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不同测试地点熟练度测试表现的差异。

Variation in proficiency testing performance by testing site.

作者信息

Stull T M, Hearn T L, Hancock J S, Handsfield J H, Collins C L

机构信息

Centers for Disease Control and Prevention, Public Health Practice Program Office, Division of Laboratory Systems, Atlanta, Ga 30341, USA.

出版信息

JAMA. 1998 Feb 11;279(6):463-7. doi: 10.1001/jama.279.6.463.

Abstract

CONTEXT

Congress enacted the Clinical Laboratory Improvement Amendments of 1988 (CLIA) to promote uniform quality and standards among all testing sites in the United States. The performance indicators specified in the legislation are proficiency testing (PT) performance and periodic inspections.

OBJECTIVE

To evaluate variation in PT performance by type of testing facility during the first year of compulsory participation under CLIA.

DESIGN

All 1994 PT score data electronically reported to the Health Care Financing Administration as a component of compliance with the CLIA regulations were obtained. Over 1.2 million PT event scores from 17058 unique testing sites were sorted into 2 groups based on the type of testing facility: hospitals and independent laboratories (HI) and all other testing sites (AOT).

MAIN OUTCOME MEASURES

Satisfactory and unsatisfactory performance rates for HI and AOT for each analyte and/or test, according to the criteria specified by the CLIA regulations.

RESULTS

The aggregate rates of satisfactory event performance for all regulated analytes, tests, and specialties were 97% and 91% for the HI and AOTgroups, respectively. The aggregate odds ratio for unsatisfactory PT event performance for the AOT group compared with the HI group was 2.89, with a range of 2.19 to 7.51 for the individual analytes.

CONCLUSION

There was a consistent difference in PT performance during the first full year of compulsory PT under the CLIA regulations based on the type of testing facility performing the analysis. Traditional testing sites achieved higher rates of satisfactory performance than newly regulated, alternative testing sites.

摘要

背景

美国国会颁布了1988年《临床实验室改进修正案》(CLIA),以促进美国所有检测场所的质量和标准统一。该立法规定的绩效指标是能力验证(PT)表现和定期检查。

目的

评估在CLIA强制参与的第一年中,不同类型检测机构的PT表现差异。

设计

获取了1994年所有以电子方式报告给医疗保健财务管理局的PT分数数据,作为符合CLIA法规的一部分。来自17058个不同检测场所的超过120万个PT项目分数,根据检测机构类型分为两组:医院和独立实验室(HI)以及所有其他检测场所(AOT)。

主要观察指标

根据CLIA法规规定的标准,HI和AOT在每种分析物和/或检测中的满意和不满意表现率。

结果

所有受监管分析物、检测和专业的满意项目表现总率,HI组和AOT组分别为97%和91%。AOT组与HI组相比,PT项目表现不满意的总体优势比为2.89,单个分析物的范围为2.19至7.51。

结论

根据进行分析的检测机构类型,在CLIA法规强制进行PT的第一个完整年度中,PT表现存在持续差异。传统检测场所的满意表现率高于新受监管的替代检测场所。

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