Vadalà Maria, Sunseri Trapani Valentina, Guarrasi Giulia, Ventura Nicasio, Castellucci Massimo, Cillino Salvatore
Biomedicine, Neuroscience and Advanced Diagnostic Department, University of Palermo, Palermo, Italy.
IEMEST, Euro-Mediterranean Institute of Science and Technology, Palermo, Italy.
Clin Ophthalmol. 2020 Sep 15;14:2657-2665. doi: 10.2147/OPTH.S257775. eCollection 2020.
There has been an increasing clinical interest in specific retinal parameters as non-invasive biomarkers of retinal inflammation in diabetic macular edema (DME) that have been shown to have prognostic value, such as hyperreflective retinal fields (HRFs) and subfoveal neuroretinal detachment (SND).
We conducted a prospective, non-comparative study of treatment-naïve patients with DME to evaluate the efficacy of a Pro Re Nata (PRN) regimen of intravitreal dexamethasone implant 0.7 mg (DexI, Ozurdex™). After administration, patients underwent subsequent injections according to PRN criteria in case of edema relapse, but not earlier than 4 months after the previous treatment. Patients were evaluated at baseline, within 15 days of injection, and every month thereafter. During all visits, best-corrected visual acuity (BCVA) was recorded; central retinal thickness (CRT), type of edema, presence of SND, and presence and number of HRFs were evaluated using swept-source optical coherence tomography (SS-OCT) 3D. Treatment outcome was defined as changes in BCVA, CRT, SND and HRFs at 12 (T12) and 24 (T24) months compared with baseline (T0).
The study enrolled 24 eyes of 18 patients. The mean duration of follow-up was 18±6.6 months; for all eyes, T12 data were available, while follow-up reached T24 for 12 eyes. BCVA improved significantly and CRT decreased significantly during treatment; the edema was no longer detectable in 13/24 eyes at T12 and 8/12 eyes at T24. No patient presented SND at T12 and T24, and the mean number of HRFs decreased significantly during treatment. Results with CRT and HRFs correlated with BCVA at 12 and 24 months. No significant adverse events were observed.
In patients with DME, the intravitreal dexamethasone implant was effective and safe in improving both functional and tomographic parameters. This result is consistent with improvement in biomarkers of inflammation.
特定视网膜参数作为糖尿病性黄斑水肿(DME)视网膜炎症的非侵入性生物标志物,如高反射视网膜区域(HRF)和黄斑下神经视网膜脱离(SND),已显示出具有预后价值,临床上对其的关注日益增加。
我们对初治DME患者进行了一项前瞻性、非对照研究,以评估0.7mg玻璃体内地塞米松植入物(DexI,Ozurdex™)按需治疗(PRN)方案的疗效。给药后,若水肿复发,患者根据PRN标准进行后续注射,但不早于前次治疗后4个月。在基线、注射后15天内以及此后每月对患者进行评估。在所有就诊时,记录最佳矫正视力(BCVA);使用扫频光学相干断层扫描(SS-OCT)3D评估中心视网膜厚度(CRT)、水肿类型、SND的存在情况以及HRF的存在情况和数量。治疗结果定义为与基线(T0)相比,在12个月(T12)和24个月(T24)时BCVA、CRT、SND和HRF的变化。
该研究纳入了18例患者的24只眼。平均随访时间为18±6.6个月;所有眼均获得了T12数据,12只眼的随访达到了T24。治疗期间BCVA显著改善,CRT显著降低;在T12时,13/24只眼中水肿不再可检测到,在T24时,8/12只眼中水肿不再可检测到。在T12和T24时,没有患者出现SND,治疗期间HRF的平均数量显著减少。CRT和HRF的结果与12个月和24个月时的BCVA相关。未观察到显著的不良事件。
在DME患者中,玻璃体内地塞米松植入物在改善功能和断层扫描参数方面有效且安全。这一结果与炎症生物标志物的改善一致。