Glaucoma Consultant, CTIG-Hospital Quirón Teknon, Barcelona, Spain.
Department of Ophthalmology, University Hospitals Leuven, Louvain, Belgium.
Ophthalmol Ther. 2016 Jun;5(1):47-61. doi: 10.1007/s40123-016-0052-8. Epub 2016 May 10.
With the increasing use of intravitreal administration of corticosteroids in macular edema, steroid-induced intraocular pressure (IOP) rise is becoming an emergent issue. However, for patients in whom intravitreal steroids are indicated, there are no specific recommendations for IOP monitoring and management after intravitreal administration of corticosteroids.
An expert panel of European ophthalmologists reviewed evidence on corticosteroid-induced IOP elevation. The objective of the panel was to propose an algorithm based on available literature and their own experience for the monitoring and management of corticosteroid-induced IOP elevation, with a focus on diabetic patients.
Data from trials including diabetic patients with a rise of IOP after intravitreal steroid administration indicate that IOP-lowering medical treatment is sufficient for a large majority of patients; only a small percentage underwent laser trabeculoplasty or filtering filtration surgery. A 2-step algorithm is proposed that is based on the basal value of IOP and evidence for glaucoma. The first step is a risk stratification before treatment. Patients normotensive at baseline (IOP ≤ 21 mmHg), do not require additional baseline diagnostic tests. However, patients with baseline ocular hypertension (OHT) (IOP > 21 mmHg) should undergo baseline imaging and visual field testing. The second step describes monitoring and treatment after steroid administration. During follow-up, patients developing OHT should have baseline and periodical imaging and visual field testing; IOP-lowering treatment is proposed only if IOP is >25 mmHg or if diagnostic tests suggest developing glaucoma.
The management and follow-up of OHT following intravitreal corticosteroid injection is similar to that of primary OHT. If OHT develops, IOP is controlled in a large proportion of patients with standard IOP treatments. The present algorithm was developed to assist ophthalmologists with guiding principles in the management of corticosteroid-induced IOP elevation.
Alimera Sciences Limited.
随着糖皮质激素在黄斑水肿患者中玻璃体腔内给药的应用日益增多,皮质类固醇引起的眼内压(IOP)升高成为一个紧急问题。然而,对于需要玻璃体内给予皮质类固醇的患者,对于玻璃体内给予皮质类固醇后 IOP 监测和管理,尚无具体的推荐意见。
一组欧洲眼科专家审查了皮质类固醇引起的IOP 升高的证据。专家组的目的是根据现有文献和他们自己的经验,提出一种用于监测和管理皮质类固醇引起的IOP 升高的算法,重点关注糖尿病患者。
包括糖尿病患者在内的接受玻璃体内皮质类固醇治疗后 IOP 升高的试验数据表明,对于大多数患者,降低 IOP 的药物治疗就足够了;只有一小部分患者需要行激光小梁成形术或滤过性手术。提出了一种两步算法,该算法基于 IOP 的基础值和青光眼的证据。第一步是治疗前的风险分层。基线时眼压正常的患者(IOP≤21mmHg),不需要额外的基线诊断性检查。然而,基线时存在眼压升高(OHT)(IOP>21mmHg)的患者应进行基线时的影像学和视野检查。第二步描述了皮质类固醇给药后的监测和治疗。在随访过程中,发生 OHT 的患者应进行基线和定期的影像学和视野检查;仅当 IOP>25mmHg 或诊断性检查提示青光眼进展时,才建议进行降眼压治疗。
玻璃体内皮质类固醇注射后 OHT 的管理和随访与原发性 OHT 相似。如果发生 OHT,在很大一部分患者中,通过标准的 IOP 治疗可以控制 IOP。本算法旨在协助眼科医生在管理皮质类固醇引起的IOP 升高方面提供指导原则。
Alimera Sciences Limited。