Kouranos Vasilios D, Karageorgopoulos Drosos E, Peppas George, Falagas Matthew E
Alfa Institute of Biomedical Sciences, Athens, Greece.
Pharmacoepidemiol Drug Saf. 2009 Oct;18(10):873-9. doi: 10.1002/pds.1809.
Some clinicians may favor a strategy of early switch to oral antimicrobial therapy for patients responding to initial intravenous therapy. An important relevant consideration refers to the comparative safety and tolerability between oral and intravenous antimicrobial therapy. LITERATURE SEARCH/STUDY SELECTION: We sought to evaluate the above-mentioned issue by performing a systematic review of randomized studies comparing the occurrence of adverse events between oral and intravenous antimicrobial therapy with the same agents.
Ten relevant studies (five randomized controlled trials, three randomized cross-over studies, and two randomized, placebo-controlled, parallel-design studies) were included. Seven of the studies evaluated antibacterials (fluoroquinolones in four, and telithromycin, amoxicillin-clavulanic acid, and linezolid in one study each, respectively), whereas two studies evaluated ganciclovir, and one evaluated isavuconazole. No difference was observed in the rate of total adverse events between oral and intravenous administration of the same antimicrobial agents in any of the included studies that reported specific relevant data. Injection site reactions were noted more frequently with intravenous treatment in one study. No serious drug-related adverse events were reported, while study withdrawals due to adverse events did not considerably differ between the compared groups in any of the included studies.
There are only limited comparative data regarding the adverse events associated with the administration of the same antimicrobial agents by the oral and intravenous route. Our review indicates that the adverse event profile of oral and intravenous antimicrobial therapy does not differ considerably; however, this issue requires validation by further studies.
对于初始静脉治疗有反应的患者,一些临床医生可能倾向于采用早期换用口服抗菌药物治疗的策略。一个重要的相关考虑因素是口服和静脉抗菌治疗之间的相对安全性和耐受性。文献检索/研究选择:我们试图通过对比较相同药物口服和静脉抗菌治疗不良事件发生率的随机研究进行系统评价来评估上述问题。
纳入了10项相关研究(5项随机对照试验、3项随机交叉试验和2项随机、安慰剂对照、平行设计试验)。其中7项研究评估了抗菌药物(4项研究评估氟喹诺酮类药物,1项研究分别评估泰利霉素、阿莫西林-克拉维酸和利奈唑胺),2项研究评估了更昔洛韦,1项研究评估了艾沙康唑。在任何报告了具体相关数据的纳入研究中,相同抗菌药物口服和静脉给药的总不良事件发生率均未观察到差异。在一项研究中,静脉治疗更常出现注射部位反应。未报告严重的药物相关不良事件,在任何纳入研究中,因不良事件导致的研究退出在比较组之间没有显著差异。
关于相同抗菌药物口服和静脉给药相关不良事件的比较数据有限。我们的综述表明,口服和静脉抗菌治疗的不良事件情况没有显著差异;然而,这个问题需要进一步研究来验证。