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Impact of specimen adequacy on the assessment of renal allograft biopsyspecimens

机译:标本充足性对同种异体肾活检评估的影响标本

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The Banff classification was introduced to achieve uniformity in the assessment of renal allograft biopsies. The primary aim of this study was to evaluate the impact of specimen adequacy on the Banff classification. All renal allograft biopsies obtained between July 2010 and June 2012 for suspicion of acute rejection were included. Pre-biopsy clinical data on suspected diagnosis and time from renal transplantation were provided to a nephropathologist who was blinded to the original pathological report. Second pathological readings were compared with the original to assess agreement stratified by specimen adequacy. Cohen's kappa test and Fisher's exact test were used for statistical analyses. Forty-nine specimens were reviewed. Among these specimens, 81.6% were classified as adequate, 6.12% as minimal, and 12.24% as unsatisfactory. The agreement analysis among the first and second readings revealed a kappa value of 0.97. Full agreement between readings was found in 75% of the adequate specimens, 66.7 and 50% for minimal and unsatisfactory specimens, respectively. There was no agreement between readings in 5% of the adequate specimens and 16.7% of the unsatisfactory specimens. For the entire sample full agreement was found in 71.4%, partial agreement in 20.4% and no agreement in 8.2% of the specimens. Statistical analysis using Fisher's exact test yielded a P value above 0.25 showing that -probably due to small sample size - the results were not statistically significant.Specimen adequacy may be a determinant of a diagnostic agreement in renal allograftspecimen assessment. While additional studies including larger case numbers arerequired to further delineate the impact of specimen adequacy on the reliability ofhistopathological assessments, specimen quality must be considered during clinicaldecision making while dealing with biopsy reports based on minimal or unsatisfactoryspecimens.
机译:引入班夫分类法是为了在评估同种异体肾活检中获得统一性。这项研究的主要目的是评估标本充足性对班夫分类的影响。包括所有在2010年7月至2012年6月之间因怀疑急性排斥反应而获得的肾脏同种异体移植活检。肾脏病理学家提供了有关肾脏病理学检查的可疑诊断和肾移植时间的活检前临床数据,而后者对原始病理报告不知情。将第二次病理学读数与原始病理学读数进行比较,以评估按样本充分性分层的一致性。统计分析使用了科恩的卡帕检验和费舍尔精确检验。审查了四十九个标本。在这些样本中,有81.6%被归类为合格,有6.12%被归类为最低,有12.24%被归类为不满意。一读和二读之间的一致性分析显示,kappa值为0.97。在75%的适当样本中,读数之间完全吻合,最小和不令人满意的样本分别为66.7和50%。在5%的适当样本和16.7%的不满意样本中,读数之间没有一致性。对于整个样品,发现全部一致性为71.4%,部分一致性为20.4%,而没有一致性为8.2%。使用Fisher精确检验进行的统计分析得出的P值大于0.25,表明-可能是由于样本量较小-结果没有统计学意义。标本的适当性可能是同种异体肾移植诊断协议的决定因素标本评估。虽然包括较大病例数在内的其他研究需要进一步描述样品充足性对样品可靠性的影响组织病理学评估,临床期间必须考虑标本质量在根据最小或不满意的结果处理活检报告时做出决策标本。

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