识别万古霉素诱发急性肾损伤的相关因素:使用通用数据模型进行回顾性分析。

IF 0.9 4区 医学 Q4 PHARMACOLOGY & PHARMACY
Sang-In Park, Jung-Kyeom Kim, Uijeong Yu, Ji In Park
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引用次数: 0

摘要

目的:以往关于万古霉素诱发急性肾损伤(AKI)预测因素的研究结果并不一致。我们旨在利用观察性医疗结果合作组织通用数据模型确定万古霉素诱发急性肾损伤的预测因素:我们分析了 2012 年 1 月 1 日至 2022 年 5 月 31 日期间接受万古霉素治疗的患者数据,这些患者的金黄色葡萄球菌呈阳性,并接受了氧青霉素药敏试验。在排除了没有万古霉素数据或血清肌酐基线水平的患者后,最终数据集中纳入了 116 名患者。为每位患者收集了截至第三次测量万古霉素浓度的数据。使用逻辑回归模型估算了与万古霉素诱发 AKI 相关的各变量的几率比和 95% 的置信区间:结果:高基线血清肌酐水平、入住重症监护室和并发肾脏疾病与万古霉素诱发的 AKI 显著相关。虽然高谷值或曲线下面积值与万古霉素诱发的 AKI 并无明显关联,但在第二次测量万古霉素浓度时,AKI 患者的谷值或曲线下面积值均明显高于未发生 AKI 的患者。在第三次测量时,有 AKI 的患者中谷浓度大于 20 mg/L 的比例高于无 AKI 的患者:我们的研究结果表明,与万古霉素药代动力学参数或剂量相比,潜在的肾脏疾病和入住重症监护室与万古霉素诱发的 AKI 有更显著的相关性,这可能是由于临床环境中基于万古霉素浓度的剂量调整造成的。我们的研究结果可能有助于制定降低万古霉素诱发 AKI 发生率的策略;然而,进一步的前瞻性研究是必不可少的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of factors associated with vancomycin-induced acute kidney injury: A retrospective analysis using the Common Data Model.

Objective: Previous findings on predictors of vancomycin-induced acute kidney injury (AKI) are inconsistent. We aimed to identify the predictors of vancomycin-induced AKI using the Observational Medical Outcome Partnership Common Data Model.

Materials and methods: We analyzed data from patients treated with vancomycin between January 1, 2012, and May 31, 2022, who were positive for Staphylococcus aureus and had undergone oxacillin susceptibility tests. After excluding patients without data for vancomycin or baseline serum creatinine levels, 116 patients were included in the final dataset. Data up to the third measured vancomycin concentration were collected for each patient. Logistic regression models were used to estimate the odds ratio and 95% confidence interval for each variable associated with vancomycin-induced AKI.

Results: High baseline serum creatinine levels, intensive care unit admission, and concurrent renal disorders were significantly associated with vancomycin-induced AKI. Although high trough levels or area under the curve values were not significantly associated with vancomycin-induced AKI, both were significantly higher in patients with AKI than in those without AKI at the second vancomycin concentration measurement. The proportion with trough levels > 20 mg/L was higher in patients with AKI than in those without AKI at the third measurement.

Conclusion: Our findings revealed that underlying renal disease and intensive care unit admission are more significantly associated with vancomycin-induced AKI than vancomycin pharmacokinetic parameters or dosage, likely due to vancomycin concentration-based dosage adjustment in clinical settings. Our findings may help develop strategies for reducing the incidence of vancomycin-induced AKI; however, further prospective studies are essential.

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来源期刊
CiteScore
1.70
自引率
12.50%
发文量
116
审稿时长
4-8 weeks
期刊介绍: The International Journal of Clinical Pharmacology and Therapeutics appears monthly and publishes manuscripts containing original material with emphasis on the following topics: Clinical trials, Pharmacoepidemiology - Pharmacovigilance, Pharmacodynamics, Drug disposition and Pharmacokinetics, Quality assurance, Pharmacogenetics, Biotechnological drugs such as cytokines and recombinant antibiotics. Case reports on adverse reactions are also of interest.
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