Hookey Lawrence C, Hurlbut David J, Day Andrew G, Manley Paul N, Depew William T
Queen's University, Kingston, Canada.
Can J Gastroenterol. 2007 Mar;21(3):164-8. doi: 10.1155/2007/851830.
Surveillance for mucosal dysplasia in patients with chronic ulcerative colitis requires numerous biopsies (often over 40). The aim of the present study was to determine if two biopsies could be obtained with jumbo forceps before removing them from the instrument (double biopsy technique), as opposed to one biopsy per pass, without sacrificing the histological quality of the biopsy material.
Twelve patients with chronic ulcerative colitis underwent colonoscopy, and four-quadrant biopsies were obtained at 10 cm intervals. For biopsies at each interval, two quadrants were obtained using the double biopsy technique and the other two quadrants were obtained individually. Two pathologists blinded to the biopsy technique examined each biopsy for technical and diagnostic qualities. The primary outcome was the histological adequacy in the evaluation of dysplasia.
A total of 468 biopsies were obtained. A higher proportion of double-biopsy specimens were inadequate for dysplasia assessment compared with single-biopsy specimens (OR=2.78, 95% CI 1.37 to 5.59; P=0.005). In the double biopsy technique group, 14 samples were deemed inadequate due to actual tissue specimen loss, compared with eight samples in the single biopsy technique. However, when analysis was repeated using only the retrieved specimens, the double biopsy technique continued to be at higher risk of obtaining inadequate specimens (OR=14.5, 95% CI 2.1 to 98.7; P=0.006).
The results of the present study suggest that the double biopsy technique is vulnerable to specimen loss and reduced histological quality, and the adoption of this technique as an equivalent method for tissue sampling may be premature.
对慢性溃疡性结肠炎患者进行黏膜发育异常监测需要多次活检(通常超过40次)。本研究的目的是确定在使用大活检钳从器械上取下活检组织之前,是否可以获取两份活检样本(双活检技术),而不是每次操作获取一份活检样本,同时不影响活检材料的组织学质量。
12例慢性溃疡性结肠炎患者接受结肠镜检查,每隔10 cm进行四象限活检。对于每个间隔的活检,两个象限采用双活检技术获取样本,另外两个象限单独获取样本。两名对活检技术不知情的病理学家检查每份活检样本的技术和诊断质量。主要结局是发育异常评估中的组织学充分性。
共获取468份活检样本。与单活检样本相比,双活检样本中发育异常评估不充分的比例更高(比值比=2.78,95%置信区间1.37至5.59;P=0.005)。在双活检技术组中,有14个样本因实际组织样本丢失而被认为不充分,而单活检技术组为8个样本。然而,仅使用获取的样本重复分析时,双活检技术获取不充分样本的风险仍然更高(比值比=14.5,95%置信区间2.1至98.7;P=0.006)。
本研究结果表明,双活检技术容易出现样本丢失和组织学质量下降的情况,将该技术作为等效的组织采样方法可能为时过早。