Moorfields Eye Hospital, London, United Kingdom.
Moorfields Eye Hospital, London, United Kingdom; UCL Institute of Ophthalmology, London, United Kingdom.
Am J Ophthalmol. 2018 Apr;188:173-180. doi: 10.1016/j.ajo.2018.02.001. Epub 2018 Feb 12.
To compare the visual outcomes of patients with acute retinal necrosis (ARN) treated initially with intravenous acyclovir vs oral valacyclovir therapy.
Retrospective, comparative, interventional case series.
Sixty-two patients (68 eyes) with ARN, treated at Moorfields Eye Hospital (United Kingdom) between 1992 and 2016, were identified through the hospital's electronic database. Exclusion criteria included insufficient patient records or follow-up (<150 days). Fifty-six patients had unilateral ARN, while 6 had bilateral ARN. Patients who received intravenous acyclovir on diagnosis (n = 33) were compared with patients treated with oral valacyclovir (n = 29) across outcomes including best-corrected visual acuity, retinal detachment, severe vision loss, and other complications. The impact of adjunctive intravitreal antiviral and prophylactic barrier laser treatment was also assessed.
Change in best-corrected visual acuity was not significantly different for eyes treated initially with intravenous therapy vs oral therapy over 5 years of follow-up data (P = .16). There was no difference in the rates of severe vision loss between the 2 groups (46% and 59%, respectively, P = .18), or of those eyes retaining good vision (28% vs 31%, respectively, P = .80). Retinal detachment occurred in 63% of cases and did not differ across treatment groups (62% vs 66%, respectively, P = .67). Barrier laser and intravitreal therapy had no effect on retinal detachment rate in either group.
Oral valacyclovir is clinically equivalent to intravenous therapy in the management of ARN. Oral valacyclovir as an outpatient therapy-with or without intravitreal foscarnet-can therefore be considered as an acceptable alternative to inpatient therapy required for intravenous treatment.
比较急性视网膜坏死(ARN)患者初始接受静脉用阿昔洛韦与口服伐昔洛韦治疗的视觉结局。
回顾性、对照、干预性病例系列研究。
通过医院的电子数据库,确定了 1992 年至 2016 年间在 Moorfields 眼科医院(英国)接受治疗的 62 例(68 只眼)ARN 患者。排除标准包括患者记录或随访不足(<150 天)。56 例患者为单侧 ARN,6 例为双侧 ARN。将诊断时接受静脉用阿昔洛韦治疗的患者(n=33)与接受口服伐昔洛韦治疗的患者(n=29)进行比较,比较结果包括最佳矫正视力、视网膜脱离、严重视力丧失和其他并发症。还评估了辅助玻璃体内抗病毒和预防性屏障激光治疗的影响。
在 5 年的随访数据中,初始接受静脉治疗的眼与初始接受口服治疗的眼之间的最佳矫正视力变化无显著差异(P=0.16)。两组严重视力丧失的发生率无差异(分别为 46%和 59%,P=0.18),保留良好视力的眼也无差异(分别为 28%和 31%,P=0.80)。视网膜脱离发生在 63%的病例中,且两组之间无差异(分别为 62%和 66%,P=0.67)。两组中,屏障激光和玻璃体内治疗对视网膜脱离率均无影响。
口服伐昔洛韦在 ARN 的治疗中与静脉治疗具有临床等效性。因此,口服伐昔洛韦作为门诊治疗(联合或不联合玻璃体内膦甲酸)可被视为静脉治疗所需住院治疗的可接受替代方案。