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Nongynecologic cytology practice patterns: A survey of participants in the college of american pathologists interlaboratory comparison program in nongynecologic cytopathology

机译:非妇科细胞学实践模式:美国妇产科学院非妇科细胞病理学实验室间比较计划参与者的调查

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Context.-Nongynecologic cytology (NGC) practices are expected to expand relative to gynecologic cytology. The College of American Pathologists attempts to track practice patterns in NGC using a self-reported questionnaire. Objective.-To analyze self-reported laboratory staffing and practices from a 2010 survey relating to NGC specimens, stains, preparation, procedures, and ancillary testing. Design.-The "NGC 2010 Demographics and Supplemental Questionnaire: Current Nongynecologic Practices in Cytopathology Laboratories" was mailed to 2059 laboratories. Results.-Survey response rate was 51% (1048 of 2059), predominantly from voluntary, nonprofit hospitals, where NGC samples were reviewed in nontraining settings by pathologists without American Board of Pathology Added Qualification in Cytopathology. Cytotechnologists reviewed NGC cases in 67.4% (675 of 1002) of laboratories. The annual mean and median volumes of NGC cases were 1927 and 858, respectively. Laboratories used more than one method to process NGCs; cell-blocks were most frequently used (930 of 1029; 90.4%) and were created with centrifugation to pellet (538 of 961; 56%). Direct smears were second in preparation frequency; discrete staining was preferred to batch staining. Nongynecologic cytology was used for molecular studies in 34.9% (350 of 1002) of laboratories, most commonly for fluorescent in situ hybridization of urine specimens. Flow cytometric immunophenotyping was performed by 55.9% (554 of 991) and immunohistochemistry by 91.9% (911 of 991) of the responding laboratories. Most laboratories (911 of 993; 91.7%) report specimen completion in 2 or fewer days. Cytohistologic correlation was performed by 71.6% (722 of 1008) of the laboratories both concurrently and retrospectively. Conclusion.-The various parameters examined in the 2010 survey provide a benchmark for future efforts in quality assurance and process improvement in NGC.
机译:背景-非妇科细胞学(NGC)实践相对于妇科细胞学有望扩大。美国病理学家学院试图使用自我报告的问卷追踪NGC中的实践模式。目的-分析2010年与NGC标本,污渍,制备,程序和辅助测试有关的自我报告的实验室人员和实践。设计-“ NGC 2010人口统计学和补充调查表:细胞病理学实验室目前的非妇科学实践”已邮寄给2059个实验室。结果:调查的回应率为51%(2059年为1048),主要来自自愿,非营利性医院,在这些医院中,病理学家在非培训情况下对NGC样本进行了审查,而美国病理学委员会并没有增加细胞病理学的资格。细胞技术专家审查了67.4%(1002的675)实验室中的NGC病例。 NGC病例的年平均量和中位数分别为1927和858。实验室使用了不止一种方法来处理NGC。细胞块是最常用的(1029的930; 90.4%),是通过离心沉淀形成的(约538的961; 56%)。直接涂片的准备频率次之;离散染色优于批量染色。 Nongynecologic细胞学用于34.9%(1002中的350)实验室的分子研究,最常用于尿液样本的荧光原位杂交。在有反应的实验室中,流式细胞仪免疫表型分型为55.9%(991,共554),免疫组织化学为91.9%(991,共911)。大多数实验室(993的911; 91.7%)报告标本在2天或更短时间内完成。 71.6%(1008中的722)实验室同时进行和回顾性进行细胞组织学相关性分析。结论:-2010年调查中检查的各种参数为NGC的质量保证和流程改进的未来工作提供了基准。

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