Jaegu Kang, Jisoo Song, SeungHwan Lee, Kyung-Sang Yu, Ki Young Huh
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Recipients were categorized into high trough (> 15 mg/dL) or non-high trough (≤ 15 mg/dL) groups based on the 1st vancomycin trough concentration after surgery. The estimated glomerular filtration rates (eGFRs) based on creatinine alone (eGFR<sub>Cr</sub>), combined with cystatin C (eGFR<sub>Cr-Cys-C</sub>), and their differences (eGFR<sub>diff</sub>) were compared between the 2 groups. The association between the eGFRs and vancomycin trough concentrations was evaluated using Pearson's method. Among the 20 recipients, 13 were the high trough group and 7 were the non-high trough group. The high trough group had a significantly higher eGFR<sub>diff</sub> than non-high trough group (8.9 vs. -5.1 mL/min/1.73 m<sup>2</sup>, <i>p</i> = 0.0265), while other eGFRs were comparable. Among the three eGFR estimates, eGFR<sub>diff</sub> showed the strongest correlation (<i>r</i> = 0.41) with the first measured vancomycin trough levels. In conclusion, creatinine-based eGFR might not fully capture vancomycin pharmacokinetics in VAD recipients. The difference between eGFR<sub>Cr</sub> and eGFR<sub>Cr-Cys-C</sub> is associated with vancomycin trough concentration in VAD recipients.</p>","PeriodicalId":23288,"journal":{"name":"Translational and Clinical Pharmacology","volume":"33 2","pages":"80-89"},"PeriodicalIF":1.1000,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12242392/pdf/","citationCount":"0","resultStr":"{\"title\":\"Association between the difference in creatinine-based and creatinine-cystatin C-based estimated glomerular filtration rates and vancomycin systemic exposure after ventricular assist device surgery.\",\"authors\":\"Jaegu Kang, Jisoo Song, SeungHwan Lee, Kyung-Sang Yu, Ki Young Huh\",\"doi\":\"10.12793/tcp.2025.33.e8\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Vancomycin is widely used as a prophylactic antibiotic for ventricular assist device (VAD) implantation to prevent infections, the most common complication. As vancomycin is renally eliminated, an accurate renal function estimation is essential. However, it has been reported that creatinine-based models inaccurately estimate renal function in VAD recipients, and cystatin C could alleviate the limitation. This study analyzed the association between renal function estimation methods and vancomycin trough concentrations in VAD recipients. Clinical data of VAD recipients who received prophylactic vancomycin at Seoul National University Hospital between 2014 and 2023 were retrospectively analyzed. Recipients were categorized into high trough (> 15 mg/dL) or non-high trough (≤ 15 mg/dL) groups based on the 1st vancomycin trough concentration after surgery. The estimated glomerular filtration rates (eGFRs) based on creatinine alone (eGFR<sub>Cr</sub>), combined with cystatin C (eGFR<sub>Cr-Cys-C</sub>), and their differences (eGFR<sub>diff</sub>) were compared between the 2 groups. The association between the eGFRs and vancomycin trough concentrations was evaluated using Pearson's method. Among the 20 recipients, 13 were the high trough group and 7 were the non-high trough group. The high trough group had a significantly higher eGFR<sub>diff</sub> than non-high trough group (8.9 vs. -5.1 mL/min/1.73 m<sup>2</sup>, <i>p</i> = 0.0265), while other eGFRs were comparable. Among the three eGFR estimates, eGFR<sub>diff</sub> showed the strongest correlation (<i>r</i> = 0.41) with the first measured vancomycin trough levels. In conclusion, creatinine-based eGFR might not fully capture vancomycin pharmacokinetics in VAD recipients. The difference between eGFR<sub>Cr</sub> and eGFR<sub>Cr-Cys-C</sub> is associated with vancomycin trough concentration in VAD recipients.</p>\",\"PeriodicalId\":23288,\"journal\":{\"name\":\"Translational and Clinical Pharmacology\",\"volume\":\"33 2\",\"pages\":\"80-89\"},\"PeriodicalIF\":1.1000,\"publicationDate\":\"2025-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12242392/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Translational and Clinical Pharmacology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.12793/tcp.2025.33.e8\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/6/24 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q4\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Translational and Clinical Pharmacology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.12793/tcp.2025.33.e8","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/6/24 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0
摘要
万古霉素被广泛用作心室辅助装置(VAD)植入的预防性抗生素,以防止感染,这是最常见的并发症。由于万古霉素是肾脏消除,准确的肾功能估计是必不可少的。然而,有报道称,基于肌酐的模型不能准确地估计VAD受者的肾功能,胱抑素C可以减轻这一局限性。本研究分析了VAD受者肾功能评估方法与万古霉素谷浓度之间的关系。回顾性分析2014 - 2023年在首尔大学医院接受预防性万古霉素治疗的VAD患者的临床资料。根据术后万古霉素第一谷浓度分为高谷(≤15mg /dL)组和非高谷(≤15mg /dL)组。比较两组间单纯肌酐(eGFRCr)联合胱抑素C (eGFRCr- cys -C)估算的肾小球滤过率(eGFRs)及其差异(eGFRdiff)。使用Pearson方法评估egfr与万古霉素谷浓度之间的关系。20例患者中,高低谷组13例,非高低谷组7例。高谷组eGFRdiff显著高于非高谷组(8.9 vs. -5.1 mL/min/1.73 m2, p = 0.0265),而其他egfr具有可比性。在三种eGFR估计中,eGFRdiff与第一次测量的万古霉素谷水平相关性最强(r = 0.41)。总之,基于肌酐的eGFR可能不能完全捕获VAD受体万古霉素的药代动力学。eGFRCr和eGFRCr- cys - c之间的差异与VAD受体万古霉素谷浓度有关。
Association between the difference in creatinine-based and creatinine-cystatin C-based estimated glomerular filtration rates and vancomycin systemic exposure after ventricular assist device surgery.
Vancomycin is widely used as a prophylactic antibiotic for ventricular assist device (VAD) implantation to prevent infections, the most common complication. As vancomycin is renally eliminated, an accurate renal function estimation is essential. However, it has been reported that creatinine-based models inaccurately estimate renal function in VAD recipients, and cystatin C could alleviate the limitation. This study analyzed the association between renal function estimation methods and vancomycin trough concentrations in VAD recipients. Clinical data of VAD recipients who received prophylactic vancomycin at Seoul National University Hospital between 2014 and 2023 were retrospectively analyzed. Recipients were categorized into high trough (> 15 mg/dL) or non-high trough (≤ 15 mg/dL) groups based on the 1st vancomycin trough concentration after surgery. The estimated glomerular filtration rates (eGFRs) based on creatinine alone (eGFRCr), combined with cystatin C (eGFRCr-Cys-C), and their differences (eGFRdiff) were compared between the 2 groups. The association between the eGFRs and vancomycin trough concentrations was evaluated using Pearson's method. Among the 20 recipients, 13 were the high trough group and 7 were the non-high trough group. The high trough group had a significantly higher eGFRdiff than non-high trough group (8.9 vs. -5.1 mL/min/1.73 m2, p = 0.0265), while other eGFRs were comparable. Among the three eGFR estimates, eGFRdiff showed the strongest correlation (r = 0.41) with the first measured vancomycin trough levels. In conclusion, creatinine-based eGFR might not fully capture vancomycin pharmacokinetics in VAD recipients. The difference between eGFRCr and eGFRCr-Cys-C is associated with vancomycin trough concentration in VAD recipients.
期刊介绍:
Translational and Clinical Pharmacology (Transl Clin Pharmacol, TCP) is the official journal of the Korean Society for Clinical Pharmacology and Therapeutics (KSCPT). TCP is an interdisciplinary journal devoted to the dissemination of knowledge relating to all aspects of translational and clinical pharmacology. The categories for publication include pharmacokinetics (PK) and drug disposition, drug metabolism, pharmacodynamics (PD), clinical trials and design issues, pharmacogenomics and pharmacogenetics, pharmacometrics, pharmacoepidemiology, pharmacovigilence, and human pharmacology. Studies involving animal models, pharmacological characterization, and clinical trials are appropriate for consideration.