A Risk-Based Clinical Decision Support System for Patient-Specific Antimicrobial Therapy (iBiogram): Design and Retrospective Analysis

被引:9
|
作者
Muller, Lars [1 ]
Srinivasan, Aditya [1 ]
Abeles, Shira R. [2 ]
Rajagopal, Amutha [2 ]
Torriani, Francesca J. [2 ]
Aronoff-Spencer, Eliah [1 ,2 ]
机构
[1] Univ Calif San Diego, Design Lab, 9500 Gilman Dr,MC0436 Atkinson Hall, La Jolla, CA 92093 USA
[2] UC San Diego Hlth, Div Infect Dis & Global Publ Hlth, Dept Med, La Jolla, CA USA
基金
美国国家卫生研究院;
关键词
antimicrobial resistance; clinical decision support; antibiotic stewardship; data visualization; PRESCRIBING DECISIONS; ANTIBIOGRAMS; RESISTANCE; MANAGEMENT; MORTALITY; NETWORK;
D O I
10.2196/23571
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Background: There is a pressing need for digital tools that can leverage big data to help clinicians select effective antibiotic treatments in the absence of timely susceptibility data. Clinical presentation and local epidemiology can inform therapy selection to balance the risk of antimicrobial resistance and patient risk. However, data and clinical expertise must be appropriately integrated into clinical workflows. Objective: The aim of this study is to leverage available data in electronic health records, to develop a data-driven, user-centered, clinical decision support system to navigate patient safety and population health. Methods: We analyzed 5 years of susceptibility testing (1,078,510 isolates) and patient data (30,761 patients) across a large academic medical center. After curating the data according to the Clinical and Laboratory Standards Institute guidelines, we analyzed and visualized the impact of risk factors on clinical outcomes. On the basis of this data-driven understanding, we developed a probabilistic algorithm that maps these data to individual cases and implemented iBiogram, a prototype digital empiric antimicrobial clinical decision support system, which we evaluated against actual prescribing outcomes. Results: We determined patient-specific factors across syndromes and contexts and identified relevant local patterns of antimicrobial resistance by clinical syndrome. Mortality and length of stay differed significantly depending on these factors and could be used to generate heuristic targets for an acceptable risk of underprescription. Combined with the developed remaining risk algorithm, these factors can be used to inform clinicians' reasoning. A retrospective comparison of the iBiogram-suggested therapies versus the actual prescription by physicians showed similar performance for low-risk diseases such as urinary tract infections, whereas iBiogram recognized risk and recommended more appropriate coverage in high mortality conditions such as sepsis. Conclusions: The application of such data-driven, patient-centered tools may guide empirical prescription for clinicians to balance morbidity and mortality with antimicrobial stewardship.
引用
收藏
页数:14
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