纠正医疗机构中艰难梭菌归属的新方法

Hunter Doyle, Abby L. Valek, Theresa Murillo, Ashley M. Ayres, Julie Slaughter, Madeline L. Berg, Graham M. Snyder
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摘要

摘要 目的:描述一种新的归因指标,该指标可估算出与医疗相关的艰难梭菌的因果源位置,并将其与当前的美国国家医疗安全网络(NHSN)监测报告标准进行比较。设计:质量改进研究。地点:两家急症护理机构两家急症护理机构。方法一种新的归因衡量标准将归因天数分配到患者确诊艰难梭菌病前 14 天和确诊当天所在的地点。我们将 NHSN 分配的单位归因与新型归因指标进行了关联,并比较了分配给住院单位的归因比例。结果:在 30 个月的时间里,共发生了 727 例 NHSN 艰难梭菌医护相关感染 (HAI) 和 409 例非 HAI;新指标的归因天数为 17,034 天。在设施 A 和 B 中,非重症监护病房的 NHSN 和新型归因相关系数分别为 0.79(95% CI,0.76-0.82)和 0.74(95% CI,0.70-0.78),重症监护病房的相关系数分别为 0.70(95% CI,0.63-0.76)和 0.69(95% CI,0.60-0.77)。归因百分比差异的分布显示,使用 NHSN 指标的住院病房归因高于使用新归因指标的住院病房:设施 A 中 38% 的 ICU 病房和 15% 的非 ICU 病房、设施 B 中 20% 的 ICU 病房和 25% 的非 ICU 病房的中位数差异大于 0;使用新归因指标的住院病房归因均未超过 0。结论:新型归因指标将归因从住院病房转移到了其他环境,并与 NHSN 的归因方法略有关联。如果得到验证,该归因指标可以更准确地确定减少艰难梭菌感染的目标。
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A novel approach to correcting attribution of Clostridioides difficile in a healthcare setting
Abstract Objective: To describe a novel attribution metric estimating the causal source location of healthcare-associated Clostridioides difficile and compare it with the current US National Healthcare Safety Network (NHSN) surveillance reporting standard. Design: Quality improvement study. Setting: Two acute care facilities. Methods: A novel attribution metric assigned days of attribution to locations where patients were located for 14 days before and the day of their C. difficile diagnosis. We correlated the NHSN-assigned unit attribution with the novel attribution measure and compared the proportion of attribution assigned to inpatient units. Results: During a 30-month period, there were 727 NHSN C. difficile healthcare-associated infections (HAIs) and 409 non-HAIs; the novel metric attributed 17,034 days. The correlation coefficients for NHSN and novel attributions among non-ICU units were 0.79 (95% CI, 0.76–0.82) and 0.74 (95% CI, 0.70–0.78) and among ICU units were 0.70 (95% CI, 0.63–0.76) and 0.69 (95% CI, 0.60–0.77) at facilities A and B, respectively. The distribution of difference in percent attribution showed higher inpatient unit attribution using NHSN measure than the novel attribution metric: 38% of ICU units and 15% of non-ICU units in facility A, and 20% of ICU units and 25% of non-ICU units in facility B had a median difference >0; no inpatient units showed a greater attribution using the novel attribution metric. Conclusion: The novel attribution metric shifts attribution from inpatient units to other settings and correlates modestly with NHSN methodology of attribution. If validated, the attribution metric may more accurately target C. difficile reduction efforts.
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