Rohner P, Pepey B, Auckenthaler R
Laboratoire Central de Bactériologie, Hôpital Cantonal Universitaire de Genève, Switzerland.
J Clin Microbiol. 1996 Jan;34(1):126-9. doi: 10.1128/jcm.34.1.126-129.1996.
The BACTEC 9240 (Becton Dickinson, Sparks, Md.) automated blood culture system is based on the continuous monitoring of CO2 production by means of a fluorescent sensor attached to the bottom of culture vials. We compared the performance of the BACTEC aerobic Plus/F medium to that of the Septi-Chek Release medium (Becton Dickinson, Sparks, Md.), a manual biphasic blood culture system. Sets consisting of BACTEC aerobic Plus/F and Septi-Chek Release vials inoculated with similar volumes (7 +/- 2 ml) were evaluated. In the laboratory, systems were equipped and analyzed according to the manufacturer's recommendations. The BACTEC and Septi-Chek vials were incubated at 35 degrees C for 5 days. A total of 6,116 compliant sets were obtained from 1,972 adult patients (3.1 cultures per patient). Of these, 731 (12%) were culture positive, including 612 (10%) that yielded at least one pathogen, and 143 (2%) were considered to be contaminated. Of the 672 pathogenic organisms detected, 524 were isolated from the BACTEC aerobic Plus/F medium and 574 were isolated from the Septi-Chek Release medium, 428 organisms grew in both media, 96 organisms grew only in the BACTEC aerobic Plus/F medium, and 146 organisms grew only in the Septi-Chek Release medium (P = 0.001). Haemophilus spp. were isolated more often (P = 0.03) from the BACTEC aerobic Plus/F medium; however, more Streptococcus anginosus organisms (P = 0.02), members of the Enterobacteriaceae family (P < 0.03), and gram-negative anaerobes (P = 0.03) were isolated from the Septi-Chek Release medium. Pathogenic organisms were detected significantly earlier (P < 0.0001) with the BACTEC aerobic Plus/F medium in conjunction with the BACTEC 9240 instrument than with the Septi-Chek Release medium.
BACTEC 9240(美国马里兰州斯帕克斯市贝克顿·迪金森公司)自动化血培养系统基于通过连接在培养瓶底部的荧光传感器对二氧化碳产生进行连续监测。我们将BACTEC需氧加/F培养基与Septi-Chek Release培养基(美国马里兰州斯帕克斯市贝克顿·迪金森公司)(一种手动双相血培养系统)的性能进行了比较。对接种了相似体积(7±2毫升)的BACTEC需氧加/F和Septi-Chek Release培养瓶组成的套装进行了评估。在实验室中,按照制造商的建议对系统进行了配备和分析。BACTEC和Septi-Chek培养瓶在35℃下孵育5天。从1972名成年患者中总共获得了6116套合格样本(每位患者3.1次培养)。其中,731套(12%)培养呈阳性,包括612套(10%)培养出至少一种病原体,143套(2%)被认为受到污染。在检测到的672种致病微生物中,524种从BACTEC需氧加/F培养基中分离得到,574种从Septi-Chek Release培养基中分离得到,428种微生物在两种培养基中均生长,96种微生物仅在BACTEC需氧加/F培养基中生长,146种微生物仅在Septi-Chek Release培养基中生长(P = 0.001)。嗜血杆菌属从BACTEC需氧加/F培养基中分离得更频繁(P = 0.03);然而,更多的咽峡炎链球菌微生物(P = 0.02)、肠杆菌科成员(P < 0.03)和革兰氏阴性厌氧菌(P = 0.03)从Septi-Chek Release培养基中分离得到。与Septi-Chek Release培养基相比,使用BACTEC需氧加/F培养基结合BACTEC 9240仪器能显著更早地检测到致病微生物(P < 0.0001)。