Instant confocal histology for the evaluation of kidney transplant procurement biopsies.

IF 3.1 3区 医学 Q1 PATHOLOGY
Angela Ernst, Volker Aßfalg, Wolfgang Arns, Luca Cicalese, Avery Koi, Giovanni Gambaro, Albino Eccher, Francesco Pesce, Geoffrey Funk, Matilin Rigsby, Doug Butler, Gavin J Pettigrew, Michael Ströhlein, Alexander Hapfelmeier, Michael Thomas, Dirk Ludger Stippel, Jan U Becker
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引用次数: 0

Abstract

Prognostic outcome models might help to minimise the discard rates of renal transplants from deceased donors. To this end, we published 2-Step Scores for both delayed graft function and transplant loss with optional histology. With conventional paraffin PAS histology taking at least 3 h excluding transport time, we tested whether fast, mobile confocal histology with portable VivaScope® 2500 systems might offer a viable and more rapid alternative. After omitting 17 biopsies with less than 12 glomeruli and 1 artery, we collected 14 0-h and 16 renal transplant indication (Tx) biopsies for a combined cohort. All biopsies were scanned in less than 10 min with a VivaScope® 2500, rendering pseudo-HE images, and then underwent our regular paraffin work-up. Banff Lesion Scores ct and cv were assessed on the granular ordinal scale and binary as (ct ≤ 1 vs. ct ≥ 2 and cv ≤ 2 vs. cv3) together with the number of glomeruli as used in the previously published 2-Step Scores in a blinded fashion by an expert nephropathologist on the paraffin sections (P) and VivaScope® 2500 scans (V). Additionally, we examined the ratio of globally sclerotic glomeruli. Correlation and mixed effects linear regressions, as well as Fleiss' kappa statistics, comparing P and V on the combined cohort were applied, supplemented with Bland-Altman statistics providing limits of agreement. Between P and V, granular Banff ct correlated with a kappa of 0.513 (p = 8.38e-05) and a Kendall's W of 0.706 (p = 0.0694) on the combined cohort; binary Banff ct correlated with a kappa of 0.869 (p = 1.92e-06). We had to exclude two more biopsies in which no artery was found in the scanning plane in V. Granular Banff cv correlated with a kappa of 0.109 (p = 0.345) and a W of 0.677 (p = 0.103) between P and V on the combined cohort and binary Banff cv with a kappa of 0.24 (p = 0.204). The total number of glomeruli correlated between P and V with an R of 0.75 (p = 2.3e-06), the number of globally sclerotic glomeruli with an R of 0.82 (p = 4.1e-08), and the ratio thereof with an R of 0.86 (p = 8.6e-10). Instant, decentralised VivaScope® 2500 histology might deliver Banff ct and the number of glomeruli with sufficient accuracy for the 2-Step Scores to predict the risk of delayed graft function and 1-year death-censored transplant loss in deceased heart-beating donors. In contrast, VivaScope® 2500 assessment of Banff cv might not be accurate enough for use in 2-Step Scores.

即时共聚焦组织学评估肾移植采购活检。
预后结果模型可能有助于将已故供者肾移植的弃肾率降至最低。为此,我们发表了移植延迟功能和移植损失的2步评分,组织学可选。常规石蜡PAS组织学至少需要3小时(不包括运输时间),我们测试了便携式VivaScope®2500系统的快速移动共聚焦组织学是否可能提供一种可行且更快速的替代方法。在省略了17例小于12个肾小球和1条动脉的活检后,我们收集了14例0-h和16例肾移植指征(Tx)活检。所有活检组织在不到10分钟的时间内用VivaScope®2500扫描,绘制假he图像,然后进行常规石蜡检查。Banff病变评分ct和cv采用颗粒顺序量表和二值量表(ct≤1 vs. ct≥2,cv≤2 vs. cv3),以及肾小球的数量,如先前发表的2步评分中使用的,由肾脏病理学专家对石蜡切片(P)和VivaScope®2500扫描(V)进行盲法评估。此外,我们检查了全球硬化性肾小球的比例。应用相关和混合效应线性回归,以及Fleiss kappa统计,比较联合队列的P和V,并补充Bland-Altman统计,提供了一致性的限制。在P和V之间,颗粒Banff ct与联合队列的kappa为0.513 (P = 8.38e-05), Kendall's W为0.706 (P = 0.0694)相关;二值Banff ct相关kappa为0.869 (p = 1.92 -06)。我们必须排除另外两个在V扫描平面上未发现动脉的活检。在联合队列和二元班夫cv中,颗粒班夫cv的kappa为0.109 (p = 0.345), p和V之间的W为0.677 (p = 0.103), kappa为0.24 (p = 0.204)。肾小球总数P与V的相关R为0.75 (P = 2.3e-06),全局硬化肾小球数量的相关R为0.82 (P = 4.1e-08),其比值的相关R为0.86 (P = 8.6e-10)。即时,分散的VivaScope®2500组织学可以提供Banff ct和肾小球数量,具有足够的2步评分准确性,以预测死亡心脏供者移植功能延迟的风险和1年死亡审查移植损失。相比之下,VivaScope®2500对班夫cv的评估可能不够准确,无法用于两步评分。
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
Virchows Archiv
Virchows Archiv 医学-病理学
CiteScore
7.40
自引率
2.90%
发文量
204
审稿时长
4-8 weeks
期刊介绍: Manuscripts of original studies reinforcing the evidence base of modern diagnostic pathology, using immunocytochemical, molecular and ultrastructural techniques, will be welcomed. In addition, papers on critical evaluation of diagnostic criteria but also broadsheets and guidelines with a solid evidence base will be considered. Consideration will also be given to reports of work in other fields relevant to the understanding of human pathology as well as manuscripts on the application of new methods and techniques in pathology. Submission of purely experimental articles is discouraged but manuscripts on experimental work applicable to diagnostic pathology are welcomed. Biomarker studies are welcomed but need to abide by strict rules (e.g. REMARK) of adequate sample size and relevant marker choice. Single marker studies on limited patient series without validated application will as a rule not be considered. Case reports will only be considered when they provide substantial new information with an impact on understanding disease or diagnostic practice.
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