浸润性乳腺癌组织病理学报告的审计,参考充分性和修订

Victoria Liza, G. Ravikumar, R. Tirumalae
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摘要

背景:对乳腺癌组织病理学报告(HPR)进行定期审计,监测其合规性,提高报告标准。本研究的目的是根据CAP方案审核乳腺癌HPR的完整性,并分析肿瘤摘要的修订。方法:回顾性分析2016-2020年浸润性乳腺癌切除术的HPR。使用CAP协议评估核心(CE)和非核心元素(NCE)。分析的结果测量:(i) CE的总体报告完整性(ii)所有报告的要素特定完整性。对修正案进行了审查。结果:乳腺癌报告包括246例手术。最常见的组织学变异为导管型(NOS),总体完全性为87%。83.1%的人有生物标志物状态。报告格式为类概要的结构化格式。CAP协议在2016-2019年期间经历了五次修订,CE和NCE之间的参数发生了变化。充分代表CE:手术、肿瘤大小和类型、诺丁汉评分、分级、分期、DCIS、边缘状态、淋巴结和淋巴血管侵袭。不常报道的CE:侧边、受累范围、最大转移灶的大小和结外延伸。经常报道的NCE: LVI, DCIS的结构/分级,邻近乳腺的发现。所有报告的生物标志物报告和治疗效果均完整。修正报告为4.8%。大多数是转录错误。结论:普通CE的代表性较好。缺陷的原因是CAP协议的频繁变化和类天气的结构化格式相对于天气格式的灵活性。该研究强调了定期审计乳腺癌摘要的必要性,以监测CE报告中的差距。带有附加自由文本字段的概要报告将提高遵从性并克服缺陷。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An Audit of Histopathology Reports of Invasive Breast Carcinomas with Reference to Adequacy and Amendments
Background: Periodic auditing of histopathology report (HPR) of breast cancer, monitors compliance and increases the standards of reporting. This study was done to audit the completeness of breast cancer HPR in accordance with the CAP protocol and to analyse the amendments in tumour summaries. Methods: Retrospective review of HPR of invasive breast carcinoma resections from 2016-2020. Core (CE) and non-core elements (NCE) evaluated using CAP protocols. Outcome measures analyzed: (i) overall report completeness for CE (ii) element specific completeness for all reports. Amendments were reviewed. Results: Breast cancer reports included 246 resections. Most common histological variant was ductal type, NOS. Overall completeness was seen in 87%. Biomarker status was available in 83.1%. Reporting format was synoptic-like structured format. CAP protocol underwent five revisions between 2016-2019 with shifting of parameters between CE and NCE. Adequately represented CE: procedure, tumour size & type, Nottingham score, grade, stage, DCIS, margin status, lymph nodes and lymphovascular invasion. Less commonly reported CE: laterality, extent of involvement, size of largest metastatic deposit and extranodal extension. Frequently reported NCE: LVI, architecture/grade of DCIS, findings in adjacent breast. Biomarker reporting and treatment effect was complete in all reports. Amended reports were 4.8%. Majority were transcriptional errors. Conclusion: Common CE were satisfactorily represented in majority. Reasons for deficiencies were frequent change in CAP protocols and flexibility in synoptic-like structured format over synoptic format. The study underscores the need for periodic auditing of breast cancer summaries to monitor gaps in CE reporting. Synoptic reporting with additional free text field will improve compliance and overcome deficiencies.
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