O'Connor D, Hynes P, Cormican M, Collins E, Corbett-Feeney G, Cassidy M
Microbiology Laboratory, Portiuncula Hospital, Ballinasloe, County Galway, Galway, Ireland.
J Clin Microbiol. 2001 Aug;39(8):2846-9. doi: 10.1128/JCM.39.8.2846-2849.2001.
Clostridium difficile is the principal pathogen associated with hospital-acquired acute diarrheal disease. We have evaluated the performances of six approaches for diagnosis of C. difficile-associated diarrhea (CDAD). Consecutive stool specimens (n = 200) from 133 patients were examined by cytotoxin assay, by culture of C. difficile on cycloserine-cefoxitin-fructose agar, and by toxin detection using four rapid immunoassay systems (Oxoid Toxin A test, ImmunoCard Toxin A test, TechLab Tox A/B II test, and Premier Toxins A&B test). A diagnosis of CDAD was established for 35 (27%) patients (representing 29% of specimens). The adjusted sensitivity and specificity of the methods were, respectively, 98 and 99% for the cytotoxin assay, 54 and 99% for ImmunoCard, 50 and 98% for Oxoid, 79 and 98% for TechLab, 80 and 98% for Premier, and 57 and 100% for culture. The TechLab and Premier assays are acceptable tests for diagnosis of CDAD but are not equivalent to the cytotoxin assay.
艰难梭菌是与医院获得性急性腹泻病相关的主要病原体。我们评估了六种诊断艰难梭菌相关性腹泻(CDAD)方法的性能。对133例患者连续采集的粪便标本(n = 200)进行了细胞毒素检测、在环丝氨酸-头孢西丁-果糖琼脂上培养艰难梭菌以及使用四种快速免疫测定系统(Oxoid毒素A检测、免疫卡毒素A检测、TechLab毒素A/B II检测和Premier毒素A&B检测)进行毒素检测。确诊35例(27%)患者患有CDAD(占标本的29%)。这些方法调整后的敏感性和特异性分别为:细胞毒素检测为98%和99%,免疫卡检测为54%和99%,Oxoid检测为50%和98%,TechLab检测为79%和98%,Premier检测为80%和98%,培养法为57%和100%。TechLab和Premier检测是诊断CDAD的可接受检测方法,但不等同于细胞毒素检测。