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首页> 外文期刊>Bone marrow transplantation >Impact of choice, timing, sequence and combination of broad-spectrum antibiotics on the outcome of allogeneic haematopoietic stem cell transplantation
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Impact of choice, timing, sequence and combination of broad-spectrum antibiotics on the outcome of allogeneic haematopoietic stem cell transplantation

机译:广谱抗生素的选择,时序,序列和组合对同种异体造血干细胞移植的结果

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摘要

Recent data link the incidence of intestinal GvHD (iGvHD) after allogeneic haematopoietic stem cell transplantation (aSCT) to exposure with piperacillin-tazobactam or imipenem-cilastatin. To assess relevance of timing, duration, sequence and combination of antibiotic treatment in this setting, we applied a time-dependent model to our aSCT cohort. Patients from the prospective Cologne Cohort of Neutropenic Patients (CoCoNut) undergoing aSCT from January 2007 to April 2013 were included into a time-dependent multivariate Cox proportional hazards regression model with backward-stepwise selection. In 399 eligible patients, cumulative antibiotic exposure (hazard ratio (HR) 2.46; 95% confidence interval (95% CI) 1.59-3.81; P 0.001) and exposure to sequential treatment with penicillin derivatives and carbapenems (HR 6.22, 95% CI 1.27-30.31), but not to the individual classes, were associated with iGvHD at day 100. Glycopeptides were assessed as a risk factor (HR 3.73, 95% CI 1.51-9.19), but not considered independent, since their use was dependent on previous exposure to penicillin derivatives and carbapenems. Patients with iGvHD presented with increased non-relapse mortality at day 365 (HR 3.51; 95% CI 2.10-5.89; P 0.001). We identified sequential exposure to penicillin derivatives and carbapenems as well as overall exposure to antibiotics as independent risk factors for iGVHD. Confirmation of these findings in larger, prospective cohorts is necessary.
机译:最近的数据链在同种异体造血干细胞移植(ASCT)与哌啶蛋白-TaZobactam或ImipeNem-Cilastatin接触后的肠GVHD(IgVHD)的发生率。为了评估在该设置中的时序,持续时间,序列和抗生素治疗组合的相关性,我们将时间依赖模型应用于我们的ASCT队列。从2007年1月到2013年1月到2013年1月至2013年4月的前瞻性科隆群体(椰子)的患者被纳入时间依赖于逐步选择的时间多变量Cox比例危险回归模型。在399名符合条件的患者中,累积抗生素暴露(危害比(HR)2.46; 95%置信区间(95%CI)1.59-3.81; P <0.001)和用青霉素衍生物和碳癌烯胺(HR 6.22,95%)的顺序治疗CI 1.27-30.31)但不是个体类别,在100天的IgVHD中与IgVHD相关。糖肽被评估为危险因素(HR 3.73,95%CI 1.51-9.19),但由于它们的使用依赖,因此不被认为是独立的以前暴露于青霉素衍生物和CarbapeNems。 IGVHD患者在365天(HR 3.51; 95%CI 2.10-5.89; P <0.001)增加,患有IGVHD的非复发死亡率增加。我们鉴定了对青霉素衍生物和肉豆蔻衍生物和碳青霉素的连续接触,以及整体暴露于抗生素作为IGVHD的独立危险因素。在更大的预期队列中确认这些发现是必要的。

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  • 来源
    《Bone marrow transplantation》 |2018年第1期|共6页
  • 作者单位

    Univ Hosp Cologne Dept Internal Med 1 Cologne Germany;

    Univ Hosp Cologne Dept Internal Med 1 Cologne Germany;

    Univ Hosp Cologne Dept Internal Med 1 Cologne Germany;

    Univ Hosp Cologne Dept Internal Med 1 Cologne Germany;

    Univ Hosp Cologne Dept Internal Med 1 Cologne Germany;

    Univ Hosp Cologne Dept Internal Med 1 Cologne Germany;

    Univ Hosp Cologne Dept Internal Med 1 Cologne Germany;

    German Ctr Infect Res DZIF Partner Site Bonn Cologne Cologne Germany;

    Univ Hosp Cologne Inst Med Microbiol Immunol &

    Hyg Cologne Germany;

    Univ Hosp Cologne Dept Internal Med 1 Cologne Germany;

    Univ Hosp Cologne Dept Internal Med 1 Cologne Germany;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 治疗学;
  • 关键词

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