Flemming J A, Hurlbut D J, Mussari B, Hookey L C
Gastrointestinal Diseases Research Unit, Queen's University, Kingston, Canada.
Can J Gastroenterol. 2009 Jun;23(6):425-30. doi: 10.1155/2009/370651.
BACKGROUND/OBJECTIVE: Liver biopsy has been the gold standard for grading and staging chronic hepatitis C virus (HCV)- mediated liver injury. Traditionally, this has been performed by trained practitioners using a nonimage-guided percutaneous technique at the bedside. Recent literature suggests an expanding role for radiologists in obtaining biopsies using an ultrasound (US)-guided technique. The present study was undertaken study to determine if the two techniques produced liver biopsy specimens of similar quality and hypothesized that at our institution, non-US-guided percutaneous liver biopsies for HCV would be of higher quality than US-guided specimens.
Liver biopsies from 100 patients with chronic HCV infection (50 consecutive US-guided and 50 consecutive non-US-guided), were retrospectively identified using a hospital histopathology database. All original biopsy slides were coded and prospectively reanalyzed by a single hepatopathologist who was blinded to the technique used in obtaining the biopsy. Additionally, all liver biopsies for chronic HCV infection completed at the centre from 1998 to 2007 were identified and the technique used was recorded. Biopsy quality was determined primarily by the number of complete portal tracts (CPTs) identifiable in the slides. The total length of specimen and the degree of fragmentation were secondary outcome measures.
There was a slight difference observed between the US-guided and non-US-guided groups in mean age (46.3 years versus 42.5 years, respectively; P=0.018) but no differences in sex, presence of cirrhosis, bilirubin, creatinine, international normalized ratio, and grade or stage of disease. Biopsies obtained using the US-guided technique produced higher quality specimens than the non-US-guided technique based on our primary outcome of number of CPTs in the biopsy (11.8 versus 7.4; P<0.001). US-guided specimens also were longer (24.4 mm versus 19.7 mm; P=0.001), had less fragmentation (P=0.016), and a higher overall histopathological quality assessment (P=0.026) than the non-US-guided biopsies. However, there was no significant difference between the two groups in the ability to grade and stage the disease (96% US-guided versus 90% in non-US-guided (P=0.20). Over a 10-year period, 763 biopsies for chronic HCV infection were identified with an obvious trend toward the increased use of US-guided technique observed at 2% in 1998 to 85% in 2007.
US-guided liver biopsies for chronic HCV are the most common method of obtaining specimens at the Kingston General Hospital, Kingston, Ontario, and are of higher quality than non-US-guided specimens. However, there is no significant difference in the two techniques in the ability to grade and stage chronic HCV.
背景/目的:肝活检一直是慢性丙型肝炎病毒(HCV)介导的肝损伤分级和分期的金标准。传统上,这是由经过培训的医生在床边使用非影像引导的经皮技术进行的。最近的文献表明,放射科医生在使用超声(US)引导技术获取活检样本方面的作用在不断扩大。本研究旨在确定这两种技术所获取的肝活检样本质量是否相似,并假设在我们机构,HCV的非超声引导经皮肝活检样本质量会高于超声引导样本。
利用医院组织病理学数据库回顾性确定100例慢性HCV感染患者的肝活检情况(50例连续的超声引导活检和50例连续的非超声引导活检)。所有原始活检玻片均进行编码,由一位对获取活检所使用技术不知情的单一肝脏病理学家进行前瞻性重新分析。此外,确定了1998年至2007年在该中心完成的所有慢性HCV感染肝活检,并记录所使用的技术。活检质量主要由玻片上可识别的完整门静脉分支(CPT)数量决定。样本总长度和破碎程度是次要观察指标。
超声引导组和非超声引导组在平均年龄上存在轻微差异(分别为46.3岁和42.5岁;P = 0.018),但在性别、肝硬化情况、胆红素、肌酐、国际标准化比值以及疾病分级或分期方面无差异。基于活检中CPT数量这一主要观察指标,使用超声引导技术获取的活检样本质量高于非超声引导技术(11.8对7.4;P < 0.001)。超声引导样本也更长(24.4毫米对19.7毫米;P = 0.001),破碎程度更低(P = 0.016),总体组织病理学质量评估更高(P = 0.026)。然而,两组在疾病分级和分期能力上无显著差异(超声引导组为96%,非超声引导组为90%(P = 0.20)。在10年期间,共确定763例慢性HCV感染的活检病例,观察到超声引导技术的使用有明显增加趋势,从1998年的2%增至2007年的85%。
在安大略省金斯顿的金斯顿综合医院,超声引导下的慢性HCV肝活检是获取样本最常用的方法,且质量高于非超声引导样本。然而,两种技术在慢性HCV分级和分期能力上无显著差异。