Laine L, Chun D, Stein C, El-Beblawi I, Sharma V, Chandrasoma P
Departments of Medicine and Pathology, University of Southern California School of Medicine, Los Angeles, USA.
Gastrointest Endosc. 1996 Jan;43(1):49-53. doi: 10.1016/s0016-5107(96)70260-2.
The optimal number or size of endoscopic biopsies for use in rapid urease testing has not been established. Postulating that increasing the amount of tissue sampled would improve diagnostic yield and hasten development of a positive test, we compared urease testing with one regular biopsy, two regular biopsies, and one "jumbo" forceps biopsy.
One hundred fifty patients undergoing endoscopy had three sets of prepyloric biopsies placed in a CLOtest: one regular forceps biopsy, two regular forceps biopsy, and one large-channel jumbo forceps biopsy. Biopsies were then taken for two independent histologic examinations. Disagreements were resolved by another examiner.
Eighty-nine patients (59%) had Helicobacter pylori infection by histology; interobserver agreement was 90% with kappa = 0.78. The mean time to a positive test was 5.3 +/- 0.9 hours for one regular biopsy, 3.2 +/- 0.7 hours for two regular biopsies, and 3.8 +/- 0.8 hours for one jumbo biopsy (p < 0.01 for two regular, one jumbo vs. one regular biopsy). Compared to one regular biopsy, the urease test was positive at least 30 minutes earlier in 56% of the patients with two regular biopsies and 54% with one jumbo biopsy. Sensitivities for one regular versus two regular biopsies were 1 hour, 19% versus 33% (p = 0.059); 2 hours, 38% versus 49% (p = 0.17); 3 hours, 48% versus 60% (p = 0.18); and 24 hours, 75% versus 79% (p > 0.20).
Doubling the amount of tissue in the CLOtest hastens the development of a positive test by approximately 1 1/2 to 2 hours; tests become positive at least 30 minutes earlier in over 50% of the patients. Low cost, ease, and excellent specificity make the rapid urease test a valuable diagnostic tool. Nevertheless, if used as a "rapid" diagnostic test (read within 3 hours of biopsy), it is associated with a false negative rate of approximately 40%.
用于快速尿素酶检测的内镜活检的最佳数量或大小尚未确定。我们推测增加取样组织的量会提高诊断率并加速阳性检测结果的出现,因此我们比较了使用一次常规活检、两次常规活检以及一次“大钳道”活检进行尿素酶检测的情况。
150例接受内镜检查的患者在CLO检测中进行了三组胃幽门活检:一次常规钳取活检、两次常规钳取活检以及一次大通道大钳道活检。然后取活检组织进行两项独立的组织学检查。分歧由另一位检查者解决。
89例患者(59%)经组织学检查确诊为幽门螺杆菌感染;观察者间一致性为90%,kappa值为0.78。一次常规活检检测出阳性的平均时间为5.3±0.9小时,两次常规活检为3.2±0.7小时,一次大钳道活检为3.8±0.8小时(两次常规活检和一次大钳道活检与一次常规活检相比,p<0.01)。与一次常规活检相比,56%接受两次常规活检的患者和54%接受一次大钳道活检的患者尿素酶检测阳性时间至少提前30分钟。一次常规活检与两次常规活检的敏感度在1小时时分别为19%和33%(p=0.059);2小时时分别为38%和49%(p=0.17);3小时时分别为48%和60%(p=0.18);24小时时分别为75%和79%(p>0.20)。
在CLO检测中使组织量翻倍可使阳性检测结果的出现时间提前约1.5至2小时;超过50%的患者检测阳性时间至少提前30分钟。低成本、操作简便以及高特异性使快速尿素酶检测成为一种有价值的诊断工具。然而,如果将其用作“快速”诊断检测(活检后3小时内读取结果),其假阴性率约为40%。