John O O Ayorinde, Xavier Loizeau, Victoria Bardsley, Spencer Angus Thomas, Marina Romanchikova, Alex Samoshkin, Gavin J Pettigrew
{"title":"测量很重要:肾移植前活检评估的计量学方法,解决器官选择的不确定性。","authors":"John O O Ayorinde, Xavier Loizeau, Victoria Bardsley, Spencer Angus Thomas, Marina Romanchikova, Alex Samoshkin, Gavin J Pettigrew","doi":"10.1097/TXD.0000000000001708","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Preimplantation biopsy combines measurements of injury into a composite index to inform organ acceptance. The uncertainty in these measurements remains poorly characterized, raising concerns variability may contribute to inappropriate clinical decisions.</p><p><strong>Methods: </strong>We adopted a metrological approach to evaluate biopsy score reliability. Variability was assessed by performing repeat biopsies (n = 293) on discarded allografts (n = 16) using 3 methods (core, punch, and wedge). Uncertainty was quantified using a bootstrapping analysis. Observer effects were controlled by semi-blinded scoring, and the findings were validated by comparison with standard glass evaluation.</p><p><strong>Results: </strong>The surgical method strongly determined the size (core biopsy area 9.04 mm<sup>2</sup>, wedge 37.9 mm<sup>2</sup>) and, therefore, yield (glomerular yield <i>r</i> = 0.94, arterial <i>r</i> = 0.62) of each biopsy. Core biopsies yielded inadequate slides most frequently. Repeat biopsy of the same kidney led to marked variation in biopsy scores. In 10 of 16 cases, scores were contradictory, crossing at least 1 decision boundary (ie, to transplant or to discard). Bootstrapping demonstrated significant uncertainty associated with single-slide assessment; however, scores were similar for paired kidneys from the same donor.</p><p><strong>Conclusions: </strong>Our investigation highlights the risks of relying on single-slide assessment to quantify organ injury. Biopsy evaluation is subject to uncertainty, meaning each slide is better conceptualized as providing an estimate of the kidney's condition rather than a definitive result. Pooling multiple assessments could improve the reliability of biopsy analysis, enhancing confidence. Where histological quantification is necessary, clinicians should seek to develop new protocols using more tissue and consider automated methods to assist pathologists in delivering analysis within clinical time frames.</p>","PeriodicalId":23225,"journal":{"name":"Transplantation Direct","volume":"10 11","pages":"e1708"},"PeriodicalIF":1.9000,"publicationDate":"2024-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11469905/pdf/","citationCount":"0","resultStr":"{\"title\":\"Measurement Matters: A Metrological Approach to Renal Preimplantation Biopsy Evaluation to Address Uncertainty in Organ Selection.\",\"authors\":\"John O O Ayorinde, Xavier Loizeau, Victoria Bardsley, Spencer Angus Thomas, Marina Romanchikova, Alex Samoshkin, Gavin J Pettigrew\",\"doi\":\"10.1097/TXD.0000000000001708\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Preimplantation biopsy combines measurements of injury into a composite index to inform organ acceptance. The uncertainty in these measurements remains poorly characterized, raising concerns variability may contribute to inappropriate clinical decisions.</p><p><strong>Methods: </strong>We adopted a metrological approach to evaluate biopsy score reliability. Variability was assessed by performing repeat biopsies (n = 293) on discarded allografts (n = 16) using 3 methods (core, punch, and wedge). Uncertainty was quantified using a bootstrapping analysis. Observer effects were controlled by semi-blinded scoring, and the findings were validated by comparison with standard glass evaluation.</p><p><strong>Results: </strong>The surgical method strongly determined the size (core biopsy area 9.04 mm<sup>2</sup>, wedge 37.9 mm<sup>2</sup>) and, therefore, yield (glomerular yield <i>r</i> = 0.94, arterial <i>r</i> = 0.62) of each biopsy. Core biopsies yielded inadequate slides most frequently. Repeat biopsy of the same kidney led to marked variation in biopsy scores. In 10 of 16 cases, scores were contradictory, crossing at least 1 decision boundary (ie, to transplant or to discard). Bootstrapping demonstrated significant uncertainty associated with single-slide assessment; however, scores were similar for paired kidneys from the same donor.</p><p><strong>Conclusions: </strong>Our investigation highlights the risks of relying on single-slide assessment to quantify organ injury. Biopsy evaluation is subject to uncertainty, meaning each slide is better conceptualized as providing an estimate of the kidney's condition rather than a definitive result. Pooling multiple assessments could improve the reliability of biopsy analysis, enhancing confidence. Where histological quantification is necessary, clinicians should seek to develop new protocols using more tissue and consider automated methods to assist pathologists in delivering analysis within clinical time frames.</p>\",\"PeriodicalId\":23225,\"journal\":{\"name\":\"Transplantation Direct\",\"volume\":\"10 11\",\"pages\":\"e1708\"},\"PeriodicalIF\":1.9000,\"publicationDate\":\"2024-10-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11469905/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Transplantation Direct\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1097/TXD.0000000000001708\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/11/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q3\",\"JCRName\":\"TRANSPLANTATION\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Transplantation Direct","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1097/TXD.0000000000001708","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/11/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"TRANSPLANTATION","Score":null,"Total":0}
引用次数: 0
摘要
背景:胚胎植入前活检将损伤测量结果合并成一个综合指数,为器官接受提供依据。这些测量结果的不确定性仍未得到充分描述,因此人们担心其可变性可能会导致不恰当的临床决策:我们采用计量学方法评估活检评分的可靠性。通过对废弃的同种异体移植物(n = 16)进行重复活检(n = 293),使用3种方法(核心活检、打孔活检和楔形活检)对变异性进行评估。不确定性通过引导分析进行量化。通过半盲评分控制观察者效应,并通过与标准玻璃评估进行比较验证结果:结果:手术方法极大地决定了每例活检的大小(核心活检面积为 9.04 平方毫米,楔形活检面积为 37.9 平方毫米),因此也决定了活检率(肾小球活检率 r = 0.94,动脉活检率 r = 0.62)。核心活检最常见的情况是切片结果不足。同一肾脏的重复活检导致活检评分差异显著。在 16 个病例中,有 10 个病例的评分是相互矛盾的,至少跨越了一个决策边界(即移植还是放弃)。Bootstrapping表明,单个切片评估具有显著的不确定性;但是,来自同一供体的配对肾脏的评分相似:我们的调查强调了依靠单滑动评估来量化器官损伤的风险。活检评估存在不确定性,这意味着每张切片最好被视为提供了肾脏状况的估计值,而不是确定的结果。汇集多项评估结果可提高活检分析的可靠性,增强信心。在有必要进行组织学量化的情况下,临床医生应设法使用更多的组织制定新的方案,并考虑采用自动化方法协助病理学家在临床时限内完成分析。
Measurement Matters: A Metrological Approach to Renal Preimplantation Biopsy Evaluation to Address Uncertainty in Organ Selection.
Background: Preimplantation biopsy combines measurements of injury into a composite index to inform organ acceptance. The uncertainty in these measurements remains poorly characterized, raising concerns variability may contribute to inappropriate clinical decisions.
Methods: We adopted a metrological approach to evaluate biopsy score reliability. Variability was assessed by performing repeat biopsies (n = 293) on discarded allografts (n = 16) using 3 methods (core, punch, and wedge). Uncertainty was quantified using a bootstrapping analysis. Observer effects were controlled by semi-blinded scoring, and the findings were validated by comparison with standard glass evaluation.
Results: The surgical method strongly determined the size (core biopsy area 9.04 mm2, wedge 37.9 mm2) and, therefore, yield (glomerular yield r = 0.94, arterial r = 0.62) of each biopsy. Core biopsies yielded inadequate slides most frequently. Repeat biopsy of the same kidney led to marked variation in biopsy scores. In 10 of 16 cases, scores were contradictory, crossing at least 1 decision boundary (ie, to transplant or to discard). Bootstrapping demonstrated significant uncertainty associated with single-slide assessment; however, scores were similar for paired kidneys from the same donor.
Conclusions: Our investigation highlights the risks of relying on single-slide assessment to quantify organ injury. Biopsy evaluation is subject to uncertainty, meaning each slide is better conceptualized as providing an estimate of the kidney's condition rather than a definitive result. Pooling multiple assessments could improve the reliability of biopsy analysis, enhancing confidence. Where histological quantification is necessary, clinicians should seek to develop new protocols using more tissue and consider automated methods to assist pathologists in delivering analysis within clinical time frames.