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Effect of Switching Therapy to Pegaptanib in Eyes With the Persistent Cases of Exudative Age-Related Macular Degeneration

机译:持续性渗出性年龄相关性黄斑变性病例中转用培加他尼治疗的效果

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摘要

Purpose of this study was to evaluate the efficacy of switching to pegaptanib monotherapy for persistent cases of exudative age-related macular degeneration (AMD).Out of 296 eyes of 296 patients treated with ranibizumab or ranibizumab combined with photodynamic therapy (PDT), 50 eyes of 50 AMD patients were found to be resistant to these treatments. Over a 12-month period, intravitreal pegaptanib (IVP) 0.3 mg was administered at intervals of 6 weeks until the exudation disappeared prospectively. All patients were examined with the following tests: best-corrected visual acuity (BCVA) and central retinal thickness (CRT), determined at the initial visit, before the first IVP (baseline), and at 12 months. The factors responsible for achieving dry macula with IVP were examined statistically.The rate of persistent cases with intravitreal ranibizumab (IVR) and/or PDT was 17.0%. The mean number of IVPs administered was 5.4 (range, 2–9). Logarithm of the minimal angle of resolution BCVA at 12 months was stable or improved by ≥0.3 in 49 eyes (98.0%), with a significant improvement noted between the baseline and final BCVA (P = 0.01, paired t test). The CRT (mean ± standard deviation) was 446.9 ± 150.6 µm at the initial visit, 414.5 ± 146.5 µm at baseline, and 318.7 ± 99.0 µm at 12 months. There was a significant decrease in the mean CRT between the measurements at baseline and at 12 months after the first IVP (P = 0.002, Bonferroni correction). At 12 months, the exudative change was completely resolved in 27 eyes (54.0%) and reduced in 21 eyes (42.0%). The number of previous IVR treatments was significantly correlated with dry macula at 12 months.After switching therapy to pegaptanib in persistent cases of AMD, most patients maintained or improved their BCVA and exhibited a positive treatment response at 12 months.
机译:这项研究的目的是评估改用培加他尼单药治疗持续性渗出性年龄相关性黄斑变性(AMD)的疗效.296例雷珠单抗或雷珠单抗联合光动力疗法(PDT)治疗的296眼中,有50眼发现50名AMD患者对这些治疗有抵抗力。在12个月的时间内,每6周注射一次玻璃体内培加他尼(IVP)0.3μmg,直至前瞻性渗出消失。所有患者均接受以下检查:最佳矫正视力(BCVA)和视网膜中央厚度(CRT),在首次就诊时,第一次IVP之前(基线)和12个月时确定。统计分析了使用IVP实现干性黄斑的因素。玻璃体腔内兰尼单抗(IVR)和/或PDT持续性病例的发生率为17.0%。 IVP的平均给药次数为5.4(范围2–9)。 49眼(98.0%)的12个月时BCVA最小分辨角的对数稳定或提高了≥0.3,在基线和最终BCVA之间有显着改善(P = 0.01,配对t检验)。初次就诊时的CRT(平均±标准偏差)为446.9±150.6μm,基线时为414.5±146.5μm,而在12个月时为318.7±99.0μm。在基线和第一次IVP后12个月之间的测量之间,平均CRT显着下降(P = 0.002,Bonferroni校正)。在12个月时,渗出性改变在27眼(54.0%)中得到了完全解决,而在21眼(42.0%)中得到了减轻。先前的IVR治疗次数与12个月时的干性黄斑显着相关。在持续性AMD病例中,将治疗改为培加他尼后,大多数患者在12个月时保持或改善了BCVA,并显示出积极的治疗反应。

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