Suppr超能文献

利奈唑胺在婴儿和儿童中的临床经验。

Clinical experience with linezolid in infants and children.

机构信息

Department of Paediatrics, University of Turin, Regina Margherita Children's Hospital, Infectious Diseases Unit, Piazza Polonia 94, Turin, Italy.

出版信息

J Antimicrob Chemother. 2011 May;66 Suppl 4:iv23-iv41. doi: 10.1093/jac/dkr074.

Abstract

The worldwide spread of multidrug-resistant organisms has required the development of new antimicrobials. Linezolid, the first oxazolidinone, has a broad spectrum of activity against Gram-positive bacteria, including resistant strains. Although approved by the Food and Drug Administration in 2002, the clinical experience with linezolid in the paediatric population is still limited, also given the fact that in most European countries the paediatric use of linezolid is off-label. In this paper we summarize the actual evidence on both licensed and off-label clinical uses of linezolid in children, including efficacy, safety and tolerability issues. Taking into account the potential bias in comparing heterogeneous clinical trials and reports, the available literature data suggest that linezolid is a safe and effective agent for the treatment of serious Gram-positive bacterial infections in neonates and children. At present, linezolid is reserved for those children who are intolerant to or fail conventional agents. A linezolid-containing regimen can be a valuable option for treating multidrug-resistant and extensively drug-resistant tuberculosis in children as well as disseminated non-tuberculous mycobacterial infections. Given the rare occurrence of serious side effects, careful monitoring of haematological parameters, possible drug interactions and neurological manifestations is recommended in linezolid-treated children, especially in case of prolonged treatments. Appropriate linezolid dosage and hospital infection control measures are essential to avoid the spread of linezolid resistance. Further studies are needed to establish novel paediatric indications for linezolid use and to assess the tolerability of long-term treatments.

摘要

全球范围内耐多药生物的传播要求开发新的抗菌药物。利奈唑胺是第一个噁唑烷酮类药物,对革兰氏阳性菌具有广泛的活性,包括耐药菌株。尽管利奈唑胺于 2002 年获得美国食品和药物管理局批准,但在儿科人群中的临床应用经验仍然有限,这主要是因为在大多数欧洲国家,儿科使用利奈唑胺是超适应证的。本文总结了利奈唑胺在儿童中的许可和超适应证临床应用的实际证据,包括疗效、安全性和耐受性问题。考虑到比较异质临床试验和报告时可能存在的偏倚,现有文献数据表明,利奈唑胺是治疗新生儿和儿童严重革兰氏阳性菌感染的安全有效的药物。目前,利奈唑胺仅保留给那些对常规药物不耐受或无效的儿童。利奈唑胺方案对于治疗儿童耐多药和广泛耐药结核病以及播散性非结核分枝杆菌感染也是一种有价值的选择。由于严重副作用的发生罕见,在利奈唑胺治疗的儿童中,建议仔细监测血液学参数、可能的药物相互作用和神经表现,尤其是在长期治疗的情况下。适当的利奈唑胺剂量和医院感染控制措施对于避免利奈唑胺耐药的传播至关重要。需要进一步的研究来确定利奈唑胺在儿科中的新适应证,并评估长期治疗的耐受性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验