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Unsatisfactory reporting rates: 2006 practices of participants in the college of american pathologists interlaboratory comparison program in gynecologic cytology.

机译:报告率不理想:2006年美国病理学家学院妇科细胞学实验室间比较计划参与者的实践。

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CONTEXT: -Minimum cellular criteria for satisfactory Papanicolaou tests were established with the Bethesda System in 2001, and unsatisfactory rates are used as a quality-reporting measure. OBJECTIVE: -To evaluate practices and unsatisfactory rates from laboratories responding to the 2007 College of American Pathologists supplemental questionnaire survey. DESIGN: -In 2007, a supplemental questionnaire was mailed to 1621 laboratories enrolled in the 2006 College of American Pathologists Interlaboratory Comparison Program in Gynecologic Cytology (PAP Education), requesting data from the 2006 calendar year. Unsatisfactory rates, reasons for unsatisfactory specimens, laboratory size, and specimen preparation type were analyzed. RESULTS: -A total of 42% of the laboratories responded to the survey. Most of those laboratories (637 of 674; 94.5%) used the Bethesda System minimum cellularity criteria. Of those laboratories responding, 79% (527 of 667) used the Bethesda System criteria for atrophic or postirradiation specimens. Unsatisfactory rates have increased since 1996. SurePath preparations were associated with the lowest unsatisfactory rate (50th percentile, 0.30; 95th percentile, 1.3), conventional Papanicolaou tests had the highest 95th percentile rates (50th percentile, 1.0; 95th percentile, 5.90), and ThinPrep specimens had the highest median percentile (50th percentile, 1.1; 95th percentile, 3.4). The most-common reason for unsatisfactory Papanicolaou tests was too few squamous cells. Air-drying artifact was the least-common reason for unsatisfactory reporting for liquid-based preparations. CONCLUSIONS: -Use of the Bethesda System criteria for unsatisfactory specimens is widespread. Unsatisfactory rates have increased since 1996; however, the median rates are 1.1% or less for all preparations. Results from the College of American Pathologists PAP Education supplemental questionnaire continue to provide valuable benchmarking data for cytologic quality-improvement programs in laboratories.
机译:背景:-2001年,贝塞斯达系统建立了令人满意的Papanicolaou测试的最低细胞标准,不良率被用作质量报告指标。目的:-评估实验室对2007年美国病理学家学院补充问卷调查的回答和不满意率。设计:-2007年,一份补充调查表邮寄给了2006年美国病理学家学院妇科细胞学实验室间比较计划(PAP教育)的1621个实验室,要求提供2006日历年的数据。分析了不满意率,不满意标本的原因,实验室规模和标本制备类型。结果:-共有42%的实验室对调查做出了回应。这些实验室中的大多数(674个实验室中的637个; 94.5%)使用Bethesda系统的最低细胞度标准。在做出回应的这些实验室中,有79%(667个中的527个)对萎缩或辐照后的样本使用了贝塞斯达系统标准。自1996年以来,不满意率上升。SurePath制剂的不满意率最低(50%,0.30; 95%,1.3),常规的Papanicolaou测试最高,为95%(50%,1.0; 95%,5.90),以及ThinPrep标本的中位数百分比最高(第50个百分点为1.1;第95个百分点为3.4)。 Papanicolaou检验不满意的最常见原因是鳞状细胞太少。风干制品是液体制剂报告不令人满意的最不常见原因。结论:-对不满意的标本使用贝塞斯达系统标准是普遍的。自1996年以来,不良率上升了;但是,所有制剂的中位发生率均为1.1%或更低。美国病理学家学院PAP教育补充调查表的结果继续为实验室的细胞学质量改进计划提供有价值的基准数据。

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