Frizziero Luisa, Parrozzani Raffaele, Trainiti Sara, Pilotto Elisabetta, Miglionico Giacomo, Pulze Serena, Midena Edoardo
Department of Ophthalmology, University of Padova, Padova, Italy.
G.B. Bietti Foundation, IRCCS, Ocular Oncology and Toxicology Research Unit, Roma, Italy.
Br J Ophthalmol. 2017 Dec;101(12):1699-1703. doi: 10.1136/bjophthalmol-2017-310220. Epub 2017 Apr 12.
To evaluate the efficacy and duration of activity of a single intravitreal dexamethasone implant in patients affected by radiation maculopathy.
Thirteen consecutive eyes of 13 patients affected by radiation maculopathy secondary to eye irradiation for a primary uveal melanoma (Iodine-125 brachytherapy) and treated with a single intravitreal 0.7 mg dexamethasone implant were retrospectively evaluated. Each patient underwent full ophthalmological examination, including fluorescein angiography and spectral domain optical coherence tomography (SD-OCT), even in en-face modality. Follow-up was performed monthly over a 6-month period.
At preinjection visit, the median central subfield thickness (CST) by SD-OCT was 407 µm (IQR, 357-524 µm) and the median best-corrected visual acuity (BCVA) was 61 ETDRS score (IQR, 54-67). The median gain of ETDRS letter at 1 month was 6.5 (IQR, 4-15) (p<0.01). The median CST showed a reduction of 120 µm (IQR, 62-134) (p<0.01). Further CST reduction was reported at 2 months' follow-up, with CST stabilisation at 3 months and maintenance of BCVA. At 4, 5 and 6 months' follow-up, all patients presented progressive retinal thickening (p<0.01) and BCVA reduction (p<0.01). No side effects were documented.
Intravitreal dexamethasone implant reduces macular oedema secondary to radiation maculopathy and also improved visual acuity in a consistent proportion of patients. Signs of macular oedema recurrence may be detected at a median of 4 months after injection.
评估单次玻璃体内注射地塞米松植入物对放射性黄斑病变患者的疗效及作用持续时间。
回顾性评估13例因原发性葡萄膜黑色素瘤接受眼内照射(碘-125近距离放疗)继发放射性黄斑病变并接受单次玻璃体内注射0.7mg地塞米松植入物治疗的患者的13只连续眼。每位患者均接受了全面的眼科检查,包括荧光素血管造影和频域光学相干断层扫描(SD-OCT),甚至包括表面成像模式。在6个月的时间里每月进行随访。
注射前检查时,SD-OCT测量的中央子野厚度(CST)中位数为407μm(四分位间距,357 - 524μm),最佳矫正视力(BCVA)中位数为61 ETDRS评分(四分位间距,54 - 67)。1个月时ETDRS字母数的中位数增加为6.5(四分位间距,4 - 15)(p<0.01)。CST中位数减少了120μm(四分位间距,62 - 134)(p<0.01)。在2个月随访时报告CST进一步降低,3个月时CST稳定,BCVA维持不变。在4、5和6个月随访时,所有患者均出现视网膜逐渐增厚(p<0.01)和BCVA下降(p<0.01)。未记录到副作用。
玻璃体内注射地塞米松植入物可减轻放射性黄斑病变继发的黄斑水肿,并使相当比例的患者视力得到改善。黄斑水肿复发的迹象可能在注射后中位数4个月时被检测到。