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首页> 外文期刊>Archives of pathology & laboratory medicine >Proficiency testing performance in US laboratories: results reported to the Centers for Medicare & Medicaid Services, 1994 through 2006.
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Proficiency testing performance in US laboratories: results reported to the Centers for Medicare & Medicaid Services, 1994 through 2006.

机译:美国实验室的能力验证表现:1994年至2006年向医疗保险和医疗补助服务中心报告的结果。

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CONTEXT: Beginning in 1994, clinical laboratories performing nonwaived testing were required, under the regulations implementing the Clinical Laboratory Improvement Amendments of 1988 (CLIA), to enroll and participate in a proficiency testing (PT) program approved by the Centers for Medicare & Medicaid Services. Successful PT performance is a requirement for maintaining CLIA certification to perform testing in certain specialties and subspecialties and for specific analytes. OBJECTIVE: To evaluate the PT performance from 1994 through 2006 of hospital and independent laboratories (HI) compared with all other testing sites (AOT) for selected commonly performed tests and analytes. DESIGN: Proficiency testing data, from 1994 through 2006, were electronically reported to the Centers for Medicare & Medicaid Services by approved PT programs as required by CLIA regulations. Approximately 16 million PT event scores from 36 000 unique testing sites were sorted into 2 groups based on the type of testing facility: HI or AOT. RESULTS: The PT performance scores for 15 of the most commonly performed tests demonstrated a decline in failure rates for both HI and AOT laboratory groups during 1994 through 2006 (analyte/test values reported in this article include alanine aminotransferase, amylase, bilirubin, cholesterol, digoxin, glucose, hemoglobin, leukocyte count, potassium, prothrombin time, theophylline, thyroxine, triglycerides, white blood cell differential, and uric acid). For most analytes, the difference in failure rates between HI and AOT was statistically significant. The AOT group started with higher failure rates, and remained higher for all analytes, during most years when compared with the HI group; although, over time, that difference diminished. The AOT group showed a greater decline in PT failure than the HI group. For all analytes, the AOT group performance improved during this period. CONCLUSIONS: The PT performance improved dramatically for the AOT group from 1994 through 2006 as measured by a decrease in the percentage of laboratories with unsatisfactory performance for 15 selected analytes. The PT performance in the HI group improved modestly for some analytes during this same period, whereas, for other analytes, the group showed no apparent improvement.
机译:背景:自1994年起,根据实施1988年临床实验室改进修正案(CLIA)的规定,要求临床实验室必须进行未经豁免的测试,才能注册并参加由Medicare&Medicaid Services中心批准的能力验证(PT)计划。 。成功的PT性能是保持CLIA认证以对某些专业和亚专业以及特定分析物进行测试的要求。目的:评估1994年至2006年期间医院和独立实验室(HI)与所有其他测试地点(AOT)的常用性能测试和分析物的PT性能。设计:1994年至2006年的能力验证数据通过CLIA法规要求的批准的PT程序以电子方式报告给Medicare和Medicaid Services中心。根据测试设施的类型(HI或AOT),将来自36000个唯一测试站点的大约1600万个PT事件得分分为2组。结果:1994年至2006年期间,HI和AOT实验室组中15个最常用的测试的PT性能得分均出现下降(本文报道的分析物/测试值包括丙氨酸转氨酶,淀粉酶,胆红素,胆固醇,地高辛,葡萄糖,血红蛋白,白细胞计数,钾,凝血酶原时间,茶碱,甲状腺素,甘油三酸酯,白细胞分化和尿酸)。对于大多数分析物,HI和AOT的故障率差异有统计学意义。与HI组相比,在大多数年份中,AOT组的故障率较高,而所有分析物的故障率仍较高。尽管随着时间的流逝,这种差异逐渐减少。与HI组相比,AOT组的PT衰竭下降更大。对于所有分析物,在此期间AOT组的性能均得到改善。结论:从1994年到2006年,AOT组的PT性能显着提高,这是通过对15种选定分析物的性能不满意的实验室所占百分比的下降来衡量的。 HI组中的PT性能在同一时期内对某些分析物有所改善,而对于其他分析物,该组没有表现出明显的改善。

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