Cannon Joan P, Lee Todd A, Clark Nina M, Setlak Paul, Grim Shellee A
Pharmacy Services, Hines VA Hospital, Hines, IL, USA.
Department of Pharmacy Systems, Outcomes and Policy, College of Pharmacy, University of Illinois at Chicago, Chicago, IL, USA.
J Antimicrob Chemother. 2014 Aug;69(8):2043-55. doi: 10.1093/jac/dku111. Epub 2014 Apr 16.
A consensus exists among clinicians that imipenem/cilastatin is the most epileptogenic carbapenem, despite inconsistencies in the literature.
We conducted a meta-analysis of all randomized controlled trials comparing carbapenems with each other or with non-carbapenem antibiotics to assess the risk of seizures for imipenem, meropenem, ertapenem and doripenem.
In the risk difference (RD) analysis, there were increased patients with seizure (2 per 1000 persons, 95% CI 0.001, 0.004) among recipients of carbapenems versus non-carbapenem antibiotics. This difference was largely attributed to imipenem as its use was associated with an additional 4 patients per 1000 with seizure (95% CI 0.002, 0.007) compared with non-carbapenem antibiotics, whereas none of the other carbapenems was associated with increased seizure. Similarly, in the pooled OR analysis, carbapenems were associated with a significant increase in the risk of seizures relative to non-carbapenem comparator antibiotics (OR 1.87, 95% CI 1.35, 2.59). The ORs for risk of seizures from imipenem, meropenem, ertapenem and doripenem compared with other antibiotics were 3.50 (95% CI 2.23, 5.49), 1.04 (95% CI 0.61, 1.77), 1.32 (95% CI 0.22, 7.74) and 0.44 (95% CI 0.13, 1.53), respectively. In studies directly comparing imipenem and meropenem, there was no difference in epileptogenicity in either RD or pooled OR analyses.
The absolute risk of seizures with carbapenems was low, albeit higher than with non-carbapenem antibiotics. Although imipenem was more epileptogenic than non-carbapenem antibiotics, there was no statistically significant difference in the imipenem versus meropenem head-to-head comparison.
尽管文献报道存在不一致,但临床医生们已达成共识,即亚胺培南/西司他丁是最易引发癫痫的碳青霉烯类药物。
我们对所有比较碳青霉烯类药物之间或与非碳青霉烯类抗生素的随机对照试验进行了荟萃分析,以评估亚胺培南、美罗培南、厄他培南和多利培南引发癫痫的风险。
在风险差异(RD)分析中,与非碳青霉烯类抗生素相比,碳青霉烯类药物使用者中癫痫发作患者有所增加(每1000人中有2例,95%CI为0.001,0.004)。这种差异主要归因于亚胺培南,因为与非碳青霉烯类抗生素相比,使用亚胺培南会使每1000人中有额外4例癫痫发作患者(95%CI为0.002,0.007),而其他碳青霉烯类药物均未显示与癫痫发作增加有关。同样,在汇总的比值比(OR)分析中,与非碳青霉烯类对照抗生素相比,碳青霉烯类药物与癫痫发作风险显著增加相关(OR为1.87,95%CI为1.35,2.59)。与其他抗生素相比,亚胺培南、美罗培南、厄他培南和多利培南引发癫痫的OR分别为3.50(95%CI为2.23,5.49)、1.04(95%CI为0.61,1.77)、1.32(95%CI为0.22,7.74)和0.44(95%CI为0.13,1.53)。在直接比较亚胺培南和美罗培南的研究中,在RD分析或汇总OR分析中,二者在致癫痫性方面均无差异。
碳青霉烯类药物引发癫痫的绝对风险较低,尽管高于非碳青霉烯类抗生素。虽然亚胺培南比非碳青霉烯类抗生素更易引发癫痫,但在亚胺培南和美罗培南的直接对比中,在统计学上无显著差异。