头孢他啶-阿维巴坦治疗耐碳青霉烯类肺炎克雷伯菌感染:头孢他啶-阿维巴坦治疗耐碳青霉烯类肺炎克雷伯菌感染。
Ceftazidime-avibactam in the treatment of infections from carbapenem-resistant Klebsiella pneumoniae: Ceftazidime-avibactam against CR-KP infections.
作者信息
Gu Jie, Xu Jie, Zuo Ting-Ting, Chen Yan-Bin
机构信息
Department of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Soochow University, 899#, Pinghai Road, Suzhou, Jiangsu Province, 215000, China.
Center for Clinical Laboratory, The First Affiliated Hospital of Soochow University, 899#, Pinghai Road, Suzhou, Jiangsu Province, 215000, China.
出版信息
J Glob Antimicrob Resist. 2021 Sep;26:20-25. doi: 10.1016/j.jgar.2021.04.022. Epub 2021 May 18.
OBJECTIVES
Clinical experience with ceftazidime-avibactam (CAZ-AVI) for the treatment of carbapenem-resistant Klebsiella pneumoniae (CR-KP) infections is not well evaluated. The aim of this study was to assess its efficacy in a single-centre cohort of patients infected with CR-KP.
METHODS
We conducted a retrospective observational study of consecutive patients treated for >72 h with CAZ-AVI or other active antibiotics (OAAs) for CR-KP infections. The primary outcome was 30-d mortality. The secondary outcomes were 14-d clinical failure and 14-d microbiological failure. Multivariate regression and propensity score matching were used to evaluate the relationship between CAZ-AVI treatment and outcomes.
RESULTS
Ninety infections caused by CR-KP were documented in our study. Forty-two patients were treated with CAZ-AVI and 48 with OAAs. The crude 30-d mortality (8/42 vs. 22/48, P=0.007), 14-d clinical failure (14/42 vs. 24/48, P=0.046) and 14-d microbiological failure (11/42 vs. 15/48, P=0.034) were significantly lower in patients with CAZ-AVI treatment. The Kaplan-Meier survival curves of 30-d mortality confirmed the findings (logrank=0.004). In the multivariable models, the odds ratio (OR) of 30-d mortality (OR 0.23 95% CI 0.10-0.51, P<0.000), 14-d clinical failure (OR 0.37, 95% CI 0.14-0.95, P=0.039) and 14-d microbiological failure (OR 0.17, 95% CI 0.08-0.93, P=0.038) remain consistently significant. In the subgroup analysis, CAZ-AVI was associated with decreased 30-d mortality in the positive blood culture (OR 0.23, 95% CI 0.08-0.63, P=0.004), septic shock (OR 0.23, 95% CI 0.07-0.78, P=0.019), SOFA score (>5, OR 0.13, 95% CI 0.04-0.36, P<0.000), mechanical ventilation (OR 0.13, 95% CI 0.04-0.36, p<0.000) and Charlson comorbidity index (>3, OR 0.15, 95% CI 0.04-0.55, P=0.004). After propensity score matching, 29 cases from each group were well matched. The 30-d mortality remained significantly lower in the CAZ-AVI group (6/29 vs. 13/29, P=0.05).
CONCLUSION
CAZ-AVI may be a more valuable therapeutic option for severe CR-KP infections than for mild cases and further randomized controlled trials are needed to evaluate the efficacy.
目的
头孢他啶-阿维巴坦(CAZ-AVI)治疗耐碳青霉烯类肺炎克雷伯菌(CR-KP)感染的临床经验尚未得到充分评估。本研究的目的是评估其在单中心CR-KP感染患者队列中的疗效。
方法
我们对连续接受CAZ-AVI或其他活性抗生素(OAAs)治疗>72小时的CR-KP感染患者进行了回顾性观察研究。主要结局是30天死亡率。次要结局是14天临床失败和14天微生物学失败。采用多变量回归和倾向评分匹配来评估CAZ-AVI治疗与结局之间的关系。
结果
本研究记录了90例由CR-KP引起的感染。42例患者接受CAZ-AVI治疗,48例接受OAAs治疗。接受CAZ-AVI治疗的患者,其30天粗死亡率(8/42对22/48,P=0.007)、14天临床失败率(14/42对24/48,P=0.046)和14天微生物学失败率(11/42对15/48,P=0.034)显著更低。30天死亡率的Kaplan-Meier生存曲线证实了这一结果(对数秩检验=0.004)。在多变量模型中,30天死亡率的比值比(OR)(OR 0.23,95%CI 0.10-0.51,P<0.000)、14天临床失败率(OR 0.37,95%CI 0.14-0.95,P=0.039)和14天微生物学失败率(OR 0.17,95%CI 0.08-0.93,P=0.038)仍然具有显著意义。在亚组分析中,CAZ-AVI与血培养阳性患者30天死亡率降低相关(OR 0.23,95%CI 0.08-0.63,P=0.004)、感染性休克(OR 0.23,95%CI 0.07-0.78,P=0.019)、序贯器官衰竭评估(SOFA)评分(>5,OR 0.13,95%CI 0.04-0.36,P<0.000)、机械通气(OR 0.13,95%CI 0.04-0.36,P<0.000)和Charlson合并症指数(>3,OR 0.15,95%CI 0.04-0.55,P=0.004)。倾向评分匹配后,每组29例病例匹配良好。CAZ-AVI组的30天死亡率仍然显著更低(6/29对13/29,P=0.05)。
结论
对于严重的CR-KP感染,CAZ-AVI可能是比轻度病例更有价值的治疗选择,需要进一步的随机对照试验来评估其疗效。