Paras P
Ric Clin Lab. 1981 Oct-Dec;11(4):357-77. doi: 10.1007/BF02909035.
In conclusion, the minimum requirements (after instrument acceptance or initial testing) for a satisfactory quality control program for each data acquisition system in nuclear medicine are: a. quality control tests should be performed routinely and should take no more than 15 min; b. protocols for each counting instrument and imaging system should be defined for the routine tests described in this paper. Test procedures may be adopted from the literature; c. the resulting data (numerical data and images) should be carefully scrutinized, compared with information (reference data) obtained initially under similar conditions, and used to decide whether to proceed with clinical studies (see scheme 1); d. all test images should be properly labeled and retained for immediate reference, preferably in the form of a logbook; e. a review of these data should be made on a weekly basis to detect long-term deterioration. A review image recording and its quality control is included in the Appendix.
总之,核医学中每个数据采集系统的质量控制程序要达到令人满意的最低要求(仪器验收或初始测试后)如下:a. 质量控制测试应定期进行,且耗时不超过15分钟;b. 应为本篇论文所述的常规测试定义每个计数仪器和成像系统的方案。测试程序可借鉴文献;c. 所得数据(数值数据和图像)应仔细审查,与在类似条件下最初获得的信息(参考数据)进行比较,并用于决定是否继续进行临床研究(见方案1);d. 所有测试图像都应妥善标注并留存以供即时参考,最好采用日志形式;e. 应每周对这些数据进行审查,以检测长期劣化情况。附录中包含审查图像记录及其质量控制内容。