Wellstood S A
J Clin Microbiol. 1986 Jun;23(6):1068-71. doi: 10.1128/jcm.23.6.1068-1071.1986.
A total of 1,800 urine specimens were screened by Gram stain to detect bacteriuria. Pellets of bacteria were obtained by centrifuging specimens containing greater than or equal to 1 gram-negative bacillus of a single morphological type per oil immersion field. Direct susceptibility tests and identifications were performed from pellets by using the AutoMicrobic system (AMS). Results were compared with culture results by routine AMS methods. Of the 145 specimens showing only gram-negative bacilli on Gram stain, 113 grew greater than or equal to 10(5) CFU of a single species per ml. Compared with routine AMS identifications, the direct method correctly identified 105 (92.9%) of the isolates. Identifications were available within 8 h for 77% of the isolates. When compared by MICs, 93.2% of the direct susceptibility test results agreed with routine AMS results within one twofold dilution. Comparisons by category call indicated that overall complete and essential agreements were 89.9 and 97.8%, respectively, with 1.0% very major, 1.0% major, and 8.1% minor errors. Cefamandole and cephalothin had the lowest correlations by both comparisons. Within 8 h, susceptibility results were available for 94.3% of the isolates. This method offers the advantage of rapid detection, prompt processing, and earlier reporting of complete results for positive urine specimens.
共对1800份尿液标本进行革兰氏染色筛查以检测菌尿症。通过对每油镜视野中含有大于或等于1株单一形态类型革兰氏阴性杆菌的标本进行离心来获取细菌沉淀。使用自动微生物系统(AMS)对沉淀进行直接药敏试验和鉴定。将结果与常规AMS方法的培养结果进行比较。在革兰氏染色仅显示革兰氏阴性杆菌的145份标本中,113份每毫升培养出大于或等于10(5) CFU的单一菌种。与常规AMS鉴定相比,直接法正确鉴定了105株(92.9%)分离株。77%的分离株在8小时内获得鉴定结果。通过最小抑菌浓度(MIC)比较,93.2%的直接药敏试验结果与常规AMS结果在一个两倍稀释度范围内一致。按类别比较表明,总体完全一致和基本一致率分别为89.9%和97.8%,非常主要误差为1.0%,主要误差为1.0%,次要误差为8.1%。头孢孟多和头孢噻吩在两种比较中的相关性最低。8小时内,94.3%的分离株获得药敏结果。该方法具有快速检测、及时处理以及更早报告阳性尿液标本完整结果的优点。