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Laboratory sanctions for proficiency testing sample referral and result communication: a review of actions from 1993-2006.

机译:实验室对能力验证样品的推荐和结果通报的制裁:1993-2006年行动回顾。

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摘要

CONTEXT: The Clinical Laboratory Improvement Amendments of 1988 (CLIA) regulations for proficiency testing (PT) include prohibitions against intentional PT sample referral or result communication, and specify sanctions against laboratories that violate these regulations. There has been little published analysis of sanctions against clinical laboratories because of PT violations. OBJECTIVE: To examine the application of principal sanctions as reported by the Centers for Medicare and Medicaid Services annually in the Laboratory Registry and to examine relevant aspects of judicial hearings and appeals in these cases. DESIGN: The Laboratory Registry was examined for all available years (1993-2006) to determine the incidence of application of principal sanctions for PT violations. In addition, the decisions from the US Department of Health and Human Services hearings and appeals were reviewed to better understand the judicial disposition of these cases. RESULTS: During the 14-year period examined, 78 laboratories received a principal sanction for a PT violation involving sample referral or result communication. During the same period, the number of laboratories in nonexempt states that would be expected to have participated in PT averaged 45 983. The interpretive meaning of the key terms intentional and referral, and the implications for sanctioned laboratories and their owners and operators are discussed. CONCLUSIONS: Applications of a principal sanction for a PT violation were rare during the period of this study. However, the consequences of the imposition of such a sanction are severe. Suggestions are offered on policies and practices to minimize the risk of a PT sample referral or result communication.
机译:背景:《 1988年临床实验室改进修正案》(CLIA)关于能力验证(PT)的法规包括禁止故意转让PT样本或结果通报的规定,并规定了对违反这些法规的实验室的制裁。由于违反PT,对临床实验室制裁的分析很少发表。目的:审查实验室登记处每年由医疗保险和医疗补助服务中心报告的主要制裁措施的适用性,并审查这些案件中司法听证和上诉的有关方面。设计:对实验室注册处的所有可用年份(1993年至2006年)进行了检查,以确定对违反PT实施主要制裁的发生率。此外,审查了美国卫生与公共服务部听证会和上诉案的决定,以更好地了解这些案件的司法处理。结果:在审查的14年期间,有78个实验室因涉及样本转诊或结果通报的PT违规而受到主要制裁。在同一时期,预计将参加PT的非豁免州的实验室数量平均为45983。讨论了有意和推荐的关键术语的解释性含义,以及对受制裁的实验室及其所有者和经营者的影响。结论:在本研究期间,很少有人因违反PT而受到主要制裁。但是,实行这种制裁的后果是严重的。提供有关政策和实践的建议,以最大程度地降低PT样本转诊或结果沟通的风险。

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