Kueht Michael, Kharsa Ahmad, Mujtaba Muhammad, Kulkarni Rupak, Britt Rachel, Lea A Scott, Hafiz Ghani, Fair Jeffery, Reynoso David
Division of Transplant Surgery, Department of Surgery.
School of Medicine.
Transplant Proc. 2022 Apr;54(3):605-609. doi: 10.1016/j.transproceed.2021.10.034. Epub 2022 Mar 3.
Diarrhea among recipients of solid organ transplants is a commonly encountered problem and is often multifactorial in etiology. Owing to the combination of perioperative antibiotic administration and the immunosuppressed status of transplant recipients, a high degree of suspicion for Clostridioides difficile (C. difficile) colitis is prudent. The purpose of this study is to demonstrate the association of an institutional integrated stewardship program with C. difficile testing practices after abdominal solid organ transplantation.
Starting in July 2017, a diagnostic stewardship was enacted in our institution requiring the ordering provider to answer a series of questions within the electronic medical record before ordering a C. difficile toxin test. The charts were reviewed for all solid organ transplant recipients on whom a test was ordered between January 2016 and September 2019.
Orders for C. difficile toxin per quarter significantly decreased in the postintervention era (18 vs 8.5, P = .038). Median cost of inpatient treatment and days of therapy per thousand patient days was significantly lower in the postintervention era (median cost, $2,944.55 vs $416.92; P = .01) (days of therapy per thousand patient days, 521.9 vs 300.5; P < .01). Quarterly rates of negative tests were similar between the pre- and postintervention eras (65% vs 73%, P = .38).
Although no orders were blocked based on the responses, this multilevel intervention was associated with a 47% decrease in C. difficile testing without effecting the rate of negative testing. These results suggest that we have achieved significant cost savings, in testing and isolation, without sacrificing critical aspects of clinical care.
实体器官移植受者腹泻是一个常见问题,病因通常是多因素的。由于围手术期使用抗生素以及移植受者的免疫抑制状态,对艰难梭菌结肠炎高度怀疑是谨慎的做法。本研究的目的是证明机构综合管理计划与腹部实体器官移植后艰难梭菌检测实践之间的关联。
从2017年7月开始,我们机构制定了一项诊断管理措施,要求开单医生在开具艰难梭菌毒素检测单之前,在电子病历中回答一系列问题。对2016年1月至2019年9月期间接受检测的所有实体器官移植受者的病历进行了回顾。
干预后时期每季度艰难梭菌毒素检测单显著减少(18份对8.5份,P = 0.038)。干预后时期住院治疗的中位数费用和每千患者日的治疗天数显著降低(中位数费用,2944.55美元对416.92美元;P = 0.01)(每千患者日的治疗天数,521.9天对300.5天;P < 0.01)。干预前后时期每季度的阴性检测率相似(65%对73%,P = 0.38)。
尽管没有根据回答阻止任何检测单开具,但这种多层面干预与艰难梭菌检测减少47%相关,且未影响阴性检测率。这些结果表明,我们在检测和隔离方面实现了显著的成本节约,同时没有牺牲临床护理的关键方面。