Laboratory of Clinical Microbiology, Department of Infectious Diseases, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico.
Department of Medicine, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico.
Microb Drug Resist. 2022 Jun;28(6):744-749. doi: 10.1089/mdr.2021.0333. Epub 2022 Mar 23.
We aimed to assess the factors associated with 30-day mortality in patients with vancomycin-resistant (VREf) bloodstream infection (BSI) who received treatment with linezolid in an 11-year retrospective cohort of patients with VREf BSI. A univariate and stepwise multivariate logistic regression analysis was performed to determine 30-day mortality factors. Moreover, a Cox proportional hazards analysis of predictor covariates of mortality was performed. Eighty patients were included in the final analysis; 42 (53%) died and 38 (47%) survived 30 days after the index bacteremia. Thirteen patients of 42 (31%) died in the first 7 days. The Acute Physiology and Chronic Health Evaluation II (APACHE II) score was significantly associated with 30-day mortality (adjusted odds ratio [aOR], 1.46; 95% confidence interval [CI]: 1.22-1.76; < 0.001) in the multivariate analysis. Moreover, VREf BSI persisting for more than 48 hours was a strong factor related to 30-day mortality (aOR, 19.6; 95% CI: 1.46-263; = 0.01). Adequate control of infection source showed a trend to be protective without reaching significance in the multivariate analysis (aOR, 0.19; 95% CI: 0.04-1.0; = 0.05). The Cox proportional hazards analysis confirmed the same significant mortality predictor besides linezolid treatment within the first 48 hours as a protective factor (hazard ratio 0.46; 95% CI: 0.23-0.92, = 0.02). Severely ill patients with high APACHE II score and persistent bacteremia have a higher risk of failure with linezolid therapy.
我们旨在评估在接受利奈唑胺治疗的万古霉素耐药(VREf)血流感染(BSI)患者中,与 30 天死亡率相关的因素,这是一项针对 VREf BSI 患者的 11 年回顾性队列研究。进行了单变量和逐步多变量逻辑回归分析,以确定 30 天死亡率的因素。此外,还对死亡率预测变量协变量进行了 Cox 比例风险分析。最终分析纳入 80 例患者;42 例(53%)在指数菌血症后 30 天死亡,38 例(47%)存活。42 例中有 13 例(31%)在第 7 天前死亡。急性生理学和慢性健康评估 II (APACHE II)评分与 30 天死亡率显著相关(调整优势比[aOR],1.46;95%置信区间[CI]:1.22-1.76; < 0.001)在多变量分析中。此外,VREf BSI 持续超过 48 小时是与 30 天死亡率相关的强因素(aOR,19.6;95% CI:1.46-263; = 0.01)。感染源的充分控制显示出在多变量分析中具有保护作用的趋势,但没有达到显著性(aOR,0.19;95% CI:0.04-1.0; = 0.05)。Cox 比例风险分析除了在 48 小时内首次使用利奈唑胺治疗外,还确认了相同的显著死亡预测因子(危险比 0.46;95% CI:0.23-0.92, = 0.02)。APACHE II 评分高且持续菌血症的重病患者使用利奈唑胺治疗失败的风险更高。