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Ultrasound transducer function: annual testing is not sufficient.

机译:超声换能器功能:仅年度测试是不够的。

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AIMS: The objective was to follow-up the study 'High incidence of defective ultrasound transducers in use in routine clinical practice' and evaluate if annual testing is good enough to reduce the incidence of defective ultrasound transducers in routine clinical practice to an acceptable level. METHODS AND RESULTS: A total of 299 transducers were tested in 13 clinics at five hospitals in the Stockholm area. Approximately 7000-15,000 ultrasound examinations are carried out at these clinics every year. The transducers tested in the study had been tested and classified as fully operational 1 year before and since then been in normal use in the routine clinical practice. The transducers were tested with the Sonora FirstCall Test System. There were 81 (27.1%) defective transducers found; giving a 95% confidence interval ranging from 22.1 to 32.1%. The most common transducer errors were 'delamination' of the ultrasound lens and 'break in the cable' which together constituted 82.7% of all transducer errors found. The highest error rate was found at the radiological clinics with a mean error rate of 36.0%. There was a significant difference in error rate between two observed ways the clinics handled the transducers. There was no significant difference in the error rates of the transducer brands or the transducers models. CONCLUSION: Annual testing is not sufficient to reduce the incidence of defective ultrasound transducers in routine clinical practice to an acceptable level and it is strongly advisable to create a user routine that minimizes the handling of the transducers.
机译:目的:目的是跟踪研究“常规临床实践中使用的故障超声换能器的高发生率”,并评估年度测试是否足够好,以将常规临床实践中有缺陷的超声换能器的发生率降至可接受的水平。方法和结果:在斯德哥尔摩地区五家医院的13家诊所中共测试了299个换能器。每年在这些诊所进行大约7000-15,000次超声检查。在这项研究中测试的换能器在常规临床实践中正常使用之前和之后的一年内已经过测试并分类为完全可操作。传感器已通过Sonora FirstCall测试系统进行了测试。发现了81个(27.1%)换能器有缺陷;给出95%的置信区间,范围从22.1到32.1%。换能器最常见的错误是超声透镜的“分层”和“电缆断裂”,它们共占发现的所有换能器错误的82.7%。放射科的错误率最高,平均错误率为36.0%。在诊所观察到的两种换能器方式之间,错误率存在显着差异。换能器品牌或换能器型号的错误率没有显着差异。结论:年度测试不足以将常规临床实践中有缺陷的超声换能器的发生率降低到可接受的水平,强烈建议创建一个使换能器的处理最小化的用户程序。

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