El Chehab H, Le Corre A, Giraud J-M, Ract-Madoux G, Swalduz B, Dot C
Service d'ophtalmologie, HIA Desgenettes, 108, boulevard Pinel, 69003 Lyon, France.
J Fr Ophtalmol. 2012 Oct;35(8):614-21. doi: 10.1016/j.jfo.2012.02.009. Epub 2012 Jul 23.
The purpose of this study was to evaluate intraocular pressure increase after intravitreal injections (IVIs) and the effect of prophylactic pressure-lowering medications.
A prospective study of 210 anti-vascular endothelial growth factor (VEGF) IVI (0.05 mL of bevacizumab or ranibizumab), that were divided into five groups, group 1: no intraocular pressure (IOP)-lowering medication (n=50); group 2: apraclonidine 1 % one drop 2 hours prior to IVI (n=50); group 3: acetazolamide 250 mg 2 hours prior (n=50); group 4: fixed combination brimonidine+timolol (n=30); group 5: fixed combination dorzolamide+timolol (n=30). IOP was measured before, immediately after (T1), 15 min after (T15) and 45 min after (T45) the IVI using a Perkins tonometer.
The mean IOP peak in group 1 was 46.4 ± 4.8 mmHg at T1, 21.7 ± 5.7 mmHg at T15 and 15.4 ± 4.3 mmHg at T45. Apraclonidine 1 % and the fixed combinations produced a significant reduction of IOP at every time point, of around 9 mmHg at T1. The reduction in IOP obtained with acetazolamide was not significant versus group 1 at T1 (-1.6 mmHg, P=0.12), but became significant at T15 and T45 (respectively, P=0.011 and P=0.015).
IOP spikes are high but transient following IVI. Acetazolamide proved to be ineffective in preventing this spike. Topical medications, however, produced a significant reduction in IOP spike as well as in the duration of the increased pressure, with no significant difference between fixed combinations and 1 % apraclonidine at T1. It would seem advisable to prevent this IOP spike in the case of repeated injections, particularly in patients with glaucoma.
本研究旨在评估玻璃体内注射(IVI)后眼压升高情况以及预防性降压药物的效果。
对210次抗血管内皮生长因子(VEGF)玻璃体内注射(0.05 mL贝伐单抗或雷珠单抗)进行前瞻性研究,分为五组,第1组:未使用降低眼压(IOP)药物(n = 50);第2组:在玻璃体内注射前2小时滴用1%阿可乐定一滴(n = 50);第3组:在注射前2小时服用250 mg乙酰唑胺(n = 50);第4组:布林佐胺+噻吗洛尔固定复方制剂(n = 30);第5组:多佐胺+噻吗洛尔固定复方制剂(n = 30)。使用珀金氏眼压计在玻璃体内注射前(T0)、注射后即刻(T1)、注射后15分钟(T15)和注射后45分钟(T45)测量眼压。
第1组眼压峰值在T1时为46.4±4.8 mmHg,T15时为21.7±5.7 mmHg,T45时为15.4±4.3 mmHg。1%阿可乐定和固定复方制剂在每个时间点均使眼压显著降低,T1时约降低9 mmHg。乙酰唑胺在T1时与第1组相比眼压降低不显著(-1.6 mmHg,P = 0.12),但在T15和T45时变得显著(分别为P = 0.011和P = 0.015)。
玻璃体内注射后眼压峰值较高但为一过性。乙酰唑胺在预防眼压峰值方面无效。然而,局部用药可使眼压峰值以及眼压升高持续时间显著降低,在T1时固定复方制剂与1%阿可乐定之间无显著差异。对于重复注射的情况,尤其是青光眼患者,预防这种眼压峰值似乎是可取的。