Bascomb S, Abbott S L, Bobolis J D, Bruckner D A, Connell S J, Cullen S K, Daugherty M, Glenn D, Janda J M, Lentsch S J, Lindquist D, Mayhew P B, Nothaft D M, Skinner J R, Williams G B, Wong J, Zimmer B L
Dade MicroScan Inc., West Sacramento, California 95691, USA.
J Clin Microbiol. 1997 Oct;35(10):2531-6. doi: 10.1128/jcm.35.10.2531-2536.1997.
The accuracy and performance of the revised MicroScan Rapid Gram-Negative Identification Type 3 Panel (Dade MicroScan Inc., West Sacramento, Calif.) were examined in a multicenter evaluation. The revised panel database includes data for 119 taxa covering a total of 150 species, with data for 12 new species added. Testing was performed in three phases: the efficacy, challenge, and reproducibility testing phases. A total of 405 fresh and stock gram-negative isolates comprising 54 species were tested in the efficacy phase; 96.8% of these species were identified correctly in comparison to the identification obtained either with the API 20E system (bioMérieux Vitek, Hazelwood, Mo.) or by the conventional tube method. The number of correctly identified isolates in the challenge phase, including new species added to the database, was 221 of 247, or 89.5%, in comparison to the number correctly identified by the conventional tube method. A total of 465 isolates were examined for intra- and interlaboratory identification reproducibility and gave an agreement of 464 of 465, or 99.8%. The overall reproducibility of each individual identification test or substrate was 14,373 of 14,384, or 99.9%. The new Rapid Gram-Negative Identification Type 3 Panel gave accurate and highly reproducible results in this multiple-laboratory evaluation.
在一项多中心评估中,对修订后的MicroScan快速革兰氏阴性菌鉴定3型板(达德MicroScan公司,加利福尼亚州西萨克拉门托)的准确性和性能进行了检测。修订后的板数据库包含119个分类单元的数据,涵盖总共150个物种,新增了12个新物种的数据。测试分三个阶段进行:效能测试、挑战测试和再现性测试阶段。在效能阶段,共对包含54个物种的405株新鲜和保存的革兰氏阴性菌分离株进行了测试;与使用API 20E系统(生物梅里埃Vitek公司,密苏里州黑兹尔伍德)或传统试管法获得的鉴定结果相比,这些物种中有96.8%被正确鉴定。在挑战阶段,包括数据库中新增的新物种,与传统试管法正确鉴定的数量相比,正确鉴定的分离株数量为247株中的221株,即89.5%。共对465株分离株进行了实验室内部和实验室间鉴定再现性检测,465株中有464株结果一致,即99.8%。每个单独鉴定试验或底物的总体再现性为14384次中的14373次,即99.9%。在这项多实验室评估中,新的快速革兰氏阴性菌鉴定3型板给出了准确且高度可重复的结果。