Division of Pharmacy Practice and Administration, University of Missouri-Kansas City School of Pharmacy, Kansas City, Missouri, USA; Department of Pharmacy, Centerpoint Medical Center, Independence, Missouri, USA.
Microbes Infect. 2023 Mar-Apr;25(3):105041. doi: 10.1016/j.micinf.2022.105041. Epub 2022 Sep 1.
Probiotic prophylaxis for Clostridioides difficile infection (CDI) is controversial stemming from deficits in strain and disease specificity considerations and concern for adverse effects. Here risk for healthcare facility-onset CDI (HO-CDI) dependent on concomitant antibiotic and infectious indication is assessed to identify opportunities for targeted prophylaxis.
Retrospective matched-cohort study from January 2016 through March 2019. Patient-admissions administered high risk antibiotics were categorized by Saccharomyces boulardii administration and matched 1:1 to non-recipients. Unadjusted and adjusted HO-CDI risk estimated using Cox proportional hazards regression.
S. boulardii administration was associated with 48% risk reduction for HO-CDI compared to non-recipients (aHR 0.52, 95% CI: 0.31-0.87). Patient-admissions administered antibiotics and S. boulardii for a pneumonia indication exhibited a 57% reduction in risk for HO-CDI (aHR 0.43, 95% CI: 0.19-0.95). Administration of S. boulardii with ceftriaxone was associated with a 76% reduced risk of HO-CDI (aHR 0.24, 95% CI: 0.11-0.53) compared to ceftriaxone without S. boulardii, number needed to treat of 100.
S. boulardii administration is associated with a significant HO-CDI risk reduction for inpatients receiving antibiotics associated with CDI. Institutions interested in targeted use of S. boulardii to limit potential adverse effects may consider prophylaxis for inpatients with pneumonia or receiving ceftriaxone.
由于缺乏对菌株和疾病特异性的考虑以及对不良反应的担忧,益生菌预防艰难梭菌感染(CDI)存在争议。在这里,评估了与抗生素和感染指征相关的医疗机构获得性 CDI(HO-CDI)的风险,以确定有针对性预防的机会。
这是一项回顾性匹配队列研究,时间从 2016 年 1 月到 2019 年 3 月。根据是否给予布拉氏酵母菌进行分类,并将接受高风险抗生素治疗的患者与未接受布拉氏酵母菌治疗的患者进行 1:1 匹配。使用 Cox 比例风险回归估计未调整和调整后的 HO-CDI 风险。
与未接受布拉氏酵母菌治疗的患者相比,给予布拉氏酵母菌治疗可使 HO-CDI 的风险降低 48%(aHR 0.52,95%CI:0.31-0.87)。接受抗生素和布拉氏酵母菌治疗肺炎的患者,HO-CDI 的风险降低了 57%(aHR 0.43,95%CI:0.19-0.95)。与未给予布拉氏酵母菌治疗的患者相比,给予头孢曲松和布拉氏酵母菌治疗可使 HO-CDI 的风险降低 76%(aHR 0.24,95%CI:0.11-0.53),需要治疗的患者数为 100。
对于接受与 CDI 相关的抗生素治疗的住院患者,给予布拉氏酵母菌治疗与显著降低 HO-CDI 风险相关。对于有兴趣通过靶向使用布拉氏酵母菌来限制潜在不良反应的机构,可能考虑对患有肺炎或接受头孢曲松治疗的住院患者进行预防。