Department of Pharmacy, Gifu University Hospital, Gifu, Japan.
Center for Nutrition Support & Infection Control, Gifu University Hospital, Gifu, Japan.
J Clin Pharm Ther. 2019 Jun;44(3):454-462. doi: 10.1111/jcpt.12809. Epub 2019 Feb 5.
Implementation of an antifungal stewardship programme is a recognized need. However, there is insufficient information to confirm the impact of antifungal stewardship interventions. Further, few studies have evaluated the clinical effects of an antifungal stewardship intervention using 1-3, β-D-glucan (βDG) testing. The aim of the present study was to evaluate the impact of implementing an antifungal stewardship with monitoring of βDG values on antifungal use and clinical outcomes.
A single institutional prospective cohort study was conducted to evaluate the impact of implementing daily reviews of antifungal agents and monitoring patients who measured βDG values since August 2013. Antifungal consumption and clinical outcomes in patients with Candida bloodstream infection were compared before and after the intervention.
After implementation of the programme, parental antifungal use was significantly reduced compared to that before intervention (P = 0.006). In the after-intervention group, the rate of 60-day clinical failure in patients with Candida bloodstream infection was significantly reduced, from 80.0% (28/35) to 36.4% (8/22) (P < 0.001), and the rate of 60-day mortality associated with Candida bloodstream infection tended to be reduced, from 42.9% (15/35) to 18.2% (4/22) (P = 0.081) compared to the before-intervention group. The incidence of adverse events associated with antifungal agents was significantly lower in the after-intervention group than in the before-intervention group (51.4% [18/35] vs 13.6% [3/22], P = 0.004).
Our findings suggest that daily review of the use of antifungal agents and monitoring of measured βDG values was highly effective in reducing antifungal consumption and improving the clinical outcomes of patients with Candida bloodstream infection.
实施抗真菌药物管理计划是公认的需要。然而,目前尚缺乏信息来确认抗真菌药物管理干预的影响。此外,很少有研究使用 1-3-β-D-葡聚糖(βDG)检测评估抗真菌药物管理干预的临床效果。本研究旨在评估实施抗真菌药物管理并监测βDG 值对抗真菌药物使用和临床结果的影响。
进行了一项单机构前瞻性队列研究,以评估自 2013 年 8 月以来,每天审查抗真菌药物并监测βDG 值的患者对使用抗真菌药物和临床结果的影响。比较了念珠菌血流感染患者在干预前后的抗真菌药物消耗和临床结局。
方案实施后,与干预前相比,父母代抗真菌药物使用明显减少(P=0.006)。在干预后组中,念珠菌血流感染患者 60 天临床失败率显著降低,从 80.0%(28/35)降至 36.4%(8/22)(P<0.001),念珠菌血流感染相关 60 天死亡率也呈降低趋势,从 42.9%(15/35)降至 18.2%(4/22)(P=0.081),与干预前组相比。干预后组抗真菌药物相关不良事件发生率明显低于干预前组(51.4%[18/35] vs 13.6%[3/22],P=0.004)。
我们的研究结果表明,每天审查抗真菌药物的使用情况并监测βDG 值可以显著减少抗真菌药物的使用,并改善念珠菌血流感染患者的临床结局。