Carlson Travis J, Endres Bradley T, Le Pham Julie, Gonzales-Luna Anne J, Alnezary Faris S, Nebo Kimberly, Miranda Julie, Lancaster Chris, Bassères Eugénie, Begum Khurshida, Alam M Jahangir, Reveles Kelly R, Garey Kevin W
Department of Pharmacy Practice and Translational Research, University of Houston College of Pharmacy, Houston, Texas, USA.
Department of Clinical and Hospital Pharmacy, College of Pharmacy, Taibah University, Medinah, Saudi Arabia.
Open Forum Infect Dis. 2020 Jan 4;7(1):ofz552. doi: 10.1093/ofid/ofz552. eCollection 2020 Jan.
Patients with infection (CDI) with either eosinopenia or infected with a binary toxin strain have increased likelihood of mortality. However, the relationship between binary toxin and eosinopenia to synergistically increase mortality has not been studied in humans. We hypothesized that patients with CDI due to binary toxin strains and concomitant peripheral eosinopenia would have a higher likelihood of inpatient mortality.
This multicenter, retrospective cohort study included adult patients with CDI of known ribotypes stratified by eosinopenia, defined as an absence of eosinophils in the peripheral blood (Houston cohort). The primary outcome was inpatient mortality. Results were supported by a separate national cohort of veterans with CDI (Veterans' cohort).
In the Houston cohort, a total of 688 patients from 13 institutions in 6 cities were included. Of these, 132 (19%) had an eosinophil count of 0.0 cells/µL (0.0 cells*10/L) and 109 (16%) were infected with a binary toxin strain. After adjusting for covariates, the combination of eosinopenia and infection with a binary toxin strain was an independent predictor of inpatient mortality (odds ratio [OR], 7.8; 95% confidence interval [CI], 1.9-33.2; = .005). In the separate Veterans' cohort (n = 790), this combination was also a significant predictor of inpatient mortality (OR, 6.1; 95% CI, 1.5-23.9; = .009).
In conclusion, the combination of eosinopenia and CDI due to a binary toxin strain was correlated with increased mortality in hospitalized patients from 2 independent cohorts. Prospective studies should further study this important subset of patients at the time of CDI diagnosis.
患有艰难梭菌感染(CDI)且伴有嗜酸性粒细胞减少或感染二元毒素菌株的患者死亡可能性增加。然而,二元毒素与嗜酸性粒细胞减少协同增加死亡率之间的关系尚未在人类中进行研究。我们假设,因二元毒素菌株导致CDI且伴有外周嗜酸性粒细胞减少的患者住院死亡率更高。
这项多中心回顾性队列研究纳入了已知核糖体分型的成年CDI患者,根据嗜酸性粒细胞减少进行分层,嗜酸性粒细胞减少定义为外周血中无嗜酸性粒细胞(休斯顿队列)。主要结局是住院死亡率。结果得到了一个单独的全国性退伍军人CDI队列(退伍军人队列)的支持。
在休斯顿队列中,纳入了来自6个城市13家机构的688例患者。其中,132例(19%)嗜酸性粒细胞计数为0.0个细胞/微升(0.0个细胞×10⁹/L),109例(16%)感染了二元毒素菌株。在调整协变量后,嗜酸性粒细胞减少与二元毒素菌株感染的组合是住院死亡率的独立预测因素(比值比[OR],7.8;95%置信区间[CI],1.9 - 33.2;P = 0.005)。在单独的退伍军人队列(n = 790)中,这种组合也是住院死亡率的显著预测因素(OR,6.1;95% CI,1.5 - 23.9;P = 0.009)。
总之,嗜酸性粒细胞减少与二元毒素菌株导致的CDI的组合与来自2个独立队列的住院患者死亡率增加相关。前瞻性研究应在CDI诊断时进一步研究这一重要的患者亚组。