CEN TR 16386-2013 Dentistry - Guidelines for handling methacrylate-based materials in the dental laboratory《牙科 在牙科实验室处理甲基丙烯酸酯材料指南》.pdf

《CEN TR 16386-2013 Dentistry - Guidelines for handling methacrylate-based materials in the dental laboratory《牙科 在牙科实验室处理甲基丙烯酸酯材料指南》.pdf》由会员分享，可在线阅读，更多相关《CEN TR 16386-2013 Dentistry - Guidelines for handling methacrylate-based materials in the dental laboratory《牙科 在牙科实验室处理甲基丙烯酸酯材料指南》.pdf（12页珍藏版）》请在麦多课文档分享上搜索。

1、raising standards worldwideNO COPYING WITHOUT BSI PERMISSION EXCEPT AS PERMITTED BY COPYRIGHT LAWBSI Standards PublicationPD CEN/TR 16386:2013Dentistry Guidelines for handling methacrylate-based materials in the dental laboratoryPD CEN/TR 16386:2013 PUBLISHED DOCUMENTNational forewordThis Published

2、Document is the UK implementation of CEN/TR 16386:2013.The UK participation in its preparation was entrusted to Technical Committee CH/106, Dentistry.A list of organizations represented on this committee can be obtained on request to its secretary.This publication does not purport to include all the

3、 necessary provisions of a contract. Users are responsible for its correct application. The British Standards Institution 2013. Published by BSI Standards Limited 2013ISBN 978 0 580 77382 2 ICS 11.060.10 Compliance with a British Standard cannot confer immunity from legal obligations.This Published

4、Document was published under the authority of the Standards Policy and Strategy Committee on 28 February 2013.Amendments issued since publicationDate Text affectedPD CEN/TR 16386:2013TECHNICAL REPORT RAPPORT TECHNIQUE TECHNISCHER BERICHT CEN/TR 16386 January 2013 ICS 11.060.10 English Version Dentis

5、try - Guidelines for handling methacrylate-based materials in the dental laboratory Mdecine bucco-dentaire - Lignes directrices relatives la manipulation des matriaux base de mthacrylate en laboratoire dentaire Zahnheilkunde - Leitlinien zur Handhabung von methacrylatbasierenden Materialien im zahnt

6、echnischen Labor This Technical Report was approved by CEN on 10 June 2012. It has been drawn up by the Technical Committee CEN/TC 55. CEN members are the national standards bodies of Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, Finland, Former Yugoslav Republic of

7、Macedonia, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and United Kingdom. EUROPEAN COMMITTEE FOR STANDARDIZATION COMIT EUROPEN DE NORMALISATION

8、 EUROPISCHES KOMITEE FR NORMUNG Management Centre: Avenue Marnix 17, B-1000 Brussels 2013 CEN All rights of exploitation in any form and by any means reserved worldwide for CEN national Members. Ref. No. CEN/TR 16386:2013: EPD CEN/TR 16386:2013CEN/TR 16386:2013 (E) 2 Contents Page Foreword . 3 Intro

9、duction 3 1 Scope 4 2 Normative references . 4 3 Terms and definitions 4 4 Risk management. 4 4.1 Risk assessment 4 4.2 Health surveillance . 4 4.3 Medical advice 4 4.4 Reduction of risks 5 4.4.1 General . 5 4.4.2 Skin . 5 4.4.3 Airways . 5 4.4.4 Eye protection 5 Annex A (informative) Use of gloves

10、6 A.1 General . 6 A.2 Recommendations . 6 Bibliography 7 PD CEN/TR 16386:2013CEN/TR 16386:2013 (E) 3 Foreword This document (CEN/TR 16386:2013) has been prepared by Technical Committee CEN/TC 055 “Dentistry”, the secretariat of which is held by DIN. Attention is drawn to the possibility that some of

11、 the elements of this document may be the subject of patent rights. CEN and/or CENELEC shall not be held responsible for identifying any or all such patent rights. This document has been prepared by Working Group 8 Occupational risk assessments of CEN/TC 55 Dentistry. Introduction In 2008 CEN/TC 55

12、established a new working group WG 8 Occupational risk assessments. The rationale for the group was concern about occupational health issues for personnel working with methacrylate-based products in dentistry. These materials (e.g. removable denture and orthodontic base materials, tray materials, de

13、ntal repair materials etc.) may pose a risk because of the presence of methacrylate monomers. The objective of WG 8 was to review the present status regarding the prevalence and awareness of the risk of methacrylate based materials among dental personnel. In addition the occupational health and safe

14、ty regulations in different countries were considered. Based on the results of the survey carried out by the group, this Technical Report has been produced as a guideline for handling methacrylate based materials in dental laboratories to maintain the safety of the occupational environment. Aspects

15、of this report may be applicable to dental practises. After reviewing the scientific literature and making an investigation among European dental technicians, adverse effects on the skin seem to be the main occupational risk for dental technicians. Uncured methyl methacrylate is a risk factor for sk

16、in disease and it has been defined by The European Chemicals Bureau as a risk substance 1. The report concluded that there is a risk for toxic, neurotoxic as well as sensitising reactions to personnel in dental laboratories and there is need for limiting the risks. Other risk factors for occupationa

17、l related skin reactions as eczema are wet work, handling of different chemicals and plaster. Dust from grinding polymer-based materials and vapour of monomers may also be a risk to the airways. PD CEN/TR 16386:2013CEN/TR 16386:2013 (E) 4 1 Scope This Technical Report gives guidance for handling all

18、 methacrylate-based materials for dental purposes used in dental laboratories. The intention is to lower the risk of adverse effects on skin and airways when working with such materials. Aspects of this document may be applicable for other areas in Dentistry. 2 Normative references The following doc

19、uments, in whole or in part, are normatively referenced in this document and are indispensable for its application. For dated references, only the edition cited applies. For undated references, the latest edition of the referenced document (including any amendments) applies. EN 374-1, Protective glo

20、ves against chemicals and micro-organisms Part 1: Terminology and performance requirements EN ISO 1942, Dentistry Vocabulary (ISO 1942) EN ISO 14971, Medical devices Application of risk management to medical devices (ISO 14971) 3 Terms and definitions For the purposes of this document, the terms and

21、 definitions given in EN ISO 1942, EN 374-1 and the following apply. 3.1 methacrylate ester of methacrylic acid 3.2 local exhaust ventilation engineering control system to reduce exposures to airborne contaminants such as dust, mist, fume, vapour or gas in a work place 4 Risk management 4.1 Risk ass

22、essment Risk assessments for each material and procedure shall be compiled and documented by a responsible person in the dental laboratory. This shall be in accordance with European regulation 2, national regulation/legislation and/or EN ISO 14971 as appropriate. Information from instructions for us

23、e or other sources (e.g. material safety data sheets) shall be incorporated in the risk assessment. 4.2 Health surveillance Regular health surveillance shall be carried out according to the risk assessment 4.3 Medical advice Medical advice is required: PD CEN/TR 16386:2013CEN/TR 16386:2013 (E) 5 a)

24、when a person has a pre-existing condition and enhanced risk of adverse effects from methacrylate-based materials; b) if there is evidence of disease after handling these materials. 4.4 Reduction of risks 4.4.1 General Uncured methacrylate-based materials constitute a risk to skin and airways. All p

25、ersonnel handling uncured materials shall be provided with suitable information about risks. Handling instructions and appropriate training shall be provided. Appropriate warning signs and a summary of safety precautions shall be displayed at each workstation 3. 4.4.2 Skin Avoid direct skin contact

26、wherever possible. When handling uncured methacrylate-based materials, use gloves and change them after each procedure. Do not reuse the gloves. If skin contact has occurred, immediately wash the affected area carefully with soap and water and dry thoroughly. Avoid the use of alcoholic solutions for

27、 disinfection. Use skin protection and care procedures (e.g. barrier creams). NOTE Important information about gloves is given in Annex A. 4.4.3 Airways Local exhaust ventilation capable of reducing the concentration of dust particles and methacrylate vapour to below the European4/national recommend

28、ed safety levels shall be installed and used according to the manufacturers instructions. 4.4.4 Eye protection When handling uncured or cured methacrylates, use eye protection such as safety glasses, visors or goggles. PD CEN/TR 16386:2013CEN/TR 16386:2013 (E) 6 Annex A (informative) Use of gloves A

29、.1 General When working with uncured methacrylates, the use of ordinary protective gloves can be insufficient due to their permeability to monomers. The time taken to penetrate the glove material will depend upon its composition, the type of chemicals and the length of exposure 5. Users should be aw

30、are of symptoms associated with glove use and latex including the possibility of type 1 allergy caused by latex. For risk assessment on permeability of methacrylate monomers penetrating gloves, appropriate information shall be collected from the manufacturer NOTE: Current information 6,7 suggests th

31、at most gloves useful in dental laboratories, are ineffective after 2 minutes of exposure to methacrylates. A.2 Recommendations The following recommendations are given: a) Use gloves when handling methacrylates. b) Do not to use gloves for a longer period of time as recommended by the manufacturer.

32、Change gloves at this point. c) The use of two gloves on each hand may increase the usage period by a factor of two. d) Change gloves immediately if contamination by monomers has occurred. e) Do not reuse gloves. f) Do not clean gloves with alcohol-based detergents, solvents containing alcohol and/o

33、r acetone, which can increase the permeability of gloves PD CEN/TR 16386:2013CEN/TR 16386:2013 (E) 7 Bibliography 1 European Union Risk Assesment Report, Methyl methacrylate CAS no 80-62 6, EINECS 201 297-1 Risk assessment. 2002. Office for Official Publications of the European Communities. ISBN. 92

34、-894-1253-4. Luxemburg 2 Medical Device Directive 93/42/EEC 1993 of the European Parliament and of the Council of 14 June 1993 3 Directive 89/686/EEC on Personal Protective Equipment (PPE) 4 Directive 2009/161/EU. Establishing a 3:rd list of indicative occupational exposure limit values in implement

35、ation of council directive 98/24/EC and amending commission directive 2000/39/EC 5 Protective gloves against chemicals and microorganisms Part 3: Determination of resistance to permeation by chemicals 6 Lnnroth EC, Wellendorf H, Ruyter IE. Permeability of different types of medical protective gloves

36、 to acrylic monomers. Eur J Oral Sci 2003; 111: 440-446 7 Lnnroth EC, Ruyter IE. Resistance of medical gloves to permeation by methyl methacrylate (MMA), ethylene glycol dimethacrylate (EGDMA) and 1,4-Butanediol dimetahcrylate (1,4-BDMA). Eur. J Oral Sci 2003;9(3):289-299 This page deliberately left

37、 blankThis page deliberately left blankBSI is the independent national body responsible for preparing British Standards and other standards-related publications, information and services. It presents the UK view on standards in Europe and at the international level. BSI is incorporated by Royal Char

38、ter. British Standards and other standardisation products are published by BSI Standards Limited.British Standards Institution (BSI)raising standards worldwideBSI389 Chiswick High Road London W4 4AL UKTel +44 (0)20 8996 9001Fax +44 (0)20 8996 Standards and PASs are periodically updated by amendment

39、 or revision. Users of British Standards and PASs should make sure that they possess the latest amendments or editions.It is the constant aim of BSI to improve the quality of our products and services. We would be grateful if anyone finding an inaccuracy or ambiguity while using British Standards wo

40、uld inform the Secretary of the technical committee responsible, the identity of which can be found on the inside frontcover. Similary for PASs, please notify BSI Customer Services.Tel: +44 (0)20 8996 9001 Fax: +44 (0)20 8996 7001BSI offers BSI Subscribing Members an individual updating service call

41、ed PLUS which ensures that subscribers automatically receive the latest editions of British Standards and PASs.Tel: +44 (0)20 8996 7669 Fax: +44 (0)20 8996 7001Email: Buying standardsYou may buy PDF and hard copy versions of standards directly using acredit card from the BSI Shop on the website add

42、ition all orders for BSI, international and foreign standards publicationscan be addressed to BSI Customer Services.Tel: +44 (0)20 8996 9001 Fax: +44 (0)20 8996 7001Email: In response to orders for international standards, BSI will supply the British Standard implementation of the relevant internati

43、onal standard, unless otherwise requested.Information on standardsBSI provides a wide range of information on national, Europeanand international standards through its Knowledge Centre.Tel: +44 (0)20 8996 7004 Fax: +44 (0)20 8996 7005Email: BSI Subscribing Members are kept up to date with standards

44、developments and receive substantial discounts on the purchase priceof standards. For details of these and other benefits contact Membership Administration. Tel: +44 (0)20 8996 7002 Fax: +44 (0)20 8996 7001 Email: Information regarding online access to British Standards and PASs via British Standar

45、ds Online can be found at information about British Standards is available on the BSI website at www.bsi- the data, software and documentation set out in all British Standards and other BSI publications are the property of and copyrighted by BSI, or some person or entity that own copyright in the i

46、nformation used (such as the international standardisation bodies) has formally licensed such information to BSI for commerical publication and use. Except as permitted under the Copyright, Designs and Patents Act 1988 no extract may be reproduced, stored in a retrieval system or transmitted in any

47、form or by any means electronic, photocopying, recording or otherwise without prior written permission from BSI. This does not preclude the free use, in the course of implementing the standard, of necessary details such as symbols, and size, type or grade designations. If these details are to be used for any other purpose than implementation then the prior written permission of BSI must be obtained. Details and advice can be obtained from the Copyright & Licensing Department.Tel: +44 (0)20 8996 7070Email: