Hubbard W A, Shalis P J, McClatchey K D
J Clin Microbiol. 1983 Feb;17(2):327-31. doi: 10.1128/jcm.17.2.327-331.1983.
A total of 100 random clinical urine specimens were divided and used to compare Becton, Dickinson & Co. B-D Urine Culture Kit-treated urine (BDU) with refrigerated urine (RU). Each RU-BDU pair was cultured with the standard calibrated loop-plate method and also screened with the Abbott Laboratories MS-2 system at 0, 5, and 24 h. An additional 158 positive urine specimens containing greater than 10(5) CFU/ml were tested by standard culturing and MS-2 at 0 and 24 h. In addition, growth curves were run for Escherichia coli containing RU-BDU pairs at 0 and 24 h, and MS-2 detection time frequencies were analyzed. Culture results showed few changes in colony counts at 0 and 5 h for RU and BDU specimens. At 24 h, there were decreased colony counts for 7.0% of RU and 17.7% of BDU specimens. MS-2 results showed detection rates at 0 h of 100% for RU and 82.9% for BDU specimens and at 24 h of 91.1% for RU and 63.3% for BDU specimens. The organisms most frequently missed at 24 h were E. coli, Pseudomonas aeruginosa, and Staphylococcus epidermidis. Growth curve analysis showed a 1-h delay of logarithmic growth in BDU specimens. MS-2 detection time analysis showed delayed positive reports owing to be extended detection time for BDU specimens. The B-D Urine Culture Kit is a convenient transport system; however, some difficulty in recovering organisms at 24 h with the standard culture method and increased difficulty with the MS-2 system were recognized.
总共100份随机临床尿液标本被分成两组,用于比较BD尿液培养试剂盒处理的尿液(BDU)和冷藏尿液(RU)。每对RU-BDU标本均采用标准校准环板法进行培养,并在0、5和24小时时用雅培公司的MS-2系统进行筛查。另外158份菌落形成单位(CFU)/毫升大于10⁵的阳性尿液标本在0和24小时时通过标准培养法和MS-2系统进行检测。此外,对0和24小时时含RU-BDU对的大肠杆菌进行生长曲线测定,并分析MS-2检测时间频率。培养结果显示,RU和BDU标本在0和5小时时菌落计数变化不大。在24小时时,7.0%的RU标本和17.7%的BDU标本菌落计数减少。MS-2检测结果显示,RU标本在0小时时的检测率为100%,BDU标本为82.9%;在24小时时,RU标本的检测率为91.1%,BDU标本为63.3%。24小时时最常漏检的微生物是大肠杆菌、铜绿假单胞菌和表皮葡萄球菌。生长曲线分析显示BDU标本对数生长期延迟1小时。MS-2检测时间分析显示,由于BDU标本检测时间延长,阳性报告延迟。BD尿液培养试剂盒是一种方便的运输系统;然而,人们认识到,使用标准培养法在24小时时回收微生物存在一些困难,而使用MS-2系统时困难更大。