反概率加权法可更准确地估算重症监护室医护相关感染的发病率,这是两个国家监测系统得出的结果。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-10-29 DOI:10.1016/j.jhin.2024.10.009
Costanza Vicentini, Roberta Bussolino, Matilde Perego, Daniela Silengo, Fortunato D'Ancona, Stefano Finazzi, Carla M Zotti
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引用次数: 0

摘要

背景:监测医疗相关感染(HAIs)主要采用两种方法:纵向监测(可测量发病率)和点流行率调查(PPS)。点流行率调查耗时较少,但受长度偏差采样的影响,可通过反概率加权法加以纠正。我们通过分析意大利两个国家监测系统的数据,评估了这种方法的准确性:通过前瞻性监控系统(GiViTI)测得的呼吸机相关肺炎(VAP)和中心管路相关血流感染(CLABSI)发病率与通过 PPS 测得的重症监护病房(ICU)中相同 HAIs 的粗略和反概率加权流行率换算得出的发病率估计值进行了比较。加权患病率是根据所有患者的风险时间按反比例加权得出的。使用改编版的 Rhame 和 Sudderth 公式将流行率转换为每 100 例住院的发病率:总共纳入了 30988 名通过 GiViTI 监测的患者和 1435 名通过 PPS 监测的患者。根据粗略 VAP 和 CLABSI 感染率估算的发病率与通过 GiViTI 测定的发病率之间存在明显差异(相对风险,RR 分别为 2.5 和 3.36;95% 置信区间,CI 分别为 1.42 - 4.39 和 1.33 - 8.53,p = 0.006 和 0.05)。相反,根据加权 VAP 和 CLABSI 感染率估算的发病率与通过 GiViTI 测量的发病率之间没有发现明显差异(p = 0.927 和 0.503):结论:在前瞻性监测不可行的情况下,我们的简单方法可用于从 PPS 数据中获得更准确的发病率。
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Inverse probability weighting leads to more accurate incidence estimates for healthcare associated infections in intensive care units, results from two national surveillance systems.

Background: Two main approaches are employed to monitor healthcare associated infections (HAIs): longitudinal surveillance, which allows to measure incidence rates, and point prevalence surveys (PPS). PPS are less time-consuming; however, they are affected by length-biased sampling, which can be corrected through inverse probability weighting. We assessed the accuracy of this method by analysing data from two Italian national surveillance systems.

Methods: Ventilator associated pneumonia (VAP) and central-line associated bloodstream infection (CLABSI) incidence measured through a prospective surveillance system (GiViTI) was compared to incidence estimates obtained through conversion of crude and inverse probability weighted prevalence of the same HAIs in intensive care units (ICUs) measured through a PPS. Weighted prevalence rates were obtained after weighting all patients inversely proportional to their time-at-risk. Prevalence rates were converted into incidence per 100 admissions using an adapted version of the Rhame and Sudderth formula.

Results: Overall, 30988 patients monitored through GiViTI, and 1435 patients monitored through the PPS were included. A significant difference was found between incidence rates estimated based on crude VAP and CLABSI prevalence and measured through GiViTI (relative risk, RR 2.5 and 3.36; 95% confidence interval, CI 1.42 - 4.39 and 1.33 - 8.53, p = 0.006 and 0.05 respectively). Conversely, no significant difference was found between incidence rates estimated based on weighted VAP and CLABSI prevalence and measured through GiViTI (p = 0.927 and 0.503 respectively).

Conclusion: When prospective surveillance is not feasible, our simple method could be useful to obtain more accurate incidence rates from PPS data.

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