Meier Frederick A, Zarbo Richard J, Varney Ruan C, Bonsal Mona, Schultz Daniel S, Vrbin Colleen M, Grzybicki Dana M, Raab Stephen S
Department of Pathology and Laboratory Medicine, Henry Ford Hospital, Detroit, MI 48202, USA.
Am J Clin Pathol. 2008 Aug;130(2):238-46. doi: 10.1309/9UPELFVQU5WLCUHX.
Amended pathology reports produce rework, confusion, and distrust. To develop a reproducible amendment taxonomy we derived a classification from 141 amended reports, then validated it with 130 new cases before 4 observers independently reviewed 430 cases measuring agreement (k). Next, agreement in classifying 30 other amended reports in 7 institutions was measured. We further tracked amendment rates, defect categories, defect discoverers, and discovery mechanisms. In the 430-case validation set agreement was excellent (k = 0.8780 [range, 0.8416-0.9144]). Among the 7 institutions, agreement was good (k = 0.6235 [range, 0.3105-0.8975]). Amendment rates ranged from 2.6 to 4.8 per 1,000 reports. Misinterpretation fractions varied least (23%-29%). Misidentification fractions ranged more widely (20%-38%). Specimen defects were least frequent (4%-10%) and report defects most frequent (29%-48%). Misidentifications and report defects inversely correlated. Pathologists discovered most misinterpretations, and clinicians found most misidentifications. Conference review revealed 40% to 80% of misinterpretations. This taxonomy produced excellent reproducibility and good agreement across institutions.
修正后的病理报告导致返工、混乱和不信任。为了制定一个可重复的修正分类法,我们从141份修正报告中得出了一个分类,然后在4名观察者独立审查430例病例以测量一致性(k值)之前,用130个新病例对其进行了验证。接下来,测量了7家机构对其他30份修正报告进行分类的一致性。我们还进一步跟踪了修正率、缺陷类别、缺陷发现者和发现机制。在430例病例的验证集中,一致性极佳(k = 0.8780[范围为0.8416 - 0.9144])。在7家机构中,一致性良好(k = 0.6235[范围为0.3105 - 0.8975])。修正率为每1000份报告2.6至4.8例。错误解读比例变化最小(23% - 29%)。错误识别比例范围更广(20% - 38%)。标本缺陷最少见(4% - 10%),报告缺陷最常见(29% - 48%)。错误识别与报告缺陷呈负相关。病理学家发现了大多数错误解读,而临床医生发现了大多数错误识别。会议审查揭示了40%至80%的错误解读。这种分类法具有出色的可重复性,且各机构之间一致性良好。