Sun Michelle T, Wood Megan K, Chan WengOnn, Selva Dinesh, Sanders Prashanthan, Casson Robert J, Wong Christopher X
South Australian Institute of Ophthalmology, The University of Adelaide and Royal Adelaide Hospital, Adelaide.
Centre for Heart Rhythm Disorders, South Australian Health and Medical Research Institute, The University of Adelaide and Royal Adelaide Hospital, Adelaide.
JAMA Ophthalmol. 2017 Aug 1;135(8):864-870. doi: 10.1001/jamaophthalmol.2017.2199.
It is unclear if the risk of intraocular bleeding with novel oral anticoagulants differs compared with warfarin.
To characterize the risk of intraocular bleeding with novel oral anticoagulants compared with warfarin.
A systematic review and meta-analysis was undertaken in an academic medical setting. MEDLINE and ClinicalTrials.gov were searched for randomized clinical trials published up until August 2016. This search was supplemented by manual bibliography searches of identified trials and other review articles.
Studies were eligible for inclusion if they were phase 3 randomized clinical trials, enrolled patients with atrial fibrillation or venous thromboembolism, compared a novel oral anticoagulant (dabigatran, rivaroxaban, apixaban, or edoxaban) with warfarin, and recorded event data on intraocular bleeding. Data on intraocular bleeding were pooled using inverse-variance, weighted, fixed-effects meta-analysis.
The PRISMA guidelines were used for abstracting data and assessing quality. Independent extraction was performed by 2 investigators.
Intraocular bleeding events and associated risk ratio for novel oral anticoagulants compared with warfarin.
Twelve trials investigating 102 627 patients were included. Randomization to novel oral anticoagulants was associated with a 22% relative reduction in intraocular bleeding compared with warfarin (risk ratio, 0.78; 95% CI, 0.61-0.99). There was no significant heterogeneity observed (I2 = 4.8%, P = .40). Comparably lower risks of intraocular bleeding with novel oral anticoagulants were seen in subgroup analyses, with no significant difference according to the indication for anticoagulation (P for heterogeneity = .49) or the novel oral anticoagulant type (P for heterogeneity = .15). Summary estimates did not differ materially when random-effects meta-analytic techniques were used.
These results suggest that novel oral anticoagulants reduce the risk of intraocular bleeding by approximately one-fifth compared with warfarin. Similar benefits were seen in both patients with atrial fibrillation and venous thromboembolism. Our data have particular relevance for patients at higher risk of spontaneous retinal and subretinal bleeding. These findings may also have important implications in the perioperative period, in which the use of novel oral anticoagulants may be superior. Future studies are required to better characterize the optimal management of patients with both ophthalmic disease and cardiovascular comorbidities requiring anticoagulation.
新型口服抗凝药导致眼内出血的风险与华法林相比是否存在差异尚不清楚。
对比新型口服抗凝药与华法林导致眼内出血的风险。
在学术性医疗环境中进行了一项系统评价和荟萃分析。检索了MEDLINE和ClinicalTrials.gov,以查找截至2016年8月发表的随机临床试验。通过对已识别试验和其他综述文章的参考文献进行手动检索对此次检索进行补充。
如果研究为3期随机临床试验,纳入心房颤动或静脉血栓栓塞患者,对比新型口服抗凝药(达比加群、利伐沙班、阿哌沙班或依度沙班)与华法林,并记录眼内出血的事件数据,则这些研究符合纳入标准。使用逆方差加权固定效应荟萃分析汇总眼内出血数据。
采用PRISMA指南提取数据并评估质量。由2名研究人员独立进行提取。
新型口服抗凝药与华法林相比的眼内出血事件及相关风险比。
纳入了12项研究102627例患者的试验。与华法林相比,随机分配至新型口服抗凝药组的患者眼内出血相对减少22%(风险比,0.78;95%CI,0.61 - 0.99)。未观察到显著的异质性(I² = 4.8%,P = 0.40)。在亚组分析中,新型口服抗凝药的眼内出血风险同样较低,根据抗凝适应证(异质性P = 0.49)或新型口服抗凝药类型(异质性P = 0.15)未观察到显著差异。使用随机效应荟萃分析技术时,汇总估计值无实质性差异。
这些结果表明,与华法林相比,新型口服抗凝药可使眼内出血风险降低约五分之一。在心房颤动和静脉血栓栓塞患者中均观察到类似益处。我们的数据对视网膜和视网膜下自发出血风险较高的患者具有特殊意义。这些发现可能在围手术期也具有重要意义,在此期间使用新型口服抗凝药可能更具优势。未来需要开展研究以更好地明确患有眼科疾病且合并需要抗凝治疗的心血管疾病患者的最佳管理方法。