Department of Pharmacy Practice, Albany College of Pharmacy and Health Sciences, Albany, NY, USA.
Chicago College of Pharmacy, Department of Pharmacy Practice, Midwestern University, Downers Grove, IL, USA; Department of Pharmacy, Northwestern Memorial Hospital, Chicago, IL, USA.
Int J Antimicrob Agents. 2018 Oct;52(4):451-458. doi: 10.1016/j.ijantimicag.2018.04.011. Epub 2018 Apr 14.
Carbapenems have shown efficacy in treating nosocomial pneumonias in clinical trials despite a reported low lung penetration compared with other β-lactams. Preserving the clinical activity of carbapenems through stewardship efforts is essential. The aim of this review was to identify any differences in outcomes potentially as a function of decreased penetration.
PubMed and the Cochrane Library were systematically searched for clinical trials comparing carbapenems with other anti-pseudomonal β-lactams for treatment of nosocomial pneumonia through to end December 2016. Trials reporting clinical and microbiological outcomes associated with treatment were included. Pediatric studies and those with uneven comparators (e.g., carbapenem vs. combination Gram-negative therapy) were excluded. Fixed effects models were used to evaluate the impact of treatment on the odds of clinical failure, death, or microbiological failure.
252 unique articles were identified; five met inclusion criteria and comprised 640 patients in the carbapenem group and 634 patients in the β-lactam group. No differences in clinical failure (odds ratio [OR] 1.08, 95% confidence interval [CI] [0.81-1.44], I=16%) or mortality (OR 0.75, CI 0.57-1.11, I=0%) were noted between groups. Patients infected with P. aeruginosa and treated with imipenem were more likely to experience clinical failure (OR 4.21, CI 1.51-11.12, I=44%) and to develop resistance to the study carbapenem (OR 2.86, CI 1.08-6.44, I= 13%) than those treated with alternative β-lactams.
No differences in clinical outcomes were observed between carbapenems and non-carbapenem β-lactams in nosocomial pneumonias. Those infected with P. aeruginosa fared worse and were more likely to have resistance develop if they were treated with imipenem. Additional studies are warranted.
尽管碳青霉烯类药物与其他β-内酰胺类药物相比,肺部穿透率较低,但在临床试验中已显示出对医院获得性肺炎的疗效。通过管理措施来维持碳青霉烯类药物的临床活性至关重要。本综述的目的是确定由于穿透率降低而导致的任何结果差异。
通过系统检索 PubMed 和 Cochrane 图书馆,检索截止至 2016 年 12 月底的比较碳青霉烯类药物与其他抗假单胞菌β-内酰胺类药物治疗医院获得性肺炎的临床试验。纳入报告与治疗相关的临床和微生物学结局的试验。排除儿科研究和不均衡对照(例如,碳青霉烯类药物与革兰氏阴性联合治疗)的研究。使用固定效应模型评估治疗对临床失败、死亡或微生物学失败的可能性的影响。
确定了 252 篇独特的文章;其中 5 篇符合纳入标准,包括碳青霉烯组 640 例患者和β-内酰胺组 634 例患者。两组之间临床失败(比值比 [OR] 1.08,95%置信区间 [CI] [0.81-1.44],I=16%)或死亡率(OR 0.75,CI 0.57-1.11,I=0%)无差异。感染铜绿假单胞菌并接受亚胺培南治疗的患者更有可能出现临床失败(OR 4.21,CI 1.51-11.12,I=44%)和对研究碳青霉烯类药物产生耐药性(OR 2.86,CI 1.08-6.44,I=13%),而接受其他β-内酰胺类药物治疗的患者则没有。
在医院获得性肺炎中,碳青霉烯类药物与非碳青霉烯类β-内酰胺类药物的临床结局无差异。感染铜绿假单胞菌的患者如果接受亚胺培南治疗,预后更差,更有可能产生耐药性。需要进一步研究。