硬停止艰难梭菌检测的效果:提供者的吸收和患者的结果

Danielle Doughman, David Weber, Nikolaos Mavrogiorgos, Shelley Summerlin-Long, Michael Swartwood, Alexander Commanday, Lisa Stancill, Nicholas Kane, Emily Sickbert-Bennett Vavalle
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引用次数: 0

摘要

背景:艰难梭菌感染(CDI)是一种严重的卫生保健相关感染,每年导致美国12,000人死亡。当患者被梭状芽胞杆菌定植,但未被感染,但尚未治疗时,过度检测可能导致抗生素的过度使用和潜在的患者伤害。国家指南建议何时进行适当的检测;偶尔,不符合指南的测试(GNCT)可能是必要的。北卡罗来纳大学医学中心(UNCMC)的一个多学科小组,包括抗菌剂管理计划(ASP),在2020年使用了最佳实践警报来改善诊断管理,但没有效果。有证据支持为此目的使用硬止流器,尽管对提供者的接受程度知之甚少。方法:从2022年5月开始,UNCMC在其电子病历系统(EMR)中实施了艰难梭菌GNCT订单的硬性停止,但由ASP主治医生批准的例外情况除外。回顾性审查了2022年5月至11月的请求,以监测不良患者结局和提供者硬停依从性。该团队从EMR (Epic Systems)导出数据,并在Microsoft Excel中生成描述性统计数据。结果:研究期间共有85个GNCT目。大多数测试(62%)由ASP审查,38%寻求非ASP或没有批准。在ASP审查的测试中,33项(62%)获得批准,20项(38%)未获得批准。在未被ASP批准的测试中,没有患者随后接受了CDI指导的抗生素,1名患者(5%)需要同一入院进行CDI测试(阴性)。在规避ASP审查的测试中,18家(56%)订购提供商收到了副首席医疗官的后续电子邮件,以确定理由。没有单一的反应类型占主导地位:3人(17%)不知道ASP审查要求,2人(11%)表示他们的患者未知地拒绝泻药,2人(11%)表示其他患者特有的原因。供应商对ASP审批机制的回避减少了38%,从第1个月53%的不合规测试减少到第6个月33%的不合规测试。总测试订单从2021年同期的1129个下降到研究期间的954个,下降了15.5% (95% CI, 13.4%-17.7%)。CDI检测前至少48小时无泻药间隔的指导成分依从性从85% (95% CI, 83%-87%)增加到95% (95% CI, 93%-96%)。CDI的发病率从0.52 / 1000患者日(95% CI, 0.41 - 0.65)下降到0.41 / 1000患者日(95% CI, 0.32-0.53),尽管变化在P = 0.05时并不显著,也不能归因于任何1次干预。结论:随着时间的推移和对规避例外流程的提供者的反馈,提供者接受并使用了硬停止,改善了诊断管理并避免了不必要的治疗。披露:没有
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of a hard stop for C. difficile testing: Provider uptake and patient outcomes
Background: Clostridioides difficile infection (CDI) is a serious healthcare-associated infection responsible for >12,000 US deaths annually. Overtesting can lead to antibiotic overuse and potential patient harm when patients are colonized with C. difficile , but not infected, yet treated. National guidelines recommend when testing is appropriate; occasionally, guideline-noncompliant testing (GNCT) may be warranted. A multidisciplinary group at UNC Medical Center (UNCMC) including the antimicrobial stewardship program (ASP) used a best-practice alert in 2020 to improve diagnostic stewardship, to no effect. Evidence supports use of hard stops for this purpose, though less is known about provider acceptance. Methods: Beginning in May 2022, UNCMC implemented a hard stop in its electronic medical record system (EMR) for C. difficile GNCT orders, with exceptions to be approved by an ASP attending physician. Requests were retrospectively reviewed May–November 2022 to monitor for adverse patient outcomes and provider hard-stop compliance. The team exported data from the EMR (Epic Systems) and generated descriptive statistics in Microsoft Excel. Results: There were 85 GNCT orders during the study period. Most tests (62%) were reviewed by the ASP, and 38% sought non-ASP or no approval. Of the tests reviewed by the ASP, 33 (62%) were approved and 20 (38%) were not. Among tests not approved by the ASP, no patients subsequently received CDI-directed antibiotics, and 1 patient (5%) warranted same-admission CDI testing (negative). Of tests that circumvented ASP review, 18 (56%) ordering providers received a follow-up email from an associate chief medical officer to determine the rationale. No single response type dominated: 3 (17%) were unaware of the ASP review requirement, 2 (11%) indicated their patient’s uncharted refusal of laxatives, 2 (11%) indicated another patient-specific reason. Provider avoidance of the ASP approval mechanism decreased 38%, from 53% of noncompliant tests in month 1 to 33% of tests in month 6. Total tests orders dropped 15.5% from 1,129 during the same period in 2021 to 954 during the study period (95% CI, 13.4%–17.7%). Compliance with the guideline component requiring at least a 48-hour laxative-free interval prior to CDI testing increased from 85% (95% CI, 83%–87%) to 95% (95% CI, 93%–96%). CDI incidence rates decreased from 0.52 per 1,000 patient days (95% CI, 0.41–0.65) to 0.41 (95% CI, 0.32–0.53), though the change was neither significant at P = .05 nor attributable to any 1 intervention. Conclusions: Over time and with feedback to providers circumventing the exception process, providers accepted and used the hard stop, improving diagnostic stewardship and avoiding unneeded treatment. Disclosures: None
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