McCafferty Sean, Harris April, Kew Corin, Kassm Tala, Lane Lisa, Levine Jason, Raven Meisha
Arizona Eye Consultants, 355 N. Silverbell Ave, Tucson, AZ, 85745, USA.
University of Arizona, 6422 E. Speedway Ave, Tucson, AZ, 85710, USA.
BMC Ophthalmol. 2017 Feb 20;17(1):16. doi: 10.1186/s12886-017-0405-7.
Define the effectiveness of a topical non-steroidal anti-inflammatory drug (NSAID) added to topical steroid use after uncomplicated phacoemulsification for the prevention of pseudophakic cystoid macular edema (PCME) using a prospective, randomized, double-masked, placebo-controlled clinical study.
Eyes (1000) were randomized to placebo (497) or nepafenac 0.3% (503) used once daily, post-operatively for 5 weeks at two ophthalmology clinics. Diagnosis of PCME was made by clinical, ocular coherence tomography (OCT), and with fluorescein angiography confirmation. Correlation of PCME to NSAID use and the presence of pre-operative risk factors for PCME were assessed including, contralateral PCME, diabetic retinopathy, retinal vein occlusion, macular hole, epiretinal membrane, macular degeneration, retinal detachment repair, and prostaglandin use.
PCME was the most common complication associated with routine cataract surgery (4.2% with PCME risk factors, 2.0% with risk factors excluded). Topical nepafenac 0.3% significantly reduces the incidence of PCME compared to placebo when used after routine cataract surgery (p = .0001). When patients with pre-operative risk factors are excluded, the incidence of PCME between treatment and placebo groups is equivalent (p = 0.31). PCME relative risk (RR) was most significant in contralateral PCME (RR 19.5), diabetic retinopathy (RR 13.1), retinal vein occlusion (RR 12.9), macular hole (RR 7.7), and epiretinal membrane (RR 5.7). Prostaglandin use and previous retinal detachment were not shown to increase risk.
Pseudophakic cystoid macular edema is common after phacoemulsification cataract surgery. Topical nepafenac 0.3% reduces PCME in patients with pre-operative risk factors for PCME compared to placebo but shows no benefit in patients without pre-operative risk factors.
NIH ClincalTrials.gov retrospectively registered January 15, 2017, NCT03025945 .
采用前瞻性、随机、双盲、安慰剂对照临床研究,确定在单纯性白内障超声乳化术后,局部使用非甾体抗炎药(NSAID)联合局部使用类固醇预防人工晶状体性黄斑囊样水肿(PCME)的有效性。
在两家眼科诊所,将1000只眼睛随机分为安慰剂组(497只)或0.3%萘非那酮组(503只),术后每天使用一次,持续5周。通过临床检查、光学相干断层扫描(OCT)以及荧光素血管造影确认来诊断PCME。评估PCME与NSAID使用以及PCME术前危险因素的相关性,包括对侧PCME、糖尿病视网膜病变、视网膜静脉阻塞、黄斑裂孔、视网膜前膜、黄斑变性、视网膜脱离修复以及前列腺素的使用情况。
PCME是与常规白内障手术相关的最常见并发症(有PCME危险因素的患者中发生率为4.2%,排除危险因素的患者中发生率为2.0%)。常规白内障手术后使用时,0.3%的局部萘非那酮与安慰剂相比,显著降低了PCME的发生率(p = 0.0001)。排除术前有危险因素的患者后,治疗组和安慰剂组的PCME发生率相当(p = 0.31)。PCME相对风险(RR)在对侧PCME(RR 19.5)、糖尿病视网膜病变(RR 13.1)、视网膜静脉阻塞(RR 12.9)、黄斑裂孔(RR 7.7)和视网膜前膜(RR 5.7)中最为显著。未显示使用前列腺素和既往视网膜脱离会增加风险。
白内障超声乳化术后人工晶状体性黄斑囊样水肿很常见。与安慰剂相比,0.3%的局部萘非那酮可降低有PCME术前危险因素患者的PCME发生率,但对无术前危险因素的患者无益处。
美国国立卫生研究院临床研究注册库,于2017年1月15日进行回顾性注册,NCT03025945 。