Real-Life Management of Central and Branch Retinal Vein Occlusion: A Seven-Year Follow-Up Study

被引:15
作者
Arrigo, Alessandro [1 ]
Crepaldi, Anna [1 ]
Vigano, Chiara [1 ]
Aragona, Emanuela [1 ]
Lattanzio, Rosangela [1 ]
Scalia, Giovanni [1 ]
Resti, Antonio Giordano [1 ]
Calcagno, Francesca [1 ]
Pina, Adelaide [1 ]
Rashid, Hassan Farah [1 ]
Bandello, Francesco [1 ]
Battaglia Parodi, Maurizio [1 ]
机构
[1] Univ Vita Salute, IRCCS San Raffaele Hosp, Dept Ophthalmol, Milan, Italy
关键词
central retinal vein occlusion; branch retinal vein occlusion; optical coherence tomography; real-life study; intravitreal injection; MACULAR EDEMA SECONDARY; INTRAVITREAL AFLIBERCEPT INJECTION; SUSTAINED BENEFITS; 12-MONTH OUTCOMES; TRAP-EYE; RANIBIZUMAB; IMPLANT; LASER;
D O I
10.1055/s-0041-1725197
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Retinal vein occlusion is the second most common retinal vascular pathology after diabetic retinopathy and a major cause of vision impairment. Nowadays, both central retinal vein occlusion (CRVO) and branch retinal vein occlusion (BRVO) can be well-managed by intravitreal treatments. However, considering the long-life expectance of the patients, few data are present in the literature about the very long-term outcome of CRVO and BRVO. The present study was an interventional, retrospective analysis of the morphological and functional long-term outcome of CRVO and BRVO patients, followed in an Italian referral center. We collected data from 313 eyes (178 CRVO eyes and 135 BRVO eyes). Mean follow-up was 45 +/- 25 months (range 12-84 months). Both CRVO and BRVO eyes experience a significant visual acuity improvement secondary to anti-vascular endothelial growth factor/dexamethasone treatments (from 0.57 +/- 0.25 to 0.41 +/- 0.24 LogMAR in CRVO and from 0.53 +/- 0.42 to 0.30 +/- 0.41 LogMAR in BRVO, respectively) ( p <0.01). Also, central macular thickness (CMT) resulted significant recovery at the end of the follow-up (from 585.54<plus/minus>131.43 to 447.88 +/- 245.07 mu m in CRVO and from 585.54 +/- 131.43 to 447.88 +/- 245.07 mu m in BRVO, respectively) ( p <0.01). CRVO eyes received a mean of 10.70<plus/minus>4.76 intravitreal treatments, whereas BRVO underwent 9.80 +/- 5.39 injections over the entire 7-year follow-up. Our analyses highlighted different time points indicating the best obtainable improvement. This was the first year for CRVO (12-month follow-up) and the second year for BRVO (24-month follow-up). After these two time points, both visual acuity and CMT resulted stable up to the end of the follow-up. Ischemia was associated with significantly worse outcome.
引用
收藏
页码:1361 / 1366
页数:6
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