The Efficacy and Influencing Factors of Polymyxin B in High-Level Carbapenem-Resistant Klebsiella pneumoniae Infections

被引:2
|
作者
Jia, Xuedong [1 ,2 ,3 ]
Yin, Zhao [1 ,2 ]
Zhang, Wan [1 ,2 ]
Du, Shuzhang [1 ,2 ,3 ]
机构
[1] Zhengzhou Univ, Dept Pharm, Affiliated Hosp 1, Zhengzhou, Peoples R China
[2] Precis Clin Pharm Key Lab Henan Prov, Zhengzhou, Peoples R China
[3] Zhengzhou Univ, Dept Pharm, Affiliated Hosp 1, 1 Jianshe Dong Rd, Zhengzhou 450052, Henan, Peoples R China
来源
关键词
efficacy; influencing factors; polymyxin B; carbapenem-resistant Klebsiella pneumoniae; CLINICAL-USE; MORTALITY;
D O I
10.2147/IDR.S409090
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Polymyxin B (PMB) is a remedial treatment for carbapenem-resistant Klebsiella pneumoniae (CRKP) infection; however, there is a paucity of reports on the treatment of high-level CRKP infections with polymyxin B. Studies are needed to explore its treatment efficacy and associated influencing factors. Methods: Patients with high-level CRKP infections treated with PMB during hospitalization from June 2019 to June 2021 in a hospital were retrospectively studied, and risk factors affecting the efficacy were explored by subgroup analysis. Results: A total of 92 patients were enrolled, and the results showed that the PMB-based regimen had a bacterial clearance rate of 45.7%, an all-cause discharge mortality rate of 22.8%, and an incidence of acute kidney injury (AKI) of 27.2% for high-level CRKP treatment. The combination of beta-lactams other than carbapenems facilitated bacterial clearance, and the combination of electrolyte disturbances and higher APACHE II scores was detrimental to microbial clearance. Risk factors for all-cause discharge mortality were advanced age, concomitant antifungal drugs, concomitant tigecycline and incidence of AKI. Conclusion: PMB-based regimens are an effective option for the treatment of high-level CRKP infections. However, the optimal dose of treatment and the choice of combination regimens need to be explored in further studies.
引用
收藏
页码:4177 / 4187
页数:11
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