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重新定义艰难梭菌感染的抗生素反应和临床结局。

Redefining Clostridioides difficile infection antibiotic response and clinical outcomes.

机构信息

Department of Pharmacy Practice and Translational Research, University of Houston College of Pharmacy, Houston, TX, USA.

Department of Medicine, Loyola University Medical Center, Maywood, IL, USA; Department of Medicine and Department of Research, Edward Hines Jr Veterans Administration Hospital, Hines, IL, USA.

出版信息

Lancet Infect Dis. 2023 Jul;23(7):e259-e265. doi: 10.1016/S1473-3099(23)00047-6. Epub 2023 Apr 14.

Abstract

With the approval and development of narrow-spectrum antibiotics for the treatment of Clostridioides difficile infection (CDI), the primary endpoint for treatment success of CDI antibiotic treatment trials has shifted from treatment response at end of therapy to sustained response 30 days after completed therapy. The current definition of a successful response to treatment (three or fewer unformed bowel movements [UBMs] per day for 1-2 days) has not been validated, does not reflect CDI management, and could impair assessments for successful treatment at 30 days. We propose new definitions to optimise trial design to assess sustained response. Primarily, we suggest that the initial response at the end of treatment be defined as (1) three or fewer UBMs per day, (2) a reduction in UBMs of more than 50% per day, (3) a decrease in stool volume of more than 75% for those with ostomy, or (4) attainment of bowel movements of Bristol Stool Form Scale types 1-4, on average, by day 2 after completion of primary CDI therapy (ie, assessed on day 11 and day 12 of a 10-day treatment course) and following an investigator determination that CDI treatment can be ceased.

摘要

随着窄谱抗生素治疗艰难梭菌感染 (CDI) 的批准和发展,CDI 抗生素治疗试验的主要治疗成功终点已从治疗结束时的治疗反应转移到完成治疗后 30 天的持续反应。目前对治疗成功反应的定义(治疗 1-2 天每天排便 3 次或更少的未成形粪便[UBM])尚未得到验证,不能反映 CDI 的管理,并且可能会影响 30 天治疗成功的评估。我们提出了新的定义来优化试验设计,以评估持续反应。首先,我们建议将治疗结束时的初始反应定义为:(1)每天排便 3 次或更少,(2)每天 UBM 减少超过 50%,(3)对于那些有造口的人,粪便量减少超过 75%,或(4)在完成原发性 CDI 治疗后第 2 天(即在 10 天疗程的第 11 天和第 12 天),平均达到布里斯托粪便形态量表 1-4 型,并且经研究者确定可以停止 CDI 治疗。

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