First Review of the Dust Diseases Scheme
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No. 26705 MULTILATERAL Convention (No. 162) Concerning
No. 26705 MULTILATERAL Convention (No. 162) concerning safety in the use of asbestos. Adopted by the General Conference of the International Labour Organisation at its seventy- second session, Geneva, 24 June 1986 Authentic texts: English and French. Registered by the International Labour Organisation on 27 June 1989. MULTILATERAL Convention (n° 162) concernant la sécurité dans l'utilisation de l'amiante. Adoptée par la Conférence générale de l'Organisation internationale du Travail à sa soixante- douzième session, Genève, 24 juin 1986 Textes authentiques : anglais et français. Enregistrée par l'Organisation internationale du Travail le 27 juin 1989. Vol. 1539, 1-26705 316______United Nations — Treaty Series • Nations Unies — Recueil des Traités 1989 CONVENTION1 CONCERNING SAFETY IN THE USE OF AS BESTOS The General Conference of the International Labour Organisation, Having been convened at Geneva by the Governing Body of the International Labour Office, and having met in its Seventy-second Session of 4 June 1986, and Noting the relevant international labour Conventions and Recommendations, and in particular the Occupational Cancer Convention and Recommendations, 1974,2 the Working Environment (Air Pollution, Noise and Vibration) Convention and Recommendation, 1977,3 the Occupational Safety and Health Convention and Recommendation, 1981,4 the Occupational Health Services Convention and Recommendation, 1985,3 the list of occupational diseases as revised in 1980 appended to the Employment Injury Benefits Convention, 1964,6 as well as the -
Interstitial Lung Diseases in Developing Countries
Rivera-Ortega P and Molina-Molina M. Interstitial Lung Diseases in Developing Countries. Annals of Global Health. 2019; 85(1): 4, 1–14. DOI: https://doi.org/10.5334/aogh.2414 REVIEW Interstitial Lung Diseases in Developing Countries Pilar Rivera-Ortega*,† and Maria Molina-Molina*,† More than 100 different conditions are grouped under the term interstitial lung disease (ILD). A diag- nosis of an ILD primarily relies on a combination of clinical, radiological, and pathological criteria, which should be evaluated by a multidisciplinary team of specialists. Multiple factors, such as environmental and occupational exposures, infections, drugs, radiation, and genetic predisposition have been implicated in the pathogenesis of these conditions. Asbestosis and other pneumoconiosis, hypersensitivity pneumonitis (HP), chronic beryllium disease, and smoking-related ILD are specifically linked to inhalational exposure of environmental agents. The recent Global Burden of Disease Study reported that ILD rank 40th in relation to global years of life lost in 2013, which represents an increase of 86% compared to 1990. Idiopathic pulmonary fibrosis (IPF) is the prototype of fibrotic ILD. A recent study from the United States reported that the incidence and prevalence of IPF are 14.6 per 100,000 person-years and 58.7 per 100,000 persons, respectively. These data suggests that, in large populated areas such as Brazil, Russia, India, and China (the BRIC region), there may be approximately 2 million people living with IPF. However, studies from South America found much lower rates (0.4–1.2 cases per 100,000 per year). Limited access to high- resolution computed tomography and spirometry or to multidisciplinary teams for accurate diagnosis and optimal treatment are common challenges to the management of ILD in developing countries. -
When Is Asbestos Dangerous?
When is Asbestos Dangerous? The most common way for asbestos fibers to enter the body is through breathing. In fact, asbestos containing material is not generally considered to be harmful unless it is releasing dust or fibers into the air where they can be inhaled or ingested. Many of the fibers will become trapped in the mucous membranes of the nose and throat where they can then be removed, but some may pass deep into the lungs, or, if swallowed, into the digestive tract. Once they are trapped in the body, the fibers can cause health problems. Asbestos is most hazardous when it is friable. The term "friable" means that the asbestos is easily crumbled by hand, releasing fibers into the air. Asbestos-containing ceiling tiles, floor tiles, undamaged laboratory cabinet tops, shingles, fire doors, siding shingles, etc. are not highly friable and will not typically release asbestos fibers unless they are disturbed or damaged in some way. Health Effects Since it is difficult to destroy asbestos fibers, the body cannot break them down or remove them once they are lodged in lung or body tissues. There are three primary diseases associated with asbestos exposure: Asbestosis Asbestosis is a serious, chronic, non-cancerous respiratory disease. Inhaled asbestos fibers aggravate lung tissues, which cause them to scar. The risk of asbestosis is minimal for those who do not work with asbestos; the disease is rarely caused by neighborhood or family exposure. Those who renovate or demolish buildings that contain asbestos may be at significant risk, depending on the nature of the exposure and precautions taken. -
Exposure to Asbestos a Resource for Veterans, Service Members, and Their Families
War Related Illness and Injury Study Center WRIISC Office of Public Health Department of Veterans Affairs EXPOSURE TO ASBESTOS A RESOURCE FOR VETERANS, SERVICE MEMBERS, AND THEIR FAMILIES WHAT IS ASBESTOS? other areas below deck for fire safety widely used in ship building and Asbestos is a fibrous mineral that purposes. ACMs also were used in construction materials during that occurs naturally in the environment. navigation rooms, sleeping quarters, time frame. There are six different types and mess halls. • Navy personnel who worked of asbestos fibers, each with a below deck before the early 1990s HOW ARE SERVICE MEMBERS somewhat different size, width, since asbestos was often used EXPOSED TO ASBESTOS? length, and shape. Asbestos minerals below deck and the ventilation have good heat resistant properties. Because asbestos has been so widely was often poor. used in our society, most people Given these characteristics, asbestos • Navy Seamen who were have been exposed to some asbestos has been used for a wide range of frequently tasked with removing at some point in time. Asbestos is manufactured goods, including damaged asbestos lagging in most hazardous when it is friable. building materials (roofing shingles, engine rooms and then using This means that the asbestos material ceiling and floor tiles, paper products, asbestos paste to re-wrap the is easily crumbled by hand, thus and asbestos cement products), pipes, often with no respiratory releasing fibers into the air. People friction products (automobile clutch, protection and no other personal are exposed to asbestos when ACMs brake, and transmission parts), heat- protective equipment especially are disturbed or damaged, and resistant fabrics, packaging, gaskets, if wet technique was not used in small asbestos fibers are dispersed and coatings. -
National Programmes for Elimination of Asbestos-Related Diseases
Outline for the Development of National Programmes for Elimination of Asbestos-Related Diseases Contacts for further information on development of national programmes for elimination of asbestos-related diseases: Programme for Safety and Health at Work and the Environment Department of Public Health, Environmental and (SAFEWORK) Social Determinants of Health (PHE) International Labour Organization (ILO) World Health Organization (WHO) 4, route des Morillons, CH-1211 Geneva 22, Switzerland 20, avenue Appia, CH1211, Geneva 22, E-mail: [email protected] Switzerland E-mail: [email protected] Copyright © International Labour Organization and World Health Organization 2007 The designations employed in ILO and WHO publications, which are in conformity with United Nations practice, and the presentation of material therein do not imply the expression of any opinion whatsoever on the part of the International Labour Office and the World Health Organization concerning the legal status of any country, area or territory or of its authorities, or concerning the delimitation of its frontiers. Reference to names of firms and commercial products and processes does not imply their endorsement by the International Labour Office or the World Health Organization, and any failure to mention a particular firm, commercial product or process is not a sign of disapproval. All reasonable precautions have been taken by the International Labour Office and 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 express or implied. The responsibility for the interpre- tation and use of the material lies with the reader. In no event shall the International Labour Office and the World Health Organization be liable for damages arising from its use. -
Are Serum Aluminum Levels a Risk Factor in the Appearance of Spontaneous Pneumothorax?
Turk J Med Sci 2010; 40 (3): 459-463 Original Article © TÜBİTAK E-mail: [email protected] doi:10.3906/sag-0901-11 Are serum aluminum levels a risk factor in the appearance of spontaneous pneumothorax? Serdar HAN1, Rasih YAZKAN2, Bülent KOÇER3,*, Gültekin GÜLBAHAR3, Serdal Kenan KÖSE4, Koray DURAL3, Ünal SAKINCI3 Aim: To investigate the relationship between aluminum and spontaneous pneumothorax (SP) development. Materials and methods: A patient group and a control group were formed with 100 individuals in each. The serum aluminum levels of the groups were determined and statistically compared. Results: The mean serum aluminum levels were 5.6 ± 2.4 μg/L (1.6-11.9) and 23.2 ± 15.4 μg/L (2-81) in the control and SP groups, respectively (P < 0.001). The specificity and sensitivity of the measurement of aluminum level were 74.4% and 86.4% in the SP group. The risk of SP development was found to be 18 times higher in individuals with high serum levels of aluminum compared to that in individuals with low serum levels of aluminum. Conclusion: A high level of aluminum is a risk factor for the development of SP. Key words: Aluminum, pneumothorax, public health Spontan pnömotoraks gelişiminde serum aluminyum seviyeleri bir risk faktörü müdür? Amaç: Bu çalışmada spontan pnömotoraks (SP) gelişimi ile serum aluminyum düzeyleri arasındaki ilişkinin analiz edilmesi amaçlandı. Yöntem ve gereç: Yüz SP hastasından oluşan hasta grubunun yanı sıra 100 kişiden oluşan sağlıklı kontrol grubu çalışmaya dahil edildi. Gruplar serum aluminyum düzeyleri açısından istatistiksel olarak kıyaslandı. Bulgular: Ortalama serum aluminyum düzeyleri SP ve kontrol grupları için sırasıyla 5,6 ± 2,4 μg/L (1,6-11,9) ve 23,2 ± 15,4 μg/L (2-81) bulundu (P < 0,001). -
Asbestos in Drinking-Water
Asbestos in Drinking-water Background document for development of WHO Guidelines for Drinking-water Quality 14 December 2020 Version for public review © World Health Organization 202X Preface To be completed by WHO Secretariat Acknowledgements To be completed by WHO Secretariat Abbreviations used in the text A/C Asbestos-cement ATSDR Agency for Toxic Substances and Disease Registry (USA) CHO Chinese hamster ovary FT-IR Fourier-transform infrared spectroscopy GI Gastrointestinal LECR Lifetime excess cancer risk MFL Million Fibres per Litre PCM Phase contrast microscopy SHE Syrian hamster embryo SIR Standardised incidence ratio F-yr/mL Total number of fibres in one year per mL of air (More potential abbreviations) CI Confidence interval NTU Nephelometric turbidity units TEM Transmission electron microscopy SAED Selected-area electron diffraction ROS Reactive oxygen species Table of Contents 1.0 EXECUTIVE SUMMARY ..................................................................................................................................... 1 2.0 GENERAL DESCRIPTION .................................................................................................................................... 1 2.1 Identity ................................................................................................................................................................. 1 2.2 Physicochemical properties ................................................................................................................................. 1 2.3 -
Nebulizers: Diagnosis Codes – Medicare Advantage Policy Appendix
UnitedHealthcare® Medicare Advantage Policy Appendix: Applicable Code List Nebulizers: Diagnosis Codes This list of codes applies to the Medicare Advantage Policy Guideline titled Approval Date: September 8, 2021 Nebulizers. Applicable Codes The following list(s) of procedure and/or diagnosis codes is provided for reference purposes only and may not be all inclusive. The listing of a code does not imply that the service described by the code is a covered or non-covered health service. Benefit coverage for health services is determined by the member specific benefit plan document and applicable laws that may require coverage for a specific service. The inclusion of a code does not imply any right to reimbursement or guarantee claim payment. Other Policies and Guidelines may apply. Diagnosis Code Description For HCPCS Codes A7003, A7004, and E0570 A15.0 Tuberculosis of lung A22.1 Pulmonary anthrax A37.01 Whooping cough due to Bordetella pertussis with pneumonia A37.11 Whooping cough due to Bordetella parapertussis with pneumonia A37.81 Whooping cough due to other Bordetella species with pneumonia A37.91 Whooping cough, unspecified species with pneumonia A48.1 Legionnaires' disease B20 Human immunodeficiency virus [HIV] disease B25.0 Cytomegaloviral pneumonitis B44.0 Invasive pulmonary aspergillosis B59 Pneumocystosis B77.81 Ascariasis pneumonia E84.0 Cystic fibrosis with pulmonary manifestations J09.X1 Influenza due to identified novel influenza A virus with pneumonia J09.X2 Influenza due to identified novel influenza A virus with other -
Differential Diagnosis of Granulomatous Lung Disease: Clues and Pitfalls
SERIES PATHOLOGY FOR THE CLINICIAN Differential diagnosis of granulomatous lung disease: clues and pitfalls Shinichiro Ohshimo1, Josune Guzman2, Ulrich Costabel3 and Francesco Bonella3 Number 4 in the Series “Pathology for the clinician” Edited by Peter Dorfmüller and Alberto Cavazza Affiliations: 1Dept of Emergency and Critical Care Medicine, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan. 2General and Experimental Pathology, Ruhr-University Bochum, Bochum, Germany. 3Interstitial and Rare Lung Disease Unit, Ruhrlandklinik, University of Duisburg-Essen, Essen, Germany. Correspondence: Francesco Bonella, Interstitial and Rare Lung Disease Unit, Ruhrlandklinik, University of Duisburg-Essen, Tueschener Weg 40, 45239 Essen, Germany. E-mail: [email protected] @ERSpublications A multidisciplinary approach is crucial for the accurate differential diagnosis of granulomatous lung diseases http://ow.ly/FxsP30cebtf Cite this article as: Ohshimo S, Guzman J, Costabel U, et al. Differential diagnosis of granulomatous lung disease: clues and pitfalls. Eur Respir Rev 2017; 26: 170012 [https://doi.org/10.1183/16000617.0012-2017]. ABSTRACT Granulomatous lung diseases are a heterogeneous group of disorders that have a wide spectrum of pathologies with variable clinical manifestations and outcomes. Precise clinical evaluation, laboratory testing, pulmonary function testing, radiological imaging including high-resolution computed tomography and often histopathological assessment contribute to make -
BERYLLIUM DISEASE by I
Postgrad Med J: first published as 10.1136/pgmj.34.391.262 on 1 May 1958. Downloaded from 262 BERYLLIUM DISEASE By I. B. SNEDDON, M.B., Ch.B., F.R.C.P. Consultant Dermatologist, Rupert Hallam Department of Dermatology, Sheffield It is opportune in a symposium on sarcoidosis monary berylliosis which fulfilled the most to discuss beryllium disease because it mimics so stringent diagnostic criteria. closely the naturally occurring Boecks sarcoid and A beryllium case registry set up at the Massa- yet carries a far graver prognosis. chusetts General Hospital by Dr. Harriet Hardy Beryllium was first reported to possess toxic had collected by 1956 309 examples of the disease, properties by Weber and Englehardt (I933) in of whom 84 had died. The constant finding of Germany. They described bronchitis and acute beryllium in autopsy material from the fatal cases respiratory disease in workers extracting beryllium had proved beyond doubt the association between from ore. Similar observations were made by the granulomatous reaction and the metal. Marradi Fabroni (I935) in Italy and Gelman It is difficult to reconcile the paucity of accounts (I936) in Russia. Further reports came from of beryllium disease in this country with the large Germany in I942 where beryllium poisoning was amount of beryllium compounds which have been recognized as a compensatable disease. Towards used in the last ten The in the end of World War II the production and use years. only reports the medical literature are those of Agate (I948),copyright. of beryllium salts increased greatly in the United Sneddon (i955), and Rogers (1957), but several States, and in 1943 Van Ordstrand et al. -
European Respiratory Society Classification of the Idiopathic
This copy is for personal use only. To order printed copies, contact [email protected] 1849 CHEST IMAGING American Thoracic Society– European Respiratory Society Classification of the Idiopathic Interstitial Pneumonias: Advances in Knowledge since 20021 Nicola Sverzellati, MD, PhD David A. Lynch, MB In the updated American Thoracic Society–European Respira- David M. Hansell, MD, FRCP, FRCR tory Society classification of the idiopathic interstitial pneumonias Takeshi Johkoh, MD, PhD (IIPs), the major entities have been preserved and grouped into Talmadge E. King, Jr, MD (a) “chronic fibrosing IIPs” (idiopathic pulmonary fibrosis and id- William D. Travis, MD iopathic nonspecific interstitial pneumonia), (b) “smoking-related IIPs” (respiratory bronchiolitis–associated interstitial lung disease Abbreviations: H-E = hematoxylin-eosin, and desquamative interstitial pneumonia), (c) “acute or subacute IIP = idiopathic interstitial pneumonia, IPF = IIPs” (cryptogenic organizing pneumonia and acute interstitial idiopathic pulmonary fibrosis, NSIP = nonspe- cific interstitial pneumonia, RB-ILD = respi- pneumonia), and (d) “rare IIPs” (lymphoid interstitial pneumonia ratory bronchiolitis–associated interstitial lung and idiopathic pleuroparenchymal fibroelastosis). Furthermore, it disease, UIP = usual interstitial pneumonia has been acknowledged that a final diagnosis is not always achiev- RadioGraphics 2015; 35:1849–1872 able, and the category “unclassifiable IIP” has been proposed. The Published online 10.1148/rg.2015140334 diagnostic interpretation of -
Pulmonary Fibrosis with Cholesterol Granulomata in a Patient Working in a Fireworks Factory K M D J Rodrigo1, D a V Rathnapala1, W V Senaratne1, S R Constantine2
Picture stories The sputum culture was negative. Post operatively she polymerase chain reaction (PCR) to detect mycobacterial was treated with anti-tuberculous medications. The wound DNA and enzyme-linked immunosorbent assays (ELISAs) completely healed after 10 months. [4]. Tuberculosis (TB) remains a major global health problem. Isolated sacral tuberculosis usually presents Conflicts of interest as chronic back pain in adults and discharging sinuses We declare that there are no conflicts of interest. or abscess formation in children, with or without neurological deficit [2]. References Definitive diagnosis of tuberculosis involves de- monstration of Mycobacterium tuberculosis by microbio- 1. Kumar A, Varshney MK, Trikha V, Khan SA. Isolated tuberculosis of the coccyx. J Bone Joint Surg Br 2006; 88: logical, cytopathological or histopathological methods. 1388-9. Histological examination of the biopsy usually shows epithelioid granulomas, Langhans’ type multinucleated 2. KimDoUn, Kim SW, Ju CL. Isolated coccygeal tubercu- giant cells and caseous necrosis, as in this patient’s losis. J Korean Neurosurg Soc 2012; 52: 495-7. biopsy specimen [3]. Demonstration of acid fast bacilli 3. Kumar V, Abbas A, Fausto N, Aster J. Robbins and Cotran by special stains is also possible. Only 35-60% of cases Pathologic Basis of Disease: Chronic inflammation. th8 can be diagnosed by demonstrating acid-fast bacilli in edition. China: Saunders Elsevier 2010. the biopsy specimen. Culture of the biopsy material 4. Barker JA, Conway AM, Hill J. Supralevator fistula-in-ano