Zou Iris, Abate Daniel, Newman Michelle, Heil Emily L, Leekha Surbhi, Claeys Kimberly C
Department of Nursing, University of Maryland Medical Center, Baltimore, Maryland, USA.
Department of Pharmacy, Baltimore Washington Medical Center, Baltimore, Maryland, USA.
Open Forum Infect Dis. 2023 Oct 12;10(10):ofad512. doi: 10.1093/ofid/ofad512. eCollection 2023 Oct.
Early detection of multidrug-resistant (MDRP) remains challenging. Existing risk prediction tools are difficult to translate to bedside application. The goal of this study was to develop a simple electronic medical record (EMR)-integrated tool for prediction of MDRP infection.
This was a mixed-methods study. We conducted a split-sample cohort study of adult critical care patients with infections. Two previously published tools were validated using c-statistic. A subset of variables based on strength of association and ease of EMR extraction was selected for further evaluation. A simplified tool was developed using multivariable logistic regression. Both c-statistic and theoretical trade-off of over- versus underprescribing of broad-spectrum MDRP therapy were assessed in the validation cohort. A qualitative survey of frontline clinicians assessed understanding of risks for MDRP and potential usability of an EMR-integrated tool to predict MDRP.
The 2 previous risk prediction tools demonstrated similar accuracy in the derivation cohort (c-statistic of 0.76 [95% confidence interval {CI}, .69-.83] and 0.73 [95% CI, .66-.8]). A simplified tool based on 4 variables demonstrated reasonable accuracy (c-statistic of 0.71 [95% CI, .57-.85]) without significant overprescribing in the validation cohort. The risk factors were prior MDRP infection, ≥4 antibiotics prior to culture, infection >3 days after admission, and dialysis. Fourteen clinicians completed the survey. An alert providing context regarding individual patient risk factors for MDRP was preferred.
These results can be used to develop a local EMR-integrated tool to improve timeliness of effective therapy in those at risk of MDRP infections.
多重耐药病原体(MDRP)的早期检测仍然具有挑战性。现有的风险预测工具难以转化为床边应用。本研究的目的是开发一种简单的、整合电子病历(EMR)的工具来预测MDRP感染。
这是一项混合方法研究。我们对成年重症感染患者进行了一项分样本队列研究。使用c统计量对两个先前发表的工具进行了验证。基于关联强度和EMR提取的简易程度选择了一组变量进行进一步评估。使用多变量逻辑回归开发了一种简化工具。在验证队列中评估了c统计量以及广谱MDRP治疗过度处方与处方不足的理论权衡。对一线临床医生进行了定性调查,以评估他们对MDRP风险的理解以及EMR整合工具预测MDRP的潜在可用性。
之前的2种风险预测工具在推导队列中显示出相似的准确性(c统计量分别为0.76 [95%置信区间{CI},0.69 - 0.83]和0.73 [95% CI,0.66 - 0.8])。基于4个变量的简化工具显示出合理的准确性(c统计量为0.71 [95% CI,0.57 - 0.85]),在验证队列中没有明显的过度处方。风险因素为既往MDRP感染、培养前使用≥4种抗生素、入院后3天以上感染以及透析。14名临床医生完成了调查。他们更倾向于一种能提供个体患者MDRP风险因素背景信息的警报。
这些结果可用于开发一种本地EMR整合工具,以提高对有MDRP感染风险患者进行有效治疗的及时性。