• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Quantitative Analysis of Gentamicin Exposure in Neonates and Infants Calls into Question Its Current Dosing Recommendations.对新生儿和婴儿庆大霉素暴露情况的定量分析对其目前的推荐剂量提出了质疑。
Antimicrob Agents Chemother. 2018 Mar 27;62(4). doi: 10.1128/AAC.02004-17. Print 2018 Apr.
2
Optimizing gentamicin conventional and extended interval dosing in neonates using Monte Carlo simulation - a retrospective study.利用蒙特卡罗模拟优化新生儿庆大霉素常规和延长间隔给药 - 一项回顾性研究。
BMC Pediatr. 2019 Sep 6;19(1):318. doi: 10.1186/s12887-019-1676-3.
3
Extended-interval Dosing of Gentamicin in Premature Neonates Born at <32 Weeks' Gestation and >7 Days of age.孕周<32周且日龄>7天的早产新生儿庆大霉素延长给药间隔方案
Clin Ther. 2017 Jun;39(6):1233-1241. doi: 10.1016/j.clinthera.2017.05.343. Epub 2017 May 31.
4
Validation of a dosage individualization table for extended-interval gentamicin in neonates.验证新生儿延长间隔时间使用庆大霉素的剂量个体化表。
Ann Pharmacother. 2012 Jul-Aug;46(7-8):935-42. doi: 10.1345/aph.1R029. Epub 2012 Jun 26.
5
Pharmacokinetic outcomes of a simplified, weight-based, extended-interval gentamicin dosing protocol in critically ill neonates.危重新生儿简化、基于体重、延长间隔的庆大霉素给药方案的药代动力学结果。
Pharmacotherapy. 2009 Nov;29(11):1297-305. doi: 10.1592/phco.29.11.1297.
6
Extended-Interval Dosing of Gentamicin Aiming for a Drug-Free Period in Neonates: A Prospective Cohort Study.以新生儿无药期为目标的庆大霉素延长给药间隔:一项前瞻性队列研究。
Ther Drug Monit. 2016 Jun;38(3):402-6. doi: 10.1097/FTD.0000000000000283.
7
Gentamicin pharmacokinetics and dosing in neonates with hypoxic ischemic encephalopathy receiving hypothermia.新生儿缺氧缺血性脑病行低温治疗时的庆大霉素药代动力学和剂量。
Pharmacotherapy. 2013 Jul;33(7):718-26. doi: 10.1002/phar.1263. Epub 2013 Apr 1.
8
Comparison of two gentamicin dosing schedules in very low birth weight infants.极低出生体重儿两种庆大霉素给药方案的比较。
Pediatr Infect Dis J. 2002 Mar;21(3):234-40. doi: 10.1097/00006454-200203000-00014.
9
Dose Optimization of Gentamicin in Critically Ill Neonates.危重新生儿庆大霉素的剂量优化。
Curr Drug Metab. 2020;21(4):270-280. doi: 10.2174/1389200221666200512111131.
10
Application of Physiologically Based Pharmacokinetic-Pharmacodynamic Modeling in Preterm Neonates to Guide Gentamicin Dosing Decisions and Predict Antibacterial Effect.生理药代动力学-药效动力学模型在指导早产儿中庆大霉素剂量决策和预测抗菌效果中的应用。
J Clin Pharmacol. 2021 Oct;61(10):1356-1365. doi: 10.1002/jcph.1890. Epub 2021 Jun 8.

引用本文的文献

1
A Quantitative Examination and Comparison of the Ability of Australian Gentamicin Dosing Guidelines to Achieve Target Therapeutic Concentrations in Neonates.澳大利亚庆大霉素给药指南在新生儿中达到目标治疗浓度能力的定量检测与比较
Antibiotics (Basel). 2025 Jan 8;14(1):48. doi: 10.3390/antibiotics14010048.
2
Pharmacokinetic model-guided enoxaparin dosing in the Neonatal ICU: Retrospective cohort study to plan for prospective feasibility trial.药代动力学模型指导新生儿重症监护室依诺肝素给药:为前瞻性可行性试验而进行的回顾性队列研究。
Clin Transl Sci. 2024 Oct;17(10):e70040. doi: 10.1111/cts.70040.
3
Physiologically Based Pharmacokinetic Modeling in Neonates: Current Status and Future Perspectives.新生儿基于生理学的药代动力学建模:现状与未来展望。
Pharmaceutics. 2023 Dec 12;15(12):2765. doi: 10.3390/pharmaceutics15122765.
4
Pragmatic physiologically-based pharmacokinetic modeling to support clinical implementation of optimized gentamicin dosing in term neonates and infants: proof-of-concept.基于生理学的实用药代动力学建模,以支持足月儿和婴儿优化庆大霉素给药方案的临床实施:概念验证
Front Pediatr. 2023 Nov 21;11:1288376. doi: 10.3389/fped.2023.1288376. eCollection 2023.
5
Evaluation of Dosing Guidelines for Gentamicin in Neonates and Children.新生儿及儿童庆大霉素给药指南的评估
Antibiotics (Basel). 2023 Apr 25;12(5):810. doi: 10.3390/antibiotics12050810.
6
Use of Antibiotics in Preterm Newborns.早产儿抗生素的使用
Antibiotics (Basel). 2022 Aug 23;11(9):1142. doi: 10.3390/antibiotics11091142.
7
Exposure to an Extended-Interval, High-Dose Gentamicin Regimen in the Neonatal Period Is Not Associated With Long-Term Nephrotoxicity.新生儿期接受延长间隔、高剂量庆大霉素治疗方案与长期肾毒性无关。
Front Pediatr. 2021 Nov 30;9:779827. doi: 10.3389/fped.2021.779827. eCollection 2021.
8
Gentamicin Population Pharmacokinetics in Pediatric Patients-A Prospective Study with Data Analysis Using the saemix Package in R.儿科患者庆大霉素群体药代动力学——一项使用R语言中的saemix软件包进行数据分析的前瞻性研究
Pharmaceutics. 2021 Oct 1;13(10):1596. doi: 10.3390/pharmaceutics13101596.
9
Saliva as a sampling matrix for therapeutic drug monitoring of gentamicin in neonates: A prospective population pharmacokinetic and simulation study.唾液作为新生儿庆大霉素治疗药物监测的采样基质:一项前瞻性群体药代动力学和模拟研究。
Br J Clin Pharmacol. 2022 Feb;88(4):1845-1855. doi: 10.1111/bcp.15105. Epub 2021 Nov 7.
10
Recent advances in the ontogeny of drug disposition.药物处置的个体发育中最近的进展。
Br J Clin Pharmacol. 2022 Oct;88(10):4267-4284. doi: 10.1111/bcp.14821. Epub 2021 Apr 15.

本文引用的文献

1
Surviving Sepsis Campaign: International Guidelines for Management of Sepsis and Septic Shock: 2016.拯救脓毒症运动:脓毒症和脓毒性休克管理国际指南:2016 年版。
Intensive Care Med. 2017 Mar;43(3):304-377. doi: 10.1007/s00134-017-4683-6. Epub 2017 Jan 18.
2
A description of medication errors reported by pharmacists in a neonatal intensive care unit.描述药剂师在新生儿重症监护病房报告的药物错误。
Int J Clin Pharm. 2017 Feb;39(1):88-94. doi: 10.1007/s11096-016-0399-x. Epub 2016 Nov 30.
3
Global, regional, and national causes of under-5 mortality in 2000-15: an updated systematic analysis with implications for the Sustainable Development Goals.2000 - 2015年全球、区域和国家五岁以下儿童死亡原因:一项最新的系统分析及其对可持续发展目标的启示
Lancet. 2016 Dec 17;388(10063):3027-3035. doi: 10.1016/S0140-6736(16)31593-8. Epub 2016 Nov 11.
4
High target attainment for β-lactam antibiotics in intensive care unit patients when actual minimum inhibitory concentrations are applied.当应用实际最低抑菌浓度时,重症监护病房患者对β-内酰胺类抗生素的高目标达成率。
Eur J Clin Microbiol Infect Dis. 2017 Mar;36(3):553-563. doi: 10.1007/s10096-016-2832-4. Epub 2016 Nov 4.
5
Population Pharmacokinetics and Dosing Considerations for Gentamicin in Newborns with Suspected or Proven Sepsis Caused by Gram-Negative Bacteria.疑似或确诊革兰氏阴性菌败血症新生儿庆大霉素的群体药代动力学及给药考量
Antimicrob Agents Chemother. 2016 Dec 27;61(1). doi: 10.1128/AAC.01304-16. Print 2017 Jan.
6
What do I need to know about aminoglycoside antibiotics?关于氨基糖苷类抗生素我需要了解些什么?
Arch Dis Child Educ Pract Ed. 2017 Apr;102(2):89-93. doi: 10.1136/archdischild-2015-309069. Epub 2016 Aug 9.
7
Gentamicin Exposure and Sensorineural Hearing Loss in Preterm Infants.早产儿中庆大霉素暴露与感音神经性听力损失
PLoS One. 2016 Jul 8;11(7):e0158806. doi: 10.1371/journal.pone.0158806. eCollection 2016.
8
Development and Evaluation of a Gentamicin Pharmacokinetic Model That Facilitates Opportunistic Gentamicin Therapeutic Drug Monitoring in Neonates and Infants.促进新生儿和婴儿机会性庆大霉素治疗药物监测的庆大霉素药代动力学模型的开发与评估。
Antimicrob Agents Chemother. 2016 Jul 22;60(8):4869-77. doi: 10.1128/AAC.00577-16. Print 2016 Aug.
9
Neonatal gram-negative infections, antibiotic susceptibility and clinical outcome: an observational study.新生儿革兰氏阴性菌感染、抗生素敏感性及临床结局:一项观察性研究。
Arch Dis Child Fetal Neonatal Ed. 2016 Nov;101(6):F507-F512. doi: 10.1136/archdischild-2015-309554. Epub 2016 Mar 7.
10
Assessment of kidney function in preterm infants: lifelong implications.早产儿肾功能评估:对一生的影响
Pediatr Nephrol. 2016 Dec;31(12):2213-2222. doi: 10.1007/s00467-016-3320-x. Epub 2016 Feb 4.

对新生儿和婴儿庆大霉素暴露情况的定量分析对其目前的推荐剂量提出了质疑。

Quantitative Analysis of Gentamicin Exposure in Neonates and Infants Calls into Question Its Current Dosing Recommendations.

机构信息

Paediatric Pharmacology and Pharmacometrics Research, University of Basel Children's Hospital, Basel, Switzerland.

Quantitative Solutions, a Certara Company, London, United Kingdom.

出版信息

Antimicrob Agents Chemother. 2018 Mar 27;62(4). doi: 10.1128/AAC.02004-17. Print 2018 Apr.

DOI:10.1128/AAC.02004-17
PMID:29358294
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5913996/
Abstract

Optimal dosing of gentamicin in neonates is still a matter of debate despite its common use. We identified gentamicin dosing regimens from eight international guidelines and seven Swiss neonatal intensive care units. The dose per administration, the dosing interval, the total daily dose, and the demographic characteristics between guidelines were compared. There was considerable variability with respect to dose (4 to 6 mg/kg), dosing interval (24 h to 48 h), total daily dose (2.5 to 6 mg/kg/day), and patient demographic characteristics that were used to calculate individualized dosing regimens. A model-based simulation study in 1071 neonates was performed to determine the achievement of efficacious peak gentamicin concentrations according to predefined MICs (/MIC ≥ 10) and safe trough concentrations ( ≤ 2 mg/liter) with recommended dosing regimens. MIC targets of 0.5 and 1 mg/liter were used. Dosing optimization was performed giving priority to the first day of treatment and with the goal of simplifying dosing. Current gentamicin neonatal guidelines allow to achieve effective peak concentrations for MICs ≤ 0.5 mg/liter but not higher. Model-based simulations indicate that to attain peak gentamicin concentrations of ≥10 mg/liter, a dose of 7.5 mg/kg should be administered using an extended dosing interval regimen. Trough concentrations of ≤2 mg/liter can be maintained with a dosing interval of 36 to 48 h in neonates according to gestational and postnatal age. For treatment beyond 3 days, therapeutic drug monitoring is advised to maintain adequate serum concentrations.

摘要

尽管庆大霉素被广泛应用,但在新生儿中的最佳剂量仍存在争议。我们从八项国际指南和七家瑞士新生儿重症监护病房中确定了庆大霉素的给药方案。比较了每次给药剂量、给药间隔、总日剂量以及指南之间的人口统计学特征。在剂量(4 至 6mg/kg)、给药间隔(24 小时至 48 小时)、总日剂量(2.5 至 6mg/kg/天)和用于计算个体化给药方案的患者人口统计学特征方面存在相当大的差异。在 1071 名新生儿中进行了基于模型的模拟研究,以确定根据预定 MIC(/MIC≥10)和安全谷浓度(≤2mg/L)以及推荐的给药方案实现有效庆大霉素峰值浓度的情况。使用了 0.5 和 1mg/L 的 MIC 目标。优先考虑治疗的第一天进行剂量优化,并以简化给药为目标。目前的新生儿庆大霉素指南可以实现 MIC≤0.5mg/L 的有效峰值浓度,但不能更高。基于模型的模拟表明,要达到≥10mg/L 的庆大霉素峰值浓度,应使用延长的给药间隔方案给予 7.5mg/kg 的剂量。根据胎龄和出生后年龄,36 至 48 小时的给药间隔可维持≤2mg/L 的谷浓度。对于 3 天以上的治疗,建议进行治疗药物监测以维持足够的血清浓度。