Saiman Lisa, Goldfarb Johhanna, Kaplan Sheldon A, Wible Kenneth, Edge-Padbury Barbara, Naberhuis-Stehouwer Sharon, Bruss Jon B
Columbia University, New York, NY, USA.
Pediatr Infect Dis J. 2003 Sep;22(9 Suppl):S193-200. doi: 10.1097/01.inf.0000087022.58089.d8.
Linezolid, an oxazolidinone, is effective in the treatment of adults and children with community-acquired and nosocomial pneumonia and uncomplicated and complicated skin and skin structure infections (SSSIs), including infections caused by Gram-positive resistant pathogens. Because of the increasing use of linezolid, it is important to review the common adverse events (AEs) associated with its use in children with the use of data from clinical trials.
The safety and tolerability of linezolid in pediatric patients with Gram-positive infections were determined in four pediatric clinical studies. Study I included pediatric patients with community-acquired pneumonia; Study II included otitis media; Study III included SSSIs; and Study IV included complicated SSSIs, nosocomial pneumonia and bacteremia.
Studies I and II had no comparator arm. Study III was randomized and compared linezolid with cefadroxil. Study IV also was randomized and compared linezolid with vancomycin. Patients <12 years of age received linezolid 10 mg/kg; patients age 12 years and older received 600 mg (intravenous/oral). Dosing frequency (two to three times daily) varied depending on age and clinical diagnosis. The primary safety endpoints were AEs, drug-related AEs, serious AEs and selected laboratory tests.
In the 4 studies 958 patients were included in the intent-to-treat analysis. In the linezolid vs. cefadroxil study (Study III), the most common AEs in patients treated with linezolid were diarrhea (7.8%), headache (6.5%) and upper respiratory tract infection (3.7%). In the linezolid vs. vancomycin study (Study IV), the most common AEs in the linezolid group were fever (14.1%), diarrhea (10.8%) and vomiting (9.4%). The most common drug-related AEs for linezolid in all 4 studies were diarrhea, vomiting, loose stools and nausea. None of these common AEs or drug-related AEs occurred more frequently in patients treated with linezolid than in those in the comparator group.
Linezolid was safe and well-tolerated in pediatric patients with community-acquired pneumonia, otitis media, SSSIs and infections caused by Gram-positive resistant pathogens.
利奈唑胺是一种恶唑烷酮类药物,对治疗成人和儿童的社区获得性肺炎及医院获得性肺炎、单纯性和复杂性皮肤及皮肤结构感染(SSSI)有效,包括由革兰氏阳性耐药病原体引起的感染。由于利奈唑胺的使用日益增多,利用临床试验数据回顾其在儿童中使用时常见的不良事件(AE)很重要。
在四项儿科临床研究中确定利奈唑胺在患有革兰氏阳性感染的儿科患者中的安全性和耐受性。研究I纳入了患有社区获得性肺炎的儿科患者;研究II纳入了中耳炎患者;研究III纳入了SSSI患者;研究IV纳入了复杂性SSSI、医院获得性肺炎和菌血症患者。
研究I和II没有对照臂。研究III是随机对照试验,将利奈唑胺与头孢羟氨苄进行比较。研究IV也是随机对照试验,将利奈唑胺与万古霉素进行比较。12岁以下患者接受10mg/kg利奈唑胺;12岁及以上患者接受600mg(静脉注射/口服)。给药频率(每日两至三次)因年龄和临床诊断而异。主要安全性终点为不良事件、药物相关不良事件、严重不良事件和选定的实验室检查。
在这4项研究中,958例患者纳入意向性分析。在利奈唑胺与头孢羟氨苄的研究(研究III)中,接受利奈唑胺治疗的患者中最常见的不良事件为腹泻(7.8%)、头痛(6.5%)和上呼吸道感染(3.7%)。在利奈唑胺与万古霉素的研究(研究IV)中,利奈唑胺组最常见的不良事件为发热(14.1%)、腹泻(10.8%)和呕吐(9.4%)。在所有4项研究中,利奈唑胺最常见的药物相关不良事件为腹泻、呕吐、稀便和恶心。这些常见不良事件或药物相关不良事件在接受利奈唑胺治疗的患者中发生频率均未高于对照组患者。
利奈唑胺在患有社区获得性肺炎、中耳炎、SSSI以及由革兰氏阳性耐药病原体引起的感染的儿科患者中安全且耐受性良好。