Managing Hazardous Materials Incidents
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Responding to a Chemical Warfare Agent Incident: from Sampling and Analysis to Decontamination and Waste Management Stuart Willi
Responding to a Chemical Warfare Agent Incident: from sampling and analysis to decontamination and waste management Stuart Willison & Lukas Oudejans U. S. EPA National Homeland Security Research Center 1 Outline • Homeland Security Relevance to Chemical (Warfare Agent) Incidents and Incident Response Cycle • Identification of Gaps/Needs: PARTNER Process and Stakeholder Priorities • Current High Stakeholder Priorities • Research Efforts to meet these Needs/Gaps Selected Analytical Methods (SAM) Document CWA Method Development and Wipe Efficiency Studies on Surfaces Fate and Transport of CWAs Natural Attenuation of VX Decontamination of Vesicant/Blister CWAs HD, L, HL Analytical Method Development: Lewisite; EA 2192 Best Practices Document for Waste Media from Remediation Activities • Summary 2 Response to Contamination Events Since 9/11, multiple chemical/biotoxin contamination events have occurred in the United States and worldwide: • Several ricin incidents (2002-2014) • Deepwater Horizon oil spill (April 2010) • Kalamazoo River oil spill (July 2010) • CWA sulfur mustard clam shells (2010) • CWA chemical attacks (Syria, Middle East) (March-August 2013 and April 2014-current) • Elk River chemical spill in West Virginia (January 2014) • Toxic algae blooms in Toledo, OH (August 2014) • Arsenic-contaminated soil in Kentucky potentially containing CWA Lewisite (March 2015) • (Organophosphate-) Pesticide over- or misuse across USA in relation to bed bug epidemic (current) 3 Response Cycle Contaminant Release Reduce Vulnerabilities Lessons -
Skin As a Mirror of Gastrointestinal Diseases
Review article Skin as a mirror of gastrointestinal diseases Sunil Kumar Gupta1, Amanjot Kaur Arora1, Jasveen Kaur1, Veenu Gupta2, Deepinder Kaur2 Department of Dermatology, Venerology and Leprology1, Department of Microbiology2, Dayanand Medical College and Hospital, Ludhiana, Punjab, India ABSTRACT The closely related origins of the skin and the gastrointestinal system make for a fascinating grouping of diseases with concomitant involvement of these two important organ systems. The dermatologic manifestations may precede clinically evident gastrointestinal disease and help in early diagnosis, saving unnecessary wastage of time and resources. In this overview, we review the cutaneous manifestations of various hereditary, neoplastic and inflammatory gastrointestinal diseases including the various polyposis syndromes, hereditary colorectal cancers, inflammatory bowel diseases, etc. Dermatologic manifestations of acute and chronic hepatic and pancreatic diseases have also been discussed. This review underscores the importance of collaboration between dermatologists and gastroenterologists for better and efficient management of the affected patients. Keywords: Gastrointestinal diseases, Genodermatoses, Hepatitis, Inflammatory bowel disease, Pancreatic diseases, Polyposis syndromes INTRODUCTION diseases with skin and GIT involvement, genodermatoses, and the various hereditary Skin is the largest organ of the body. With a wide surface gastrointestinal cancers. area and being the outermost covering of the human body, skin has proven to be of good diagnostic help or atleast II.Cutaneous manifestations of liver diseases raise the index of suspicion that something inside the covering is wrong. Like many other systemic diseases, III.Cutaneous manifestations of pancreatic diseases. ,gastrointestinal tract (GIT) diseases may present with I. CUTANEOUS MANIFESTATIONS OF cutaneous symptoms, either primarily or secondarily as a GASTROINTESTINAL DISEASES sequalae to gut pathology, embryologic development being responsible for such clinically important associations. -
Wound Classification
Wound Classification Presented by Dr. Karen Zulkowski, D.N.S., RN Montana State University Welcome! Thank you for joining this webinar about how to assess and measure a wound. 2 A Little About Myself… • Associate professor at Montana State University • Executive editor of the Journal of the World Council of Enterstomal Therapists (JWCET) and WCET International Ostomy Guidelines (2014) • Editorial board member of Ostomy Wound Management and Advances in Skin and Wound Care • Legal consultant • Former NPUAP board member 3 Today We Will Talk About • How to assess a wound • How to measure a wound Please make a note of your questions. Your Quality Improvement (QI) Specialists will follow up with you after this webinar to address them. 4 Assessing and Measuring Wounds • You completed a skin assessment and found a wound. • Now you need to determine what type of wound you found. • If it is a pressure ulcer, you need to determine the stage. 5 Assessing and Measuring Wounds This is important because— • Each type of wound has a different etiology. • Treatment may be very different. However— • Not all wounds are clear cut. • The cause may be multifactoral. 6 Types of Wounds • Vascular (arterial, venous, and mixed) • Neuropathic (diabetic) • Moisture-associated dermatitis • Skin tear • Pressure ulcer 7 Mixed Etiologies Many wounds have mixed etiologies. • There may be both venous and arterial insufficiency. • There may be diabetes and pressure characteristics. 8 Moisture-Associated Skin Damage • Also called perineal dermatitis, diaper rash, incontinence-associated dermatitis (often confused with pressure ulcers) • An inflammation of the skin in the perineal area, on and between the buttocks, into the skin folds, and down the inner thighs • Scaling of the skin with papule and vesicle formation: – These may open, with “weeping” of the skin, which exacerbates skin damage. -
Pressure Ulcer Staging Cards and Skin Inspection Opportunities.Indd
Pressure Ulcer Staging Pressure Ulcer Staging Suspected Deep Tissue Injury (sDTI): Purple or maroon localized area of discolored Suspected Deep Tissue Injury (sDTI): Purple or maroon localized area of discolored intact skin or blood-fi lled blister due to damage of underlying soft tissue from pressure intact skin or blood-fi lled blister due to damage of underlying soft tissue from pressure and/or shear. The area may be preceded by tissue that is painful, fi rm, mushy, boggy, and/or shear. The area may be preceded by tissue that is painful, fi rm, mushy, boggy, warmer or cooler as compared to adjacent tissue. warmer or cooler as compared to adjacent tissue. Stage 1: Intact skin with non- Stage 1: Intact skin with non- blanchable redness of a localized blanchable redness of a localized area usually over a bony prominence. area usually over a bony prominence. Darkly pigmented skin may not have Darkly pigmented skin may not have visible blanching; its color may differ visible blanching; its color may differ from surrounding area. from surrounding area. Stage 2: Partial thickness loss of Stage 2: Partial thickness loss of dermis presenting as a shallow open dermis presenting as a shallow open ulcer with a red pink wound bed, ulcer with a red pink wound bed, without slough. May also present as without slough. May also present as an intact or open/ruptured serum- an intact or open/ruptured serum- fi lled blister. fi lled blister. Stage 3: Full thickness tissue loss. Stage 3: Full thickness tissue loss. Subcutaneous fat may be visible but Subcutaneous fat may be visible but bone, tendon or muscle are not exposed. -
Angina Bullosa Haemorrhagica (Oral Blood Blister) (PDF)
Patient Information Maxillo-facial Angina Bullosa Haemorrhagica (Oral Blood Blister) What is Angina Bullosa Haemorrhagica? Angina Bullosa Hemorrhagica (ABH) is a condition where an often painful, but benign blood-filled blister suddenly develops in the mouth. The blisters are generally not due to a blood clotting disorder or any other medical disorder. It is a fairly common, sudden onset and benign blood blistering oral (mouth) disorder. It mainly affects people over 45 years and both males and females are equally affected. Usually there is no family history of the condition. It may be associated with Type 2 Diabetes, a family history of diabetes or Hyperglycaemia. What are the signs and symptoms of ABH? The first indication is a stinging pain or burning sensation just before the appearance of a blood blister The blisters last only a few minutes and then spontaneously rupture (burst), leaving a shallow ulcer that heals without scarring, discomfort or pain They can reach an average size of one to three centimetres in diameter The Soft Palate (back of the mouth) is the most affected site If they occur on the palate and are relatively big, they may need to be de-roofed (cut and drained) to ease the sensation of choking Patient Information Occasionally blisters can occur in the buccal mucosa (cheek) and tongue Approximately one third of the patients have blood blisters in more than one location. What are the causes of ABH? More than 50% of cases are related to minor trauma caused by: hot foods, restorative dentistry (fillings, crowns etc) or Periodontal Therapy (treatment of gum disease). -
Kinetic Modeling of the Thermal Destruction of Nitrogen Mustard
Kinetic Modeling of the Thermal Destruction of Nitrogen Mustard Gas Juan-Carlos Lizardo-Huerta, Baptiste Sirjean, Laurent Verdier, René Fournet, Pierre-Alexandre Glaude To cite this version: Juan-Carlos Lizardo-Huerta, Baptiste Sirjean, Laurent Verdier, René Fournet, Pierre-Alexandre Glaude. Kinetic Modeling of the Thermal Destruction of Nitrogen Mustard Gas. Journal of Physical Chemistry A, American Chemical Society, 2017, 121 (17), pp.3254-3262. 10.1021/acs.jpca.7b01238. hal-01708219 HAL Id: hal-01708219 https://hal.archives-ouvertes.fr/hal-01708219 Submitted on 13 Feb 2018 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Kinetic Modeling of the Thermal Destruction of Nitrogen Mustard Gas Juan-Carlos Lizardo-Huerta†, Baptiste Sirjean†, Laurent Verdier‡, René Fournet†, Pierre-Alexandre Glaude†,* †Laboratoire Réactions et Génie des Procédés, CNRS, Université de Lorraine, 1 rue Grandville BP 20451 54001 Nancy Cedex, France ‡DGA Maîtrise NRBC, Site du Bouchet, 5 rue Lavoisier, BP n°3, 91710 Vert le Petit, France *corresponding author: [email protected] Abstract The destruction of stockpiles or unexploded ammunitions of nitrogen mustard (tris (2- chloroethyl) amine, HN-3) requires the development of safe processes. -
CLINICAL RESEARCH PROJECT Protocol #11-H-0134 Drug Name: Eltrombopag (Promacta®) IND Number: 104,877 IND Holder: NHLBI OCD Date: January 2, 2019
CLINICAL RESEARCH PROJECT Protocol #11-H-0134 Drug Name: eltrombopag (Promacta®) IND number: 104,877 IND holder: NHLBI OCD Date: January 2, 2019 Title: A Pilot Study of a Thrombopoietin-receptor Agonist (TPO-R agonist), Eltrombopag, in Moderate Aplastic Anemia Patients Other Identifying Words: Hematopoiesis, autoimmunity, thrombocytopenia, neutropenia, anemia, stem cells, cytokine, Promacta® (eltrombopag) Protocol Principal Investigator: *Cynthia E. Dunbar, M.D., TSCBB, NHLBI (E) Medically and Scientifically Responsible Investigator: *Cynthia E. Dunbar, M.D., TSCBB, NHLBI (E) Associate Investigators: *Georg Aue, M.D., OCD, NHLBI (E) *Neal S. Young, M.D., Chief, HB, NHLBI (E) *André Larochelle, M.D., Ph.D., CMTB, NHLBI (E) David Young, M.D., TSCBB, NHLBI (E) Susan Soto, M.S.N., R.N., Research Nurse, OCD, NHLBI(E) Olga Rios, RN, Research Nurse, OCD, NHLBI (E) Evette Barranta, R.N, Research Nurse, OCD, NHLBI (E) Jennifer Jo Kyte, DNP, Research Nurse, OCD, NHLBI (E) Colin Wu, PhD, Biostatistician, OBR, NHLBI (E) Xin Tian, PhD, Biostatistician, OBR/NHLBI (E) *Janet Valdez, MS, PAC, OCD, NHLBI (E) *Jennifer Lotter, MSHS, PA-C., OCD, NHLBI (E) Qian Sun, Ph.D., DLM, CC (F) Xing Fan, M.D., HB, NHLBI (F) Non-NIH, Non-Enrolling Engaged Investigators: Thomas Winkler, M.D., NHLBI, HB (V)# # Covered under the NIH FWA Independent Medical Monitor: John Tisdale, MD, NHLBI, OSD 402-6497 Bldg. 10, 9N116 * asterisk denotes who can obtain informed consent on this protocol Subjects of Study: Number Sex Age-range 38 Either ≥ 2 years and weight >12 kg Project Involves Ionizing Radiation? No (only when medically indicated) Off-Site Project? No Multi center trial? No DSMB Involvement? Yes 11-H-0134 1 Cynthia E. -
Study About the Efficacy of an Aerosol Plastic Dressing in Wound
1.0 ANCC CE Contact Hours Study About the Effi cacy of an Aerosol Plastic Dressing in Wound Prevention After Compressive Adhesive Dressing Application in Plastic Surgery Procedures Enrique Salmerón-González , MD Elena García-Vilariño , MD Pilar Vilariño-López , MD Cristina García-Pons , MD Cristina Escalante-Ibáñez , MD Alfonso A. Valverde-Navarro , MD The use of compressive adhesive bandages is widely men placed over a layer of an aerosol plastic dressing and extended in the fi eld of plastic, aesthetic, and reconstruc- another bandage placed directly over the skin. A statisti- tive surgery, and the apparition of skin damage after its cally signifi cant decrease in skin damage incidence was removal is a relatively frequent complication. The aim observed in areas in which the aerosol plastic dressing of this study was to evaluate the capacity of an aerosol was applied as a layer between the adhesive dressing and plastic dressing for protecting the skin from the apparition the skin. Furthermore, a reduction in symptoms associ- of damage caused by adhesive dressings. A prospective, ated with the use of these adhesive dressings was found. randomized, simple-blind study was performed, evaluating The results of this study support the use of aerosol plastic skin damage incidence after removal of adhesive compres- dressings as a barrier for skin protection in patients in sive bandages in 80 subjects. The patients carried for whom an adhesive compressive dressing is applied to 48 hr an adhesive compressive dressing on their abdo- reduce the incidence of skin damage. he use of adhesive compressive dressings is established seromas ( Rogliani, Gentile, & Cervelli, 2008 ). -
Hand Blisters in Major League Baseball Pitchers: Current Concepts and Management
A Review Paper Hand Blisters in Major League Baseball Pitchers: Current Concepts and Management Andrew R. McNamara, MD, Scott Ensell, MS, ATC, and Timothy D. Farley, MD Abstract Friction blisters are a common sequela of spent time on the DL due to blisters. More- many athletic activities. Their significance can over, there have been several documented range from minor annoyance to major per- and publicized instances of professional formance disruptions. The latter is particularly baseball pitchers suffering blisters that did true in baseball pitchers, who sustain repeat- not require placement on the DL but did ed trauma between the baseball seams and result in injury time and missed starts. the fingers of the pitching hand, predominate- The purpose of this article is to review ly at the tips of the index and long fingers. the etiology and pathophysiology of friction Since 2010, 6 Major League Baseball blisters with particular reference to baseball (MLB) players accounted for 7 stints on the pitchers; provide an overview of past and disabled list (DL) due to blisters. These inju- current prevention methods; and discuss ries resulted in a total of 151 days spent on our experience in treating friction blisters the DL. Since 2012, 8 minor league players in MLB pitchers. riction blisters result from repetitive friction of rubbing (erythroderma). This is followed by a and strain forces that develop between the pale, narrow demarcation, which forms around the F skin and various objects. Blisters form in reddened region. Subsequently, this pale area fills areas where the stratum corneum and stratum in toward the center to occupy the entire affected granulosum are sufficiently robust (Figure), such area, which becomes the blister lesion.1,2 as the palmar and plantar surfaces of the hand and Hydrostatic pressure then causes blister fluid feet. -
44 Xenobiotic: Vesicant, WMD Blister Agent, Lewisite, Phosgene, Sulfur Mustard, Nitrogen Mustard Expected States of Matter: Liqu
44 Xenobiotic: Vesicant, WMD Blister Agent, Lewisite, Phosgene, Sulfur mustard, Nitrogen mustard Expected states of matter: Liquid, Vapor, Gas Purpose: Vesicants typically begin having chemical effects on the body within minutes through a complex mechanism of action but signs and symptoms do not present for 4-6 hours depending on exposure concentrations & time. Treatment begins with early recognition and limiting exposure. Otherwise, treatment is dependant on route of exposure and should be addressed symptomatically. Signs & Symptoms: Conjunctivitis, Corneal opacification or ulceration. Erythema to the skin, Vesicles. Laryngeal edema, dyspnea or respiratory obstruction. Coagulation necrosis of the skin. Warmth and humidity increase dermal damage, Targets groin and axilla General Response: Establish zones of control to protect responders & the public Protect responders with appropriate PPE Entry: Level A Decon: Level C Transport: Street level PPE Decon victims with high volume of water Specialized dedon: Soap & water Does victim present risk of secondary contamination? No Specific Treatments: ● There is no specific antidote available for blister agents. Treatment should be symptomatic and similar to thermal burns. Albuterol 2.5mg/3mL nebulized over 5-10 minutes For bronchoconstriction Diphenhydramine 50mg IM/IV over 1-2 min Relieves itching due to dermal damage Treat pain according to PAIN MANAGEMENT PROTOCOL Alkaline Gargle 5mL normal saline with 5mL of sodium bicarbonate. Treats pharyngitis Gargle for 10-15 seconds without swallowing 45 ● For vapor/gas exposure or liquid exposure to the eyes - Tetracaine Hydrochloride 1-2 gtts/eye. Analgesic Rationale for Treatment: Exposure to blister agents are rarely fatal, but designed to incapacitate. They require long periods of convalescence with some of the major threats being infection through multiple routes. -
MADSTONES with an ACCOUNT of SEVERAL from VIRGINIA* by WYNDHAM B
MADSTONES WITH AN ACCOUNT OF SEVERAL FROM VIRGINIA* By WYNDHAM B. BLANTON, M.D. RICHMOND, VA. MBEDDED in the folklore more, though it often adhered of of many nations is a belief its own accord. It was then removed in the efficacy of all sorts of and placed in warm milk. If bubbles medicinal stones and among and a greenish color appeared in the them the madstone is of particularmilk the stone was supposed to be interest.E Madstones have been vari- giving up the poison it had extracted. ously known as snakestones, Chinese The stone was then reapplied to the snakestones, Indian snakestones, ser- surface and theoretically the process pent stones, adder stones, sucking was kept up until no further bubbles stones and bezoar stones. Typical and no more discolorations of the specimens are usually small, light, milk were to be observed. porous, stonelike objects, often with The theory upon which these porous one surface flattened. They possess stones were used was clearly one definite absorptive qualities and are of physical absorption. Some have believed to be capable of extracting been shown to increase their weight the poison from a poisonous bite, as much as 5 per cent when applied especially the poison of a mad dog. Ob- to a wet surface, but in a number of jects from many sources and of many instances well-controlled experiments different compositions have been con- with animals injected with snake sidered to possess the miraculous venom have clearly demonstrated the powers ascribed to madstones, but utter worthlessness of the madstone. in general real madstones are com- The explanation of the popularity posed of (i) a light porous substance of the madstone is due to the fact made by a secret process such as was that contrary to common belief most known to certain natives of India; dog bites are inflicted by animals (2) some porous form of calcareous who are not mad and are therefore rock, such as halloysite, a mineral of themselves harmless. -
Covalent Protein Adduction of Nitrogen Mustards and Related Compounds Vanessa R
Florida International University FIU Digital Commons FIU Electronic Theses and Dissertations University Graduate School 2-28-2014 Covalent Protein Adduction of Nitrogen Mustards and Related Compounds Vanessa R. Thompson Florida International University, [email protected] DOI: 10.25148/etd.FI14040835 Follow this and additional works at: https://digitalcommons.fiu.edu/etd Part of the Amino Acids, Peptides, and Proteins Commons, and the Analytical Chemistry Commons Recommended Citation Thompson, Vanessa R., "Covalent Protein Adduction of Nitrogen Mustards and Related Compounds" (2014). FIU Electronic Theses and Dissertations. 1152. https://digitalcommons.fiu.edu/etd/1152 This work is brought to you for free and open access by the University Graduate School at FIU Digital Commons. It has been accepted for inclusion in FIU Electronic Theses and Dissertations by an authorized administrator of FIU Digital Commons. For more information, please contact [email protected]. FLORIDA INTERNATIONAL UNIVERSITY Miami, Florida COVALENT PROTEIN ADDUCTION OF NITROGEN MUSTARDS AND RELATED COMPOUNDS A dissertation submitted in partial fulfillment of the requirements for the degree of DOCTOR OF PHILOSOPHY in CHEMISTRY by Vanessa Thompson 2014 To: Dean Kenneth G. Furton College of Arts and Sciences This dissertation, written by Vanessa Thompson, and entitled Covalent Protein Adduction of Nitrogen Mustards and Related Compounds, having been approved in respect to style and intellectual content, is referred to you for judgment. We have read this dissertation and recommend that it be approved. _______________________________________ Fenfei Leng _______________________________________ Watson Lees _______________________________________ Dietrich Lorke _______________________________________ Bruce McCord _______________________________________ Anthony DeCaprio, Major Professor Date of Defense: February 27, 2014 The dissertation of Vanessa Thompson is approved.