Eli Lilly and Company, Indianapolis, IN.
Ann Epidemiol. 2014 Apr;24(4):279-85. doi: 10.1016/j.annepidem.2013.12.009. Epub 2014 Jan 2.
Peripheral neuropathy (PN) is an identified risk of systemic antibacterial therapy with fluoroquinolones. The risk and its severity, including the development of Guillain-Barré syndrome (GBS) between individual agents is uncertain. This study examines the association between fluoroquinolones and PN and GBS in cases spontaneously reported to the FDA Adverse Event Reporting System.
Cases reported to FDA Adverse Event Reporting System between 1997 and 2012 were retrieved. The Medical Dictionary for Regulatory Activities Preferred Term was used to define PN and GBS. Individual fluoroquinolones were identified by generic names and route of administration. Empirical Bayes Geometric Mean (EBGM) with 95% confidence interval (EB05-EB95) was calculated as disproportionality measure. Safety signals with EB05 2 or more was considered a significant disproportional increase in the event reporting of at least twice times higher than that expected.
There were 539 PN reports out of 46,257 adverse event reports submitted for fluoroquinolones. Nine percent of PN reports were for GBS. Significant disproportionality of PN (EBGM 2.70; EB05-EB95 2.51-2.90) and GBS (EBGM 3.22; EB05-EB95 2.55-4.02) was identified for fluoroquinolones. Signals of PN were detected for ciprofloxacin (EBGM 3.24; EB05-EB95 2.87-3.66) and levofloxacin (EBGM 3.36; EB05-EB95 3.02-3.72). A GBS signal was detected for ciprofloxacin (EBGM 4.15; EB05-EB95 2.94-5.74). GBS and PN, respectively, ranked 6th and 8th among reported neurologic events.
This study re-emphasizes the link between fluoroquinolones and PN and shows the potential association with more severe forms of nerve damage, for example, GBS. Unless the benefit of fluoroquinolone therapy (e.g., overwhelming infection or development of bacterial resistance) outweighs PN risk, treatment with alternative antibacterial agents is recommended.
周围神经病变(PN)是全身抗菌治疗中氟喹诺酮类药物的一个确定风险。各个药物之间的风险和严重程度,包括格林-巴利综合征(GBS)的发生情况并不明确。本研究通过美国食品和药物管理局不良事件报告系统(FDA Adverse Event Reporting System)自发报告的病例,来研究氟喹诺酮类药物与 PN 和 GBS 之间的相关性。
检索了 1997 年至 2012 年期间向 FDA 不良事件报告系统报告的病例。采用监管活动医学词典首选术语来定义 PN 和 GBS。通过通用名和给药途径来确定各个氟喹诺酮类药物。计算经验贝叶斯几何均数(EBGM)及其 95%置信区间(EB05-EB95)作为不成比例的衡量标准。如果 EB05 2 或更高,则认为该事件的报告存在显著不成比例的增加,至少是预期的两倍以上。
在提交的 46257 例氟喹诺酮类药物不良事件报告中,有 539 例报告出现 PN。9%的 PN 报告为 GBS。氟喹诺酮类药物的 PN(EBGM 2.70;EB05-EB95 2.51-2.90)和 GBS(EBGM 3.22;EB05-EB95 2.55-4.02)存在显著的不成比例。环丙沙星(EBGM 3.24;EB05-EB95 2.87-3.66)和左氧氟沙星(EBGM 3.36;EB05-EB95 3.02-3.72)的 PN 信号被检测到。环丙沙星(EBGM 4.15;EB05-EB95 2.94-5.74)的 GBS 信号被检测到。PN 和 GBS 分别排在报告的神经事件中的第 6 位和第 8 位。
本研究再次强调了氟喹诺酮类药物与 PN 之间的联系,并表明其与更严重形式的神经损伤(例如 GBS)之间存在潜在的关联。除非氟喹诺酮类药物治疗的益处(例如,严重感染或细菌耐药性的发展)超过 PN 风险,否则建议使用替代的抗菌药物进行治疗。