Division of Clinical Microbiology, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.
J Clin Microbiol. 2011 Feb;49(2):725-7. doi: 10.1128/JCM.01028-10. Epub 2010 Dec 1.
We compared two commercial PCR assays, the Prodesse ProGastro CD assay and the BD GeneOhm Cdiff assay, with a laboratory-developed Clostridium difficile toxin PCR assay with previously established performance characteristics. Results of all methods were in agreement for 333 (96%) of 346 stool specimens. No significant difference in performance among the assays was found (P values, >0.05).
我们将两种商业 PCR 检测方法,Prodesse ProGastro CD 检测法和 BD GeneOhm Cdiff 检测法,与实验室开发的具有先前建立的性能特征的艰难梭菌毒素 PCR 检测法进行了比较。所有方法的结果在 346 份粪便标本中的 333 份(96%)中是一致的。在检测方法之间没有发现性能的显著差异(P 值均>0.05)。