Alfa Institute of Biomedical Sciences, Athens, Greece.
J Antimicrob Chemother. 2011 Feb;66(2):251-9. doi: 10.1093/jac/dkq451. Epub 2010 Dec 3.
Once daily dosing (ODD) of aminoglycosides has become a standard of care for most patient populations. However, the use of ODD of aminoglycosides has not been clarified in febrile neutropenia.
We performed a systematic review and meta-analysis of randomized controlled trials (RCTs) that compared the effectiveness and safety of ODD versus multiple daily dosing (MDD) of aminoglycosides in patients with febrile neutropenia. We searched the PubMed, Scopus, Cochrane Central Register of Trials and clinicaltrials.gov databases up to July 2010.
A total of five and eight RCTs were included in the effectiveness and safety analyses, respectively. We observed a trend towards better effectiveness of the ODD regimen in the clinically evaluable population {five RCTs, 403 patient-episodes, risk ratio (RR) = 1.18 [95% confidence interval (95% CI): 0.98, 1.42]}, but not in the microbiologically evaluable population [three RCTs, 119 patient-episodes, RR = 1.11 (95% CI: 0.84, 1.48)]. The occurrence of nephrotoxicity was similar between the two groups [seven RCTs, 1643 patient-episodes, RR = 0.74 (95% CI: 0.36, 1.50)], as was ototoxicity [six RCTs, 862 patient-episodes, RR = 1.05 (95% CI: 0.51, 2.19)]. There was no difference in mortality [four RCTs, 403 patient-episodes, RR = 0.77 (95% CI: 0.21, 2.78)].
Although the generalization of our findings may be restricted by the relatively small sample size and other methodological limitations of the included RCTs, ODD appears to be at least as effective and as safe as MDD in patients with febrile neutropenia. RCTs comparing ODD versus MDD in patients with bacteraemia and profound or prolonged neutropenia would be of additional value.
氨基糖苷类药物的每日一次给药(ODD)已成为大多数患者群体的标准治疗方法。然而,在发热性中性粒细胞减少症中,ODD 用法尚未明确。
我们对比较发热性中性粒细胞减少症患者中 ODD 与多次每日剂量(MDD)氨基糖苷类药物的有效性和安全性的随机对照试验(RCT)进行了系统评价和荟萃分析。我们检索了 PubMed、Scopus、Cochrane 临床试验中心注册库和 clinicaltrials.gov 数据库,检索时间截至 2010 年 7 月。
有效性分析纳入了 5 项 RCT,安全性分析纳入了 8 项 RCT。我们观察到 ODD 方案在临床可评估人群中的有效性有提高趋势(5 项 RCT,403 例患者-发作,风险比[RR] = 1.18 [95%置信区间(95%CI):0.98,1.42]),但在微生物可评估人群中则不然(3 项 RCT,119 例患者-发作,RR = 1.11 [95%CI:0.84,1.48])。两组的肾毒性发生率相似(7 项 RCT,1643 例患者-发作,RR = 0.74 [95%CI:0.36,1.50]),耳毒性也相似(6 项 RCT,862 例患者-发作,RR = 1.05 [95%CI:0.51,2.19])。两组死亡率无差异(4 项 RCT,403 例患者-发作,RR = 0.77 [95%CI:0.21,2.78])。
尽管我们的发现可能受到纳入 RCT 样本量较小和其他方法学限制的限制,但是 ODD 似乎至少与 MDD 一样有效和安全,可用于发热性中性粒细胞减少症患者。比较 ODD 与 MDD 在菌血症和严重或持续中性粒细胞减少症患者中的疗效的 RCT 将具有额外价值。