Palmoplantar Eruption in a Patient with Mercury Poisoning
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
10Neurodevelopmental Effects of Childhood Exposure to Heavy
Neurodevelopmental E¤ects of Childhood Exposure to Heavy Metals: 10 Lessons from Pediatric Lead Poisoning Theodore I. Lidsky, Agnes T. Heaney, Jay S. Schneider, and John F. Rosen Increasing industrialization has led to increased exposure to neurotoxic metals. By far the most heavily studied of these metals is lead, a neurotoxin that is particularly dangerous to the developing nervous system of children. Awareness that lead poison- ing poses a special risk for children dates back over 100 years, and there has been increasing research on the developmental e¤ects of this poison over the past 60 years. Despite this research and growing public awareness of the dangers of lead to chil- dren, government regulation has lagged scientific knowledge; legislation has been in- e¤ectual in critical areas, and many new cases of poisoning occur each year. Lead, however, is not the only neurotoxic metal that presents a danger to children. Several other heavy metals, such as mercury and manganese, are also neurotoxic, have adverse e¤ects on the developing brain, and can be encountered by children. Al- though these other neurotoxic metals have not been as heavily studied as lead, there has been important research describing their e¤ects on the brain. The purpose of the present chapter is to review the neurotoxicology of lead poisoning as well as what is known concerning the neurtoxicology of mercury and manganese. The purpose of this review is to provide information that might be of some help in avoiding repeti- tion of the mistakes that were made in attempting to protect children from the dan- gers of lead poisoning. -
Approach to the Poisoned Patient
PED-1407 Chocolate to Crystal Methamphetamine to the Cinnamon Challenge - Emergency Approach to the Intoxicated Child BLS 08 / ALS 75 / 1.5 CEU Target Audience: All Pediatric and adolescent ingestions are common reasons for 911 dispatches and emergency department visits. With greater availability of medications and drugs, healthcare professionals need to stay sharp on current trends in medical toxicology. This lecture examines mind altering substances, initial prehospital approach to toxicology and stabilization for transport, poison control center resources, and ultimate emergency department and intensive care management. Pediatric Toxicology Dr. James Burhop Pediatric Emergency Medicine Children’s Hospital of the Kings Daughters Objectives • Epidemiology • History of Poisoning • Review initial assessment of the child with a possible ingestion • General management principles for toxic exposures • Case Based (12 common pediatric cases) • Emerging drugs of abuse • Cathinones, Synthetics, Salvia, Maxy/MCAT, 25I, Kratom Epidemiology • 55 Poison Centers serving 295 million people • 2.3 million exposures in 2011 – 39% are children younger than 3 years – 52% in children younger than 6 years • 1-800-222-1222 2011 Annual report of the American Association of Poison Control Centers Toxic Exposure Surveillance System Introduction • 95% decline in the number of pediatric poisoning deaths since 1960 – child resistant packaging – heightened parental awareness – more sophisticated interventions – poison control centers Epidemiology • Unintentional (1-2 -
Mercury Poisoning Manifested Acrodynia, Reported in Four Old Boy in Michigan Ten Day After the Inside of His Heme Painted
TOXIC INFECTIVE DISORDERS MERCURY POISONING AND LATEX PAINT Mercury poisoning manifested as acrodynia, reported in a four year old boy in Michigan ten day after the inside of his heme was painted with 64 liters of interior latex paint containing phenylmercurie acetate, prompted an investigation by the Division of Environmental Hazards and Health Effects, Centers for Disease Control, Atlanta, GA. Nineteen families were recruited from a list of more than 100 persons who called the Michigan Department of Public Health after a press release announced that some interior latex paint contained more than the recommended limit of mercury of 1.5 nmol per liter. Ihe median mercury content of the paint in 29 cans sanpled from the exposed households was 3.8 nmol per liter. Hie concentrations of mercury in the air sanples obtained from homes of exposed families were significantly higher than in the unexposed households. Urinary mercury concentrations were significantly higher among the exposed persons than among unexposed persons (4.7 nmol of mercury per millimole of creatinine compared to 1.1 nmol per millimole). These mercury concentrations in exposed persons have been associated with synptcmatic mercury poisoning. (Agocs MM, Etzel RA et al. Mercury exposure from interior latex paint. N Engl J Med Oct 18, 1990; 323:1096-1101). OCMVENT. Exposed children had the highest urinary mercury concentrations and young children may be at increased risk since vapors containing mercury are heavier than indoor air and tend to settle toward the floor. Individual exposure to mercury varies with the time spent in painted rooms, the depth and frequency of inhalation, the degree of ventilation in the room, and the likely decrease in mercury vapors over time. -
Sound Management of Pesticides and Diagnosis and Treatment Of
* Revision of the“IPCS - Multilevel Course on the Safe Use of Pesticides and on the Diagnosis and Treatment of Presticide Poisoning, 1994” © World Health Organization 2006 All rights reserved. The designations employed and the presentation of the material in this publication do not imply the expression of any opinion whatsoever on the part of the World Health Organization concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. Dotted lines on maps represent approximate border lines for which there may not yet be full agreement. The mention of specific companies or of certain manufacturers’ products does not imply that they are endorsed or recommended by the World Health Organization in preference to others of a similar nature that are not mentioned. Errors and omissions excepted, the names of proprietary products are distinguished by initial capital letters. All reasonable precautions have been taken by the World Health Organization to verify the information contained in this publication. However, the published material is being distributed without warranty of any kind, either expressed or implied. The responsibility for the interpretation and use of the material lies with the reader. In no event shall the World Health Organization be liable for damages arising from its use. CONTENTS Preface Acknowledgement Part I. Overview 1. Introduction 1.1 Background 1.2 Objectives 2. Overview of the resource tool 2.1 Moduledescription 2.2 Training levels 2.3 Visual aids 2.4 Informationsources 3. Using the resource tool 3.1 Introduction 3.2 Training trainers 3.2.1 Organizational aspects 3.2.2 Coordinator’s preparation 3.2.3 Selection of participants 3.2.4 Before training trainers 3.2.5 Specimen module 3.3 Trainers 3.3.1 Trainer preparation 3.3.2 Selection of participants 3.3.3 Organizational aspects 3.3.4 Before a course 4. -
Indoor Air Mercury May 2003
Indoor Air Mercury May 2003 Why is Mercury a Problem in Indoor Air? Mercury is a potent neurotoxin found in a variety of products. It affects the brain, liver and kidneys and can cause developmental disorders in children. Young children and developing fetuses are especially at risk. Metallic, or elemental mercury, is a liquid at room temperature and like any other liquid it evaporates into the air, where it can be inhaled. Exposures can occur in the home when a mercury-containing item, such as a thermometer, breaks and is not properly cleaned up. They can occur in the workplace when mercury or mercury-containing device/materials are not carefully handled and safely managed or when workplace or storage areas are not properly ventilated. Exposures can also occur when children find and play with improperly stored mercury; many cases of mercury poisoning result for this reason.1 When spilled in a small, poorly-ventilated room, mercury can pose significant health threats. Very small amounts of metallic mercury, released into an enclosed space, (i.e., a few drops) can raise air concentrations of mercury to levels that may be harmful to health. The longer people breathe the contaminated air, the greater the risk to their health. In addition, metallic mercury and its vapors are extremely difficult to remove from clothes, furniture, carpet, and other porous items. If these items are not properly disposed or cleaned, the mercury can linger for months or years, continuing to pose a health threat. The risk of exposure to mercury from indoor air is not insignificant. -
Compendium of Chemical Hazards: Mercury
Inorganic Mercury/Elemental Mercury Toxicological Overview Key Points Kinetics and metabolism the main route of exposure to elemental mercury is inhalation and to inorganic mercury compounds is ingestion mercury is distributed to all tissues but mainly accumulates in the kidneys elemental mercury may readily cross the blood-brain barrier elimination predominantly occurs through the urine and faeces Health effects of acute exposure inhalation of elemental mercury may cause respiratory, central nervous system and cardiovascular effects, renal damage and gastrointestinal disturbances ingestion of inorganic mercury compounds may affect the digestive tract, and cause renal damage, cardiovascular effects and skin/eye effects Health effects of chronic exposure inhalation of elemental mercury vapour may cause neurotoxicity, nephrotoxicity and effects on the oral cavity ingestion of inorganic mercury compounds may cause neurotoxicity, digestive tract effects or renal failure the International Agency for Research on Cancer (IARC) classified elemental mercury and mercury compounds as a category 3 carcinogen, ie not classifiable as to the carcinogenicity to humans PHE publications gateway number: 2014790 Published: June 2016 Compendium of Chemical Hazards: Inorganic Mercury/Elemental Mercury Summary of Health Effects The main target organs of elemental and inorganic mercury toxicity are the central nervous system (CNS) and the kidneys. Inhalation is the significant route of exposure to elemental mercury. It is poorly absorbed from the gastrointestinal (GI) tract and is therefore unlikely to cause serious adverse health effects following ingestion. The majority of data available on the toxicity of inorganic mercury compounds concerns exposure by ingestion. Acute inhalation of elemental mercury vapour may cause respiratory effects such as cough, dyspnoea, chest tightness, bronchitis and decreased pulmonary function. -
Mercury Intoxication and Arterial Hypertension: Report of Two Patients and Review of the Literature
Mercury Intoxication and Arterial Hypertension: Report of Two Patients and Review of the Literature Alfonso D. Torres, MD*; Ashok N. Rai, MD‡; and Melissa L. Hardiek, MD‡ ABSTRACT. Two children in the same household with evere systemic arterial hypertension in infants symptomatic arterial hypertension simulating pheochro- and children is usually secondary to an under- mocytoma were found to be intoxicated with elemental lying disease process. The most frequent causes mercury. The first child was a 4-year-old boy who pre- S of hypertension in this group include renal paren- sented with new-onset seizures, rash, and painful ex- chymal disease, obstructive uropathy, chronic pyelo- tremities, who was found to have a blood pressure of nephritis associated with reflux, and renal artery ste- 171/123 mm Hg. An extensive investigation ensued. Ele- vated catecholamines were demonstrated in plasma and nosis. Less frequent causes include adrenal tumors, urine; studies did not confirm pheochromocytoma. Mer- pheochromocytomas, neurofibromas, and an in- cury levels were elevated. These findings prompted an creasing number of familial forms of hypertension. evaluation of the family. A foster sister had similar find- Other causes are medications and drugs of ingestion ings of rash and hypertension. Both had been exposed to or abuse, especially cocaine and sympathomimetics. elemental mercury in the home. The family was tempo- Heavy metal intoxication is also implicated.1 We rarily relocated and chelation therapy was started. present 2 patients with an infrequent cause of hyper- A Medline search for mercury intoxication with hyper- tension. tension found 6 reports of patients ranging from 11 months to 17 years old. -
Chemical Pollution and Marine Mammals
PROCEEDINGS OF THE ECS/ASCOBANS/ACCOBAMS JOINT WORKSHOP ON CHEMICAL POLLUTION AND MARINE MAMMALS Held at the European Cetacean Society’s 25th Annual Conference Cádiz, Spain, 20th March 2011 Editor: Peter G.H. Evans ECS SPECIAL PUBLICATION SERIES NO. 55 Cover photo credits: Right: © Ron Wooten/Marine Photobank Left: © Peter G.H. Evans PROCEEDINGS OF THE ECS/ASCOBANS/ACCOBAMS JOINT WORKSHOP ON CHEMICAL POLLUTION AND MARINE MAMMALS Held at the European Cetacean Society’s 25th Annual Conference Cádiz, Spain, 20th March 2011 Editor: Peter G.H. Evans1, 2 1Sea Watch Foundation, Ewyn y Don, Bull Bay, Amlwch, Isle of Anglesey LL68 9SD 2 School of Ocean Sciences, University of Bangor, Menai Bridge, Isle of Anglesey, LL59 5AB, UK ECS SPECIAL PUBLICATION SERIES NO. 55 AUG 2013 a a CONTENTS Reijnders, Peter.J.H. Foreword: Some encouraging successes despite the never ending story ........... 2 Evans, Peter G.H. Introduction ...................................................................................................... 3 Simmonds, Mark P. European cetaceans and pollutants: an historical perspective ........................... 4 Insights from long-term datasets Law, Robin and Barry, Jon. Long-term time-trends in organohalogen concentrations in blubber of porpoises from the UK .................................................................................................................. 9 Jepson, Paul D., Deaville, Rob, Barnett, James, Davison, Nick J., Paterson, Ian A.P., Penrose, Rod, S., Perkins, M.P., Reid, Robert J., and Law, Robin J. Persisent -
Evidence-Based Management of Kawasaki Disease in the Emergency Department
January 2015 Evidence-Based Management Volume 12, Number 1 Authors Of Kawasaki Disease In The Kara K. Seaton, MD Fellow, Pediatric Emergency Medicine, Children’s Hospital and Clinics of Minnesota, Minneapolis, MN Emergency Department Anupam Kharbanda, MD Director of Research, Emergency and Trauma Services, Abstract Children’s Hospital and Clinics of Minnesota, Minneapolis, MN Peer Reviewers Kawasaki disease, also known as mucocutaneous lymph node syn- Catherine Sellinger, MD, FAAP Associate Director, Pediatric Emergency Services, Children’s drome, was first described in Japan in 1967. It is currently the leading Hospital at Montefiore; Assistant Professor of Pediatrics, Albert cause of acquired heart disease in children in the United States. Un- Einstein College of Medicine, Bronx, NY treated Kawasaki disease may lead to the formation of coronary artery Michael J. Stoner, MD Assistant Professor of Pediatrics, The Ohio State University aneurysms and sudden cardiac death in children. This vasculitis pres- College of Medicine; Attending Physician, Pediatric Emergency ents with fever for ≥ 5 days, plus a combination of key criteria. Because Medicine, Nationwide Children’s Hospital, Columbus, OH each of the symptoms commonly occurs in other childhood illnesses, CME Objectives the disease can be difficult to diagnose, especially in children who Upon completion of this article, you should be able to: present with an incomplete form of the disease. At this time, the etiol- 1. Describe the clinical features and risks associated with ogy of the disease remains unknown, and there is no single diagnostic Kawasaki disease. 2. Identify epidemiologic trends in Kawasaki disease in high- test to confirm the diagnosis. This issue reviews the presentation, diag- risk populations. -
PINK DISEASE MENU Heather Thiele
pink2a PINK DISEASE MENU most of these articles were gathered by Heather Thiele. http://www.users.bigpond.com/difarnsworth/pink2a.htm (1 of 2) [05/28/2000 1:42:05 AM] pink2a ACRODYNIA-Nelson's book of poisons & drugs. MERCURY & PINK DISEASE-Lancet 1951 THE MEDICAL JOURNAL OF AUSTRALIA (June 11-1960) MORTALITY FROM PINK DISEASE in 1923-1947 DISEASES KNOWN TO BE CAUSED BY THE DIET Dr. CHEEK...discoverer of possible CAUSE/linkage with Hg & Enzyme. PINK DISEASE-10 YEARS AFTER (The Epilogue) A LONG TERM STUDY OF 62 CASES YOUNG'S SYNDROME & PINK DISEASE. BMJ December 1993 Back to Top MAIN MENU http://www.users.bigpond.com/difarnsworth/pink2a.htm (2 of 2) [05/28/2000 1:42:05 AM] pink34 Acrodynia. Pink Disease, Swift Disease, Feer Disease, Erythodema, Dermatopolyneuritus Nelson’s Textbook Chemical and Drug Poisoning http://www.users.bigpond.com/difarnsworth/pink34.htm (1 of 4) [05/28/2000 1:42:21 AM] pink34 Acrodynia (the term derived from the Greek, denotes painful extremities) is principally a syndrome of chronic mercury poisoning in infants and young children consisting of many unusual symptoms which, in the well established cases, are so distinctive that there is practically no difficult diagnosis. In few other conditions is extreme and persistent misery such prominent part of the clinical picture. The condition was recognised in Australia as early as 1890 and established as a clinical entity in the British and American literature by Byfield and Bilderback in 1920. Etiology. Most and perhaps all cases of acrodynia represent the clinical response to repeated contact with or ingestion of mercury in products such as house paints, wallpapers, teething powders, vermifuges and diaper rinses. -
Implications for Inositol 1,4,5-Trip
Review http://dx.doi.org/10.4070/kcj.2013.43.9.581 Print ISSN 1738-5520 • On-line ISSN 1738-5555 Korean Circulation Journal Mercury Promotes Catecholamines Which Potentiate Mercurial Autoimmunity and Vasodilation: Implications for Inositol 1,4,5-Triphosphate 3-Kinase C Susceptibility in Kawasaki Syndrome Deniz Yeter, MD1, Richard Deth, PhD2, and Ho-Chang Kuo, MD3 1Shawnee, KS, 2Department of Pharmaceutical Sciences, Northeastern University, Boston, MA, USA 3Division of Allergy, Immunology and Rheumatology, Department of Pediatrics, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, Taiwan Previously, we reviewed biological evidence that mercury could induce autoimmunity and coronary arterial wall relaxation as observed in Kawasaki syndrome (KS) through its effects on calcium signaling, and that inositol 1,4,5-triphosphate 3-kinase C (ITPKC) susceptibility in KS would predispose patients to mercury by increasing Ca2+ release. Hg2+ sensitizes inositol 1,4,5-triphosphate (IP3) receptors at low doses, which release Ca2+ from intracellular stores in the sarcoplasmic reticulum, resulting in delayed, repetitive calcium influx. ITPKC prevents IP3 from triggering IP3 receptors to release calcium by converting IP3 to inositol 1,3,4,5-tetrakisphosphate. Defective IP3 phosphorylation re- sulting from reduced genetic expressions of ITPKC in KS would promote IP3, which increases Ca2+ release. Hg2+ increases catecholamine levels through the inhibition of S-adenosylmethionine and subsequently catechol-O-methyltransferase (COMT), while a single nucleotide polymorphism of the COMT gene (rs769224) was recently found to be significantly associated with the development of coronary artery le- sions in KS. Accumulation of norepinephrine or epinephrine would potentiate Hg2+-induced calcium influx by increasing IP3 production and increasing the permeability of cardiac sarcolemma to Ca2+. -
An NGO Introduction to Mercury Pollution
INTERNATIONAL POPs ELIMINATION NETWORK An NGO Introduction to Mercury Pollution By Jack Weinberg Senior Policy Advisor International POPs Elimination Network INTERNATIONAL POPs ELIMINATION NETWORK The International POPs Elimination Network (IPEN) is a global network of health and environmental organizations working in more than a hundred countries. The network was originally founded to promote the negotiation of a global treaty to protect human health and the environment from a class of toxic chemicals called Persistent Organic Pollutants (POPs). Then, following adoption by Governments of the Stockholm Convention on POPs, IPEN expanded its mission beyond POPs and now supports local, national, regional and international efforts to protect health and the environment from harms caused by exposure to toxic chemicals. This booklet may only be reproduced for non-commercial purposes with the permission of IPEN. Cover photos top to bottom: 1) Shutterstock® Images, 2) Shutterstock® Images, 3) iStockphoto®, 4) Global Mercury Project, 2007, 5) iStockphoto®, 6) iStockphoto® List of Abbreviations and Acronyms AAP American Academy of Pediatrics ALMR Association of Lamp and Mercury Recyclers AMDE Atmospheric Mercury Depletion Event APCD Air Pollution Control Device ASGM Artisanal and Small-Scale Gold Mining BAT Best Available Techniques BPOM Indonesian Food and Drug Control Agency CDC United States Centers for Disease Control and Prevention CFL Compact Fluorescent Lamp COP Conference of Parties CSO Civil Society Organization EMEA European Agency for