Medical electrical equipment - Dosimeters with ionization chambers as used in radiotherapy

Establishes requirements for a satisfactory level of performance of dosimeters with ionization chambers intended for the measurement of absorbed dose to water or air kerma (and their rates) in photon or electron radiation fields as used in radiotherapy. Standardizes methods for the determination of compliance with this level of performance.

Medizinische elektrische Geräte - Dosimeter mit Ionisationskammern zur Anwendung in der Strahlentherapie

Appareils électromédicaux - Dosimètres à chambre d'ionisation utilisés en radiothérapie

Etablit les prescriptions pour un niveau de performance satisfaisant des dosimètres à chambres d'ionisation destinés à mesurer les doses absorbées dans l'eau ou les kerma dans l'air (et les débits correspondants) dans les champs de rayonnement de photons ou d'électrons utilisés en radiothérapie. Normalise les méthodes servant à déterminer la conformité à ce niveau de performance.

Medical electrical equipment - Dosimeters with ionization chambers as used in radiotherapy (IEC 60731:1997)

General Information

Status
Withdrawn
Publication Date
16-Oct-1997
Withdrawal Date
30-Jun-1998
Current Stage
9960 - Withdrawal effective - Withdrawal
Start Date
14-Mar-2015
Completion Date
14-Mar-2015

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SLOVENSKI STANDARD
01-september-1998
Medical electrical equipment - Dosimeters with ionization chambers as used in
radiotherapy (IEC 60731:1997)
Medical electrical equipment - Dosimeters with ionization chambers as used in
radiotherapy
Medizinische elektrische Geräte - Dosimeter mit Ionisationskammern zur Anwendung in
der Strahlentherapie
Appareils électromédicaux - Dosimètres à chambre d'ionisation utilisés en radiothérapie
Ta slovenski standard je istoveten z: EN 60731:1997
ICS:
11.040.50 Radiografska oprema Radiographic equipment
17.240 Merjenje sevanja Radiation measurements
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

NORME
CEI
INTERNATIONALE
IEC
INTERNATIONAL
Deuxième édition
STANDARD
Second edition
1997-07
Appareils électromédicaux –
Dosimètres à chambres d’ionisation
utilisés en radiothérapie
Medical electrical equipment –
Dosimeters with ionization chambers
as used in radiotherapy
 IEC 1997 Droits de reproduction réservés  Copyright - all rights reserved
Aucune partie de cette publication ne peut être reproduite ni No part of this publication may be reproduced or utilized in
utilisée sous quelque forme que ce soit et par aucun any form or by any means, electronic or mechanical,
procédé, électronique ou mécanique, y compris la photo- including photocopying and microfilm, without permission in
copie et les microfilms, sans l'accord écrit de l'éditeur. writing from the publisher.
International Electrotechnical Commission 3, rue de Varembé Geneva, Switzerland
Telefax: +41 22 919 0300 e-mail: inmail@iec.ch IEC web site http: //www.iec.ch
CODE PRIX
Commission Electrotechnique Internationale
XD
PRICE CODE
International Electrotechnical Commission
Pour prix, voir catalogue en vigueur
For price, see current catalogue

60731 © IEC:1997 – 3 –
CONTENTS
Page
FOREWORD . 11
INTRODUCTION . 13
Clause
1 Scope and object. 15
2 Normative references . 17
3 Terminology and definitions . 19
4 General requirements . 31
4.1 Performance requirements . 31
4.2 REFERENCE VALUES and STANDARD TEST VALUES . 31
4.3 General test conditions and methods . 33
4.3.1 STANDARD TEST CONDITIONS . 33
4.3.2 Test of components. 33
4.3.3 RATED or EFFECTIVE RANGE of DOSE (or KERMA) RATES. 33
4.3.4 Uncertainty of measurement . 35
4.3.5 Adjustments during test . 35
4.3.6 Test conditions particular to CHAMBER ASSEMBLIES. 35
4.3.7 Test conditions particular to MEASURING ASSEMBLIES. 35
4.3.8 Test conditions particular to STABILITY CHECK DEVICES . 37
4.3.9 Use of STABILITY CHECK DEVICES. 37
4.4 Summary tables . 37
Table 1 – REFERENCE CONDITIONS and STANDARD TEST CONDITIONS
1a – CHAMBER ASSEMBLY . 39
1b – MEASURING ASSEMBLY . 39
Table 2 – Limits of PERFORMANCE CHARACTERISTICS at STANDARD TEST CONDITIONS
2a – CHAMBER ASSEMBLY . 41
2b – MEASURING ASSEMBLY . 41
Table 3 – LIMITS OF VARIATION of PERFORMANCE CHARACTERISTICS for effects of
INFLUENCE QUANTITIES and INSTRUMENT PARAMETERS
3a – CHAMBER ASSEMBLY . 43
3b – MEASURING ASSEMBLY . 47
3c – CHAMBER and MEASURING ASSEMBLIES combined . 49
4.5 Classification of equipment according to LIMITS OF VARIATION. 49
4.5.1 FIELD-CLASS DOSIMETER. 49
4.5.2 REFERENCE-CLASS DOSIMETER. 49

60731 © IEC:1997 – 5 –
Clause Page
5 CHAMBER ASSEMBLY performance requirements. 51
5.1 General performance requirements for (RADIOTHERAPY) IONIZATION CHAMBERS . 51
5.1.1 CHAMBER ASSEMBLY LEAKAGE CURRENT without irradiation . 51
5.1.2 Stability. 51
5.1.3 STABILIZATION TIME . 53
5.1.4 Post-irradiation leakage. 53
5.1.5 RATED or EFFECTIVE RANGE of DOSE RATE (continuous radiation) . 55
5.1.6 Maximum RATED DOSE per pulse (pulsed radiation) . 57
5.1.7 STRAY RADIATION . 59
5.1.8 Guard/collector insulation. 61
5.1.9 Cable microphony . 61
5.1.10 Polarity of polarizing voltage effect . 61
5.1.11 Electromagnetic compatibility . 63
5.2 Performance requirements particular to SHELL CHAMBERS . 63
5.2.1 Dependence on radiation quality. 65
5.2.2 RATED RANGE of field sizes . 69
5.2.3 CHAMBER orientation. 73
5.3 Performance requirements particular to PARALLEL-PLATE CHAMBERS . 73
5.3.1 Dependence on radiation quality. 75
5.3.2 RATED RANGE of field sizes. 77
HAMBER
5.3.3 C orientation. 77
5.4 Performance requirements particular to VENTED CHAMBERS. 79
5.4.1 Atmospheric pressure change . 79
5.4.2 Temperature . 79
5.4.3 Humidity. 81
5.5 Performance requirements particular to SEALED CHAMBERS . 81
5.5.1 Atmospheric pressure change . 81
5.5.2 Temperature . 83
6. MEASURING ASSEMBLY performance requirements. 83
6.1 General performance requirements for (RADIOTHERAPY) DOSIMETERS . 85
6.1.1 EFFECTIVE RANGES . 85
6.1.2 RESOLUTION of the display. 85
6.1.3 Repeatability . 87
6.1.4 Long-term stability. 87
6.1.5 STABILIZATION TIME. 89
6.1.6 Electromagnetic compatibility . 89
6.2 Performance requirements particular to DOSIMETERS . 91
6.2.1 ZERO DRIFT . 91
6.2.2 ZERO SHIFT . 93
6.2.3 NON-LINEARITY . 95

60731 © IEC:1997 – 7 –
Clause Page
6.2.4 Range changing . 97
6.2.5 Dead time . 99
6.2.6 Temperature . 99
6.2.7 Humidity. 101
6.2.8 STRAY RADIATION effect. 101
6.2.9 Charge leakage. 103
6.2.10 DOSE RATE dependence of DOSIMETERS . 103
6.3 Performance requirements particular to DOSE RATEMETERS . 105
6.3.1 ZERO DRIFT . 105
6.3.2 ZERO SHIFT . 107
6.3.3 NON-LINEARITY . 109
6.3.4 Range changing . 111
6.3.5 RESPONSE TIME . 113
6.3.6 Temperature . 115
6.3.7 Humidity. 115
6.3.8 STRAY RADIATION effect. 117
6.4 Performance requirements particular to battery-operated MEASURING ASSEMBLIES 119
6.4.1 Operating battery life. 119
MEASURING
6.5 Performance requirements particular to supply mains-operated
ASSEMBLIES . 119
6.5.1 Mains voltage – static. 119
6.5.2 Mains voltage – variation during a measurement . 119
7 STABILITY CHECK DEVICE performance requirements . 121
7.1 General performance requirements for STABILITY CHECK DEVICES . 121
7.1.1 Long-term stability. 121
7.1.2 Repeatability . 121
8 Constructional requirements as related to PERFORMANCE CHARACTERISTICS . 123
8.1 Constructional requirements on CHAMBER ASSEMBLIES . 123
8.2 Constructional requirements on MEASURING ASSEMBLIES . 123
8.2.1 Adjustment of RESPONSE . 123
8.2.2 Display device. 123
8.2.3 Battery indication and compensation . 125
8.2.4 Input current threshold . 125
8.2.5 Automatic termination of measurement in the DOSE mode. 125
8.3 Constructional requirements on STABILITY CHECK DEVICES . 127
8.3.1 General constructional requirements on STABILITY CHECK DEVICES . 127
8.3.2 Constructional requirements particular to a radioactive type STABILITY
CHECK DEVICE . 127
8.3.3 Constructional requirements particular to an overall STABILITY CHECK
DEVICE. 127

60731 © IEC:1997 – 9 –
Clause Page
8.4 Constructional requirements on PHANTOMs and build-up caps. 127
8.4.1 PHANTOMs . 127
9 Marking . 129
9.1 Marking required on CHAMBER ASSEMBLY . 129
9.2 Marking required on MEASURING ASSEMBLY . 129
9.3 Marking required on STABILITY CHECK DEVICE . 131
9.4 Marking required on PHANTOM or build-up cap .
...

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