Shafiq Ayad, Hillier Roxane, Hearn Richard
Ophthalmology, Royal Victoria Infirmary, Newcastle, UK
Ophthalmology, Royal Victoria Infirmary, Newcastle, UK.
BMJ Case Rep. 2020 Mar 12;13(3):e232359. doi: 10.1136/bcr-2019-232359.
An extremely premature baby boy born at 23 weeks' gestational age was treated with unilateral low dose of 0.16 mg/0.025 mL intravitreal bevacizumab in the left eye for aggressive retinopathy of prematurity (ROP). He developed photographically documented changes in his contralateral right eye on imaging 5 days later. Second eye treatment was at 12 days. He has development assessment and ophthalmic review beyond age 2, which is normal. Systemic absorption of the drug caused an end organ effect to slow down and reverse ROP in his untreated right eye. Both eyes vascularised fully. His normal Bayley III developmental score at age 2 is uncommon for a 23-week gestation baby. Even at a low dose, bevacizumab has the potential for end organ effect on the second eye, and therefore other organs. In this case, there are no medium-term measurable neurodevelopmental side-effects. We suggest longer term follow-up is required before excluding unwanted side-effects.
一名孕23周出生的极早产儿因严重早产儿视网膜病变(ROP)接受了左眼0.16毫克/0.025毫升玻璃体腔注射低剂量贝伐单抗治疗。5天后,其对侧右眼在影像学上出现了经照片记录的变化。12天时进行了对侧眼治疗。他在2岁以后接受了发育评估和眼科检查,结果均正常。药物的全身吸收导致未治疗的右眼ROP进展减缓并逆转。双眼均完全血管化。对于一名孕23周的婴儿来说,其2岁时贝利婴幼儿发展量表第三版(Bayley III)发育评分正常并不常见。即使是低剂量,贝伐单抗也有可能对侧眼以及其他器官产生终末器官效应。在本病例中,尚无中期可测量的神经发育副作用。我们建议在排除不良副作用之前需要进行长期随访。