Department of Pediatrics, University of Florence, Florence, Italy.
Clin Ther. 2010 Jan;32(1):66-88. doi: 10.1016/j.clinthera.2010.01.019.
Linezolid is marketed for the treatment of severe, vancomycin-resistant infections with gram-positive bacteria in adults. Most information regarding the pharmacokinetic profile, efficacy, and tolerability of linezolid is derived from adult studies.
The aim of this review was to summarize evidence regarding the use of linezolid in infants and children, focusing on the drug's clinical efficacy data and tolerability profile.
A literature search was conducted of the Cochrane Library, EMBASE, and MEDLINE databases, from their inception through July 20, 2009, using the following terms: linezolid, newborn, infant, child, pediatrics, adolescent, human, clinical trial, and case report. Articles were excluded if they were redundant or not pertinent. (Articles that did not focus on the use of linezolid in children were considered not pertinent.) Bibliographies of all relevant articles were also evaluated.
Forty-seven publications regarding the use of linezolid in children were included in the review: 5 pharmacokinetic studies, 32 case reports, 6 randomized clinical trials (RCTs), 2 uncontrolled trials, 1 subanalysis of 2 published RCTs, and 1 subanalysis of published data about linezolid's tolerability. Pharmacokinetic data on linezolid use in children were derived from studies that enrolled 447 children. Plasma pharmacokinetics of linezolid in pediatric patients were found to be age dependent. Results from 6 vancomycinor cefadroxil-controlled RCTs (including 1480 children) evaluating linezolid treatment in children reported variable clinical cure rates, ranging from 75.0% to 93.2% in children with skin and skin-structure infections and from 77.5% to 90.0% in children with bacteremia or pneumonia. No significant difference in clinical cure rates between the linezolid group and the comparator group was observed in any study. The most frequently reported adverse events were diarrhea (from 3.1% to 16.8%), nausea and/or vomiting (from 2.9% to 11.9%), and thrombocytopenia (from 1.9% to 4.7%). To date, 3 cases of neuropathy have been described in children.
The reviewed pediatric studies in skin and skin-structure infections, bacteremia, or pneumonia found that linezolid was associated with high clinical cure rates (75.0%-93.2%) that did not differ significantly from those of vancomycin or cefadroxil. RCTs enrolling children with other types of infection (eg, osteomyelitis, endocarditis), as well as long-term studies, are needed to draw definitive conclusions about linezolid's efficacy and tolerability in pediatric patients. Careful monitoring for adverse events and possible linezolid resistance continues to be essential.
利奈唑胺在临床上用于治疗成人严重的、耐万古霉素的革兰氏阳性菌感染。大多数关于利奈唑胺药代动力学、疗效和耐受性的信息都来源于成人研究。
本综述的目的在于总结利奈唑胺在婴儿和儿童中的应用,重点是药物的临床疗效数据和耐受性。
检索 Cochrane 图书馆、EMBASE 和 MEDLINE 数据库,从建库到 2009 年 7 月 20 日,使用以下检索词:利奈唑胺、新生儿、婴儿、儿童、青少年、人类、临床试验、病例报告。如果文章重复或不相关则将其排除(未聚焦于儿童利奈唑胺应用的文章被认为是不相关的)。也评估了所有相关文章的参考文献。
综述中纳入了 47 篇关于儿童利奈唑胺应用的文献:5 项药代动力学研究、32 个病例报告、6 项随机对照试验(RCT)、2 项非对照试验、2 项发表 RCT 的亚分析、1 项利奈唑胺耐受性发表数据的亚分析。在纳入 447 名儿童的研究中得出了利奈唑胺在儿童中应用的药代动力学数据。儿童患者的利奈唑胺血浆药代动力学是年龄依赖性的。6 项万古霉素或头孢羟氨苄对照 RCT(包括 1480 名儿童)的结果显示,不同的临床治愈率在皮肤和皮肤结构感染的儿童中为 75.0%至 93.2%,在菌血症或肺炎的儿童中为 77.5%至 90.0%。在任何研究中,利奈唑胺组与对照组之间的临床治愈率均无显著差异。最常报告的不良事件是腹泻(3.1%至 16.8%)、恶心和/或呕吐(2.9%至 11.9%)和血小板减少症(1.9%至 4.7%)。迄今为止,已有 3 例儿童神经病变的病例报告。
皮肤和皮肤结构感染、菌血症或肺炎的儿科研究表明,利奈唑胺的临床治愈率高(75.0%至 93.2%),与万古霉素或头孢羟氨苄无显著差异。需要 RCT 研究纳入患有其他类型感染(如骨髓炎、心内膜炎)的儿童,以及长期研究,才能对利奈唑胺在儿科患者中的疗效和耐受性得出明确的结论。对不良事件和可能的利奈唑胺耐药性的持续密切监测仍然至关重要。