Rare and severe complications following surgical treatment of retinopathy of prematurity according to the vitrectomy method – case report

M. Modrzejewska, Wiktoria Bosy, Patrycja Woźniak
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Abstract

Abstract Introduction: Retinopathy of preterm infants is a serious condition that can lead to various complications, such as severe vision loss, blindness, and other sequelae of progressive disease in premature infants. In this paper, we report the complication of ciliary body hernias resulting from high intraocular pressure in the afflicted eye combined with secondary glaucoma after vitrectomy due to retinopathy of prematurity (ROP), a condition previously not described in the literature (PubMed or Google Scholar from 2014–2022). Material and methods: The infant underwent photocoagulation treatment twice due to ROP due to ROP stage 4/5. At 4th months of life, the baby underwent posterior vitrectomy with lensectomy, with the final injection of sodium hyaluronate to the vitreous chamber. The child did not suffer from any autoimmune diseases or keratitis. The only risk factors included photocoagulation and vitrectomy with the reconstruction of both the anterior chambers and the pupil. Results: Following posterior vitrectomy, the child manifested multiple complications, such as hernia of the ciliary body, secondary glaucoma, leucoma, hemorrhage to the anterior eye chamber, keratomalacia, and advanced keratopathy. Autoimmune diseases, avitaminosis, the inflammatory of the cornea (of no iatrogenic etiology) and viral or bacterial infections were excluded. Nevertheless, positive bacterial cultures from natural body orifices obtained in routine examinations during hospitalization could cause a severe course of ROP as well as complicated outcomes of surgical treatment. Conclusions: Vitrectomy is the last resort therapeutic option (ROP stage 4A, 4B, 5), as it might result in keratopathy, cataract, glaucoma, strabismus, or severe hyperopia. Due to severe damage to the eye structures that may occur after surgical vitrectomy in premature infants in the course of ROP, this technique should only be used by experienced vitrectomists with great care and caution, especially in extremely low-birthweight children.
采用玻璃体切除术治疗早产儿视网膜病变的并发症少见且严重
摘要简介:早产儿视网膜病变是一种严重的疾病,可导致各种并发症,如严重的视力丧失、失明和其他早产儿进行性疾病的后遗症。在这篇论文中,我们报道了早产儿视网膜病变(ROP)引起的玻璃体切除术后,患眼高眼压合并继发性青光眼引起的睫状体疝的并发症,这种情况以前没有在文献中描述过(PubMed或Google Scholar,2014–2022)。材料和方法:婴儿因ROP 4/5期ROP接受了两次光凝治疗。在出生4个月时,婴儿接受了后部玻璃体切除术和晶状体切除术,最后向玻璃体腔注射透明质酸钠。该儿童没有任何自身免疫性疾病或角膜炎。唯一的危险因素包括光凝和玻璃体切除术,同时重建前房和瞳孔。结果:玻璃体切除术后,患儿出现多种并发症,如睫状体疝、继发性青光眼、白带瘤、前房出血、角膜软化和晚期角膜病变。排除自身免疫性疾病、维生素缺乏症、角膜炎症(无医源性病因)和病毒或细菌感染。然而,在住院期间的常规检查中获得的来自自然身体孔口的阳性细菌培养物可能会导致严重的ROP过程以及复杂的手术治疗结果。结论:玻璃体切除术是最后的治疗选择(ROP 4A、4B、5期),因为它可能导致角膜病变、白内障、青光眼、斜视或严重远视。由于早产儿在ROP过程中进行玻璃体切除术后可能会对眼睛结构造成严重损伤,因此只有有经验的玻璃体切除术者才能非常小心地使用这项技术,尤其是在极低出生体重的儿童中。
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