Hayakawa Kayoko, Mezaki Kazuhisa, Kobayakawa Masao, Yamamoto Kei, Mutoh Yoshikazu, Tsuboi Motoyuki, Hasimoto Takehiro, Nagamatsu Maki, Kutsuna Satoshi, Takeshita Nozomi, Katanami Yuichi, Ishikane Masahiro, Ohmagari Norio
Disease Control and Prevention Center, National Center for Global Health and Medicine, Tokyo, Japan.
Department of Clinical Laboratory, National Center for Global Health and Medicine, Tokyo, Japan.
PLoS One. 2017 Jul 24;12(7):e0181548. doi: 10.1371/journal.pone.0181548. eCollection 2017.
Rapid identification of positive blood cultures is important for initiation of optimal treatment in septic patients. Effects of automated, microarray-based rapid identification systems on antibiotic prescription against community-onset bacteremia (COB) remain unclear.
We prospectively enrolled 177 patients with 185 COB episodes (occurring within 72 h of admission) over 17 months. Bacteremia episodes due to gram-positive bacteria (GP) and gram-negative bacteria (GN) in the same patient were counted separately. For GP bacteremia, patients with ≥2 sets of positive blood cultures were included. The primary study objective was evaluating the rates of antibiotic prescription changes within 2 days of rapid identification using the Verigene system.
Bacteremia due to GN and GP included 144/185 (77.8%) and 41/185 (22.2%) episodes, respectively. Antibiotic prescription changes occurred in 51/185 cases (27.6% [95%CI:21.3-34.6%]) after Verigene analysis and 70/185 cases (37.8% [30.8-45.2%]) after conventional identification and susceptibility testing. Prescription changes after Verigene identification were more frequent in GP (17/41[41.5%]) than in GN (34/144[23.5%]). Among bacteremia due to single pathogen targeted by Verigene test, bacterial identification agreement between the two tests was high (GP: 38/39[97.4%], GN: 116/116[100%]). The Verigene test correctly predicted targeted antimicrobial resistance. The durations between the initiation of incubation and reporting of the results for the Verigene system and conventional test was 28.3 h (IQR: 25.8-43.4 h) and 90.6 h (68.3-118.4 h), respectively. In only four of the seven episodes of COB in which two isolates were identified by conventional tests, the Verigene test correctly identified both organisms.
We observed a high rate of antibiotic prescription changes after the Verigene test in a population with COB especially in GP. The Verigene test would be a useful tool in antimicrobial stewardship programs among patients with COB.
快速鉴定血培养阳性结果对于脓毒症患者启动最佳治疗至关重要。基于微阵列的自动化快速鉴定系统对社区获得性菌血症(COB)抗生素处方的影响尚不清楚。
我们前瞻性纳入了177例患者,在17个月内发生了185次COB发作(入院72小时内)。同一患者革兰氏阳性菌(GP)和革兰氏阴性菌(GN)引起的菌血症发作分别计数。对于GP菌血症,纳入血培养阳性≥2套的患者。主要研究目标是评估使用Verigene系统在快速鉴定后2天内抗生素处方的更改率。
GN和GP引起的菌血症分别包括144/185例(77.8%)和41/185例(22.2%)发作。Verigene分析后,51/185例(27.6%[95%CI:21.3 - 34.6%])发生抗生素处方更改,常规鉴定和药敏试验后,70/185例(37.8%[30.8 - 45.2%])发生更改。Verigene鉴定后,GP菌血症的处方更改(17/41[41.5%])比GN菌血症(34/144[23.5%])更频繁。在Verigene检测针对的单一病原体引起的菌血症中,两种检测之间的细菌鉴定一致性很高(GP:38/39[97.4%],GN:116/116[100%])。Verigene检测正确预测了目标抗菌药物耐药性。Verigene系统和常规检测从开始孵育到报告结果的时间分别为28.3小时(IQR:25.8 - 43.4小时)和90.6小时(68.3 - 118.4小时)。在常规检测鉴定出两种分离株的7例COB发作中,只有4例Verigene检测正确鉴定出两种病原体。
我们观察到在COB患者中,尤其是GP菌血症患者,Verigene检测后抗生素处方更改率很高。Verigene检测将是COB患者抗菌药物管理计划中的一个有用工具。