Near-Real-Time Surveillance of Illnesses Related to Shellfish Consumption in British Columbia: Analysis of Poison Center Data
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News and Notes 97
96 Injury Prevention 1998;4:96–97 ... while in Canada, helmet laws nated eVorts. It sets targets for the reduction Inj Prev: first published as 10.1136/ip.4.2.96 on 1 June 1998. Downloaded from knocked of deaths and injuries requiring hospitalisa- NEWS AND tion for traYc collisions, fires, drownings, and As summer approached, the debate over those in the workplace and home. Recognis- NOTES bicycle helmets in Canada was heating up. ing the lack of information on sport and rec- Countering a growing movement to get reational injuries the report notes that this helmet laws passed in every province is an area requires further attention. Further details: organization called the Ontario Coalition for Minister’s Injury Prevention Committee, c/o Better Cycling whose web site applauds the OYce for Injury Prevention, Environmental Revised injury control manual from failures of helmet law lobbyists and the Health Assessment and Safety Branch, BC Ministry of Health, 7-1 1515 Blanshard AAP watering down of Ontario’s law (only cyclists younger than 18 must wear helmets or face a Street, Victoria BC V8V 3C8, Canada (fax: The new injury control manual from the fine in that province). The group argues that +1 250 952 1342). American Academy of Pediatrics (AAP) is the government should instead mandate now available and by all accounts is well cycling education in schools, on the grounds Our Healthier Nation worth looking at. It contains new chapters on that more crashes and injuries can be violence, sports injuries, agricultural injuries, prevented “by getting children to appreciate A Contract for Health is how the UK govern- the need to cycle responsibly”. -
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 -
Allergic and Toxic Reactions to Seafood
Allergic and toxic reactions to seafood ASCIA EDUCATION RESOURCES (AER) PATIENT INFORMATION Seafood allergy occurs most commonly where seafood is an important part of the diet, such as Asia and Scandinavia. It is more common in adults than children. Seafood allergy usually remains a life long problem. Some conditions caused by toxins or parasites in seafood can resemble allergic reactions to seafood. Seafood allergy is not rare While estimates vary from country to country, approximately 1% of the population is estimated to suffer from seafood allergy, which is more common in teenage and adult life than very early childhood. An estimated 20% will grow out of their allergy with time. Symptoms of seafood allergy are usually obvious Many allergic reactions to seafood are mild and cause hives (urticaria), swelling (angioedema) and/or gut reactions (vomiting, diarrhoea). The most dangerous symptoms are breathing difficulties or collapse [a drop in blood pressure (shock)], either of which can be life threatening. This is known as anaphylaxis, which is the most severe type of allergic reaction. Occasionally, breathing difficulties may occur from inhaling fumes when seafood is being cooked, and in seafood processing factories. Children with a history of asthma may be more likely to have severe allergic reactions to seafood. There are many varieties of seafood The major groups of seafood that can trigger allergic reactions are: • VERTEBRATES Fish including salmon, cod, mackerel, sardines, herring, anchovies, tuna, trout, haddock, John Dory, eels, rays. • INVERTEBTRATES (SHELLFISH) Crustaceans including prawns/shrimps, lobster, crab, crayfish, yabbies. Molluscs including oysters, mussels, clams, octopus, squid, calamari, abalone, sea slugs. -
Cyanobacterial Toxins: Saxitoxins
WHO/SDE/WSH/xxxxx English only Cyanobacterial toxins: Saxitoxins Background document for development of WHO Guidelines for Drinking-water Quality and Guidelines for Safe Recreational Water Environments Version for Public Review Nov 2019 © World Health Organization 20XX Preface Information on cyanobacterial toxins, including saxitoxins, is comprehensively reviewed in a recent volume to be published by the World Health Organization, “Toxic Cyanobacteria in Water” (TCiW; Chorus & Welker, in press). This covers chemical properties of the toxins and information on the cyanobacteria producing them as well as guidance on assessing the risks of their occurrence, monitoring and management. In contrast, this background document focuses on reviewing the toxicological information available for guideline value derivation and the considerations for deriving the guideline values for saxitoxin in water. Sections 1-3 and 8 are largely summaries of respective chapters in TCiW and references to original studies can be found therein. To be written by WHO Secretariat Acknowledgements To be written by WHO Secretariat 5 Abbreviations used in text ARfD Acute Reference Dose bw body weight C Volume of drinking water assumed to be consumed daily by an adult GTX Gonyautoxin i.p. intraperitoneal i.v. intravenous LOAEL Lowest Observed Adverse Effect Level neoSTX Neosaxitoxin NOAEL No Observed Adverse Effect Level P Proportion of exposure assumed to be due to drinking water PSP Paralytic Shellfish Poisoning PST paralytic shellfish toxin STX saxitoxin STXOL saxitoxinol -
Methadone Poisonings in France
2019 Extended Abstract Clinical Pharmacology & Toxicology Journal Vol. 3 No.2 Methadone Poisonings in France: A Seven-Year Experience of the French Poison Control Center Network Katharina von Fabeck1, Romain Torrents1, 2, Mathieu Glaizal1, Luc de Haro1, Nicolas Simon 1 Centre Antipoison et de Toxicovigilance, Service de Pharmacologie Clinique, Hôpital Sainte Marguerite, APHM, Marseille, France 2 Aix-Marseille University, Marseille, France Methadone is an opioid agonist prescribed in France for the methadone must be considered as a highly toxic medicine. treatment of opioid dependency. In order to evaluate the This investigation is a review examination of methadone exposures clinical toxicity of methadone, the authors present a seven- answered to the nine FPCC between October 15, 2010 and October year experience of the French Poison Control Center (FPCC) 15, 2017. The two pharmaceutical structures (case and syrup) Network at the national level. This study is a retrospective were thought of. Youth inadvertent poisonings were prohibited analysis of methadone exposures reported to the nine FPCC (diverse examination). 1415 instances of methadone harming between October 15th 2010 and October 15th 2017. The two were incorporated (29% female, 71% male, normal age 34 +/ - pharmaceutical forms (capsule and syrup) were considered. 10). 90% of the patients had history of compulsion and 69% were Childhood accidental poisonings were excluded (different treated with methadone (31% were gullible patients). The two study). 1415 cases of methadone poisoning were included (29% primary conditions were addictions (47% of the cases) and self- female, 71% male, average age 34 +/-10). 90% of the patients destruction endeavors (41%). In 45% of the cases it was containers, had history of addiction and 69% were treated with methadone in 35% syrup, obscure for 20%. -
(Slide 1) Lesson 3: Seafood-Borne Illnesses and Risks from Eating
Introductory Slide (slide 1) Lesson 3: Seafood-borne Illnesses and Risks from Eating Seafood (slide 2) Lesson 3 Goals (slide 3) The goal of lesson 3 is to gain a better understanding of the potential health risks of eating seafood. Lesson 3 covers a broad range of topics. Health risks associated specifically with seafood consumption include bacterial illness associated with eating raw seafood, particularly raw molluscan shellfish, natural marine toxins, and mercury contamination. Risks associated with seafood as well as other foods include microorganisms, allergens, and environmental contaminants (e.g., PCBs). A section on carotenoid pigments (“color added”) explains the use of these essential nutrients in fish feed for particular species. Dyes are not used by the seafood industry and color is not added to fish—a common misperception among the public. The lesson concludes with a discussion on seafood safety inspection, country of origin labeling (COOL) requirements, and a summary. • Lesson 3 Objectives (slide 4) The objectives of lesson 3 are to increase your knowledge of the potential health risks of seafood consumption, to provide context about the potential risks, and to inform you about seafood safety inspection programs and country of origin labeling for seafood required by U.S. law. Before we begin, I would like you to take a few minutes to complete the pretest. Instructor: Pass out lesson 3 pretest. Foodborne Illnesses (slide 5) Although many people are complacent about foodborne illnesses (old risk, known to science, natural, usually not fatal, and perceived as controllable), the risk is serious. The Centers for Disease Control and Prevention (CDC) estimates 48 million people suffer from foodborne illnesses annually, resulting in about 128,000 hospitalizations and 3,000 deaths. -
Amnesic Shellfish Poisoning Pseudo-Nitzschia Seen Unde a Microscope
Amnesic Shellfish Poisoning Pseudo-nitzschia seen unde a microscope. Photo credit: Associated Press What is Amnesic Shellfish Poisoning? Amnesic Shellfish Poisoning (ASP) is caused by domoic acid, a toxin produced by marine phytoplankton known as Pseudo-nitzschia. When shellfish filter out large amounts of domoic acid and A satellite picture showing the amount of chloro- Pseudo-nitzschia, they can become contaminated phyll in the North Pacific in summer 2015. Darker with enough toxin to cause ASP. Humans then green areas correspond to higher concentrations get ASP by eating those contaminated shellfish of plankton. (including clams, mussels, oysters, and crabs). Symptoms of ASP develop within 48 hours and Deadly Myths include vomiting, nausea, and diarrhea. Symptoms • Shellfish are safe to eat during months containing the for more severe cases include headaches, dizziness, letter “r”. In November 2015, the entire California confusion, and permanent short-term memory loss. crab fishery was shut down due to high levels of In rare cases, ASP can lead to coma and death. There domoic acid. is no antidote for domoic acid, but patients with ASP should be taken to a hospital for supportive medical • If the water is clear, there is no danger of shellfish care until the toxin passes through their system. poisoning. Many harmful algal blooms are colorless, including most Pseudo-nitzschia blooms. Some shellfish can also retain their toxins for months after a bloom. • If wildlife has been eating the shellfish, it must be safe. Every animal has a different tolerance to ASP toxins. Do not assume shellfish is safe on the basis of animal observations. -
Botulism Guide for Health Care Professionals
Botulism Guide for Health Care Professionals This information requires knowledgeable interpretation and is intended primarily for use by health care workers and facilities/organizations providing health care including pharmacies, hospitals, long-term care homes, community-based health care service providers and pre-hospital emergency services. Population and Public Health Division Ministry of Health and Long-Term Care March 2017 AT A GLANCE A Quick Response Guide to Botulism Botulism – The treatment of botulism is guided by clinical diagnosis The initial diagnosis of botulism should be based on a history of recent exposure, consistent clinical symptoms and elimination of other illnesses in the differential. Treatment should not wait for laboratory confirmation. All treatment and management decisions should be made based on clinical diagnosis. Initial Presentation and evaluation of signs and symptoms There are several clinically distinct forms of botulism. All forms produce the same neurological signs and symptoms of symmetrical cranial nerve palsies followed by descending, symmetric flaccid paralysis of voluntary muscles, which may progress to respiratory compromise and death. Additional symptoms (e.g., gastrointestinal signs in foodborne cases) may also be seen in some forms. Read more on the disease on page 2 Reading the section on Differential Diagnosis and the referenced articles will assist with making the diagnosis of botulism – you will find this on page 3 Place a request for Botulinum Antitoxin (BAT) or BabyBIG® Ministry of Health and Long-Term Care (ministry) staff will arrange for the shipment of BAT. Information on ordering BAT and BabyBIG (BabyBIG has a different ordering process) is on page 5 Laboratory Diagnosis and Specimen Collection Clinical specimens must be obtained prior to administering treatment with botulinum antitoxin. -
2003 Annual Report of the American Association of Poison Control Centers Toxic Exposure Surveillance System
Toxicology A special contribution from the American Association of Poison Control Centers. 2003 Annual Report of the American Association of Poison Control Centers Toxic Exposure Surveillance System WILLIAM A. WATSON, PHARMD, TOBY L. LITOVITZ, MD, WENDY KLEIN-SCHWARTZ, PHARMD, MPH, GEORGE C. RODGERS, JR, MD, PHD, JESSICA YOUNISS, MBA, NICOLE REID, MED, WAYNE G. ROUSE, MCSD, REBECCA S. REMBERT, BS, DOUGLAS BORYS, BSPHARM Toxic Exposure Surveillance System (TESS) data are used to support regulatory actions; and form the basis of compiled by the American Association of Poison Control postmarketing surveillance of newly released drugs and Centers (AAPCC) on behalf of US poison centers. These products. data are used to identify hazards early, focus prevention From its inception in 1983, TESS has grown dramati- education, guide clinical research, direct training, and detect cally, with increases in the number of participating poison chem/bioterrorism incidents. TESS data have prompted centers, population served by those centers, and reported product reformulations, repackaging, recalls, and bans; are human exposures (Table 1A).1-20 The American Association of Poison Control Centers gratefully acknowledges the generous financial contribution of McNeil Consumer and Specialty Pharmaceuticals in support of the compilation and production of this report. The compilation of these data was also supported, in part, by the US Centers for Disease Control and Prevention, Cooperative Agreement U50/CCU323406-01. US poison centers make possible the compilation -
Inhibition of Diarrheal Shellfish Toxins Accumulation in the Mussel Perna Viridis by Curcumin and Underlying Mechanisms
toxins Article Inhibition of Diarrheal Shellfish Toxins Accumulation in the Mussel Perna viridis by Curcumin and Underlying Mechanisms Kuan-Kuan Yuan † , Guo-Fang Duan †, Qing-Yuan Liu, Hong-Ye Li and Wei-Dong Yang * Key Laboratory of Aquatic Eutrophication and Control of Harmful Algal Blooms of Guangdong Higher Education Institute, College of Life Science and Technology, Jinan University, Guangzhou 510632, China; [email protected] (K.-K.Y.); [email protected] (G.-F.D.); [email protected] (Q.-Y.L.); [email protected] (H.-Y.L.) * Correspondence: [email protected] † Equal contributors. Abstract: Diarrheal shellfish toxins (DSTs) are among the most widely distributed phytotoxins, and are associated with diarrheal shellfish poisoning (DSP) events in human beings all over the world. Therefore, it is urgent and necessary to identify an effective method for toxin removal in bivalves. In this paper, we found that curcumin (CUR), a phytopolylphenol pigment, can inhibit the accumulation of DSTs (okadaic acid-eq) in the digestive gland of Perna viridis after Prorocentrum lima exposure. qPCR results demonstrated that CUR inhibited the induction of DSTs on the aryl hydrocarbon receptor (AhR), hormone receptor 96 (HR96) and CYP3A4 mRNA, indicating that the CUR-induced reduction in DSTs may be correlated with the inhibition of transcriptional induction of AhR, HR96 and CYP3A4. The histological examination showed that P. lima cells caused severe damage to the digestive gland of P. viridis, and the addition of curcumin effectively alleviated the damage induced by P. lima. In conclusion, our findings provide a potential method for the effective removal of toxins from DST-contaminated shellfish. -
Studies in the Use of Magnetic Microspheres for Immunoaffinity Extraction of Paralytic Shellfish Poisoning Toxins from Shellfish
Toxins 2011, 3, 1-16; doi:10.3390/toxins3010001 OPEN ACCESS toxins ISSN 2072-6651 www.mdpi.com/journal/toxins Article Studies in the Use of Magnetic Microspheres for Immunoaffinity Extraction of Paralytic Shellfish Poisoning Toxins from Shellfish Raymond Devlin 1, Katrina Campbell 1, Kentaro Kawatsu 2 and Christopher Elliott 1,* 1 Institute of Agri-Food and Land Use, School of Biological Sciences, Queen’s University Belfast, Stranmillis Road, Belfast, BT9 5AG, Northern Ireland, UK; E-Mails: [email protected] (R.D.); [email protected] (K.C.) 2 Division of Bacteriology, Osaka Prefectural Institute of Public Health, Osaka, Japan; E-Mail: [email protected] * Author to whom correspondence should be addressed; E-Mail: [email protected]; Tel.: +44-28-9097-6549; Fax: +44-28-9097-6513. Received: 19 November 2010; in revised form: 10 December 2010 / Accepted: 14 December 2010 / Published: 4 January 2011 Abstract: Paralytic shellfish poisoning (PSP) is a potentially fatal human health condition caused by the consumption of shellfish containing high levels of PSP toxins. Toxin extraction from shellfish and from algal cultures for use as standards and analysis by alternative analytical monitoring methods to the mouse bioassay is extensive and laborious. This study investigated whether a selected MAb antibody could be coupled to a novel form of magnetic microsphere (hollow glass magnetic microspheres, brand name Ferrospheres-N) and whether these coated microspheres could be utilized in the extraction of low concentrations of the PSP toxin, STX, from potential extraction buffers and spiked mussel extracts. The feasibility of utilizing a mass of 25 mg of Ferrospheres-N, as a simple extraction procedure for STX from spiked sodium acetate buffer, spiked PBS buffer and spiked mussel extracts was determined. -
Fda and Epa Safety Levels in Regulations and Guidance
APPENDIX 5: FDA AND EPA SAFETY LEVELS IN REGULATIONS AND GUIDANCE This guidance represents the Food and Drug Administration’s (FDA’s) current thinking on this topic. It does not create or confer any rights for or on any person and does not operate to bind FDA or the public. You can use an alternative approach if the approach satisfies the requirements of the applicable statutes and regulations. If you want to discuss an alternative approach, contact the FDA staff responsible for implementing this guidance. If you cannot identify the appropriate FDA staff, call the telephone number listed on the title page of this guidance. This appendix lists FDA and EPA levels relating to safety attributes of fish and fishery products. In many cases, these levels represent the point at which the agency could take legal action to include removing product from market. Consequently, the levels contained in this table may not always be suitable for critical limits. Regardless of an established level or not, FDA may take legal action against food deemed to be adulterated as defined by the Federal Food, Drug and Cosmetic Act (FD&C Act) [21 U.S.C. 342]. A food is adulterated if the food bears or contains any poisonous or deleterious substance which may render it injurious to health under section 402 (a)(1) of the FD&C Act. Additionally, a food is adulterated if the food has been prepared, packed or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health under section 402 (a)(4) of the FD&C Act.