GPT-4-based AI agents-the new expert system for detection of antimicrobial resistance mechanisms?

IF 6.1 2区 医学 Q1 MICROBIOLOGY Journal of Clinical Microbiology Pub Date : 2024-11-13 Epub Date: 2024-10-17 DOI:10.1128/jcm.00689-24
Christian G Giske, Michelle Bressan, Farah Fiechter, Vladimira Hinic, Stefano Mancini, Oliver Nolte, Adrian Egli
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Abstract

The European Committee on Antimicrobial Susceptibility Testing (EUCAST) recommends two steps for detecting beta-lactamases in Gram-negative bacteria. Screening for potential extended-spectrum beta-lactamase (ESBL), plasmid-mediated AmpC beta-lactamase, or carbapenemase production is confirmed. We aimed to validate generative pre-trained transformer (GPT)-4 and GPT-agent for pre-classification of disk diffusion to indicate potential beta-lactamases. We assigned 225 Gram-negative isolates based on phenotypic resistances against beta-lactam antibiotics and additional tests to one or more resistance mechanisms as follows: "none," "ESBL," "AmpC," or "carbapenemase." Next, we customized a GPT-agent with EUCAST guidelines and breakpoint table (v13.1). We compared routine diagnostics (reference) to those of (i) EUCAST-GPT-expert, (ii) microbiologists, and (iii) non-customized GPT-4. We determined sensitivities and specificities to flag suspect resistances. Three microbiologists showed concordance in 814/862 (94.4%) phenotypic categories and were used in median eight words (interquartile range [IQR] 4-11) for reasoning. Median sensitivity/specificity for ESBL, AmpC, and carbapenemase were 98%/99.1%, 96.8%/97.1%, and 95.5%/98.5%, respectively. Three prompts of EUCAST-GPT-expert showed concordance in 706/862 (81.9%) categories but were used in median 158 words (IQR 140-174) for reasoning. Sensitivity/specificity for ESBL, AmpC, and carbapenemase prediction were 95.4%/69.23%, 96.9%/86.3%, and 100%/98.8%, respectively. Non-customized GPT-4 could interpret 169/862 (19.6%) categories, and 137/169 (81.1%) agreed with routine diagnostics. Non-customized GPT-4 was used in median 85 words (IQR 72-105) for reasoning. Microbiologists showed higher concordance and shorter argumentations compared to GPT-agents. Humans showed higher specificities compared to GPT-agents. GPT-agent's unspecific flagging of ESBL and AmpC potentially results in additional testing, diagnostic delays, and higher costs. GPT-4 is not approved by regulatory bodies, but validation of large language models is needed.

Importance: The study titled "GPT-4-based AI agents-the new expert system for detection of antimicrobial resistance mechanisms?" is critically important as it explores the integration of advanced artificial intelligence (AI) technologies, like generative pre-trained transformer (GPT)-4, into the field of laboratory medicine, specifically in the diagnostics of antimicrobial resistance (AMR). With the growing challenge of AMR, there is a pressing need for innovative solutions that can enhance diagnostic accuracy and efficiency. This research assesses the capability of AI to support the existing two-step confirmatory process recommended by the European Committee on Antimicrobial Susceptibility Testing for detecting beta-lactamases in Gram-negative bacteria. By potentially speeding up and improving the precision of initial screenings, AI could reduce the time to appropriate treatment interventions. Furthermore, this study is vital for validating the reliability and safety of AI tools in clinical settings, ensuring they meet stringent regulatory standards before they can be broadly implemented. This could herald a significant shift in how laboratory diagnostics are performed, ultimately leading to better patient outcomes.

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基于 GPT-4 的人工智能代理--检测抗菌素耐药性机制的新专家系统?
欧洲抗菌药物敏感性检测委员会(EUCAST)建议采用两个步骤检测革兰氏阴性细菌中的β-内酰胺酶。对潜在的广谱β-内酰胺酶(ESBL)、质粒介导的 AmpC β-内酰胺酶或碳青霉烯酶的产生进行筛选确认。我们的目的是验证生成式预训练转换器(GPT)-4 和 GPT-agent,通过对磁盘扩散进行预分类来指示潜在的β-内酰胺酶。根据对β-内酰胺类抗生素的表型耐药性和其他测试结果,我们将 225 个革兰氏阴性分离株归入一种或多种耐药机制,具体如下:无"、"ESBL"、"AmpC "或 "碳青霉烯酶"。接下来,我们根据 EUCAST 指南和断点表(v13.1)定制了 GPT 试剂。我们将常规诊断(参考)与 (i) EUCAST GPT 专家、(ii) 微生物学家和 (iii) 非定制 GPT-4 的诊断进行了比较。我们确定了标记可疑耐药性的敏感性和特异性。三位微生物学家在 814/862 个(94.4%)表型类别中显示出一致性,并以中位数 8 个字(四分位数间距 [IQR] 4-11)进行推理。ESBL、AmpC和碳青霉烯酶的敏感性/特异性中位数分别为98%/99.1%、96.8%/97.1%和95.5%/98.5%。EUCAST-GPT-expert 的三个提示在 706/862 个(81.9%)类别中显示出一致性,但推理所用字数中位数为 158 个(IQR 140-174)。ESBL、AmpC和碳青霉烯酶预测的灵敏度/特异性分别为95.4%/69.23%、96.9%/86.3%和100%/98.8%。非定制 GPT-4 可解释 169/862(19.6%)个类别,137/169(81.1%)个类别与常规诊断一致。非定制 GPT-4 的推理用词中位数为 85 个(IQR 72-105)。与 GPT 代理相比,微生物学家显示出更高的一致性和更短的论证时间。与 GPT 代理相比,人类表现出更高的特异性。GPT-agent 对 ESBL 和 AmpC 的非特异性标记可能会导致额外的检测、诊断延迟和更高的成本。监管机构尚未批准 GPT-4,但需要对大型语言模型进行验证:这项题为 "基于 GPT-4 的人工智能代理--检测抗菌素耐药性机制的新专家系统?"的研究具有极其重要的意义,因为它探讨了将生成式预训练转换器(GPT)-4 等先进的人工智能(AI)技术融入实验室医学领域,特别是抗菌素耐药性(AMR)诊断领域的问题。随着 AMR 的挑战日益严峻,人们迫切需要能够提高诊断准确性和效率的创新解决方案。这项研究评估了人工智能支持欧洲抗菌药敏感性测试委员会推荐的现有两步确证流程的能力,以检测革兰氏阴性细菌中的β-内酰胺酶。人工智能有可能加快并提高初步筛查的精确度,从而缩短采取适当治疗干预措施的时间。此外,这项研究对于验证人工智能工具在临床环境中的可靠性和安全性至关重要,它能确保人工智能工具在广泛应用之前符合严格的监管标准。这可能预示着实验室诊断方式的重大转变,最终为患者带来更好的治疗效果。
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来源期刊
Journal of Clinical Microbiology
Journal of Clinical Microbiology 医学-微生物学
CiteScore
17.10
自引率
4.30%
发文量
347
审稿时长
3 months
期刊介绍: The Journal of Clinical Microbiology® disseminates the latest research concerning the laboratory diagnosis of human and animal infections, along with the laboratory's role in epidemiology and the management of infectious diseases.
期刊最新文献
Characterization of carbapenem-resistant Enterobacterales and Pseudomonas aeruginosa carrying multiple carbapenemase genes-Antimicrobial Resistance Laboratory Network, 2018-2022. A simplified pyrazinamidase test for Mycobacterium tuberculosis pyrazinamide antimicrobial susceptibility testing. Retrospective analysis of antimicrobial susceptibility profiles of non-diphtheriae Corynebacterium species from a tertiary hospital and reference laboratory, 2012-2023. Performance evaluation of the Specific Reveal system for rapid antibiotic susceptibility testing from positive blood cultures containing Gram-negative pathogens. Evaluation of the KPC/IMP/NDM/VIM/OXA-48 Combo Test Kit and Carbapenem-Resistant K.N.I.V.O. Detection K-Set in detecting KPC variants.
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