Department of Ophthalmology, Copenhagen University Hospital, Rigshospitalet-Glostrup, Glostrup, Denmark.
Department of Drug Design and Pharmacology, University of Copenhagen, Copenhagen, Denmark.
Br J Ophthalmol. 2020 Nov;104(11):1512-1518. doi: 10.1136/bjophthalmol-2019-315623. Epub 2020 Feb 12.
BACKGROUND/AIMS: This systematic review compared the efficacy and safety of benzalkonium chloride (BAK)-preserved eye-drops with alternatively preserved (AP) and preservative-free (PF) eye-drops.
PubMed, EMBASE and MEDLINE were searched for randomised controlled trials in June and October 2019. Study selection, data extraction and risk of bias assessment were made by two independent reviewers using the Cochrane Handbook. Studies on prostaglandin analogue or beta-blocker eye-drops and patients with glaucoma or ocular hypertension were included. Primary outcome was change in intraocular pressure (IOP). Secondary outcomes were safety measures as assessed in original study.
Of 433 articles screened, 16 studies were included. IOP meta-analysis was conducted on 13 studies (4201 patients) ranging from 15 days to 6 months. No significant differences between BAK versus PF and AP were identified (95% CI -0.00 to 0.30 mm Hg, p=0.05). Meta-analyses revealed no differences between BAK versus AP and PF with regards to conjunctival hyperaemia (risk ratio (RR) 1.05, 95% CI 0.91 to 1.22, 3800 patients, 9 studies), ocular hyperaemia (RR 1.31, 95% CI 0.96 to 1.78, 2268 patients, 5 studies), total ocular adverse events (RR 1.03, 95% CI 0.88 to 1.20, 1906 patients, 5 studies) or tear break-up time (mean difference 0.89, 95% CI -0.03 to 1.81, 130 patients, 3 studies). Diverse reporting on safety measures made comparison challenging. Risk of bias was assessed as high or unclear in many relevant domains, suggesting potential selective reporting or under-reporting.
No clinically significant differences on efficacy or safety could be determined between BAK versus AP and PF. However, there were substantial uncertainties on safety.CRD42019139692.
背景/目的:本系统评价比较了苯扎氯铵(BAK)保存的滴眼液与替代保存(AP)和无防腐剂(PF)滴眼液的疗效和安全性。
2019 年 6 月和 10 月,我们在 PubMed、EMBASE 和 MEDLINE 上检索了随机对照试验。使用 Cochrane 手册,由两名独立评审员进行研究选择、数据提取和偏倚风险评估。纳入了前列腺素类似物或β受体阻滞剂滴眼液和青光眼或高眼压患者的研究。主要结局是眼压(IOP)的变化。次要结局是原始研究中评估的安全性措施。
在筛选出的 433 篇文章中,有 16 项研究被纳入。对 13 项研究(4201 例患者)进行了 IOP 荟萃分析,研究时间从 15 天到 6 个月不等。BAK 与 PF 和 AP 之间未发现显著差异(95%CI-0.00 至 0.30mmHg,p=0.05)。荟萃分析显示,BAK 与 AP 和 PF 之间在结膜充血(风险比(RR)1.05,95%CI0.91 至 1.22,3800 例患者,9 项研究)、眼充血(RR1.31,95%CI0.96 至 1.78,2268 例患者,5 项研究)、总眼部不良事件(RR1.03,95%CI0.88 至 1.20,1906 例患者,5 项研究)或泪膜破裂时间(平均差异 0.89,95%CI-0.03 至 1.81,130 例患者,3 项研究)方面均无差异。由于安全性措施的报告方式多种多样,因此比较具有挑战性。在许多相关领域,偏倚风险评估为高或不明确,这表明可能存在选择性报告或报告不足。
在疗效或安全性方面,BAK 与 AP 和 PF 之间没有发现有临床意义的差异。但是,安全性方面存在很大的不确定性。CRD42019139692。