病理学助理对常规妊娠中期和晚期单胎胎盘进行大体检查所需的时间。

IF 1.3 4区 医学 Q3 PATHOLOGY Pediatric and Developmental Pathology Pub Date : 2023-09-01 Epub Date: 2023-09-06 DOI:10.1177/10935266231196015
Christopher Horn, Nicole Engel, Dominique Drouin, John Haley, Cameron Holder, Lina Hung, Lorraine Royall, Patricia McInnis, Lawrence de Koning, Elaine S Chan
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引用次数: 0

摘要

在加拿大和美国,解剖病理学工作量的测量主要基于标本的复杂性和临床意义,其中大体检查是一个相当大的贡献。虽然病理学家助理(PAs)在大体检查中发挥着越来越大的作用,但对于PAs完成总体检查任务所需的时间知之甚少。这些信息对于病理实验室有效的人员配置和工作量管理至关重要。我们研究的目的是确定在一家具有重要围产期病理服务的大型三级医院中,PAs检查妊娠中期和晚期单胎胎盘所需的时间。材料和方法:在我们的研究中,7名经过认证的PAs使用标准胎盘检查方案、电子实验室信息系统和语音识别听写软件,每人检查至少10个妊娠中期和晚期单胎胎盘。胎盘标本需要摄影,取样辅助研究,或立即病理咨询排除。我们使用混合线性回归模型计算了每个PA的平均票房时间和标准差,总平均票房时间和95%置信区间。我们在多变量分析中分析了PA工作经验,获得的学位和总体平均准备的区块数量的影响。结果:每个PA的平均发病时间为11.0(标准差[sd] = 2.0)至17.8 (sd = 4.5) min。总体平均票房时间为14.5分钟,95%置信区间为11.7至17.3分钟。在多变量分析中,制备的块数量的增加与较长的总体平均总收入时间显着相关。如果连续准备4个块,该模型预测的总体平均时间略低,为13.3分钟,95%置信区间为10.9至15.7分钟。讨论:据我们所知,我们的研究首次客观地报告了PAs对常规妊娠中期和晚期单胎胎盘进行粗检查所需的时间。我们的研究方法是可复制的,可以应用于其他标本类型和实验室设置。以前,标本的估计总时间主要基于回顾性调查,容易出现回忆错误和主观性。然而,我们的研究表明,客观的数据收集是可以实现的。此外,从本研究中收集的数据为以前和现在的中期和晚期单胎胎盘病理工作量模型的准确性提供了有价值的见解。
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Time Required for Gross Examination of Routine Second and Third Trimester Singleton Placentas by Pathologists' Assistants.

Introduction: In both Canada and the United States, workload measurement for anatomic pathology is mainly based on complexity and clinical significance of specimens, with gross examination being a considerable contributor. While Pathologists' Assistants (PAs) play an increasing role in gross examination, there is little known regarding the time required for PAs to complete grossing tasks. This information is essential for effective staffing and workload management in pathology laboratories. The objective of our study was to determine the time required for PAs to gross second and third trimester singleton placentas in a large tertiary hospital with a significant perinatal pathology service.

Materials and methods: For our study, 7 certified PAs each grossed a minimum of 10 second and third trimester singleton placentas using a standard placental grossing protocol, an electronic laboratory information system, and voice recognition dictation software. Placental specimens requiring photography, sampling for ancillary studies, or immediate pathologist's consultation were excluded. We calculated average and standard deviation of grossing times for each PA, overall average grossing time, and 95% confidence interval using a mixed linear regression model. We analyzed the impact of PA job experience, degree obtained, and number of blocks prepared on overall average in a multivariate analysis.

Results: The mean grossing times for each PA ranged from 11.0 (standard deviation [sd] = 2.0) to 17.8 (sd = 4.5) minutes. The overall average grossing time was 14.5 minutes, with a 95% confidence interval of 11.7 to 17.3 minutes. In multivariate analysis, an increase in the number of blocks prepared was significantly associated with longer overall average grossing time. If 4 blocks were prepared consistently, the model predicted a slightly lower overall average of 13.3 minutes, with a 95% confidence interval of 10.9 to 15.7 minutes.

Discussion: To our knowledge, our study is the first to objectively report time required for PAs to perform gross examinations of routine second and third trimester singleton placentas. The methodology of our study is replicable and can be applied to other specimen types and laboratory settings. Previously, estimated grossing times for specimens were primarily based on retrospective surveys, which were susceptible to recall errors and subjectivity. However, our study demonstrates objective data collection is achievable. Furthermore, the data collected from this study offer valuable insights into the accuracy of previous and current pathology workload models for second and third trimester singleton placentas.

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来源期刊
CiteScore
3.70
自引率
5.30%
发文量
59
审稿时长
6-12 weeks
期刊介绍: The Journal covers the spectrum of disorders of early development (including embryology, placentology, and teratology), gestational and perinatal diseases, and all diseases of childhood. Studies may be in any field of experimental, anatomic, or clinical pathology, including molecular pathology. Case reports are published only if they provide new insights into disease mechanisms or new information.
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