Newsom S W, Palsingh J, Wells F C, Kelly H C
Papworth Hospital, Cambridge, UK.
J Antimicrob Chemother. 1995 Jul;36 Suppl A:57-62. doi: 10.1093/jac/36.suppl_a.57.
Thirty-three patients requiring cardiac valve surgery were administered meropenem 1000 mg by a 5 to 10 min iv injection. Samples of blood, cardiac valve and atrial muscle tissue were removed at valvectomy and analysed for meropenem by high performance liquid chromatography (HPLC) with UV detection. The plasma concentrations observed in the samples from these patients were higher than those reported when meropenem 1000 mg was administered to healthy volunteers by 5 min iv injection. No clinical adverse events attributable to meropenem were reported and the single 1000 mg dose was well tolerated. The penetration of meropenem into cardiac muscle and valve tissue was rapid and in excess of that expected solely on the basis of distribution into extracellular fluid. The concentrations achieved in the tissues were in excess of the MICs of the pathogens commonly causing endocarditis.
33例需要进行心脏瓣膜手术的患者接受了美罗培南治疗,通过静脉注射5至10分钟给予1000mg。在瓣膜切除术中采集血液、心脏瓣膜和心房肌肉组织样本,并通过带有紫外检测的高效液相色谱法(HPLC)分析美罗培南。这些患者样本中观察到的血浆浓度高于通过静脉注射5分钟给予1000mg美罗培南时健康志愿者所报告的浓度。未报告任何可归因于美罗培南的临床不良事件,单次1000mg剂量耐受性良好。美罗培南进入心肌和瓣膜组织的速度很快,且超过仅基于分布到细胞外液所预期的水平。组织中达到的浓度超过了通常引起心内膜炎的病原体的最低抑菌浓度。