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首页> 外文期刊>International journal of infectious diseases : >The effect of colistin resistance and other predictors on fatality among patients with bloodstream infections due to Klebsiella pneumoniae in an OXA-48 dominant region
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The effect of colistin resistance and other predictors on fatality among patients with bloodstream infections due to Klebsiella pneumoniae in an OXA-48 dominant region

机译:牛瘟抗血管患者血流感染患者患者患者患者患者患者的疗效

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Background The aim of this study was to determine the effect of colistin resistance and other predictors on fatality among patients with Klebsiella pneumoniae bloodstream infections (Kp-BSI) and to describe the effect of amikacin and tigecycline on the outcome in an OXA-48 dominant country. Method This was a retrospective study performed among patients 16 years of age in a tertiary hospital with 465 beds. All cases had ≥1 positive blood culture for K. pneumoniae 48?h after admission. Results Among 210 patients with Kp-BSI, the 30-day mortality rate after isolation of the microorganism was 58%. The rate of carbapenem resistance was higher (64% vs. 38%, p ??0.001) and the colistin minimum inhibitory concentration (MIC) was elevated (7 vs. 4, p ??0.029) among the patients who died. Among the colistin-resistant K. pneumoniae , the rates of OXA-48, ST101, and NDM-1 were 78%, 67%, and 35%, respectively. Amikacin was added to the treatment of 13 patients with carbapenem and colistin-resistant Kp-BSI and 77% survived ( p ??0.001). Tigecycline was added to the treatment of 24 patients with carbapenem and colistin-resistant Kp-BSI, and the 30-day mortality rate was 71% ( p ?=?0.576). In the multivariate analysis, carbapenem resistance (odds ratio (OR) 5.2, 95% confidence interval (CI) 2.47–10.9, p ??0.001) and increasing APACHE II score (OR 1.19, 95% CI 1.12–1.26, p ??0.001) were significantly associated with 30-day mortality. The addition of amikacin to the treatment regimen (OR 0.05, 95% CI 0.01–0.23, p ??0.001) was significantly beneficial. Conclusions Carbapenem resistance, increasing MIC of colistin, and the lungs as the source of the infection were significantly associated with 30-day mortality. The empirical use of combined active aminoglycosides was found to be beneficial in the treatment of colistin-resistant K. pneumoniae infections.
机译:背景技术本研究的目的是确定Colistin抗性和其他预测因子对肺炎肺炎血管感染(KP-BSI)患者的死亡作用,并描述Amikacin和Tigecycline对Oxa-48主导国家的结果的影响。方法这是一个回顾性研究,在患者中患有16岁的患者,患有465张床。所有病例均为K.1肺炎肺炎肺炎入院后48?H.结果210例KP-BSI患者中,分离微生物后的30天死亡率为58%。鲤鱼抗性的速率较高(64%vs.38%,p≤0.001),并且升高的Colistin最小抑制浓度(MIC)在死亡的患者中升高(7 vs.4,p?0.029)。在耐菌抗性K.肺炎中,牛-48,ST101和Ndm-1的速率分别为78%,67%和35%。加入Amikacin治疗13名患有Carbapenem和Colistin抗性KP-BSI的患者,77%存活(p?<0.001)。将替霉素加入到治疗24例Carbapenem和Colistin抗性KP-BSI患者中,30天死亡率为71%(P?= 0.576)。在多变量分析中,鲤鱼抗性(OTS比(或)5.2,95%置信区间(CI)2.47-10.9,P?<〜0.001)和增加Apache II得分(或1.19,95%CI 1.12-1.26,P? <?0.001)与30天死亡率显着相关。加入Amikacin至治疗方案(或0.05,95%CI 0.01-0.23,p≤0.001)显着有益。结论Carbapenem抗性,增加Colistin的MIC和肺部作为感染源与30天死亡率显着相关。发现合并的活性氨基糖苷的经验用途是有益于治疗Colistin抗性K.肺炎的感染。

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