Yogev Ram, Patterson Lori E, Kaplan Sheldon L, Adler Stuart, Morfin Maria Rayo, Martin Amando, Edge-Padbury Barbara, Naberhuis-Stehouwer Sharon, Bruss Jon B
Children's Memorial Hospital, Chicago, IL, USA.
Pediatr Infect Dis J. 2003 Sep;22(9 Suppl):S172-7. doi: 10.1097/01.inf.0000088671.35064.7c.
Gram-positive pathogens are a major cause of complicated skin and skin structure infections (CSSSIs) in children. Many pathogens are developing decreased susceptibility to currently used antibiotics, increasing the need for new therapies. Linezolid is well-tolerated and effective in the treatment of these infections in adults.
To evaluate the clinical efficacy and safety of iv/oral linezolid and iv vancomycin in children with Gram-positive CSSSIs.
Hospitalized children <12 years of age were randomized (2:1 ratio) to receive either linezolid 10 mg/kg iv every 8 h (with the option to change treatment to oral linezolid suspension 10 mg/kg every 8 h) or iv vancomycin 10 to 15 mg/kg every 6 to 24 h (according to age). Clinical response, tolerance and safety were evaluated at follow-up. The results of a subset analysis of patients with CSSSIs are presented here.
One hundred twenty intent-to-treat patients (linezolid 80, vancomycin 40) with CSSSI were included in this analysis. Clinical cure rates for clinically evaluable patients with CSSSI did not differ between treatment groups (linezolid, 93.2% vs. vancomycin, 90.0%; P = 0.594). Significantly fewer linezolid-treated patients experienced drug-related adverse events than did vancomycin-treated patients (23% vs. 48%; P = 0.006). The percentages of patients with laboratory abnormalities, including selected hematologic parameters, were generally low and similar between the treatment groups.
Linezolid given iv or orally was well-tolerated and safe. It was as effective as vancomycin in treating children with Gram-positive CSSSIs.
革兰氏阳性病原体是儿童复杂性皮肤和皮肤结构感染(CSSSI)的主要病因。许多病原体对目前使用的抗生素敏感性降低,因此对新疗法的需求不断增加。利奈唑胺耐受性良好,对成人这些感染的治疗有效。
评估静脉注射/口服利奈唑胺和静脉注射万古霉素治疗革兰氏阳性CSSSI儿童的临床疗效和安全性。
将12岁以下住院儿童按2:1比例随机分组,分别接受每8小时静脉注射10mg/kg利奈唑胺(可选择改为每8小时口服10mg/kg利奈唑胺混悬液)或每6至24小时静脉注射10至15mg/kg万古霉素(根据年龄)。随访时评估临床反应、耐受性和安全性。本文展示了CSSSI患者亚组分析的结果。
本分析纳入了一百二十例意向性治疗的CSSSI患者(利奈唑胺组80例,万古霉素组40例)。CSSSI临床可评估患者的临床治愈率在治疗组之间无差异(利奈唑胺组为93.2%,万古霉素组为90.0%;P = 0.594)。与万古霉素治疗的患者相比,接受利奈唑胺治疗的患者发生药物相关不良事件的比例显著更低(23%对48%;P = 0.006)。包括选定血液学参数在内的实验室异常患者百分比总体较低,且在治疗组之间相似。
静脉注射或口服利奈唑胺耐受性良好且安全。在治疗革兰氏阳性CSSSI儿童方面,它与万古霉素一样有效。