白蛋白-胆红素-纤维化-4评分预测接受治疗药物监测的患者teicoplanin诱导的异常肝酶水平:一项多中心回顾性队列研究。

IF 2.3 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Hayahide Ooi, Yuki Asai, Yoshihiro Kondo, Takumi Tashiro, Nobuyuki Zakoji, Maria Aoki, Yoshiki Koriyama, Takuya Iwamoto, Masaaki Takahashi
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引用次数: 0

摘要

背景:虽然治疗性药物监测(TDM)可维持血清teicoplanin (TEIC)浓度在15 ~ 30 μg/mL之间,但TEIC诱导的肝损伤仍可能发生。白蛋白-胆红素(ALBI)-纤维化-4 (FIB-4)评分可能有助于预测TDM患者teic诱导的肝损伤。目的:本初步研究旨在探讨ALBI-FIB4评分是否可以预测TDM患者teic诱导的肝酶异常水平。方法:采用多中心回顾性队列研究,纳入140例TEIC稳态TDM患者。主要终点是teic诱导的肝酶水平异常。采用受试者工作特征曲线检测丙氨酸转氨酶(ALT)、ALBI评分、FIB-4指数和ALBI- fib4评分的临界值。采用Kaplan-Meier曲线分析log-rank检验评价teic诱导的肝酶水平异常的累积风险。结果:TEIC诱导的肝酶水平异常发生率为14.3%(20/140)。ALT的临界值为24 IU/L(敏感性0.800;特异性:0.692;曲线下面积[AUC]: 0.753), ALBI评分为-1.33(敏感性:0.550;特异性:0.617;AUC: 0.539), FIB-4指数为2.73(灵敏度:0.700;特异性:0.475;AUC: 0.550), ALBI-FIB4评分为-0.85(敏感性:0.800;特异性:0.467;AUC: 0.572)。ALT≥24 IU/L、ALBI-FIB4评分≥-0.85时(P = 0.042) teic诱导肝酶水平异常的累积风险较高。患者血清TEIC浓度P = 0.058)。结论及相关性:ALBI-FIB4评分≥-0.85可能是TDM患者teic诱导的肝酶水平异常的潜在预测因子。然而,支持这一阈值的证据需要使用更大的数据集进行进一步的统计验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Albumin-Bilirubin-Fibrosis-4 Score for Predicting Teicoplanin-Induced Abnormal Liver Enzyme Levels in Patients Undergoing Therapeutic Drug Monitoring: A Multicentral Retrospective Cohort Study.

Background: Although therapeutic drug monitoring (TDM) maintains serum teicoplanin (TEIC) concentration between 15 and 30 μg/mL, TEIC-induced liver injury may still occur. The albumin-bilirubin (ALBI)-fibrosis-4 (FIB-4) score may be useful for predicting TEIC-induced liver injury in patients undergoing TDM.

Objective: This pilot study aimed to investigate whether the ALBI-FIB4 score can predict TEIC-induced abnormal liver enzyme levels in patients undergoing TDM.

Methods: The multicenter retrospective cohort study included 140 patients undergoing TDM of TEIC at steady state. The primary outcome was TEIC-induced abnormal liver enzyme levels. Cut-off values for the alanine aminotransferase (ALT), ALBI score, FIB-4 index, and ALBI-FIB4 score were detected using receiver-operating characteristic curves. The cumulative risk of TEIC-induced abnormal liver enzyme levels was evaluated using Kaplan-Meier curves analyzed log-rank test. Subgroup analysis was performed to examine cumulative risk in patients with serum TEIC concentration of <30 μg/mL.

Results: The incidence of TEIC-induced abnormal liver enzyme levels was 14.3% (20/140). Cut-off values were 24 IU/L for ALT (sensitivity: 0.800; specificity: 0.692; area under the curve [AUC]: 0.753), -1.33 for the ALBI score (sensitivity: 0.550; specificity: 0.617; AUC: 0.539), 2.73 for the FIB-4 index (sensitivity: 0.700; specificity: 0.475; AUC: 0.550), and -0.85 for the ALBI-FIB4 score (sensitivity: 0.800; specificity: 0.467; AUC: 0.572). The cumulative risk of TEIC-induced abnormal liver enzyme levels was significantly higher for patients with ALT ≥24 IU/L (P < 0.01) and ALBI-FIB4 score ≥-0.85 (P = 0.042). Patients with a serum TEIC concentration of <30 µg/mL exhibited a similar trend, with a higher cumulative risk for patients with ALBI-FIB4 score ≥-0.85 (P = 0.058).

Conclusion and relevance: An ALBI-FIB4 score ≥-0.85 may serve as a potential predictor for TEIC-induced abnormal liver enzyme levels in patients undergoing TDM. However, evidence supporting this threshold requires further statistical validation using a larger dataset.

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来源期刊
CiteScore
5.70
自引率
0.00%
发文量
166
审稿时长
3-8 weeks
期刊介绍: Annals of Pharmacotherapy (AOP) is a peer-reviewed journal that advances pharmacotherapy throughout the world by publishing high-quality research and review articles to achieve the most desired health outcomes.The articles provide cutting-edge information about the most efficient, safe and cost-effective pharmacotherapy for the treatment and prevention of various illnesses. This journal is a member of the Committee on Publication Ethics (COPE). Average time from submission to first decision: 14 days
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