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Vancomycin Therapeutic Regime Adjustment in Newborns and Infants with Bacterial Infection: Case Series

机译:万古霉素治疗细菌性感染新生儿和婴儿的治疗方式调整:病例系列

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摘要

Background: Vancomycin is used mostly to overcome infections caused by methicillin-resistant microorganisms. There are no well-established administration protocols for neonates and infants, so the leak of a specific administration regime in that population may lead to serum concentrations beyond the specified range.Objective: This case series evaluated the pharmacokinetics adjustment from a vancomycin therapeutic regimen prescribed to neonates and infants with bacterial infection at a neonatal public hospital intensive- care-unit, with the primary purpose to verify cases of nephrotoxicity.Methods: Three neonates and four infants taking vancomycin therapy, hospitalized in a public hospital from November 2014 to March 2015, were included in the study. Vancomycin serum concentrations were determined by particle-enhanced-turbidimetric inhibition-immunoassay. The vancomycin concentrations were used for dose adjustment by USC*Pack-PC-Collection((R)), a non-parametric maximization program. The trough serum concentration range of 10 to 20mg.L-1 was considered therapeutic.Results: Three patients had serum concentration outside the reference-range, one with subtherapeutic, and two with supratherapeutic concentrations. All patients had concomitant use of drugs which interfered with vancomycin distribution and excretion pharmacokinetics parameters, including drugs that may enhance nephrotoxicity. One patient showed signs of acute renal damage, by low vancomycin and creatinine estimated clearances.Conclusion: The pharmacokinetic adjustment has been proven to be a useful and necessary tool to increase therapeutic efficacy and treatment benefits. The standard dose of vancomycin can be used to initiate therapy in neonates and infants admitted to the ICU, but after reaching the drug steady state, the dosing regimen should be individualized and guided by pharmacokinetic parameters.
机译:背景:万古霉素主要用于克服由耐甲氧西林的微生物引起的感染。目前尚无针对新生儿和婴儿的完善给药方案,因此该人群中特定给药方案的泄漏可能导致血清浓度超出规定范围。目的:本病例系列评估了根据万古霉素治疗方案规定的药代动力学调整方法:从2014年11月至2015年3月在一家公立医院住院的三名新生儿和四名接受万古霉素治疗的婴儿,在新生儿公立医院重症监护病房接受细菌感染的新生儿和婴儿。被纳入研究。万古霉素血清浓度通过颗粒增强比浊抑制-免疫测定法测定。万古霉素的浓度用于通过非参数最大化程序USC *Pack-PC-Collection®进行剂量调整。结果:低血脂血清浓度范围在10至20mg.L-1被认为是治疗性的。结果:三名患者的血药浓度超出参考范围,一例为亚治疗浓度,二例为超治疗浓度。所有患者均同时使用会干扰万古霉素分布和排泄药代动力学参数的药物,包括可能增强肾毒性的药物。一名患者由于万古霉素和肌酐估计清除率低而显示出急性肾损害的迹象。结论:药代动力学调整已被证明是增加治疗功效和治疗益处的有用且必要的工具。万古霉素的标准剂量可用于接受ICU的新生儿和婴儿中的治疗,但在达到药物稳态后,应根据药物动力学参数对给药方案进行个性化指导。

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  • 来源
    《Current Pharmaceutical Biotechnology》 |2019年第4期|346-351|共6页
  • 作者单位

    Fed Univ Bahia UFBA, Fac Pharm, Pharm Postgrad Program, Salvador, BA, Brazil;

    Fed Univ Bahia UFBA, Clin Biochem Lab, Dept Clin & Toxicol Anal, Fac Pharm, Univ Campus,Barao Jeremoabo St, BR-40170115 Salvador, BA, Brazil;

    Univ Ctr Estacio Bahia, Salvador, BA, Brazil;

    Poison Informat Ctr Ciave Bahia, Salvador, BA, Brazil;

    Hosp Roberto Santos, Dept Pediat, Salvador, BA, Brazil;

    Fed Univ Bahia UFBA, Fac Pharm, Pharm Postgrad Program, Salvador, BA, Brazil|Fed Univ Bahia UFBA, Clin Biochem Lab, Dept Clin & Toxicol Anal, Fac Pharm, Univ Campus,Barao Jeremoabo St, BR-40170115 Salvador, BA, Brazil;

    Fed Univ Bahia UFBA, Fac Pharm, Pharm Postgrad Program, Salvador, BA, Brazil|Fed Univ Bahia UFBA, Fac Pharm, Dept Drug, Salvador, BA, Brazil;

    Fed Univ Bahia UFBA, Fac Pharm, Pharm Postgrad Program, Salvador, BA, Brazil|Fed Univ Bahia UFBA, Clin Biochem Lab, Dept Clin & Toxicol Anal, Fac Pharm, Univ Campus,Barao Jeremoabo St, BR-40170115 Salvador, BA, Brazil;

    Fed Univ Bahia UFBA, Fac Pharm, Pharm Postgrad Program, Salvador, BA, Brazil|Fed Univ Bahia UFBA, Clin Biochem Lab, Dept Clin & Toxicol Anal, Fac Pharm, Univ Campus,Barao Jeremoabo St, BR-40170115 Salvador, BA, Brazil;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Vancomycin therapy; pharmacokinetics; drug monitoring; nephrotoxicity; neonates; infants;

    机译:万古霉素治疗;药代动力学;药物监测;肾毒性;新生儿;婴儿;

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