Kosaka Tadashi, Kokufu Takatoshi, Shime Nobuaki, Sugioka Nobuyuki, Kato Ryuichi, Hamaoka Kenji, Fujita Naohisa
Department of Pharmacy, Kyoto Prefectural University, School of Medicine, Kamigyo-ku, Kyoto 602-8566, Japan.
Int J Antimicrob Agents. 2009 Apr;33(4):368-70. doi: 10.1016/j.ijantimicag.2008.10.006. Epub 2008 Dec 18.
Here we report our experience with four paediatric patients with mediastinitis due to meticillin-resistant Staphylococcus aureus (MRSA) following cardiac surgery refractory to glycopeptide treatment and treated by linezolid. The pharmacokinetics and tolerance of linezolid administered orally or intravenously were analysed. Linezolid was administered intravenously at a dosage of 10 mg/kg every 8 h and then orally. In oral administration, 10 mg/kg or 15 mg/kg was given every 8 h as a powder made by crushing tablets. The linezolid serum trough concentration was >or=3.5 mg/L in patients treated by intravenous administration. However, with oral administration lower trough levels were detected, including patients with an undetectable level (<0.1 mg/L). No significant intolerance or drug-related haematological events were reported. We conclude that linezolid, with a switch from intravenous to oral administration, could be an effective and safe option in paediatric mediastinitis refractory to conventional glycopeptides, whilst care must be taken to maintain an adequate dose by monitoring the trough concentration.
在此,我们报告4例心脏手术后因耐甲氧西林金黄色葡萄球菌(MRSA)引起纵隔炎的儿科患者的治疗经验,这些患者对糖肽类治疗无效,随后接受利奈唑胺治疗。我们分析了口服或静脉给予利奈唑胺的药代动力学和耐受性。利奈唑胺静脉给药剂量为每8小时10mg/kg,随后改为口服给药。口服给药时,将片剂碾碎制成粉末,每8小时给予10mg/kg或15mg/kg。静脉给药治疗的患者中,利奈唑胺血清谷浓度≥3.5mg/L。然而,口服给药时检测到较低的谷浓度水平,包括未检测到浓度(<0.1mg/L)的患者。未报告明显的不耐受情况或与药物相关的血液学事件。我们得出结论,利奈唑胺从静脉给药改为口服给药,对于常规糖肽类治疗无效的儿科纵隔炎可能是一种有效且安全的选择,同时必须通过监测谷浓度来确保维持足够的剂量。