Children's Hospital Los Angeles, University of Southern California, Los Angeles, CA, USA; Roski Eye Institute, University of Southern California, Los Angeles, CA, USA.
Children's Hospital Los Angeles, University of Southern California, Los Angeles, CA, USA; Roski Eye Institute, University of Southern California, Los Angeles, CA, USA.
Surv Ophthalmol. 2020 Nov-Dec;65(6):708-724. doi: 10.1016/j.survophthal.2020.03.001. Epub 2020 Mar 19.
Cortical/cerebral visual impairment (CVI) is the most frequent cause of pediatric visual impairment in developed countries and is increasing in prevalence in developing nations. The most common underlying etiology is hypoxic-ischemic encephalopathy, particularly in premature children. Other causes include seizures, hydrocephalus, trauma, and infections. Because of neurologic comorbidities, children with CVI often present challenges in diagnosis and characterization of visual deficits. Caregiver questionnaires may aid in assessment of visual functioning, while newer types of neuroimaging, including functional neuroimaging and diffusion tensor magnetic resonance imaging, may provide further insights on structure-function relationships. Genetic testing may assist in identification of underlying genetic or metabolic syndromes. Although no standard therapy for pediatric CVI exists, advances in care of preterm children and those with hypoxic-ischemic encephalopathy may in future reduce the incidence of this disorder. In addition, various methods of visual stimulation and stem cells have been advocated as treatment for pediatric CVI. Future controlled trials using standardized methods of visual assessment are necessary to establish whether these interventions are superior to observation. Practitioners should work with families and teachers of children with CVI to optimize their environment for visual functioning. Comorbid ocular and systemic disorders, which are common, should be managed appropriately.
皮质/大脑视觉障碍(CVI)是发达国家儿童视力障碍最常见的原因,在发展中国家的患病率也在增加。最常见的潜在病因是缺氧缺血性脑病,特别是在早产儿中。其他原因包括癫痫、脑积水、创伤和感染。由于神经合并症,患有 CVI 的儿童在诊断和特征描述视觉缺陷方面经常面临挑战。护理人员调查问卷可能有助于评估视觉功能,而包括功能神经影像学和弥散张量磁共振成像在内的新型神经影像学可能提供关于结构-功能关系的进一步见解。基因检测可能有助于确定潜在的遗传或代谢综合征。尽管目前尚无治疗儿童 CVI 的标准疗法,但早产儿和缺氧缺血性脑病患者护理方面的进步可能会降低这种疾病的发生率。此外,已经提倡使用各种视觉刺激和干细胞的方法来治疗儿童 CVI。需要使用标准化视觉评估方法进行未来的对照试验,以确定这些干预措施是否优于观察。从业者应与患有 CVI 的儿童的家庭和教师合作,为他们的视觉功能优化环境。常见的伴发性眼部和系统性疾病应得到适当治疗。