Training Module for Management of Snake Bite & Common Poisons
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Abhijit Preliminary Report of Reptilian 1541
CASE REPORT ZOOS' PRINT JOURNAL 22(7): 2742-2744 A PRELIMINARY REPORT OF REPTILIAN MORTALITY ON ROAD DUE TO VEHICULAR MOVEMENTS NEAR KAZIRANGA NATIONAL PARK, ASSAM, INDIA Abhijit Das¹, M. Firoz Ahmed², Bibhuti P. Lahkar and Pranjit Sharma ¹ ²Division of Herpetology, Aaranyak, Sommonoy Path, Survey, Beltola, Guwahati, Assam 781028, India ¹Email: [email protected] ABSTRACT STUDY AREA We report road mortality of reptiles on a highway segment The study was carried out during May 2004 to September passing along the southern boundary of Kaziranga National 2004 on a 60km road segment of National Highway 37, passing Park, Assam, India. A total of 68 instances of road kills of 0 0 0 reptiles belonging to 21 species and seven families were recorded. adjacent to Kaziranga National Park (26 34'-26 46'N & 93 08'- There was a greater mortality among snakes compared to lizards. 93036'E) (KNP), Assam, India. The 7.5m wide paved road The arboreal reptiles were the most affected, the highest percent separates the southern side of Kaziranga National Park from being those that were diurnal followed by the nocturnal, Karbi Anglong Hills (KAH) and passes through tea gardens, crepuscular and both day and night active species. Possible human habitations, paddy fields, teak plantations besides forest explanations of such differences in mortality among reptile groups are discussed. It is feared that such kind of persistent habitats of KNP at Panbari, Haldibari, Kanchanjuri and loss can be detrimental to the local reptilian population. Ghorakati (Fig. 1). All these adjacent forest habitats are animal corridors and are frequently used by megamammals like KEYWORDS Elephants, Indian One-horned Rhinoceros, Water Buffalo, Assam, India, Kaziranga National Park, reptile, road kill Tiger, Leopard and Hog Deer during their to and fro movement between KNP and KAH. -
Pharmacology/Therapeutics Ii Block 1 Handouts – 2015-16
PHARMACOLOGY/THERAPEUTICS II BLOCK 1 HANDOUTS – 2015‐16 55. H2 Blockers, PPls – Moorman 56. Palliation of Contipation & Nausea/Vomiting – Kristopaitis 57. On‐Line Only – Principles of Clinical Toxicology – Kennedy 58. Anti‐Parasitic Agents – Johnson Histamine Antagonists and PPIs January 6, 2016 Debra Hoppensteadt Moorman, Ph.D. Histamine Antagonists and PPIs Debra Hoppensteadt Moorman, Ph.D. Office # 64625 Email: [email protected] KEY CONCEPTS AND LEARNING OBJECTIVES . 1 To understand the clinical uses of H2 receptor antagonists. 2 To describe the drug interactions associated with the use of H2 receptor antagonists. 3 To understand the mechanism of action of PPIs 4 To describe the adverse effects and drugs interactions with PPIs 5 To understand when the histamine antagonists and the PPIs are to be used for treatment 6 To describe the drugs used to treat H. pylori infection Drug List: See Summary Table. Histamine Antagonists and PPIs January 6, 2016 Debra Hoppensteadt Moorman, Ph.D. Histamine Antagonists and PPIs I. H2 Receptor Antagonists These drugs reduce gastric acid secretion, and are used to treat peptic ulcer disease and gastric acid hypersecretion. These are remarkably safe drugs, and are now available over the counter. The H2 antagonists are available OTC: 1. Cimetidine (Tagamet®) 2. Famotidine (Pepcid®) 3. Nizatidine (Axid®) 4. Ranitidine (Zantac®) All of these have different structures and, therefore, different side-effects. The H2 antagonists are rapidly and well absorbed after oral administration (bioavailability 50-90%). Peak plasma concentrations are reached in 1-3 hours, and the drugs have a t1/2 of 1-3 hours. H2 antagonists also inhibit stimulated (due to feeding, gastrin, hypoglycemia, vagal) acid secretion and are useful in controlling nocturnal acidity – useful when added to proton pump therapy to control “nocturnal acid breakthrough”. -
WHO Guidance on Management of Snakebites
GUIDELINES FOR THE MANAGEMENT OF SNAKEBITES 2nd Edition GUIDELINES FOR THE MANAGEMENT OF SNAKEBITES 2nd Edition 1. 2. 3. 4. ISBN 978-92-9022- © World Health Organization 2016 2nd Edition All rights reserved. Requests for publications, or for permission to reproduce or translate WHO publications, whether for sale or for noncommercial distribution, can be obtained from Publishing and Sales, World Health Organization, Regional Office for South-East Asia, Indraprastha Estate, Mahatma Gandhi Marg, New Delhi-110 002, India (fax: +91-11-23370197; e-mail: publications@ searo.who.int). 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. -
Poisoning in Children
ARTICLE IN PRESS Current Paediatrics (2005) 15, 563–568 www.elsevier.com/locate/cupe Poisoning in children Fiona JepsenÃ, Mary Ryan Emergency Medicine, Royal Liverpool Children’s NHS Trust, Alder Hey, Liverpool L12 2AP, UK KEYWORDS Summary Poisoning accounts for about 7% of all accidents in children under 5 Poisoning; years and is implicated in about 2% of all childhood deaths in the developed world, Child; and over 5% in the developing world (National Poisons Information Service). In Accidents; considering this topic, however, it is important to differentiate accidental overdose Home (common in the younger age groups) and deliberate overdose (more common in young adults). Although initial assessment and treatment of these groups may not differ significantly, the social issues and ongoing follow-up of these children will be totally different and the treating physician must remain aware of this difference. The initial identification and treatment of these children remains the mainstay of management, and many ingested substances do not have a specific antidote. Supportive treatment must be planned and the potential for delayed or long-term effects noted. The specific presentation and treatment of some of the commonly ingested substances will be addressed in this article, and guidance given on when to contact expert help. & 2005 Elsevier Ltd. All rights reserved. Introduction such as bleaches, detergents and turpentine sub- stitutes. More than 100 000 individuals are admitted to Toxic compounds may be ingested or inhaled hospital in England and Wales annually due to either accidentally or deliberately. Accidental poisoning, accounting for 10% of all acute admis- poisoning can occur at any age, but is much more 1 sions.1 However, the true incidence of acute common in children. -
First Record of Banded Krait, Bungarus Fasciatus (Schneider, 1801), (Reptilia: Elapidae), from Guru Ghasidas National Park, Koriya District, Chhattisgarh, India
ISSN 0375-1511 Rec. zool. Surv. India: 113(Part-2): 77-80,2013 FIRST RECORD OF BANDED KRAIT, BUNGARUS FASCIATUS (SCHNEIDER, 1801), (REPTILIA: ELAPIDAE), FROM GURU GHASIDAS NATIONAL PARK, KORIYA DISTRICT, CHHATTISGARH, INDIA KAILASH CHANDRA, ANGSHUMAN RAHA, AM ITAV A MAJUMDER, ABINASH P ARIDA AND ANIL SARSAVAN Zoological Survey of India, New Alipore, Kolkata-700053, India E-mail: [email protected] The present communication reports the restricted to the eastern part of India particularly occurrence of Banded Krait for the first time from in North-east India (Brahmaputra Basin), Andhra Guru Ghasidas National Park (GGNP) as well as Pradesh (Hyderabad, Godavari valley), Central Koriya district of Chhattisgarh. This also India (Chhattisgarh and parts of Madhya represents the significant north western range Pradesh), Orissa (Mahanadi valley), Bihar, Uttar extension of the species in Chhattisgarh. While Pradesh and West Bengal (northern part) (Wall undertaking the faunal survey of Protected Areas 1912, Kinnear 1913, Smith 1943, Sanyal 1993, of Chhattisgarh, banded krait was sighted at the Sanyal et al. 1993, Sharma 2003, Whitaker & Amapani beat, Sonhat range (23°35'12.7/1, Captain 2004). Both the snakes are common 82°29'20.7/1) of Guru Ghasidas National Park at throughou t their ranges. night (10:30 PM) on 23'd May 2012 (Fig. 1). The Physiography of GGNP snake was observed while it was crossing a Guru Ghasidas National Park is located in the narrow road from a paddy field to a water body extreme north western part of Chhattisgarh state on the opposite side. The paddy field was in Koriya district. -
615.9Barref.Pdf
INDEX Abortifacient, abortifacients bees, wasps, and ants ginkgo, 492 aconite, 737 epinephrine, 963 ginseng, 500 barbados nut, 829 blister beetles goldenseal blister beetles, 972 cantharidin, 974 berberine, 506 blue cohosh, 395 buckeye hawthorn, 512 camphor, 407, 408 ~-escin, 884 hypericum extract, 602-603 cantharides, 974 calamus inky cap and coprine toxicity cantharidin, 974 ~-asarone, 405 coprine, 295 colocynth, 443 camphor, 409-411 ethanol, 296 common oleander, 847, 850 cascara, 416-417 isoxazole-containing mushrooms dogbane, 849-850 catechols, 682 and pantherina syndrome, mistletoe, 794 castor bean 298-302 nutmeg, 67 ricin, 719, 721 jequirity bean and abrin, oduvan, 755 colchicine, 694-896, 698 730-731 pennyroyal, 563-565 clostridium perfringens, 115 jellyfish, 1088 pine thistle, 515 comfrey and other pyrrolizidine Jimsonweed and other belladonna rue, 579 containing plants alkaloids, 779, 781 slangkop, Burke's, red, Transvaal, pyrrolizidine alkaloids, 453 jin bu huan and 857 cyanogenic foods tetrahydropalmatine, 519 tansy, 614 amygdalin, 48 kaffir lily turpentine, 667 cyanogenic glycosides, 45 lycorine,711 yarrow, 624-625 prunasin, 48 kava, 528 yellow bird-of-paradise, 749 daffodils and other emetic bulbs Laetrile", 763 yellow oleander, 854 galanthamine, 704 lavender, 534 yew, 899 dogbane family and cardenolides licorice Abrin,729-731 common oleander, 849 glycyrrhetinic acid, 540 camphor yellow oleander, 855-856 limonene, 639 cinnamomin, 409 domoic acid, 214 rna huang ricin, 409, 723, 730 ephedra alkaloids, 547 ephedra alkaloids, 548 Absorption, xvii erythrosine, 29 ephedrine, 547, 549 aloe vera, 380 garlic mayapple amatoxin-containing mushrooms S-allyl cysteine, 473 podophyllotoxin, 789 amatoxin poisoning, 273-275, gastrointestinal viruses milk thistle 279 viral gastroenteritis, 205 silibinin, 555 aspartame, 24 ginger, 485 mistletoe, 793 Medical Toxicology ofNatural Substances, by Donald G. -
The Distribution of Reptiles and Amphibians in the Annapurna-Dhaulagiri Region (Nepal)
THE DISTRIBUTION OF REPTILES AND AMPHIBIANS IN THE ANNAPURNA-DHAULAGIRI REGION (NEPAL) by LURLY M.R. NANHOE and PAUL E. OUBOTER L.M.R. Nanhoe & P.E. Ouboter: The distribution of reptiles and amphibians in the Annapurna-Dhaulagiri region (Nepal). Zool. Verh. Leiden 240, 12-viii-1987: 1-105, figs. 1-16, tables 1-5, app. I-II. — ISSN 0024-1652. Key words: reptiles; amphibians; keys; Annapurna region; Dhaulagiri region; Nepal; altitudinal distribution; zoogeography. The reptiles and amphibians of the Annapurna-Dhaulagiri region in Nepal are keyed and described. Their distribution is recorded, based on both personal observations and literature data. The ecology of the species is discussed. The zoogeography and the altitudinal distribution are analysed. All in all 32 species-group taxa of reptiles and 21 species-group taxa of amphibians are treated. L.M.R. Nanhoe & P.E. Ouboter, c/o Rijksmuseum van Natuurlijke Historie Raamsteeg 2, Postbus 9517, 2300 RA Leiden, The Netherlands. CONTENTS Introduction 5 Study area 7 Climate and vegetation 9 Material and methods 12 Reptilia 13 Sauria 13 Gekkonidae 13 Hemidactylus brookii 14 Hemidactylus flaviviridis 14 Hemidactylus garnotii 15 Agamidae 15 Agama tuberculata 16 Calotes versicolor 18 Japalura major 19 Japalura tricarinata 20 Phrynocephalus theobaldi 22 Scincidae 24 Scincella capitanea 25 Scincella ladacensis ladacensis 26 3 4 ZOOLOGISCHE VERHANDELINGEN 240 (1987) Scincella ladacensis himalayana 27 2g Scincella sikimmensis ^ Sphenomorphus maculatus ^ Serpentes ^ Colubridae ^ Amphiesma platyceps ^ -
Critical Care Nursing of Infants and Children Martha A
University of Pennsylvania ScholarlyCommons Miscellaneous Papers Miscellaneous Papers 1-1-2001 Critical Care Nursing of Infants and Children Martha A. Q. Curley University of Pennsylvania, [email protected] Patricia A. Moloney-Harmon The Children's Hospital at Sinai Copyright by the author. Reprinted from Critical Care Nursing of Infants and Children, Martha A.Q. Curley and Patricia A. Moloney-Harmon (Editors), (Philadelphia: W.B. Saunders Co., 2001), 1,128 pages. NOTE: At the time of publication, the author, Martha Curley was affiliated with the Children's Hospital of Boston. Currently, she is a faculty member in the School of Nursing at the University of Pennsylvania. This paper is posted at ScholarlyCommons. http://repository.upenn.edu/miscellaneous_papers/4 For more information, please contact [email protected]. Please Note: The full version of this book and all of its chapters (below) can be found on ScholarlyCommons (from the University of Pennsylvania) at http://repository.upenn.edu/miscellaneous_papers/4/ Information page in ScholarlyCommons Full book front.pdf - Front Matter, Contributors, Forward, Preface, Acknowledgements, and Contents Chapter 1.pdf - The Essence of Pediatric Critical Care Nursing Chapter 2.pdf - Caring Practices: Providing Developmentally Supportive Care Chapter_3.pdf - Caring Practices: The Impact of the Critical Care Experience on the Family Chapter_4.pdf - Leadership in Pediatric Critical Care Chapter 5.pdf - Facilitation of Learning Chapter_6.pdf - Advocacy and Moral Agency: A Road Map for -
Chelation Therapy
Corporate Medical Policy Chelation Therapy File Name: chelation_therapy Origination: 12/1995 Last CAP Review: 2/2021 Next CAP Review: 2/2022 Last Review: 2/2021 Description of Procedure or Service Chelation therapy is an established treatment for the removal of metal toxins by converting them to a chemically inert form that can be excreted in the urine. Chelation therapy comprises intravenous or oral administration of chelating agents that remove metal ions such as lead, aluminum, mercury, arsenic, zinc, iron, copper, and calcium from the body. Specific chelating agents are used for particular heavy metal toxicities. For example, desferroxamine (not Food and Drug Administration [FDA] approved) is used for patients with iron toxicity, and calcium-ethylenediaminetetraacetic acid (EDTA) is used for patients with lead poisoning. Note that disodium-EDTA is not recommended for acute lead poisoning due to the increased risk of death from hypocalcemia. Another class of chelating agents, called metal protein attenuating compounds (MPACs), is under investigation for the treatment of Alzheimer’s disease, which is associated with the disequilibrium of cerebral metals. Unlike traditional systemic chelators that bind and remove metals from tissues systemically, MPACs have subtle effects on metal homeostasis and abnormal metal interactions. In animal models of Alzheimer’s disease, they promote the solubilization and clearance of β-amyloid protein by binding to its metal-ion complex and also inhibit redox reactions that generate neurotoxic free radicals. MPACs therefore interrupt two putative pathogenic processes of Alzheimer’s disease. However, no MPACs have received FDA approval for treating Alzheimer’s disease. Chelation therapy has also been investigated as a treatment for other indications including atherosclerosis and autism spectrum disorder. -
A Case of Mushroom Poisoning with Russula Subnigricans: Development of Rhabdomyolysis, Acute Kidney Injury, Cardiogenic Shock, and Death
CASE REPORT Nephrology http://dx.doi.org/10.3346/jkms.2016.31.7.1164 • J Korean Med Sci 2016; 31: 1164-1167 A Case of Mushroom Poisoning with Russula subnigricans: Development of Rhabdomyolysis, Acute Kidney Injury, Cardiogenic Shock, and Death Jong Tae Cho and Jin Hyung Han Mushroom exposures are increasing worldwide. The incidence and fatality of mushroom poisoning are reported to be increasing. Several new syndromes in mushroom poisoning Department of Internal Medicine, College of have been described. Rhabdomyolytic mushroom poisoning is one of new syndromes. Medicine, Dankook University, Cheonan, Korea Russula subnigricans mushroom can cause delayed-onset rhabdomyolysis with acute Received: 17 April 2015 kidney injury in the severely poisoned patient. There are few reports on the toxicity of R. Accepted: 6 June 2015 subnigricans. This report represents the first record of R. subnigricans poisoning with rhabdomyolysis in Korea, describing a 51-year-old man who suffered from rhabdomyolysis, Address for Correspondence: Jong Tae Cho, MD acute kidney injury, severe hypocalcemia, respiratory failure, ventricular tachycardia, Department of Internal Medicine, College of Medicine, cardiogenic shock, and death. Mushroom poisoning should be considered in the evaluation Dankook University, 201 Manghyang-ro, Dongnam-gu, Cheonan 31116, Korea of rhabdomyolysis of unknown cause. Furthermore, R. subnigricans should be considered E-mail: [email protected] in the mushroom poisoning with rhabdomyolysis. Keywords: Mushroom Poisoning; Rhabdomyolysis; Acute Kidney Injury; Respiratory Failure; Cardiogenic Shock INTRODUCTION in August, 2010 at the Jujak mountain located on the province of Jeollanamdo, the southern area of Korea. He was a bus driv More leisure time for hobbies, hiking, and trekking has led to er. -
Annual Report for the Year 2019-2020
MADRAS CROCODILE BANK TRUST / CENTRE FOR HERPETOLOGY Post bag No.4, Vadanemmelli Village, East Coast Road, Mamallapuram-603 104, Tamil Nadu, India Annual Report for the year 2019-2020 2 CONTENTS S.No Section Page Number 1. Report of the Officer-in-charge 5 2. History of the Zoo 6 3. Vision 6 4. Mission 7 5. Objective 7 6. About us 7 7. Organizational Chart 11 8. Human Resources 12 9. Capacity Building of the zoo personnel 13 10. Zoo Advisory Committee 13 11. Health Advisory Committee 14 12. Statement of income and expenditure of the Zoo 14 13. Daily feed Schedule of animals 15 14. Vaccination Schedule of animals 19 15. De-worming Schedule of animals 19 3 S.No Section Page Number 16. Disinfection Schedule 19 17. Health Check-up of employees for zoonotic diseases 22 18. Development Works carried out in the zoo during the year 23 19. Education and Awareness programmes during the year 24 20. Important Events and happenings in the zoo 25 21. Seasonal special arrangements for upkeep of animals 25 22. Research Work carried out and publications 26 23. Conservation Breeding Programme of the Zoo 27 24. Animal acquisition / transfer / exchange during the year 27 25. Rescue and Rehabilitation of the wild animals carried out by the zoo 28 26. Annual Inventory of animals 30 27. Mortality of animals. 39 28. Status of the Compliance with conditions stipulated by the Central Zoo 44 Authority 29. List of free living wild animals within the zoo premises 45 4 1. Report of the Officer-in-charge The year 2019-2020 was a great one for us at the Madras Crocodile Bank Trust (MCBT), although we were looking at the effects of the COVID-19 pandemic in the far end of the year. -
Venomous Snakes
Venomous Snakes - By Kedar Bhide Kedar Bhide is a snake expert from Mumbai. A postgraduate from Mumbai's Haffkine Institute, his work has resulted into first records of 2 snake species for India, Barta (Kaulback's Pit Viper) from Arunachal Pradesh and the Sind Awl-headed snake from Rajasthan. “ Moments after being bitten, the man feels a live fire germinating in the wound as if red hot tongs contorted his flesh; that which was mortified enlarges to monstrosity, and lividness invades him. The unfortunate victim witnesses his body becoming corpse piece by piece; a chill of death invades all his being, and soon bloody threads fall from his gums; and his eyes, without intending to, will also cry blood, until, beaten by suffering and anguish, he loses the sense of reality. If we then ask the unlucky man something, he may see us through blurred eyes, but we get no response; and perhaps a final sweat of red pearls or a mouthful of blackish blood warns of impending” (This is an introduction of a book written in 1931 by a Costa Rican Biologists and snakebite expert Clodomiro Picado.) INTRODUCTION Human fear of snakes is caused almost entirely by those species that can deliver a venomous bite. It is somewhat ironic that such a minority group, like venomous snakes has endangered the whole kingdom of snakes. Let us start by correcting a frequent misnomer. People often refer to poisonous snakes, and indeed by directory definition, this is not incorrect. But as a student of herpetology we should be more specific in our terminology.