Departments of Pediatrics and
Departments of Pediatrics and.
Pediatrics. 2020 Jan;145(1). doi: 10.1542/peds.2019-1814. Epub 2019 Dec 5.
Bevacizumab is a human monoclonal immunoglobulin G1 antibody to vascular endothelial growth factor indicated in several adult diseases. Emerging literature and expert opinion support the off-label use of intravitreal bevacizumab in the treatment of retinopathy of prematurity (ROP), a common disease process seen in premature neonates. One of the most common side effects of systemic therapy in adults is hypertension; however, this has not been well described in infants receiving bevacizumab for ROP. In this report, we review a case of a former 25-week premature infant treated for stage 3 ROP with administration of intravitreal bevacizumab. The immediate posttreatment course was uncomplicated; however, at 10 days posttreatment, he developed new-onset systemic hypertension. In addition, neuroimaging revealed new areas of vasogenic edema, which improved over time. To the best of our knowledge and after a review of the literature, neither of these effects has been described in neonates after intravitreal bevacizumab for ROP.
贝伐单抗是一种针对血管内皮生长因子的人源单克隆免疫球蛋白 G1 抗体,适用于多种成人疾病。新出现的文献和专家意见支持将玻璃体内注射贝伐单抗用于治疗早产儿视网膜病变(ROP),这是一种常见于早产儿的疾病。成人全身治疗最常见的副作用之一是高血压;然而,在接受贝伐单抗治疗 ROP 的婴儿中,这方面的描述并不完善。在本报告中,我们回顾了一例曾接受 25 周早产儿治疗的病例,该患儿因 ROP 接受了玻璃体内注射贝伐单抗。治疗后的即刻过程无并发症;然而,在治疗后 10 天,他出现了新的全身高血压。此外,神经影像学显示新出现的血管源性水肿区域,随着时间的推移逐渐改善。据我们所知,在对文献进行回顾后,在接受玻璃体内注射贝伐单抗治疗 ROP 的新生儿中,尚未描述过这两种影响。