Hurley J C
Division of Infectious Diseases, Children's Hospital and Medical Center, Seattle, Washington, USA.
Drug Saf. 1995 Mar;12(3):183-95. doi: 10.2165/00002018-199512030-00004.
There is clear experimental evidence that antibiotics increase the bioavailability of endotoxin from Gram-negative bacteria. In this review, data for 2 variables, level of endotoxin and level of bacteria, at the time point closest to 2 hours post-antibiotic exposure were abstracted as a change from baseline readings from each available study, to enable presentation in a graphical overview. This overview indicates that the phenomenon is not limited to beta-lactam agents nor is it apparent only for the more rapidly bactericidal agents. However, evidence that this phenomenon is of clinical importance is scant. With the Jarisch-Herxheimer reaction (JHR), there is clear evidence for an acute deterioration with the initiation of antibiotic therapy and yet uncertainty as to the nature of the bacterial mediator(s) of this reaction. There is no evidence to support the commonly stated concern that therapy with antibiotics with a more rapid bactericidal action may result in the sudden lysis of bacteria with the release of cell wall components and cause a deterioration that might be avoidable through the use of antibiotics with a slower time course of action.
有明确的实验证据表明,抗生素会增加革兰氏阴性菌内毒素的生物利用度。在本综述中,从每项可用研究中提取抗生素暴露后最接近2小时时间点的两个变量(内毒素水平和细菌水平)的数据,作为相对于基线读数的变化,以便以图形概述的形式呈现。该概述表明,这种现象不仅限于β-内酰胺类药物,也并非仅在杀菌速度较快的药物中才明显。然而,关于这种现象具有临床重要性的证据却很少。对于雅里希-赫克斯海默反应(JHR),有明确证据表明抗生素治疗开始后会出现急性恶化,但对于该反应的细菌介导物的性质仍存在不确定性。没有证据支持人们普遍表达的担忧,即使用杀菌作用更快的抗生素进行治疗可能会导致细菌突然裂解并释放细胞壁成分,从而引起恶化,而使用作用时间较慢的抗生素或许可以避免这种恶化。