Ahn Jin Young, Ann Hea Won, Jeon Yongduk, Ahn Mi Young, Oh Dong Hyun, Kim Yong Chan, Kim Eun Jin, Song Je Eun, Jung In Young, Kim Moo Hyun, Jeong Wooyoung, Ku Nam Su, Jeong Su Jin, Choi Jun Yong, Yong Dongeun, Song Young Goo, Kim June Myung
Department of Internal Medicine, Seoul Medical Center, Seoul, South Korea.
Department of Internal Medicine, Yonsei University College of Medicine, Seoul, South Korea.
BMC Infect Dis. 2017 May 3;17(1):327. doi: 10.1186/s12879-017-2431-8.
The incidence of Proteus mirabilis antimicrobial resistance, especially that mediated by extended-spectrum β-lactamases (ESBLs), has increased. We investigated the impact of ESBL production on the mortality of patients with P. mirabilis bacteremia in Korea.
Patients diagnosed with P. mirabilis bacteremia between November 2005 and December 2013 at a 2000-bed tertiary care center in South Korea were included in this study. Phenotypic and molecular analyses were performed to assess ESBL expression. Characteristics and treatment outcomes were investigated among ESBL-producing and non-ESBL-producing P. mirabilis bacteremia groups. A multivariate analysis of 28-day mortality rates was performed to evaluate the independent impact of ESBLs.
Among 62 P. mirabilis isolates from 62 patients, 14 expressed ESBLs (CTX-M, 2; TEM, 5; both, 6; other, 1), and the 28-day mortality rate of the 62 patients was 17.74%. No clinical factor was significantly associated with ESBL production. The 28-day mortality rate in the ESBL-producing group was significantly higher than that in the non-ESBL-producing group (50% vs. 8.3%, p = 0.001). A multivariate analysis showed that ESBL production (odds ratio [OR], 11.53, 95% confidence interval [CI], 2.11-63.05, p = 0.005) was independently associated with the 28-day mortality rate in patients with P. mirabilis bacteremia.
ESBL production is significantly associated with mortality in patients with bacteremia caused by P. mirabilis. Rapid detection of ESBL expression and prompt appropriate antimicrobial therapy are required to reduce mortality caused by P. mirabilis bacteremia.
奇异变形杆菌的耐药性,尤其是由超广谱β-内酰胺酶(ESBLs)介导的耐药性发生率有所上升。我们调查了ESBLs产生对韩国奇异变形杆菌菌血症患者死亡率的影响。
本研究纳入了2005年11月至2013年12月期间在韩国一家拥有2000张床位的三级医疗中心被诊断为奇异变形杆菌菌血症的患者。进行了表型和分子分析以评估ESBLs的表达。在产ESBLs和不产ESBLs的奇异变形杆菌菌血症组中调查了特征和治疗结果。对28天死亡率进行多变量分析以评估ESBLs的独立影响。
在62例患者的62株奇异变形杆菌分离株中,14株表达ESBLs(CTX-M型2株;TEM型5株;两种类型均有的6株;其他类型1株),62例患者的28天死亡率为17.74%。没有临床因素与ESBLs产生显著相关。产ESBLs组的28天死亡率显著高于不产ESBLs组(50%对8.3%,p = 0.001)。多变量分析显示,ESBLs产生(比值比[OR],11.53,95%置信区间[CI],2.11 - 63.05,p = 0.005)与奇异变形杆菌菌血症患者的28天死亡率独立相关。
ESBLs产生与奇异变形杆菌所致菌血症患者的死亡率显著相关。需要快速检测ESBLs表达并及时给予适当的抗菌治疗,以降低奇异变形杆菌菌血症所致的死亡率。