The Rotterdam Eye Hospital, Rotterdam, the Netherlands.
Rotterdam Ophthalmic Institute, Rotterdam, the Netherlands.
Acta Ophthalmol. 2018 Jun;96(4):348-355. doi: 10.1111/aos.13610. Epub 2017 Dec 7.
We aimed to determine whether intravitreal dexamethasone as an adjuvant to intravitreal antibiotics is beneficial in the treatment of suspected bacterial endophthalmitis after cataract surgery.
Randomized, placebo-controlled superiority trial in three tertiary referral centres in the Netherlands. Patients with suspected bacterial endophthalmitis within 6 weeks after cataract surgery were eligible. A diagnostic vitreous biopsy was taken for culture, and patients received intravitreal injections of 400 μg dexamethasone (without preservatives) or placebo, in addition to 0.2 mg vancomycin and 0.05 mg gentamicin. The vancomycin and dexamethasone or placebo injections were repeated once at day 3 or 4. Primary outcome measure was best-corrected visual acuity (BCVA) at 1 year.
Between 1 November 2004 and 1 March 2014 (excluding two interruptions totalling 20 months), 324 eligible patients presented. A total of 167 patients (81 dexamethasone, 86 placebo) were available for the intention-to-treat analysis. Biopsies of 114 patients (68%) were culture-positive. Final BCVA did not differ between the dexamethasone and the placebo group (logMAR 0.31 ± 0.58 versus 0.27 ± 0.50; p = 0.90), nor did the number of patients with final vision of no light perception (LP, 7 versus 13). Pain, corneal oedema, the absence of a red fundus reflex on presentation, LP on presentation and culture of virulent pathogens from biopsy were statistically significantly associated with an unfavourable visual outcome.
Intravitreal dexamethasone without preservatives as an adjuvant to intravitreal antibiotics does not improve visual acuity (VA) in patients treated for suspected bacterial endophthalmitis after cataract surgery.
我们旨在确定在白内障手术后疑似细菌性眼内炎的治疗中,玻璃体内给予地塞米松作为辅助抗生素是否有益。
这是一项在荷兰三个三级转诊中心进行的随机、安慰剂对照优势试验。白内障手术后 6 周内患有疑似细菌性眼内炎的患者符合条件。进行诊断性玻璃体内活检以进行培养,并且患者除了接受 0.2 毫克万古霉素和 0.05 毫克庆大霉素外,还接受了 400 微克(不含防腐剂)地塞米松或安慰剂的玻璃体内注射。万古霉素和地塞米松或安慰剂注射在第 3 或第 4 天重复一次。主要结局指标是 1 年时的最佳矫正视力(BCVA)。
2004 年 11 月 1 日至 2014 年 3 月 1 日(不包括两次总共 20 个月的中断),共有 324 名符合条件的患者就诊。共有 167 名患者(81 名地塞米松,86 名安慰剂)可进行意向治疗分析。114 名患者(68%)的活检标本培养阳性。地塞米松组和安慰剂组的最终 BCVA 无差异(logMAR 0.31 ± 0.58 与 0.27 ± 0.50;p = 0.90),最终无光感视力的患者数量也无差异(7 名与 13 名)。疼痛、角膜水肿、就诊时眼底无红色反射、就诊时无光感和活检培养出毒力病原体与不良视力结局有统计学显著关联。
在白内障手术后疑似细菌性眼内炎的治疗中,玻璃体内给予不含防腐剂的地塞米松作为辅助抗生素不能提高视力。