Department of Epidemiology of Health Products, The French National Agency for Medicines and Health Products Safety, Saint-Denis, France.
JAMA Ophthalmol. 2016 Apr;134(4):415-21. doi: 10.1001/jamaophthalmol.2015.6205.
Several studies have focused on the current use of oral fluoroquinolones and the risk for retinal detachment (RD), but the existence of this association is under debate. Given the widespread fluoroquinolone use, investigation of this association is essential.
To assess the association between oral fluoroquinolone use and the risk for RD, including the rhegmatogenous and exudative types.
DESIGN, SETTING, AND PARTICIPANTS: This case-crossover study included 27,540 adults with RD from French health care databases from July 1, 2010, through December 31, 2013. Patients with a history of RD or retinal break, endophthalmitis, intravitreal injection, choroidal retinal vitreal biopsy, and human immunodeficiency virus infection or those hospitalized within 6 months of RD were excluded. The risk period of primary interest was current use, defined as exposure to fluoroquinolones within 10 days immediately before RD surgery, according to previous findings. Oral fluoroquinolone use was assumed to start on the day the prescription was dispensed.
Exposure to fluoroquinolones during the risk period (1-10 days) compared with the control period (61-180 days). The association was also assessed regarding use in the recent (11-30 days) and past (31-60 days) intermediate risk period, type of fluoroquinolone, and type of RD.
Of the 27,540 eligible patients (57% men; mean [SD] age, 61.5 [13.6] years), 663 patients with RD were exposed to fluoroquinolones during the observation period, corresponding to 80 cases exposed during the 10-day risk period (≤10 days before RD) and 583 cases exposed during the control period (61-180 days). We found a significant increased risk for RD during the 10-day period after the dispensing of oral fluoroquinolones, with an adjusted odds ratio of 1.46 (95% CI, 1.15-1.87). The risk was significantly increased for rhegmatogenous and exudative RD, with adjusted odds ratios of 1.41 (95% CI, 1.04-1.92) and 2.57 (95% CI, 1.46-4.53), respectively. Recent and past use of fluoroquinolones were not associated with a higher risk for RD, with adjusted odds ratios of 0.94 (95% CI, 0.78-1.14) and 1.06 (95% CI, 0.91-1.24), respectively.
Current oral fluoroquinolone use was associated with an increased risk for RD, including the rhegmatogenous and exudative types. These findings, along with the available literature, suggest an association between fluoroquinolone use and the risk for RD. The nature of this association should be further investigated in future studies.
已有多项研究集中于当前氟喹诺酮类药物的使用与视网膜脱离(RD)风险之间的关系,但该关联仍存在争议。鉴于氟喹诺酮类药物的广泛使用,对该关联进行调查至关重要。
评估口服氟喹诺酮类药物使用与 RD 风险之间的关联,包括孔源性和渗出性 RD。
设计、设置和参与者:这项病例交叉研究纳入了来自法国医疗保健数据库的 27540 名 RD 成年患者,纳入时间为 2010 年 7 月 1 日至 2013 年 12 月 31 日。排除了有 RD 或视网膜裂孔病史、眼内炎、眼内注射、脉络膜视网膜玻璃体活检和人类免疫缺陷病毒感染病史的患者,或 RD 发病后 6 个月内住院的患者。主要关注的风险期为当前使用期,定义为根据先前的研究结果,在 RD 手术前 10 天内使用氟喹诺酮类药物。口服氟喹诺酮类药物的使用假定从处方配药之日开始。
在风险期(1-10 天)和对照期(61-180 天)内暴露于氟喹诺酮类药物的情况。还评估了近期(11-30 天)和过去(31-60 天)中等风险期、氟喹诺酮类药物类型和 RD 类型的使用与 RD 之间的关联。
在 27540 名符合条件的患者(57%为男性;平均[SD]年龄为 61.5[13.6]岁)中,有 663 名 RD 患者在观察期内使用了氟喹诺酮类药物,其中 80 例在风险期内(≤RD 前 10 天)暴露,583 例在对照期内暴露。我们发现,在口服氟喹诺酮类药物配药后 10 天内,RD 的风险显著增加,校正后的优势比为 1.46(95%CI,1.15-1.87)。孔源性和渗出性 RD 的风险显著增加,校正后的优势比分别为 1.41(95%CI,1.04-1.92)和 2.57(95%CI,1.46-4.53)。近期和过去使用氟喹诺酮类药物与 RD 风险增加无关,校正后的优势比分别为 0.94(95%CI,0.78-1.14)和 1.06(95%CI,0.91-1.24)。
当前口服氟喹诺酮类药物的使用与 RD 风险增加相关,包括孔源性和渗出性 RD。这些发现以及现有文献表明,氟喹诺酮类药物的使用与 RD 风险之间存在关联。在未来的研究中,应进一步调查这种关联的性质。