Division of Infectious Diseases, MetroHealth Medical Center, Cleveland, OH; Department of Medicine, Case Western Reserve University School of Medicine, Cleveland, OH.
Department of Pharmacy, MetroHealth Medical Center, Cleveland, OH.
Am J Infect Control. 2019 Aug;47(8):869-875. doi: 10.1016/j.ajic.2019.01.026. Epub 2019 Mar 6.
Fluoroquinolones are often prescribed unnecessarily and are an important risk factor for infection with fluoroquinolone-resistant gram-negative bacilli and Clostridioides difficile.
We conducted a quasi-experimental study to determine the impact of sequential syndrome-specific stewardship interventions on use of and resistance to fluoroquinolones in a tertiary care hospital. An initial 2-year intervention focused on reducing treatment of asymptomatic bacteriuria and ensuring concordance of urinary tract infection treatment with guidelines. A second 5-year intervention focused on limiting overuse of fluoroquinolones for health care-associated pneumonia in conjunction with a formal stewardship program. The primary outcomes were fluoroquinolone use and changes in use over time analyzed by segmented regression analysis.
The asymptomatic bacteriuria and urinary tract infection intervention resulted in a significant reduction in fluoroquinolone use, with a significant change from an increasing to a decreasing rate of use (change in slope of quarterly defined daily doses/1,000 patient days -15.3, P < .01). The health care-associated pneumonia intervention resulted in a continued significant reduction in fluoroquinolone use (rate ratio = 0.68, P < .01). During the interventions, fluoroquinolone susceptibility increased significantly in Pseudomonas aeruginosa, but not in Escherichia coli, Klebsiella spp., or C difficile.
Antimicrobial stewardship interventions focused on specific syndromes may be effective in reducing fluoroquinolone use. In our hospital, reduction in fluoroquinolone use resulted in increased fluoroquinolone susceptibility in P aeruginosa, but not other Enterobacteriaceae or C difficile.
氟喹诺酮类药物经常被不必要地开处方,是感染氟喹诺酮类耐药革兰氏阴性杆菌和艰难梭菌的一个重要危险因素。
我们进行了一项准实验研究,以确定连续综合征特异性管理干预对三级保健医院氟喹诺酮类药物使用和耐药性的影响。最初的 2 年干预侧重于减少无症状菌尿的治疗,并确保尿路感染治疗与指南一致。第二项为期 5 年的干预侧重于限制与正式管理计划一起用于医疗保健相关肺炎的氟喹诺酮类药物的过度使用。主要结局是通过分段回归分析分析氟喹诺酮类药物的使用和随时间的变化。
无症状菌尿和尿路感染干预导致氟喹诺酮类药物的使用显著减少,使用量的变化从增加变为减少(每季度定义的每日剂量/ 1000 患者天的斜率变化-15.3,P <.01)。医疗保健相关肺炎的干预导致氟喹诺酮类药物的使用持续显著减少(率比= 0.68,P <.01)。在干预期间,铜绿假单胞菌的氟喹诺酮类药物敏感性显著增加,但大肠杆菌、克雷伯菌属或艰难梭菌则没有。
针对特定综合征的抗菌药物管理干预可能有效减少氟喹诺酮类药物的使用。在我们的医院中,氟喹诺酮类药物使用量的减少导致铜绿假单胞菌的氟喹诺酮类药物敏感性增加,但其他肠杆菌科或艰难梭菌则没有。