L. Falk, MD Medical Toxicology and Banner Poison Control Center, Banner Good Samaritan Medical Center, Lewis Goldfrank, MD Phoenix, AZ (Curry); Department of Emergency Medicine, Orlando Regional Medical Center, University of Susan E. Gorman, PharmD, MS Florida, Orlando, FL (Falk); New York City Poison Center; New York University School of Medicine, New Stephen Groft, PharmD York, NY (Goldfrank); Division of Strategic National Stockpile, Centers for Disease Control and Kennon Heard, MD Prevention, Atlanta, GA (Gorman); Office of Rare Diseases Research, Bethesda, MD (Groft); Division of Ken Miller, MD, PhD Emergency Medicine, School of Medicine (Dart, Heard, Lavonas, Schaeffer) and Department of Kent R. Olson, MD Pharmaceutical Sciences, School of Pharmacy (Bogdan), University of Colorado Denver, Aurora, CO; Gerald O’Malley, DO Orange County Fire Authority and Orange County Health Care Agency Emergency Medical Services, Donna Seger, MD Irvine, CA, and National Association of EMS Physicians, Lenexa, KS, (Miller); University of California, Steven A. Seifert, MD San Francisco, and San Francisco Division, California Poison Control System, San Francisco, CA Marco L.
    [Show full text]
  • Reactions of Alcohols & Ethers 1
    REACTIONS OF ALCOHOLS & ETHERS 1. Combustion (Extreme Oxidation) alcohol + oxygen carbon dioxide + water 2 CH3CH2OH + 6 O2 4 CO2 + 6 H2O 2. Elimination (Dehydration) ° alcohol H 2 S O 4/ 1 0 0 C alkene + water H2SO4/100 ° C CH3CH2CH2OH CH3CH=CH2 + H2O 3. Condensation ° excess alcohol H 2 S O 4 / 1 4 0 C ether + water H2SO4/140 ° C 2 CH3CH2OH CH3CH2OCH2CH3 + H2O 4. Substitution Lucas Reagent alcohol + hydrogen halide Z n C l2 alkyl halide + water ZnCl2 CH3CH2OH + HCl CH3CH2Cl + H2O • This reaction with the Lucas Reagent (ZnCl2) is a qualitative test for the different types of alcohols because the rate of the reaction differs greatly for a primary, secondary and tertiary alcohol. • The difference in rates is due to the solubility of the resulting alkyl halides • Tertiary Alcohol→ turns cloudy immediately (the alkyl halide is not soluble in water and precipitates out) • Secondary Alcohol → turns cloudy after 5 minutes • Primary Alcohol → takes much longer than 5 minutes to turn cloudy 5. Oxidation • Uses an oxidizing agent such as potassium permanganate (KMnO4) or potassium dichromate (K2Cr2O7). • This reaction can also be used as a qualitative test for the different types of alcohols because there is a distinct colour change. dichromate → chromium 3+ (orange) → (green) permanganate → manganese (IV) oxide (purple) → (brown) Tertiary Alcohol not oxidized under normal conditions CH3 KMnO4 H3C C OH NO REACTION K2Cr2O7 CH3 tertbutyl alcohol Secondary Alcohol ketone + hydrogen ions H O KMnO4 H3C C CH3 + K2Cr2O7 C + 2 H H3C CH3 OH propanone 2-propanol Primary Alcohol aldehyde + water carboxylic acid + hydrogen ions O KMnO4 O H H KMnO H H 4 + CH3CH2CH2OH C C C H C C C H + 2 H K2Cr2O7 + H2O K Cr O H H H 2 2 7 HO H H 1-propanol propanal propanoic acid 6.
    [Show full text]
  • Chemical Disinfectants | Disinfection & Sterilization Guidelines | Guidelines Library | Infection Control | CDC 3/19/20, 14:52
    Chemical Disinfectants | Disinfection & Sterilization Guidelines | Guidelines Library | Infection Control | CDC 3/19/20, 14:52 Infection Control Chemical Disinfectants Guideline for Disinfection and Sterilization in Healthcare Facilities (2008) Alcohol Overview. In the healthcare setting, “alcohol” refers to two water-soluble chemical compounds—ethyl alcohol and isopropyl alcohol —that have generally underrated germicidal characteristics 482. FDA has not cleared any liquid chemical sterilant or high- level disinfectant with alcohol as the main active ingredient. These alcohols are rapidly bactericidal rather than bacteriostatic against vegetative forms of bacteria; they also are tuberculocidal, fungicidal, and virucidal but do not destroy bacterial spores. Their cidal activity drops sharply when diluted below 50% concentration, and the optimum bactericidal concentration is 60%–90% solutions in water (volume/volume) 483, 484. Mode of Action. The most feasible explanation for the antimicrobial action of alcohol is denaturation of proteins. This mechanism is supported by the observation that absolute ethyl alcohol, a dehydrating agent, is less bactericidal than mixtures of alcohol and water because proteins are denatured more quickly in the presence of water 484, 485. Protein denaturation also is consistent with observations that alcohol destroys the dehydrogenases of Escherichia coli 486, and that ethyl alcohol increases the lag phase of Enterobacter aerogenes 487 and that the lag phase e!ect could be reversed by adding certain amino acids. The bacteriostatic action was believed caused by inhibition of the production of metabolites essential for rapid cell division. Microbicidal Activity. Methyl alcohol (methanol) has the weakest bactericidal action of the alcohols and thus seldom is used in healthcare 488. The bactericidal activity of various concentrations of ethyl alcohol (ethanol) was examined against a variety of microorganisms in exposure periods ranging from 10 seconds to 1 hour 483.
    [Show full text]
  • Alcohols I 1400
    ALCOHOLS I 1400 Table 1 MW: Table 1 CAS: Table 2 RTECS: Table 2 METHOD: 1400, Issue 2 EVALUATION: PARTIAL Issue 1: 15 February 1984 Issue 2: 15 August 1994 OSHA : Table 2 PROPERTIES: Table 1 NIOSH: Table 2 ACGIH: Table 2 COMPOUNDS AND SYNONYMS: (1) ethanol: ethyl alcohol. (2) isopropyl alcohol: 2-propanol. (3) tert-butyl alcohol: 2-methyl-2-propanol. SAMPLING MEASUREMENT SAMPLER: SOLID SORBENT TUBE TECHNIQUE: GAS CHROMATOGRAPHY, FID (coconut shell charcoal, 100 mg/50 mg) ANALYTE: compounds above FLOW RATE: 0.01 to 0.2 L/min (£0.05 L/min for ethyl alcohol) DESORPTION: 1 mL 1% 2-butanol in CS 2 (1) (2) (3) INJECTION VOL-MIN: 0.1 L 0.3 L 1.0 L VOLUME: 5 µL -MAX: 1 L 3 L 10 L TEMPERATURE-INJECTION: 200 °C SHIPMENT: cooled -DETECTOR: 250-300 °C -COLUMN: 65-70 °C SAMPLE STABILITY: unknown, store in freezer CARRIER GAS: N2 or He, 30 mL/min BLANKS: 2 to 10 field blanks per set COLUMN: glass, 2 m x 4-mm ID, 0.2% Carbowax 1500 on 60/80 Carbopack C or equivalent ACCURACY CALIBRATION: solutions of analyte in eluent (internal standard optional) RANGE STUDIED: see EVALUATION OF METHOD RANGE AND BIAS: not significant [1] PRECISION: see EVALUATION OF METHOD OVERALL PRECISION (S ˆ ): see EVALUATION OF METHOD rT ESTIMATED LOD: 0.01 mg per sample [2] ACCURACY: ± 14% APPLICABILITY: The working ranges are 16 to 1000 ppm ethanol (30 to 1900 mg/m 3) for a 1-L air sample; 4 to 400 ppm isopropyl alcohol (10 to 1000 mg/m 3) for a 3-L air sample; and 1 to 100 ppm t-butyl alcohol (3 to 300 mg/m 3) for a 10-L air sample.
    [Show full text]
  • Antiseptics in the Era of Bacterial Resistance: a Focus on Povidone Iodine
    Therapeutic Perspective Antiseptics in the era of bacterial resistance: a focus on povidone iodine Jean-Marie Lachapelle*1, Olivier Castel2, Alejandro Fueyo Casado3, Bernard Leroy1, Giuseppe Micali4, Dominique Tennstedt1 & Julien Lambert5 Practice Points Increasing bacterial resistance to antibiotics makes the management of superficial skin infections a major medical challenge. Antiseptics have broader spectrums of antimicrobial activity and a reduced potential for selection of bacterial resistance, relative to antibiotics. Consequently, antiseptics are appropriate alternatives to antibiotics for the prevention and treatment of superficial skin infections. Of four widely used antiseptics (povidone iodine, polihexanide, chlorhexidine and octenidine), povidone iodine has a particularly broad spectrum of antimicrobial activity that includes Gram-positive and Gram-negative bacteria, bacterial spores, fungi, protozoa and viruses. Widespread and extended use of povidone iodine is not associated with the selection of resistant bacterial strains. In contrast, bacterial resistance to chlorhexidine, quaternary ammonium salts, silver and triclosan has been documented. Regarding duration of effect on healthy skin, chlorhexidine is active for 1–4 h, whereas solutions of povidone iodine are active for 12–14 h. Aqueous and hydroalcoholic formulations of povidone iodine have good skin tolerance. Povidone iodine scrub has better skin tolerance than soap formulations of chlorhexidine and quaternary ammonium compounds (e.g., benzalkonium chloride and
    [Show full text]
  • Nature the Enzyme-Substrate Com- Pounds of Catalase and Peroxides
    914 NATURE June 12, 1948 Vol. 161 These are valid equivalents ; but the important point is this-the agreed figure for the last two THE ENZYME-SUBSTRATE COM­ whaling seasons of 16,000 'blue whale units' for the POUNDS OF CATALASE AND contracting parties may well mean that a full catch involves the killing of many more than 16,000 PEROXIDES animals. For example, in 1945-46 the Antarctic catch was returned8 as 8,304·8 'blue whale units', By BRITTON CHANCE* but was, in fact, made up of 13,381 whales (3,604 blue, 9,184 fin, 238 humpback and 81 sei whales, as well Biochemical Department, Medical Nobel Institute, Stockholm, and Molteno Institute, University of as 239 sperm whales and 35 "sperm and others"). Cambridge This last might include some bottlenose or Berardius. The catch for 1946-47 has been returned7 as 15,230·7 'blue whale units'. This represents 8,870 blue, ATALASE is a hrematin enzyme found in 12,857 fin and 2 sei whales, a total of 21,729 C relatively large concentrations in erythrocytes, whales8 • liver, kidney, etc. Its extremely efficient catalysis There is obviously a serious danger of losing sight of the destruction of hydrogen peroxide and its of the reality of the position by continued contempla­ ability to catalyse the oxidation of alcohols by tion of the 'blue whale unit' value of a catch, since hydrogen peroxide have been recognized for some the number of animals killed will always be greater time, but very little direct evidence for the than the number of units allowed.
    [Show full text]
  • Alcohols and Phenols (Pp. 591-600)
    13.9 Reactions of Alcohols: Substitution and Elimination 591 MEDICALLYSPEAKING Phenols as Antifungal Agents >ÞÊ« iÃÊ>`ÊÌ iÀÊ`iÀÛ>ÌÛiÃÊiÝ LÌÊÌ«V>Ê>ÌvÕ}>Ê«À« / iÃiÊV«Õ`Ã]Ê>ÃÊÜiÊ>ÃÊ>ÞÊÌ iÀÃ]Ê>ÀiÊÕÃi`ÊÊ iÀÌiðÊ/ iÃiÊ>}iÌÃÊ>ÀiÊLiiÛi`ÊÌÊÌiÀviÀiÊÜÌ ÊÌ iÊViÊi Ì iÊÌÀi>ÌiÌÊvÊ>Ì iÌi½ÃÊvÌ]ÊVÊÌV ]Ê >`ÊÀ}ÜÀ°Ê LÀ>iÊvÕVÌÊvÊvÕ}°Ê/ iÊvÜ}Ê>ÀiÊÕÃÌÊ>ÊviÜÊiÝ>«ið />vÌ>ÌiÊ ÃÊ Ì iÊ >VÌÛiÊ }Ài`iÌÊ Ê />VÌ/]Ê "`ÀÊ >ÌiÀÃ/]Ê>`Ê iÃiiÝ/° OH O Cl Cl I S N O Cl I N Alcohols and Phenols Cl Cl OH para-Chloro- Haloprogin Clioquinol Tolnaftate meta-xylenol Klein, D. (2012). Alcohols and Phenols. En Organic Chemistry (pp. 591- 600). USA: Wiley. 13.9 Reactions of Alcohols: Substitution and Elimination SN1 Reactions with Alcohols !SSEENIN3ECTION TERTIARYALCOHOLSWILLUNDERGOASUBSTITUTIONREACTIONWHENTREATEDWITH a hydrogen halide. OH HX X ± H2O 7ESAWTHATTHISREACTIONPROCEEDSVIAAN3N1 mechanism. Proton transfer Loss of a leaving group Nucleophilic attack H + – – + OH H Br O H2O Br Br H Recall that an SN1 mechanism has two core steps (loss of leaving group and nucleophilic attack). 7HENTHESTARTINGMATERIALISANALCOHOL WESAWTHATANADDITIONALSTEPISREQUIREDINORDERTO PROTONATETHEHYDROXYLGROUPlRST4HISREACTIONPROCEEDSVIAACARBOCATIONINTERMEDIATEANDIS therefore most appropriate for tertiary alcohols. Secondary alcohols undergo SN1 more slowly, and primary alcohols will not undergo SNATANAPPRECIABLERATE7HENDEALINGWITHAPRIMARY alcohol, an SNPATHWAYISREQUIREDINORDERTOCONVERTANALCOHOLINTOANALKYLHALIDE SN2 Reactions with Alcohols Primary and secondary alcohols will undergo substitution reactions with
    [Show full text]
  • POISONS LIST APPENDIX Amoebicides: Carbarsone
    POISONS LIST APPENDIX Amoebicides: Carbarsone Clioquinol and other halogenated hydroxyquinoline compounds Dehydroemetine; its salts Diloxanide; its compounds Dimetridazole Emetine Ipronidazole Metronidazole Pentamidine; its salts Ronidazole Anaesthetics: Alphadolone acetate Alphaxolone Desflurane Disoprofol Enflurane Ethyl ether Etomidate; its salts Halothane Isoflurane Ketamine; its salts Local anaesthetics, the following: their salts; their homologues and analogues; their molecular compounds Amino-alcohols esterified with benzoic acid, phenylacetic acid, phenylpropionic acid, cinnamic acid or the derivatives of these acids; their salts Benzocaine Bupivacaine Butyl aminobenzoate Cinchocaine Diperodon Etidocaine Levobupivacaine Lignocaine Mepivacaine Orthocaine Oxethazaine Phenacaine Phenodianisyl Prilocaine Ropivacaine Phencyclidine; its salts Propanidid Sevoflurane Tiletamine; its salts Tribromoethanol Analeptics and Central Stimulants: Amiphenazole; its salts Amphetamine (DD) Bemegride Cathine Cathinone (DD) Dimethoxybromoamphetamine (DOB) (DD) 2, 5-Dimethoxyamphetamine (DMA) (DD) 2, 5-Dimethoxy-4-ethylamphetamine (DOET) (DD) Ethamivan N-Ethylamphetamine; its salts N-Ethyl MDA (DD) N-Hydroxy MDA (DD) Etryptamine (DD) Fencamfamine Fenetylline Lefetamine or SPA or (-)-1-dimethylamino-1, 2-diphenylethane Leptazol Lobelia, alkaloids of Meclofenoxate; its salts Methamphetamine (DD) Methcathinone (DD) 5-Methoxy-3, 4-methylenedioxyamphetamine (MMDA) (DD) Methylenedioxyamphetamine (MDA) (DD) 3, 4-Methylenedioxymetamphetamine (MDMA) (DD) Methylphenidate;
    [Show full text]
  • Version 4.1, 02/2020 SUMMARY of PRODUCT CHARACTERISTICS
    Version 4.1, 02/2020 SUMMARY OF PRODUCT CHARACTERISTICS, LABELLING AND PACKAGE LEAFLET 1 SUMMARY OF PRODUCT CHARACTERISTICS 2 1. NAME OF THE MEDICINAL PRODUCT [Nationally completed name], plaster for provocation test 2. QUALITATIVE AND QUANTITATIVE COMPOSITION Active substance microgram/cm2 microgram/patch Panel 1 1. Nickel sulphate 200 162 2. Wool alcohols 1000 810 3. Neomycin sulphate 600 486 4. Potassium dichromate 54 44 5. Caine mixa) 630 510 6. Fragrance mixb) 430 348 7. Colophony 1200 972 8. Paraben mixc) 1000 810 9. Blank patch - - 10. Balsam of Peru 800 648 11. Ethylenediamine dihydrochloride 50 41 12. Cobalt chloride 20 16 Panel 2 13. p-tert Butylphenol formaldehyde resin 45 36 14. Epoxy resin 50 41 15. Carba mixd) 250 203 16. Black rubber mixe) 75 61 17. Cl+Me-Isothiazolinone 4 3 18. Quaternium-15 100 81 19. Methyldibromoglutaronitrile 5.0 4.1 20. p-Phenylenediamine 80 65 21. Formaldehydef) 180 146 22. Mercapto mixg) 75 61 23. Thiomersal 7 6 24. Thiuram mixh) 27 22 Panel 3 25. Diazolidinyl urea 550 450 26. Quinoline mixi) 190 154 27. Tixocortol-21-pivalate 3.0 2.4 28. Gold sodium thiosulfate 75 61 29. Imidazolidinyl urea 600 490 30. Budesonide 1.0 0.81 31. Hydrocortisone-17-butyrate 20 16 32. Mercaptobenzothiazole 75 61 33. Bacitracin 600 490 3 34. Parthenolide 3.0 2.4 35. Disperse blue 106 50 41 36. 2-bromo-2-nitropropane-1,3-diol 250 200 a) Five parts of benzocaine, one part of cinchocaine hydrochloride and tetracaine hydrochloride. b) Five parts of geraniol and oak moss, four parts of hydroxycitronellal and cinnamylalcohol, two parts of cinnamaldehyde and eugenol and one part of isoeugenol and α-amylcinnamaldehyde.
    [Show full text]
  • (12) Patent Application Publication (10) Pub. No.: US 2016/0319266A1 Kolkman Et Al
    US 201603 19266A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2016/0319266A1 Kolkman et al. (43) Pub. Date: Nov. 3, 2016 (54) SERINE PROTEASES OF THE BACILLUS Related U.S. Application Data GIBSONI-CLADE (60) Provisional application No. 61/915,737, filed on Dec. (71) Applicant: DANISCO US INC., Palo Alto, CA 13, 2013, provisional application No. 62/069,200, (US) filed on Oct. 27, 2014. (72) Inventors: Marc Kolkman, Oegstgeest (NL); Rie Publication Classification Mejldal, Ostbirk (DK); Frits Goedegebuur, Vlaardingen (NL); Lilia (51) Int. Cl. Maria Babe, Emerald Hills, CA (US); CI2N 9/54 (2006.01) Anja Hemmingsen Kellett-Smith, A47L I3/00 (2006.01) Arhuc (DK); Harm Mulder. Oegstgeest CLID 3/386 (2006.01) (NL); Richard R. Bott, Burlingame, (52) U.S. Cl. CA (US); Miles Christopher Scotcher, CPC ............... CI2N 9/54 (2013.01): CI2Y 304/21 Hayward, CA (US) (2013.01): CIID 3/386 (2013.01); A47L (73) Assignee: Danisco US Inc., Palo Alto, CA (US) 15/0002 (2013.01); A47L 2601/20 (2013.01) (21) Appl. No.: 15/104,219 (57) ABSTRACT (22) PCT Filed: Dec. 12, 2014 The present disclosure relates to serine proteases cloned from Bacillus gibsonii, and variants thereof. Compositions (86). PCT No.: PCT/US1.4/70 107 containing the serine proteases are Suitable for use in clean 371 C)(1),1 1nging fabriTabr1cS andd hardnard SurTaces,Surf as wellll as i1n a Var1elyiety ofo (2) Date: Jun. 13, 2016 industrial applications. Patent Application Publication Nov. 3, 2016 Sheet 1 of 18 US 2016/0319266 A1 eft - iambda apfs promoter region signai peptide apt Tet R.
    [Show full text]
  • Hand Hygiene Factfinder
    Published November 2013 Hand Hygiene FactFinder Committed to providing helpful information to International Spine Intervention Society members about key patient safety issues, the Society’s Patient Safety Committee has developed a FactFinder series. FactFinders will explore and debunk myths surrounding patient safety issues. The intent of this FactFinder is to present the evidence regarding the importance of hand hygiene and its role in decreasing the risk of infectious complications following spinal procedures. Myth: Washing hands with soap and water is as effective as using antiseptic solutions or surgical scrubs. Fact: Non-antimicrobial soaps contain detergents that are effective in removing loose dirt, transient bacteria, and spores from skin surfaces. However, non-antimicrobial soaps have limited bactericidal activity compared to antimicrobial soap, antiseptic hand washes, or surgical scrubs. Historical In 1822, Labarraque, a French pharmacist, demonstrated that solutions containing chlorides of lime or soda could eradicate the foul odors associated with human corpses and that such solutions could be used as disinfectants and antiseptics. In an 1825 paper, he stated that physicians and other persons attending patients with contagious diseases would benefit from moistening their hands with a liquid chloride solution.1 In 1847, students and physicians working at a maternity clinic were instructed to clean their hands with a chlorine solution between each patient, which resulted in a significant reduction of the maternal mortality rate
    [Show full text]