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玻璃体腔内注射贝伐单抗治疗早产儿视网膜病变的疗效和安全性:单中心回顾性研究。

Efficacy and safety of intravitreal bevacizumab for the treatment of retinopathy of prematurity: a single-center retrospective review.

机构信息

Eye Clinic, Neuromuscular and Sense Organs Department, Careggi University Hospital, Florence, Italy.

Division of Neonatology, Careggi University Hospital of Florence, Florence, Italy.

出版信息

J Matern Fetal Neonatal Med. 2022 Sep;35(17):3337-3342. doi: 10.1080/14767058.2020.1818214. Epub 2020 Sep 15.

Abstract

PURPOSE

The aim of this study is to report our experience in the management of type 1 retinopathy of prematurity (ROP) or aggressive posterior retinopathy of prematurity (APROP) in premature infants, who received intravitreal bevacizumab (IVB) injections either as first-line monotherapy or as rescue therapy following laser therapy.

METHODS

Single-center retrospective study on 37 patients (74 eyes) affected by sight-threatening ROP that underwent treatment either with IVB alone or laser photocoagulation followed by IVB at the Neonatal Intensive Care Unit of Careggi University Hospital of Florence, between 2008 and 2015.

RESULTS

Seventeen patients were males (45.9%) and 20 were females (54.1%). The mean gestational age was 24 weeks and the mean birth weight was 610 g. Fifty-six eyes (75.7%) of 28 patients were diagnosed as type 1 ROP and 18 eyes (24.3%) of nine patients as APROP. Sixty-six eyes of 33 patients received IVB as first-line monotherapy, eight eyes of four patients were treated with IVB after laser photocoagulation treatment, as rescue therapy. The mean postmenstrual age at treatment was 33.9 weeks. All the patients received bilateral injections. None of the infants required repeat injections. The mean follow-up time was 59.6 months. All the patients achieved a good response to treatment, showing the regression of the proliferative phase and a complete peripheral retinal vascularization within 2 months from the injection of bevacizumab. One patient with a bilateral ROP had only a partial resolution of a vitreous hemorrhage in the left eye. The procedures were well tolerated without local or systemic adverse events during the follow-up. No infants showed recurrences. Ocular motility alterations appeared in four patients (10.8%), with the absence of stereopsis in six cases (16.20%). After treatment, spherical equivalent values in cycloplegic refraction ranged from -4.0 D to +5.0 D, with a mean value of +1.75 D. All the patients showed a normal neuropsychomotor development.

CONCLUSION

Our study confirms the effectiveness and safety of IVB in the treatment of ROP, both as monotherapy and rescue therapy after laser photocoagulation, according to the published literature.

摘要

目的

本研究旨在报告我们在接受玻璃体腔内注射贝伐单抗(IVB)治疗的早产儿中管理 1 型早产儿视网膜病变(ROP)或侵袭性后部早产儿视网膜病变(APROP)的经验,这些早产儿接受 IVB 治疗的方式为一线单药治疗或激光治疗后进行的挽救性治疗。

方法

这是一项单中心回顾性研究,纳入了 2008 年至 2015 年期间在佛罗伦萨 Careggi 大学医院新生儿重症监护室接受治疗的 37 名(74 只眼)患有威胁视力的 ROP 的患者。这些患者接受了单独的 IVB 治疗或激光光凝联合 IVB 治疗。

结果

17 名男性(45.9%)和 20 名女性(54.1%)纳入本研究。平均胎龄为 24 周,平均出生体重为 610 克。28 名患者的 56 只眼(75.7%)被诊断为 1 型 ROP,9 名患者的 18 只眼(24.3%)为 APROP。33 名患者中的 66 只眼接受了 IVB 作为一线单药治疗,4 名患者中的 8 只眼在激光光凝治疗后接受了 IVB 作为挽救性治疗。治疗时的平均孕龄为 33.9 周。所有患者均接受了双眼注射。没有患者需要重复注射。平均随访时间为 59.6 个月。所有患者对治疗均有良好反应,在接受贝伐单抗注射后 2 个月内,增殖期消退,视网膜周边血管完全形成。1 名双侧 ROP 患者左眼仅部分解决了玻璃体积血。在随访期间,所有患者均未出现局部或全身不良反应,治疗过程耐受良好。没有患者出现复发。4 名患者(10.8%)出现眼球运动改变,6 名患者(16.20%)出现立体视缺失。治疗后,睫状肌麻痹下的屈光球镜值范围为-4.0 D 至+5.0 D,平均为+1.75 D。所有患者的神经精神运动发育均正常。

结论

根据已发表的文献,本研究证实了 IVB 作为一线单药治疗或激光治疗后挽救性治疗在治疗 ROP 方面的有效性和安全性。

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