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Interobserver variation in the reporting of cervical colposcopic biopsy specimens: comparison of grading systems.

机译:宫颈阴道镜活检标本的报告中观察者间的差异:分级系统的比较。

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摘要

AIMS: To assess interobserver variation in reporting cervical colposcopic biopsy specimens and to determine whether a modified Bethesda grading system results in better interobserver agreement than the traditional cervical intraepithelial neoplasia (CIN) grading system. METHODS: One hundred and twenty five consecutive cervical colposcopic biopsy specimens were assessed independently by six histopathologists. Specimens were classified using the traditional CIN grading system as normal, koilocytosis, CIN I, CIN II, or CIN III. The specimens were also classified using a modified Bethesda grading system as either normal, low grade squamous intraepithelial lesion (LSIL) or high grade squamous intraepithelial lesion (HSIL). Participants were also asked to categorise biopsy specimens by the CIN system with the addition of the recently proposed category "basal abnormalities of uncertain significance (BAUS)". The degree of agreement between participants was assessed by kappa statistics. RESULTS: Using the CIN system, interobserver agreement was generally poor: unweighted and weighted kappa values between individual pairs of observers ranging from 0.05 to 0.34 (average 0.20) and from 0.20 to 0.54 (average 0.36), respectively. With the modified Bethesda system, interobserver agreement was better but still poor: unweighted and weighted kappa values ranging from 0.15 to 0.58 (average 0.30) and from 0.21 to 0.61 (average 0.36), respectively. There was little or no agreement between observers in the diagnosis of BAUS. CONCLUSIONS: Interobserver agreement in the reporting of cervical colposcopic biopsy specimens using the CIN grading system is poor. Agreement, while still poor, is better when a modified Bethesda grading system is used. There is little or no consensus in the diagnosis of BAUS.
机译:目的:评估观察者在报告宫颈阴道镜活检标本中的观察者间差异,并确定改良的贝塞斯达分级系统是否比传统的宫颈上皮内瘤变(CIN)分级系统产生更好的观察者间一致性。方法:由六位组织病理学家独立评估了一百二十五个连续的宫颈阴道镜活检标本。使用传统的CIN分级系统将标本分为正常,小细胞增多症,CIN I,CIN II或CIN III。还使用改良的Bethesda分级系统将标本分为正常,低度鳞状上皮内病变(LSIL)或高等级鳞状上皮内病变(HSIL)。还要求参与者通过CIN系统对活检标本进行分类,并增加了最近提议的类别“不确定意义的基础异常(BAUS)”。参与者之间的一致程度通过kappa统计数据进行评估。结果:使用CIN系统时,观察者之间的共识通常很差:观察者对之间的未加权和加权kappa值分别在0.05至0.34(平均0.20)和0.20至0.54(平均0.36)之间。使用改进的Bethesda系统,观察者之间的一致性更好,但仍然很差:未加权和加权kappa值分别在0.15至0.58(平均0.30)和0.21至0.61(平均0.36)之间。观察者之间在诊断BAUS方面几乎没有共识。结论:在使用CIN分级系统的宫颈阴道镜活检标本的报告中,观察者之间的一致性差。使用改良的Bethesda分级系统时,一致性虽然仍然很差,但更好。 BAUS的诊断很少或没有共识。

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