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早产儿视网膜病变中的低剂量雷珠单抗治疗。

Low-dose ranibizumab administration in retinopathy of prematurity.

机构信息

Department of Ophthalmology, Faculty of Medicine, Süleyman Demirel University Hospital, 32260, Çünür, Isparta, Turkey.

Konya Eye Private Hospital, Isparta, Turkey.

出版信息

Int Ophthalmol. 2022 May;42(5):1545-1552. doi: 10.1007/s10792-021-02145-w. Epub 2022 Jan 7.

DOI:10.1007/s10792-021-02145-w
PMID:34993841
Abstract

PURPOSE

To evaluate the efficiency of low-dose intravitreal ranibizumab therapy in the treatment of aggressive retinopathy of prematurity (A-ROP).

METHODS

A total of 124 eyes of 62 patients who underwent intravitreal ranibizumab after an A-ROP diagnosis between January 2015 and January 2021 were evaluated retrospectively. After receiving family-approved informed consent, low-dose intravitreal ranibizumab was administered, and regular follow-ups were performed.

RESULTS

Patients included in the study had a mean birth week of 26.6 (23-33 weeks), a mean birth weight of 905 (450-1970) grams, and an average injection postnatal time of 9.1 (4-19) weeks. The mean follow-up period was 63 (24-250) weeks. In all eyes, ROP regressed in the first week after injection, and no asymmetrical response was observed in the eyes of any baby. A total of 58 eyes recovered with a single dose of intravitreal injection therapy, and peripheral retinal vascularization was completed. A second injection was required in 38 eyes. Rescue treatment was applied in addition to intravitreal ranibizumab treatment in 22 eyes of 11 babies. None of the patients had any ocular or systemic side effects.

CONCLUSION

Low-dose intravitreal ranibizumab injection with close follow-up and appropriate timing is an effective treatment modality in A-ROP. Even among patients undergoing rescue laser treatment, the treatment can be completed with a wide visual field.

摘要

目的

评估小剂量玻璃体内雷珠单抗治疗早产儿侵袭性视网膜病变(A-ROP)的疗效。

方法

回顾性分析 2015 年 1 月至 2021 年 1 月期间诊断为 A-ROP 并接受玻璃体内雷珠单抗治疗的 62 例患者的 124 只眼。在获得家属同意后,给予小剂量玻璃体内雷珠单抗治疗,并进行定期随访。

结果

研究纳入的患者平均出生孕周为 26.6(23-33 周),平均出生体重为 905(450-1970)g,平均生后注射时间为 9.1(4-19)周。平均随访时间为 63(24-250)周。所有患眼在注射后第 1 周ROP 均消退,且未观察到任何婴儿的眼出现不对称反应。58 只眼单次玻璃体内注射治疗后痊愈,周边视网膜血管化完成。38 只眼需要再次注射。11 例患儿的 22 只眼除玻璃体内雷珠单抗治疗外,还进行了挽救性激光治疗。所有患者均无眼部或全身不良反应。

结论

小剂量玻璃体内雷珠单抗注射结合密切随访和适时治疗是 A-ROP 的有效治疗方法。即使在需要进行挽救性激光治疗的患者中,也可以通过广泛的视场完成治疗。

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本文引用的文献

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Ranibizumab Population Pharmacokinetics and Free VEGF Pharmacodynamics in Preterm Infants With Retinopathy of Prematurity in the RAINBOW Trial.在RAINBOW试验中,雷珠单抗在早产儿视网膜病变患儿中的群体药代动力学和游离血管内皮生长因子药效学研究。
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Intravitreal aflibercept injection in Indian eyes with retinopathy of prematurity.
玻璃体腔内注射阿柏西普治疗早产儿视网膜病变的印度人群研究。
Indian J Ophthalmol. 2019 Jun;67(6):884-888. doi: 10.4103/ijo.IJO_708_18.
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Transfer of single dose of intravitreal injection of ranibizumab and bevacizumab into milk of sheep.单剂量玻璃体内注射雷珠单抗和贝伐单抗向绵羊乳汁中的转移。
Int J Ophthalmol. 2017 Jul 18;10(7):1069-1075. doi: 10.18240/ijo.2017.07.08. eCollection 2017.
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The vascularization process after intravitreal ranibizumab injections for aggressive posterior retinopathy of prematurity.玻璃体内注射雷珠单抗治疗侵袭性早产儿视网膜病变后的血管化过程。
Arq Bras Oftalmol. 2017 Jan-Feb;80(1):30-34. doi: 10.5935/0004-2749.20170009.
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Neurodevelopmental Outcomes Following Bevacizumab Injections for Retinopathy of Prematurity.贝伐单抗注射治疗早产儿视网膜病变后的神经发育结局
Pediatrics. 2016 Apr;137(4). doi: 10.1542/peds.2015-3218. Epub 2016 Mar 17.
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Primary intravitreal ranibizumab for high-risk retinopathy of prematurity.玻璃体内注射雷珠单抗治疗高危早产儿视网膜病变
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Vascular endothelial growth factor plasma levels before and after treatment of retinopathy of prematurity with ranibizumab.雷珠单抗治疗早产儿视网膜病变前后血管内皮生长因子的血浆水平
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