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通过定期荧光血管造影和光学相干断层扫描评估玻璃体内阿柏西普单药治疗早产儿视网膜病变的疗效。

Efficacy of intravitreal aflibercept monotherapy in retinopathy of prematurity evaluated by periodic fluorescence angiography and optical coherence tomography.

作者信息

Vural Aslı, Perente İrfan, Onur İsmail Umut, Eriş Erdem, Seymen Zeynep, Hergünsel Gülsüm Oya, Salihoğlu Özgül, Yiğit Fadime Ulviye

机构信息

Ophthalmology Clinics, SBU Bakirkoy Dr. Sadi Konuk Training and Research Hospital, Bakirkoy, Istanbul, Turkey.

Ophthalmology Clinics, SBU Beyoglu Eye Training and Research Hospital, Beyoğlu, Istanbul, Turkey.

出版信息

Int Ophthalmol. 2019 Oct;39(10):2161-2169. doi: 10.1007/s10792-018-1040-x. Epub 2018 Nov 26.

Abstract

PURPOSE

To evaluate the efficacy of intravitreal aflibercept (IVA) in vascular and macular maturation in neonates with type 1 retinopathy of prematurity (ROP) and aggressive posterior retinopathy of prematurity (APROP).

MATERIALS AND METHODS

Thirty-six eyes of 18 patients with type 1 ROP or APROP in zone I or posterior zone II were enrolled in our study. At baseline, only fluorescein angiography (FA) was performed. After IVA injection, both FA and optical coherence tomography (OCT) were performed after 6.8 ± 0.8 (range 6-8) and 19 ± 0.9 (range 18-20) weeks to follow vascular and macular changes.

RESULTS

Both diffuse flat neovascularization with leakage and abnormal vascular branching at the small arteriolar level were detected in all eyes (100%) at baseline FA. Regression of the disease was observed in 34 eyes (94.4%) in the first week with binocular indirect ophthalmoscopy. Early unresponsiveness in remaining two eyes of an infant required an IVA re-treatment. Late reactivation was detected only in 19.4% of eyes, none of which required treatment during 12 months of follow-up. The most common feature after IVA injection was abnormal branching at capillary level, which was noted in 100% in the first post-injection FA and 50.0% of all eyes in the second FA. Meanwhile, the end limit of vascularization was observed in zone III in 83.3% of eyes. No vascular abnormality was also detected in 27.3% of eyes. The OCT examination at a mean postmenstrual age of 43.4 weeks revealed cystoid macular changes in four eyes of two infants (11.1%), normal foveal contour in 30 eyes of 15 infants (83.3%) and matured ellipsoid zone at the foveal center in 28 eyes of 14 infants (77.8%). Macular maturation was complete in all eyes in the last OCT analyses.

CONCLUSION

Intravitreal aflibercept monotherapy has been an effective treatment in type I ROP and APROP with much lower early and late re-treatment rates because of early unresponsiveness and late reactivation, respectively. In most of the eyes, rapid vascular outgrowth beyond zone III together with normal macular maturation was observed more precisely by periodic FA and OCT.

摘要

目的

评估玻璃体内注射阿柏西普(IVA)对1型早产儿视网膜病变(ROP)和侵袭性后部早产儿视网膜病变(APROP)新生儿血管和黄斑成熟的疗效。

材料与方法

18例1型ROP或APROP且病变位于I区或II区后部的患者的36只眼纳入本研究。基线时,仅进行荧光素血管造影(FA)。注射IVA后,分别在6.8±0.8(范围6 - 8)周和19±0.9(范围18 - 20)周进行FA和光学相干断层扫描(OCT),以观察血管和黄斑的变化。

结果

基线FA检查时,所有眼(100%)均检测到伴有渗漏的弥漫性扁平新生血管形成以及小动脉水平的异常血管分支。双眼间接检眼镜检查显示,第1周时34只眼(94.4%)病情出现消退。一名婴儿的其余两只眼早期无反应,需再次注射IVA治疗。仅19.4%的眼出现晚期复发,在12个月的随访期间均无需治疗。注射IVA后最常见的特征是毛细血管水平的异常分支,首次注射后FA检查时100%的眼出现该情况,第二次FA检查时50.0%的眼出现该情况。同时,83.3%的眼在III区观察到血管化的终点界限。27.3%的眼未检测到血管异常。平均月经后年龄43.4周时的OCT检查显示,两名婴儿的4只眼(11.1%)出现黄斑囊样改变,15名婴儿的30只眼(83.3%)黄斑中心凹轮廓正常,14名婴儿的28只眼(77.8%)黄斑中心凹处椭圆体带成熟。在最后一次OCT分析中,所有眼的黄斑均完全成熟。

结论

玻璃体内注射阿柏西普单一疗法对1型ROP和APROP是一种有效的治疗方法,由于分别存在早期无反应和晚期复发情况,其早期和晚期再次治疗率均较低。在大多数眼中,可以通过定期的FA和OCT更精确地观察到血管快速生长至III区以外以及黄斑正常成熟的情况。

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