Histopathology reporting of temporal artery biopsy specimens for giant cell arteritis: results of a modified Delphi study.

IF 2.5 4区 医学 Q2 PATHOLOGY
Dilek Taze, Arundhati Chakrabarty, Ranjana Venkateswaran, Collette Hartley, Charlotte Harden, Ann Wendy Morgan, Sarah Louise Mackie, Kathryn Jane Griffin
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Abstract

The temporal artery biopsy (TAB) is regarded as the gold-standard test in the diagnosis of giant cell arteritis (GCA). There is a lack of agreement among experienced pathologists regarding the diagnostic features and classification of inflammation observed in TAB sections in the diagnosis of GCA.

Aims: The aim of this research study was to establish consensus on the key parameters which should be included in a standardised reporting proforma for TAB specimens. We specifically investigated factors pertaining to clinical information, specimen handling and microscopic pathological features.

Methods: A modified Delphi process, comprising three survey rounds and three virtual consensus group meetings, was undertaken by 13 UK-based pathology or ophthalmology consultants, with a 100% response rate across the three rounds. Initial statements were formulated after a literature review and participants were asked to rate their agreement using a nine-point Likert scale. Consensus was defined a priori as an agreement of ≥70% and individual feedback was provided after each round, together with data on the distribution of group responses.

Results: Overall, 67 statements reached consensus and 17 statements did not. The participants agreed on the core microscopic features to be included in a pathology report and felt that a proforma would facilitate consistent reporting practices.

Conclusions: Our work revealed uncertainty surrounding the correlation between clinical parameters (eg, laboratory markers of inflammation and steroid therapy duration) and microscopic findings, and we propose areas for future research.

巨细胞动脉炎颞动脉活检标本的组织病理学报告:改良德尔菲研究的结果。
颞动脉活检(TAB)被认为是诊断巨细胞动脉炎(GCA)的金标准检测方法。目的:本研究旨在就 TAB 标本标准化报告表中应包含的关键参数达成共识。我们特别调查了与临床信息、标本处理和显微病理特征有关的因素:方法:13 位英国病理学或眼科顾问采用了改良德尔菲流程,包括三轮调查和三次虚拟共识小组会议,三轮调查的回复率均为 100%。最初的陈述是在查阅文献后制定的,并要求参与者使用九点李克特量表对其同意程度进行评分。共识的先验定义是同意率≥70%,每轮讨论后都会提供个人反馈,以及关于小组答复分布的数据:结果:总体而言,67 项陈述达成了共识,17 项陈述未达成共识。与会者就病理报告中应包含的核心显微特征达成了一致,并认为一份表格将有助于报告实践的一致性:我们的工作揭示了临床参数(如炎症的实验室标记物和类固醇治疗持续时间)与显微镜检查结果之间相关性的不确定性,并提出了未来的研究领域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.80
自引率
2.90%
发文量
113
审稿时长
3-8 weeks
期刊介绍: Journal of Clinical Pathology is a leading international journal covering all aspects of pathology. Diagnostic and research areas covered include histopathology, virology, haematology, microbiology, cytopathology, chemical pathology, molecular pathology, forensic pathology, dermatopathology, neuropathology and immunopathology. Each issue contains Reviews, Original articles, Short reports, Correspondence and more.
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