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Clinical practice guidelines for therapeutic drug monitoring of teicoplanin: a consensus review by the Japanese Society of Chemotherapy and the Japanese Society of Therapeutic Drug Monitoring.替考拉宁治疗药物监测临床实践指南:日本化疗学会和日本治疗药物监测学会的共识综述。
J Antimicrob Chemother. 2022 Mar 31;77(4):869-879. doi: 10.1093/jac/dkab499.
2
Optimal trough concentration of teicoplanin for the treatment of methicillin-resistant Staphylococcus aureus infection: A systematic review and meta-analysis.替考拉宁治疗耐甲氧西林金黄色葡萄球菌感染的最佳谷浓度:系统评价和荟萃分析。
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3
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Basic Clin Pharmacol Toxicol. 2020 Mar;126(3):277-288. doi: 10.1111/bcpt.13338. Epub 2019 Oct 28.
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Eur J Clin Microbiol Infect Dis. 2019 Nov;38(11):2113-2120. doi: 10.1007/s10096-019-03652-6. Epub 2019 Aug 1.
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Infect Drug Resist. 2018 Jan 5;11:29-36. doi: 10.2147/IDR.S146961. eCollection 2018.
10
Therapeutic Drug Monitoring of Teicoplanin in Haematological Malignancy Patients with Febrile Neutropenia and Optimizing Dosage Regimens.替考拉宁治疗血液系统恶性肿瘤合并发热性中性粒细胞减少症患者的药物监测及优化剂量方案。
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JAC Antimicrob Resist. 2025 Aug 21;7(4):dlaf151. doi: 10.1093/jacamr/dlaf151. eCollection 2025 Aug.
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Front Pharmacol. 2025 Jul 1;16:1621959. doi: 10.3389/fphar.2025.1621959. eCollection 2025.
3
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Drug Des Devel Ther. 2025 Jun 9;19:4967-4977. doi: 10.2147/DDDT.S516472. eCollection 2025.
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Population pharmacokinetics and dosing optimization of teicoplanin in renal transplant patients.替考拉宁在肾移植患者中的群体药代动力学及给药优化
Antimicrob Agents Chemother. 2025 Jun 4;69(6):e0156824. doi: 10.1128/aac.01568-24. Epub 2025 Apr 23.
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Drug Des Devel Ther. 2024 Nov 8;18:5073-5086. doi: 10.2147/DDDT.S474470. eCollection 2024.
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Adv Ther. 2024 Jul;41(7):2966-2977. doi: 10.1007/s12325-024-02884-z. Epub 2024 May 14.

本文引用的文献

1
Enhanced loading dose of teicoplanin for three days is required to achieve a target trough concentration of 20 μg/mL in patients receiving continuous venovenous haemodiafiltration with a low flow rate.对于接受低流量持续静脉-静脉血液透析滤过的患者,需要增强替考拉宁负荷剂量,连续给药 3 天,以达到目标谷浓度 20μg/mL。
J Infect Chemother. 2022 Feb;28(2):232-237. doi: 10.1016/j.jiac.2021.10.023. Epub 2021 Nov 27.
2
Performance of Area under the Concentration-Time Curve Estimations of Vancomycin with Limited Sampling by a Newly Developed Web Application.新型网络应用程序对万古霉素有限采样浓度时间曲线下面积估算性能的评估。
Pharm Res. 2021 Apr;38(4):637-646. doi: 10.1007/s11095-021-03030-y. Epub 2021 Mar 29.
3
From Therapeutic Drug Monitoring to Model-Informed Precision Dosing for Antibiotics.从治疗药物监测到抗生素模型指导下的精准给药。
Clin Pharmacol Ther. 2021 Apr;109(4):928-941. doi: 10.1002/cpt.2202. Epub 2021 Mar 16.
4
The monitoring of vancomycin: a systematic review and meta-analyses of area under the concentration-time curve-guided dosing and trough-guided dosing.万古霉素的监测:基于浓度-时间曲线下面积指导给药和谷值指导给药的系统评价和荟萃分析。
BMC Infect Dis. 2021 Feb 6;21(1):153. doi: 10.1186/s12879-021-05858-6.
5
Optimal trough concentration of teicoplanin for the treatment of methicillin-resistant Staphylococcus aureus infection: A systematic review and meta-analysis.替考拉宁治疗耐甲氧西林金黄色葡萄球菌感染的最佳谷浓度:系统评价和荟萃分析。
J Clin Pharm Ther. 2021 Jun;46(3):622-632. doi: 10.1111/jcpt.13366. Epub 2021 Feb 6.
6
Pharmacokinetic/pharmacodynamic evaluation of teicoplanin against Staphylococcus aureus in a murine thigh infection model.替考拉宁对金黄色葡萄球菌引起的小鼠大腿感染模型的药代动力学/药效学评价。
J Glob Antimicrob Resist. 2021 Mar;24:83-87. doi: 10.1016/j.jgar.2020.11.014. Epub 2020 Dec 5.
7
Clinical efficacy and safety in patients treated with teicoplanin with a target trough concentration of 20 μg/mL using a regimen of 12 mg/kg for five doses within the initial 3 days.治疗患者时采用替考拉宁目标谷浓度 20μg/mL,方案为初始 3 天内给予 12mg/kg,5 剂,观察临床疗效和安全性。
BMC Pharmacol Toxicol. 2020 Jul 8;21(1):50. doi: 10.1186/s40360-020-00424-3.
8
Prospective validation of a model-informed precision dosing tool for vancomycin in intensive care patients.前瞻性验证 ICU 患者万古霉素模型指导下精准给药工具。
Br J Clin Pharmacol. 2020 Dec;86(12):2497-2506. doi: 10.1111/bcp.14360. Epub 2020 Jun 5.
9
Population Pharmacokinetics of Teicoplanin in Preterm and Term Neonates: Is It Time for a New Dosing Regimen?替考拉宁在早产儿和足月儿中的群体药代动力学:是时候采用新的给药方案了吗?
Antimicrob Agents Chemother. 2020 Mar 24;64(4). doi: 10.1128/AAC.01971-19.
10
Optimal teicoplanin loading regimen to rapidly achieve target trough plasma concentration in critically ill patients.优化替考拉宁负荷剂量方案以快速达到危重症患者的目标谷浓度。
Basic Clin Pharmacol Toxicol. 2020 Mar;126(3):277-288. doi: 10.1111/bcpt.13338. Epub 2019 Oct 28.

替考拉宁治疗药物监测临床实践指南:日本化疗学会和日本治疗药物监测学会的共识综述。

Clinical practice guidelines for therapeutic drug monitoring of teicoplanin: a consensus review by the Japanese Society of Chemotherapy and the Japanese Society of Therapeutic Drug Monitoring.

机构信息

Department of Pharmacy, Toho University Omori Medical Center, Tokyo, Japan.

Department of Pharmacy, Hyogo College of Medicine, Nishinomiya, Japan.

出版信息

J Antimicrob Chemother. 2022 Mar 31;77(4):869-879. doi: 10.1093/jac/dkab499.

DOI:10.1093/jac/dkab499
PMID:35022752
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8969460/
Abstract

BACKGROUND

Owing to its low risk of adverse effects, teicoplanin has been extensively used in patients with infections caused by MRSA. To promote the better management of patients receiving teicoplanin, we have updated the guidelines for therapeutic drug monitoring (TDM).

METHODS

The guidelines were developed by a committee following the methodology handbook published by the Japanese Medical Information Distribution Service. Nine clinical questions were selected. The committee conducted a systematic review and meta-analysis to establish evidence-based recommendations for the target trough concentration (Cmin). An initial electronic database search returned 515 articles, and 97 articles qualified for a full review. Four and five studies were included for the efficacy evaluation of cut-off Cmin values of 15 and 20 mg/L, respectively.

RESULTS

Compared with Cmin < 15 mg/L, a target Cmin value of 15-30 mg/L resulted in increased clinical efficacy in patients with non-complicated MRSA infections (OR = 2.68; 95% CI = 1.14-6.32) without an increase in adverse effects. Although there was insufficient evidence, target Cmin values of 20-40 mg/L were suggested in patients with complicated or serious MRSA infections. A 3 day loading regimen followed by maintenance treatment according to renal function was recommended to achieve the target trough concentrations. Because of the prolonged half-life of teicoplanin, measurement of the Cmin value on Day 4 before reaching steady state was recommended.

CONCLUSIONS

The new guideline recommendations indicate the target Cmin value for TDM and the dosage regimen to achieve this concentration and suggest practices for specific subpopulations.

摘要

背景

由于替考拉宁不良反应风险低,已广泛用于治疗耐甲氧西林金黄色葡萄球菌(MRSA)感染。为了更好地管理接受替考拉宁治疗的患者,我们更新了治疗药物监测(TDM)指南。

方法

该指南由一个委员会根据日本医学信息分发服务发布的方法手册制定。选择了 9 个临床问题。委员会进行了系统评价和荟萃分析,为目标谷浓度(Cmin)建立了基于证据的推荐意见。最初的电子数据库搜索返回了 515 篇文章,其中 97 篇文章符合全文审查标准。对于截断 Cmin 值分别为 15 和 20 mg/L 的疗效评估,分别纳入了 4 项和 5 项研究。

结果

与 Cmin < 15 mg/L 相比,目标 Cmin 值为 15-30 mg/L 可提高非复杂性 MRSA 感染患者的临床疗效(OR=2.68;95%CI=1.14-6.32),而不增加不良反应。虽然证据不足,但建议复杂性或严重 MRSA 感染患者的目标 Cmin 值为 20-40 mg/L。建议采用 3 天负荷剂量方案,然后根据肾功能进行维持治疗,以达到目标谷浓度。由于替考拉宁半衰期较长,建议在达到稳态前第 4 天测量 Cmin 值。

结论

新指南建议了 TDM 的目标 Cmin 值和实现该浓度的剂量方案,并为特定亚群提出了实践建议。