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YY/T 0889-2013 PDF English

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YY/T 0889-2013: Intensity-modulated radiation treatment planning system - Functional performance characteristics and test methods
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YY/T 0889-2013: Intensity-modulated radiation treatment planning system - Functional performance characteristics and test methods


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YY ICS 11.040.60 C 43 PHARMACEUTICAL INDUSTRY STANDARD YY/T 0889-2013 Intensity-modulated radiation treatment planning system — Functional performance characteristics and test methods Issued on. OCTOBER 21, 2013 Implemented on. OCTOBER 1, 2014 Issued by. State Food and Drug Administration

Table of Contents

Foreword... 3 1 Scope... 4 2 Normative references... 4 3 Terms and Definitions... 5 4 Performance Requirements... 6 5 Test Methods... 6 Annex A (Normative) Test Cases... 9 Annex B (Informative) Test Data... 17 Bibliography... 18

Foreword

This Standard is drafted according to the rules specified in GB/T 1.1-2009. Please note that some content in the Document may involve patents. The issuing authority of this Document does not undertake the responsibility of identifying these patents. The Standard was proposed by State Food and Drug Administration. The Standard shall be under the jurisdiction of National Standardization Technical Committee of Medical Appliances Radiotherapy and Technical Committee of Nuclear Medicine and Radiation Dosimetry Equipment (SAC/TC10/SC3). Drafting organizations of this Standard. Beijing Institute of Medical Device Testing, Cancer Hospital of Chinese Academy of Medical Sciences, Nuclear Science and Technology Research Institute of Sichuan University, and Beijing Cancer Hospital. The main drafters of this Standard. Jiao Chunying, Zhang Xin, Dai Jianrong, Li Minghui, Gou Chengjun, and Wu Hao. Intensity-modulated radiation treatment planning system — Functional performance characteristics and test methods

1 Scope

This Standard specifies the terms, definitions, performance requirements and test methods of intensity-modulated radiation treatment planning system.

2 Normative references

The articles contained in the following documents have become part of this Document when they are quoted herein. For the dated documents so quoted, all the modifications (Including all corrections) or revisions made thereafter shall be applicable to this document. GB 9706.5 Medical electrical equipment - Part 2-1.Particular requirements for the safety of electron accelerators in the range 1 MeV to 50 MeV

3 Terms and Definitions

Those defined in GB 9706.5, GB 15213, GB/T 17857 and YY 0637 AND the following terms and definitions apply to this Standard. The therapeutic dose that is given to target volume according to certain time dose splitting methods.

4 Performance Requirements

For each IMRT test case specified in Appendix A, DESIGN the treatment plan in accordance with the dose target specified in this Standard; REPORT the actual situations that meet dose target.

5 Test Methods

Treatment plan shall be designed according to the requirements as stated in Appendix A. The conformance of dose target of each IMRT test case shall be checked. Dose target of test cases shall be satisfied as far as possible. Otherwise, the actual test data shall be provided for assessment, so as to determine whether the IMRT plan is acceptable.

Annex A

(Normative) Test Cases These test cases radiate die body through easily-designed fields. It is mainly used to verify the accuracy of system dose calculation prior to the design of IMRT treatment plan.

Annex B

(Informative) When designing treatment plan according to the test case requirements of Appendix A of this Document, the anatomical structure data in data package of AAPM TG119 technical report [1] is recommended to use. ......

Source: Above contents are excerpted from the full-copy PDF -- translated/reviewed by: www.ChineseStandard.net / Wayne Zheng et al.
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