Kellogg J A, Bankert D A, Manzella J P, Parsey K S, Scott S L, Cavanaugh S H
Department of Pathology, York Hospital, York, Pennsylvania 17405.
J Clin Microbiol. 1994 Sep;32(9):2050-5. doi: 10.1128/jcm.32.9.2050-2055.1994.
The recovery of pathogens and the speed of their detection were determined for our conventional blood culture system (an Isolator [Wampole] and a 100-ml Thiol bottle [Difco]) compared with automated ESP aerobic and anaerobic bottles (80 ml each; Difco). Each of the four culture devices was inoculated with approximately 10 ml of blood from symptomatic patients weighing more than 80 lb (ca. 36 kg). From 7,070 sets of cultures for 2,841 patients, 607 clinically significant isolates were recovered: 456 (75.1%) from the Isolator, 353 (58.2%) from Thiol, 377 (62.1%) from ESP aerobic bottles, and 346 (57.0%) from ESP anaerobic bottles. Of the 607 isolates, 149 (24.5%) were detected only with the conventional system (Isolator and/or Thiol), and 65 (10.7%) were detected only with the ESP two-bottle system (P < 0.001). Our conventional system allowed for detection of significantly more isolates of members of the family Enterobacteriaceae (P < 0.001), Staphylococcus aureus (P < 0.01), Staphylococcus spp. (coagulase-negative) (P < 0.01), and Enterococcus spp. (P < 0.05), and ESP facilitated detection of significantly more isolates of S. pneumoniae (P < 0.01). When all four devices in a culture set were positive for the same isolate, no microbial species or group was detected significantly earlier ( > or = 24 h) by either blood culture system. The Isolator contamination rate (4.8%) was > or = 6 times the rate for any of the bottles. Of pathogens detected by the Isolator, 50% were recovered in counts of < or = 1.0 CFU/ml and 18% were recovered only as a single colony. The ESP system offered an automated, less labor-intensive blood culture system for which routine subcultures were not required, but the important considerations of culturing large volumes of blood and of obtaining at least two sets from each patient in our population were reemphasized.
我们将传统血液培养系统(一种隔离器[Wampole公司生产]和一个100毫升硫醇瓶[Difco公司生产])与自动化的ESP需氧瓶和厌氧瓶(各80毫升;Difco公司生产)进行比较,测定了病原体的回收率及其检测速度。将四种培养装置分别接种来自体重超过80磅(约36千克)有症状患者的约10毫升血液。在对2841例患者进行的7070组培养中,共分离出607株具有临床意义的菌株:456株(75.1%)来自隔离器,353株(58.2%)来自硫醇瓶,377株(62.1%)来自ESP需氧瓶,346株(57.0%)来自ESP厌氧瓶。在这607株分离菌株中,149株(24.5%)仅在传统系统(隔离器和/或硫醇瓶)中被检测到,65株(10.7%)仅在ESP两瓶系统中被检测到(P<0.001)。我们的传统系统能检测到显著更多的肠杆菌科成员菌株(P<0.001)、金黄色葡萄球菌(P<0.01)、葡萄球菌属(凝固酶阴性)(P<0.01)和肠球菌属菌株(P<0.05),而ESP系统能更显著地检测到更多的肺炎链球菌菌株(P<0.01)。当培养组中的所有四种装置对同一菌株均呈阳性时,两种血液培养系统均未显著更早(≥24小时)检测到任何微生物种类或菌群。隔离器的污染率(4.8%)是任何一种瓶子污染率的6倍或更高。在隔离器检测到的病原体中,50%的回收率为≤1.0 CFU/ml,18%仅以单个菌落形式被回收。ESP系统提供了一种自动化、劳动强度较低的血液培养系统,但再次强调了在我们的人群中培养大量血液以及从每位患者至少获取两组培养物的重要性,且该系统无需常规传代培养。