Garcia L S, Shimizu R Y, Bernard C N
LSG & Associates, Diagnostic Medical Parasitology Consulting/Training Services, Santa Monica, California 90402, USA.
J Clin Microbiol. 2000 Sep;38(9):3337-40. doi: 10.1128/JCM.38.9.3337-3340.2000.
The Triage parasite panel (BIOSITE Diagnostics, San Diego, Calif.) is a new qualitative enzyme immunoassay (EIA) panel for the detection of Giardia lamblia, Entamoeba histolytica/E. dispar, and Cryptosporidium parvum in fresh or fresh, frozen, unfixed human fecal specimens. By using specific antibodies, antigens specific for these organisms are captured and immobilized on a membrane. Panel performance was evaluated with known positive and negative stool specimens (a total of 444 specimens) that were tested by the standard ova and parasite (O&P) examination as the "gold standard," including staining with both trichrome and modified acid-fast stains. Specimens with discrepant results between the reference and Triage methods were retested by a different method, either EIA or immunofluorescence. A number of samples with discrepant results with the Triage device were confirmed to be true positives. After resolution of discrepant results, the number of positive specimens and the sensitivity and specificity results were as follows: for G. lamblia, 170, 95.9%, and 97.4%, respectively; for E. histolytica/E. dispar, 99, 96.0%, and 99.1%, respectively; and for C. parvum, 60, 98.3%, and 99.7%, respectively. There was no cross-reactivity with other parasites found in stool specimens, including eight different protozoa (128 challenges) and three different helminths (83 challenges). The ability to perform the complete O&P examination should remain an option for those patients with negative parasite panel results but who are still symptomatic.
分诊寄生虫检测试剂盒(BIOSITE诊断公司,加利福尼亚州圣地亚哥)是一种新型定性酶免疫分析(EIA)试剂盒,用于检测新鲜或新鲜、冷冻、未固定的人类粪便标本中的蓝氏贾第鞭毛虫、溶组织内阿米巴/迪氏内阿米巴和微小隐孢子虫。通过使用特异性抗体,将这些生物体的特异性抗原捕获并固定在膜上。使用已知的阳性和阴性粪便标本(共444份标本)对试剂盒性能进行评估,这些标本通过标准的虫卵和寄生虫(O&P)检查作为“金标准”进行检测,包括用三色染色和改良抗酸染色。参考方法和分诊方法结果不一致的标本通过不同方法重新检测,即EIA或免疫荧光法。许多与分诊设备结果不一致的样本被确认为真阳性。在解决结果不一致的问题后,阳性标本数量以及灵敏度和特异性结果如下:对于蓝氏贾第鞭毛虫,分别为170例、95.9%和97.4%;对于溶组织内阿米巴/迪氏内阿米巴,分别为99例、96.0%和99.1%;对于微小隐孢子虫,分别为60例、98.3%和99.7%。未发现与粪便标本中其他寄生虫有交叉反应,包括8种不同的原生动物(128次检测)和3种不同的蠕虫(83次检测)。对于寄生虫检测试剂盒结果为阴性但仍有症状的患者,进行完整的O&P检查仍应是一种选择。