首页> 外文期刊>JAMA: the Journal of the American Medical Association >Are physicians' office laboratory results of comparable quality to those produced in other laboratory settings? (see comments)
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Are physicians' office laboratory results of comparable quality to those produced in other laboratory settings? (see comments)

机译:医师办公室的实验室结果与其他实验室设置的结果是否具有可比的质量? (看评论)

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CONTEXT: In 1995, California adopted a bill that brought laboratory laws in line with the 1988 Clinical Laboratory Improvement Amendments' standards for clinical laboratories and mandated a study comparing results in physicians' office laboratories (POLs) with other settings. OBJECTIVE: To determine whether persons conducting tests in POLs produce accurate and reliable test results comparable to those produced by non-POLs. DESIGN: Survey of clinical laboratories using proficiency testing data. SETTING: All California clinical laboratories participating in the American Association of Bioanalysts proficiency testing program in 1996 (n=1110). MAIN OUTCOME MEASURES: "Unsatisfactory" (single testing event failure) and "unsuccessful" (repeated testing event failure) on proficiency testing samples. RESULTS: The unsatisfactory failure rate for POLs was nearly 3 times (21.5% vs 8.1%) the rate for the non-POLs and about 1.5 times (21.5% vs 14.0%) for POLs that used laboratory professionals as testing or supervisory personnel (P<.001). The POL unsuccessful rate was more than 4 times (4.4% vs 0.9%) the rate for non-POLs and more than twice (4.4% vs 1.8%) the rate for the POLs using laboratory professionals (P<.001). CONCLUSIONS: Significant differences exist among POLs, POLs using licensed clinical laboratory scientists (medical technologists), and non-POLs. Testing personnel in many POLs might lack the necessary education, training, and oversight common to larger facilities. We must better understand the contributing factors that result in the poorer results of POLs relative to non-POLs. In the meantime, patients should be aware that preliminary findings suggest that differences in quality of laboratory tests based on testing site may exist. Laboratory directors at all testing sites must ensure that they understand laboratory practice sufficiently to minimize errors and maximize accuracy and reliability. Directors must understand their obligation when they elect to oversee those assigned testing responsibility. Legislators may wish to reconsider the wisdom of further easing restrictions on those to whom we entrust our laboratory specimens.
机译:背景:1995年,加利福尼亚州通过了一项法案,使实验室法律与1988年临床实验室改进修正案针对临床实验室的标准保持一致,并授权进行一项将医师办公室实验室(POLs)与其他环境的结果进行比较的研究。目的:确定在POL中进行测试的人员所产生的准确和可靠的测试结果是否可与非POL所产生的结果相媲美。设计:使用能力验证数据对临床实验室进行调查。地点:1996年,美国加利福尼亚州所有临床实验室都参加了美国生物分析家能力验证计划(n = 1110)。主要观察指标:能力验证样品的“不满意”(单次测试事件失败)和“不成功”(重复测试事件失败)。结果:以实验室专业人员作为测试或监督人员的POL的失败率不令人满意,约为非POL的3倍(21.5%比8.1%),约为1.5倍(21.5%VS 14.0%)。 <.001)。使用实验室专业人员,POL的不成功率是非POL率的4倍以上(4.4%vs. 0.9%),是非POL率的两倍以上(4.4%vs 1.8%)(P <.001)。结论:POL,使用许可的临床实验室科学家(医学技术人员)的POL和非POL之间存在显着差异。许多POL中的测试人员可能缺少大型机构所必需的必要的教育,培训和监督。我们必须更好地理解导致POL相对于非POL较差的结果的因素。同时,患者应意识到初步发现表明,基于测试地点的实验室测试质量可能存在差异。所有测试地点的实验室主管必须确保他们充分了解实验室实践,以最大程度地减少错误并最大化准确性和可靠性。董事选择监督分配的测试职责时,必须理解其义务。立法者不妨重新考虑进一步放宽对我们委托实验室标本的人的限制的智慧。

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