Schelonka R L, Chai M K, Yoder B A, Hensley D, Brockett R M, Ascher D P
Division of Neonatology, Wilford Hall United States Air Force Medical Center, Lackland Air Force Base, Texas 78236-5300, USA.
J Pediatr. 1996 Aug;129(2):275-8. doi: 10.1016/s0022-3476(96)70254-8.
To determine the minimum volume of blood and the absolute number of organisms required for detection of bacteremia and fungemia by an automated colorimetric blood culture system (BacT/Alert, Organon Teknika).
Common neonatal pathogens, Escherichia coli, Streptococcus agalactiae (group B streptococcus (GBS): one American Type Culture Collection (ATCC) strain and one clinical isolate), Staphylococcus epidermidis, and Candida albicans, were seeded into blood to produce bacteremia or fungemia with low colony counts (1 to 3 colony-forming units (CFU) per milliliter) and ultra-low colony counts (<1 CFU/ml). For each organism, 96 culture bottles were inoculated with either 0.25, 0.5, 1.0, or 4.0 ml of the two seeded blood concentrations. Blood culture bottles were incubated in the BacT/Alert device for 5 days, and time to positivity was noted when applicable. All bottles were subcultured on plated media.
The Poisson statistic was used to calculate the probability of finding at least one viable CFU per inoculated culture bottle. The fraction of culture bottles with positive findings per group was divided by the probability of one or more organisms present to give the positivity index.
Plated subculture identified no growth of organisms not detected by the colorimetric detection system. The false-positive rate for the automated device was less than 1%. The positivity index for the GBS clinical isolate was 1.13, for the GBS ATCC isolate 0.96, for S. epidermidis 0.94, for C. albicans 0.97, and for E. coli 0.95. There was a statistically significant difference with time to positivity and inocula volume (p <0.01), but the difference was not clinically important.
If one or two viable colony-forming units are in the blood inoculated into culture media, the BacT/Alert system will detect growth rapidly. Because there appears to be a sizable subset of neonates who are at risk of sepsis with a colony count less than 4 CFU/ml, then a 0.5 ml inoculum of blood into the culture media is inadequate for sensitive and timely detection of bacteremia. One to two milliliters of blood should increase microorganism recovery in the face of low-colony-count sepsis.
通过自动比色血培养系统(BacT/Alert,奥加农泰尼克公司)确定检测菌血症和真菌血症所需的最小血量及微生物绝对数量。
将常见的新生儿病原体大肠杆菌、无乳链球菌(B组链球菌[GBS]:一株美国典型培养物保藏中心[ATCC]菌株和一株临床分离株)、表皮葡萄球菌和白色念珠菌接种到血液中,以产生低菌落计数(每毫升1至3个菌落形成单位[CFU])和超低菌落计数(<1 CFU/ml)的菌血症或真菌血症。对于每种微生物,用0.25、0.5、1.0或4.0 ml两种接种血液浓度接种96个培养瓶。血培养瓶在BacT/Alert装置中孵育5天,适当时记录阳性时间。所有培养瓶均在平板培养基上进行传代培养。
采用泊松统计量计算每个接种培养瓶中至少发现一个活CFU的概率。将每组有阳性结果的培养瓶比例除以存在一个或多个微生物的概率,得出阳性指数。
平板传代培养未发现比色检测系统未检测到的微生物生长。自动装置的假阳性率小于1%。GBS临床分离株的阳性指数为1.13,GBS ATCC分离株为0.96,表皮葡萄球菌为0.94,白色念珠菌为0.97,大肠杆菌为0.95。阳性时间和接种量存在统计学显著差异(p<0.01),但该差异在临床上并不重要。
如果接种到培养基中的血液中有一两个活的菌落形成单位,BacT/Alert系统将迅速检测到生长。由于似乎有相当一部分新生儿有发生菌落计数低于4 CFU/ml的败血症风险,因此向培养基中接种0.5 ml血液不足以敏感、及时地检测菌血症。面对低菌落计数败血症,1至2 ml血液应能提高微生物回收率。