EN 60976-2007 en Medical electrical equipment - Medical electron accelerators - Functional performance characteristics (Incorporates Amendment A1 2000)《医用电气设备 医用电子加速器 功能特性 包含修改件A1-.pdf

《EN 60976-2007 en Medical electrical equipment - Medical electron accelerators - Functional performance characteristics (Incorporates Amendment A1 2000)《医用电气设备 医用电子加速器 功能特性 包含修改件A1-.pdf》由会员分享，可在线阅读，更多相关《EN 60976-2007 en Medical electrical equipment - Medical electron accelerators - Functional performance characteristics (Incorporates Amendment A1 2000)《医用电气设备 医用电子加速器 功能特性 包含修改件A1-.pdf（102页珍藏版）》请在麦多课文档分享上搜索。

1、BRITISH STANDARDBS EN 60976:2007Medical electrical equipment Medical electron accelerators Functional performance characteristicsICS 11.040.50; 13.280g49g50g3g38g50g51g60g44g49g42g3g58g44g55g43g50g56g55g3g37g54g44g3g51g40g53g48g44g54g54g44g50g49g3g40g59g38g40g51g55g3g36g54g3g51g40g53g48g44g55g55g40g

2、39g3g37g60g3g38g50g51g60g53g44g42g43g55g3g47g36g58BS EN 60976:2007This British Standard was published under the authority of the Standards Policy and Strategy Committee on 30 April 2008 BSI 2008ISBN 978 0 580 55685 2National forewordThis British Standard is the UK implementation of EN 60976:2007. It

3、 is identical to IEC 60976:2007. It supersedes BS EN 60976:2001 which is withdrawn.The UK participation in its preparation was entrusted by Technical Committee CH/62, Electromedical equipment in medical practice, to Subcommittee CH/62/3, Equipment for radiotherapy, nuclear medicine and radiation dos

4、imetry.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 necessary provisions of a contract. Users are responsible for its correct application.Compliance with a British Standard cannot confer immunit

5、y from legal obligations. Amendments/corrigenda issued since publicationDate CommentsEUROPEAN STANDARD EN 60976 NORME EUROPENNE EUROPISCHE NORM December 2007 CENELEC European Committee for Electrotechnical Standardization Comit Europen de Normalisation Electrotechnique Europisches Komitee fr Elektro

6、technische Normung Central Secretariat: rue de Stassart 35, B - 1050 Brussels 2007 CENELEC - All rights of exploitation in any form and by any means reserved worldwide for CENELEC members. Ref. No. EN 60976:2007 E ICS 11.040.50; 13.280 Supersedes EN 60976:1999 + A1:2000English version Medical electr

7、ical equipment - Medical electron accelerators - Functional performance characteristics (IEC 60976:2007) Appareils lectromdicaux - Acclrateurs mdicaux dlectrons - Caractristiques fonctionnelles de performance (CEI 60976:2007) Medizinische elektrische Gerte - Medizinische Elektronenbeschleuniger - Ap

8、parative Qualittsmerkmale (IEC 60976:2007) This European Standard was approved by CENELEC on 2007-11-01. CENELEC members are bound to comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for giving this European Standard the status of a national standard without any altera

9、tion. Up-to-date lists and bibliographical references concerning such national standards may be obtained on application to the Central Secretariat or to any CENELEC member. This European Standard exists in three official versions (English, French, German). A version in any other language made by tra

10、nslation under the responsibility of a CENELEC member into its own language and notified to the Central Secretariat has the same status as the official versions. CENELEC members are the national electrotechnical committees of Austria, Belgium, Bulgaria, Cyprus, the Czech Republic, Denmark, Estonia,

11、Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, the Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland and the United Kingdom. BS EN 60976:2007 2 Foreword The text of document 62C/429/FDIS, future e

12、dition 2 of IEC 60976, prepared by SC 62C, Equipment for radiotherapy, nuclear medicine and radiation dosimetry, of IEC TC 62, Electrical equipment in medical practice, was submitted to the IEC-CENELEC parallel vote and was approved by CENELEC as EN 60976 on 2007-11-01. This European Standard supers

13、edes EN 60976:1999 + A1:2000. EN 60976:2007 includes the addition of performance standards and test methods relating to the following new technologies: dynamic beam delivery techniques, such as MOVING BEAM RADIOTHERAPY, INTENSITY-MODULATED RADIATION THERAPY (IMRT), IMAGE-GUIDED RADIOTHERAPY (IGRT) a

14、nd PROGRAMMABLE WEDGE FIELDS (PWF); STEREOTACTIC RADIOTHERAPY (SRT) / STEREOTACTIC RADIOSURGERY (SRS); use of ELECTRONIC IMAGING DEVICES. This standard, together with IEC/TR 60977, is to be used in conjunction with EN 60601-2-1. The following dates were fixed: latest date by which the EN has to be i

15、mplemented at national level by publication of an identical national standard or by endorsement (dop) 2008-08-01 latest date by which the national standards conflicting with the EN have to be withdrawn (dow) 2010-11-01 In this standard, the following print types are used: requirements, compliance wi

16、th which can be tested, and definitions: in roman type; explanations, advice, general statements, exceptions and notes: in small roman type; test specifications and headings of sub-clauses: in italic type; TERMS USED THROUGHOUT THIS PARTICULAR STANDARD THAT HAVE BEEN LISTED IN THE INDEX OF DEFINED T

17、ERMS AND DEFINED IN CLAUSE 3, OR IN OTHER STANDARDS: SMALL CAPITALS. Annex ZA has been added by CENELEC. _ Endorsement notice The text of the International Standard IEC 60976:2007 was approved by CENELEC as a European Standard without any modification. _ 3 CONTENTS INTRODUCTION H7 1 Scope . H8 2 Nor

18、mative references H9 3 Terms and definitions H9 4 Environmental conditions. H13 4.1 General H13 4.2 Transport and storage H13 4.3 Power supply H13 5 General information to the USER. H13 5.1 Functional performance characteristics . H13 5.2 Available nominal energies and ABSORBED DOSE RATES H14 5.3 Av

19、ailable RADIATION FIELDS H14 5.4 NORMAL TREATMENT DISTANCE H14 5.5 Available WEDGE X-RAY FIELDS. H14 5.6 Available flattening FILTERS . H14 5.7 Availability H15 5.8 Influencing quantities H15 5.9 Maintenance. H15 5.10 Presentation. H15 5.11 Dimensions, clearances, within the RADIATION HEAD, and in t

20、he region RADIATION HEAD to ISOCENTRE, of BEAM LIMITING DEVICES . H15 5.12 IMRT H15 6 Standardized test conditions H16 6.1 General H16 6.2 Angle settings. H16 6.3 Properties and positioning of the PHANTOM H16 6.4 Positioning of measuring points H16 6.5 RADIATION DETECTORS . H16 6.6 STANDARD MEASUREM

21、ENT DEPTHS . H17 6.7 RADIATION FIELDS H17 6.8 Adjustments during test H17 6.9 Use of RADIOGRAPHIC FILM or alternative imaging method . H17 7 DOSE MONITORING SYSTEM. H17 7.1 General H17 7.2 Reproducibility H18 7.3 Proportionality H19 7.4 Dependence on angular positions . H20 7.5 Dependence on GANTRY

22、rotation . H21 7.6 Dependence on the shape of the RADIATION FIELD H21 7.7 Stability of calibration . H22 7.8 Stability in MOVING BEAM RADIOTHERAPY H24 8 Depth ABSORBED DOSE characteristics. H25 8.1 X-RADIATION H25 8.2 ELECTRON RADIATION . H27 9 Uniformity of RADIATION FIELDS H30 BS EN 60976:2007 4 9

23、.1 X-RADIATION H30 9.2 ELECTRON RADIATION . H35 9.3 PENUMBRA of RADIATION FIELDS H37 10 Indication of RADIATION FIELDS H38 10.1 X-RADIATION H38 10.2 ELECTRON RADIATION . H44 10.3 Geometry and motion speeds of adjustable BLDs for X-RADIATION and ELECTRON RADIATION H45 10.4 Illuminance and PENUMBRA of

24、 the LIGHT FIELD. H46 11 Indication of the RADIATION BEAM AXIS . H47 11.1 General H47 11.2 Indication on entry to the PATIENT H48 11.3 Indication on exit from the PATIENT H50 12 ISOCENTRE . H51 12.1 Displacement of the RADIATION BEAM AXIS from the ISOCENTRE H51 12.2 Indication of the ISOCENTRE . H52

25、 13 Indication of distance along the RADIATION BEAM AXIS H52 13.1 Indicating device. H52 13.2 Additional indicating device for equipment with variable distance between RADIATION SOURCE and ISOCENTRE and for non-isocentric equipment. H53 14 Zero position of rotational scales . H54 14.1 General H54 14

26、.2 Information to the USER. H54 14.3 Tests H54 15 Congruence of opposed RADIATION FIELDS. H55 15.1 Information to the USER. H55 15.2 Test . H55 16 Movements of the PATIENT table . H56 16.1 General H56 16.2 Vertical movement of the table H56 16.3 ISOCENTRIC rotation of the table. H57 16.4 Parallelism

27、 of table rotational axes H57 16.5 Rigidity of the table. H58 17 ELECTRONIC IMAGING DEVICE (e.g. EPID) H59 17.1 Information to the USER. H59 17.2 Tests H61 Annex A (informative) Format for presentation of functional performances values H74 Annex ZA (normative) Normative references to international p

28、ublications with their corresponding European publications98 Index of defined terms . H95 Figure 1 Explanatory diagram for the definition of wedge . H63 Figure 2 The rotary GANTRY . H64 Figure 3 The wall- or floor-mounted GANTRY. H65 Figure 4 The ceiling-mounted GANTRY H66 Figure 5 Flattened area (s

29、hown hatched) within the RADIATION FIELD. H67 BS EN 60976:2007 5 Figure 6 Examples of profiles of ABSORBED DOSE along the major axes or the diagonal axes H68 Figure 7 Explanatory diagram for flatness of the ELECTRON FIELD H69 Figure 8 A possible arrangement of equipment for the measurement of the IS

30、OCENTRE described in Clause 12 H70 Figure 9 Test 10.1.1.3. H71 Figure 10 RADIATION HEAD showing X-RADIATION BLDs and ACCESSORIES (see 4.11) H72 Figure 11 Multi-element BLD RADIATION FIELDS used for measurement of X-RADIATION PENUMBRA (see 8.3.2). H73 Table 1 Conditions for testing reproducibility .

31、H18 Table 2 Conditions for testing proportionality of the DOSE MONITORING SYSTEM H19 Table 3 Conditions for testing dependence of the DOSE MONITORING SYSTEM on equipment position. H20 Table 4 Conditions for testing dependence of the DOSE MONITORING SYSTEM on GANTRY rotation . H21 Table 5 Conditions

32、for testing dependence on the shape of the RADIATION FIELD . H22 Table 6 Conditions for testing stability of calibration of the DOSE MONITORING SYSTEM. H23 Table 7 Conditions for testing stability of the DOSE MONITORING SYSTEM in MOVING BEAM RADIOTHERAPY . H25 Table 8 Conditions for testing depth do

33、se characteristics. H26 Table 9 Conditions for testing depth dose characteristics. H28 Table 10 Conditions for testing stability of PENETRATIVE QUALITY of ELECTRON RADIATION H28 Table 11 Flattened area according to Figure 5 H30 Table 12 Conditions for testing flatness and symmetry of X-RAY FIELDS H3

34、1 Table 13 Conditions for testing deviation of dose distribution of X-RAY FIELDS with angular position . H32 Table 14 Conditions for testing maximum ABSORBED DOSE ratio in the RADIATION FIELD H33 Table 15 Conditions for testing WEDGE FACTORS . H34 Table 16 Conditions for testing WEDGE ANGLES. H34 Ta

35、ble 17 Conditions for testing flatness, symmetry, deviation of dose distribution with angular position, and maximum ABSORBED DOSE ratio of ELECTRON FIELDS H36 Table 18 Conditions for film calibration H40 Table 19 Conditions for testing the numerical and the LIGHT FIELD-INDICATION . H41 Table 20 Cond

36、itions for testing reproducibility of X-RAY FIELDS . H43 Table 21 Conditions for testing the LIGHT FIELD-INDICATOR for ELECTRON RADIATION. H45 Table 22 Conditions for testing geometry of the BEAM LIMITING SYSTEM. H47 Table 23 Conditions for testing the indication of the RADIATION BEAM AXIS on entry

37、to the PATIENT H49 Table 24 Conditions for testing the indication of the RADIATION BEAM AXIS on exit from the PATIENT H50 BS EN 60976:2007 6 Table 25 Conditions for testing indication of the ISOCENTRE H52 Table 26 Conditions for testing vertical movement of the table . H57 Table 27 Conditions for te

38、sting ISOCENTRIC rotation of the table . H57 Table 28 Conditions for testing the angulation of rotational axes of the table H58 Table 29 Conditions for testing lateral rigidity of the table H59 BS EN 60976:2007 7 INTRODUCTION Standards containing safety requirements for medical ELECTRON ACCELERATORS

39、 have been published by the IEC, details of which will be found in Clause 2. The present standard specifies methods of testing and methods of disclosure of functional performance of medical ELECTRON ACCELERATORS intended for RADIOTHERAPY. It permits a direct comparison between the performance data o

40、f equipment of different MANUFACTURERS. Since this standard does not contain safety requirements, it has not been numbered in the IEC 60601 publication series. It describes aspects of functional performance of medical ELECTRON ACCELERATORS and the way in which they should be presented. It also inclu

41、des test methods and conditions suitable for TYPE TESTS. These test methods are suggested test methods and alternative methods may be equally appropriate, but the specified functional performance characteristics of medical ELECTRON ACCELERATORS shall be related to these test methods and conditions.

42、Tests specified in this standard are not necessarily appropriate for ensuring that any individual medical ELECTRON ACCELERATOR conforms to the declared functional performance during the course of its working lifetime. Guidance on the values which may be expected is given in the technical report, IEC

43、 60977. This International Standard was first published in 1989. With the rapidly increasing use of medical ELECTRON ACCELERATORS equipped with multi-element BEAM LIMITING DEVICES (BLDs), amendments to both this standard and the associated report, IEC 60977, were published in 2000. Amendment 1 was i

44、ntended mainly to address the basic performance issues associated with the applications of multi-element BLDs to static RADIATION FIELDS. This second edition includes the addition of performance standards and test methods relating to several relatively new technologies introduced within the last few

45、 years, including dynamic beam delivery techniques, such as MOVING BEAM RADIOTHERAPY, INTENSITY-MODULATED RADIATION THERAPY (IMRT), IMAGE-GUIDED RADIOTHERAPY (IGRT), and PROGRAMMABLE WEDGE FIELDS (PWF). Also included are STEREOTACTIC RADIOTHERAPY (SRT)/STEREOTACTIC RADIOSURGERY (SRS) and the use of

46、certain ELECTRONIC IMAGING DEVICES. In recognition of the diversity of equipment produced by MANUFACTURERS in each of these technologies, this second edition has specified performance standards, methods of test, and methods of disclosure of functional performance, that are as basic and generic as po

47、ssible. MANUFACTURERS may add more detailed information and special tests of performance characteristics to each performance category, in their ACCOMPANYING DOCUMENTS. BS EN 60976:2007 8 MEDICAL ELECTRICAL EQUIPMENT MEDICAL ELECTRON ACCELERATORS FUNCTIONAL PERFORMANCE CHARACTERISTICS 1 Scope This In

48、ternational Standard applies to medical ELECTRON ACCELERATORS when used, for therapy purposes, in human medical practice. This standard applies to medical ELECTRON ACCELERATORS which deliver a RADIATION BEAM of either X-RADIATION or ELECTRON RADIATION with NOMINAL ENERGIES in the range 1 MeV to 50 M

49、eV at maximum ABSORBED DOSE RATES between 0,001 Gy s1and 1 Gy s1at 1 m from the RADIATION SOURCE and at NORMAL TREATMENT DISTANCES between 50 cm and 200 cm from the RADIATION SOURCE. The present standard describes measurements and test procedures to be performed by the MANUFACTURER at the design and c